Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 9679 |
|---|---|
| ensemblid | ENSG00000189319.14 |
| hgncid | 28968 |
| symbol | FAM53B |
| name | family with sequence similarity 53 member B |
| refseq_nuc | NM_014661.4 |
| refseq_prot | NP_055476.3 |
| ensembl_nuc | ENST00000337318.8 |
| ensembl_prot | ENSP00000338532.3 |
| mane_status | MANE Select |
| chr | chr10 |
| start | 124619292 |
| end | 124744378 |
| strand | - |
| ver | v1.2 |
| region | chr10:124619292-124744378 |
| region5000 | chr10:124614292-124749378 |
| regionname0 | FAM53B_chr10_124619292_124744378 |
| regionname5000 | FAM53B_chr10_124614292_124749378 |
| 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 | 422 | 326 | 75 | 48 | 153 | 14 | 34 | 115 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0002 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0003 | 0/0 | 422 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0004 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0005 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| 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 | 1/1 | 1269 | 314 | 74 | 41 | 149 | 14 | 34 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| c0002 | 0/0 | 1269 | 7 | 0 | 7 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| c0003 | 0/0 | 1269 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| c0004 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| c0005 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| c0006 | 0/0 | 1269 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| c0007 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| c0008 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| c0009 | 0/0 | 1269 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 4491 | 96 | 16 | 22 | 36 | 8 | 12 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0002 | 0/0 | 4491 | 21 | 0 | 0 | 21 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0003 | 0/0 | 4492 | 18 | 1 | 1 | 12 | 1 | 3 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0004 | 0/0 | 4491 | 11 | 11 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0005 | 0/0 | 4504 | 9 | 0 | 0 | 7 | 1 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0006 | 0/0 | 4491 | 9 | 9 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0007 | 0/0 | 4491 | 8 | 0 | 0 | 8 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0008 | 0/0 | 4495 | 7 | 0 | 0 | 7 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0009 | 0/0 | 4491 | 7 | 0 | 3 | 0 | 1 | 3 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0010 | 0/0 | 4491 | 6 | 4 | 0 | 0 | 0 | 2 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0011 | 0/0 | 4490 | 6 | 1 | 0 | 4 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0012 | 0/0 | 4491 | 5 | 5 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0013 | 0/0 | 4492 | 5 | 0 | 0 | 5 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0014 | 0/0 | 4496 | 4 | 0 | 4 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0015 | 0/0 | 4493 | 4 | 4 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0016 | 0/0 | 4491 | 4 | 0 | 3 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0017 | 0/0 | 4490 | 4 | 0 | 0 | 4 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0018 | 0/0 | 4491 | 4 | 1 | 0 | 1 | 2 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0019 | 0/0 | 4503 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0020 | 0/0 | 4504 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0021 | 0/0 | 4491 | 3 | 2 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0022 | 0/0 | 4491 | 3 | 1 | 2 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0023 | 0/0 | 4491 | 3 | 3 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0024 | 0/0 | 4491 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0025 | 0/0 | 4495 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0026 | 0/0 | 4491 | 3 | 2 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0027 | 0/0 | 4491 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0028 | 0/0 | 4490 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0029 | 0/0 | 4504 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0030 | 0/0 | 4504 | 2 | 1 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0031 | 0/0 | 4491 | 2 | 0 | 0 | 0 | 0 | 2 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0032 | 0/0 | 4491 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0033 | 0/0 | 4491 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0034 | 0/0 | 4491 | 2 | 0 | 0 | 0 | 0 | 2 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0035 | 0/0 | 4490 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0036 | 0/0 | 4492 | 2 | 0 | 1 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0037 | 0/0 | 4491 | 2 | 0 | 1 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0038 | 0/0 | 4504 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0039 | 0/0 | 4504 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0040 | 0/0 | 4503 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0041 | 0/0 | 4504 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0042 | 0/0 | 4508 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0043 | 0/0 | 4504 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0044 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0045 | 0/0 | 4491 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0046 | 0/0 | 4491 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0047 | 0/0 | 4502 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0048 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0049 | 0/0 | 4491 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0050 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0051 | 0/0 | 4492 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0052 | 0/0 | 4491 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0053 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0054 | 0/0 | 4490 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0055 | 0/0 | 4491 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0056 | 0/0 | 4501 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0057 | 0/0 | 4501 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0058 | 0/0 | 4503 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0059 | 0/0 | 4495 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0060 | 0/0 | 4491 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0061 | 0/0 | 4491 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0062 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0063 | 0/0 | 4492 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0064 | 0/0 | 4492 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0065 | 0/0 | 4494 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0066 | 0/0 | 4492 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0067 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0068 | 0/0 | 4491 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0069 | 0/0 | 4491 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0070 | 0/0 | 4492 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0071 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0072 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0073 | 0/0 | 4493 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0074 | 0/0 | 4495 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0075 | 0/0 | 4493 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0076 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0077 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0078 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0079 | 0/0 | 4491 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0080 | 0/0 | 4491 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0081 | 0/0 | 4492 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0082 | 0/0 | 4491 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0083 | 0/0 | 4492 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0084 | 0/0 | 4490 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0085 | 0/0 | 4492 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0086 | 0/0 | 4491 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0087 | 0/0 | 4491 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0088 | 0/0 | 4490 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0089 | 0/0 | 4481 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0090 | 0/0 | 4493 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| t0091 | 0/0 | 4491 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| 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 | 2 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| 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 | 1/1 | 1269 | 314 | 74 | 41 | 149 | 14 | 34 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0002 | 0/0 | 1269 | 7 | 0 | 7 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0003 | 0/0 | 1269 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0008 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0009 | 0/0 | 1269 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0002c0007 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0003c0006 | 0/0 | 1269 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0004c0005 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0005c0004 | 0/0 | 1269 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/1 | 5759 | 88 | 15 | 15 | 36 | 8 | 12 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0002 | 0/0 | 5759 | 20 | 0 | 0 | 20 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0003 | 0/0 | 5760 | 16 | 1 | 1 | 10 | 1 | 3 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0004 | 0/0 | 5759 | 11 | 11 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0005 | 0/0 | 5772 | 9 | 0 | 0 | 7 | 1 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0006 | 0/0 | 5759 | 9 | 9 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0007 | 0/0 | 5759 | 8 | 0 | 0 | 8 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0008 | 0/0 | 5763 | 7 | 0 | 0 | 7 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0009 | 0/0 | 5759 | 7 | 0 | 3 | 0 | 1 | 3 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0010 | 0/0 | 5759 | 6 | 4 | 0 | 0 | 0 | 2 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0011 | 0/0 | 5758 | 6 | 1 | 0 | 4 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0012 | 0/0 | 5759 | 5 | 5 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0013 | 0/0 | 5760 | 5 | 0 | 0 | 5 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0014 | 0/0 | 5764 | 4 | 0 | 4 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0015 | 0/0 | 5761 | 4 | 4 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0016 | 0/0 | 5759 | 4 | 0 | 3 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0017 | 0/0 | 5758 | 4 | 0 | 0 | 4 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0018 | 0/0 | 5759 | 3 | 0 | 0 | 1 | 2 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0019 | 0/0 | 5771 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0020 | 0/0 | 5772 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0021 | 0/0 | 5759 | 3 | 2 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0022 | 0/0 | 5759 | 3 | 1 | 2 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0023 | 0/0 | 5759 | 3 | 3 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0024 | 0/0 | 5759 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0025 | 0/0 | 5763 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0026 | 0/0 | 5759 | 2 | 1 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0027 | 0/0 | 5759 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0028 | 0/0 | 5758 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0029 | 0/0 | 5772 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0030 | 0/0 | 5772 | 2 | 1 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0031 | 0/0 | 5759 | 2 | 0 | 0 | 0 | 0 | 2 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0032 | 0/0 | 5759 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0033 | 0/0 | 5759 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0034 | 0/0 | 5759 | 2 | 0 | 0 | 0 | 0 | 2 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0035 | 0/0 | 5758 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0036 | 0/0 | 5760 | 2 | 0 | 1 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0037 | 0/0 | 5759 | 2 | 0 | 1 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0038 | 0/0 | 5772 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0039 | 0/0 | 5772 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0040 | 0/0 | 5771 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0041 | 0/0 | 5772 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0042 | 0/0 | 5776 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0043 | 0/0 | 5772 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0044 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0045 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0046 | 0/0 | 5759 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0047 | 0/0 | 5770 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0048 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0049 | 0/0 | 5759 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0050 | 0/0 | 5758 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0051 | 0/0 | 5760 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0052 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0053 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0054 | 0/0 | 5758 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0055 | 0/0 | 5759 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0056 | 0/0 | 5769 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0057 | 0/0 | 5769 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0059 | 0/0 | 5763 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0060 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0061 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0062 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0063 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0064 | 0/0 | 5760 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0065 | 0/0 | 5762 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0066 | 0/0 | 5760 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0067 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0068 | 0/0 | 5759 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0069 | 0/0 | 5759 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0070 | 0/0 | 5760 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0071 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0072 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0073 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0074 | 0/0 | 5763 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0075 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0076 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0077 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0078 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0079 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0080 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0081 | 0/0 | 5760 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0082 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0083 | 0/0 | 5760 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0085 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0087 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0088 | 0/0 | 5758 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0089 | 0/0 | 5749 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0090 | 0/0 | 5761 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0001t0091 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0002t0001 | 0/0 | 5759 | 7 | 0 | 7 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0003t0003 | 0/0 | 5760 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0003t0058 | 0/0 | 5771 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0008t0018 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0001c0009t0002 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0002c0007t0001 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0003c0006t0084 | 0/0 | 5758 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0004c0005t0026 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| a0005c0004t0086 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | copy fasta | chr10 | 124614292 | 124749378 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0053 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0144 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0004g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0004g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0004g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0004g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0004g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0004g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0004g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0004g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0004g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0005g0009 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0005g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0005g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0005g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0005g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0005g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0005g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0005g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0005g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0006g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0006g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0006g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0006g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0006g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0006g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0007g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0007g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0007g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0007g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0007g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0007g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0007g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0007g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0008g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0008g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0008g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0008g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0008g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0008g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0008g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0009g0284 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0009g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0009g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0009g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0009g0321 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0009g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0009g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0010g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0010g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0010g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0010g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0010g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0010g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0011g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0011g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0011g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0011g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0011g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0011g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0012g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0012g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0012g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0012g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0012g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0013g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0013g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0013g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0013g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0013g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0014g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0014g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0014g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0014g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0015g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0015g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0015g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0015g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0016g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0016g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0016g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0016g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0017g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0017g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0017g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0017g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0018g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0018g0292 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0018g0295 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0019g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0019g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0019g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0020g0007 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0020g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0020g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0021g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0021g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0021g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0022g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0022g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0022g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0023g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0023g0238 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0023g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0024g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0024g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0024g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0025g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0025g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0025g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0026g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0026g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0027g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0027g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0027g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0028g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0028g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0028g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0029g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0029g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0030g0005 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0030g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0031g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0031g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0032g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0032g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0033g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0033g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0034g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0034g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0035g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0035g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0036g0282 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0036g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0037g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0037g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0038g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0039g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0040g0008 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0041g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0042g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0043g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0044g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0045g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0046g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0047g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0048g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0049g0105 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0050g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0051g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0052g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0053g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0054g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0055g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0056g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0057g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0059g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0060g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0061g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0062g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0063g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0064g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0065g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0066g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0067g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0068g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0069g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0070g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0071g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0072g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0073g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0074g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0075g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0076g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0077g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0078g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0079g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0080g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0081g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0082g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0083g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0085g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0087g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0088g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0089g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0090g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0091g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0002t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0002t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0002t0001g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0002t0001g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0002t0001g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0002t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0003t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0003t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0003t0058g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0008t0018g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0009t0002g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0002c0007t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0003c0006t0084g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0004c0005t0026g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0005c0004t0086g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0129 | EUR | GBR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0217 | EUR | GBR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0196 | EUR | GBR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0009 | EUR | GBR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0135 | EUR | FIN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00280 | hp2 | a0001 | c0001 | t0009 | g0321 | EUR | FIN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0098 | EUR | FIN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00323 | hp2 | a0001 | c0001 | t0036 | g0282 | EUR | FIN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00408 | hp1 | a0001 | c0001 | t0038 | g0021 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00408 | hp2 | a0001 | c0001 | t0024 | g0262 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00423 | hp2 | a0001 | c0001 | t0057 | g0268 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00558 | hp1 | a0001 | c0001 | t0017 | g0185 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00558 | hp2 | a0001 | c0003 | t0003 | g0076 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00609 | hp1 | a0001 | c0001 | t0013 | g0303 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00609 | hp2 | a0001 | c0001 | t0029 | g0006 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00621 | hp1 | a0001 | c0001 | t0041 | g0013 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00621 | hp2 | a0001 | c0001 | t0048 | g0246 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00639 | hp1 | a0001 | c0001 | t0021 | g0266 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0101 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0133 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00673 | hp2 | a0001 | c0001 | t0056 | g0274 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00735 | hp1 | a0001 | c0001 | t0014 | g0038 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0195 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0293 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01069 | hp2 | a0001 | c0001 | t0016 | g0201 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01071 | hp1 | a0001 | c0001 | t0016 | g0202 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01074 | hp1 | a0001 | c0001 | t0068 | g0270 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01074 | hp2 | a0001 | c0001 | t0009 | g0320 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0207 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01099 | hp2 | a0001 | c0001 | t0051 | g0057 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01106 | hp2 | a0001 | c0001 | t0064 | g0100 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01168 | hp1 | a0001 | c0001 | t0022 | g0055 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01168 | hp2 | a0001 | c0001 | t0040 | g0008 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01169 | hp2 | a0001 | c0001 | t0022 | g0056 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01175 | hp2 | a0001 | c0001 | t0037 | g0325 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01261 | hp1 | a0001 | c0001 | t0070 | g0181 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01346 | hp1 | a0001 | c0001 | t0016 | g0177 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01361 | hp1 | a0001 | c0001 | t0066 | g0178 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01361 | hp2 | a0001 | c0001 | t0014 | g0093 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01496 | hp1 | a0001 | c0001 | t0036 | g0283 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0212 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01515 | hp1 | a0001 | c0001 | t0018 | g0295 | EUR | IBS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0151 | EUR | IBS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0166 | EUR | IBS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01517 | hp2 | a0001 | c0001 | t0018 | g0292 | EUR | IBS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0060 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01891 | hp1 | a0001 | c0001 | t0052 | g0037 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0095 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01943 | hp2 | a0001 | c0001 | t0030 | g0005 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01952 | hp2 | a0001 | c0001 | t0090 | g0285 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0213 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01975 | hp2 | a0001 | c0001 | t0009 | g0322 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01981 | hp1 | a0001 | c0001 | t0014 | g0094 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01981 | hp2 | a0001 | c0001 | t0069 | g0180 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0230 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0220 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02027 | hp1 | a0001 | c0001 | t0071 | g0210 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02027 | hp2 | a0001 | c0001 | t0024 | g0256 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02040 | hp1 | a0001 | c0001 | t0035 | g0149 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0058 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02055 | hp1 | a0001 | c0001 | t0030 | g0010 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02056 | hp1 | a0001 | c0001 | t0062 | g0132 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02056 | hp2 | a0001 | c0001 | t0007 | g0206 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0324 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02071 | hp2 | a0001 | c0001 | t0007 | g0187 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02074 | hp2 | a0001 | c0001 | t0007 | g0034 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0312 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02132 | hp1 | a0001 | c0001 | t0042 | g0012 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02145 | hp1 | a0001 | c0001 | t0063 | g0063 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02145 | hp2 | a0005 | c0004 | t0086 | g0052 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02155 | hp1 | a0001 | c0001 | t0020 | g0015 | EAS | CDX | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02155 | hp2 | a0001 | c0001 | t0013 | g0305 | EAS | CDX | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02165 | hp1 | a0001 | c0001 | t0007 | g0252 | EAS | CDX | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0078 | EAS | CDX | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0233 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0118 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0120 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02258 | hp2 | a0001 | c0001 | t0015 | g0051 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02280 | hp1 | a0001 | c0001 | t0039 | g0029 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0115 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0191 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02300 | hp2 | a0001 | c0001 | t0026 | g0241 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02451 | hp1 | a0001 | c0001 | t0054 | g0040 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0197 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02572 | hp1 | a0001 | c0001 | t0022 | g0065 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0050 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02602 | hp1 | a0001 | c0001 | t0009 | g0294 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02602 | hp2 | a0001 | c0001 | t0074 | g0156 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02615 | hp1 | a0001 | c0001 | t0021 | g0199 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02615 | hp2 | a0001 | c0001 | t0012 | g0054 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0278 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02647 | hp1 | a0001 | c0001 | t0045 | g0031 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0061 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02683 | hp2 | a0001 | c0001 | t0037 | g0319 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0143 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02698 | hp2 | a0001 | c0001 | t0011 | g0091 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0281 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02717 | hp2 | a0001 | c0001 | t0061 | g0243 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0116 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02723 | hp2 | a0001 | c0001 | t0082 | g0045 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0265 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02738 | hp2 | a0001 | c0001 | t0031 | g0106 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02809 | hp1 | a0001 | c0001 | t0023 | g0239 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0108 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0036 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02886 | hp1 | a0001 | c0001 | t0015 | g0276 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0114 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02896 | hp1 | a0001 | c0001 | t0050 | g0107 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0062 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02965 | hp1 | a0001 | c0001 | t0023 | g0237 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02965 | hp2 | a0001 | c0001 | t0075 | g0124 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02976 | hp1 | a0001 | c0001 | t0021 | g0198 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02976 | hp2 | a0001 | c0001 | t0015 | g0121 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0277 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03098 | hp2 | a0001 | c0001 | t0011 | g0244 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03130 | hp1 | a0001 | c0001 | t0085 | g0041 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03130 | hp2 | a0001 | c0001 | t0026 | g0234 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03139 | hp1 | a0001 | c0001 | t0087 | g0286 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03139 | hp2 | a0004 | c0005 | t0026 | g0236 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03209 | hp1 | a0001 | c0001 | t0015 | g0042 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03209 | hp2 | a0001 | c0001 | t0033 | g0122 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03225 | hp1 | a0001 | c0001 | t0060 | g0126 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03225 | hp2 | a0002 | c0007 | t0001 | g0102 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0103 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03486 | hp1 | a0001 | c0008 | t0018 | g0317 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03486 | hp2 | a0001 | c0001 | t0033 | g0125 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0099 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03490 | hp2 | a0001 | c0001 | t0059 | g0128 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0097 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03516 | hp1 | a0001 | c0001 | t0010 | g0066 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0089 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0110 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03579 | hp2 | a0001 | c0001 | t0012 | g0123 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03669 | hp1 | a0001 | c0001 | t0034 | g0154 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03688 | hp1 | a0001 | c0001 | t0055 | g0182 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03688 | hp2 | a0001 | c0001 | t0046 | g0032 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0155 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0077 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0242 | SAS | BEB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03834 | hp2 | a0001 | c0001 | t0049 | g0105 | SAS | BEB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03927 | hp1 | a0001 | c0001 | t0088 | g0311 | SAS | BEB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0175 | SAS | BEB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0245 | SAS | BEB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03942 | hp2 | a0001 | c0001 | t0065 | g0092 | SAS | BEB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04115 | hp1 | a0001 | c0001 | t0010 | g0222 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0225 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04184 | hp1 | a0001 | c0001 | t0009 | g0323 | SAS | BEB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04184 | hp2 | a0001 | c0001 | t0010 | g0127 | SAS | BEB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04199 | hp1 | a0001 | c0001 | t0034 | g0227 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0160 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0011 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0228 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04228 | hp1 | a0001 | c0001 | t0009 | g0284 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04228 | hp2 | a0001 | c0001 | t0031 | g0049 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0067 | AFR | YRI | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0279 | AFR | YRI | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18612 | hp1 | a0001 | c0001 | t0007 | g0205 | EAS | CHB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0300 | EAS | CHB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18747 | hp1 | a0001 | c0001 | t0047 | g0033 | EAS | CHB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18747 | hp2 | a0001 | c0001 | t0019 | g0017 | EAS | CHB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0043 | AFR | YRI | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0104 | AFR | YRI | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18939 | hp2 | a0001 | c0001 | t0011 | g0090 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18942 | hp1 | a0001 | c0001 | t0025 | g0253 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0315 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18944 | hp1 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18945 | hp1 | a0001 | c0001 | t0007 | g0204 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18946 | hp1 | a0003 | c0006 | t0084 | g0240 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18946 | hp2 | a0001 | c0001 | t0017 | g0142 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18947 | hp1 | a0001 | c0001 | t0019 | g0016 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18948 | hp2 | a0001 | c0001 | t0024 | g0250 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18949 | hp1 | a0001 | c0001 | t0017 | g0273 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18949 | hp2 | a0001 | c0001 | t0008 | g0258 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18956 | hp2 | a0001 | c0001 | t0008 | g0261 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18957 | hp1 | a0001 | c0001 | t0028 | g0288 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18960 | hp1 | a0001 | c0001 | t0028 | g0287 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18962 | hp2 | a0001 | c0001 | t0025 | g0248 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18963 | hp1 | a0001 | c0001 | t0067 | g0184 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18963 | hp2 | a0001 | c0001 | t0019 | g0027 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18964 | hp1 | a0001 | c0001 | t0011 | g0080 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18964 | hp2 | a0001 | c0001 | t0032 | g0146 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0023 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18967 | hp2 | a0001 | c0001 | t0007 | g0263 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0296 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18970 | hp2 | a0001 | c0001 | t0008 | g0260 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0232 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18973 | hp2 | a0001 | c0001 | t0011 | g0069 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18977 | hp1 | a0001 | c0001 | t0013 | g0306 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0028 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18980 | hp2 | a0001 | c0001 | t0016 | g0168 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18983 | hp1 | a0001 | c0001 | t0076 | g0255 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0039 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18986 | hp2 | a0001 | c0001 | t0032 | g0267 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18988 | hp2 | a0001 | c0001 | t0020 | g0007 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18989 | hp1 | a0001 | c0001 | t0013 | g0304 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18990 | hp1 | a0001 | c0003 | t0003 | g0073 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18995 | hp1 | a0001 | c0001 | t0008 | g0259 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18998 | hp1 | a0001 | c0001 | t0028 | g0290 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0147 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0308 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19002 | hp1 | a0001 | c0001 | t0025 | g0264 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19002 | hp2 | a0001 | c0001 | t0081 | g0200 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19003 | hp1 | a0001 | c0001 | t0029 | g0024 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19003 | hp2 | a0001 | c0001 | t0017 | g0189 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0070 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19007 | hp1 | a0001 | c0001 | t0008 | g0254 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19009 | hp1 | a0001 | c0001 | t0078 | g0194 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19010 | hp1 | a0001 | c0001 | t0007 | g0211 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0071 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19011 | hp2 | a0001 | c0001 | t0072 | g0251 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0088 | AFR | LWK | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19043 | hp2 | a0001 | c0001 | t0012 | g0046 | AFR | LWK | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19057 | hp1 | a0001 | c0001 | t0027 | g0209 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19057 | hp2 | a0001 | c0001 | t0008 | g0247 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19064 | hp2 | a0001 | c0001 | t0018 | g0289 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0068 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19066 | hp2 | a0001 | c0001 | t0083 | g0186 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19068 | hp1 | a0001 | c0001 | t0073 | g0249 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0318 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19070 | hp2 | a0001 | c0009 | t0002 | g0307 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19078 | hp1 | a0001 | c0001 | t0089 | g0310 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19078 | hp2 | a0001 | c0001 | t0077 | g0138 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19079 | hp2 | a0001 | c0001 | t0020 | g0026 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19081 | hp1 | a0001 | c0001 | t0043 | g0025 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19082 | hp2 | a0001 | c0001 | t0044 | g0030 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19083 | hp1 | a0001 | c0003 | t0058 | g0269 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19083 | hp2 | a0001 | c0001 | t0008 | g0257 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19085 | hp1 | a0001 | c0001 | t0013 | g0314 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19086 | hp1 | a0001 | c0001 | t0027 | g0223 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0020 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19087 | hp2 | a0001 | c0001 | t0035 | g0148 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19088 | hp2 | a0001 | c0001 | t0005 | g0014 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19089 | hp1 | a0001 | c0001 | t0027 | g0170 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0291 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0084 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0193 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19091 | hp2 | a0001 | c0001 | t0011 | g0072 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19240 | hp1 | a0001 | c0001 | t0012 | g0047 | AFR | YRI | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0064 | AFR | YRI | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0079 | AFR | ASW | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0280 | AFR | ASW | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0059 | EUR | TSI | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0179 | EUR | TSI | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01123 | hp1 | a0001 | c0001 | t0014 | g0096 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0203 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03471 | hp1 | a0001 | c0001 | t0023 | g0238 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG06807 | hp1 | a0001 | c0001 | t0091 | g0326 | AFR | USA | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0134 | AFR | USA | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18955 | hp1 | a0001 | c0001 | t0053 | g0275 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18955 | hp2 | a0001 | c0001 | t0079 | g0171 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | USA | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA20300 | hp2 | a0001 | c0001 | t0080 | g0109 | AFR | USA | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0144 | REF | REF | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0053 | REF | REF | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:124623306
|
G | A | 1 | a0004 | 1 | HG03139.hp2 | missense_variant | MODERATE | c.1205C>T | p.Ala402Val | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 1745/5759 | 1205/1269 | 402/422 | chr10 | 124623306 | ||
| chr10:124623309
|
C | A | 1 | a0005 | 1 | HG02145.hp2 | missense_variant | MODERATE | c.1202G>T | p.Gly401Val | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 1742/5759 | 1202/1269 | 401/422 | chr10 | 124623309 | ||
| chr10:124623313
|
G | A | 1 | a0003 | 1 | NA18946.hp1 | missense_variant | MODERATE | c.1198C>T | p.Arg400Cys | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 1738/5759 | 1198/1269 | 400/422 | chr10 | 124623313 | ||
| chr10:124681905
|
G | A | 1 | a0002 | 1 | HG03225.hp2 | missense_variant | MODERATE | c.608C>T | p.Pro203Leu | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/5 | 1148/5759 | 608/1269 | 203/422 | chr10 | 124681905 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:124623263
|
A | G | 1 | a0001c0002 | 7 | HG01099.hp1 HG01123.hp2 HG01496.hp2 others(4): Show |
synonymous_variant | LOW | c.1248T>C | p.Ile416Ile | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 1788/5759 | 1248/1269 | 416/422 | chr10 | 124623263 | ||
| chr10:124623449
|
C | T | 1 | a0005c0004 | 1 | HG02145.hp2 | synonymous_variant | LOW | c.1062G>A | p.Pro354Pro | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 1602/5759 | 1062/1269 | 354/422 | chr10 | 124623449 | ||
| chr10:124623461
|
G | A | 1 | a0001c0003 | 3 | HG00558.hp2 NA18990.hp1 NA19083.hp1 |
synonymous_variant | LOW | c.1050C>T | p.Pro350Pro | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 1590/5759 | 1050/1269 | 350/422 | chr10 | 124623461 | ||
| chr10:124682207
|
G | A | 1 | a0001c0008 | 1 | HG03486.hp1 | synonymous_variant | LOW | c.306C>T | p.Asn102Asn | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/5 | 846/5759 | 306/1269 | 102/422 | chr10 | 124682207 | ||
| chr10:124706660
|
T | A | 1 | a0001c0009 | 1 | NA19070.hp2 | synonymous_variant | LOW | c.54A>T | p.Ala18Ala | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/5 | 594/5759 | 54/1269 | 18/422 | chr10 | 124706660 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:124619357
|
G | C | 1 | a0001c0001t0023 | 3 | HG02809.hp1 HG02965.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3885C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 3885 | chr10 | 124619357 | |||||
| chr10:124619424
|
C | A | 5 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(2): Show | 15 | HG00408.hp2 HG02027.hp2 NA18942.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*3818G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 3818 | chr10 | 124619424 | |||||
| chr10:124619437
|
C | A | 1 | a0001c0001t0068 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3805G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 3805 | chr10 | 124619437 | |||||
| chr10:124619523
|
G | A | 1 | a0001c0001t0064 | 1 | HG01106.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3719C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 3719 | chr10 | 124619523 | |||||
| chr10:124619632
|
A | G | 1 | a0001c0001t0031 | 2 | HG02738.hp2 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3610T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 3610 | chr10 | 124619632 | |||||
| chr10:124619655
|
TA | T | 18 | a0001c0001t0003a0001c0001t0006a0001c0001t0011others(15): Show | 55 | HG00323.hp1 HG00558.hp1 HG00558.hp2 others(52): Show |
3_prime_UTR_variant | MODIFIER | c.*3586delT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 3586 | chr10 | 124619655 | |||||
| chr10:124619668
|
A | ATCT | 1 | a0001c0001t0014 | 4 | HG00735.hp1 HG01123.hp1 HG01361.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3573_*3574insAGA | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 3573 | chr10 | 124619668 | |||||
| chr10:124619669
|
A | T | 1 | a0001c0001t0014 | 4 | HG00735.hp1 HG01123.hp1 HG01361.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3573T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 3573 | chr10 | 124619669 | |||||
| chr10:124619720
|
C | T | 1 | a0001c0001t0080 | 1 | NA20300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3522G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 3522 | chr10 | 124619720 | |||||
| chr10:124619782
|
C | T | 2 | a0001c0001t0034a0001c0001t0046 | 3 | HG03669.hp1 HG03688.hp2 HG04199.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3460G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 3460 | chr10 | 124619782 | |||||
| chr10:124619787
|
C | T | 3 | a0001c0001t0053a0001c0001t0056a0001c0001t0067 | 3 | HG00673.hp2 NA18955.hp1 NA18963.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3455G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 3455 | chr10 | 124619787 | |||||
| chr10:124619790
|
G | A | 1 | a0001c0001t0055 | 1 | HG03688.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3452C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 3452 | chr10 | 124619790 | |||||
| chr10:124620039
|
T | C | 1 | a0001c0001t0069 | 1 | HG01981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3203A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 3203 | chr10 | 124620039 | |||||
| chr10:124620114
|
A | G | 11 | a0001c0001t0005a0001c0001t0019a0001c0001t0029others(8): Show | 23 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3128T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 3128 | chr10 | 124620114 | |||||
| chr10:124620184
|
G | A | 1 | a0001c0001t0045 | 1 | HG02647.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3058C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 3058 | chr10 | 124620184 | |||||
| chr10:124620355
|
G | GC | 13 | a0001c0001t0006a0001c0001t0013a0001c0001t0036others(10): Show | 26 | HG00323.hp2 HG00609.hp1 HG01099.hp2 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*2886dupG | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 2886 | chr10 | 124620355 | |||||
| chr10:124620355
|
G | GCC | 8 | a0001c0001t0003a0001c0001t0014a0001c0001t0015others(5): Show | 30 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*2885_*2886dupGG | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 2886 | chr10 | 124620355 | |||||
| chr10:124620355
|
G | GCCCC | 6 | a0001c0001t0008a0001c0001t0025a0001c0001t0042others(3): Show | 14 | HG02132.hp1 HG02602.hp2 HG03490.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2883_*2886dupGGGG | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 2886 | chr10 | 124620355 | |||||
| chr10:124620355
|
G | GCCCCCCC others(3): Show |
2 | a0001c0001t0056a0001c0001t0057 | 2 | HG00423.hp2 HG00673.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2886_*2887insGGGG others(6): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 2886 | chr10 | 124620355 | |||||
| chr10:124620355
|
G | GCCCCCCC others(5): Show |
1 | a0001c0003t0058 | 1 | NA19083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2886_*2887insGGGG others(8): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 2886 | chr10 | 124620355 | |||||
| chr10:124620362
|
C | G | 2 | a0001c0001t0031a0001c0001t0049 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2880G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 2880 | chr10 | 124620362 | |||||
| chr10:124620364
|
A | C | 71 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(68): Show | 198 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(195): Show |
3_prime_UTR_variant | MODIFIER | c.*2878T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 2878 | chr10 | 124620364 | |||||
| chr10:124620640
|
G | T | 11 | a0001c0001t0005a0001c0001t0019a0001c0001t0029others(8): Show | 23 | HG00140.hp2 HG00423.hp2 HG00609.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2602C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 2602 | chr10 | 124620640 | |||||
| chr10:124620666
|
A | G | 1 | a0001c0001t0033 | 2 | HG03209.hp2 HG03486.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2576T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 2576 | chr10 | 124620666 | |||||
| chr10:124620688
|
T | G | 1 | a0001c0001t0071 | 1 | HG02027.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2554A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 2554 | chr10 | 124620688 | |||||
| chr10:124620703
|
G | C | 1 | a0001c0001t0025 | 3 | NA18942.hp1 NA18962.hp2 NA19002.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2539C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 2539 | chr10 | 124620703 | |||||
| chr10:124620879
|
C | G | 69 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(66): Show | 193 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*2363G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 2363 | chr10 | 124620879 | |||||
| chr10:124620911
|
G | A | 1 | a0001c0001t0029 | 2 | HG00609.hp2 NA19003.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2331C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 2331 | chr10 | 124620911 | |||||
| chr10:124621049
|
G | A | 22 | a0001c0001t0005a0001c0001t0008a0001c0001t0010others(19): Show | 49 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2193C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 2193 | chr10 | 124621049 | |||||
| chr10:124621179
|
C | T | 1 | a0001c0001t0062 | 1 | HG02056.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2063G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 2063 | chr10 | 124621179 | |||||
| chr10:124621209
|
G | A | 1 | a0001c0001t0037 | 2 | HG01175.hp2 HG02683.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2033C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 2033 | chr10 | 124621209 | |||||
| chr10:124621221
|
C | A | 9 | a0001c0001t0002a0001c0001t0007a0001c0001t0013others(6): Show | 41 | HG00408.hp1 HG00609.hp1 HG02056.hp2 others(38): Show |
3_prime_UTR_variant | MODIFIER | c.*2021G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 2021 | chr10 | 124621221 | |||||
| chr10:124621250
|
G | A | 1 | a0001c0001t0039 | 1 | HG02280.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1992C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 1992 | chr10 | 124621250 | |||||
| chr10:124621435
|
G | A | 2 | a0001c0001t0022a0001c0001t0051 | 4 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1807C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 1807 | chr10 | 124621435 | |||||
| chr10:124621473
|
G | A | 23 | a0001c0001t0005a0001c0001t0008a0001c0001t0010others(20): Show | 50 | HG00140.hp2 HG00408.hp2 HG00423.hp2 others(47): Show |
3_prime_UTR_variant | MODIFIER | c.*1769C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 1769 | chr10 | 124621473 | |||||
| chr10:124621863
|
C | G | 1 | a0001c0001t0061 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1379G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 1379 | chr10 | 124621863 | |||||
| chr10:124622069
|
T | C | 1 | a0005c0004t0086 | 1 | HG02145.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1173A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 1173 | chr10 | 124622069 | |||||
| chr10:124622090
|
G | A | 1 | a0001c0001t0060 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1152C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 1152 | chr10 | 124622090 | |||||
| chr10:124622163
|
T | G | 9 | a0001c0001t0008a0001c0001t0024a0001c0001t0025others(6): Show | 19 | HG00408.hp2 HG00621.hp2 HG02027.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1079A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 1079 | chr10 | 124622163 | |||||
| chr10:124622212
|
C | T | 45 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(42): Show | 123 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(120): Show |
3_prime_UTR_variant | MODIFIER | c.*1030G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 1030 | chr10 | 124622212 | |||||
| chr10:124622376
|
C | T | 1 | a0001c0001t0078 | 1 | NA19009.hp1 | 3_prime_UTR_variant | MODIFIER | c.*866G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 866 | chr10 | 124622376 | |||||
| chr10:124622451
|
C | T | 1 | a0001c0001t0021 | 3 | HG00639.hp1 HG02615.hp1 HG02976.hp1 |
3_prime_UTR_variant | MODIFIER | c.*791G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 791 | chr10 | 124622451 | |||||
| chr10:124622470
|
TCAGCCTC others(3): Show |
T | 1 | a0001c0001t0089 | 1 | NA19078.hp1 | 3_prime_UTR_variant | MODIFIER | c.*762_*771delGGAGAG others(4): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 762 | chr10 | 124622470 | |||||
| chr10:124622507
|
G | A | 2 | a0001c0001t0026a0004c0005t0026 | 3 | HG02300.hp2 HG03130.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*735C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 735 | chr10 | 124622507 | |||||
| chr10:124622548
|
G | A | 1 | a0001c0001t0075 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*694C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 694 | chr10 | 124622548 | |||||
| chr10:124622590
|
G | A | 1 | a0001c0001t0091 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*652C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 652 | chr10 | 124622590 | |||||
| chr10:124622695
|
A | T | 1 | a0001c0001t0048 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*547T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 547 | chr10 | 124622695 | |||||
| chr10:124622858
|
G | A | 1 | a0001c0001t0076 | 1 | NA18983.hp1 | 3_prime_UTR_variant | MODIFIER | c.*384C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 384 | chr10 | 124622858 | |||||
| chr10:124622898
|
G | A | 1 | a0001c0001t0077 | 1 | NA19078.hp2 | 3_prime_UTR_variant | MODIFIER | c.*344C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 344 | chr10 | 124622898 | |||||
| chr10:124622926
|
G | C | 23 | a0001c0001t0002a0001c0001t0007a0001c0001t0009others(20): Show | 73 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*316C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 316 | chr10 | 124622926 | |||||
| chr10:124623012
|
G | A | 1 | a0001c0001t0085 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*230C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 5/5 | 230 | chr10 | 124623012 | |||||
| chr10:124706747
|
G | A | 1 | a0005c0004t0086 | 1 | HG02145.hp2 | 5_prime_UTR_variant | MODIFIER | c.-34C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/5 | 34 | chr10 | 124706747 | |||||
| chr10:124706829
|
T | C | 1 | a0001c0001t0043 | 1 | NA19081.hp1 | 5_prime_UTR_variant | MODIFIER | c.-116A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/5 | 116 | chr10 | 124706829 | |||||
| chr10:124744085
|
C | CCCGCCGC others(4): Show |
1 | a0001c0001t0047 | 1 | NA18747.hp1 | 5_prime_UTR_variant | MODIFIER | c.-258_-248dupACGCGC others(5): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/5 | 37373 | chr10 | 124744085 | |||||
| chr10:124744194
|
C | G | 1 | a0001c0001t0046 | 1 | HG03688.hp2 | 5_prime_UTR_variant | MODIFIER | c.-356G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/5 | 37481 | chr10 | 124744194 | |||||
| chr10:124744208
|
C | G | 1 | a0001c0001t0045 | 1 | HG02647.hp1 | 5_prime_UTR_variant | MODIFIER | c.-370G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/5 | 37495 | chr10 | 124744208 | |||||
| chr10:124744320
|
C | G | 1 | a0001c0001t0044 | 1 | NA19082.hp2 | 5_prime_UTR_variant | MODIFIER | c.-482G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/5 | 37607 | chr10 | 124744320 | |||||
| chr10:124744331
|
T | C | 13 | a0001c0001t0002a0001c0001t0009a0001c0001t0013others(10): Show | 48 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(45): Show |
5_prime_UTR_variant | MODIFIER | c.-493A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/5 | 37618 | chr10 | 124744331 | |||||
| chr10:124744338
|
G | A | 1 | a0001c0001t0091 | 1 | HG06807.hp1 | 5_prime_UTR_variant | MODIFIER | c.-500C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/5 | 37625 | chr10 | 124744338 | |||||
| chr10:124744341
|
A | AGGCGGCG others(6): Show |
11 | a0001c0001t0005a0001c0001t0019a0001c0001t0020others(8): Show | 25 | HG00140.hp2 HG00408.hp1 HG00609.hp2 others(22): Show |
5_prime_UTR_variant | MODIFIER | c.-516_-504dupGCCGCA others(7): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/5 | 37629 | chr10 | 124744341 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:124623720
|
G | A | 43 | a0001c0001t0001g0153a0001c0001t0003g0039a0001c0001t0003g0058others(40): Show | 43 | HG00558.hp2 HG00639.hp2 HG00735.hp1 others(40): Show |
intron_variant | MODIFIER | c.907-116C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124623720 | ||||||
| chr10:124623793
|
G | A | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0007g0206others(2): Show | 5 | HG02056.hp2 NA18612.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.907-189C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124623793 | ||||||
| chr10:124623813
|
C | T | 1 | a0001c0001t0030g0005 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.907-209G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124623813 | ||||||
| chr10:124623878
|
G | A | 3 | a0001c0001t0015g0042a0001c0001t0015g0051a0001c0001t0015g0276 | 3 | HG02258.hp2 HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.907-274C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124623878 | ||||||
| chr10:124623997
|
C | G | 1 | a0001c0001t0005g0018 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.907-393G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124623997 | ||||||
| chr10:124624097
|
A | G | 3 | a0001c0001t0033g0122a0001c0001t0033g0125a0001c0001t0085g0041 | 3 | HG03130.hp1 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.907-493T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124624097 | ||||||
| chr10:124624451
|
C | T | 1 | a0001c0001t0015g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.907-847G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124624451 | ||||||
| chr10:124624603
|
G | A | 1 | a0001c0001t0001g0161 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.907-999C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124624603 | ||||||
| chr10:124624667
|
A | G | 1 | a0001c0001t0006g0089 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.907-1063T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124624667 | ||||||
| chr10:124624685
|
G | A | 1 | a0001c0001t0039g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.907-1081C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124624685 | ||||||
| chr10:124624740
|
TGCACAAG others(33): Show |
T | 1 | a0001c0001t0001g0174 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.907-1176_907-1137d others(42): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124624740 | ||||||
| chr10:124624741
|
G | A | 48 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(45): Show | 50 | HG00609.hp1 HG01069.hp1 HG01943.hp2 others(47): Show |
intron_variant | MODIFIER | c.907-1137C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124624741 | ||||||
| chr10:124624817
|
T | C | 196 | a0001c0001t0001g0229a0001c0001t0001g0235a0001c0001t0002g0003others(193): Show | 198 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(195): Show |
intron_variant | MODIFIER | c.907-1213A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124624817 | ||||||
| chr10:124624862
|
C | T | 13 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0297others(10): Show | 15 | HG02135.hp1 NA18612.hp1 NA18942.hp2 others(12): Show |
intron_variant | MODIFIER | c.907-1258G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124624862 | ||||||
| chr10:124624932
|
T | C | 4 | a0001c0001t0014g0038a0001c0001t0014g0093a0001c0001t0014g0094others(1): Show | 4 | HG00735.hp1 HG01123.hp1 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.907-1328A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124624932 | ||||||
| chr10:124624952
|
G | T | 1 | a0001c0001t0078g0194 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.907-1348C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124624952 | ||||||
| chr10:124624980
|
A | G | 1 | a0001c0001t0047g0033 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.907-1376T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124624980 | ||||||
| chr10:124625009
|
G | A | 3 | a0001c0001t0005g0022a0001c0001t0005g0023a0001c0001t0043g0025 | 3 | NA18944.hp1 NA18967.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.907-1405C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124625009 | ||||||
| chr10:124625027
|
C | T | 1 | a0001c0001t0010g0222 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.907-1423G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124625027 | ||||||
| chr10:124625054
|
G | A | 1 | a0001c0001t0001g0152 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.907-1450C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124625054 | ||||||
| chr10:124625170
|
C | G | 1 | a0001c0001t0025g0248 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.907-1566G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124625170 | ||||||
| chr10:124625177
|
G | A | 1 | a0001c0001t0033g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.907-1573C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124625177 | ||||||
| chr10:124625177
|
G | T | 1 | a0001c0001t0001g0232 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.907-1573C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124625177 | ||||||
| chr10:124625538
|
C | T | 1 | a0001c0001t0024g0256 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.907-1934G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124625538 | ||||||
| chr10:124625559
|
C | T | 17 | a0001c0001t0004g0103a0001c0001t0004g0108a0001c0001t0004g0115others(14): Show | 17 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(14): Show |
intron_variant | MODIFIER | c.907-1955G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124625559 | ||||||
| chr10:124625668
|
C | T | 1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.907-2064G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124625668 | ||||||
| chr10:124625725
|
G | C | 17 | a0001c0001t0009g0284a0001c0001t0009g0320a0001c0001t0009g0321others(14): Show | 17 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.907-2121C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124625725 | ||||||
| chr10:124625770
|
A | G | 1 | a0001c0001t0025g0248 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.907-2166T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124625770 | ||||||
| chr10:124625777
|
A | C | 1 | a0001c0001t0085g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.907-2173T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124625777 | ||||||
| chr10:124625780
|
T | C | 147 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(144): Show | 147 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(144): Show |
intron_variant | MODIFIER | c.907-2176A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124625780 | ||||||
| chr10:124625906
|
C | T | 46 | a0001c0001t0001g0129a0001c0001t0001g0134a0001c0001t0001g0135others(43): Show | 46 | HG00099.hp1 HG00280.hp1 HG00621.hp1 others(43): Show |
intron_variant | MODIFIER | c.907-2302G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124625906 | ||||||
| chr10:124626085
|
A | G | 13 | a0001c0001t0001g0133a0001c0001t0001g0136a0001c0001t0001g0137others(10): Show | 13 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(10): Show |
intron_variant | MODIFIER | c.907-2481T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626085 | ||||||
| chr10:124626111
|
C | T | 1 | a0001c0001t0091g0326 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.907-2507G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626111 | ||||||
| chr10:124626147
|
C | A | 16 | a0001c0001t0004g0103a0001c0001t0004g0108a0001c0001t0004g0110others(13): Show | 16 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.907-2543G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626147 | ||||||
| chr10:124626166
|
C | T | 24 | a0001c0001t0001g0150a0001c0001t0001g0152a0001c0001t0001g0153others(21): Show | 24 | HG01169.hp1 HG01346.hp1 HG01361.hp1 others(21): Show |
intron_variant | MODIFIER | c.907-2562G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626166 | ||||||
| chr10:124626190
|
G | T | 2 | a0001c0001t0001g0070a0001c0001t0001g0078 | 2 | HG02165.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.907-2586C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626190 | ||||||
| chr10:124626196
|
G | A | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.907-2592C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626196 | ||||||
| chr10:124626206
|
C | T | 1 | a0001c0001t0003g0058 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.907-2602G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626206 | ||||||
| chr10:124626233
|
G | A | 1 | a0001c0001t0009g0321 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.907-2629C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626233 | ||||||
| chr10:124626240
|
G | A | 1 | a0001c0001t0010g0222 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.907-2636C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626240 | ||||||
| chr10:124626255
|
C | A | 1 | a0001c0001t0091g0326 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.907-2651G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626255 | ||||||
| chr10:124626305
|
G | A | 6 | a0001c0001t0001g0143a0001c0001t0001g0151a0001c0001t0001g0158others(3): Show | 6 | HG01071.hp2 HG01261.hp1 HG01515.hp2 others(3): Show |
intron_variant | MODIFIER | c.907-2701C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626305 | ||||||
| chr10:124626313
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.907-2709G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626313 | ||||||
| chr10:124626330
|
T | G | 1 | a0001c0001t0001g0235 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.907-2726A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626330 | ||||||
| chr10:124626342
|
T | C | 4 | a0001c0001t0012g0123a0001c0001t0015g0121a0001c0001t0060g0126others(1): Show | 4 | HG02965.hp2 HG02976.hp2 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.907-2738A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626342 | ||||||
| chr10:124626375
|
G | A | 1 | a0001c0001t0079g0171 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.907-2771C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626375 | ||||||
| chr10:124626388
|
G | GC | 77 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0044others(74): Show | 78 | HG00280.hp1 HG00423.hp1 HG00621.hp1 others(75): Show |
intron_variant | MODIFIER | c.907-2785dupG | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626388 | ||||||
| chr10:124626388
|
G | GCC | 34 | a0001c0001t0001g0160a0001c0001t0001g0193a0001c0001t0001g0216others(31): Show | 34 | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(31): Show |
intron_variant | MODIFIER | c.907-2786_907-2785d others(4): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626388 | ||||||
| chr10:124626388
|
G | GCCC | 17 | a0001c0001t0001g0245a0001c0001t0003g0039a0001c0001t0003g0075others(14): Show | 17 | HG00423.hp2 HG00558.hp2 HG02040.hp1 others(14): Show |
intron_variant | MODIFIER | c.907-2787_907-2785d others(5): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626388 | ||||||
| chr10:124626388
|
GC | G | 20 | a0001c0001t0001g0070a0001c0001t0001g0130a0001c0001t0001g0151others(17): Show | 20 | HG00140.hp2 HG00621.hp2 HG00673.hp1 others(17): Show |
intron_variant | MODIFIER | c.907-2785delG | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626388 | ||||||
| chr10:124626388
|
GCC | G | 27 | a0001c0001t0001g0001a0001c0001t0001g0159a0001c0001t0001g0221others(24): Show | 28 | HG01099.hp2 HG01106.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.907-2786_907-2785d others(4): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626388 | ||||||
| chr10:124626397
|
C | G | 17 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(14): Show | 18 | HG00642.hp1 HG01074.hp1 HG01884.hp2 others(15): Show |
intron_variant | MODIFIER | c.907-2793G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626397 | ||||||
| chr10:124626398
|
C | G | 1 | a0001c0001t0065g0092 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.907-2794G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626398 | ||||||
| chr10:124626575
|
C | T | 1 | a0001c0001t0002g0297 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.907-2971G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626575 | ||||||
| chr10:124626702
|
GC | G | 34 | a0001c0001t0001g0229a0001c0001t0002g0004a0001c0001t0002g0298others(31): Show | 35 | HG00140.hp2 HG00423.hp2 HG00609.hp1 others(32): Show |
intron_variant | MODIFIER | c.907-3099delG | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626702 | ||||||
| chr10:124626760
|
G | A | 5 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0007g0206others(2): Show | 5 | HG02056.hp2 NA18612.hp2 NA18945.hp2 others(2): Show |
intron_variant | MODIFIER | c.907-3156C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626760 | ||||||
| chr10:124626841
|
T | C | 15 | a0001c0001t0001g0133a0001c0001t0001g0136a0001c0001t0001g0137others(12): Show | 15 | HG00099.hp2 HG00140.hp1 HG00642.hp1 others(12): Show |
intron_variant | MODIFIER | c.907-3237A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124626841 | ||||||
| chr10:124627109
|
A | T | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.907-3505T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124627109 | ||||||
| chr10:124627309
|
C | G | 1 | a0001c0001t0001g0135 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.907-3705G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124627309 | ||||||
| chr10:124627564
|
GC | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(84): Show | 88 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(85): Show |
intron_variant | MODIFIER | c.907-3961delG | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124627564 | ||||||
| chr10:124627633
|
C | T | 1 | a0001c0001t0013g0314 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.907-4029G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124627633 | ||||||
| chr10:124627808
|
AGCCG | A | 71 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0104others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.907-4208_907-4205d others(6): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124627808 | ||||||
| chr10:124627875
|
A | T | 1 | a0001c0003t0058g0269 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.907-4271T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124627875 | ||||||
| chr10:124627876
|
T | A | 1 | a0001c0003t0058g0269 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.907-4272A>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124627876 | ||||||
| chr10:124627912
|
