Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| 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 | 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 | MVMVL others(417): Show |
chr10 | 124614292 | 124749378 |
| a0002 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | MVMVL others(417): Show |
chr10 | 124614292 | 124749378 |
| a0003 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | MVMVL others(417): Show |
chr10 | 124614292 | 124749378 |
| a0004 | 0/0 | 422 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | MVMVL others(417): Show |
chr10 | 124614292 | 124749378 |
| a0005 | 0/0 | 422 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | MVMVL others(417): Show |
chr10 | 124614292 | 124749378 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 1266 | 314 | 74 | 41 | 149 | 14 | 34 | FAM53B_chr10_124614292_124749378 | FAM53B | ATGGT others(1261): Show |
chr10 | 124614292 | 124749378 | ||
| a0001c0002 | 0/0 | 1266 | 7 | 0 | 7 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ATGGT others(1261): Show |
chr10 | 124614292 | 124749378 | ||
| a0001c0003 | 0/0 | 1266 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ATGGT others(1261): Show |
chr10 | 124614292 | 124749378 | ||
| a0001c0008 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ATGGT others(1261): Show |
chr10 | 124614292 | 124749378 | ||
| a0001c0009 | 0/0 | 1266 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ATGGT others(1261): Show |
chr10 | 124614292 | 124749378 | ||
| a0002c0004 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ATGGT others(1261): Show |
chr10 | 124614292 | 124749378 | ||
| a0003c0005 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ATGGT others(1261): Show |
chr10 | 124614292 | 124749378 | ||
| a0004c0007 | 0/0 | 1266 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ATGGT others(1261): Show |
chr10 | 124614292 | 124749378 | ||
| a0005c0006 | 0/0 | 1266 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ATGGT others(1261): Show |
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 | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0002 | 0/0 | 5759 | 20 | 0 | 0 | 20 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0003 | 0/0 | 5760 | 16 | 1 | 1 | 10 | 1 | 3 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5755): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0004 | 0/0 | 5759 | 11 | 11 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0005 | 0/0 | 5772 | 9 | 0 | 0 | 7 | 1 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5767): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0006 | 0/0 | 5759 | 9 | 9 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0007 | 0/0 | 5759 | 8 | 0 | 0 | 8 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0008 | 0/0 | 5763 | 7 | 0 | 0 | 7 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5758): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0009 | 0/0 | 5759 | 7 | 0 | 3 | 0 | 1 | 3 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0010 | 0/0 | 5759 | 6 | 4 | 0 | 0 | 0 | 2 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0011 | 0/0 | 5758 | 6 | 1 | 0 | 4 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5753): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0012 | 0/0 | 5759 | 5 | 5 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0013 | 0/0 | 5760 | 5 | 0 | 0 | 5 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5755): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0014 | 0/0 | 5764 | 4 | 0 | 4 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5759): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0015 | 0/0 | 5761 | 4 | 4 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5756): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0016 | 0/0 | 5759 | 4 | 0 | 3 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0017 | 0/0 | 5758 | 4 | 0 | 0 | 4 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5753): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0018 | 0/0 | 5759 | 3 | 0 | 0 | 1 | 2 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0019 | 0/0 | 5771 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5766): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0020 | 0/0 | 5772 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5767): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0021 | 0/0 | 5759 | 3 | 2 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0022 | 0/0 | 5759 | 3 | 1 | 2 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0023 | 0/0 | 5759 | 3 | 3 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0024 | 0/0 | 5759 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0025 | 0/0 | 5763 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5758): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0026 | 0/0 | 5759 | 2 | 1 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0027 | 0/0 | 5759 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0028 | 0/0 | 5758 | 3 | 0 | 0 | 3 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5753): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0029 | 0/0 | 5772 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5767): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0030 | 0/0 | 5772 | 2 | 1 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5767): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0031 | 0/0 | 5759 | 2 | 0 | 0 | 0 | 0 | 2 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0032 | 0/0 | 5759 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0033 | 0/0 | 5759 | 2 | 2 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0034 | 0/0 | 5759 | 2 | 0 | 0 | 0 | 0 | 2 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0035 | 0/0 | 5758 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5753): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0036 | 0/0 | 5760 | 2 | 0 | 1 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5755): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0037 | 0/0 | 5759 | 2 | 0 | 1 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0038 | 0/0 | 5772 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5767): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0039 | 0/0 | 5772 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5767): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0040 | 0/0 | 5771 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5766): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0041 | 0/0 | 5772 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5767): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0042 | 0/0 | 5776 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5771): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0043 | 0/0 | 5772 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5767): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0044 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0045 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0046 | 0/0 | 5759 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0047 | 0/0 | 5770 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5765): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0048 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0049 | 0/0 | 5759 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0050 | 0/0 | 5758 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5753): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0051 | 0/0 | 5760 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5755): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0052 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0053 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0054 | 0/0 | 5758 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5753): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0055 | 0/0 | 5759 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0056 | 0/0 | 5769 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5764): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0057 | 0/0 | 5769 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5764): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0059 | 0/0 | 5763 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5758): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0060 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0061 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0062 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0063 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5755): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0064 | 0/0 | 5760 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5755): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0065 | 0/0 | 5762 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5757): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0066 | 0/0 | 5760 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5755): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0067 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0068 | 0/0 | 5759 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0069 | 0/0 | 5759 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0070 | 0/0 | 5760 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5755): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0071 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0072 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0073 | 0/0 | 5761 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5756): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0074 | 0/0 | 5763 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5758): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0075 | 0/0 | 5761 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5756): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0076 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0077 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0078 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0079 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0080 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0081 | 0/0 | 5760 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5755): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0082 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0083 | 0/0 | 5760 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5755): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0085 | 0/0 | 5760 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5755): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0087 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0088 | 0/0 | 5758 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5753): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0089 | 0/0 | 5749 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5744): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0090 | 0/0 | 5761 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5756): Show |
chr10 | 124614292 | 124749378 |
| a0001c0001t0091 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0002t0001 | 0/0 | 5759 | 7 | 0 | 7 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0003t0003 | 0/0 | 5760 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5755): Show |
chr10 | 124614292 | 124749378 |
| a0001c0003t0058 | 0/0 | 5771 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5766): Show |
chr10 | 124614292 | 124749378 |
| a0001c0008t0018 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0001c0009t0002 | 0/0 | 5759 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0002c0004t0086 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0003c0005t0026 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0004c0007t0001 | 0/0 | 5759 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5754): Show |
chr10 | 124614292 | 124749378 |
| a0005c0006t0084 | 0/0 | 5758 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | ACTGC others(5753): Show |
chr10 | 124614292 | 124749378 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0047 | 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 |
| a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0054 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0084 | 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 |
| a0001c0001t0001g0105 | 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 |
| a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0134 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0140 | 0/1 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0170 | 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 | 1 | 0 | 0 | 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 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 1 | 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 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | 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 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 2 | 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 |
| a0001c0001t0002g0292 | 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 |
| a0001c0001t0002g0303 | 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 |
| a0001c0001t0002g0310 | 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 |
| a0001c0001t0002g0314 | 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 |
| a0001c0001t0002g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0319 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0072 | 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 |
| a0001c0001t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0003g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0003g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0004g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0004g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0004g0111 | 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 |
| a0001c0001t0004g0117 | 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 |
| a0001c0001t0004g0121 | 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 |
| a0001c0001t0004g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0005g0008 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0005g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0005g0013 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0005g0017 | 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 |
| a0001c0001t0005g0021 | 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 |
| a0001c0001t0005g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0006g0042 | 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 |
| a0001c0001t0006g0063 | 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 |
| a0001c0001t0006g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0006g0234 | 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 |
| a0001c0001t0006g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0007g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0007g0186 | 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 |
| a0001c0001t0007g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0007g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0007g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0007g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0008g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0008g0255 | 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 |
| a0001c0001t0008g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0009g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0009g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0009g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0009g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0009g0322 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0009g0323 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0009g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0010g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0010g0065 | 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 |
| a0001c0001t0010g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0010g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0010g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0011g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0011g0073 | 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 |
| a0001c0001t0011g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0011g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0011g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0012g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0012g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0012g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0012g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0012g0124 | 0/0 | 1 | 1 | 0 | 0 | 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 |
| a0001c0001t0013g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0013g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0014g0037 | 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 |
| a0001c0001t0014g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0014g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0015g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0015g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0015g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0015g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0016g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0016g0178 | 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 |
| a0001c0001t0016g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0017g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0017g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0017g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0017g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0018g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0018g0293 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0018g0296 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0019g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 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 |
| a0001c0001t0019g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0020g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0020g0014 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0020g0025 | 0/0 | 1 | 0 | 0 | 1 | 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 |
| a0001c0001t0021g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0021g0267 | 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 |
| a0001c0001t0022g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0022g0064 | 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 |
| a0001c0001t0023g0240 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0024g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0024g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0024g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0025g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0025g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0025g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0026g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0026g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0027g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0027g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0027g0222 | 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 |
