Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| Item | Value |
|---|---|
| geneid | 100507747 |
| ensemblid | ENSG00000283199.3 |
| hgncid | 53786 |
| symbol | C13orf46 |
| name | chromosome 13 open reading frame 46 |
| refseq_nuc | NM_001365455.2 |
| refseq_prot | NP_001352384.1 |
| ensembl_nuc | ENST00000636427.3 |
| ensembl_prot | ENSP00000490032.2 |
| mane_status | MANE Select |
| chr | chr13 |
| start | 113953705 |
| end | 113974076 |
| strand | - |
| ver | v1.2 |
| region | chr13:113953705-113974076 |
| region5000 | chr13:113948705-113979076 |
| regionname0 | C13orf46_chr13_113953705_113974076 |
| regionname5000 | C13orf46_chr13_113948705_113979076 |
| ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 212 | 390 | 88 | 82 | 159 | 16 | 43 | 117 | C13orf46_chr13_113948705_113979076 | C13orf46 | MEKDT others(207): Show |
chr13 | 113948705 | 113979076 |
| a0002 | 0/0 | 212 | 13 | 0 | 3 | 9 | 0 | 1 | 8 | C13orf46_chr13_113948705_113979076 | C13orf46 | MEKDT others(207): Show |
chr13 | 113948705 | 113979076 |
| a0003 | 0/0 | 212 | 6 | 5 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | MEKDT others(207): Show |
chr13 | 113948705 | 113979076 |
| a0004 | 0/0 | 212 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | MEKDT others(207): Show |
chr13 | 113948705 | 113979076 |
| a0005 | 0/0 | 212 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | MEKDT others(207): Show |
chr13 | 113948705 | 113979076 |
| a0006 | 0/0 | 212 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | MEKDT others(207): Show |
chr13 | 113948705 | 113979076 |
| a0007 | 0/0 | 224 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | MEKDT others(219): Show |
chr13 | 113948705 | 113979076 |
| achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/1 | 636 | 389 | 88 | 82 | 158 | 16 | 43 | C13orf46_chr13_113948705_113979076 | C13orf46 | ATGGA others(631): Show |
chr13 | 113948705 | 113979076 | ||
| a0001c0008 | 0/0 | 636 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | ATGGA others(631): Show |
chr13 | 113948705 | 113979076 | ||
| a0002c0002 | 0/0 | 636 | 13 | 0 | 3 | 9 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | ATGGA others(631): Show |
chr13 | 113948705 | 113979076 | ||
| a0003c0003 | 0/0 | 636 | 6 | 5 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | ATGGA others(631): Show |
chr13 | 113948705 | 113979076 | ||
| a0004c0004 | 0/0 | 636 | 2 | 1 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | ATGGA others(631): Show |
chr13 | 113948705 | 113979076 | ||
| a0005c0006 | 0/0 | 636 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | ATGGA others(631): Show |
chr13 | 113948705 | 113979076 | ||
| a0006c0007 | 0/0 | 636 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | ATGGA others(631): Show |
chr13 | 113948705 | 113979076 | ||
| a0007c0005 | 0/0 | 672 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | ATGGA others(667): Show |
chr13 | 113948705 | 113979076 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 3786 | 98 | 15 | 16 | 48 | 3 | 16 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0002 | 0/0 | 3786 | 89 | 5 | 26 | 49 | 4 | 5 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0003 | 0/0 | 3763 | 16 | 0 | 3 | 10 | 0 | 3 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3758): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0005 | 0/0 | 3789 | 10 | 2 | 4 | 0 | 1 | 3 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3784): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0006 | 0/0 | 3786 | 9 | 1 | 1 | 5 | 2 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0007 | 0/0 | 3786 | 8 | 8 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0008 | 0/0 | 3766 | 8 | 0 | 1 | 5 | 0 | 2 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3761): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0009 | 0/0 | 3786 | 8 | 0 | 0 | 8 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0010 | 0/0 | 3786 | 7 | 2 | 0 | 4 | 1 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0011 | 0/0 | 3789 | 7 | 1 | 5 | 0 | 1 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3784): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0013 | 0/0 | 3786 | 6 | 5 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0014 | 0/0 | 3783 | 6 | 6 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3778): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0015 | 0/0 | 3786 | 6 | 4 | 2 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0016 | 1/0 | 3786 | 5 | 4 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0017 | 0/0 | 3763 | 4 | 0 | 0 | 4 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3758): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0018 | 0/0 | 3789 | 4 | 2 | 2 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3784): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0019 | 0/0 | 3786 | 4 | 2 | 0 | 2 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0020 | 0/0 | 3786 | 4 | 4 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0021 | 0/0 | 3763 | 3 | 3 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3758): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0022 | 0/0 | 3740 | 3 | 3 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3735): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0023 | 0/0 | 3786 | 2 | 0 | 2 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0024 | 0/0 | 3786 | 3 | 0 | 3 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0025 | 0/0 | 3786 | 2 | 0 | 0 | 0 | 2 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0026 | 0/0 | 3746 | 2 | 0 | 1 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3741): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0027 | 0/0 | 3789 | 2 | 0 | 0 | 0 | 0 | 2 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3784): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0028 | 0/0 | 3789 | 2 | 0 | 2 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3784): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0029 | 0/0 | 3789 | 2 | 2 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3784): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0030 | 0/0 | 3786 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0031 | 0/0 | 3786 | 2 | 1 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0032 | 0/0 | 3766 | 2 | 0 | 0 | 0 | 0 | 2 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3761): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0033 | 0/0 | 3786 | 2 | 1 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0034 | 0/0 | 3789 | 2 | 0 | 2 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3784): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0035 | 0/0 | 3786 | 2 | 1 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0036 | 0/0 | 3786 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0037 | 0/0 | 3763 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3758): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0040 | 0/0 | 3786 | 1 | 0 | 0 | 0 | 1 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0041 | 0/0 | 3769 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3764): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0042 | 0/0 | 3763 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3758): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0043 | 0/0 | 3763 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3758): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0044 