TACAG | T | 71 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0104others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.907-4312_907-4309d others(6): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124627912 | ||||||
| chr10:124628035
|
C | G | 82 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(79): Show | 82 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(79): Show |
intron_variant | MODIFIER | c.907-4431G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124628035 | ||||||
| chr10:124628092
|
C | G | 1 | a0001c0003t0058g0269 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.907-4488G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124628092 | ||||||
| chr10:124628208
|
G | A | 42 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(39): Show | 42 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(39): Show |
intron_variant | MODIFIER | c.907-4604C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124628208 | ||||||
| chr10:124628248
|
G | C | 3 | a0001c0001t0010g0127a0001c0001t0010g0222a0001c0001t0059g0128 | 3 | HG03490.hp2 HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.907-4644C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124628248 | ||||||
| chr10:124628289
|
G | A | 1 | a0001c0001t0054g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.907-4685C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124628289 | ||||||
| chr10:124628382
|
C | T | 71 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0104others(68): Show | 71 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(68): Show |
intron_variant | MODIFIER | c.907-4778G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124628382 | ||||||
| chr10:124628486
|
T | G | 1 | a0001c0001t0054g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.907-4882A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124628486 | ||||||
| chr10:124628619
|
A | G | 318 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(315): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.907-5015T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124628619 | ||||||
| chr10:124628656
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.907-5052T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124628656 | ||||||
| chr10:124628700
|
G | A | 1 | a0001c0001t0008g0247 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.907-5096C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124628700 | ||||||
| chr10:124628782
|
G | A | 7 | a0001c0001t0010g0036a0001c0001t0010g0064a0001c0001t0010g0066others(4): Show | 7 | HG02818.hp2 HG03490.hp2 HG03516.hp1 others(4): Show |
intron_variant | MODIFIER | c.907-5178C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124628782 | ||||||
| chr10:124628830
|
C | T | 1 | a0001c0001t0001g0218 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.907-5226G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124628830 | ||||||
| chr10:124628876
|
G | A | 4 | a0001c0001t0010g0036a0001c0001t0010g0064a0001c0001t0010g0066others(1): Show | 4 | HG02818.hp2 HG03516.hp1 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.907-5272C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124628876 | ||||||
| chr10:124629003
|
G | A | 1 | a0001c0001t0006g0061 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.907-5399C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124629003 | ||||||
| chr10:124629062
|
T | C | 1 | a0001c0001t0001g0130 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.907-5458A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124629062 | ||||||
| chr10:124629158
|
A | T | 1 | a0001c0003t0058g0269 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.907-5554T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124629158 | ||||||
| chr10:124629215
|
C | T | 2 | a0001c0001t0018g0289a0001c0001t0028g0290 | 2 | NA18998.hp1 NA19064.hp2 |
intron_variant | MODIFIER | c.907-5611G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124629215 | ||||||
| chr10:124629258
|
G | A | 1 | a0001c0001t0054g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.907-5654C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124629258 | ||||||
| chr10:124629288
|
T | C | 270 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(267): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.907-5684A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124629288 | ||||||
| chr10:124629509
|
C | T | 1 | a0001c0001t0011g0091 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.907-5905G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124629509 | ||||||
| chr10:124630041
|
T | G | 1 | a0001c0001t0026g0241 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.907-6437A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124630041 | ||||||
| chr10:124630159
|
T | C | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.907-6555A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124630159 | ||||||
| chr10:124630229
|
A | G | 1 | a0001c0001t0004g0103 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.907-6625T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124630229 | ||||||
| chr10:124630244
|
T | C | 270 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(267): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.907-6640A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124630244 | ||||||
| chr10:124630381
|
T | C | 1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.907-6777A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124630381 | ||||||
| chr10:124630382
|
C | T | 1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.907-6778G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124630382 | ||||||
| chr10:124630422
|
A | G | 1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.907-6818T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124630422 | ||||||
| chr10:124630423
|
G | A | 1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.907-6819C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124630423 | ||||||
| chr10:124630429
|
C | T | 1 | a0001c0001t0063g0063 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.907-6825G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124630429 | ||||||
| chr10:124630584
|
G | A | 82 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(79): Show | 82 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.907-6980C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124630584 | ||||||
| chr10:124630675
|
C | G | 2 | a0001c0001t0004g0103a0002c0007t0001g0102 | 2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.907-7071G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124630675 | ||||||
| chr10:124630918
|
A | G | 161 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(158): Show | 161 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(158): Show |
intron_variant | MODIFIER | c.907-7314T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124630918 | ||||||
| chr10:124631031
|
G | A | 75 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0104others(72): Show | 75 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(72): Show |
intron_variant | MODIFIER | c.907-7427C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124631031 | ||||||
| chr10:124631155
|
G | A | 43 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(40): Show | 43 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.907-7551C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124631155 | ||||||
| chr10:124631204
|
G | A | 160 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(157): Show | 160 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(157): Show |
intron_variant | MODIFIER | c.907-7600C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124631204 | ||||||
| chr10:124631389
|
C | T | 5 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.907-7785G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124631389 | ||||||
| chr10:124631423
|
C | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0129others(135): Show | 139 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(136): Show |
intron_variant | MODIFIER | c.907-7819G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124631423 | ||||||
| chr10:124631543
|
G | A | 5 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(2): Show | 5 | HG00323.hp1 HG00639.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.907-7939C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124631543 | ||||||
| chr10:124631758
|
C | T | 3 | a0001c0001t0005g0022a0001c0001t0005g0023a0001c0001t0043g0025 | 3 | NA18944.hp1 NA18967.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.907-8154G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124631758 | ||||||
| chr10:124631784
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.907-8180C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124631784 | ||||||
| chr10:124631855
|
C | T | 1 | a0001c0001t0074g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.907-8251G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124631855 | ||||||
| chr10:124631968
|
G | T | 18 | a0001c0001t0007g0252a0001c0001t0008g0247a0001c0001t0008g0254others(15): Show | 18 | HG00408.hp2 HG00621.hp2 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.907-8364C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124631968 | ||||||
| chr10:124632071
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0172 | 2 | HG02135.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.907-8467C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124632071 | ||||||
| chr10:124632108
|
G | A | 19 | a0001c0001t0004g0108a0001c0001t0004g0110a0001c0001t0004g0115others(16): Show | 19 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.907-8504C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124632108 | ||||||
| chr10:124632152
|
C | T | 110 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0104others(107): Show | 112 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(109): Show |
intron_variant | MODIFIER | c.907-8548G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124632152 | ||||||
| chr10:124632168
|
C | CGGTGGCG others(11): Show |
1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.907-8565_907-8564i others(20): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124632168 | ||||||
| chr10:124632174
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.907-8570G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124632174 | ||||||
| chr10:124632187
|
C | T | 1 | a0001c0001t0047g0033 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.907-8583G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124632187 | ||||||
| chr10:124632333
|
C | T | 196 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(193): Show | 198 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.907-8729G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124632333 | ||||||
| chr10:124632423
|
C | T | 19 | a0001c0001t0004g0108a0001c0001t0004g0110a0001c0001t0004g0115others(16): Show | 19 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.907-8819G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124632423 | ||||||
| chr10:124632612
|
C | G | 1 | a0001c0001t0009g0320 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.907-9008G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124632612 | ||||||
| chr10:124632670
|
A | G | 1 | a0001c0001t0015g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.907-9066T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124632670 | ||||||
| chr10:124632687
|
G | A | 1 | a0001c0001t0046g0032 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.907-9083C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124632687 | ||||||
| chr10:124632857
|
G | A | 1 | a0001c0001t0033g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.907-9253C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124632857 | ||||||
| chr10:124632921
|
T | C | 311 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(308): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.907-9317A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124632921 | ||||||
| chr10:124632929
|
C | T | 1 | a0001c0001t0054g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.907-9325G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124632929 | ||||||
| chr10:124633246
|
G | GA | 28 | a0001c0001t0003g0071a0001c0001t0004g0108a0001c0001t0004g0110others(25): Show | 28 | HG00140.hp2 HG00735.hp1 HG01099.hp2 others(25): Show |
intron_variant | MODIFIER | c.907-9643dupT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124633246 | ||||||
| chr10:124633246
|
GA | G | 107 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0104others(104): Show | 109 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.907-9643delT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124633246 | ||||||
| chr10:124633246
|
GAA | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(87): Show | 91 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.907-9644_907-9643d others(4): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124633246 | ||||||
| chr10:124633289
|
A | C | 1 | a0001c0002t0001g0212 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.907-9685T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124633289 | ||||||
| chr10:124633338
|
A | G | 3 | a0001c0001t0001g0139a0001c0001t0001g0173a0001c0001t0001g0188 | 3 | NA18944.hp2 NA18948.hp1 NA18989.hp2 |
intron_variant | MODIFIER | c.907-9734T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124633338 | ||||||
| chr10:124633348
|
A | C | 1 | a0001c0001t0001g0111 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.907-9744T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124633348 | ||||||
| chr10:124633461
|
T | G | 2 | a0001c0001t0002g0299a0001c0001t0002g0309 | 2 | NA18988.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.907-9857A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124633461 | ||||||
| chr10:124633545
|
G | A | 1 | a0001c0001t0015g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.907-9941C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124633545 | ||||||
| chr10:124633579
|
C | G | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.907-9975G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124633579 | ||||||
| chr10:124633646
|
C | A | 1 | a0001c0001t0076g0255 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.907-10042G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124633646 | ||||||
| chr10:124634252
|
C | T | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.907-10648G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124634252 | ||||||
| chr10:124634360
|
A | G | 27 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(24): Show | 27 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.907-10756T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124634360 | ||||||
| chr10:124634431
|
G | A | 4 | a0001c0001t0018g0289a0001c0001t0028g0287a0001c0001t0028g0288others(1): Show | 4 | NA18957.hp1 NA18960.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.907-10827C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124634431 | ||||||
| chr10:124634442
|
G | A | 45 | a0001c0001t0001g0129a0001c0001t0001g0134a0001c0001t0001g0135others(42): Show | 45 | HG00099.hp1 HG00280.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.907-10838C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124634442 | ||||||
| chr10:124634464
|
T | C | 1 | a0001c0001t0005g0020 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.907-10860A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124634464 | ||||||
| chr10:124634561
|
G | A | 1 | a0001c0001t0091g0326 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.907-10957C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124634561 | ||||||
| chr10:124634595
|
C | T | 1 | a0001c0001t0052g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.907-10991G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124634595 | ||||||
| chr10:124634655
|
A | C | 83 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(80): Show | 83 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.907-11051T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124634655 | ||||||
| chr10:124634710
|
C | T | 111 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(108): Show | 112 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.907-11106G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124634710 | ||||||
| chr10:124634840
|
T | C | 1 | a0001c0001t0030g0005 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.907-11236A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124634840 | ||||||
| chr10:124635086
|
TTTTTTA | T | 111 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0104others(108): Show | 113 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.907-11488_907-1148 others(10): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124635086 | ||||||
| chr10:124635131
|
C | T | 45 | a0001c0001t0001g0129a0001c0001t0001g0134a0001c0001t0001g0135others(42): Show | 45 | HG00099.hp1 HG00280.hp1 HG01071.hp2 others(42): Show |
intron_variant | MODIFIER | c.907-11527G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124635131 | ||||||
| chr10:124635197
|
A | G | 111 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(108): Show | 112 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.907-11593T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124635197 | ||||||
| chr10:124635325
|
T | C | 1 | a0001c0001t0004g0116 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.907-11721A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124635325 | ||||||
| chr10:124635327
|
G | A | 2 | a0001c0001t0004g0103a0002c0007t0001g0102 | 2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.907-11723C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124635327 | ||||||
| chr10:124635333
|
T | C | 309 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(306): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.907-11729A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124635333 | ||||||
| chr10:124635386
|
C | T | 1 | a0001c0001t0002g0313 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.907-11782G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124635386 | ||||||
| chr10:124635387
|
G | A | 19 | a0001c0001t0004g0108a0001c0001t0004g0110a0001c0001t0004g0115others(16): Show | 19 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(16): Show |
intron_variant | MODIFIER | c.907-11783C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124635387 | ||||||
| chr10:124635450
|
A | G | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.907-11846T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124635450 | ||||||
| chr10:124635508
|
G | A | 111 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(108): Show | 112 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.907-11904C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124635508 | ||||||
| chr10:124635575
|
C | T | 5 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(2): Show | 5 | HG01884.hp2 HG02109.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.907-11971G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124635575 | ||||||
| chr10:124635640
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.907-12036C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124635640 | ||||||
| chr10:124635769
|
C | T | 3 | a0001c0001t0005g0022a0001c0001t0005g0023a0001c0001t0043g0025 | 3 | NA18944.hp1 NA18967.hp1 NA19081.hp1 |
intron_variant | MODIFIER | c.907-12165G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124635769 | ||||||
| chr10:124635778
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.907-12174G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124635778 | ||||||
| chr10:124635792
|
A | G | 323 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0044others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.907-12188T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124635792 | ||||||
| chr10:124635919
|
C | T | 1 | a0001c0001t0052g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.907-12315G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124635919 | ||||||
| chr10:124636053
|
G | A | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.907-12449C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124636053 | ||||||
| chr10:124636165
|
C | T | 2 | a0001c0001t0004g0103a0002c0007t0001g0102 | 2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.907-12561G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124636165 | ||||||
| chr10:124636166
|
A | G | 309 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(306): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.907-12562T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124636166 | ||||||
| chr10:124636714
|
G | A | 2 | a0001c0001t0004g0103a0002c0007t0001g0102 | 2 | HG03225.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.907-13110C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124636714 | ||||||
| chr10:124636732
|
G | A | 4 | a0001c0001t0002g0300a0001c0001t0002g0301a0001c0001t0007g0206others(1): Show | 4 | HG02056.hp2 NA18612.hp2 NA18945.hp2 others(1): Show |
intron_variant | MODIFIER | c.907-13128C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124636732 | ||||||
| chr10:124636781
|
G | A | 1 | a0001c0001t0073g0249 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.907-13177C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124636781 | ||||||
| chr10:124636937
|
T | C | 1 | a0001c0001t0043g0025 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.907-13333A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124636937 | ||||||
| chr10:124636989
|
T | C | 1 | a0001c0001t0013g0305 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.907-13385A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124636989 | ||||||
| chr10:124637278
|
G | A | 1 | a0001c0001t0052g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.907-13674C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124637278 | ||||||
| chr10:124637312
|
T | C | 311 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(308): Show | 314 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(311): Show |
intron_variant | MODIFIER | c.907-13708A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124637312 | ||||||
| chr10:124637430
|
C | T | 1 | a0001c0001t0028g0287 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.907-13826G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124637430 | ||||||
| chr10:124637476
|
C | T | 5 | a0001c0001t0004g0108a0001c0001t0004g0115a0001c0001t0004g0118others(2): Show | 5 | HG02257.hp2 HG02280.hp2 HG02818.hp1 others(2): Show |
intron_variant | MODIFIER | c.907-13872G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124637476 | ||||||
| chr10:124637725
|
G | A | 2 | a0001c0001t0004g0110a0001c0001t0004g0120 | 2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.907-14121C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124637725 | ||||||
| chr10:124637794
|
G | A | 35 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(32): Show | 35 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.907-14190C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124637794 | ||||||
| chr10:124637835
|
T | C | 1 | a0001c0001t0052g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.907-14231A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124637835 | ||||||
| chr10:124638037
|
T | C | 112 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0104others(109): Show | 114 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(111): Show |
intron_variant | MODIFIER | c.907-14433A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124638037 | ||||||
| chr10:124638086
|
C | T | 1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.907-14482G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124638086 | ||||||
| chr10:124638095
|
C | T | 1 | a0001c0001t0054g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.907-14491G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124638095 | ||||||
| chr10:124638117
|
C | G | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.907-14513G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124638117 | ||||||
| chr10:124638145
|
G | A | 1 | a0001c0001t0065g0092 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.907-14541C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124638145 | ||||||
| chr10:124638353
|
G | A | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.907-14749C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124638353 | ||||||
| chr10:124638374
|
A | AAAAAC | 85 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(82): Show | 85 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(82): Show |
intron_variant | MODIFIER | c.907-14775_907-1477 others(9): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124638374 | ||||||
| chr10:124638535
|
G | A | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.907-14931C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124638535 | ||||||
| chr10:124638699
|
G | A | 6 | a0001c0001t0002g0291a0001c0001t0002g0300a0001c0001t0002g0301others(3): Show | 6 | HG02056.hp2 NA18612.hp2 NA18945.hp2 others(3): Show |
intron_variant | MODIFIER | c.907-15095C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124638699 | ||||||
| chr10:124638785
|
A | G | 88 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(85): Show | 88 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.907-15181T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124638785 | ||||||
| chr10:124638913
|
G | A | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.907-15309C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124638913 | ||||||
| chr10:124638962
|
G | A | 1 | a0001c0001t0021g0266 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.907-15358C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124638962 | ||||||
| chr10:124639181
|
G | A | 5 | a0001c0002t0001g0191a0001c0002t0001g0203a0001c0002t0001g0207others(2): Show | 5 | HG01099.hp1 HG01123.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.907-15577C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124639181 | ||||||
| chr10:124639255
|
G | A | 1 | a0001c0001t0004g0279 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.907-15651C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124639255 | ||||||
| chr10:124639421
|
C | G | 1 | a0001c0001t0015g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.907-15817G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124639421 | ||||||
| chr10:124639526
|
C | T | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.907-15922G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124639526 | ||||||
| chr10:124639602
|
G | A | 1 | a0001c0001t0033g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.907-15998C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124639602 | ||||||
| chr10:124639675
|
T | C | 1 | a0001c0001t0049g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.907-16071A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124639675 | ||||||
| chr10:124639816
|
G | C | 2 | a0001c0001t0009g0293a0001c0001t0009g0294 | 2 | HG01069.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.907-16212C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124639816 | ||||||
| chr10:124639959
|
T | C | 1 | a0001c0001t0015g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.907-16355A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124639959 | ||||||
| chr10:124640120
|
A | G | 195 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(192): Show | 197 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(194): Show |
intron_variant | MODIFIER | c.907-16516T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124640120 | ||||||
| chr10:124640195
|
G | A | 1 | a0001c0001t0003g0039 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.907-16591C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124640195 | ||||||
| chr10:124640414
|
G | A | 3 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0030g0010 | 3 | HG00140.hp2 HG02055.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.907-16810C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124640414 | ||||||
| chr10:124640468
|
T | C | 309 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(306): Show | 312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): Show |
intron_variant | MODIFIER | c.907-16864A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124640468 | ||||||
| chr10:124640574
|
C | T | 1 | a0001c0001t0001g0161 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.907-16970G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124640574 | ||||||
| chr10:124640619
|
G | A | 1 | a0001c0001t0014g0093 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.907-17015C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124640619 | ||||||
| chr10:124640710
|
G | C | 1 | a0001c0001t0054g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.907-17106C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124640710 | ||||||
| chr10:124640884
|
C | T | 1 | a0001c0001t0015g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.907-17280G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124640884 | ||||||
| chr10:124641004
|
G | A | 3 | a0001c0001t0001g0221a0001c0001t0010g0066a0001c0001t0010g0067 | 3 | HG03516.hp1 NA18522.hp1 NA18956.hp1 |
intron_variant | MODIFIER | c.907-17400C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124641004 | ||||||
| chr10:124641130
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.907-17526G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124641130 | ||||||
| chr10:124641144
|
C | T | 1 | a0001c0001t0024g0250 | 1 | NA18948.hp2 | intron_variant | MODIFIER | c.907-17540G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124641144 | ||||||
| chr10:124641882
|
C | T | 1 | a0001c0001t0033g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.907-18278G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124641882 | ||||||
| chr10:124641936
|
T | C | 1 | a0001c0001t0008g0258 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.907-18332A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124641936 | ||||||
| chr10:124641995
|
C | A | 1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.907-18391G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124641995 | ||||||
| chr10:124641996
|
C | T | 101 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0104others(98): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.907-18392G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124641996 | ||||||
| chr10:124641997
|
G | A | 1 | a0001c0001t0079g0171 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.907-18393C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124641997 | ||||||
| chr10:124642001
|
G | C | 3 | a0001c0001t0001g0035a0001c0001t0001g0183a0001c0001t0001g0216 | 3 | NA18975.hp1 NA18983.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.907-18397C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124642001 | ||||||
| chr10:124642036
|
C | T | 301 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(298): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.907-18432G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124642036 | ||||||
| chr10:124642038
|
T | C | 1 | a0001c0001t0037g0325 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.907-18434A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124642038 | ||||||
| chr10:124642047
|
G | A | 1 | a0001c0001t0009g0322 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.907-18443C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124642047 | ||||||
| chr10:124642051
|
G | A | 1 | a0001c0001t0008g0257 | 1 | NA19083.hp2 | intron_variant | MODIFIER | c.907-18447C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124642051 | ||||||
| chr10:124642172
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0015g0121 | 2 | HG02976.hp2 NA18957.hp2 |
intron_variant | MODIFIER | c.907-18568G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124642172 | ||||||
| chr10:124642189
|
C | T | 7 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0159others(4): Show | 7 | HG00735.hp2 HG01069.hp2 HG01071.hp1 others(4): Show |
intron_variant | MODIFIER | c.907-18585G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124642189 | ||||||
| chr10:124642229
|
C | T | 1 | a0001c0001t0004g0118 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.907-18625G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124642229 | ||||||
| chr10:124642391
|
T | C | 307 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(304): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.907-18787A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124642391 | ||||||
| chr10:124642445
|
G | A | 1 | a0001c0001t0024g0262 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.907-18841C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124642445 | ||||||
| chr10:124642545
|
T | C | 307 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(304): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.907-18941A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124642545 | ||||||
| chr10:124642654
|
G | C | 1 | a0001c0001t0059g0128 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.907-19050C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124642654 | ||||||
| chr10:124642669
|
C | T | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.907-19065G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124642669 | ||||||
| chr10:124642832
|
G | A | 4 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0034g0227others(1): Show | 4 | HG03669.hp2 HG03688.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.907-19228C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124642832 | ||||||
| chr10:124642856
|
C | G | 1 | a0005c0004t0086g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.907-19252G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124642856 | ||||||
| chr10:124642936
|
G | A | 1 | a0001c0001t0012g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.907-19332C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124642936 | ||||||
| chr10:124642986
|
C | T | 86 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(83): Show | 86 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.907-19382G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124642986 | ||||||
| chr10:124643063
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.907-19459C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124643063 | ||||||
| chr10:124643316
|
G | A | 5 | a0001c0002t0001g0191a0001c0002t0001g0203a0001c0002t0001g0207others(2): Show | 5 | HG01099.hp1 HG01123.hp2 HG01496.hp2 others(2): Show |
intron_variant | MODIFIER | c.907-19712C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124643316 | ||||||
| chr10:124643551
|
G | T | 1 | a0001c0001t0057g0268 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.907-19947C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124643551 | ||||||
| chr10:124643743
|
A | G | 20 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(17): Show | 20 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.907-20139T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124643743 | ||||||
| chr10:124643747
|
G | C | 32 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(29): Show | 32 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.907-20143C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124643747 | ||||||
| chr10:124643774
|
A | C | 1 | a0001c0001t0012g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.907-20170T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124643774 | ||||||
| chr10:124643793
|
A | G | 307 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(304): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.907-20189T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124643793 | ||||||
| chr10:124643824
|
G | A | 1 | a0001c0001t0009g0320 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.907-20220C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124643824 | ||||||
| chr10:124643828
|
A | G | 307 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(304): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.907-20224T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124643828 | ||||||
| chr10:124643912
|
C | G | 1 | a0001c0001t0082g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.907-20308G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124643912 | ||||||
| chr10:124643917
|
C | A | 1 | a0001c0001t0012g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.907-20313G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124643917 | ||||||
| chr10:124644008
|
G | A | 20 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(17): Show | 20 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.907-20404C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124644008 | ||||||
| chr10:124644054
|
AG | A | 307 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(304): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.907-20451delC | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124644054 | ||||||
| chr10:124644201
|
A | T | 307 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(304): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.907-20597T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124644201 | ||||||
| chr10:124644365
|
T | A | 20 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(17): Show | 20 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.907-20761A>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124644365 | ||||||
| chr10:124644588
|
C | A | 1 | a0001c0001t0001g0133 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.907-20984G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124644588 | ||||||
| chr10:124644715
|
G | C | 1 | a0001c0001t0012g0046 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.907-21111C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124644715 | ||||||
| chr10:124645066
|
A | G | 2 | a0001c0001t0003g0068a0001c0001t0011g0069 | 2 | NA18973.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.907-21462T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124645066 | ||||||
| chr10:124645098
|
G | A | 1 | a0001c0001t0050g0107 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.907-21494C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124645098 | ||||||
| chr10:124645130
|
T | C | 307 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(304): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.907-21526A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124645130 | ||||||
| chr10:124645168
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.907-21564G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124645168 | ||||||
| chr10:124645270
|
T | C | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.907-21666A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124645270 | ||||||
| chr10:124645305
|
A | C | 91 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(88): Show | 91 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(88): Show |
intron_variant | MODIFIER | c.907-21701T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124645305 | ||||||
| chr10:124645482
|
G | A | 1 | a0001c0001t0001g0140 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.907-21878C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124645482 | ||||||
| chr10:124645493
|
C | T | 1 | a0001c0001t0003g0079 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.907-21889G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124645493 | ||||||
| chr10:124645658
|
G | T | 1 | a0001c0001t0007g0204 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.907-22054C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124645658 | ||||||
| chr10:124645845
|
G | C | 1 | a0001c0001t0001g0195 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.907-22241C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124645845 | ||||||
| chr10:124645897
|
C | A | 1 | a0001c0001t0004g0103 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.907-22293G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124645897 | ||||||
| chr10:124646161
|
G | A | 1 | a0005c0004t0086g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.907-22557C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124646161 | ||||||
| chr10:124646387
|
T | C | 1 | a0001c0001t0001g0265 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.907-22783A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124646387 | ||||||