| a0001c0001t0028g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0028g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0029g0005 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0029g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0030g0004 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0030g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0031g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0031g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0032g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0032g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0033g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0033g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0034g0155 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0034g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | 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 |
| a0001c0001t0035g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0036g0283 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0036g0284 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0037g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0037g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0038g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0039g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0040g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0041g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0042g0011 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0043g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0044g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0045g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0046g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0047g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0048g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0049g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0050g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0051g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0052g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0053g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0054g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0055g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0056g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0057g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0059g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0060g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0061g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0062g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0063g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0064g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0065g0093 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0066g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0067g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0068g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0069g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0070g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0071g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0072g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0073g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0074g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0075g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0076g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0077g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0078g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0079g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0080g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0081g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0082g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0083g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0085g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0087g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0088g0312 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0089g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0090g0286 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0001t0091g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0002t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0002t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0002t0001g0208 | 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 |
| a0001c0002t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0002t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0003t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0003t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0003t0058g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0008t0018g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0001c0009t0002g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0002c0004t0086g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0003c0005t0026g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0004c0007t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| a0005c0006t0084g0241 | 0/0 | 1 | 0 | 0 | 1 | 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 | g0130 | EUR | GBR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00099 | hp2 | a0001 | c0001 | t0001 | g0218 | EUR | GBR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00140 | hp1 | a0001 | c0001 | t0001 | g0197 | EUR | GBR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00140 | hp2 | a0001 | c0001 | t0005 | g0008 | EUR | GBR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0136 | EUR | FIN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00280 | hp2 | a0001 | c0001 | t0009 | g0322 | EUR | FIN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00323 | hp1 | a0001 | c0001 | t0003 | g0099 | EUR | FIN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00323 | hp2 | a0001 | c0001 | t0036 | g0283 | EUR | FIN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00408 | hp1 | a0001 | c0001 | t0038 | g0020 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00408 | hp2 | a0001 | c0001 | t0024 | g0263 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00423 | hp2 | a0001 | c0001 | t0057 | g0269 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00558 | hp1 | a0001 | c0001 | t0017 | g0188 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00558 | hp2 | a0001 | c0003 | t0003 | g0077 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00609 | hp1 | a0001 | c0001 | t0013 | g0304 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00609 | hp2 | a0001 | c0001 | t0029 | g0005 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00621 | hp1 | a0001 | c0001 | t0041 | g0012 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00621 | hp2 | a0001 | c0001 | t0048 | g0247 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00639 | hp1 | a0001 | c0001 | t0021 | g0267 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00639 | hp2 | a0001 | c0001 | t0003 | g0102 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00642 | hp1 | a0001 | c0001 | t0001 | g0134 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00642 | hp2 | a0001 | c0001 | t0001 | g0193 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0131 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00673 | hp2 | a0001 | c0001 | t0056 | g0275 | EAS | CHS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00735 | hp1 | a0001 | c0001 | t0014 | g0037 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0196 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01069 | hp1 | a0001 | c0001 | t0009 | g0294 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01069 | hp2 | a0001 | c0001 | t0016 | g0202 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01071 | hp1 | a0001 | c0001 | t0016 | g0203 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01071 | hp2 | a0001 | c0001 | t0001 | g0160 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01074 | hp1 | a0001 | c0001 | t0068 | g0271 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01074 | hp2 | a0001 | c0001 | t0009 | g0321 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01081 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01081 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0208 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01099 | hp2 | a0001 | c0001 | t0051 | g0058 | 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 | g0101 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01168 | hp1 | a0001 | c0001 | t0022 | g0056 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01168 | hp2 | a0001 | c0001 | t0040 | g0007 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01169 | hp1 | a0001 | c0001 | t0001 | g0225 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01169 | hp2 | a0001 | c0001 | t0022 | g0057 | 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 | g0326 | AMR | PUR | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01261 | hp1 | a0001 | c0001 | t0070 | g0182 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0216 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01346 | hp1 | a0001 | c0001 | t0016 | g0178 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01346 | hp2 | a0001 | c0001 | t0001 | g0137 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01361 | hp1 | a0001 | c0001 | t0066 | g0179 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01361 | hp2 | a0001 | c0001 | t0014 | g0094 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01496 | hp1 | a0001 | c0001 | t0036 | g0284 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0213 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01515 | hp1 | a0001 | c0001 | t0018 | g0296 | EUR | IBS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0152 | EUR | IBS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01517 | hp1 | a0001 | c0001 | t0001 | g0167 | EUR | IBS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01517 | hp2 | a0001 | c0001 | t0018 | g0293 | EUR | IBS | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01884 | hp1 | a0001 | c0001 | t0006 | g0061 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0112 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01891 | hp1 | a0001 | c0001 | t0052 | g0036 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01934 | hp1 | a0001 | c0002 | t0001 | g0096 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01934 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0154 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01943 | hp2 | a0001 | c0001 | t0030 | g0004 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01952 | hp1 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01952 | hp2 | a0001 | c0001 | t0090 | g0286 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01975 | hp1 | a0001 | c0002 | t0001 | g0214 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01975 | hp2 | a0001 | c0001 | t0009 | g0323 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01981 | hp1 | a0001 | c0001 | t0014 | g0095 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01981 | hp2 | a0001 | c0001 | t0069 | g0181 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02004 | hp1 | a0001 | c0002 | t0001 | g0231 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02004 | hp2 | a0001 | c0001 | t0001 | g0221 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02027 | hp1 | a0001 | c0001 | t0071 | g0211 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02027 | hp2 | a0001 | c0001 | t0024 | g0257 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02040 | hp1 | a0001 | c0001 | t0035 | g0150 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02040 | hp2 | a0001 | c0001 | t0003 | g0059 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02055 | hp1 | a0001 | c0001 | t0030 | g0009 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02055 | hp2 | a0001 | c0001 | t0004 | g0120 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02056 | hp1 | a0001 | c0001 | t0062 | g0133 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02056 | hp2 | a0001 | c0001 | t0007 | g0207 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02071 | hp1 | a0001 | c0001 | t0002 | g0325 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02071 | hp2 | a0001 | c0001 | t0007 | g0186 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02074 | hp2 | a0001 | c0001 | t0007 | g0033 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02080 | hp1 | a0001 | c0001 | t0002 | g0313 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02129 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02132 | hp1 | a0001 | c0001 | t0042 | g0011 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02132 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02135 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02135 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | KHV | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02145 | hp1 | a0001 | c0001 | t0063 | g0066 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02145 | hp2 | a0002 | c0004 | t0086 | g0053 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02155 | hp1 | a0001 | c0001 | t0020 | g0014 | EAS | CDX | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02155 | hp2 | a0001 | c0001 | t0013 | g0306 | EAS | CDX | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02165 | hp1 | a0001 | c0001 | t0007 | g0253 | EAS | CDX | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | CDX | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02257 | hp1 | a0001 | c0001 | t0006 | g0234 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02257 | hp2 | a0001 | c0001 | t0004 | g0119 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02258 | hp1 | a0001 | c0001 | t0004 | g0121 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02258 | hp2 | a0001 | c0001 | t0015 | g0052 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02280 | hp1 | a0001 | c0001 | t0039 | g0028 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02280 | hp2 | a0001 | c0001 | t0004 | g0116 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02300 | hp1 | a0001 | c0002 | t0001 | g0192 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02300 | hp2 | a0001 | c0001 | t0026 | g0242 | AMR | PEL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02451 | hp1 | a0001 | c0001 | t0054 | g0039 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02451 | hp2 | a0001 | c0001 | t0001 | g0198 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02572 | hp1 | a0001 | c0001 | t0022 | g0064 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02572 | hp2 | a0001 | c0001 | t0012 | g0051 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02602 | hp1 | a0001 | c0001 | t0009 | g0295 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02602 | hp2 | a0001 | c0001 | t0074 | g0157 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02615 | hp1 | a0001 | c0001 | t0021 | g0200 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02615 | hp2 | a0001 | c0001 | t0012 | g0055 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02622 | hp1 | a0001 | c0001 | t0006 | g0279 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02622 | hp2 | a0001 | c0001 | t0001 | g0168 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02647 | hp1 | a0001 | c0001 | t0045 | g0030 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02647 | hp2 | a0001 | c0001 | t0006 | g0062 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02683 | hp1 | a0001 | c0001 | t0001 | g0272 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02683 | hp2 | a0001 | c0001 | t0037 | g0320 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02698 | hp1 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02698 | hp2 | a0001 | c0001 | t0011 | g0092 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02717 | hp1 | a0001 | c0001 | t0004 | g0282 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02717 | hp2 | a0001 | c0001 | t0061 | g0244 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02723 | hp1 | a0001 | c0001 | t0004 | g0117 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02723 | hp2 | a0001 | c0001 | t0082 | g0043 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0266 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02738 | hp2 | a0001 | c0001 | t0031 | g0107 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02809 | hp1 | a0001 | c0001 | t0023 | g0240 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02809 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02818 | hp1 | a0001 | c0001 | t0004 | g0109 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02818 | hp2 | a0001 | c0001 | t0010 | g0035 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02886 | hp1 | a0001 | c0001 | t0015 | g0277 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02886 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02896 | hp1 | a0001 | c0001 | t0050 | g0108 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02896 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | GWD | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02965 | hp1 | a0001 | c0001 | t0023 | g0238 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02965 | hp2 | a0001 | c0001 | t0075 | g0125 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02976 | hp1 | a0001 | c0001 | t0021 | g0199 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02976 | hp2 | a0001 | c0001 | t0015 | g0122 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03098 | hp1 | a0001 | c0001 | t0006 | g0278 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03098 | hp2 | a0001 | c0001 | t0011 | g0245 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03130 | hp1 | a0001 | c0001 | t0085 | g0040 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03130 | hp2 | a0001 | c0001 | t0026 | g0235 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03139 | hp1 | a0001 | c0001 | t0087 | g0287 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03139 | hp2 | a0003 | c0005 | t0026 | g0237 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03209 | hp1 | a0001 | c0001 | t0015 | g0041 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03209 | hp2 | a0001 | c0001 | t0033 | g0123 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03225 | hp1 | a0001 | c0001 | t0060 | g0127 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03225 | hp2 | a0004 | c0007 | t0001 | g0103 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03453 | hp1 | a0001 | c0001 | t0004 | g0104 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03453 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03486 | hp1 | a0001 | c0008 | t0018 | g0318 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03486 | hp2 | a0001 | c0001 | t0033 | g0126 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03490 | hp1 | a0001 | c0001 | t0003 | g0100 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03490 | hp2 | a0001 | c0001 | t0059 | g0129 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0175 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03492 | hp2 | a0001 | c0001 | t0003 | g0098 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03516 | hp1 | a0001 | c0001 | t0010 | g0065 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03516 | hp2 | a0001 | c0001 | t0006 | g0090 | AFR | ESN | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03579 | hp1 | a0001 | c0001 | t0004 | g0111 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03579 | hp2 | a0001 | c0001 | t0012 | g0124 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03669 | hp1 | a0001 | c0001 | t0034 | g0155 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03669 | hp2 | a0001 | c0001 | t0001 | g0227 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03688 | hp1 | a0001 | c0001 | t0055 | g0183 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03688 | hp2 | a0001 | c0001 | t0046 | g0031 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03704 | hp1 | a0001 | c0001 | t0001 | g0156 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03704 | hp2 | a0001 | c0001 | t0003 | g0078 | SAS | PJL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03834 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | BEB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03834 | hp2 | a0001 | c0001 | t0049 | g0106 | SAS | BEB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03927 | hp1 | a0001 | c0001 | t0088 | g0312 | SAS | BEB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03927 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | BEB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | BEB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03942 | hp2 | a0001 | c0001 | t0065 | g0093 | SAS | BEB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04115 | hp1 | a0001 | c0001 | t0010 | g0224 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04115 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04184 | hp1 | a0001 | c0001 | t0009 | g0324 | SAS | BEB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04184 | hp2 | a0001 | c0001 | t0010 | g0128 | SAS | BEB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04199 | hp1 | a0001 | c0001 | t0034 | g0228 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0161 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04204 | hp1 | a0001 | c0001 | t0005 | g0010 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0229 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04228 | hp1 | a0001 | c0001 | t0009 | g0285 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG04228 | hp2 | a0001 | c0001 | t0031 | g0050 | SAS | STU | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18522 | hp1 | a0001 | c0001 | t0010 | g0068 | AFR | YRI | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18522 | hp2 | a0001 | c0001 | t0004 | g0280 | AFR | YRI | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18612 | hp1 | a0001 | c0001 | t0007 | g0206 | EAS | CHB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18612 | hp2 | a0001 | c0001 | t0002 | g0301 | EAS | CHB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18747 | hp1 | a0001 | c0001 | t0047 | g0032 | EAS | CHB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18747 | hp2 | a0001 | c0001 | t0019 | g0016 | EAS | CHB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18906 | hp1 | a0001 | c0001 | t0006 | g0042 | AFR | YRI | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18906 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | YRI | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18939 | hp2 | a0001 | c0001 | t0011 | g0091 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18942 | hp1 | a0001 | c0001 | t0025 | g0254 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18942 | hp2 | a0001 | c0001 | t0002 | g0316 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18944 | hp1 | a0001 | c0001 | t0005 | g0021 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18944 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18945 | hp1 | a0001 | c0001 | t0007 | g0205 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0302 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18946 | hp1 | a0005 | c0006 | t0084 | g0241 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18946 | hp2 | a0001 | c0001 | t0017 | g0144 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18947 | hp1 | a0001 | c0001 | t0019 | g0015 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18947 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18948 | hp2 | a0001 | c0001 | t0024 | g0251 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18949 | hp1 | a0001 | c0001 | t0017 | g0274 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18949 | hp2 | a0001 | c0001 | t0008 | g0259 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18956 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18956 | hp2 | a0001 | c0001 | t0008 | g0262 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18957 | hp1 | a0001 | c0001 | t0028 | g0289 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18957 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18960 | hp1 | a0001 | c0001 | t0028 | g0288 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18960 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18962 | hp2 | a0001 | c0001 | t0025 | g0249 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18963 | hp1 | a0001 | c0001 | t0067 | g0185 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18963 | hp2 | a0001 | c0001 | t0019 | g0026 | 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 | g0147 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18967 | hp1 | a0001 | c0001 | t0005 | g0022 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18967 | hp2 | a0001 | c0001 | t0007 | g0264 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18969 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18969 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18970 | hp1 | a0001 | c0001 | t0002 | g0297 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18970 | hp2 | a0001 | c0001 | t0008 | g0261 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18973 | hp1 | a0001 | c0001 | t0001 | g0233 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18973 | hp2 | a0001 | c0001 | t0011 | g0070 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18977 | hp1 | a0001 | c0001 | t0013 | g0307 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18977 | hp2 | a0001 | c0001 | t0005 | g0027 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18980 | hp1 | a0001 | c0001 | t0002 | g0299 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18980 | hp2 | a0001 | c0001 | t0016 | g0169 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18982 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18982 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18983 | hp1 | a0001 | c0001 | t0076 | g0256 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18983 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18984 | hp1 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18984 | hp2 | a0001 | c0001 | t0003 | g0038 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18986 | hp1 | a0001 | c0001 | t0002 | g0314 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18986 | hp2 | a0001 | c0001 | t0032 | g0268 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18988 | hp1 | a0001 | c0001 | t0002 | g0310 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18988 | hp2 | a0001 | c0001 | t0020 | g0006 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18989 | hp1 | a0001 | c0001 | t0013 | g0305 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18990 | hp1 | a0001 | c0003 | t0003 | g0074 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18990 | hp2 | a0001 | c0001 | t0002 | g0317 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18995 | hp1 | a0001 | c0001 | t0008 | g0260 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18995 | hp2 | a0001 | c0001 | t0003 | g0082 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18998 | hp1 | a0001 | c0001 | t0028 | g0291 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18998 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18999 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18999 | hp2 | a0001 | c0001 | t0002 | g0309 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19002 | hp1 | a0001 | c0001 | t0025 | g0265 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19002 | hp2 | a0001 | c0001 | t0081 | g0201 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19003 | hp1 | a0001 | c0001 | t0029 | g0023 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19003 | hp2 | a0001 | c0001 | t0017 | g0187 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19005 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19005 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19007 | hp1 | a0001 | c0001 | t0008 | g0255 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19007 | hp2 | a0001 | c0001 | t0003 | g0076 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19009 | hp1 | a0001 | c0001 | t0078 | g0195 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19009 | hp2 | a0001 | c0001 | t0003 | g0081 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19010 | hp1 | a0001 | c0001 | t0007 | g0212 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0034 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19011 | hp1 | a0001 | c0001 | t0003 | g0072 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19011 | hp2 | a0001 | c0001 | t0072 | g0252 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19043 | hp1 | a0001 | c0001 | t0006 | g0089 | AFR | LWK | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19043 | hp2 | a0001 | c0001 | t0012 | g0044 | AFR | LWK | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19057 | hp1 | a0001 | c0001 | t0027 | g0210 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19057 | hp2 | a0001 | c0001 | t0008 | g0248 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19064 | hp1 | a0001 | c0001 | t0005 | g0018 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19064 | hp2 | a0001 | c0001 | t0018 | g0290 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19065 | hp2 | a0001 | c0001 | t0003 | g0069 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19066 | hp1 | a0001 | c0001 | t0002 | g0300 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19066 | hp2 | a0001 | c0001 | t0083 | g0189 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19068 | hp1 | a0001 | c0001 | t0073 | g0250 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19068 | hp2 | a0001 | c0001 | t0002 | g0319 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19070 | hp2 | a0001 | c0009 | t0002 | g0308 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19078 | hp1 | a0001 | c0001 | t0089 | g0311 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19078 | hp2 | a0001 | c0001 | t0077 | g0139 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19079 | hp2 | a0001 | c0001 | t0020 | g0025 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19081 | hp1 | a0001 | c0001 | t0043 | g0024 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19081 | hp2 | a0001 | c0001 | t0003 | g0075 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19082 | hp1 | a0001 | c0001 | t0002 | g0303 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19082 | hp2 | a0001 | c0001 | t0044 | g0029 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19083 | hp1 | a0001 | c0003 | t0058 | g0270 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19083 | hp2 | a0001 | c0001 | t0008 | g0258 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19085 | hp1 | a0001 | c0001 | t0013 | g0315 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0017 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19086 | hp1 | a0001 | c0001 | t0027 | g0222 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19086 | hp2 | a0001 | c0001 | t0003 | g0088 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19087 | hp1 | a0001 | c0001 | t0005 | g0019 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19087 | hp2 | a0001 | c0001 | t0035 | g0149 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19088 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19088 | hp2 | a0001 | c0001 | t0005 | g0013 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19089 | hp1 | a0001 | c0001 | t0027 | g0171 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19089 | hp2 | a0001 | c0001 | t0002 | g0292 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19090 | hp1 | a0001 | c0001 | t0003 | g0083 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19091 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19091 | hp2 | a0001 | c0001 | t0011 | g0073 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19240 | hp1 | a0001 | c0001 | t0012 | g0045 | AFR | YRI | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA19240 | hp2 | a0001 | c0001 | t0010 | g0067 | AFR | YRI | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA20129 | hp1 | a0001 | c0001 | t0003 | g0087 | AFR | ASW | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA20129 | hp2 | a0001 | c0001 | t0004 | g0281 | AFR | ASW | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0060 | EUR | TSI | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA20752 | hp2 | a0001 | c0001 | t0001 | g0180 | EUR | TSI | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01123 | hp1 | a0001 | c0001 | t0014 | g0097 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG01123 | hp2 | a0001 | c0002 | t0001 | g0204 | AMR | CLM | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02109 | hp1 | a0001 | c0001 | t0001 | g0114 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02109 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02559 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG02559 | hp2 | a0001 | c0001 | t0001 | g0113 | AFR | ACB | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03471 | hp1 | a0001 | c0001 | t0023 | g0239 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG03471 | hp2 | a0001 | c0001 | t0001 | g0236 | AFR | MSL | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG06807 | hp1 | a0001 | c0001 | t0091 | g0327 | AFR | USA | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| HG06807 | hp2 | a0001 | c0001 | t0001 | g0135 | AFR | USA | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18955 | hp1 | a0001 | c0001 | t0053 | g0276 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA18955 | hp2 | a0001 | c0001 | t0079 | g0172 | EAS | JPT | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA20300 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | USA | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| NA20300 | hp2 | a0001 | c0001 | t0080 | g0110 | AFR | USA | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0001 | g0140 | REF | REF | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0001 | g0054 | REF | REF | FAM53B_chr10_124614292_124749378 | FAM53B | chr10 | 124614292 | 124749378 |
| view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:124623306 | G | A | 1 | a0003 | 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 | a0002 | 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 | a0005 | 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 | a0004 | 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 |
| view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0002c0004 | 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 |
| view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 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 | a0001c0001t0008 a0001c0001t0024 a0001c0001t0025 others(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 | a0001c0001t0003 a0001c0001t0006 a0001c0001t0011 others(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 | a0001c0001t0034 a0001c0001t0046 |
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 | a0001c0001t0053 a0001c0001t0056 a0001c0001t0067 |
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 | a0001c0001t0005 a0001c0001t0019 a0001c0001t0029 others(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 | a0001c0001t0006 a0001c0001t0013 a0001c0001t0036 others(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 | a0001c0001t0003 a0001c0001t0014 a0001c0001t0015 others(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 | a0001c0001t0008 a0001c0001t0025 a0001c0001t0042 others(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 | a0001c0001t0056 a0001c0001t0057 |
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 | a0001c0001t0031 a0001c0001t0049 |
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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(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 | a0001c0001t0005 a0001c0001t0019 a0001c0001t0029 others(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 | a0001c0001t0002 a0001c0001t0003 a0001c0001t0004 others(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 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0010 others(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 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0013 others(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 | a0001c0001t0022 a0001c0001t0051 |
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 | a0001c0001t0005 a0001c0001t0008 a0001c0001t0010 others(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 | a0002c0004t0086 | 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 | a0001c0001t0008 a0001c0001t0024 a0001c0001t0025 others(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 | a0001c0001t0002 a0001c0001t0004 a0001c0001t0005 others(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 | a0001c0001t0026 a0003c0005t0026 |
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 | a0001c0001t0002 a0001c0001t0007 a0001c0001t0009 others(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 | a0002c0004t0086 | 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 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0013 others(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 | a0001c0001t0005 a0001c0001t0019 a0001c0001t0020 others(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 |
| view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr10:124623720 | G | A | 43 | a0001c0001t0001g0154 a0001c0001t0003g0038 a0001c0001t0003g0059 others(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 | a0001c0001t0002g0301 a0001c0001t0002g0302 a0001c0001t0007g0207 others(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 | a0001c0001t0030g0004 | 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 | a0001c0001t0015g0041 a0001c0001t0015g0052 a0001c0001t0015g0277 |
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 | a0001c0001t0005g0017 | 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 | a0001c0001t0033g0123 a0001c0001t0033g0126 a0001c0001t0085g0040 |
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 | a0001c0001t0015g0122 | 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0006g0090 | 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 | a0001c0001t0039g0028 | 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | a0001c0001t0001g0230 a0001c0001t0001g0236 a0001c0001t0002g0002 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0298 others(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 | a0001c0001t0014g0037 a0001c0001t0014g0094 a0001c0001t0014g0095 others(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 | a0001c0001t0078g0195 | 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 | a0001c0001t0047g0032 | 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 | a0001c0001t0005g0021 a0001c0001t0005g0022 a0001c0001t0043g0024 |
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 | a0001c0001t0010g0224 | 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 | a0001c0001t0001g0153 | 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 | a0001c0001t0025g0249 | 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 | a0001c0001t0033g0126 | 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0024g0257 | 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 | a0001c0001t0004g0104 a0001c0001t0004g0109 a0001c0001t0004g0116 others(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 | a0001c0001t0089g0311 | 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 | a0001c0001t0009g0285 a0001c0001t0009g0321 a0001c0001t0009g0322 others(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 | a0001c0001t0025g0249 | 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 | a0001c0001t0085g0040 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | 45 | a0001c0001t0001g0130 a0001c0001t0001g0135 a0001c0001t0001g0136 others(42): Show |