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0045 | 0/0 | 3786 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0046 | 0/1 | 3746 | 1 | 0 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3741): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0047 | 0/0 | 3726 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3721): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0048 | 0/0 | 3789 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3784): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0049 | 0/0 | 3789 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3784): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0050 | 0/0 | 3766 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3761): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0051 | 0/0 | 3789 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3784): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0052 | 0/0 | 3789 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3784): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0053 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0054 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0055 | 0/0 | 3763 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3758): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0056 | 0/0 | 3786 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0057 | 0/0 | 3786 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0058 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0059 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0060 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0061 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0062 | 0/0 | 3786 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0063 | 0/0 | 3786 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0064 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0065 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0066 | 0/0 | 3786 | 1 | 0 | 0 | 0 | 1 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0067 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0068 | 0/0 | 3786 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0069 | 0/0 | 3740 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3735): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0070 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0071 | 0/0 | 3786 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0072 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0073 | 0/0 | 3760 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3755): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0074 | 0/0 | 3740 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3735): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0075 | 0/0 | 3763 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3758): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0076 | 0/0 | 3746 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3741): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0077 | 0/0 | 3520 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3515): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0078 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0079 | 0/0 | 3786 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0080 | 0/0 | 3786 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0081 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0082 | 0/0 | 3786 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0083 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0084 | 0/0 | 3763 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3758): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0085 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3784): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0086 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0087 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0088 | 0/0 | 2744 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(2739): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0089 | 0/0 | 3789 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3784): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0090 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0091 | 0/0 | 3766 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3761): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0092 | 0/0 | 3763 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3758): Show |
chr13 | 113948705 | 113979076 |
| a0001c0001t0093 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0001c0008t0002 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0002c0002t0004 | 0/0 | 3812 | 11 | 0 | 3 | 7 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3807): Show |
chr13 | 113948705 | 113979076 |
| a0002c0002t0038 | 0/0 | 3789 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3784): Show |
chr13 | 113948705 | 113979076 |
| a0002c0002t0039 | 0/0 | 3812 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3807): Show |
chr13 | 113948705 | 113979076 |
| a0003c0003t0012 | 0/0 | 3789 | 6 | 5 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3784): Show |
chr13 | 113948705 | 113979076 |
| a0004c0004t0001 | 0/0 | 3786 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0004c0004t0023 | 0/0 | 3786 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0005c0006t0002 | 0/0 | 3786 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0006c0007t0002 | 0/0 | 3786 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3781): Show |
chr13 | 113948705 | 113979076 |
| a0007c0005t0002 | 0/0 | 3822 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | GCACC others(3817): Show |
chr13 | 113948705 | 113979076 |
| actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 27 | 5 | 3 | 15 | 0 | 4 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0004 | 0/0 | 16 | 1 | 2 | 11 | 0 | 2 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0013 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0016 | 0/0 | 4 | 0 | 4 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0029 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0032 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0036 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0037 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0038 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0039 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0040 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0045 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0049 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0002 | 0/0 | 20 | 0 | 4 | 14 | 1 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0003 | 0/0 | 18 | 0 | 5 | 12 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0005 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0023 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0024 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0025 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0051 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0054 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0057 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0058 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0059 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0184 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0209 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0222 