| chr10:124646465
|
T | C | 1 | a0001c0001t0049g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.907-22861A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124646465 | ||||||
| chr10:124646597
|
C | T | 1 | a0001c0001t0033g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.907-22993G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124646597 | ||||||
| chr10:124646631
|
T | G | 1 | a0001c0001t0008g0254 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.907-23027A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124646631 | ||||||
| chr10:124646646
|
G | A | 1 | a0001c0001t0060g0126 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.907-23042C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124646646 | ||||||
| chr10:124646793
|
A | G | 7 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(4): Show | 8 | NA18947.hp2 NA18975.hp2 NA18984.hp1 others(5): Show |
intron_variant | MODIFIER | c.907-23189T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124646793 | ||||||
| chr10:124647017
|
T | C | 106 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0104others(103): Show | 108 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.907-23413A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124647017 | ||||||
| chr10:124647023
|
CAGA | C | 4 | a0001c0001t0010g0127a0001c0001t0010g0222a0001c0001t0059g0128others(1): Show | 4 | HG03130.hp1 HG03490.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.907-23422_907-2342 others(7): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124647023 | ||||||
| chr10:124647128
|
G | A | 35 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(32): Show | 35 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.907-23524C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124647128 | ||||||
| chr10:124647299
|
G | A | 1 | a0001c0001t0005g0011 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.907-23695C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124647299 | ||||||
| chr10:124647520
|
G | A | 1 | a0001c0001t0085g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.907-23916C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124647520 | ||||||
| chr10:124647561
|
A | G | 1 | a0005c0004t0086g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.907-23957T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124647561 | ||||||
| chr10:124647589
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(82): Show | 86 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(83): Show |
intron_variant | MODIFIER | c.907-23985C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124647589 | ||||||
| chr10:124647694
|
T | TG | 4 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105others(1): Show | 4 | HG02738.hp2 HG03490.hp2 HG03834.hp2 others(1): Show |
intron_variant | MODIFIER | c.907-24091dupC | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124647694 | ||||||
| chr10:124647750
|
T | C | 1 | a0001c0001t0015g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.907-24146A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124647750 | ||||||
| chr10:124647814
|
G | A | 2 | a0001c0001t0029g0006a0001c0001t0029g0024 | 2 | HG00609.hp2 NA19003.hp1 |
intron_variant | MODIFIER | c.907-24210C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124647814 | ||||||
| chr10:124647963
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.907-24359C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124647963 | ||||||
| chr10:124647987
|
G | A | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.907-24383C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124647987 | ||||||
| chr10:124648278
|
T | C | 1 | a0001c0001t0055g0182 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.907-24674A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124648278 | ||||||
| chr10:124648345
|
G | A | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.907-24741C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124648345 | ||||||
| chr10:124648470
|
G | C | 318 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(315): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.907-24866C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124648470 | ||||||
| chr10:124648491
|
T | C | 157 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(154): Show | 159 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.907-24887A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124648491 | ||||||
| chr10:124648512
|
C | T | 1 | a0001c0001t0062g0132 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.907-24908G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124648512 | ||||||
| chr10:124648621
|
C | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(86): Show | 90 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.907-25017G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124648621 | ||||||
| chr10:124648774
|
G | T | 3 | a0001c0001t0010g0127a0001c0001t0010g0222a0001c0001t0059g0128 | 3 | HG03490.hp2 HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.907-25170C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124648774 | ||||||
| chr10:124648781
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.907-25177G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124648781 | ||||||
| chr10:124648836
|
G | A | 2 | a0001c0001t0016g0177a0001c0001t0066g0178 | 2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.907-25232C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124648836 | ||||||
| chr10:124649303
|
C | T | 1 | a0001c0001t0037g0325 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.907-25699G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124649303 | ||||||
| chr10:124649524
|
C | T | 156 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(153): Show | 158 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.907-25920G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124649524 | ||||||
| chr10:124649566
|
A | T | 1 | a0001c0001t0021g0266 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.907-25962T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124649566 | ||||||
| chr10:124649637
|
G | A | 1 | a0001c0001t0014g0094 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.907-26033C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124649637 | ||||||
| chr10:124649717
|
C | T | 2 | a0001c0001t0023g0238a0001c0001t0023g0239 | 2 | HG02809.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.907-26113G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124649717 | ||||||
| chr10:124649745
|
G | C | 19 | a0001c0001t0007g0252a0001c0001t0007g0263a0001c0001t0008g0247others(16): Show | 19 | HG00408.hp2 HG00621.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.907-26141C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124649745 | ||||||
| chr10:124649873
|
C | T | 1 | a0001c0001t0034g0154 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.907-26269G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124649873 | ||||||
| chr10:124649874
|
G | A | 1 | a0001c0001t0083g0186 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.907-26270C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124649874 | ||||||
| chr10:124649875
|
C | T | 305 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(302): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.907-26271G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124649875 | ||||||
| chr10:124649885
|
T | G | 2 | a0001c0001t0001g0145a0001c0001t0017g0142 | 2 | NA18946.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.907-26281A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124649885 | ||||||
| chr10:124649916
|
A | G | 1 | a0001c0001t0038g0021 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.907-26312T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124649916 | ||||||
| chr10:124650088
|
A | G | 158 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(155): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.907-26484T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124650088 | ||||||
| chr10:124650326
|
C | G | 1 | a0001c0001t0046g0032 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.907-26722G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124650326 | ||||||
| chr10:124650371
|
C | T | 1 | a0001c0001t0006g0233 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.907-26767G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124650371 | ||||||
| chr10:124650461
|
G | A | 1 | a0001c0001t0001g0175 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.907-26857C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124650461 | ||||||
| chr10:124650833
|
T | G | 9 | a0001c0001t0001g0035a0001c0001t0001g0183a0001c0001t0001g0193others(6): Show | 9 | HG00423.hp1 NA18939.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.907-27229A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124650833 | ||||||
| chr10:124650961
|
C | CA | 35 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(32): Show | 35 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(32): Show |
intron_variant | MODIFIER | c.907-27358dupT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124650961 | ||||||
| chr10:124651207
|
C | G | 1 | a0001c0001t0005g0028 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.907-27603G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124651207 | ||||||
| chr10:124651293
|
G | C | 2 | a0001c0001t0052g0037a0001c0001t0060g0126 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.907-27689C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124651293 | ||||||
| chr10:124651698
|
C | A | 156 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(153): Show | 158 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(155): Show |
intron_variant | MODIFIER | c.907-28094G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124651698 | ||||||
| chr10:124651768
|
G | A | 2 | a0001c0001t0016g0168a0001c0001t0077g0138 | 2 | NA18980.hp2 NA19078.hp2 |
intron_variant | MODIFIER | c.907-28164C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124651768 | ||||||
| chr10:124652147
|
C | T | 3 | a0001c0001t0004g0279a0001c0001t0004g0280a0001c0001t0004g0281 | 3 | HG02717.hp1 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.907-28543G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124652147 | ||||||
| chr10:124652323
|
C | T | 279 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(276): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.907-28719G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124652323 | ||||||
| chr10:124652382
|
G | A | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.907-28778C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124652382 | ||||||
| chr10:124652396
|
T | C | 1 | a0001c0001t0001g0140 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.907-28792A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124652396 | ||||||
| chr10:124652776
|
A | C | 1 | a0001c0001t0074g0156 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.906+28831T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124652776 | ||||||
| chr10:124652804
|
C | T | 1 | a0001c0001t0004g0110 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.906+28803G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124652804 | ||||||
| chr10:124652902
|
C | T | 1 | a0001c0001t0001g0131 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.906+28705G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124652902 | ||||||
| chr10:124653211
|
G | GGA | 47 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0143others(44): Show | 47 | HG00099.hp1 HG00280.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.906+28394_906+2839 others(6): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124653211 | ||||||
| chr10:124653217
|
G | A | 1 | a0001c0001t0017g0142 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.906+28390C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124653217 | ||||||
| chr10:124653218
|
C | G | 1 | a0001c0001t0017g0142 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.906+28389G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124653218 | ||||||
| chr10:124653280
|
G | A | 1 | a0001c0001t0009g0322 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.906+28327C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124653280 | ||||||
| chr10:124653453
|
C | T | 302 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(299): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.906+28154G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124653453 | ||||||
| chr10:124653465
|
C | A | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.906+28142G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124653465 | ||||||
| chr10:124653719
|
C | A | 304 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(301): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.906+27888G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124653719 | ||||||
| chr10:124654005
|
C | G | 4 | a0001c0001t0022g0055a0001c0001t0022g0056a0001c0001t0022g0065others(1): Show | 4 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+27602G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124654005 | ||||||
| chr10:124654191
|
G | A | 1 | a0001c0001t0001g0112 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.906+27416C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124654191 | ||||||
| chr10:124654239
|
G | A | 2 | a0001c0001t0048g0246a0001c0001t0076g0255 | 2 | HG00621.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.906+27368C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124654239 | ||||||
| chr10:124654350
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.906+27257C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124654350 | ||||||
| chr10:124654400
|
G | A | 3 | a0001c0001t0010g0127a0001c0001t0010g0222a0001c0001t0059g0128 | 3 | HG03490.hp2 HG04115.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.906+27207C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124654400 | ||||||
| chr10:124654484
|
C | G | 304 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(301): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.906+27123G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124654484 | ||||||
| chr10:124654562
|
G | A | 1 | a0001c0001t0012g0123 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.906+27045C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124654562 | ||||||
| chr10:124654734
|
G | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0130a0001c0001t0001g0131others(14): Show | 18 | HG00558.hp1 HG00673.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.906+26873C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124654734 | ||||||
| chr10:124654817
|
A | G | 1 | a0001c0001t0049g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.906+26790T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124654817 | ||||||
| chr10:124654836
|
G | A | 4 | a0001c0001t0001g0059a0001c0001t0001g0134a0001c0001t0001g0192others(1): Show | 4 | HG00642.hp2 HG03834.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+26771C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124654836 | ||||||
| chr10:124654882
|
T | C | 1 | a0001c0001t0060g0126 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.906+26725A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124654882 | ||||||
| chr10:124655052
|
C | T | 1 | a0001c0002t0001g0203 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.906+26555G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124655052 | ||||||
| chr10:124655197
|
T | A | 3 | a0001c0001t0032g0267a0001c0001t0057g0268a0001c0003t0058g0269 | 3 | HG00423.hp2 NA18986.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.906+26410A>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124655197 | ||||||
| chr10:124655362
|
C | T | 158 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(155): Show | 160 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(157): Show |
intron_variant | MODIFIER | c.906+26245G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124655362 | ||||||
| chr10:124655469
|
A | G | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.906+26138T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124655469 | ||||||
| chr10:124655620
|
G | C | 1 | a0001c0001t0009g0323 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.906+25987C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124655620 | ||||||
| chr10:124655826
|
T | C | 32 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(29): Show | 32 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.906+25781A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124655826 | ||||||
| chr10:124655917
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.906+25690A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124655917 | ||||||
| chr10:124656055
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.906+25552G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124656055 | ||||||
| chr10:124656091
|
T | C | 2 | a0001c0001t0001g0161a0001c0001t0027g0209 | 2 | HG02132.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.906+25516A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124656091 | ||||||
| chr10:124656293
|
C | A | 14 | a0001c0001t0007g0263a0001c0001t0008g0247a0001c0001t0008g0254others(11): Show | 14 | HG02027.hp2 NA18942.hp1 NA18948.hp2 others(11): Show |
intron_variant | MODIFIER | c.906+25314G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124656293 | ||||||
| chr10:124656663
|
A | C | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.906+24944T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124656663 | ||||||
| chr10:124656680
|
G | A | 1 | a0001c0001t0006g0061 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.906+24927C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124656680 | ||||||
| chr10:124656895
|
G | T | 1 | a0001c0001t0001g0078 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.906+24712C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124656895 | ||||||
| chr10:124657040
|
ATATATAT others(13): Show |
A | 4 | a0001c0001t0001g0104a0001c0001t0004g0103a0001c0001t0033g0122others(1): Show | 4 | HG03209.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+24547_906+2456 others(24): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657040 | ||||||
| chr10:124657052
|
GTATATAT others(5): Show |
G | 89 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(86): Show | 90 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.906+24543_906+2455 others(16): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657052 | ||||||
| chr10:124657052
|
GTATATAT others(7): Show |
G | 1 | a0001c0001t0001g0218 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.906+24541_906+2455 others(18): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657052 | ||||||
| chr10:124657059
|
T | G | 1 | a0001c0001t0085g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.906+24548A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657059 | ||||||
| chr10:124657062
|
A | G | 2 | a0001c0001t0011g0091a0001c0001t0065g0092 | 2 | HG02698.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.906+24545T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657062 | ||||||
| chr10:124657063
|
T | C | 1 | a0001c0001t0006g0061 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.906+24544A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657063 | ||||||
| chr10:124657068
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.906+24539T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657068 | ||||||
| chr10:124657070
|
A | G | 1 | a0001c0001t0001g0218 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.906+24537T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657070 | ||||||
| chr10:124657108
|
A | ATG | 89 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(86): Show | 90 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.906+24497_906+2449 others(6): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657108 | ||||||
| chr10:124657108
|
A | G | 1 | a0001c0001t0085g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.906+24499T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657108 | ||||||
| chr10:124657108
|
ATG | A | 54 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(51): Show | 54 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.906+24497_906+2449 others(6): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657108 | ||||||
| chr10:124657108
|
ATGTGTG | A | 7 | a0001c0001t0001g0059a0001c0001t0001g0134a0001c0001t0001g0192others(4): Show | 7 | HG00642.hp2 HG02717.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.906+24493_906+2449 others(10): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657108 | ||||||
| chr10:124657112
|
G | GTATATA | 95 | a0001c0001t0001g0035a0001c0001t0001g0133a0001c0001t0001g0136others(92): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.906+24494_906+2449 others(10): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657112 | ||||||
| chr10:124657114
|
G | A | 95 | a0001c0001t0001g0035a0001c0001t0001g0133a0001c0001t0001g0136others(92): Show | 97 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(94): Show |
intron_variant | MODIFIER | c.906+24493C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657114 | ||||||
| chr10:124657114
|
G | GTATATAC others(5): Show |
2 | a0001c0001t0053g0275a0001c0001t0056g0274 | 2 | HG00673.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.906+24492_906+2449 others(16): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657114 | ||||||
| chr10:124657116
|
G | A | 2 | a0001c0001t0053g0275a0001c0001t0056g0274 | 2 | HG00673.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.906+24491C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657116 | ||||||
| chr10:124657116
|
G | GTATATAT others(21): Show |
1 | a0001c0001t0085g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.906+24490_906+2449 others(32): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657116 | ||||||
| chr10:124657120
|
A | ATATATAT others(23): Show |
27 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(24): Show | 27 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.906+24457_906+2448 others(34): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657120 | ||||||
| chr10:124657120
|
A | ATATATAT others(53): Show |
1 | a0001c0001t0029g0006 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.906+24486_906+2448 others(64): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657120 | ||||||
| chr10:124657120
|
A | G | 3 | a0001c0001t0053g0275a0001c0001t0056g0274a0001c0001t0085g0041 | 3 | HG00673.hp2 HG03130.hp1 NA18955.hp1 |
intron_variant | MODIFIER | c.906+24487T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657120 | ||||||
| chr10:124657132
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0009g0322 | 2 | HG00140.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.906+24475C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657132 | ||||||
| chr10:124657139
|
C | T | 2 | a0001c0001t0001g0196a0001c0001t0009g0322 | 2 | HG00140.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.906+24468G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657139 | ||||||
| chr10:124657140
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.906+24467T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657140 | ||||||
| chr10:124657142
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.906+24465T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657142 | ||||||
| chr10:124657144
|
A | G | 1 | a0001c0001t0001g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.906+24463T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657144 | ||||||
| chr10:124657148
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.906+24459C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657148 | ||||||
| chr10:124657150
|
G | A | 1 | a0001c0001t0001g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.906+24457C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657150 | ||||||
| chr10:124657151
|
T | C | 1 | a0001c0001t0001g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.906+24456A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657151 | ||||||
| chr10:124657152
|
A | G | 8 | a0001c0001t0001g0135a0001c0001t0001g0144a0001c0001t0001g0158others(5): Show | 8 | HG00280.hp1 HG01071.hp2 HG01106.hp1 others(5): Show |
intron_variant | MODIFIER | c.906+24455T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657152 | ||||||
| chr10:124657158
|
G | A | 2 | a0001c0001t0001g0196a0001c0001t0009g0322 | 2 | HG00140.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.906+24449C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657158 | ||||||
| chr10:124657164
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0172 | 2 | HG02135.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.906+24443T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657164 | ||||||
| chr10:124657165
|
TATATATA others(5): Show |
T | 144 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(141): Show | 146 | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(143): Show |
intron_variant | MODIFIER | c.906+24430_906+2444 others(16): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657165 | ||||||
| chr10:124657167
|
TATATATG others(3): Show |
T | 4 | a0001c0001t0001g0190a0001c0001t0001g0208a0001c0001t0027g0209others(1): Show | 4 | HG03688.hp2 NA19057.hp1 NA19079.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+24430_906+2443 others(14): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657167 | ||||||
| chr10:124657169
|
T | C | 4 | a0001c0001t0018g0289a0001c0001t0028g0287a0001c0001t0028g0288others(1): Show | 4 | NA18957.hp1 NA18960.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+24438A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657169 | ||||||
| chr10:124657170
|
A | G | 2 | a0001c0001t0001g0196a0001c0001t0009g0322 | 2 | HG00140.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.906+24437T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657170 | ||||||
| chr10:124657172
|
A | ATATATGT others(11): Show |
4 | a0001c0001t0018g0289a0001c0001t0028g0287a0001c0001t0028g0288others(1): Show | 4 | NA18957.hp1 NA18960.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+24434_906+2443 others(22): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657172 | ||||||
| chr10:124657172
|
A | G | 2 | a0001c0001t0001g0196a0001c0001t0009g0322 | 2 | HG00140.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.906+24435T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657172 | ||||||
| chr10:124657177
|
C | CAT | 80 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(77): Show | 81 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.906+24428_906+2442 others(6): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657177 | ||||||
| chr10:124657177
|
C | CATAT | 7 | a0001c0001t0001g0152a0001c0001t0001g0161a0001c0001t0007g0263others(4): Show | 7 | HG01952.hp1 HG02040.hp1 HG02132.hp2 others(4): Show |
intron_variant | MODIFIER | c.906+24426_906+2442 others(8): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657177 | ||||||
| chr10:124657177
|
C | CATATATA others(19): Show |
1 | a0001c0001t0001g0159 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.906+24429_906+2443 others(30): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657177 | ||||||
| chr10:124657177
|
C | T | 6 | a0001c0001t0001g0196a0001c0001t0009g0322a0001c0001t0018g0289others(3): Show | 6 | HG00140.hp1 HG01975.hp2 NA18957.hp1 others(3): Show |
intron_variant | MODIFIER | c.906+24430G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657177 | ||||||
| chr10:124657253
|
T | C | 1 | a0001c0001t0013g0306 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.906+24354A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657253 | ||||||
| chr10:124657288
|
T | G | 1 | a0001c0001t0003g0058 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.906+24319A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657288 | ||||||
| chr10:124657310
|
T | C | 1 | a0001c0001t0001g0197 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.906+24297A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657310 | ||||||
| chr10:124657380
|
A | C | 3 | a0001c0001t0001g0104a0001c0001t0004g0103a0002c0007t0001g0102 | 3 | HG03225.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.906+24227T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657380 | ||||||
| chr10:124657398
|
G | A | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | NA18957.hp2 NA18962.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+24209C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657398 | ||||||
| chr10:124657575
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.906+24032G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657575 | ||||||
| chr10:124657780
|
C | T | 299 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(296): Show | 302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): Show |
intron_variant | MODIFIER | c.906+23827G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124657780 | ||||||
| chr10:124658034
|
C | T | 53 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(50): Show | 53 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.906+23573G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124658034 | ||||||
| chr10:124658065
|
G | C | 2 | a0001c0001t0001g0272a0001c0001t0044g0030 | 2 | NA18960.hp2 NA19082.hp2 |
intron_variant | MODIFIER | c.906+23542C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124658065 | ||||||
| chr10:124658090
|
A | G | 1 | a0004c0005t0026g0236 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.906+23517T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124658090 | ||||||
| chr10:124658188
|
C | T | 1 | a0001c0001t0010g0222 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.906+23419G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124658188 | ||||||
| chr10:124658189
|
G | A | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.906+23418C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124658189 | ||||||
| chr10:124658218
|
T | C | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.906+23389A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124658218 | ||||||
| chr10:124658641
|
G | A | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.906+22966C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124658641 | ||||||
| chr10:124658713
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.906+22894G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124658713 | ||||||
| chr10:124658746
|
G | A | 1 | a0001c0001t0024g0262 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.906+22861C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124658746 | ||||||
| chr10:124658836
|
C | G | 32 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(29): Show | 32 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.906+22771G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124658836 | ||||||
| chr10:124659039
|
C | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0130a0001c0001t0001g0131others(14): Show | 18 | HG00558.hp1 HG00673.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.906+22568G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124659039 | ||||||
| chr10:124659119
|
T | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(86): Show | 90 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.906+22488A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124659119 | ||||||
| chr10:124659190
|
T | C | 1 | a0001c0001t0063g0063 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.906+22417A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124659190 | ||||||
| chr10:124659466
|
T | C | 10 | a0001c0001t0009g0284a0001c0001t0009g0320a0001c0001t0009g0321others(7): Show | 10 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(7): Show |
intron_variant | MODIFIER | c.906+22141A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124659466 | ||||||
| chr10:124659468
|
G | A | 4 | a0001c0001t0018g0289a0001c0001t0028g0287a0001c0001t0028g0288others(1): Show | 4 | NA18957.hp1 NA18960.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+22139C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124659468 | ||||||
| chr10:124659492
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.906+22115G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124659492 | ||||||
| chr10:124659705
|
A | G | 103 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0133others(100): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.906+21902T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124659705 | ||||||
| chr10:124659797
|
G | A | 2 | a0001c0001t0012g0050a0001c0001t0012g0054 | 2 | HG02572.hp2 HG02615.hp2 |
intron_variant | MODIFIER | c.906+21810C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124659797 | ||||||
| chr10:124659996
|
G | A | 190 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(187): Show | 192 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(189): Show |
intron_variant | MODIFIER | c.906+21611C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124659996 | ||||||
| chr10:124660192
|
T | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(86): Show | 90 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.906+21415A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124660192 | ||||||
| chr10:124660252
|
C | T | 3 | a0001c0001t0007g0263a0001c0001t0008g0259a0001c0001t0008g0260 | 3 | NA18967.hp2 NA18970.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.906+21355G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124660252 | ||||||
| chr10:124660299
|
A | G | 1 | a0001c0001t0045g0031 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.906+21308T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124660299 | ||||||
| chr10:124660578
|
C | G | 1 | a0001c0001t0011g0072 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.906+21029G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124660578 | ||||||
| chr10:124660708
|
T | A | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.906+20899A>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124660708 | ||||||
| chr10:124660822
|
G | A | 1 | a0001c0001t0013g0306 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.906+20785C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124660822 | ||||||
| chr10:124660823
|
C | A | 1 | a0001c0001t0013g0306 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.906+20784G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124660823 | ||||||
| chr10:124660847
|
T | C | 1 | a0001c0001t0025g0248 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.906+20760A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124660847 | ||||||
| chr10:124660880
|
T | G | 2 | a0001c0001t0009g0293a0001c0001t0009g0294 | 2 | HG01069.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.906+20727A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124660880 | ||||||
| chr10:124660962
|
C | T | 1 | a0001c0001t0002g0298 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.906+20645G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124660962 | ||||||
| chr10:124660974
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0004g0103a0002c0007t0001g0102 | 3 | HG03225.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.906+20633C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124660974 | ||||||
| chr10:124661056
|
T | TA | 28 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(25): Show | 28 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.906+20550dupT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124661056 | ||||||
| chr10:124661056
|
T | TAA | 6 | a0001c0001t0005g0028a0001c0001t0010g0036a0001c0001t0010g0064others(3): Show | 6 | HG02145.hp1 HG02818.hp2 NA18522.hp1 others(3): Show |
intron_variant | MODIFIER | c.906+20549_906+2055 others(6): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124661056 | ||||||
| chr10:124661056
|
T | TAAAA | 8 | a0001c0001t0003g0039a0001c0001t0003g0098a0001c0001t0006g0062others(5): Show | 8 | HG00323.hp1 HG01099.hp2 HG01169.hp2 others(5): Show |
intron_variant | MODIFIER | c.906+20547_906+2055 others(8): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124661056 | ||||||
| chr10:124661056
|
T | TAAAAA | 34 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(31): Show | 34 | HG00558.hp2 HG00639.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.906+20546_906+2055 others(9): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124661056 | ||||||
| chr10:124661056
|
T | TAAAAAA | 7 | a0001c0001t0003g0058a0001c0001t0003g0082a0001c0001t0006g0061others(4): Show | 7 | HG02040.hp2 HG02572.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.906+20545_906+2055 others(10): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124661056 | ||||||
| chr10:124661056
|
TA | T | 104 | a0001c0001t0001g0002a0001c0001t0001g0111a0001c0001t0001g0112others(101): Show | 105 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(102): Show |
intron_variant | MODIFIER | c.906+20550delT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124661056 | ||||||
| chr10:124661056
|
TAA | T | 8 | a0001c0001t0001g0131a0001c0001t0001g0166a0001c0001t0004g0280others(5): Show | 8 | HG01517.hp1 HG02896.hp1 NA18954.hp1 others(5): Show |
intron_variant | MODIFIER | c.906+20549_906+2055 others(6): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124661056 | ||||||
| chr10:124661056
|
TAAA | T | 99 | a0001c0001t0001g0035a0001c0001t0001g0133a0001c0001t0001g0134others(96): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.906+20548_906+2055 others(7): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124661056 | ||||||
| chr10:124661058
|
A | T | 1 | a0001c0001t0031g0049 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.906+20549T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124661058 | ||||||
| chr10:124661060
|
A | T | 1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.906+20547T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124661060 | ||||||
| chr10:124661434
|
A | G | 3 | a0001c0001t0015g0042a0001c0001t0015g0051a0001c0001t0015g0276 | 3 | HG02258.hp2 HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.906+20173T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124661434 | ||||||
| chr10:124661440
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0140a0001c0001t0001g0141others(3): Show | 7 | NA18947.hp2 NA18975.hp2 NA18984.hp1 others(4): Show |
intron_variant | MODIFIER | c.906+20167C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124661440 | ||||||
| chr10:124661772
|
A | G | 32 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(29): Show | 32 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.906+19835T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124661772 | ||||||
| chr10:124661847
|
C | T | 4 | a0001c0001t0002g0003a0001c0001t0002g0297a0001c0001t0002g0318others(1): Show | 5 | NA18969.hp2 NA19068.hp2 NA19085.hp1 others(2): Show |
intron_variant | MODIFIER | c.906+19760G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124661847 | ||||||
| chr10:124661883
|
G | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(87): Show | 91 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.906+19724C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124661883 | ||||||
| chr10:124662412
|
G | A | 1 | a0001c0001t0001g0272 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.906+19195C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124662412 | ||||||
| chr10:124662448
|
A | C | 38 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(35): Show | 38 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.906+19159T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124662448 | ||||||
| chr10:124662461
|
CCCATCCA others(1): Show |
C | 13 | a0001c0001t0001g0035a0001c0001t0001g0217a0001c0001t0007g0034others(10): Show | 13 | HG00099.hp2 HG01891.hp1 HG02074.hp2 others(10): Show |
intron_variant | MODIFIER | c.906+19138_906+1914 others(12): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124662461 | ||||||
| chr10:124662461
|
CCCATCCA others(5): Show |
C | 91 | a0001c0001t0001g0059a0001c0001t0001g0133a0001c0001t0001g0134others(88): Show | 93 | HG00140.hp1 HG00280.hp2 HG00323.hp2 others(90): Show |
intron_variant | MODIFIER | c.906+19134_906+1914 others(16): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124662461 | ||||||