45 | HG00099.hp1 HG00280.hp1 HG00621.hp1 others(42): 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 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0138 others(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 | a0001c0001t0091g0327 | 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 | a0001c0001t0004g0104 a0001c0001t0004g0109 a0001c0001t0004g0111 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0153 a0001c0001t0001g0154 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0079 |
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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0003g0059 | 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 | a0001c0001t0009g0322 | 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 | a0001c0001t0010g0224 | 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 | a0001c0001t0091g0327 | 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 | a0001c0001t0001g0145 a0001c0001t0001g0152 a0001c0001t0001g0160 others(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 | a0001c0001t0001g0115 | 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 | a0001c0001t0001g0236 | 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 | a0001c0001t0012g0124 a0001c0001t0015g0122 a0001c0001t0060g0127 others(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 | a0001c0001t0079g0172 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0047 others(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 | a0001c0001t0001g0161 a0001c0001t0001g0194 a0001c0001t0001g0217 others(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 | a0001c0001t0001g0246 a0001c0001t0003g0038 a0001c0001t0003g0076 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0131 a0001c0001t0001g0152 others(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 | 28 | a0001c0001t0001g0046 a0001c0001t0001g0049 a0001c0001t0001g0159 others(25): 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0065g0093 | 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 | a0001c0001t0002g0298 | 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 | a0001c0001t0001g0230 a0001c0001t0002g0003 a0001c0001t0002g0299 others(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 | a0001c0001t0002g0301 a0001c0001t0002g0302 a0001c0001t0007g0207 others(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 | a0001c0001t0001g0134 a0001c0001t0001g0137 a0001c0001t0001g0138 others(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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0001g0136 | 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 | 86 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(83): Show |
87 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(84): Show |
intron_variant | MODIFIER | c.907-3961delG | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124627564 | |||||||
| chr10:124627633 | C | T | 1 | a0001c0001t0013g0315 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0105 others(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 | a0001c0003t0058g0270 | 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 | a0001c0003t0058g0270 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0105 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0003t0058g0270 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0010g0128 a0001c0001t0010g0224 a0001c0001t0059g0129 |
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 | a0001c0001t0054g0039 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0105 others(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 | a0001c0001t0054g0039 | 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 | 317 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(314): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): 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 | a0001c0001t0001g0217 | 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 | a0001c0001t0008g0248 | 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 | a0001c0001t0010g0035 a0001c0001t0010g0065 a0001c0001t0010g0067 others(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 | a0001c0001t0001g0219 | 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 | a0001c0001t0010g0035 a0001c0001t0010g0065 a0001c0001t0010g0067 others(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 | a0001c0001t0006g0062 | 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 | a0001c0001t0001g0131 | 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 | a0001c0003t0058g0270 | 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 | a0001c0001t0018g0290 a0001c0001t0028g0291 |
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 | a0001c0001t0054g0039 | 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 | 269 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(266): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | a0001c0001t0011g0092 | 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 | a0001c0001t0026g0242 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0004g0104 | 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 | 269 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(266): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): 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 | a0001c0001t0089g0311 | 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 | a0001c0001t0089g0311 | 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 | a0001c0001t0089g0311 | 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 | a0001c0001t0089g0311 | 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 | a0001c0001t0063g0066 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0004g0104 a0004c0007t0001g0103 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0105 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | 137 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0130 others(134): Show |
138 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(135): 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 | a0001c0001t0003g0098 a0001c0001t0003g0099 a0001c0001t0003g0100 others(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 | a0001c0001t0005g0021 a0001c0001t0005g0022 a0001c0001t0043g0024 |
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 | a0001c0001t0001g0079 | 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 | a0001c0001t0074g0157 | 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 | a0001c0001t0007g0253 a0001c0001t0008g0248 a0001c0001t0008g0255 others(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 | a0001c0001t0001g0151 a0001c0001t0001g0173 |
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 | a0001c0001t0004g0109 a0001c0001t0004g0111 a0001c0001t0004g0116 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0105 others(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 | a0001c0001t0089g0311 | 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 | a0001c0001t0001g0118 | 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 | a0001c0001t0047g0032 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0004g0109 a0001c0001t0004g0111 a0001c0001t0004g0116 others(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 | a0001c0001t0009g0321 | 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 | a0001c0001t0015g0122 | 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 | a0001c0001t0046g0031 | 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 | a0001c0001t0033g0123 | 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 | 310 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(307): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): 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 | a0001c0001t0054g0039 | 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 | a0001c0001t0003g0072 a0001c0001t0004g0109 a0001c0001t0004g0111 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0105 others(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 | 89 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(86): Show |
90 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(87): 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 | a0001c0002t0001g0213 | 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 | a0001c0001t0001g0141 a0001c0001t0001g0174 a0001c0001t0001g0190 |
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 | a0001c0001t0001g0112 | 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 | a0001c0001t0002g0300 a0001c0001t0002g0310 |
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 | a0001c0001t0015g0122 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0076g0256 | 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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0018g0290 a0001c0001t0028g0288 a0001c0001t0028g0289 others(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 | 44 | a0001c0001t0001g0130 a0001c0001t0001g0135 a0001c0001t0001g0136 others(41): Show |
44 | HG00099.hp1 HG00280.hp1 HG01071.hp2 others(41): 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 | a0001c0001t0005g0019 | 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 | a0001c0001t0091g0327 | 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 | a0001c0001t0052g0036 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | 110 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(107): Show |
111 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(108): 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 | a0001c0001t0030g0004 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0105 others(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 | 44 | a0001c0001t0001g0130 a0001c0001t0001g0135 a0001c0001t0001g0136 others(41): Show |
44 | HG00099.hp1 HG00280.hp1 HG01071.hp2 others(41): Show |
intron_variant | MODIFIER | c.907-11527G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124635131 | |||||||
| chr10:124635197 | A | G | 110 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(107): Show |
111 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(108): 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 | a0001c0001t0004g0117 | 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 | a0001c0001t0004g0104 a0004c0007t0001g0103 |
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 | 308 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(305): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): 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 | a0001c0001t0002g0314 | 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 | a0001c0001t0004g0109 a0001c0001t0004g0111 a0001c0001t0004g0116 others(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 | a0001c0001t0001g0191 | 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 | 110 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(107): Show |
111 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(108): 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | 87 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(84): Show |
88 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(85): 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 | a0001c0001t0005g0021 a0001c0001t0005g0022 a0001c0001t0043g0024 |
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 | a0001c0001t0001g0130 | 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 | 322 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0047 others(319): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): 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 | a0001c0001t0052g0036 | 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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0004g0104 a0004c0007t0001g0103 |
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 | 308 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(305): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): 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 | a0001c0001t0004g0104 a0004c0007t0001g0103 |
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 | a0001c0001t0002g0301 a0001c0001t0002g0302 a0001c0001t0007g0207 others(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 | a0001c0001t0073g0250 | 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 | a0001c0001t0043g0024 | 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 | a0001c0001t0013g0306 | 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 | a0001c0001t0052g0036 | 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 | 310 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(307): Show |
313 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(310): 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 | a0001c0001t0028g0288 | 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 | a0001c0001t0004g0109 a0001c0001t0004g0116 a0001c0001t0004g0119 others(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 | a0001c0001t0004g0111 a0001c0001t0004g0121 |
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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0052g0036 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0105 others(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 | a0001c0001t0089g0311 | 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 | a0001c0001t0054g0039 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0065g0093 | 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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0002g0292 a0001c0001t0002g0301 a0001c0001t0002g0302 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0021g0267 | 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 | a0001c0002t0001g0192 a0001c0002t0001g0204 a0001c0002t0001g0208 others(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 | a0001c0001t0004g0280 | 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 | a0001c0001t0015g0122 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0033g0126 | 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 | a0001c0001t0049g0106 | 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 | a0001c0001t0009g0294 a0001c0001t0009g0295 |
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 | a0001c0001t0015g0122 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0003g0038 | 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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0030g0009 |
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 | 308 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(305): Show |
311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): 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 | a0001c0001t0001g0162 | 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 | a0001c0001t0014g0094 | 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 | a0001c0001t0054g0039 | 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 | a0001c0001t0015g0122 | 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 | a0001c0001t0001g0223 a0001c0001t0010g0065 a0001c0001t0010g0068 |
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 | a0001c0001t0001g0272 | 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 | a0001c0001t0024g0251 | 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 | a0001c0001t0033g0123 | 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 | a0001c0001t0008g0259 | 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 | a0001c0001t0089g0311 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0105 others(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 | a0001c0001t0079g0172 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0184 a0001c0001t0001g0217 |
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 | 300 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(297): Show |
303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): 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 | a0001c0001t0037g0326 | 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 | a0001c0001t0009g0323 | 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 | a0001c0001t0008g0258 | 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 | a0001c0001t0001g0166 a0001c0001t0015g0122 |
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 | a0001c0001t0001g0137 a0001c0001t0001g0138 a0001c0001t0001g0159 others(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 | a0001c0001t0004g0119 | 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 | 306 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0024g0263 | 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 | 306 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0059g0129 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0034g0228 others(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 | a0002c0004t0086g0053 | 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 | a0001c0001t0012g0045 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0151 | 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 | a0001c0002t0001g0192 a0001c0002t0001g0204 a0001c0002t0001g0208 others(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 | a0001c0001t0057g0269 | 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0012g0045 | 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 | 306 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0009g0321 | 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 | 306 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0082g0043 | 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 | a0001c0001t0012g0045 | 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | 306 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.907-20451delC | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124644054 | |||||||
| chr10:124644201 | A | T | 306 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0134 | 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 | a0001c0001t0012g0044 | 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 | a0001c0001t0003g0069 a0001c0001t0011g0070 |
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 | a0001c0001t0050g0108 | 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 | 306 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0001g0168 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0142 | 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 | a0001c0001t0003g0087 | 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 | a0001c0001t0007g0205 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0004g0104 | 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 | a0002c0004t0086g0053 | 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0049g0106 | 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 | a0001c0001t0033g0123 | 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 | a0001c0001t0008g0255 | 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 | a0001c0001t0060g0127 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0105 others(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 | a0001c0001t0010g0128 a0001c0001t0010g0224 a0001c0001t0059g0129 others(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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0005g0010 | 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 | a0001c0001t0085g0040 | 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 | a0002c0004t0086g0053 | 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 | 84 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(81): Show |