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0003g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0003g0019 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0003g0047 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0003g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0003g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0003g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0003g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0003g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0005g0006 | 0/0 | 6 | 0 | 4 | 0 | 1 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0005g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0005g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0005g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0006g0014 | 0/0 | 4 | 1 | 0 | 3 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0006g0044 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0006g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0006g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0006g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0007g0008 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0007g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0007g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0008g0007 | 0/0 | 6 | 0 | 1 | 3 | 0 | 2 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0008g0033 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0009g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0009g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0009g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0009g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0010g0055 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0010g0190 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0010g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0010g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0010g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0010g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0011g0018 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0011g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0011g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0011g0078 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0013g0034 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0013g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0013g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0013g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0013g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0014g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0014g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0014g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0014g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0014g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0015g0015 | 0/0 | 4 | 2 | 2 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0015g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0015g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0016g0022 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0016g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0016g0168 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0017g0052 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0017g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0017g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0018g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0018g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0018g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0018g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0019g0041 | 0/0 | 2 | 1 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0019g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0019g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0020g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0020g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0020g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0021g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0021g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0022g0020 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0023g0042 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0024g0021 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0025g0053 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0026g0093 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0026g0097 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0027g0030 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0028g0031 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0029g0050 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0030g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0030g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0031g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0031g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0032g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0032g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0033g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0033g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0034g0046 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0035g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0035g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0036g0043 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0037g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0040g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0041g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0042g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0043g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0044g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0045g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0046g0071 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0047g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0048g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0049g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0050g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0051g0077 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0052g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0053g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0054g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0055g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0056g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0057g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0058g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0059g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0060g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0061g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0062g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0063g0208 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0064g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0065g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0066g0191 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0067g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0068g0218 