| chr10:124662461
|
CCCATCCA others(9): Show |
C | 38 | a0001c0001t0001g0104a0001c0001t0004g0103a0001c0001t0005g0009others(35): Show | 38 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.906+19130_906+1914 others(20): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124662461 | ||||||
| chr10:124662461
|
CCCATCCA others(13): Show |
C | 161 | a0001c0001t0001g0002a0001c0001t0001g0070a0001c0001t0001g0078others(158): Show | 162 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.906+19126_906+1914 others(24): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124662461 | ||||||
| chr10:124662461
|
CCCATCCA others(21): Show |
C | 3 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0002g0324 | 3 | HG02071.hp1 HG02080.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.906+19118_906+1914 others(32): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124662461 | ||||||
| chr10:124662481
|
T | C | 38 | a0001c0001t0001g0104a0001c0001t0004g0103a0001c0001t0005g0009others(35): Show | 38 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(35): Show |
intron_variant | MODIFIER | c.906+19126A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124662481 | ||||||
| chr10:124662485
|
T | C | 86 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(83): Show | 87 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.906+19122A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124662485 | ||||||
| chr10:124662489
|
T | C | 2 | a0001c0001t0001g0131a0001c0001t0007g0187 | 2 | HG02071.hp2 NA18954.hp1 |
intron_variant | MODIFIER | c.906+19118A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124662489 | ||||||
| chr10:124662511
|
C | A | 32 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(29): Show | 32 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.906+19096G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124662511 | ||||||
| chr10:124662545
|
G | T | 1 | a0001c0001t0030g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.906+19062C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124662545 | ||||||
| chr10:124662668
|
T | G | 1 | a0001c0001t0071g0210 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.906+18939A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124662668 | ||||||
| chr10:124663251
|
T | C | 51 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(48): Show | 51 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(48): Show |
intron_variant | MODIFIER | c.906+18356A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124663251 | ||||||
| chr10:124663630
|
G | A | 1 | a0001c0001t0001g0245 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.906+17977C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124663630 | ||||||
| chr10:124663833
|
A | G | 304 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(301): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.906+17774T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124663833 | ||||||
| chr10:124663840
|
G | A | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG01081.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.906+17767C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124663840 | ||||||
| chr10:124663995
|
A | C | 5 | a0001c0001t0008g0257a0001c0001t0008g0258a0001c0001t0008g0261others(2): Show | 5 | HG02027.hp2 NA18948.hp2 NA18949.hp2 others(2): Show |
intron_variant | MODIFIER | c.906+17612T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124663995 | ||||||
| chr10:124664111
|
C | T | 47 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0143others(44): Show | 47 | HG00099.hp1 HG00280.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.906+17496G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124664111 | ||||||
| chr10:124664152
|
C | T | 1 | a0001c0001t0045g0031 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.906+17455G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124664152 | ||||||
| chr10:124664356
|
G | A | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.906+17251C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124664356 | ||||||
| chr10:124664398
|
C | G | 31 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.906+17209G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124664398 | ||||||
| chr10:124664788
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0231 | 2 | HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.906+16819T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124664788 | ||||||
| chr10:124665245
|
A | G | 1 | a0001c0001t0001g0179 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.906+16362T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124665245 | ||||||
| chr10:124665296
|
G | A | 67 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0143others(64): Show | 67 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(64): Show |
intron_variant | MODIFIER | c.906+16311C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124665296 | ||||||
| chr10:124665386
|
A | G | 1 | a0001c0001t0009g0320 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.906+16221T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124665386 | ||||||
| chr10:124665494
|
C | T | 1 | a0001c0001t0059g0128 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.906+16113G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124665494 | ||||||
| chr10:124665916
|
T | A | 54 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(51): Show | 54 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.906+15691A>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124665916 | ||||||
| chr10:124665917
|
CGGCTACG others(11): Show |
C | 54 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(51): Show | 54 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.906+15672_906+1568 others(22): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124665917 | ||||||
| chr10:124665923
|
C | T | 30 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.906+15684G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124665923 | ||||||
| chr10:124665985
|
G | C | 103 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0133others(100): Show | 105 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(102): Show |
intron_variant | MODIFIER | c.906+15622C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124665985 | ||||||
| chr10:124666169
|
T | C | 308 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(305): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.906+15438A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124666169 | ||||||
| chr10:124666256
|
G | A | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.906+15351C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124666256 | ||||||
| chr10:124666560
|
C | T | 178 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(175): Show | 180 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(177): Show |
intron_variant | MODIFIER | c.906+15047G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124666560 | ||||||
| chr10:124666567
|
G | T | 4 | a0001c0001t0001g0104a0001c0001t0004g0103a0001c0001t0033g0122others(1): Show | 4 | HG03209.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+15040C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124666567 | ||||||
| chr10:124666671
|
C | A | 1 | a0001c0001t0085g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.906+14936G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124666671 | ||||||
| chr10:124666767
|
G | A | 1 | a0001c0001t0001g0153 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.906+14840C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124666767 | ||||||
| chr10:124666801
|
G | A | 1 | a0001c0001t0009g0293 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.906+14806C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124666801 | ||||||
| chr10:124666864
|
C | A | 1 | a0001c0001t0009g0293 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.906+14743G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124666864 | ||||||
| chr10:124666908
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.906+14699C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124666908 | ||||||
| chr10:124667015
|
G | C | 4 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(1): Show | 4 | NA18957.hp2 NA18962.hp1 NA18969.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+14592C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124667015 | ||||||
| chr10:124667093
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.906+14514G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124667093 | ||||||
| chr10:124667185
|
T | C | 1 | a0001c0001t0001g0193 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.906+14422A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124667185 | ||||||
| chr10:124667212
|
C | A | 1 | a0001c0001t0003g0077 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.906+14395G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124667212 | ||||||
| chr10:124667324
|
A | G | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.906+14283T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124667324 | ||||||
| chr10:124667464
|
CCCCCACC others(21): Show |
C | 1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.906+14115_906+1414 others(32): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124667464 | ||||||
| chr10:124667532
|
G | A | 2 | a0001c0001t0002g0315a0001c0001t0002g0316 | 2 | NA18942.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.906+14075C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124667532 | ||||||
| chr10:124667693
|
T | C | 302 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(299): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.906+13914A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124667693 | ||||||
| chr10:124667727
|
A | G | 3 | a0001c0001t0004g0116a0001c0001t0004g0119a0001c0001t0050g0107 | 3 | HG02055.hp2 HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.906+13880T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124667727 | ||||||
| chr10:124667754
|
G | A | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.906+13853C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124667754 | ||||||
| chr10:124667907
|
G | A | 1 | a0001c0001t0001g0059 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.906+13700C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124667907 | ||||||
| chr10:124668243
|
G | A | 1 | a0001c0001t0085g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.906+13364C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124668243 | ||||||
| chr10:124668271
|
T | G | 143 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0111others(140): Show | 144 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(141): Show |
intron_variant | MODIFIER | c.906+13336A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124668271 | ||||||
| chr10:124668637
|
T | C | 1 | a0001c0001t0031g0049 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.906+12970A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124668637 | ||||||
| chr10:124668672
|
G | A | 1 | a0001c0001t0001g0165 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.906+12935C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124668672 | ||||||
| chr10:124668709
|
T | C | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.906+12898A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124668709 | ||||||
| chr10:124668781
|
G | A | 31 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.906+12826C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124668781 | ||||||
| chr10:124668783
|
T | C | 107 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0133others(104): Show | 109 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(106): Show |
intron_variant | MODIFIER | c.906+12824A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124668783 | ||||||
| chr10:124668800
|
T | TA | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.906+12806dupT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124668800 | ||||||
| chr10:124669007
|
G | A | 1 | a0001c0001t0020g0007 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.906+12600C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669007 | ||||||
| chr10:124669041
|
C | A | 2 | a0001c0001t0006g0277a0001c0001t0006g0278 | 2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.906+12566G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669041 | ||||||
| chr10:124669065
|
C | T | 9 | a0001c0001t0001g0035a0001c0001t0001g0183a0001c0001t0001g0193others(6): Show | 9 | HG00423.hp1 NA18939.hp1 NA18949.hp1 others(6): Show |
intron_variant | MODIFIER | c.906+12542G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669065 | ||||||
| chr10:124669088
|
G | A | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.906+12519C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669088 | ||||||
| chr10:124669129
|
G | T | 1 | a0001c0001t0010g0222 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.906+12478C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669129 | ||||||
| chr10:124669351
|
C | G | 31 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.906+12256G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669351 | ||||||
| chr10:124669394
|
C | A | 243 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(240): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(243): Show |
intron_variant | MODIFIER | c.906+12213G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669394 | ||||||
| chr10:124669412
|
T | C | 101 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0133others(98): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.906+12195A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669412 | ||||||
| chr10:124669477
|
G | A | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.906+12130C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669477 | ||||||
| chr10:124669492
|
C | A | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.906+12115G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669492 | ||||||
| chr10:124669504
|
G | T | 150 | a0001c0001t0001g0002a0001c0001t0001g0070a0001c0001t0001g0078others(147): Show | 151 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(148): Show |
intron_variant | MODIFIER | c.906+12103C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669504 | ||||||
| chr10:124669519
|
G | A | 1 | a0001c0001t0033g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906+12088C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669519 | ||||||
| chr10:124669525
|
G | A | 112 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(109): Show | 112 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(109): Show |
intron_variant | MODIFIER | c.906+12082C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669525 | ||||||
| chr10:124669605
|
T | C | 89 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(86): Show | 90 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.906+12002A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669605 | ||||||
| chr10:124669631
|
G | A | 1 | a0001c0001t0031g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.906+11976C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669631 | ||||||
| chr10:124669745
|
C | T | 58 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0133others(55): Show | 58 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(55): Show |
intron_variant | MODIFIER | c.906+11862G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669745 | ||||||
| chr10:124669787
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.906+11820C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669787 | ||||||
| chr10:124669844
|
G | A | 89 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(86): Show | 90 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.906+11763C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669844 | ||||||
| chr10:124669911
|
TAGGGTGG others(11): Show |
T | 261 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(258): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.906+11678_906+1169 others(22): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669911 | ||||||
| chr10:124669913
|
GGGTGGGT others(10): Show |
G | 1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.906+11677_906+1169 others(21): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669913 | ||||||
| chr10:124669929
|
C | CAGGGTGG others(11): Show |
1 | a0001c0001t0004g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.906+11677_906+1167 others(22): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669929 | ||||||
| chr10:124669974
|
T | C | 4 | a0001c0001t0001g0175a0001c0001t0031g0049a0001c0001t0031g0106others(1): Show | 4 | HG02738.hp2 HG03834.hp2 HG03927.hp2 others(1): Show |
intron_variant | MODIFIER | c.906+11633A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124669974 | ||||||
| chr10:124670154
|
C | G | 31 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.906+11453G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124670154 | ||||||
| chr10:124670190
|
G | A | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.906+11417C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124670190 | ||||||
| chr10:124670193
|
CCTGA | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(87): Show | 91 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(88): Show |
intron_variant | MODIFIER | c.906+11410_906+1141 others(8): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124670193 | ||||||
| chr10:124670233
|
C | G | 1 | a0001c0001t0015g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.906+11374G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124670233 | ||||||
| chr10:124670264
|
C | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(86): Show | 90 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(87): Show |
intron_variant | MODIFIER | c.906+11343G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124670264 | ||||||
| chr10:124670283
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.906+11324G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124670283 | ||||||
| chr10:124670296
|
A | C | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.906+11311T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124670296 | ||||||
| chr10:124670321
|
G | A | 5 | a0001c0001t0001g0152a0001c0001t0001g0153a0001c0001t0001g0160others(2): Show | 5 | HG01934.hp2 HG01943.hp1 HG01952.hp1 others(2): Show |
intron_variant | MODIFIER | c.906+11286C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124670321 | ||||||
| chr10:124670531
|
C | A | 88 | a0001c0001t0001g0129a0001c0001t0001g0145a0001c0001t0001g0150others(85): Show | 88 | HG00099.hp1 HG00140.hp2 HG00408.hp1 others(85): Show |
intron_variant | MODIFIER | c.906+11076G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124670531 | ||||||
| chr10:124670554
|
G | A | 9 | a0001c0001t0005g0028a0001c0001t0015g0121a0001c0001t0030g0005others(6): Show | 9 | HG01943.hp2 HG02280.hp1 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.906+11053C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124670554 | ||||||
| chr10:124670563
|
G | A | 4 | a0001c0001t0001g0130a0001c0001t0018g0289a0001c0001t0028g0288others(1): Show | 4 | HG00673.hp1 NA18957.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+11044C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124670563 | ||||||
| chr10:124670572
|
G | A | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.906+11035C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124670572 | ||||||
| chr10:124670689
|
C | T | 1 | a0001c0003t0003g0076 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.906+10918G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124670689 | ||||||
| chr10:124670707
|
T | C | 2 | a0001c0001t0016g0177a0001c0001t0066g0178 | 2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.906+10900A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124670707 | ||||||
| chr10:124670812
|
G | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0172 | 2 | HG02135.hp2 NA18998.hp2 |
intron_variant | MODIFIER | c.906+10795C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124670812 | ||||||
| chr10:124671006
|
G | A | 53 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(50): Show | 53 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.906+10601C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124671006 | ||||||
| chr10:124671025
|
G | C | 1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.906+10582C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124671025 | ||||||
| chr10:124671026
|
C | G | 1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.906+10581G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124671026 | ||||||
| chr10:124671058
|
G | A | 1 | a0001c0001t0009g0322 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.906+10549C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124671058 | ||||||
| chr10:124671189
|
T | G | 1 | a0001c0001t0001g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.906+10418A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124671189 | ||||||
| chr10:124671354
|
G | A | 2 | a0001c0001t0002g0291a0001c0001t0002g0302 | 2 | NA19082.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.906+10253C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124671354 | ||||||
| chr10:124671585
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.906+10022C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124671585 | ||||||
| chr10:124671695
|
C | T | 2 | a0001c0001t0002g0291a0001c0001t0002g0302 | 2 | NA19082.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.906+9912G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124671695 | ||||||
| chr10:124671823
|
G | A | 2 | a0001c0001t0016g0177a0001c0001t0066g0178 | 2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.906+9784C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124671823 | ||||||
| chr10:124671933
|
C | T | 302 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(299): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.906+9674G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124671933 | ||||||
| chr10:124672018
|
C | T | 1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.906+9589G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124672018 | ||||||
| chr10:124672020
|
G | A | 30 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.906+9587C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124672020 | ||||||
| chr10:124672187
|
T | C | 4 | a0001c0001t0001g0104a0001c0001t0004g0103a0001c0001t0033g0122others(1): Show | 4 | HG03209.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+9420A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124672187 | ||||||
| chr10:124672265
|
G | A | 1 | a0001c0001t0008g0260 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.906+9342C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124672265 | ||||||
| chr10:124672340
|
G | C | 3 | a0001c0001t0022g0055a0001c0001t0022g0056a0001c0001t0051g0057 | 3 | HG01099.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.906+9267C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124672340 | ||||||
| chr10:124672382
|
G | A | 2 | a0001c0001t0003g0097a0001c0001t0003g0099 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.906+9225C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124672382 | ||||||
| chr10:124672476
|
A | G | 1 | a0001c0001t0033g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.906+9131T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124672476 | ||||||
| chr10:124672906
|
A | G | 1 | a0001c0001t0008g0259 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.906+8701T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124672906 | ||||||
| chr10:124672990
|
G | A | 2 | a0001c0001t0016g0201a0001c0001t0016g0202 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.906+8617C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124672990 | ||||||
| chr10:124673143
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.906+8464G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124673143 | ||||||
| chr10:124673374
|
G | A | 1 | a0001c0001t0006g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.906+8233C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124673374 | ||||||
| chr10:124673394
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.906+8213G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124673394 | ||||||
| chr10:124673414
|
G | A | 1 | a0001c0001t0033g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.906+8193C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124673414 | ||||||
| chr10:124673469
|
G | A | 1 | a0001c0001t0039g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.906+8138C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124673469 | ||||||
| chr10:124673525
|
A | G | 1 | a0001c0001t0004g0280 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.906+8082T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124673525 | ||||||
| chr10:124673798
|
G | A | 2 | a0001c0001t0027g0223a0003c0006t0084g0240 | 2 | NA18946.hp1 NA19086.hp1 |
intron_variant | MODIFIER | c.906+7809C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124673798 | ||||||
| chr10:124673895
|
C | T | 1 | a0001c0001t0030g0005 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.906+7712G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124673895 | ||||||
| chr10:124673984
|
G | C | 1 | a0001c0001t0006g0043 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.906+7623C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124673984 | ||||||
| chr10:124674079
|
C | G | 76 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(73): Show | 76 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(73): Show |
intron_variant | MODIFIER | c.906+7528G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124674079 | ||||||
| chr10:124674178
|
C | T | 1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.906+7429G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124674178 | ||||||
| chr10:124674180
|
T | C | 1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.906+7427A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124674180 | ||||||
| chr10:124674294
|
C | T | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.906+7313G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124674294 | ||||||
| chr10:124674451
|
G | A | 13 | a0001c0001t0001g0135a0001c0001t0001g0144a0001c0001t0001g0158others(10): Show | 13 | HG00280.hp1 HG01071.hp2 HG01106.hp1 others(10): Show |
intron_variant | MODIFIER | c.906+7156C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124674451 | ||||||
| chr10:124674583
|
C | T | 2 | a0001c0001t0002g0302a0001c0001t0025g0248 | 2 | NA18962.hp2 NA19082.hp1 |
intron_variant | MODIFIER | c.906+7024G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124674583 | ||||||
| chr10:124674616
|
G | A | 1 | a0001c0001t0002g0318 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.906+6991C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124674616 | ||||||
| chr10:124674669
|
C | G | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.906+6938G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124674669 | ||||||
| chr10:124674694
|
A | C | 1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.906+6913T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124674694 | ||||||
| chr10:124674694
|
A | G | 2 | a0001c0001t0018g0292a0001c0001t0018g0295 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.906+6913T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124674694 | ||||||
| chr10:124674836
|
A | G | 1 | a0001c0001t0068g0270 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.906+6771T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124674836 | ||||||
| chr10:124675267
|
G | C | 1 | a0001c0001t0085g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.906+6340C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124675267 | ||||||
| chr10:124675575
|
T | C | 2 | a0001c0001t0016g0201a0001c0001t0016g0202 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.906+6032A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124675575 | ||||||
| chr10:124675601
|
G | A | 1 | a0001c0001t0030g0005 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.906+6006C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124675601 | ||||||
| chr10:124675775
|
C | A | 2 | a0001c0001t0019g0016a0001c0001t0019g0027 | 2 | NA18947.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.906+5832G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124675775 | ||||||
| chr10:124675904
|
A | G | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.906+5703T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124675904 | ||||||
| chr10:124675997
|
C | T | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.906+5610G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124675997 | ||||||
| chr10:124676070
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.906+5537C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124676070 | ||||||
| chr10:124676076
|
C | T | 1 | a0001c0001t0014g0094 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.906+5531G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124676076 | ||||||
| chr10:124676174
|
C | T | 1 | a0001c0001t0015g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.906+5433G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124676174 | ||||||
| chr10:124676204
|
A | C | 31 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.906+5403T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124676204 | ||||||
| chr10:124676212
|
T | G | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.906+5395A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124676212 | ||||||
| chr10:124676217
|
T | C | 23 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0112others(20): Show | 23 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.906+5390A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124676217 | ||||||
| chr10:124676501
|
C | A | 1 | a0001c0001t0005g0018 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.906+5106G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124676501 | ||||||
| chr10:124676521
|
G | C | 2 | a0001c0001t0003g0068a0001c0001t0011g0069 | 2 | NA18973.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.906+5086C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124676521 | ||||||
| chr10:124676556
|
C | G | 304 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(301): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.906+5051G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124676556 | ||||||
| chr10:124676615
|
G | A | 27 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(24): Show | 27 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.906+4992C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124676615 | ||||||
| chr10:124676618
|
TG | T | 308 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(305): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.906+4988delC | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124676618 | ||||||
| chr10:124676678
|
T | C | 1 | a0001c0001t0014g0094 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.906+4929A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124676678 | ||||||
| chr10:124677041
|
G | C | 1 | a0001c0001t0027g0170 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.906+4566C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124677041 | ||||||
| chr10:124677109
|
C | A | 2 | a0001c0001t0019g0016a0001c0001t0019g0027 | 2 | NA18947.hp1 NA18963.hp2 |
intron_variant | MODIFIER | c.906+4498G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124677109 | ||||||
| chr10:124677118
|
G | A | 1 | a0001c0001t0052g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.906+4489C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124677118 | ||||||
| chr10:124677138
|
C | A | 1 | a0001c0001t0001g0129 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.906+4469G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124677138 | ||||||
| chr10:124677163
|
C | T | 5 | a0001c0001t0014g0038a0001c0001t0014g0093a0001c0001t0014g0094others(2): Show | 5 | HG00735.hp1 HG01123.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.906+4444G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124677163 | ||||||
| chr10:124677255
|
A | G | 16 | a0001c0001t0003g0039a0001c0001t0003g0068a0001c0001t0003g0071others(13): Show | 16 | HG00558.hp2 HG02132.hp1 NA18939.hp2 others(13): Show |
intron_variant | MODIFIER | c.906+4352T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124677255 | ||||||
| chr10:124677444
|
G | A | 245 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(242): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.906+4163C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124677444 | ||||||
| chr10:124677509
|
G | A | 1 | a0001c0001t0040g0008 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.906+4098C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124677509 | ||||||
| chr10:124677518
|
A | C | 1 | a0001c0001t0001g0218 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.906+4089T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124677518 | ||||||
| chr10:124677669
|
T | C | 38 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(35): Show | 38 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.906+3938A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124677669 | ||||||
| chr10:124677760
|
G | A | 1 | a0001c0001t0050g0107 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.906+3847C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124677760 | ||||||
| chr10:124677888
|
C | G | 1 | a0001c0001t0001g0175 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.906+3719G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124677888 | ||||||
| chr10:124677889
|
G | A | 11 | a0001c0001t0001g0002a0001c0001t0001g0130a0001c0001t0001g0139others(8): Show | 12 | HG00673.hp1 NA18944.hp2 NA18947.hp2 others(9): Show |
intron_variant | MODIFIER | c.906+3718C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124677889 | ||||||
| chr10:124678232
|
G | C | 1 | a0001c0001t0002g0301 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.906+3375C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124678232 | ||||||
| chr10:124678362
|
T | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(190): Show | 196 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(193): Show |
intron_variant | MODIFIER | c.906+3245A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124678362 | ||||||
| chr10:124678603
|
T | A | 318 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(315): Show | 321 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(318): Show |
intron_variant | MODIFIER | c.906+3004A>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124678603 | ||||||
| chr10:124678728
|
G | A | 2 | a0001c0001t0003g0068a0001c0001t0011g0069 | 2 | NA18973.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.906+2879C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124678728 | ||||||
| chr10:124678808
|
C | T | 4 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0030g0010others(1): Show | 4 | HG00140.hp2 HG01168.hp2 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.906+2799G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124678808 | ||||||
| chr10:124679153
|
G | A | 3 | a0001c0001t0032g0267a0001c0001t0057g0268a0001c0003t0058g0269 | 3 | HG00423.hp2 NA18986.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.906+2454C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124679153 | ||||||
| chr10:124679238
|
G | A | 1 | a0001c0001t0028g0287 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.906+2369C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124679238 | ||||||
| chr10:124679249
|
C | T | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.906+2358G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124679249 | ||||||
| chr10:124679353
|
G | A | 1 | a0001c0001t0004g0279 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.906+2254C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124679353 | ||||||
| chr10:124679365
|
C | T | 1 | a0001c0001t0001g0179 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.906+2242G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124679365 | ||||||
| chr10:124679387
|
C | A | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.906+2220G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124679387 | ||||||
| chr10:124679399
|
C | T | 29 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(26): Show | 29 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.906+2208G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124679399 | ||||||
| chr10:124679481
|
C | G | 2 | a0001c0001t0006g0088a0001c0001t0006g0089 | 2 | HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.906+2126G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124679481 | ||||||
| chr10:124679550
|
C | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.906+2057G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124679550 | ||||||
| chr10:124679589
|
A | G | 29 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(26): Show | 29 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.906+2018T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124679589 | ||||||
| chr10:124679797
|
C | T | 191 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(188): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.906+1810G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124679797 | ||||||
| chr10:124679809
|
G | A | 1 | a0005c0004t0086g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.906+1798C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124679809 | ||||||
| chr10:124680006
|
G | C | 1 | a0001c0001t0088g0311 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.906+1601C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124680006 | ||||||
| chr10:124680171
|
A | C | 1 | a0001c0001t0001g0232 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.906+1436T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124680171 | ||||||
| chr10:124680181
|
G | A | 2 | a0001c0001t0012g0046a0001c0001t0082g0045 | 2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.906+1426C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124680181 | ||||||
| chr10:124680230
|
G | C | 17 | a0001c0001t0001g0002a0001c0001t0001g0130a0001c0001t0001g0131others(14): Show | 18 | HG00558.hp1 HG00673.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.906+1377C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124680230 | ||||||
| chr10:124680583
|
G | A | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.906+1024C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124680583 | ||||||
| chr10:124680887
|
A | G | 2 | a0001c0001t0012g0046a0001c0001t0082g0045 | 2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.906+720T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124680887 | ||||||
| chr10:124680897
|
C | T | 3 | a0001c0001t0004g0116a0001c0001t0004g0119a0001c0001t0050g0107 | 3 | HG02055.hp2 HG02723.hp1 HG02896.hp1 |
intron_variant | MODIFIER | c.906+710G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124680897 | ||||||
| chr10:124680950
|
C | T | 5 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(2): Show | 5 | NA18957.hp2 NA18962.hp1 NA18969.hp1 others(2): Show |
intron_variant | MODIFIER | c.906+657G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124680950 | ||||||
| chr10:124681045
|
T | C | 5 | a0001c0001t0014g0038a0001c0001t0014g0093a0001c0001t0014g0094others(2): Show | 5 | HG00735.hp1 HG01123.hp1 HG01361.hp2 others(2): Show |
intron_variant | MODIFIER | c.906+562A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124681045 | ||||||
| chr10:124681157
|
G | A | 1 | a0004c0005t0026g0236 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.906+450C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124681157 | ||||||
| chr10:124681202
|
G | A | 1 | a0001c0001t0054g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.906+405C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124681202 | ||||||
| chr10:124681260
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0004g0103a0002c0007t0001g0102 | 3 | HG03225.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.906+347C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124681260 | ||||||
| chr10:124681430
|