85 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(82): 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 others(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 | a0001c0001t0015g0122 | 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 | a0001c0001t0029g0005 a0001c0001t0029g0023 |
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 | a0001c0001t0001g0174 | 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0055g0183 | 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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | 317 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(314): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0062g0133 | 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 | 88 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(85): Show |
89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): 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 | a0001c0001t0010g0128 a0001c0001t0010g0224 a0001c0001t0059g0129 |
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 | 87 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(84): Show |
88 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(85): 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 | a0001c0001t0016g0178 a0001c0001t0066g0179 |
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 | a0001c0001t0037g0326 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0021g0267 | 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 | a0001c0001t0014g0095 | 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 | a0001c0001t0023g0239 a0001c0001t0023g0240 |
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 | a0001c0001t0007g0253 a0001c0001t0007g0264 a0001c0001t0008g0248 others(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 | a0001c0001t0034g0155 | 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 | a0001c0001t0083g0189 | 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 | 304 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(301): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): 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 | a0001c0001t0001g0146 a0001c0001t0017g0144 |
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 | a0001c0001t0038g0020 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0046g0031 | 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 | a0001c0001t0006g0234 | 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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0184 a0001c0001t0001g0194 others(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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0005g0027 | 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 | a0001c0001t0052g0036 a0001c0001t0060g0127 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0016g0169 a0001c0001t0077g0139 |
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 | a0001c0001t0004g0280 a0001c0001t0004g0281 a0001c0001t0004g0282 |
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 | 278 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(275): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0142 | 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 | a0001c0001t0074g0157 | 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 | a0001c0001t0004g0111 | 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 | a0001c0001t0001g0132 | 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 | 46 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0145 others(43): Show |
46 | HG00099.hp1 HG00280.hp1 HG01071.hp2 others(43): 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 | a0001c0001t0017g0144 | 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 | a0001c0001t0017g0144 | 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 | a0001c0001t0009g0323 | 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 | 301 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(298): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): 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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | 303 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(300): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): 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 | a0001c0001t0022g0056 a0001c0001t0022g0057 a0001c0001t0022g0064 others(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 | a0001c0001t0001g0113 | 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 | a0001c0001t0048g0247 a0001c0001t0076g0256 |
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 | 87 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(84): Show |
88 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(85): 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 | a0001c0001t0010g0128 a0001c0001t0010g0224 a0001c0001t0059g0129 |
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 | 303 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(300): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): 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 | a0001c0001t0012g0124 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0131 a0001c0001t0001g0132 others(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 | a0001c0001t0049g0106 | 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 | a0001c0001t0001g0060 a0001c0001t0001g0135 a0001c0001t0001g0193 others(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 | a0001c0001t0060g0127 | 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 | a0001c0002t0001g0204 | 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 | a0001c0001t0032g0268 a0001c0001t0057g0269 a0001c0003t0058g0270 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0009g0324 | 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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0001g0194 | 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 | 87 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(84): Show |
88 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(85): 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 | a0001c0001t0001g0162 a0001c0001t0027g0210 |
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 | a0001c0001t0007g0264 a0001c0001t0008g0248 a0001c0001t0008g0255 others(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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0006g0062 | 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 | a0001c0001t0001g0079 | 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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0001c0001t0033g0123 others(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 | 88 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(85): Show |
89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): 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 | a0001c0001t0001g0219 | 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 | a0001c0001t0085g0040 | 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 | a0001c0001t0011g0092 a0001c0001t0065g0093 |
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 | a0001c0001t0006g0062 | 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 | a0001c0001t0001g0219 | 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 | a0001c0001t0001g0219 | 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 | 88 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(85): Show |
89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): 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 | a0001c0001t0085g0040 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0135 a0001c0001t0001g0193 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0134 a0001c0001t0001g0137 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0134 a0001c0001t0001g0137 others(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 | a0001c0001t0053g0276 a0001c0001t0056g0275 |
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 | a0001c0001t0053g0276 a0001c0001t0056g0275 |
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 | a0001c0001t0085g0040 | 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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0029g0005 | 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 | a0001c0001t0053g0276 a0001c0001t0056g0275 a0001c0001t0085g0040 |
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 | a0001c0001t0001g0197 a0001c0001t0009g0323 |
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 | a0001c0001t0001g0197 a0001c0001t0009g0323 |
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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0001g0197 | 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 | 7 | a0001c0001t0001g0136 a0001c0001t0001g0159 a0001c0001t0001g0160 others(4): Show |
7 | HG00280.hp1 HG01071.hp2 HG01106.hp1 others(4): 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 | a0001c0001t0001g0197 a0001c0001t0009g0323 |
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 | a0001c0001t0001g0151 a0001c0001t0001g0173 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0191 a0001c0001t0001g0209 a0001c0001t0027g0210 others(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 | a0001c0001t0018g0290 a0001c0001t0028g0288 a0001c0001t0028g0289 others(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 | a0001c0001t0001g0197 a0001c0001t0009g0323 |
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 | a0001c0001t0018g0290 a0001c0001t0028g0288 a0001c0001t0028g0289 others(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 | a0001c0001t0001g0197 a0001c0001t0009g0323 |
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 | 79 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(76): Show |
80 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(77): 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 | a0001c0001t0001g0153 a0001c0001t0001g0162 a0001c0001t0007g0264 others(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 | a0001c0001t0001g0197 a0001c0001t0009g0323 a0001c0001t0018g0290 others(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 | a0001c0001t0013g0307 | 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 | a0001c0001t0003g0059 | 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 | a0001c0001t0001g0198 | 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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0004c0007t0001g0103 |
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 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0001t0001g0175 | 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 | 298 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(295): Show |
301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0273 a0001c0001t0044g0029 |
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 | a0003c0005t0026g0237 | 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 | a0001c0001t0010g0224 | 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0024g0263 | 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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0001g0001 a0001c0001t0001g0131 a0001c0001t0001g0132 others(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 | 88 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(85): Show |
89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): 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 | a0001c0001t0063g0066 | 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 | a0001c0001t0009g0285 a0001c0001t0009g0321 a0001c0001t0009g0322 others(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 | a0001c0001t0018g0290 a0001c0001t0028g0288 a0001c0001t0028g0289 others(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 | 87 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(84): Show |
88 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(85): 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0134 others(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 | a0001c0001t0012g0051 a0001c0001t0012g0055 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | 88 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(85): Show |
89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): 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 | a0001c0001t0007g0264 a0001c0001t0008g0260 a0001c0001t0008g0261 |
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 | a0001c0001t0045g0030 | 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 | a0001c0001t0011g0073 | 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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0013g0307 | 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 | a0001c0001t0013g0307 | 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 | a0001c0001t0025g0249 | 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 | a0001c0001t0009g0294 a0001c0001t0009g0295 |
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 | a0001c0001t0002g0299 | 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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0004c0007t0001g0103 |
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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0005g0027 a0001c0001t0010g0035 a0001c0001t0010g0067 others(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 | a0001c0001t0003g0038 a0001c0001t0003g0099 a0001c0001t0006g0063 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0003g0059 a0001c0001t0003g0081 a0001c0001t0006g0062 others(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 | 103 | a0001c0001t0001g0001 a0001c0001t0001g0112 a0001c0001t0001g0113 others(100): Show |
104 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(101): Show |
intron_variant | MODIFIER | c.906+20550delT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124661056 | |||||||
| chr10:124661056 | TAA | T | 8 | a0001c0001t0001g0132 a0001c0001t0001g0167 a0001c0001t0004g0281 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0134 a0001c0001t0001g0135 others(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 | a0001c0001t0031g0050 | 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 | a0001c0001t0089g0311 | 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 | a0001c0001t0015g0041 a0001c0001t0015g0052 a0001c0001t0015g0277 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0142 a0001c0001t0001g0143 others(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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0298 a0001c0001t0002g0319 others(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 | 89 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(86): Show |
90 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(87): 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 | a0001c0001t0001g0273 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0218 a0001c0001t0007g0033 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0134 a0001c0001t0001g0135 others(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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0001c0001t0005g0008 others(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 | 160 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0079 others(157): Show |
161 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(158): 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 | a0001c0001t0002g0313 a0001c0001t0002g0314 a0001c0001t0002g0325 |
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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0001c0001t0005g0008 others(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 | 85 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(82): Show |
86 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(83): 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 | a0001c0001t0001g0132 a0001c0001t0007g0186 |
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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0030g0009 | 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 | a0001c0001t0071g0211 | 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0246 | 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 | 303 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(300): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): 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 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
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 | a0001c0001t0008g0258 a0001c0001t0008g0259 a0001c0001t0008g0262 others(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 | 46 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0145 others(43): Show |
46 | HG00099.hp1 HG00280.hp1 HG01071.hp2 others(43): 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 | a0001c0001t0045g0030 | 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 | a0001c0001t0001g0047 | 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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0001g0191 a0001c0001t0001g0232 |
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 | a0001c0001t0001g0180 | 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 | 66 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0145 others(63): Show |
66 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(63): 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 | a0001c0001t0009g0321 | 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 | a0001c0001t0059g0129 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0134 others(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 | 307 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(304): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0001c0001t0033g0123 others(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 | a0001c0001t0085g0040 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0009g0294 | 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 | a0001c0001t0009g0294 | 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 | 87 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(84): Show |
88 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(85): 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 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | 87 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(84): Show |
88 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(85): 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 | a0001c0001t0001g0194 | 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 | a0001c0001t0003g0078 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0089g0311 | 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 | a0001c0001t0002g0316 a0001c0001t0002g0317 |
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 | 301 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(298): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): 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 | a0001c0001t0004g0117 a0001c0001t0004g0120 a0001c0001t0050g0108 |
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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0001g0060 | 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 | a0001c0001t0085g0040 | 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 | 142 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0112 others(139): Show |