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0069g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0070g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0071g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0072g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0073g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0074g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0075g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0076g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0077g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0078g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0079g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0080g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0081g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0082g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0083g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0084g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0085g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0086g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0087g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0088g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0089g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0090g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0091g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0092g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0001t0093g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0001c0008t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0002c0002t0004g0012 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0002c0002t0004g0017 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0002c0002t0004g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0002c0002t0004g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0002c0002t0004g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0002c0002t0004g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0002c0002t0038g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0002c0002t0039g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0003c0003t0012g0009 | 0/0 | 5 | 4 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0003c0003t0012g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0004c0004t0001g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0004c0004t0023g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0005c0006t0002g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0006c0007t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| a0007c0005t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0001 | t0001 | g0037 | EUR | GBR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00099 | hp2 | a0001 | c0001 | t0006 | g0044 | EUR | GBR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00140 | hp1 | a0001 | c0001 | t0040 | g0169 | EUR | GBR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0049 | EUR | GBR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00280 | hp1 | a0001 | c0001 | t0002 | g0023 | EUR | FIN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00280 | hp2 | a0001 | c0001 | t0002 | g0188 | EUR | FIN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00323 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | FIN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0037 | EUR | FIN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00408 | hp1 | a0001 | c0001 | t0002 | g0195 | EAS | CHS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00408 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00423 | hp1 | a0001 | c0001 | t0042 | g0226 | EAS | CHS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00423 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00544 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00544 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | CHS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00558 | hp1 | a0001 | c0001 | t0002 | g0181 | EAS | CHS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00558 | hp2 | a0001 | c0001 | t0003 | g0136 | EAS | CHS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00597 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | CHS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00597 | hp2 | a0001 | c0001 | t0083 | g0117 | EAS | CHS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00609 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | CHS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00621 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00621 | hp2 | a0001 | c0001 | t0003 | g0010 | EAS | CHS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00639 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00639 | hp2 | a0001 | c0001 | t0049 | g0176 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0024 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00642 | hp2 | a0001 | c0001 | t0050 | g0073 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00673 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | CHS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00673 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | CHS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00733 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00733 | hp2 | a0001 | c0001 | t0003 | g0126 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00735 | hp1 | a0001 | c0001 | t0089 | g0165 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00735 | hp2 | a0001 | c0001 | t0001 | g0132 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00738 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00738 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00741 | hp1 | a0001 | c0001 | t0018 | g0070 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG00741 | hp2 | a0001 | c0001 | t0043 | g0224 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01069 | hp1 | a0001 | c0001 | t0015 | g0015 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01069 | hp2 | a0001 | c0001 | t0045 | g0183 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01070 | hp1 | a0001 | c0001 | t0034 | g0046 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01070 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01071 | hp1 | a0001 | c0001 | t0015 | g0015 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01071 | hp2 | a0001 | c0001 | t0034 | g0046 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0173 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01074 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01081 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01081 | hp2 | a0001 | c0001 | t0011 | g0018 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01099 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01099 | hp2 | a0001 | c0001 | t0002 | g0215 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01106 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01106 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01109 | hp1 | a0001 | c0001 | t0013 | g0034 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01109 | hp2 | a0001 | c0001 | t0052 | g0075 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01167 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01167 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01168 | hp1 | a0001 | c0001 | t0001 | g0049 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01168 | hp2 | a0001 | c0001 | t0028 | g0031 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01169 | hp1 | a0001 | c0001 | t0002 | g0054 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01169 | hp2 | a0001 | c0001 | t0028 | g0031 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01175 