C | T | 1 | a0001c0001t0037g0325 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.906+177G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124681430 | ||||||
| chr10:124681498
|
C | T | 53 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(50): Show | 53 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.906+109G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124681498 | ||||||
| chr10:124682429
|
C | T | 1 | a0001c0001t0002g0296 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.134-50G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124682429 | ||||||
| chr10:124682461
|
G | A | 2 | a0001c0001t0018g0292a0001c0001t0018g0295 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.134-82C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124682461 | ||||||
| chr10:124682505
|
T | A | 1 | a0001c0001t0008g0260 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.134-126A>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124682505 | ||||||
| chr10:124682551
|
G | C | 1 | a0001c0001t0033g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.134-172C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124682551 | ||||||
| chr10:124682583
|
T | C | 1 | a0001c0001t0024g0262 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.134-204A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124682583 | ||||||
| chr10:124683388
|
C | T | 88 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(85): Show | 89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): Show |
intron_variant | MODIFIER | c.134-1009G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124683388 | ||||||
| chr10:124683428
|
C | T | 1 | a0001c0001t0033g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.134-1049G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124683428 | ||||||
| chr10:124683494
|
C | A | 1 | a0001c0001t0085g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.134-1115G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124683494 | ||||||
| chr10:124683561
|
C | G | 1 | a0001c0001t0004g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.134-1182G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124683561 | ||||||
| chr10:124683737
|
CCTGA | C | 99 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0133others(96): Show | 101 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(98): Show |
intron_variant | MODIFIER | c.134-1362_134-1359d others(6): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124683737 | ||||||
| chr10:124683933
|
T | G | 4 | a0001c0001t0001g0104a0001c0001t0004g0103a0001c0001t0033g0122others(1): Show | 4 | HG03209.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-1554A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124683933 | ||||||
| chr10:124683997
|
A | C | 1 | a0001c0001t0082g0045 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.134-1618T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124683997 | ||||||
| chr10:124684356
|
G | A | 2 | a0001c0001t0001g0035a0001c0001t0007g0211 | 2 | NA19010.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.134-1977C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124684356 | ||||||
| chr10:124684449
|
C | A | 1 | a0001c0001t0033g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.134-2070G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124684449 | ||||||
| chr10:124684491
|
G | A | 1 | a0001c0001t0066g0178 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.134-2112C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124684491 | ||||||
| chr10:124684552
|
C | T | 2 | a0001c0001t0034g0227a0001c0001t0046g0032 | 2 | HG03688.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.134-2173G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124684552 | ||||||
| chr10:124684676
|
G | A | 4 | a0001c0001t0001g0139a0001c0001t0001g0173a0001c0001t0001g0188others(1): Show | 4 | NA18944.hp2 NA18948.hp1 NA18989.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-2297C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124684676 | ||||||
| chr10:124684744
|
C | T | 53 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(50): Show | 53 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.134-2365G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124684744 | ||||||
| chr10:124685270
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.134-2891G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124685270 | ||||||
| chr10:124685510
|
G | A | 1 | a0001c0001t0001g0151 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.134-3131C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124685510 | ||||||
| chr10:124685558
|
G | A | 2 | a0001c0001t0017g0189a0004c0005t0026g0236 | 2 | HG03139.hp2 NA19003.hp2 |
intron_variant | MODIFIER | c.134-3179C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124685558 | ||||||
| chr10:124685777
|
T | C | 5 | a0001c0001t0010g0036a0001c0001t0010g0064a0001c0001t0010g0066others(2): Show | 5 | HG02145.hp1 HG02818.hp2 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.134-3398A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124685777 | ||||||
| chr10:124685861
|
T | C | 29 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(26): Show | 29 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.134-3482A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124685861 | ||||||
| chr10:124685885
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.134-3506G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124685885 | ||||||
| chr10:124686056
|
A | C | 1 | a0001c0001t0008g0259 | 1 | NA18995.hp1 | intron_variant | MODIFIER | c.134-3677T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124686056 | ||||||
| chr10:124686114
|
C | G | 1 | a0001c0001t0001g0141 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.134-3735G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124686114 | ||||||
| chr10:124686122
|
T | C | 2 | a0001c0001t0011g0244a0001c0001t0061g0243 | 2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.134-3743A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124686122 | ||||||
| chr10:124686239
|
T | G | 1 | a0001c0001t0001g0070 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.134-3860A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124686239 | ||||||
| chr10:124686328
|
TAC | T | 4 | a0001c0001t0001g0104a0001c0001t0004g0103a0001c0001t0033g0122others(1): Show | 4 | HG03209.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.134-3951_134-3950d others(4): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124686328 | ||||||
| chr10:124686343
|
T | C | 1 | a0001c0001t0067g0184 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.134-3964A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124686343 | ||||||
| chr10:124686536
|
A | C | 1 | a0001c0001t0033g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.134-4157T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124686536 | ||||||
| chr10:124686627
|
G | T | 305 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(302): Show | 308 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
intron_variant | MODIFIER | c.134-4248C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124686627 | ||||||
| chr10:124686683
|
C | T | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.134-4304G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124686683 | ||||||
| chr10:124686710
|
C | A | 1 | a0001c0001t0012g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.134-4331G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124686710 | ||||||
| chr10:124686734
|
T | C | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.134-4355A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124686734 | ||||||
| chr10:124687039
|
G | C | 101 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0133others(98): Show | 103 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(100): Show |
intron_variant | MODIFIER | c.134-4660C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124687039 | ||||||
| chr10:124687217
|
G | A | 4 | a0001c0001t0022g0055a0001c0001t0022g0056a0001c0001t0022g0065others(1): Show | 4 | HG01099.hp2 HG01168.hp1 HG01169.hp2 others(1): Show |
intron_variant | MODIFIER | c.134-4838C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124687217 | ||||||
| chr10:124687354
|
T | C | 1 | a0001c0001t0091g0326 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.134-4975A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124687354 | ||||||
| chr10:124687561
|
C | T | 3 | a0001c0001t0001g0215a0001c0001t0016g0201a0001c0001t0016g0202 | 3 | HG01069.hp2 HG01071.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.134-5182G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124687561 | ||||||
| chr10:124688110
|
A | T | 54 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(51): Show | 54 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.134-5731T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124688110 | ||||||
| chr10:124688152
|
A | G | 1 | a0001c0001t0028g0288 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.134-5773T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124688152 | ||||||
| chr10:124688313
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.134-5934G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124688313 | ||||||
| chr10:124688743
|
T | C | 1 | a0001c0001t0030g0005 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.134-6364A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124688743 | ||||||
| chr10:124688997
|
A | T | 2 | a0001c0001t0004g0115a0001c0001t0004g0118 | 2 | HG02257.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.134-6618T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124688997 | ||||||
| chr10:124689116
|
A | G | 304 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(301): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.134-6737T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124689116 | ||||||
| chr10:124689128
|
G | A | 1 | a0001c0003t0003g0076 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.134-6749C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124689128 | ||||||
| chr10:124689254
|
C | T | 2 | a0001c0001t0001g0139a0001c0001t0001g0161 | 2 | HG02132.hp2 NA18948.hp1 |
intron_variant | MODIFIER | c.134-6875G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124689254 | ||||||
| chr10:124689272
|
G | C | 31 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.133+6886C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124689272 | ||||||
| chr10:124689678
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.133+6480C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124689678 | ||||||
| chr10:124689837
|
T | A | 1 | a0001c0001t0009g0323 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.133+6321A>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124689837 | ||||||
| chr10:124689992
|
A | G | 1 | a0001c0001t0004g0116 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.133+6166T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124689992 | ||||||
| chr10:124689997
|
C | A | 1 | a0001c0001t0003g0071 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.133+6161G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124689997 | ||||||
| chr10:124690115
|
C | A | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.133+6043G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124690115 | ||||||
| chr10:124690263
|
C | A | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.133+5895G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124690263 | ||||||
| chr10:124690638
|
T | G | 4 | a0001c0001t0016g0168a0001c0001t0017g0185a0001c0001t0067g0184others(1): Show | 4 | HG00558.hp1 NA18963.hp1 NA18980.hp2 others(1): Show |
intron_variant | MODIFIER | c.133+5520A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124690638 | ||||||
| chr10:124690820
|
G | A | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.133+5338C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124690820 | ||||||
| chr10:124690834
|
T | G | 34 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(31): Show | 34 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(31): Show |
intron_variant | MODIFIER | c.133+5324A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124690834 | ||||||
| chr10:124691043
|
T | C | 1 | a0001c0001t0012g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.133+5115A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124691043 | ||||||
| chr10:124691166
|
C | T | 1 | a0001c0001t0033g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.133+4992G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124691166 | ||||||
| chr10:124691608
|
G | C | 6 | a0001c0001t0001g0104a0001c0001t0004g0103a0001c0001t0033g0122others(3): Show | 6 | HG01891.hp1 HG03209.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.133+4550C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124691608 | ||||||
| chr10:124691693
|
T | C | 1 | a0001c0001t0054g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.133+4465A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124691693 | ||||||
| chr10:124691706
|
G | C | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.133+4452C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124691706 | ||||||
| chr10:124691769
|
G | A | 54 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(51): Show | 54 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.133+4389C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124691769 | ||||||
| chr10:124691834
|
C | T | 2 | a0001c0001t0005g0009a0001c0001t0005g0011 | 2 | HG00140.hp2 HG04204.hp1 |
intron_variant | MODIFIER | c.133+4324G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124691834 | ||||||
| chr10:124691910
|
A | C | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.133+4248T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124691910 | ||||||
| chr10:124692095
|
T | C | 1 | a0001c0001t0054g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.133+4063A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124692095 | ||||||
| chr10:124692332
|
G | T | 53 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0112others(50): Show | 53 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.133+3826C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124692332 | ||||||
| chr10:124692360
|
G | T | 3 | a0001c0001t0001g0104a0001c0001t0004g0103a0002c0007t0001g0102 | 3 | HG03225.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.133+3798C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124692360 | ||||||
| chr10:124692500
|
A | T | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.133+3658T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124692500 | ||||||
| chr10:124692714
|
C | CA | 81 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0129others(78): Show | 82 | HG00099.hp1 HG00408.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.133+3443dupT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124692714 | ||||||
| chr10:124692714
|
C | CAA | 33 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(30): Show | 33 | HG00280.hp1 HG01071.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.133+3442_133+3443d others(4): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124692714 | ||||||
| chr10:124692714
|
CA | C | 97 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0133others(94): Show | 99 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(96): Show |
intron_variant | MODIFIER | c.133+3443delT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124692714 | ||||||
| chr10:124692714
|
CAA | C | 10 | a0001c0001t0001g0193a0001c0001t0001g0197a0001c0001t0001g0219others(7): Show | 10 | HG00423.hp1 HG01074.hp1 HG01517.hp2 others(7): Show |
intron_variant | MODIFIER | c.133+3442_133+3443d others(4): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124692714 | ||||||
| chr10:124692714
|
CAAAAAAA others(6): Show |
C | 2 | a0001c0001t0006g0277a0001c0001t0006g0278 | 2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.133+3431_133+3443d others(15): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124692714 | ||||||
| chr10:124692860
|
C | T | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.133+3298G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124692860 | ||||||
| chr10:124693026
|
A | G | 1 | a0001c0001t0005g0028 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.133+3132T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693026 | ||||||
| chr10:124693121
|
C | T | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.133+3037G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693121 | ||||||
| chr10:124693137
|
A | G | 3 | a0001c0001t0001g0183a0001c0001t0001g0216a0001c0001t0029g0006 | 3 | HG00609.hp2 NA18975.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.133+3021T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693137 | ||||||
| chr10:124693190
|
C | T | 1 | a0001c0001t0039g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.133+2968G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693190 | ||||||
| chr10:124693194
|
G | A | 4 | a0001c0001t0001g0104a0001c0001t0004g0103a0001c0001t0033g0122others(1): Show | 4 | HG03209.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+2964C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693194 | ||||||
| chr10:124693367
|
G | C | 1 | a0001c0001t0012g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.133+2791C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693367 | ||||||
| chr10:124693383
|
C | T | 304 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(301): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.133+2775G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693383 | ||||||
| chr10:124693388
|
T | C | 54 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0112others(51): Show | 54 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(51): Show |
intron_variant | MODIFIER | c.133+2770A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693388 | ||||||
| chr10:124693405
|
C | T | 1 | a0001c0001t0001g0114 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.133+2753G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693405 | ||||||
| chr10:124693431
|
C | T | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.133+2727G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693431 | ||||||
| chr10:124693454
|
G | T | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.133+2704C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693454 | ||||||
| chr10:124693466
|
CA | C | 32 | a0001c0001t0001g0113a0001c0001t0002g0313a0001c0001t0005g0009others(29): Show | 32 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.133+2691delT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693466 | ||||||
| chr10:124693513
|
G | A | 1 | a0001c0001t0085g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.133+2645C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693513 | ||||||
| chr10:124693625
|
C | T | 1 | a0001c0001t0009g0322 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.133+2533G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693625 | ||||||
| chr10:124693630
|
C | T | 2 | a0001c0001t0009g0293a0001c0001t0009g0294 | 2 | HG01069.hp1 HG02602.hp1 |
intron_variant | MODIFIER | c.133+2528G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693630 | ||||||
| chr10:124693706
|
T | C | 300 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(297): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.133+2452A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693706 | ||||||
| chr10:124693783
|
C | T | 28 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(25): Show | 28 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(25): Show |
intron_variant | MODIFIER | c.133+2375G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693783 | ||||||
| chr10:124693784
|
G | A | 53 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(50): Show | 53 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.133+2374C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693784 | ||||||
| chr10:124693862
|
G | C | 47 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0143others(44): Show | 47 | HG00099.hp1 HG00280.hp1 HG01071.hp2 others(44): Show |
intron_variant | MODIFIER | c.133+2296C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693862 | ||||||
| chr10:124693899
|
C | T | 1 | a0001c0001t0083g0186 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.133+2259G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124693899 | ||||||
| chr10:124694113
|
C | T | 247 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(244): Show | 250 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(247): Show |
intron_variant | MODIFIER | c.133+2045G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124694113 | ||||||
| chr10:124694114
|
G | A | 245 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(242): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(245): Show |
intron_variant | MODIFIER | c.133+2044C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124694114 | ||||||
| chr10:124694121
|
C | T | 54 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(51): Show | 54 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(51): Show |
intron_variant | MODIFIER | c.133+2037G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124694121 | ||||||
| chr10:124694221
|
T | C | 1 | a0002c0007t0001g0102 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.133+1937A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124694221 | ||||||
| chr10:124694265
|
G | A | 2 | a0001c0001t0018g0292a0001c0001t0018g0295 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.133+1893C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124694265 | ||||||
| chr10:124694342
|
C | T | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.133+1816G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124694342 | ||||||
| chr10:124694519
|
C | A | 141 | a0001c0001t0001g0002a0001c0001t0001g0070a0001c0001t0001g0078others(138): Show | 142 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.133+1639G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124694519 | ||||||
| chr10:124694651
|
C | T | 1 | a0001c0001t0085g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.133+1507G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124694651 | ||||||
| chr10:124694700
|
G | A | 3 | a0001c0001t0006g0060a0001c0001t0006g0061a0001c0001t0006g0062 | 3 | HG01884.hp1 HG02647.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.133+1458C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124694700 | ||||||
| chr10:124694746
|
C | T | 4 | a0001c0001t0001g0104a0001c0001t0004g0103a0001c0001t0033g0122others(1): Show | 4 | HG03209.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+1412G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124694746 | ||||||
| chr10:124694794
|
T | C | 106 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0133others(103): Show | 108 | HG00099.hp2 HG00140.hp1 HG00280.hp2 others(105): Show |
intron_variant | MODIFIER | c.133+1364A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124694794 | ||||||
| chr10:124695109
|
G | A | 3 | a0001c0001t0001g0193a0001c0001t0027g0223a0003c0006t0084g0240 | 3 | NA18946.hp1 NA19086.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.133+1049C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124695109 | ||||||
| chr10:124695192
|
G | A | 1 | a0001c0001t0001g0193 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.133+966C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124695192 | ||||||
| chr10:124695288
|
C | T | 59 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0133others(56): Show | 59 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(56): Show |
intron_variant | MODIFIER | c.133+870G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124695288 | ||||||
| chr10:124695375
|
A | G | 2 | a0001c0001t0060g0126a0001c0001t0091g0326 | 2 | HG03225.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.133+783T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124695375 | ||||||
| chr10:124695377
|
C | T | 4 | a0001c0001t0001g0104a0001c0001t0004g0103a0001c0001t0075g0124others(1): Show | 4 | HG02965.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+781G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124695377 | ||||||
| chr10:124695628
|
C | G | 4 | a0001c0001t0001g0104a0001c0001t0004g0103a0001c0001t0033g0122others(1): Show | 4 | HG03209.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.133+530G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124695628 | ||||||
| chr10:124695714
|
G | GGTAA | 23 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0112others(20): Show | 23 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.133+440_133+443dup others(4): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124695714 | ||||||
| chr10:124695763
|
A | G | 1 | a0001c0001t0029g0024 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.133+395T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124695763 | ||||||
| chr10:124695817
|
C | G | 1 | a0001c0001t0085g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.133+341G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124695817 | ||||||
| chr10:124695904
|
G | A | 1 | a0003c0006t0084g0240 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.133+254C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124695904 | ||||||
| chr10:124696041
|
G | A | 49 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(46): Show | 51 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.133+117C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124696041 | ||||||
| chr10:124696575
|
C | A | 1 | a0001c0001t0065g0092 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.79-363G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124696575 | ||||||
| chr10:124696688
|
C | T | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.79-476G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124696688 | ||||||
| chr10:124696731
|
C | G | 1 | a0001c0001t0002g0301 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.79-519G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124696731 | ||||||
| chr10:124696761
|
G | A | 1 | a0001c0001t0031g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.79-549C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124696761 | ||||||
| chr10:124696948
|
C | G | 4 | a0001c0001t0001g0104a0001c0001t0004g0103a0001c0001t0033g0122others(1): Show | 4 | HG03209.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-736G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124696948 | ||||||
| chr10:124697083
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.79-871C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124697083 | ||||||
| chr10:124697346
|
C | T | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.79-1134G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124697346 | ||||||
| chr10:124697459
|
T | C | 1 | a0001c0001t0001g0160 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.79-1247A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124697459 | ||||||
| chr10:124697557
|
G | C | 28 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0112others(25): Show | 28 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.79-1345C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124697557 | ||||||
| chr10:124697560
|
G | A | 1 | a0001c0001t0003g0084 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.79-1348C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124697560 | ||||||
| chr10:124697611
|
G | A | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.79-1399C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124697611 | ||||||
| chr10:124697701
|
G | C | 3 | a0001c0001t0001g0104a0001c0001t0004g0103a0002c0007t0001g0102 | 3 | HG03225.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.79-1489C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124697701 | ||||||
| chr10:124697701
|
G | T | 1 | a0001c0001t0001g0272 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.79-1489C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124697701 | ||||||
| chr10:124697775
|
C | G | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.79-1563G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124697775 | ||||||
| chr10:124697930
|
C | CA | 49 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(46): Show | 49 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.79-1719dupT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124697930 | ||||||
| chr10:124698042
|
T | C | 308 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(305): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.79-1830A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124698042 | ||||||
| chr10:124698147
|
G | A | 1 | a0001c0001t0030g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.79-1935C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124698147 | ||||||
| chr10:124698218
|
G | A | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.79-2006C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124698218 | ||||||
| chr10:124698265
|
G | A | 1 | a0001c0001t0085g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.79-2053C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124698265 | ||||||
| chr10:124698474
|
G | A | 49 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(46): Show | 51 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.79-2262C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124698474 | ||||||
| chr10:124698494
|
C | A | 1 | a0001c0001t0054g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.79-2282G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124698494 | ||||||
| chr10:124698569
|
T | C | 107 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(104): Show | 107 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(104): Show |
intron_variant | MODIFIER | c.79-2357A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124698569 | ||||||
| chr10:124698736
|
C | G | 4 | a0001c0001t0018g0289a0001c0001t0028g0287a0001c0001t0028g0288others(1): Show | 4 | NA18957.hp1 NA18960.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.79-2524G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124698736 | ||||||
| chr10:124698844
|
C | G | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.79-2632G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124698844 | ||||||
| chr10:124698874
|
C | T | 1 | a0001c0001t0004g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.79-2662G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124698874 | ||||||
| chr10:124699021
|
G | A | 1 | a0001c0001t0054g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.79-2809C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124699021 | ||||||
| chr10:124699158
|
C | T | 1 | a0001c0001t0001g0112 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.79-2946G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124699158 | ||||||
| chr10:124699405
|
G | A | 1 | a0001c0001t0009g0293 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.79-3193C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124699405 | ||||||
| chr10:124699564
|
G | A | 1 | a0001c0001t0037g0325 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.79-3352C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124699564 | ||||||
| chr10:124699567
|
A | G | 23 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0112others(20): Show | 23 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.79-3355T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124699567 | ||||||
| chr10:124699669
|
C | A | 3 | a0001c0001t0001g0104a0001c0001t0004g0103a0002c0007t0001g0102 | 3 | HG03225.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.79-3457G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124699669 | ||||||
| chr10:124699781
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.79-3569C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124699781 | ||||||
| chr10:124699854
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG01081.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.79-3642G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124699854 | ||||||
| chr10:124699862
|
G | A | 2 | a0001c0001t0010g0066a0001c0001t0010g0067 | 2 | HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.79-3650C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124699862 | ||||||
| chr10:124700020
|
C | T | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.79-3808G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124700020 | ||||||
| chr10:124700027
|
G | T | 2 | a0001c0001t0003g0097a0001c0001t0003g0099 | 2 | HG03490.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.79-3815C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124700027 | ||||||
| chr10:124700229
|
G | C | 1 | a0001c0001t0031g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.79-4017C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124700229 | ||||||
| chr10:124700373
|
CAGGCCGA others(5): Show |
C | 1 | a0001c0001t0001g0129 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.79-4173_79-4162del others(12): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124700373 | ||||||
| chr10:124700386
|
C | T | 1 | a0001c0001t0001g0129 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.79-4174G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124700386 | ||||||
| chr10:124700694
|
T | C | 1 | a0001c0008t0018g0317 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.79-4482A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124700694 | ||||||
| chr10:124700790
|
A | C | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.79-4578T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124700790 | ||||||
| chr10:124700816
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0004g0103 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.79-4604C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124700816 | ||||||
| chr10:124700910
|
C | G | 1 | a0001c0001t0001g0130 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.79-4698G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124700910 | ||||||
| chr10:124700999
|
G | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0130a0001c0001t0001g0131others(14): Show | 18 | HG00558.hp1 HG00673.hp1 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.79-4787C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124700999 | ||||||
| chr10:124701072
|
G | C | 1 | a0001c0001t0001g0228 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.79-4860C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124701072 | ||||||
| chr10:124701240
|
A | C | 1 | a0001c0001t0001g0048 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.79-5028T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124701240 | ||||||
| chr10:124701419
|
G | A | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.79-5207C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124701419 | ||||||
| chr10:124701509
|
G | A | 2 | a0001c0001t0004g0110a0001c0001t0004g0120 | 2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.78+5127C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124701509 | ||||||
| chr10:124701650
|
T | C | 1 | a0001c0001t0033g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.78+4986A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124701650 | ||||||
| chr10:124701694
|
G | A | 1 | a0001c0001t0076g0255 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.78+4942C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124701694 | ||||||
| chr10:124701702
|
G | A | 1 | a0001c0001t0033g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.78+4934C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124701702 | ||||||
| chr10:124701780
|
AG | A | 101 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.78+4855delC | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124701780 | ||||||
| chr10:124701852
|
T | G | 3 | a0001c0001t0015g0042a0001c0001t0015g0051a0001c0001t0015g0276 | 3 | HG02258.hp2 HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.78+4784A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124701852 | ||||||
| chr10:124701855
|
T | C | 101 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(98): Show | 101 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(98): Show |
intron_variant | MODIFIER | c.78+4781A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124701855 | ||||||
| chr10:124701977
|
C | G | 1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.78+4659G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124701977 | ||||||
| chr10:124702043
|
G | A | 18 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0114others(15): Show | 18 | HG02055.hp2 HG02109.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.78+4593C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124702043 | ||||||
| chr10:124702189
|
G | A | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.78+4447C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124702189 | ||||||
| chr10:124702358
|
G | A | 2 | a0001c0001t0033g0122a0001c0001t0091g0326 | 2 | HG03209.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.78+4278C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124702358 | ||||||
| chr10:124702499
|
C | T | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG02074.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.78+4137G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124702499 | ||||||
| chr10:124702532
|
C | G | 1 | a0001c0001t0088g0311 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.78+4104G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124702532 | ||||||
| chr10:124702718
|
G | T | 3 | a0001c0001t0007g0263a0001c0001t0008g0259a0001c0001t0008g0260 | 3 | NA18967.hp2 NA18970.hp2 NA18995.hp1 |
intron_variant | MODIFIER | c.78+3918C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124702718 | ||||||
| chr10:124703048
|
C | T | 1 | a0001c0001t0067g0184 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.78+3588G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124703048 | ||||||
| chr10:124703114
|
G | A | 1 | a0005c0004t0086g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.78+3522C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124703114 | ||||||
| chr10:124703190
|
G | A | 1 | a0001c0001t0029g0006 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.78+3446C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124703190 | ||||||
| chr10:124703241
|
G | A | 29 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(26): Show | 29 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(26): Show |
intron_variant | MODIFIER | c.78+3395C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124703241 | ||||||
| chr10:124703241
|
G | T | 1 | a0001c0001t0034g0227 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.78+3395C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124703241 | ||||||
| chr10:124703243
|
C | T | 279 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(276): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.78+3393G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124703243 | ||||||
| chr10:124703275
|
C | T | 1 | a0001c0001t0010g0036 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.78+3361G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124703275 | ||||||
| chr10:124703328
|
G | A | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.78+3308C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124703328 | ||||||
| chr10:124703364
|
T | C | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.78+3272A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124703364 | ||||||
| chr10:124703433
|
C | T | 1 | a0001c0001t0003g0058 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.78+3203G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124703433 | ||||||
| chr10:124703435
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0004g0103 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.78+3201A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124703435 | ||||||
| chr10:124703520
|
C | G | 23 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0112others(20): Show | 23 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.78+3116G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124703520 | ||||||
| chr10:124703530
|
G | A | 31 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.78+3106C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124703530 | ||||||
| chr10:124703558
|