143 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(140): 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 | a0001c0001t0031g0050 | 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 | a0001c0001t0001g0166 | 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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0134 others(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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0020g0006 | 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 | a0001c0001t0006g0278 a0001c0001t0006g0279 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0184 a0001c0001t0001g0194 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0010g0224 | 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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | 242 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(239): Show |
245 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(242): 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0134 others(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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | 149 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0079 others(146): Show |
150 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(147): 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 | a0001c0001t0033g0123 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | 88 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(85): Show |
89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): 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 | a0001c0001t0031g0107 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0158 | 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 | 88 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(85): Show |
89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): 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 | 260 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(257): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0001c0001t0089g0311 | 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 | a0001c0001t0004g0120 | 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 | a0001c0001t0001g0176 a0001c0001t0031g0050 a0001c0001t0031g0107 others(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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | 89 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(86): Show |
90 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(87): 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 | a0001c0001t0015g0122 | 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 | 88 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(85): Show |
89 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(86): 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 | a0001c0001t0001g0193 | 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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0001g0153 a0001c0001t0001g0154 a0001c0001t0001g0161 others(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 | a0001c0001t0001g0130 a0001c0001t0001g0146 a0001c0001t0001g0151 others(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 | a0001c0001t0005g0027 a0001c0001t0015g0122 a0001c0001t0030g0004 others(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 | a0001c0001t0001g0131 a0001c0001t0018g0290 a0001c0001t0028g0289 others(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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0003t0003g0077 | 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 | a0001c0001t0016g0178 a0001c0001t0066g0179 |
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 | a0001c0001t0001g0151 a0001c0001t0001g0173 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0089g0311 | 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 | a0001c0001t0089g0311 | 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 | a0001c0001t0009g0323 | 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 | a0001c0001t0001g0197 | 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 | a0001c0001t0002g0292 a0001c0001t0002g0303 |
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 | a0001c0001t0001g0216 | 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 | a0001c0001t0002g0292 a0001c0001t0002g0303 |
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 | a0001c0001t0016g0178 a0001c0001t0066g0179 |
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 | 301 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(298): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): 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 | a0001c0001t0089g0311 | 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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0001c0001t0033g0123 others(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 | a0001c0001t0008g0261 | 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 | a0001c0001t0022g0056 a0001c0001t0022g0057 a0001c0001t0051g0058 |
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 | a0001c0001t0003g0098 a0001c0001t0003g0100 |
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 | a0001c0001t0033g0126 | 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 | a0001c0001t0008g0260 | 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 | a0001c0001t0016g0202 a0001c0001t0016g0203 |
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 | a0001c0001t0001g0131 | 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 | a0001c0001t0006g0061 | 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 | a0001c0001t0001g0158 | 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 | a0001c0001t0033g0123 | 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 | a0001c0001t0039g0028 | 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 | a0001c0001t0004g0281 | 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 | a0001c0001t0027g0222 a0005c0006t0084g0241 |
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 | a0001c0001t0030g0004 | 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 | a0001c0001t0006g0042 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0089g0311 | 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 | a0001c0001t0089g0311 | 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | 12 | a0001c0001t0001g0136 a0001c0001t0001g0159 a0001c0001t0001g0160 others(9): Show |
12 | HG00280.hp1 HG01071.hp2 HG01106.hp1 others(9): 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 | a0001c0001t0002g0303 a0001c0001t0025g0249 |
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 | a0001c0001t0002g0319 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0089g0311 | 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 | a0001c0001t0018g0293 a0001c0001t0018g0296 |
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 | a0001c0001t0068g0271 | 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 | a0001c0001t0085g0040 | 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 | a0001c0001t0016g0202 a0001c0001t0016g0203 |
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 | a0001c0001t0030g0004 | 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 | a0001c0001t0019g0015 a0001c0001t0019g0026 |
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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0001g0229 | 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 | a0001c0001t0014g0095 | 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 | a0001c0001t0015g0277 | 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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0113 others(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 | a0001c0001t0005g0017 | 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 | a0001c0001t0003g0069 a0001c0001t0011g0070 |
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 | 303 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(300): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): 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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | 307 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(304): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.906+4988delC | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124676618 | |||||||
| chr10:124676678 | T | C | 1 | a0001c0001t0014g0095 | 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 | a0001c0001t0027g0171 | 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 | a0001c0001t0019g0015 a0001c0001t0019g0026 |
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 | a0001c0001t0052g0036 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0014g0037 a0001c0001t0014g0094 a0001c0001t0014g0095 others(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 | a0001c0001t0003g0038 a0001c0001t0003g0069 a0001c0001t0003g0072 others(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 | 244 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(241): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): 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 | a0001c0001t0040g0007 | 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 | a0001c0001t0001g0219 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0050g0108 | 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 | a0001c0001t0001g0176 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0131 a0001c0001t0001g0141 others(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 | a0001c0001t0002g0302 | 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 | 192 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(189): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.906+3245A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 4/4 | chr10 | 124678362 | |||||||
| chr10:124678603 | T | A | 317 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(314): Show |
320 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(317): 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 | a0001c0001t0003g0069 a0001c0001t0011g0070 |
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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0030g0009 others(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 | a0001c0001t0032g0268 a0001c0001t0057g0269 a0001c0003t0058g0270 |
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 | a0001c0001t0028g0288 | 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0004g0280 | 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 | a0001c0001t0001g0180 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0006g0089 a0001c0001t0006g0090 |
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 | 87 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(84): Show |
88 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(85): 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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | 190 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(187): Show |
193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): 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 | a0002c0004t0086g0053 | 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 | a0001c0001t0088g0312 | 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 | a0001c0001t0001g0233 | 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 | a0001c0001t0012g0044 a0001c0001t0082g0043 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0131 a0001c0001t0001g0132 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0012g0044 a0001c0001t0082g0043 |
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 | a0001c0001t0004g0117 a0001c0001t0004g0120 a0001c0001t0050g0108 |
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 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0001t0014g0037 a0001c0001t0014g0094 a0001c0001t0014g0095 others(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 | a0003c0005t0026g0237 | 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 | a0001c0001t0054g0039 | 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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0004c0007t0001g0103 |
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 | a0001c0001t0037g0326 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0002g0297 | 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 | a0001c0001t0018g0293 a0001c0001t0018g0296 |
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 | a0001c0001t0008g0261 | 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 | a0001c0001t0033g0123 | 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 | a0001c0001t0024g0263 | 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 | 87 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(84): Show |
88 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(85): 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 | a0001c0001t0033g0123 | 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 | a0001c0001t0085g0040 | 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 | a0001c0001t0004g0121 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0001c0001t0033g0123 others(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 | a0001c0001t0082g0043 | 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 | a0001c0001t0001g0034 a0001c0001t0007g0212 |
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 | a0001c0001t0033g0123 | 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 | a0001c0001t0066g0179 | 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 | a0001c0001t0034g0228 a0001c0001t0046g0031 |
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 | a0001c0001t0001g0141 a0001c0001t0001g0174 a0001c0001t0001g0190 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0227 | 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 | a0001c0001t0001g0152 | 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 | a0001c0001t0017g0187 a0003c0005t0026g0237 |
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 | a0001c0001t0010g0035 a0001c0001t0010g0065 a0001c0001t0010g0067 others(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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0001g0174 | 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 | a0001c0001t0008g0260 | 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 | a0001c0001t0001g0143 | 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 | a0001c0001t0011g0245 a0001c0001t0061g0244 |
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 | a0001c0001t0001g0071 | 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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0001c0001t0033g0123 others(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 | a0001c0001t0067g0185 | 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 | a0001c0001t0033g0126 | 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 | 304 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(301): Show |
307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0012g0045 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0134 others(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 | a0001c0001t0022g0056 a0001c0001t0022g0057 a0001c0001t0022g0064 others(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 | a0001c0001t0091g0327 | 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 | a0001c0001t0001g0216 a0001c0001t0016g0202 a0001c0001t0016g0203 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0028g0289 | 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 | a0001c0001t0001g0272 | 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 | a0001c0001t0030g0004 | 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 | a0001c0001t0004g0116 a0001c0001t0004g0119 |
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 | 303 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(300): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): 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 | a0001c0003t0003g0077 | 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 | a0001c0001t0001g0141 a0001c0001t0001g0162 |
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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0001g0079 | 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 | a0001c0001t0009g0324 | 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 | a0001c0001t0004g0117 | 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 | a0001c0001t0003g0072 | 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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0016g0169 a0001c0001t0017g0188 a0001c0001t0067g0185 others(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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0012g0051 | 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 | a0001c0001t0033g0123 | 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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0001c0001t0033g0123 others(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 | a0001c0001t0054g0039 | 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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0005g0008 a0001c0001t0005g0010 |
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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0054g0039 | 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 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0004c0007t0001g0103 |
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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0001g0001 a0001c0001t0001g0048 a0001c0001t0001g0130 others(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 | 32 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(29): Show |
32 | HG00280.hp1 HG01071.hp2 HG01081.hp1 others(29): 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0194 a0001c0001t0001g0198 a0001c0001t0001g0220 others(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 | a0001c0001t0006g0278 a0001c0001t0006g0279 |
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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0005g0027 | 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0184 a0001c0001t0001g0217 a0001c0001t0029g0005 |
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 | a0001c0001t0039g0028 | 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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0001c0001t0033g0123 others(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 | a0001c0001t0012g0045 | 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 | 303 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(300): Show |
306 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(303): 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 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0115 | 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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0001g0114 a0001c0001t0002g0314 a0001c0001t0005g0008 others(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 | a0001c0001t0085g0040 | 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 | a0001c0001t0009g0323 | 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 | a0001c0001t0009g0294 a0001c0001t0009g0295 |
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 | 299 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(296): Show |
302 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(299): 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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | 46 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0145 others(43): Show |
46 | HG00099.hp1 HG00280.hp1 HG01071.hp2 others(43): 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 | a0001c0001t0083g0189 | 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 | 246 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(243): Show |