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01175 | hp2 | a0001 | c0001 | t0002 | g0222 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01192 | hp1 | a0001 | c0001 | t0002 | g0186 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01192 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01243 | hp1 | a0001 | c0001 | t0033 | g0145 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0057 | AMR | PUR | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01255 | hp1 | a0001 | c0001 | t0062 | g0193 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01255 | hp2 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01256 | hp1 | a0001 | c0001 | t0024 | g0021 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01256 | hp2 | a0001 | c0001 | t0051 | g0077 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01258 | hp1 | a0001 | c0001 | t0024 | g0021 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01261 | hp1 | a0001 | c0001 | t0005 | g0006 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01261 | hp2 | a0001 | c0001 | t0002 | g0051 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01346 | hp1 | a0001 | c0001 | t0068 | g0218 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01346 | hp2 | a0001 | c0001 | t0024 | g0021 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01358 | hp1 | a0001 | c0001 | t0002 | g0192 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01358 | hp2 | a0001 | c0001 | t0026 | g0093 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01361 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01433 | hp1 | a0001 | c0001 | t0011 | g0018 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01433 | hp2 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01496 | hp1 | a0001 | c0001 | t0011 | g0026 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01496 | hp2 | a0003 | c0003 | t0012 | g0009 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01515 | hp1 | a0001 | c0001 | t0006 | g0044 | EUR | IBS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01515 | hp2 | a0001 | c0001 | t0025 | g0053 | EUR | IBS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01516 | hp1 | a0001 | c0001 | t0010 | g0190 | EUR | IBS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01516 | hp2 | a0001 | c0001 | t0011 | g0078 | EUR | IBS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01517 | hp1 | a0001 | c0001 | t0066 | g0191 | EUR | IBS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01517 | hp2 | a0001 | c0001 | t0025 | g0053 | EUR | IBS | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01884 | hp1 | a0001 | c0001 | t0018 | g0069 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01884 | hp2 | a0001 | c0001 | t0002 | g0023 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01891 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01891 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01928 | hp1 | a0001 | c0001 | t0023 | g0042 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01928 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01934 | hp1 | a0001 | c0001 | t0002 | g0194 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01934 | hp2 | a0001 | c0001 | t0002 | g0211 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01943 | hp1 | a0001 | c0001 | t0006 | g0155 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01943 | hp2 | a0001 | c0001 | t0003 | g0047 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01952 | hp1 | a0004 | c0004 | t0023 | g0237 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01952 | hp2 | a0001 | c0001 | t0011 | g0076 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01975 | hp2 | a0001 | c0001 | t0002 | g0005 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01978 | hp1 | a0005 | c0006 | t0002 | g0189 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01978 | hp2 | a0001 | c0001 | t0002 | g0024 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01981 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01993 | hp1 | a0002 | c0002 | t0004 | g0062 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01993 | hp2 | a0001 | c0001 | t0008 | g0007 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02004 | hp1 | a0001 | c0001 | t0063 | g0208 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02004 | hp2 | a0002 | c0002 | t0004 | g0064 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02040 | hp1 | a0001 | c0001 | t0030 | g0182 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02040 | hp2 | a0002 | c0002 | t0038 | g0065 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02056 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02056 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02071 | hp1 | a0006 | c0007 | t0002 | g0197 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02071 | hp2 | a0001 | c0001 | t0010 | g0204 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02074 | hp1 | a0001 | c0001 | t0070 | g0196 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02074 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02080 | hp1 | a0001 | c0001 | t0008 | g0007 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02083 | hp1 | a0001 | c0001 | t0064 | g0202 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02083 | hp2 | a0001 | c0001 | t0008 | g0007 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02129 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02129 | hp2 | a0001 | c0001 | t0008 | g0007 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02132 | hp1 | a0001 | c0001 | t0030 | g0180 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02132 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02135 | hp1 | a0001 | c0001 | t0081 | g0120 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02135 | hp2 | a0001 | c0001 | t0010 | g0219 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02145 | hp1 | a0001 | c0001 | t0076 | g0089 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02145 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02148 | hp2 | a0001 | c0001 | t0002 | g0184 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02155 | hp1 | a0001 | c0001 | t0003 | g0138 | EAS | CDX | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02155 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | CDX | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02165 | hp1 | a0001 | c0001 | t0002 | g0214 | EAS | CDX | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02165 | hp2 | a0001 | c0001 | t0009 | g0154 | EAS | CDX | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02257 | hp1 | a0001 | c0001 | t0007 | g0174 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02257 | hp2 | a0001 | c0001 | t0055 | g0103 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02258 | hp1 | a0001 | c0001 | t0060 | g0102 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02258 | hp2 | a0001 | c0001 | t0015 | g0133 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02273 | hp1 | a0002 | c0002 | t0004 | g0063 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02273 | hp2 | a0001 | c0001 | t0002 | g0209 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02280 | hp1 | a0001 | c0001 | t0015 | g0234 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02280 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02293 | hp1 | a0001 | c0001 | t0002 | g0023 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0127 