G | A | 1 | a0001c0001t0009g0322 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.78+3078C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124703558 | ||||||
| chr10:124703595
|
G | A | 1 | a0001c0001t0091g0326 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.78+3041C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124703595 | ||||||
| chr10:124703705
|
C | T | 1 | a0001c0001t0054g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.78+2931G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124703705 | ||||||
| chr10:124703727
|
G | A | 1 | a0001c0001t0091g0326 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.78+2909C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124703727 | ||||||
| chr10:124703983
|
G | A | 1 | a0001c0001t0005g0022 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.78+2653C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124703983 | ||||||
| chr10:124704087
|
A | T | 1 | a0001c0001t0044g0030 | 1 | NA19082.hp2 | intron_variant | MODIFIER | c.78+2549T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124704087 | ||||||
| chr10:124704148
|
CCTT | C | 3 | a0001c0001t0001g0085a0001c0001t0001g0086a0001c0001t0001g0087 | 3 | HG02074.hp1 HG02080.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.78+2485_78+2487del others(3): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124704148 | ||||||
| chr10:124704191
|
G | A | 1 | a0001c0001t0034g0227 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.78+2445C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124704191 | ||||||
| chr10:124704324
|
A | C | 2 | a0001c0001t0017g0185a0001c0001t0067g0184 | 2 | HG00558.hp1 NA18963.hp1 |
intron_variant | MODIFIER | c.78+2312T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124704324 | ||||||
| chr10:124704397
|
C | T | 307 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(304): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.78+2239G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124704397 | ||||||
| chr10:124704537
|
T | A | 1 | a0001c0001t0001g0174 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.78+2099A>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124704537 | ||||||
| chr10:124704538
|
A | G | 308 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(305): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.78+2098T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124704538 | ||||||
| chr10:124704551
|
G | T | 1 | a0001c0001t0001g0245 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.78+2085C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124704551 | ||||||
| chr10:124704669
|
G | A | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.78+1967C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124704669 | ||||||
| chr10:124704703
|
CCATGTAC others(17): Show |
C | 1 | a0001c0001t0002g0291 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.78+1909_78+1932del others(24): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124704703 | ||||||
| chr10:124704710
|
C | A | 1 | a0001c0001t0012g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.78+1926G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124704710 | ||||||
| chr10:124704747
|
T | C | 1 | a0001c0001t0005g0009 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.78+1889A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124704747 | ||||||
| chr10:124704872
|
C | T | 2 | a0001c0001t0011g0091a0001c0001t0065g0092 | 2 | HG02698.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.78+1764G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124704872 | ||||||
| chr10:124704908
|
G | A | 1 | a0001c0001t0004g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.78+1728C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124704908 | ||||||
| chr10:124705030
|
G | A | 3 | a0001c0001t0004g0279a0001c0001t0004g0280a0001c0001t0004g0281 | 3 | HG02717.hp1 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.78+1606C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124705030 | ||||||
| chr10:124705042
|
C | A | 1 | a0001c0008t0018g0317 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.78+1594G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124705042 | ||||||
| chr10:124705138
|
T | G | 19 | a0001c0001t0007g0252a0001c0001t0007g0263a0001c0001t0008g0247others(16): Show | 19 | HG00408.hp2 HG00621.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.78+1498A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124705138 | ||||||
| chr10:124705254
|
A | G | 307 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(304): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.78+1382T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124705254 | ||||||
| chr10:124705285
|
G | C | 1 | a0001c0002t0001g0213 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.78+1351C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124705285 | ||||||
| chr10:124705306
|
G | GGAAGGC | 94 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(91): Show | 95 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.78+1324_78+1329dup others(6): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124705306 | ||||||
| chr10:124705359
|
T | A | 1 | a0005c0004t0086g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.78+1277A>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124705359 | ||||||
| chr10:124705374
|
A | C | 105 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.78+1262T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124705374 | ||||||
| chr10:124705395
|
G | A | 5 | a0001c0001t0001g0183a0001c0001t0001g0193a0001c0001t0001g0216others(2): Show | 5 | HG00423.hp1 NA18949.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.78+1241C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124705395 | ||||||
| chr10:124705701
|
C | T | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.78+935G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124705701 | ||||||
| chr10:124705724
|
G | A | 1 | a0001c0001t0036g0282 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.78+912C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124705724 | ||||||
| chr10:124705802
|
G | C | 31 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.78+834C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124705802 | ||||||
| chr10:124705864
|
G | A | 1 | a0001c0001t0055g0182 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.78+772C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124705864 | ||||||
| chr10:124706007
|
T | G | 1 | a0001c0001t0012g0046 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.78+629A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124706007 | ||||||
| chr10:124706042
|
A | G | 1 | a0001c0001t0004g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.78+594T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124706042 | ||||||
| chr10:124706095
|
A | G | 1 | a0001c0001t0033g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.78+541T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124706095 | ||||||
| chr10:124706185
|
A | G | 1 | a0001c0001t0001g0265 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.78+451T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124706185 | ||||||
| chr10:124706229
|
G | A | 1 | a0001c0001t0001g0231 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.78+407C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124706229 | ||||||
| chr10:124706276
|
T | C | 307 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(304): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.78+360A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124706276 | ||||||
| chr10:124706294
|
C | A | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.78+342G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124706294 | ||||||
| chr10:124706424
|
C | G | 32 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(29): Show | 32 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.78+212G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124706424 | ||||||
| chr10:124706488
|
G | C | 1 | a0001c0001t0005g0028 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.78+148C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124706488 | ||||||
| chr10:124706554
|
T | C | 308 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(305): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.78+82A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124706554 | ||||||
| chr10:124706565
|
G | A | 1 | a0001c0001t0005g0018 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.78+71C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124706565 | ||||||
| chr10:124706575
|
C | T | 2 | a0001c0001t0001g0151a0001c0001t0001g0166 | 2 | HG01515.hp2 HG01517.hp1 |
intron_variant | MODIFIER | c.78+61G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124706575 | ||||||
| chr10:124706624
|
C | T | 1 | a0001c0008t0018g0317 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.78+12G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124706624 | ||||||
| chr10:124706625
|
C | T | 1 | a0001c0001t0068g0270 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.78+11G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 2/4 | chr10 | 124706625 | ||||||
| chr10:124706933
|
C | T | 4 | a0001c0001t0001g0104a0001c0001t0004g0103a0001c0001t0033g0122others(1): Show | 4 | HG03209.hp2 HG03225.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.-174-46G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124706933 | ||||||
| chr10:124707055
|
C | A | 1 | a0001c0001t0025g0264 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.-174-168G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124707055 | ||||||
| chr10:124707119
|
G | C | 49 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(46): Show | 51 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-174-232C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124707119 | ||||||
| chr10:124707170
|
G | T | 4 | a0001c0001t0001g0197a0001c0001t0021g0198a0001c0001t0021g0199others(1): Show | 4 | HG00639.hp1 HG02451.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-174-283C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124707170 | ||||||
| chr10:124707482
|
A | T | 1 | a0001c0001t0030g0010 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.-174-595T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124707482 | ||||||
| chr10:124707547
|
G | T | 1 | a0001c0001t0004g0279 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-174-660C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124707547 | ||||||
| chr10:124707941
|
C | T | 1 | a0001c0001t0002g0318 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-174-1054G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124707941 | ||||||
| chr10:124707942
|
C | G | 86 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(83): Show | 88 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
intron_variant | MODIFIER | c.-174-1055G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124707942 | ||||||
| chr10:124707976
|
C | T | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-174-1089G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124707976 | ||||||
| chr10:124708079
|
G | A | 1 | a0001c0001t0014g0096 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-174-1192C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124708079 | ||||||
| chr10:124708767
|
G | A | 1 | a0001c0001t0001g0215 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.-174-1880C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124708767 | ||||||
| chr10:124708897
|
A | G | 3 | a0001c0001t0022g0055a0001c0001t0022g0056a0001c0001t0051g0057 | 3 | HG01099.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-174-2010T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124708897 | ||||||
| chr10:124708912
|
T | C | 4 | a0001c0001t0001g0145a0001c0001t0001g0161a0001c0001t0001g0229others(1): Show | 4 | HG02129.hp1 HG02132.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.-174-2025A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124708912 | ||||||
| chr10:124708964
|
G | A | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-174-2077C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124708964 | ||||||
| chr10:124708996
|
G | T | 1 | a0001c0001t0006g0277 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.-174-2109C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124708996 | ||||||
| chr10:124709002
|
TG | T | 53 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(50): Show | 53 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.-174-2116delC | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124709002 | ||||||
| chr10:124709046
|
G | A | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-174-2159C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124709046 | ||||||
| chr10:124709138
|
G | A | 1 | a0001c0001t0030g0005 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-174-2251C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124709138 | ||||||
| chr10:124709242
|
C | A | 275 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(272): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.-174-2355G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124709242 | ||||||
| chr10:124709261
|
G | A | 1 | a0001c0001t0050g0107 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-174-2374C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124709261 | ||||||
| chr10:124709274
|
G | A | 2 | a0001c0001t0011g0091a0001c0001t0065g0092 | 2 | HG02698.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-174-2387C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124709274 | ||||||
| chr10:124709386
|
C | T | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-174-2499G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124709386 | ||||||
| chr10:124709458
|
G | A | 1 | a0001c0001t0001g0173 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-174-2571C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124709458 | ||||||
| chr10:124709609
|
C | T | 307 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(304): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.-174-2722G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124709609 | ||||||
| chr10:124709701
|
T | C | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-174-2814A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124709701 | ||||||
| chr10:124709725
|
G | A | 1 | a0001c0001t0001g0141 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.-174-2838C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124709725 | ||||||
| chr10:124709843
|
G | GA | 54 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(51): Show | 56 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(53): Show |
intron_variant | MODIFIER | c.-174-2957dupT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124709843 | ||||||
| chr10:124709993
|
T | TA | 4 | a0001c0001t0001g0235a0001c0001t0006g0233a0001c0001t0026g0234others(1): Show | 4 | HG02257.hp1 HG03130.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.-174-3107dupT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124709993 | ||||||
| chr10:124710127
|
G | A | 1 | a0001c0001t0047g0033 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-174-3240C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124710127 | ||||||
| chr10:124710205
|
A | G | 4 | a0001c0001t0009g0284a0001c0001t0036g0282a0001c0001t0036g0283others(1): Show | 4 | HG00323.hp2 HG01496.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.-174-3318T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124710205 | ||||||
| chr10:124710208
|
C | A | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-174-3321G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124710208 | ||||||
| chr10:124710317
|
G | A | 302 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(299): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.-174-3430C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124710317 | ||||||
| chr10:124710358
|
A | G | 93 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(90): Show | 94 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.-174-3471T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124710358 | ||||||
| chr10:124710590
|
A | C | 49 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(46): Show | 51 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-174-3703T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124710590 | ||||||
| chr10:124710666
|
T | C | 4 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0034g0227others(1): Show | 4 | HG03669.hp2 HG03688.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-174-3779A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124710666 | ||||||
| chr10:124710677
|
C | A | 2 | a0001c0001t0001g0086a0001c0001t0001g0087 | 2 | HG02074.hp1 HG02129.hp2 |
intron_variant | MODIFIER | c.-174-3790G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124710677 | ||||||
| chr10:124710757
|
C | T | 1 | a0001c0001t0012g0047 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-174-3870G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124710757 | ||||||
| chr10:124710981
|
G | C | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-174-4094C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124710981 | ||||||
| chr10:124710993
|
T | A | 1 | a0001c0001t0001g0245 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-174-4106A>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124710993 | ||||||
| chr10:124710997
|
T | C | 307 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(304): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.-174-4110A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124710997 | ||||||
| chr10:124711033
|
A | G | 1 | a0001c0001t0015g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-174-4146T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124711033 | ||||||
| chr10:124711065
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.-174-4178G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124711065 | ||||||
| chr10:124711160
|
C | T | 1 | a0001c0001t0024g0262 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.-174-4273G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124711160 | ||||||
| chr10:124711329
|
G | A | 6 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(3): Show | 6 | NA18957.hp2 NA18962.hp1 NA18969.hp1 others(3): Show |
intron_variant | MODIFIER | c.-174-4442C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124711329 | ||||||
| chr10:124711342
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.-174-4455C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124711342 | ||||||
| chr10:124711361
|
G | A | 105 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.-174-4474C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124711361 | ||||||
| chr10:124711542
|
A | T | 4 | a0001c0001t0001g0197a0001c0001t0021g0198a0001c0001t0021g0199others(1): Show | 4 | HG00639.hp1 HG02451.hp2 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.-174-4655T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124711542 | ||||||
| chr10:124711674
|
G | A | 1 | a0001c0001t0008g0258 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.-174-4787C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124711674 | ||||||
| chr10:124711685
|
A | T | 1 | a0001c0001t0052g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-174-4798T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124711685 | ||||||
| chr10:124711709
|
G | A | 1 | a0005c0004t0086g0052 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.-174-4822C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124711709 | ||||||
| chr10:124711788
|
C | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(89): Show | 93 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-174-4901G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124711788 | ||||||
| chr10:124711816
|
T | C | 32 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(29): Show | 32 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(29): Show |
intron_variant | MODIFIER | c.-174-4929A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124711816 | ||||||
| chr10:124712112
|
C | T | 2 | a0001c0001t0006g0277a0001c0001t0006g0278 | 2 | HG02622.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-174-5225G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124712112 | ||||||
| chr10:124712304
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-174-5417G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124712304 | ||||||
| chr10:124712400
|
A | T | 1 | a0001c0001t0006g0233 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.-174-5513T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124712400 | ||||||
| chr10:124712447
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-174-5560T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124712447 | ||||||
| chr10:124712501
|
C | T | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-174-5614G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124712501 | ||||||
| chr10:124712630
|
C | T | 279 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(276): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.-174-5743G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124712630 | ||||||
| chr10:124712680
|
T | C | 1 | a0001c0001t0006g0062 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-174-5793A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124712680 | ||||||
| chr10:124712928
|
A | G | 2 | a0001c0001t0004g0110a0001c0001t0004g0120 | 2 | HG02258.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-174-6041T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124712928 | ||||||
| chr10:124712962
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.-174-6075C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124712962 | ||||||
| chr10:124713048
|
G | T | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-174-6161C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124713048 | ||||||
| chr10:124713049
|
A | T | 19 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(16): Show | 19 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.-174-6162T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124713049 | ||||||
| chr10:124713189
|
C | G | 1 | a0001c0001t0003g0077 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-174-6302G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124713189 | ||||||
| chr10:124713227
|
A | G | 47 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(44): Show | 47 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(44): Show |
intron_variant | MODIFIER | c.-174-6340T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124713227 | ||||||
| chr10:124713243
|
G | A | 1 | a0001c0001t0085g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-174-6356C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124713243 | ||||||
| chr10:124713371
|
G | C | 1 | a0001c0001t0045g0031 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.-174-6484C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124713371 | ||||||
| chr10:124713395
|
G | T | 307 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(304): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.-174-6508C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124713395 | ||||||
| chr10:124713408
|
G | A | 1 | a0001c0001t0054g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-174-6521C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124713408 | ||||||
| chr10:124713425
|
G | A | 2 | a0001c0001t0004g0118a0001c0001t0045g0031 | 2 | HG02257.hp2 HG02647.hp1 |
intron_variant | MODIFIER | c.-174-6538C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124713425 | ||||||
| chr10:124713515
|
C | G | 1 | a0001c0001t0089g0310 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.-174-6628G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124713515 | ||||||
| chr10:124713531
|
C | T | 92 | a0001c0001t0001g0002a0001c0001t0001g0129a0001c0001t0001g0130others(89): Show | 93 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(90): Show |
intron_variant | MODIFIER | c.-174-6644G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124713531 | ||||||
| chr10:124713613
|
T | C | 3 | a0001c0001t0006g0043a0001c0001t0012g0050a0001c0001t0012g0054 | 3 | HG02572.hp2 HG02615.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.-174-6726A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124713613 | ||||||
| chr10:124713741
|
G | T | 323 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0044others(320): Show | 326 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(323): Show |
intron_variant | MODIFIER | c.-174-6854C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124713741 | ||||||
| chr10:124714107
|
G | A | 27 | a0001c0001t0001g0193a0001c0001t0005g0009a0001c0001t0005g0011others(24): Show | 27 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.-174-7220C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124714107 | ||||||
| chr10:124714428
|
C | T | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-174-7541G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124714428 | ||||||
| chr10:124714561
|
C | A | 2 | a0001c0001t0001g0192a0001c0001t0068g0270 | 2 | HG00642.hp2 HG01074.hp1 |
intron_variant | MODIFIER | c.-174-7674G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124714561 | ||||||
| chr10:124714652
|
G | A | 3 | a0001c0001t0001g0104a0001c0001t0004g0103a0002c0007t0001g0102 | 3 | HG03225.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-174-7765C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124714652 | ||||||
| chr10:124714757
|
T | A | 1 | a0001c0001t0026g0241 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-174-7870A>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124714757 | ||||||
| chr10:124714758
|
C | CA | 48 | a0001c0001t0001g0002a0001c0001t0001g0130a0001c0001t0001g0131others(45): Show | 49 | HG00408.hp2 HG00558.hp1 HG00621.hp2 others(46): Show |
intron_variant | MODIFIER | c.-174-7872dupT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124714758 | ||||||
| chr10:124714758
|
C | CAA | 53 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0143others(50): Show | 53 | HG00099.hp1 HG00280.hp1 HG00735.hp1 others(50): Show |
intron_variant | MODIFIER | c.-174-7873_-174-787 others(6): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124714758 | ||||||
| chr10:124714758
|
CA | C | 53 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0133others(50): Show | 53 | HG00099.hp2 HG00140.hp1 HG00323.hp2 others(50): Show |
intron_variant | MODIFIER | c.-174-7872delT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124714758 | ||||||
| chr10:124714775
|
A | G | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-174-7888T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124714775 | ||||||
| chr10:124714776
|
A | C | 30 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(27): Show | 30 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(27): Show |
intron_variant | MODIFIER | c.-174-7889T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124714776 | ||||||
| chr10:124714834
|
C | A | 1 | a0001c0001t0022g0065 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.-174-7947G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124714834 | ||||||
| chr10:124714851
|
C | G | 1 | a0001c0001t0001g0174 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.-174-7964G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124714851 | ||||||
| chr10:124715337
|
T | C | 1 | a0001c0001t0001g0217 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.-174-8450A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124715337 | ||||||
| chr10:124715572
|
G | A | 204 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(201): Show | 205 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(202): Show |
intron_variant | MODIFIER | c.-174-8685C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124715572 | ||||||
| chr10:124715635
|
G | A | 282 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(279): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-174-8748C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124715635 | ||||||
| chr10:124715742
|
G | A | 20 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(17): Show | 20 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.-174-8855C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124715742 | ||||||
| chr10:124715875
|
A | G | 1 | a0001c0001t0015g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-174-8988T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124715875 | ||||||
| chr10:124715952
|
C | A | 1 | a0001c0001t0001g0218 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-174-9065G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124715952 | ||||||
| chr10:124715958
|
G | A | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-174-9071C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124715958 | ||||||
| chr10:124716034
|
C | T | 1 | a0001c0001t0010g0222 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-174-9147G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124716034 | ||||||
| chr10:124716278
|
G | A | 1 | a0001c0001t0054g0040 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-174-9391C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124716278 | ||||||
| chr10:124716597
|
T | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0231 | 2 | HG02809.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.-174-9710A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124716597 | ||||||
| chr10:124716667
|
A | G | 307 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(304): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.-174-9780T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124716667 | ||||||
| chr10:124716840
|
G | A | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-174-9953C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124716840 | ||||||
| chr10:124716842
|
T | TC | 19 | a0001c0001t0007g0252a0001c0001t0007g0263a0001c0001t0008g0247others(16): Show | 19 | HG00408.hp2 HG00621.hp2 HG02027.hp2 others(16): Show |
intron_variant | MODIFIER | c.-174-9956dupG | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124716842 | ||||||
| chr10:124717037
|
G | C | 2 | a0001c0001t0052g0037a0001c0001t0060g0126 | 2 | HG01891.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.-174-10150C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124717037 | ||||||
| chr10:124717043
|
A | G | 4 | a0001c0001t0018g0289a0001c0001t0028g0287a0001c0001t0028g0288others(1): Show | 4 | NA18957.hp1 NA18960.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.-174-10156T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124717043 | ||||||
| chr10:124717330
|
C | T | 1 | a0001c0001t0005g0009 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.-174-10443G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124717330 | ||||||
| chr10:124717692
|
G | A | 1 | a0001c0001t0015g0042 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-174-10805C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124717692 | ||||||
| chr10:124717893
|
G | A | 1 | a0001c0001t0020g0007 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-174-11006C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124717893 | ||||||
| chr10:124718065
|
G | T | 1 | a0001c0001t0002g0291 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-174-11178C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124718065 | ||||||
| chr10:124718840
|
G | C | 49 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(46): Show | 51 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-174-11953C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124718840 | ||||||
| chr10:124718870
|
A | G | 3 | a0001c0001t0002g0312a0001c0001t0002g0313a0001c0001t0002g0324 | 3 | HG02071.hp1 HG02080.hp1 NA18986.hp1 |
intron_variant | MODIFIER | c.-174-11983T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124718870 | ||||||
| chr10:124719047
|
T | A | 3 | a0001c0001t0010g0036a0001c0001t0010g0066a0001c0001t0010g0067 | 3 | HG02818.hp2 HG03516.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.-174-12160A>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124719047 | ||||||
| chr10:124719047
|
T | TA | 194 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(191): Show | 195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.-174-12161dupT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124719047 | ||||||
| chr10:124719124
|
G | C | 1 | a0001c0001t0047g0033 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.-174-12237C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124719124 | ||||||
| chr10:124719375
|
C | T | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-174-12488G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124719375 | ||||||
| chr10:124719577
|
A | C | 49 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(46): Show | 51 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-174-12690T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124719577 | ||||||
| chr10:124719726
|
A | G | 1 | a0001c0001t0033g0125 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.-174-12839T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124719726 | ||||||
| chr10:124719867
|
C | A | 1 | a0001c0001t0001g0219 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-174-12980G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124719867 | ||||||
| chr10:124719891
|
A | C | 2 | a0001c0001t0012g0046a0001c0001t0082g0045 | 2 | HG02723.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.-174-13004T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124719891 | ||||||
| chr10:124719937
|
C | T | 1 | a0001c0001t0078g0194 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.-174-13050G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124719937 | ||||||
| chr10:124720089
|
G | A | 31 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.-174-13202C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124720089 | ||||||
| chr10:124720197
|
C | T | 1 | a0001c0001t0028g0287 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.-174-13310G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124720197 | ||||||
| chr10:124720208
|
G | C | 49 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(46): Show | 51 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-174-13321C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124720208 | ||||||
| chr10:124720300
|
T | G | 49 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(46): Show | 51 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-174-13413A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124720300 | ||||||
| chr10:124720306
|
C | CA | 197 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(194): Show | 198 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(195): Show |
intron_variant | MODIFIER | c.-174-13420dupT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124720306 | ||||||
| chr10:124720517
|
G | A | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-174-13630C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124720517 | ||||||
| chr10:124720656
|
C | T | 1 | a0001c0001t0001g0173 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.-174-13769G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124720656 | ||||||
| chr10:124720771
|
C | T | 1 | a0001c0001t0017g0142 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.-174-13884G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124720771 | ||||||
| chr10:124720898
|
C | T | 1 | a0001c0001t0033g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-174-14011G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124720898 | ||||||
| chr10:124720910
|
G | C | 23 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0112others(20): Show | 23 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.-174-14023C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124720910 | ||||||
| chr10:124721095
|
G | T | 1 | a0001c0001t0001g0151 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.-174-14208C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124721095 | ||||||
| chr10:124721116
|
C | T | 12 | a0001c0001t0003g0039a0001c0001t0003g0068a0001c0001t0003g0074others(9): Show | 12 | HG00558.hp2 NA18939.hp2 NA18964.hp1 others(9): Show |
intron_variant | MODIFIER | c.-174-14229G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124721116 | ||||||
| chr10:124721451
|
G | A | 1 | a0001c0001t0075g0124 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.-174-14564C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124721451 | ||||||
| chr10:124721543
|
T | C | 2 | a0001c0001t0001g0104a0001c0001t0004g0103 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-174-14656A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124721543 | ||||||
| chr10:124721610
|
A | T | 1 | a0001c0001t0085g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-174-14723T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124721610 | ||||||
| chr10:124721839
|
T | C | 1 | a0001c0001t0006g0060 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.-174-14952A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124721839 | ||||||
| chr10:124722041
|
G | C | 106 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(103): Show | 106 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.-174-15154C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124722041 | ||||||
| chr10:124722049
|
G | A | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-174-15162C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124722049 | ||||||
| chr10:124722123
|
G | C | 1 | a0001c0001t0049g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-174-15236C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124722123 | ||||||
| chr10:124722235
|
C | T | 81 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(78): Show | 83 | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(80): Show |
intron_variant | MODIFIER | c.-174-15348G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124722235 | ||||||
| chr10:124722351
|
A | G | 23 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0112others(20): Show | 23 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.-174-15464T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124722351 | ||||||
| chr10:124722352
|
A | C | 23 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0112others(20): Show | 23 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.-174-15465T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124722352 | ||||||
| chr10:124722446
|
T | C | 106 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(103): Show | 106 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.-174-15559A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124722446 | ||||||
| chr10:124722791
|
C | T | 1 | a0001c0001t0002g0318 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-174-15904G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124722791 | ||||||
| chr10:124723355
|
G | A | 105 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.-174-16468C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124723355 | ||||||
| chr10:124723738
|
AG | A | 12 | a0001c0001t0002g0291a0001c0001t0002g0301a0001c0001t0002g0302others(9): Show | 12 | HG00609.hp1 HG02071.hp1 HG02080.hp1 others(9): Show |
intron_variant | MODIFIER | c.-174-16852delC | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124723738 | ||||||
| chr10:124723742
|
C | G | 1 | a0001c0001t0061g0243 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-174-16855G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124723742 | ||||||
| chr10:124723754
|
C | T | 105 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(102): Show | 105 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.-174-16867G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124723754 | ||||||
| chr10:124723761
|
G | C | 1 | a0001c0001t0088g0311 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-174-16874C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124723761 | ||||||
| chr10:124723839
|
G | A | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-174-16952C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124723839 | ||||||
| chr10:124723906
|
G | A | 31 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(28): Show | 31 | HG00140.hp2 HG00408.hp1 HG00423.hp2 others(28): Show |
intron_variant | MODIFIER | c.-174-17019C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124723906 | ||||||