249 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(246): Show |
intron_variant | MODIFIER | c.133+2045G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 3/4 | chr10 | 124694113 | |||||||
| chr10:124694114 | G | A | 244 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(241): Show |
247 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(244): 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0004c0007t0001g0103 | 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 | a0001c0001t0018g0293 a0001c0001t0018g0296 |
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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | 140 | a0001c0001t0001g0001 a0001c0001t0001g0071 a0001c0001t0001g0079 others(137): Show |
141 | HG00099.hp1 HG00280.hp1 HG00323.hp1 others(138): 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 | a0001c0001t0085g0040 | 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 | a0001c0001t0006g0061 a0001c0001t0006g0062 a0001c0001t0006g0063 |
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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0001c0001t0033g0123 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0194 a0001c0001t0027g0222 a0005c0006t0084g0241 |
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 | a0001c0001t0001g0194 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0134 others(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 | a0001c0001t0060g0127 a0001c0001t0091g0327 |
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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0001c0001t0075g0125 others(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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0001c0001t0033g0123 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0113 others(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 | a0001c0001t0029g0023 | 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 | a0001c0001t0085g0040 | 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 | a0005c0006t0084g0241 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | a0001c0001t0065g0093 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0002g0302 | 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 | a0001c0001t0031g0107 | 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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0001c0001t0033g0123 others(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 | a0001c0001t0001g0243 | 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0161 | 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 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0113 others(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 | a0001c0001t0003g0083 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0004c0007t0001g0103 |
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 | a0001c0001t0001g0273 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | 307 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(304): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): 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 | a0001c0001t0030g0009 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0085g0040 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | a0001c0001t0054g0039 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0018g0290 a0001c0001t0028g0288 a0001c0001t0028g0289 others(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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0004g0120 | 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 | a0001c0001t0054g0039 | 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 | a0001c0001t0001g0113 | 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 | a0001c0001t0009g0294 | 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 | a0001c0001t0037g0326 | 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 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0004c0007t0001g0103 |
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 | a0001c0001t0001g0232 | 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 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
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 | a0001c0001t0010g0065 a0001c0001t0010g0068 |
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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0003g0098 a0001c0001t0003g0100 |
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 | a0001c0001t0031g0107 | 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 | a0001c0001t0001g0130 | 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 | a0001c0001t0001g0130 | 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 | a0001c0008t0018g0318 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0001g0105 a0001c0001t0004g0104 |
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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0131 a0001c0001t0001g0132 others(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 | a0001c0001t0001g0229 | 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0004g0111 a0001c0001t0004g0121 |
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 | a0001c0001t0033g0123 | 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 | a0001c0001t0076g0256 | 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 | a0001c0001t0033g0123 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0015g0041 a0001c0001t0015g0052 a0001c0001t0015g0277 |
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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0089g0311 | 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 | a0001c0001t0001g0113 a0001c0001t0001g0114 a0001c0001t0001g0115 others(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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0033g0123 a0001c0001t0091g0327 |
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 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
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 | a0001c0001t0088g0312 | 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 | a0001c0001t0007g0264 a0001c0001t0008g0260 a0001c0001t0008g0261 |
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 | a0001c0001t0067g0185 | 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 | a0002c0004t0086g0053 | 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 | a0001c0001t0029g0005 | 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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0034g0228 | 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 | 278 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(275): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): 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 | a0001c0001t0010g0035 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0003g0059 | 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 | a0001c0001t0001g0105 a0001c0001t0004g0104 |
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 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0113 others(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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0009g0323 | 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 | a0001c0001t0091g0327 | 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 | a0001c0001t0054g0039 | 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 | a0001c0001t0091g0327 | 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 | a0001c0001t0005g0021 | 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 | a0001c0001t0044g0029 | 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 | a0001c0001t0001g0084 a0001c0001t0001g0085 a0001c0001t0001g0086 |
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 | a0001c0001t0034g0228 | 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 | a0001c0001t0017g0188 a0001c0001t0067g0185 |
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 | 306 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0001g0175 | 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 | 307 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(304): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): 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 | a0001c0001t0001g0246 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0002g0292 | 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 | a0001c0001t0012g0045 | 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 | a0001c0001t0005g0008 | 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 | a0001c0001t0011g0092 a0001c0001t0065g0093 |
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 | a0001c0001t0004g0120 | 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 | a0001c0001t0004g0280 a0001c0001t0004g0281 a0001c0001t0004g0282 |
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 | a0001c0008t0018g0318 | 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 | a0001c0001t0007g0253 a0001c0001t0007g0264 a0001c0001t0008g0248 others(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 | 306 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0002t0001g0214 | 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 | 93 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(90): Show |
94 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(91): 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 | a0002c0004t0086g0053 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0184 a0001c0001t0001g0194 a0001c0001t0001g0217 others(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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0036g0283 | 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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0055g0183 | 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 | a0001c0001t0012g0044 | 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 | a0001c0001t0004g0120 | 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 | a0001c0001t0033g0123 | 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 | a0001c0001t0001g0266 | 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 | a0001c0001t0001g0232 | 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 | 306 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0005g0027 | 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 | 307 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(304): Show |
310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): 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 | a0001c0001t0005g0017 | 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 | a0001c0001t0001g0152 a0001c0001t0001g0167 |
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 | a0001c0008t0018g0318 | 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 | a0001c0001t0068g0271 | 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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0001c0001t0033g0123 others(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 | a0001c0001t0025g0265 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | a0001c0001t0001g0198 a0001c0001t0021g0199 a0001c0001t0021g0200 others(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 | a0001c0001t0030g0009 | 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 | a0001c0001t0004g0280 | 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 | a0001c0001t0002g0319 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0014g0097 | 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 | a0001c0001t0001g0216 | 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 | a0001c0001t0022g0056 a0001c0001t0022g0057 a0001c0001t0051g0058 |
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 | a0001c0001t0001g0146 a0001c0001t0001g0162 a0001c0001t0001g0230 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0006g0278 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0030g0004 | 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 | 274 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(271): Show |
277 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(274): 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 | a0001c0001t0050g0108 | 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 | a0001c0001t0011g0092 a0001c0001t0065g0093 |
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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0174 | 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 | 306 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0001g0143 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | a0001c0001t0001g0236 a0001c0001t0006g0234 a0001c0001t0026g0235 others(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 | a0001c0001t0047g0032 | 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 | a0001c0001t0009g0285 a0001c0001t0036g0283 a0001c0001t0036g0284 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | 301 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(298): Show |
304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.-174-3430C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124710317 | |||||||
| chr10:124710358 | A | G | 92 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(89): Show |
93 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(90): 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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0034g0228 others(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 | a0001c0001t0001g0085 a0001c0001t0001g0086 |
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 | a0001c0001t0012g0045 | 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0246 | 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 | 306 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0015g0122 | 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 | a0001c0001t0001g0154 | 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 | a0001c0001t0024g0263 | 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 | a0001c0001t0001g0163 a0001c0001t0001g0164 a0001c0001t0001g0165 others(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 | a0001c0001t0001g0167 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0001g0198 a0001c0001t0021g0199 a0001c0001t0021g0200 others(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 | a0001c0001t0008g0259 | 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 | a0001c0001t0052g0036 | 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 | a0002c0004t0086g0053 | 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 | 91 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(88): Show |
92 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(89): 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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0006g0278 a0001c0001t0006g0279 |
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 | a0001c0001t0001g0197 | 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 | a0001c0001t0006g0234 | 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 | a0001c0001t0001g0196 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | 278 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(275): Show |
281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): 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 | a0001c0001t0006g0063 | 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 | a0001c0001t0004g0111 a0001c0001t0004g0121 |
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 | a0001c0001t0001g0217 | 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0003g0078 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0085g0040 | 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 | a0001c0001t0045g0030 | 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 | 306 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0054g0039 | 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 | a0001c0001t0004g0119 a0001c0001t0045g0030 |
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 | a0001c0001t0089g0311 | 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 | 91 | a0001c0001t0001g0001 a0001c0001t0001g0130 a0001c0001t0001g0131 others(88): Show |
92 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(89): 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 | a0001c0001t0006g0042 a0001c0001t0012g0051 a0001c0001t0012g0055 |
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 | 322 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0047 others(319): Show |
325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): 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 | a0001c0001t0001g0194 a0001c0001t0005g0008 a0001c0001t0005g0010 others(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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0001g0193 a0001c0001t0068g0271 |
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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0004c0007t0001g0103 |
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 | a0001c0001t0026g0242 | 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 | a0001c0001t0001g0001 a0001c0001t0001g0131 a0001c0001t0001g0132 others(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 | 52 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0145 others(49): Show |
52 | HG00099.hp1 HG00280.hp1 HG00735.hp1 others(49): 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0134 others(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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0022g0064 | 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 | a0001c0001t0001g0175 | 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 | a0001c0001t0001g0218 | 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 | 203 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(200): Show |
204 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(201): Show |
intron_variant | MODIFIER | c.-174-8685C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124715572 | |||||||
| chr10:124715635 | G | A | 281 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(278): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0015g0122 | 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 | a0001c0001t0001g0219 | 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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0010g0224 | 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 | a0001c0001t0054g0039 | 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 | a0001c0001t0001g0191 a0001c0001t0001g0232 |
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 | 306 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(303): Show |
309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): 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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0007g0253 a0001c0001t0007g0264 a0001c0001t0008g0248 others(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 | a0001c0001t0052g0036 a0001c0001t0060g0127 |
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 | a0001c0001t0018g0290 a0001c0001t0028g0288 a0001c0001t0028g0289 others(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 | a0001c0001t0005g0008 | 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 | a0001c0001t0015g0041 | 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 | a0001c0001t0020g0006 | 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 | a0001c0001t0002g0292 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | a0001c0001t0002g0313 a0001c0001t0002g0314 a0001c0001t0002g0325 |
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 | a0001c0001t0010g0035 a0001c0001t0010g0065 a0001c0001t0010g0068 |
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 | 193 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(190): Show |
194 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(191): Show |
intron_variant | MODIFIER | c.-174-12161dupT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124719047 | |||||||
| chr10:124719124 | G | C | 1 | a0001c0001t0047g0032 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | a0001c0001t0033g0126 | 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 | a0001c0001t0001g0220 | 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 | a0001c0001t0012g0044 a0001c0001t0082g0043 |
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 | a0001c0001t0078g0195 | 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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0028g0288 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | 196 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(193): Show |
197 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(194): Show |
intron_variant | MODIFIER | c.-174-13420dupT | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124720306 | |||||||
| chr10:124720517 | G | A | 2 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0001g0174 | 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 | a0001c0001t0017g0144 | 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 | a0001c0001t0033g0123 | 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 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0152 | 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 | a0001c0001t0003g0038 a0001c0001t0003g0069 a0001c0001t0003g0075 others(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 | a0001c0001t0075g0125 | 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 | a0001c0001t0001g0105 a0001c0001t0004g0104 |
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 | a0001c0001t0085g0040 | 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 | a0001c0001t0006g0061 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0049g0106 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0002g0319 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0002g0292 a0001c0001t0002g0302 a0001c0001t0002g0303 others(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 | a0001c0001t0061g0244 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | a0001c0001t0088g0312 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0003g0087 | 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 | a0001c0001t0005g0021 a0001c0001t0005g0022 |
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 | a0001c0001t0001g0151 a0001c0001t0001g0173 a0001c0001t0035g0149 others(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 | a0001c0001t0077g0139 | 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 | a0001c0001t0077g0139 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0134 others(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 | a0001c0001t0001g0194 a0001c0001t0017g0274 |
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 | a0001c0001t0007g0253 a0001c0001t0007g0264 a0001c0001t0008g0248 others(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 | 115 | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0112 others(112): Show |
116 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(113): 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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | a0001c0001t0001g0193 | 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 | a0001c0001t0002g0310 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | a0001c0002t0001g0192 | 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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0134 others(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 | a0001c0001t0009g0285 a0001c0001t0009g0321 a0001c0001t0009g0322 others(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 | a0001c0001t0032g0268 a0001c0001t0057g0269 a0001c0003t0058g0270 |
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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0001g0191 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0001g0229 | 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 | a0001c0001t0031g0050 a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0047 | 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 | a0001c0008t0018g0318 | 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 | 81 | a0001c0001t0001g0130 a0001c0001t0001g0136 a0001c0001t0001g0145 others(78): Show |
81 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(78): Show |
intron_variant | MODIFIER | c.-175+16787A>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124727226 | |||||||
| chr10:124727330 | T | TG | 17 | a0001c0001t0001g0047 a0001c0001t0001g0048 a0001c0001t0001g0049 others(14): Show |
17 | HG00558.hp1 HG01175.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.-175+16682dupC | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124727330 | |||||||
| chr10:124727330 | TG | T | 89 | a0001c0001t0001g0079 a0001c0001t0001g0105 a0001c0001t0001g0112 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0071 others(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 | 26 | a0001c0001t0001g0001 a0001c0001t0001g0141 a0001c0001t0001g0142 others(23): Show |
27 | HG00140.hp2 HG00621.hp1 HG00673.hp2 others(24): 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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0113 others(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 | a0001c0001t0001g0034 a0001c0001t0001g0060 a0001c0001t0001g0134 others(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 | a0001c0001t0077g0139 | 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 | a0001c0001t0004g0109 a0001c0001t0080g0110 a0001c0001t0087g0287 |
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 | a0001c0001t0015g0041 a0001c0001t0015g0052 a0001c0001t0015g0277 |
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 | a0001c0001t0002g0292 | 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 | a0001c0001t0061g0244 | 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 | a0001c0001t0052g0036 | 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 | a0001c0001t0088g0312 | 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 | a0001c0001t0003g0069 a0001c0001t0011g0070 |
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 | a0001c0001t0001g0223 | 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 | a0001c0001t0001g0105 a0001c0001t0004g0104 a0004c0007t0001g0103 |
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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0054g0039 a0001c0001t0085g0040 |
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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0010g0224 | 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 | a0001c0001t0014g0097 | 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 | a0001c0001t0031g0050 | 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 | a0001c0001t0091g0327 | 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 | a0001c0001t0049g0106 | 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 | a0001c0001t0004g0120 | 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 | a0001c0001t0011g0092 a0001c0001t0065g0093 |
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 | 148 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(145): Show |
149 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(146): 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0006g0089 a0001c0001t0006g0090 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0272 | 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 | a0001c0001t0050g0108 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | a0001c0001t0001g0225 | 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 | a0001c0001t0033g0123 | 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 | a0001c0001t0046g0031 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | 160 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(157): Show |
161 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(158): 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 | a0001c0001t0077g0139 | 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 | a0001c0001t0077g0139 | 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 | a0001c0001t0077g0139 | 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 | a0001c0001t0001g0060 a0001c0001t0001g0134 a0001c0001t0001g0135 others(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 | a0001c0008t0018g0318 | 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 | a0001c0001t0008g0248 | 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 | a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0001g0134 | 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0011g0091 | 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 | a0001c0001t0037g0326 | 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 | a0001c0001t0015g0122 | 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 | a0001c0001t0011g0092 a0001c0001t0065g0093 |
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 | a0001c0001t0040g0007 | 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 | a0001c0001t0048g0247 | 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 | a0001c0001t0030g0004 | 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 | a0001c0001t0011g0245 a0001c0001t0061g0244 |
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 | a0001c0001t0001g0137 a0001c0001t0001g0138 |
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 | a0001c0001t0012g0051 | 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 | a0001c0001t0001g0226 | 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 | a0001c0001t0001g0227 a0001c0001t0001g0229 a0001c0001t0034g0228 others(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 | a0001c0001t0015g0122 | 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 | a0001c0001t0001g0246 | 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 | a0001c0001t0001g0136 | 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 | a0001c0001t0001g0230 | 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 | a0001c0002t0001g0231 | 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 | a0001c0001t0001g0232 | 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 | a0001c0001t0002g0319 | 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 | a0001c0001t0065g0093 | 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 | a0001c0001t0001g0060 a0001c0001t0001g0134 a0001c0001t0001g0135 others(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 | a0001c0001t0012g0124 a0001c0001t0075g0125 |
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 | a0001c0001t0062g0133 | 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 | a0001c0001t0005g0013 a0001c0001t0005g0017 a0001c0001t0005g0018 others(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 | a0001c0001t0001g0233 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0004g0121 | 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 | a0001c0001t0015g0052 | 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 | 146 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(143): Show |
147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): 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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0037g0320 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0005c0006t0084g0241 | 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 | a0001c0001t0009g0285 a0001c0001t0009g0321 a0001c0001t0009g0322 others(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 | 154 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(151): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): Show |
intron_variant | MODIFIER | c.-175+7759C>T | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124736254 | |||||||
| chr10:124736266 | C | T | 153 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(150): Show |
154 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(151): 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 | a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0026g0242 a0001c0001t0037g0326 |
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 | a0001c0001t0004g0121 | 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 | a0001c0001t0020g0006 | 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 | a0001c0001t0019g0026 | 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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0018g0290 a0001c0001t0028g0288 a0001c0001t0028g0289 others(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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | a0001c0001t0001g0105 a0001c0001t0004g0104 |
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 | a0001c0001t0012g0124 a0001c0001t0033g0126 a0001c0001t0075g0125 |
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 | a0001c0001t0001g0071 a0001c0001t0001g0079 a0001c0001t0001g0084 others(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 | a0001c0001t0001g0132 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0292 others(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 | 312 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(309): Show |
315 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(312): 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 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0046 others(321): Show |
327 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(324): 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 | a0001c0001t0087g0287 | 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 | a0001c0001t0001g0243 | 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 | a0001c0001t0085g0040 | 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 | 175 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0105 others(172): Show |
176 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(173): 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 | a0001c0001t0005g0027 | 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 | a0001c0001t0032g0268 | 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 | a0001c0001t0039g0028 | 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 | a0001c0001t0001g0246 a0001c0001t0007g0253 a0001c0001t0007g0264 others(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 | a0001c0001t0091g0327 | 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 | a0001c0001t0003g0059 | 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 | a0001c0001t0049g0106 | 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 | a0001c0001t0001g0131 | 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 | a0001c0001t0001g0266 a0001c0001t0014g0094 a0001c0001t0014g0095 others(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 | a0001c0001t0001g0130 | 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 | a0001c0001t0030g0004 | 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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0032g0268 a0001c0001t0057g0269 a0001c0003t0058g0270 |
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 | a0001c0001t0068g0271 | 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 | a0001c0001t0001g0272 | 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 | a0001c0001t0001g0273 | 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 | 262 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(259): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): Show |
intron_variant | MODIFIER | c.-175+4437C>G | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124739576 | |||||||
| chr10:124739605 | C | G | 262 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(259): Show |
263 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(260): 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 | a0001c0001t0031g0107 | 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 | a0001c0001t0003g0098 a0001c0001t0003g0099 a0001c0001t0003g0100 others(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 | a0001c0001t0012g0124 a0001c0001t0033g0123 a0001c0001t0033g0126 others(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 | a0001c0001t0003g0098 a0001c0001t0003g0099 a0001c0001t0003g0100 others(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 | a0001c0001t0001g0060 a0001c0001t0001g0071 a0001c0001t0001g0079 others(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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | a0001c0001t0002g0325 | 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 | a0001c0001t0009g0285 a0001c0001t0036g0283 a0001c0001t0036g0284 others(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 | 309 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(306): Show |
312 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(309): 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 | a0001c0001t0031g0107 a0001c0001t0049g0106 |
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 | a0001c0001t0022g0056 a0001c0001t0022g0057 a0001c0001t0051g0058 |
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 | a0001c0001t0012g0055 | 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 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0114 others(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 | 261 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0060 others(258): Show |
262 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(259): 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 | a0001c0001t0003g0038 | 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 | a0001c0001t0053g0276 a0001c0001t0056g0275 |
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 | a0001c0001t0015g0122 | 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 | a0001c0001t0012g0124 a0001c0001t0033g0123 a0001c0001t0033g0126 others(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 | a0001c0001t0017g0274 | 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 | 154 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0130 others(151): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): 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 | a0001c0001t0010g0128 a0001c0001t0059g0129 |
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 | 154 | a0001c0001t0001g0001 a0001c0001t0001g0034 a0001c0001t0001g0130 others(151): Show |
155 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(152): 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 | a0001c0001t0014g0037 | 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 | a0001c0001t0005g0008 a0001c0001t0005g0010 a0001c0001t0005g0013 others(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 | a0001c0001t0053g0276 a0001c0001t0056g0275 |
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 | a0001c0001t0006g0278 a0001c0001t0006g0279 a0001c0001t0015g0277 |
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 | a0001c0001t0004g0280 a0001c0001t0004g0281 a0001c0001t0004g0282 |
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 | a0001c0001t0052g0036 | 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 | a0001c0001t0010g0035 | 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 | a0001c0001t0001g0034 a0001c0001t0007g0033 |
2 | HG02074.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.-175+20G>A | FAM53B | ENSG00000189319.14 | transcript | ENST00000337318.8 | protein_coding | 1/4 | chr10 | 124743993 |