| chr10:124723986
|
C | T | 1 | a0001c0001t0003g0079 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-174-17099G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124723986 | ||||||
| chr10:124724145
|
A | C | 2 | a0001c0001t0005g0022a0001c0001t0005g0023 | 2 | NA18944.hp1 NA18967.hp1 |
intron_variant | MODIFIER | c.-174-17258T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124724145 | ||||||
| chr10:124724218
|
A | T | 6 | a0001c0001t0001g0150a0001c0001t0001g0172a0001c0001t0035g0148others(3): Show | 6 | HG02040.hp1 HG02056.hp1 HG02135.hp2 others(3): Show |
intron_variant | MODIFIER | c.-174-17331T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124724218 | ||||||
| chr10:124724223
|
G | T | 1 | a0001c0001t0077g0138 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-174-17336C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124724223 | ||||||
| chr10:124724383
|
C | A | 1 | a0001c0001t0077g0138 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-174-17496G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124724383 | ||||||
| chr10:124724422
|
C | T | 52 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0133others(49): Show | 52 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.-174-17535G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124724422 | ||||||
| chr10:124725062
|
C | G | 2 | a0001c0001t0001g0193a0001c0001t0017g0273 | 2 | NA18949.hp1 NA19090.hp2 |
intron_variant | MODIFIER | c.-174-18175G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124725062 | ||||||
| chr10:124725099
|
G | A | 20 | a0001c0001t0007g0252a0001c0001t0007g0263a0001c0001t0008g0247others(17): Show | 20 | HG00408.hp2 HG00621.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.-174-18212C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124725099 | ||||||
| chr10:124725204
|
C | A | 116 | a0001c0001t0001g0002a0001c0001t0001g0104a0001c0001t0001g0111others(113): Show | 117 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(114): Show |
intron_variant | MODIFIER | c.-174-18317G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124725204 | ||||||
| chr10:124725410
|
CTA | C | 49 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(46): Show | 51 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(48): Show |
intron_variant | MODIFIER | c.-174-18525_-174-18 others(8): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124725410 | ||||||
| chr10:124725428
|
C | T | 1 | a0001c0001t0001g0192 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.-174-18541G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124725428 | ||||||
| chr10:124725483
|
G | A | 1 | a0001c0001t0002g0309 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.-175+18530C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124725483 | ||||||
| chr10:124725515
|
C | T | 47 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(44): Show | 49 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.-175+18498G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124725515 | ||||||
| chr10:124725760
|
A | G | 1 | a0001c0002t0001g0191 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-175+18253T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124725760 | ||||||
| chr10:124725883
|
G | A | 52 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0133others(49): Show | 52 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(49): Show |
intron_variant | MODIFIER | c.-175+18130C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124725883 | ||||||
| chr10:124725941
|
G | A | 14 | a0001c0001t0009g0284a0001c0001t0009g0320a0001c0001t0009g0321others(11): Show | 14 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(11): Show |
intron_variant | MODIFIER | c.-175+18072C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124725941 | ||||||
| chr10:124726151
|
AT | A | 3 | a0001c0001t0032g0267a0001c0001t0057g0268a0001c0003t0058g0269 | 3 | HG00423.hp2 NA18986.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-175+17861delA | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124726151 | ||||||
| chr10:124726288
|
C | T | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-175+17725G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124726288 | ||||||
| chr10:124726362
|
A | T | 1 | a0001c0001t0001g0190 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.-175+17651T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124726362 | ||||||
| chr10:124726395
|
G | T | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-175+17618C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124726395 | ||||||
| chr10:124726921
|
T | C | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-175+17092A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124726921 | ||||||
| chr10:124727082
|
G | A | 1 | a0001c0001t0001g0228 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-175+16931C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124727082 | ||||||
| chr10:124727083
|
A | T | 3 | a0001c0001t0031g0049a0001c0001t0031g0106a0001c0001t0049g0105 | 3 | HG02738.hp2 HG03834.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.-175+16930T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124727083 | ||||||
| chr10:124727100
|
C | G | 1 | a0001c0001t0001g0225 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-175+16913G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124727100 | ||||||
| chr10:124727129
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.-175+16884G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124727129 | ||||||
| chr10:124727220
|
G | A | 1 | a0001c0008t0018g0317 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-175+16793C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124727220 | ||||||
| chr10:124727226
|
T | C | 82 | a0001c0001t0001g0129a0001c0001t0001g0135a0001c0001t0001g0143others(79): Show | 82 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(79): Show |
intron_variant | MODIFIER | c.-175+16787A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124727226 | ||||||
| chr10:124727330
|
TG | T | 89 | a0001c0001t0001g0078a0001c0001t0001g0104a0001c0001t0001g0111others(86): Show | 89 | HG00323.hp1 HG00408.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.-175+16682delC | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124727330 | ||||||
| chr10:124727330
|
TGG | T | 147 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0070others(144): Show | 149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): Show |
intron_variant | MODIFIER | c.-175+16681_-175+16 others(8): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124727330 | ||||||
| chr10:124727330
|
TGGG | T | 27 | a0001c0001t0001g0002a0001c0001t0001g0139a0001c0001t0001g0140others(24): Show | 28 | HG00140.hp2 HG00621.hp1 HG00673.hp2 others(25): Show |
intron_variant | MODIFIER | c.-175+16680_-175+16 others(9): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124727330 | ||||||
| chr10:124727332
|
G | T | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-175+16681C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124727332 | ||||||
| chr10:124727339
|
G | T | 23 | a0001c0001t0001g0104a0001c0001t0001g0111a0001c0001t0001g0112others(20): Show | 23 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.-175+16674C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124727339 | ||||||
| chr10:124727341
|
G | C | 80 | a0001c0001t0001g0035a0001c0001t0001g0059a0001c0001t0001g0133others(77): Show | 82 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.-175+16672C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124727341 | ||||||
| chr10:124727344
|
G | T | 1 | a0001c0001t0077g0138 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-175+16669C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124727344 | ||||||
| chr10:124727392
|
A | G | 3 | a0001c0001t0004g0108a0001c0001t0080g0109a0001c0001t0087g0286 | 3 | HG02818.hp1 HG03139.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.-175+16621T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124727392 | ||||||
| chr10:124728104
|
C | T | 3 | a0001c0001t0015g0042a0001c0001t0015g0051a0001c0001t0015g0276 | 3 | HG02258.hp2 HG02886.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.-175+15909G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124728104 | ||||||
| chr10:124728185
|
A | T | 1 | a0001c0001t0002g0291 | 1 | NA19089.hp2 | intron_variant | MODIFIER | c.-175+15828T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124728185 | ||||||
| chr10:124728328
|
C | T | 1 | a0001c0001t0061g0243 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.-175+15685G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124728328 | ||||||
| chr10:124728412
|
C | T | 1 | a0001c0001t0052g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-175+15601G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124728412 | ||||||
| chr10:124728612
|
C | A | 1 | a0001c0001t0088g0311 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-175+15401G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124728612 | ||||||
| chr10:124728701
|
C | T | 2 | a0001c0001t0003g0068a0001c0001t0011g0069 | 2 | NA18973.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.-175+15312G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124728701 | ||||||
| chr10:124728741
|
G | C | 1 | a0001c0001t0001g0221 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.-175+15272C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124728741 | ||||||
| chr10:124728882
|
T | C | 3 | a0001c0001t0001g0104a0001c0001t0004g0103a0002c0007t0001g0102 | 3 | HG03225.hp2 HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-175+15131A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124728882 | ||||||
| chr10:124729151
|
C | T | 18 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(15): Show | 18 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-175+14862G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124729151 | ||||||
| chr10:124729183
|
C | T | 2 | a0001c0001t0054g0040a0001c0001t0085g0041 | 2 | HG02451.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.-175+14830G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124729183 | ||||||
| chr10:124729345
|
G | A | 52 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(49): Show | 54 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-175+14668C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124729345 | ||||||
| chr10:124729429
|
A | C | 18 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(15): Show | 18 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-175+14584T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124729429 | ||||||
| chr10:124729804
|
G | C | 1 | a0001c0001t0010g0222 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-175+14209C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124729804 | ||||||
| chr10:124729828
|
G | A | 1 | a0001c0001t0014g0096 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.-175+14185C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124729828 | ||||||
| chr10:124729861
|
T | C | 1 | a0001c0001t0031g0049 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.-175+14152A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124729861 | ||||||
| chr10:124730001
|
G | C | 1 | a0001c0001t0091g0326 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-175+14012C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124730001 | ||||||
| chr10:124730108
|
A | G | 1 | a0001c0001t0049g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-175+13905T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124730108 | ||||||
| chr10:124730109
|
T | C | 1 | a0001c0001t0004g0119 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.-175+13904A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124730109 | ||||||
| chr10:124730182
|
C | T | 2 | a0001c0001t0011g0091a0001c0001t0065g0092 | 2 | HG02698.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-175+13831G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124730182 | ||||||
| chr10:124730213
|
C | T | 149 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(146): Show | 150 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(147): Show |
intron_variant | MODIFIER | c.-175+13800G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124730213 | ||||||
| chr10:124730217
|
T | A | 18 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(15): Show | 18 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-175+13796A>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124730217 | ||||||
| chr10:124730402
|
T | C | 2 | a0001c0001t0006g0088a0001c0001t0006g0089 | 2 | HG03516.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.-175+13611A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124730402 | ||||||
| chr10:124730584
|
T | C | 86 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(83): Show | 86 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(83): Show |
intron_variant | MODIFIER | c.-175+13429A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124730584 | ||||||
| chr10:124730714
|
C | T | 1 | a0001c0001t0001g0271 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-175+13299G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124730714 | ||||||
| chr10:124730813
|
C | T | 1 | a0001c0001t0050g0107 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.-175+13200G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124730813 | ||||||
| chr10:124730815
|
G | A | 52 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(49): Show | 54 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-175+13198C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124730815 | ||||||
| chr10:124730831
|
T | C | 1 | a0001c0001t0001g0224 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.-175+13182A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124730831 | ||||||
| chr10:124730960
|
C | T | 1 | a0001c0001t0033g0122 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-175+13053G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124730960 | ||||||
| chr10:124730985
|
A | G | 1 | a0001c0001t0046g0032 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-175+13028T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124730985 | ||||||
| chr10:124731174
|
G | C | 52 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(49): Show | 54 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(51): Show |
intron_variant | MODIFIER | c.-175+12839C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124731174 | ||||||
| chr10:124731205
|
C | T | 18 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(15): Show | 18 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-175+12808G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124731205 | ||||||
| chr10:124731258
|
T | A | 36 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(33): Show | 36 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(33): Show |
intron_variant | MODIFIER | c.-175+12755A>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124731258 | ||||||
| chr10:124731272
|
C | T | 161 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(158): Show | 162 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(159): Show |
intron_variant | MODIFIER | c.-175+12741G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124731272 | ||||||
| chr10:124731572
|
T | C | 1 | a0001c0001t0077g0138 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-175+12441A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124731572 | ||||||
| chr10:124731573
|
C | A | 1 | a0001c0001t0077g0138 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-175+12440G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124731573 | ||||||
| chr10:124731575
|
A | C | 1 | a0001c0001t0077g0138 | 1 | NA19078.hp2 | intron_variant | MODIFIER | c.-175+12438T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124731575 | ||||||
| chr10:124731577
|
C | CT | 51 | a0001c0001t0001g0059a0001c0001t0001g0133a0001c0001t0001g0134others(48): Show | 53 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(50): Show |
intron_variant | MODIFIER | c.-175+12435dupA | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124731577 | ||||||
| chr10:124731632
|
G | C | 1 | a0001c0008t0018g0317 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.-175+12381C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124731632 | ||||||
| chr10:124731716
|
C | T | 1 | a0001c0001t0008g0247 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-175+12297G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124731716 | ||||||
| chr10:124731810
|
T | C | 2 | a0001c0001t0031g0106a0001c0001t0049g0105 | 2 | HG02738.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-175+12203A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124731810 | ||||||
| chr10:124731956
|
C | T | 1 | a0001c0001t0001g0133 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.-175+12057G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124731956 | ||||||
| chr10:124732002
|
T | C | 18 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(15): Show | 18 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-175+12011A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124732002 | ||||||
| chr10:124732203
|
G | A | 1 | a0001c0001t0011g0090 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.-175+11810C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124732203 | ||||||
| chr10:124732256
|
A | G | 1 | a0001c0001t0037g0325 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.-175+11757T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124732256 | ||||||
| chr10:124732335
|
C | T | 1 | a0001c0001t0015g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-175+11678G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124732335 | ||||||
| chr10:124732341
|
G | A | 2 | a0001c0001t0011g0091a0001c0001t0065g0092 | 2 | HG02698.hp2 HG03942.hp2 |
intron_variant | MODIFIER | c.-175+11672C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124732341 | ||||||
| chr10:124732368
|
A | C | 1 | a0001c0001t0040g0008 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.-175+11645T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124732368 | ||||||
| chr10:124732448
|
C | T | 1 | a0001c0001t0048g0246 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.-175+11565G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124732448 | ||||||
| chr10:124732479
|
G | A | 1 | a0001c0001t0030g0005 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-175+11534C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124732479 | ||||||
| chr10:124732685
|
C | G | 2 | a0001c0001t0011g0244a0001c0001t0061g0243 | 2 | HG02717.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.-175+11328G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124732685 | ||||||
| chr10:124732997
|
C | T | 2 | a0001c0001t0001g0136a0001c0001t0001g0137 | 2 | HG01081.hp2 HG01346.hp2 |
intron_variant | MODIFIER | c.-175+11016G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124732997 | ||||||
| chr10:124733333
|
G | A | 1 | a0001c0001t0012g0050 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-175+10680C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124733333 | ||||||
| chr10:124733563
|
T | G | 1 | a0001c0001t0001g0225 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.-175+10450A>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124733563 | ||||||
| chr10:124733598
|
G | C | 4 | a0001c0001t0001g0226a0001c0001t0001g0228a0001c0001t0034g0227others(1): Show | 4 | HG03669.hp2 HG03688.hp2 HG04199.hp1 others(1): Show |
intron_variant | MODIFIER | c.-175+10415C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124733598 | ||||||
| chr10:124733605
|
C | T | 1 | a0001c0001t0015g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-175+10408G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124733605 | ||||||
| chr10:124733747
|
A | G | 1 | a0001c0001t0001g0245 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.-175+10266T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124733747 | ||||||
| chr10:124733807
|
C | T | 1 | a0001c0001t0001g0135 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.-175+10206G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124733807 | ||||||
| chr10:124733924
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.-175+10089A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124733924 | ||||||
| chr10:124734177
|
T | A | 1 | a0001c0002t0001g0230 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.-175+9836A>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124734177 | ||||||
| chr10:124734255
|
T | C | 1 | a0001c0001t0001g0231 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.-175+9758A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124734255 | ||||||
| chr10:124734425
|
C | A | 1 | a0001c0001t0002g0318 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.-175+9588G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124734425 | ||||||
| chr10:124734551
|
T | C | 1 | a0001c0001t0065g0092 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.-175+9462A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124734551 | ||||||
| chr10:124734653
|
C | T | 4 | a0001c0001t0001g0059a0001c0001t0001g0133a0001c0001t0001g0134others(1): Show | 4 | HG00642.hp1 HG03834.hp1 HG06807.hp2 others(1): Show |
intron_variant | MODIFIER | c.-175+9360G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124734653 | ||||||
| chr10:124734825
|
G | T | 2 | a0001c0001t0012g0123a0001c0001t0075g0124 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-175+9188C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124734825 | ||||||
| chr10:124734961
|
A | C | 1 | a0001c0001t0062g0132 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-175+9052T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124734961 | ||||||
| chr10:124735023
|
G | A | 18 | a0001c0001t0005g0014a0001c0001t0005g0018a0001c0001t0005g0019others(15): Show | 18 | HG00408.hp1 HG00621.hp1 HG00673.hp2 others(15): Show |
intron_variant | MODIFIER | c.-175+8990C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124735023 | ||||||
| chr10:124735080
|
G | A | 1 | a0001c0001t0001g0232 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.-175+8933C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124735080 | ||||||
| chr10:124735137
|
G | A | 53 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(50): Show | 53 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.-175+8876C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124735137 | ||||||
| chr10:124735265
|
C | T | 1 | a0001c0001t0004g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-175+8748G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124735265 | ||||||
| chr10:124735555
|
C | A | 1 | a0001c0001t0015g0051 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.-175+8458G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124735555 | ||||||
| chr10:124735568
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(144): Show | 148 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(145): Show |
intron_variant | MODIFIER | c.-175+8445G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124735568 | ||||||
| chr10:124735730
|
T | C | 26 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(23): Show | 26 | HG00140.hp2 HG00408.hp1 HG00621.hp1 others(23): Show |
intron_variant | MODIFIER | c.-175+8283A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124735730 | ||||||
| chr10:124735749
|
G | C | 18 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(15): Show | 18 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-175+8264C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124735749 | ||||||
| chr10:124735770
|
C | T | 1 | a0001c0001t0037g0319 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.-175+8243G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124735770 | ||||||
| chr10:124735775
|
GGGCT | G | 134 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(131): Show | 136 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.-175+8234_-175+823 others(8): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124735775 | ||||||
| chr10:124736062
|
G | A | 1 | a0003c0006t0084g0240 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.-175+7951C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124736062 | ||||||
| chr10:124736183
|
T | A | 13 | a0001c0001t0009g0284a0001c0001t0009g0320a0001c0001t0009g0321others(10): Show | 13 | HG00280.hp2 HG00323.hp2 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.-175+7830A>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124736183 | ||||||
| chr10:124736254
|
G | A | 155 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-175+7759C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124736254 | ||||||
| chr10:124736266
|
C | T | 154 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(151): Show | 155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.-175+7747G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124736266 | ||||||
| chr10:124736413
|
T | C | 2 | a0001c0001t0031g0106a0001c0001t0049g0105 | 2 | HG02738.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-175+7600A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124736413 | ||||||
| chr10:124736633
|
T | C | 2 | a0001c0001t0026g0241a0001c0001t0037g0325 | 2 | HG01175.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.-175+7380A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124736633 | ||||||
| chr10:124736634
|
G | C | 1 | a0001c0001t0004g0120 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-175+7379C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124736634 | ||||||
| chr10:124736832
|
C | T | 1 | a0001c0001t0020g0007 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.-175+7181G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124736832 | ||||||
| chr10:124736836
|
C | A | 1 | a0001c0001t0019g0027 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.-175+7177G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124736836 | ||||||
| chr10:124736968
|
G | C | 78 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(75): Show | 78 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(75): Show |
intron_variant | MODIFIER | c.-175+7045C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124736968 | ||||||
| chr10:124737224
|
C | T | 4 | a0001c0001t0018g0289a0001c0001t0028g0287a0001c0001t0028g0288others(1): Show | 4 | NA18957.hp1 NA18960.hp1 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.-175+6789G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124737224 | ||||||
| chr10:124737297
|
G | A | 50 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(47): Show | 52 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(49): Show |
intron_variant | MODIFIER | c.-175+6716C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124737297 | ||||||
| chr10:124737398
|
G | A | 2 | a0001c0001t0001g0104a0001c0001t0004g0103 | 2 | HG03453.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.-175+6615C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124737398 | ||||||
| chr10:124737399
|
G | A | 3 | a0001c0001t0012g0123a0001c0001t0033g0125a0001c0001t0075g0124 | 3 | HG02965.hp2 HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.-175+6614C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124737399 | ||||||
| chr10:124737418
|
C | A | 51 | a0001c0001t0001g0070a0001c0001t0001g0078a0001c0001t0001g0085others(48): Show | 51 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(48): Show |
intron_variant | MODIFIER | c.-175+6595G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124737418 | ||||||
| chr10:124737441
|
G | T | 1 | a0001c0001t0001g0131 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-175+6572C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124737441 | ||||||
| chr10:124737579
|
G | C | 47 | a0001c0001t0002g0003a0001c0001t0002g0004a0001c0001t0002g0291others(44): Show | 49 | HG00280.hp2 HG00323.hp2 HG00609.hp1 others(46): Show |
intron_variant | MODIFIER | c.-175+6434C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124737579 | ||||||
| chr10:124737900
|
T | C | 313 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(310): Show | 316 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(313): Show |
intron_variant | MODIFIER | c.-175+6113A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124737900 | ||||||
| chr10:124738101
|
GAGC | G | 324 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0035others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.-175+5909_-175+591 others(7): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124738101 | ||||||
| chr10:124738205
|
C | T | 1 | a0001c0001t0087g0286 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.-175+5808G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124738205 | ||||||
| chr10:124738206
|
G | A | 1 | a0001c0001t0001g0242 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.-175+5807C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124738206 | ||||||
| chr10:124738296
|
G | A | 1 | a0001c0001t0085g0041 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.-175+5717C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124738296 | ||||||
| chr10:124738468
|
G | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0104others(173): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(174): Show |
intron_variant | MODIFIER | c.-175+5545C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124738468 | ||||||
| chr10:124738627
|
C | A | 1 | a0001c0001t0005g0028 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.-175+5386G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124738627 | ||||||
| chr10:124738636
|
A | T | 1 | a0001c0001t0032g0267 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.-175+5377T>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124738636 | ||||||
| chr10:124738654
|
C | A | 1 | a0001c0001t0039g0029 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.-175+5359G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124738654 | ||||||
| chr10:124738695
|
T | C | 20 | a0001c0001t0001g0245a0001c0001t0007g0252a0001c0001t0007g0263others(17): Show | 20 | HG00408.hp2 HG00621.hp2 HG02027.hp2 others(17): Show |
intron_variant | MODIFIER | c.-175+5318A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124738695 | ||||||
| chr10:124738715
|
G | A | 1 | a0001c0001t0091g0326 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.-175+5298C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124738715 | ||||||
| chr10:124738880
|
G | T | 1 | a0001c0001t0003g0058 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.-175+5133C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124738880 | ||||||
| chr10:124738915
|
G | T | 1 | a0001c0001t0049g0105 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-175+5098C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124738915 | ||||||
| chr10:124738995
|
A | C | 1 | a0001c0001t0001g0130 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-175+5018T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124738995 | ||||||
| chr10:124739043
|
C | CA | 7 | a0001c0001t0001g0265a0001c0001t0014g0093a0001c0001t0014g0094others(4): Show | 7 | HG00639.hp1 HG01123.hp1 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.-175+4969dupT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124739043 | ||||||
| chr10:124739056
|
A | C | 1 | a0001c0001t0001g0129 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.-175+4957T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124739056 | ||||||
| chr10:124739061
|
A | C | 1 | a0001c0001t0030g0005 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-175+4952T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124739061 | ||||||
| chr10:124739064
|
C | A | 27 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(24): Show | 27 | HG00140.hp2 HG00408.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.-175+4949G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124739064 | ||||||
| chr10:124739122
|
T | C | 3 | a0001c0001t0032g0267a0001c0001t0057g0268a0001c0003t0058g0269 | 3 | HG00423.hp2 NA18986.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.-175+4891A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124739122 | ||||||
| chr10:124739275
|
G | A | 1 | a0001c0001t0068g0270 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-175+4738C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124739275 | ||||||
| chr10:124739280
|
T | C | 1 | a0001c0001t0001g0271 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-175+4733A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124739280 | ||||||
| chr10:124739416
|
T | C | 1 | a0001c0001t0001g0272 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.-175+4597A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124739416 | ||||||
| chr10:124739576
|
G | C | 263 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(260): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-175+4437C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124739576 | ||||||
| chr10:124739605
|
C | G | 263 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(260): Show | 264 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(261): Show |
intron_variant | MODIFIER | c.-175+4408G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124739605 | ||||||
| chr10:124740035
|
T | A | 1 | a0001c0001t0031g0106 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.-175+3978A>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124740035 | ||||||
| chr10:124740038
|
G | A | 5 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(2): Show | 5 | HG00323.hp1 HG00639.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.-175+3975C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124740038 | ||||||
| chr10:124740064
|
C | T | 4 | a0001c0001t0012g0123a0001c0001t0033g0122a0001c0001t0033g0125others(1): Show | 4 | HG02965.hp2 HG03209.hp2 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.-175+3949G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124740064 | ||||||
| chr10:124740105
|
G | A | 5 | a0001c0001t0003g0097a0001c0001t0003g0098a0001c0001t0003g0099others(2): Show | 5 | HG00323.hp1 HG00639.hp2 HG01106.hp2 others(2): Show |
intron_variant | MODIFIER | c.-175+3908C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124740105 | ||||||
| chr10:124740196
|
C | T | 52 | a0001c0001t0001g0059a0001c0001t0001g0070a0001c0001t0001g0078others(49): Show | 52 | HG00323.hp1 HG00558.hp2 HG00639.hp2 others(49): Show |
intron_variant | MODIFIER | c.-175+3817G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124740196 | ||||||
| chr10:124740312
|
CA | C | 18 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(15): Show | 18 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-175+3700delT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124740312 | ||||||
| chr10:124740627
|
C | A | 1 | a0001c0001t0002g0324 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-175+3386G>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124740627 | ||||||
| chr10:124740635
|
C | T | 4 | a0001c0001t0009g0284a0001c0001t0036g0282a0001c0001t0036g0283others(1): Show | 4 | HG00323.hp2 HG01496.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.-175+3378G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124740635 | ||||||
| chr10:124740752
|
A | G | 310 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(307): Show | 313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): Show |
intron_variant | MODIFIER | c.-175+3261T>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124740752 | ||||||
| chr10:124740865
|
G | A | 2 | a0001c0001t0031g0106a0001c0001t0049g0105 | 2 | HG02738.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.-175+3148C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124740865 | ||||||
| chr10:124740906
|
G | T | 3 | a0001c0001t0022g0055a0001c0001t0022g0056a0001c0001t0051g0057 | 3 | HG01099.hp2 HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.-175+3107C>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124740906 | ||||||
| chr10:124740907
|
G | A | 1 | a0001c0001t0012g0054 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-175+3106C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124740907 | ||||||
| chr10:124741060
|
G | A | 18 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(15): Show | 18 | HG01884.hp2 HG02055.hp2 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.-175+2953C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124741060 | ||||||
| chr10:124741306
|
G | A | 262 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0059others(259): Show | 263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.-175+2707C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124741306 | ||||||
| chr10:124741458
|
C | T | 1 | a0001c0001t0003g0039 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.-175+2555G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124741458 | ||||||
| chr10:124741902
|
T | C | 2 | a0001c0001t0053g0275a0001c0001t0056g0274 | 2 | HG00673.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.-175+2111A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124741902 | ||||||
| chr10:124742029
|
G | A | 1 | a0001c0001t0015g0121 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.-175+1984C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124742029 | ||||||
| chr10:124742116
|
G | A | 6 | a0001c0001t0012g0123a0001c0001t0033g0122a0001c0001t0033g0125others(3): Show | 6 | HG01891.hp1 HG02965.hp2 HG03209.hp2 others(3): Show |
intron_variant | MODIFIER | c.-175+1897C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124742116 | ||||||
| chr10:124742125
|
T | C | 1 | a0001c0001t0017g0273 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.-175+1888A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124742125 | ||||||
| chr10:124742712
|
G | C | 155 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0129others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-175+1301C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124742712 | ||||||
| chr10:124743014
|
A | C | 2 | a0001c0001t0010g0127a0001c0001t0059g0128 | 2 | HG03490.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.-175+999T>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124743014 | ||||||
| chr10:124743142
|
G | A | 155 | a0001c0001t0001g0002a0001c0001t0001g0035a0001c0001t0001g0129others(152): Show | 156 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(153): Show |
intron_variant | MODIFIER | c.-175+871C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124743142 | ||||||
| chr10:124743315
|
C | T | 1 | a0001c0001t0014g0038 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.-175+698G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124743315 | ||||||
| chr10:124743442
|
GC | G | 25 | a0001c0001t0005g0009a0001c0001t0005g0011a0001c0001t0005g0014others(22): Show | 25 | HG00140.hp2 HG00408.hp1 HG00609.hp2 others(22): Show |
intron_variant | MODIFIER | c.-175+570delG | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124743442 | ||||||
| chr10:124743606
|
G | A | 2 | a0001c0001t0053g0275a0001c0001t0056g0274 | 2 | HG00673.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.-175+407C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124743606 | ||||||
| chr10:124743730
|
AGCCAG | A | 3 | a0001c0001t0006g0277a0001c0001t0006g0278a0001c0001t0015g0276 | 3 | HG02622.hp1 HG02886.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.-175+278_-175+282d others(7): Show |
FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124743730 | ||||||
| chr10:124743775
|
G | A | 3 | a0001c0001t0004g0279a0001c0001t0004g0280a0001c0001t0004g0281 | 3 | HG02717.hp1 NA18522.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.-175+238C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124743775 | ||||||
| chr10:124743799
|
C | G | 1 | a0001c0001t0052g0037 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-175+214G>C | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124743799 | ||||||
| chr10:124743894
|
C | T | 1 | a0001c0001t0010g0036 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.-175+119G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124743894 | ||||||
| chr10:124743993
|
C | T | 2 | a0001c0001t0001g0035a0001c0001t0007g0034 | 2 | HG02074.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-175+20G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124743993 |