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02300 | hp1 | a0001 | c0001 | t0018 | g0074 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02300 | hp2 | a0001 | c0001 | t0023 | g0042 | AMR | PEL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02451 | hp1 | a0001 | c0001 | t0075 | g0235 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02451 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02523 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02523 | hp2 | a0001 | c0001 | t0009 | g0143 | EAS | KHV | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02572 | hp1 | a0001 | c0001 | t0035 | g0166 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02572 | hp2 | a0001 | c0001 | t0086 | g0148 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02602 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02602 | hp2 | a0001 | c0001 | t0082 | g0147 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02615 | hp1 | a0001 | c0001 | t0020 | g0158 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02622 | hp1 | a0001 | c0001 | t0013 | g0034 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02622 | hp2 | a0001 | c0001 | t0019 | g0041 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02630 | hp1 | a0001 | c0001 | t0014 | g0084 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02630 | hp2 | a0001 | c0001 | t0022 | g0020 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02647 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02647 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02698 | hp1 | a0001 | c0001 | t0080 | g0146 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0128 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02717 | hp1 | a0001 | c0001 | t0053 | g0112 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02717 | hp2 | a0004 | c0004 | t0001 | g0236 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02735 | hp2 | a0001 | c0001 | t0001 | g0032 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0091 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02738 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02809 | hp1 | a0001 | c0001 | t0054 | g0111 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02809 | hp2 | a0003 | c0003 | t0012 | g0009 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02818 | hp1 | a0003 | c0003 | t0012 | g0067 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02818 | hp2 | a0001 | c0001 | t0016 | g0022 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02886 | hp1 | a0001 | c0001 | t0013 | g0110 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02886 | hp2 | a0001 | c0001 | t0006 | g0014 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02895 | hp1 | a0001 | c0001 | t0001 | g0039 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02895 | hp2 | a0001 | c0001 | t0031 | g0221 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02896 | hp1 | a0001 | c0001 | t0021 | g0056 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02896 | hp2 | a0001 | c0001 | t0020 | g0048 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02897 | hp1 | a0001 | c0001 | t0020 | g0048 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02897 | hp2 | a0001 | c0001 | t0021 | g0056 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02922 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | ESN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02922 | hp2 | a0003 | c0003 | t0012 | g0009 | AFR | ESN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02965 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02965 | hp2 | a0001 | c0001 | t0088 | g0149 | AFR | ESN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02970 | hp1 | a0003 | c0003 | t0012 | g0009 | AFR | ESN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02970 | hp2 | a0001 | c0001 | t0014 | g0083 | AFR | ESN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02976 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02976 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ESN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03017 | hp2 | a0001 | c0001 | t0001 | g0004 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03041 | hp1 | a0001 | c0001 | t0011 | g0026 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03041 | hp2 | a0001 | c0001 | t0041 | g0177 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03098 | hp1 | a0001 | c0001 | t0029 | g0050 | AFR | MSL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03098 | hp2 | a0001 | c0001 | t0048 | g0178 | AFR | MSL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03130 | hp1 | a0001 | c0001 | t0014 | g0028 | AFR | ESN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03130 | hp2 | a0001 | c0001 | t0016 | g0022 | AFR | ESN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03139 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | ESN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03139 | hp2 | a0001 | c0001 | t0058 | g0100 | AFR | ESN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03195 | hp1 | a0001 | c0001 | t0010 | g0232 | AFR | ESN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03195 | hp2 | a0001 | c0001 | t0033 | g0141 | AFR | ESN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03209 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | MSL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03209 | hp2 | a0001 | c0001 | t0029 | g0050 | AFR | MSL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03225 | hp1 | a0001 | c0001 | t0061 | g0109 | AFR | MSL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03225 | hp2 | a0001 | c0001 | t0092 | g0099 | AFR | MSL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0005 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03239 | hp2 | a0001 | c0001 | t0079 | g0171 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03486 | hp1 | a0001 | c0001 | t0007 | g0105 | AFR | MSL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03486 | hp2 | a0001 | c0001 | t0019 | g0129 | AFR | MSL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03490 | hp1 | a0001 | c0001 | t0031 | g0200 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03490 | hp2 | a0001 | c0001 | t0008 | g0007 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03491 | hp1 | a0001 | c0001 | t0005 | g0095 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03491 | hp2 | a0001 | c0001 | t0032 | g0123 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03492 | hp1 | a0001 | c0001 | t0008 | g0007 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03492 | hp2 | a0001 | c0001 | t0005 | g0006 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03516 | hp1 | a0001 | c0001 | t0022 | g0020 | AFR | ESN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03516 | hp2 | a0001 | c0001 | t0015 | g0015 | AFR | ESN | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03540 | hp1 | a0001 | c0001 | t0021 | g0220 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03540 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | GWD | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03579 | hp1 | a0001 | c0001 | t0059 | g0106 | AFR | MSL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03579 | hp2 | a0001 | c0001 | t0013 | g0101 | AFR | MSL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03669 | hp1 | a0001 | c0001 | t0071 | g0108 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03669 | hp2 | a0001 | c0001 | t0069 | g0205 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03688 | hp1 | a0001 | c0001 | t0001 | g0121 | SAS | STU | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | STU | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03704 | hp1 | a0001 | c0001 | t0056 | g0175 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03710 | hp1 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03710 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | PJL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03831 | hp1 | a0001 | c0001 | t0027 | g0030 | SAS | BEB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03831 | hp2 | a0001 | c0001 | t0002 | g0223 | SAS | BEB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03834 | hp1 | a0002 | c0002 | t0004 | g0012 | SAS | BEB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03834 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | BEB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03927 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03927 | hp2 | a0001 | c0001 | t0002 | g0002 | SAS | BEB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03942 | hp1 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03942 | hp2 | a0001 | c0001 | t0003 | g0019 | SAS | BEB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG04115 | hp1 | a0001 | c0001 | t0057 | g0107 | SAS | STU | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG04115 | hp2 | a0001 | c0001 | t0003 | g0019 | SAS | STU | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG04184 | hp1 | a0001 | c0001 | t0026 | g0097 | SAS | BEB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG04184 | hp2 | a0001 | c0001 | t0032 | g0124 | SAS | BEB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0115 | SAS | STU | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG04204 | hp2 | a0001 | c0001 | t0047 | g0092 | SAS | STU | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG04228 | hp1 | a0001 | c0001 | t0027 | g0030 | SAS | STU | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | STU | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18522 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | YRI | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18522 | hp2 | a0001 | c0001 | t0001 | g0156 | AFR | YRI | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18612 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | CHB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18612 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | CHB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18747 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | CHB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18747 | hp2 | a0001 | c0001 | t0084 | g0118 | EAS | CHB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18906 | hp1 | a0001 | c0001 | t0001 | g0137 | AFR | YRI | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18906 | hp2 | a0001 | c0001 | t0014 | g0081 | AFR | YRI | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18939 | hp1 | a0001 | c0001 | t0087 | g0135 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18939 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18940 | hp1 | a0001 | c0008 | t0002 | g0198 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18940 | hp2 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18942 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18943 | hp1 | a0001 | c0001 | t0072 | g0206 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18943 | hp2 | a0001 | c0001 | t0090 | g0119 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18944 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18944 | hp2 | a0001 | c0001 | t0017 | g0207 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18945 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18945 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18946 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18947 | hp1 | a0002 | c0002 | t0004 | g0017 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18947 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18948 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18949 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18949 | hp2 | a0001 | c0001 | t0002 | g0229 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18950 | hp1 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18950 | hp2 | a0001 | c0001 | t0019 | g0116 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18951 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18952 | hp1 | a0001 | c0001 | t0002 | g0187 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18954 | hp1 | a0002 | c0002 | t0004 | g0066 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18954 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18957 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18957 | hp2 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18960 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18960 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18961 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18961 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18962 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18962 | hp2 | a0001 | c0001 | t0074 | g0125 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18964 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18964 | hp2 | a0001 | c0001 | t0001 | g0163 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18965 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18965 | hp2 | a0001 | c0001 | t0044 | g0212 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18966 | hp1 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18966 | hp2 | a0001 | c0001 | t0008 | g0033 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18967 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18967 | hp2 | a0001 | c0001 | t0006 | g0140 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18970 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0122 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18971 | hp1 | a0002 | c0002 | t0004 | g0017 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18971 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18972 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18972 | hp2 | a0001 | c0001 | t0002 | g0233 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18973 | hp1 | a0001 | c0001 | t0078 | g0088 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18973 | hp2 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18974 | hp1 | a0001 | c0001 | t0010 | g0055 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18974 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18975 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18975 | hp2 | a0001 | c0001 | t0017 | g0227 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18977 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18981 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18981 | hp2 | a0001 | c0001 | t0006 | g0134 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18983 | hp1 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18983 | hp2 | a0001 | c0001 | t0002 | g0005 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18986 | hp1 | a0001 | c0001 | t0019 | g0041 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18986 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18989 | hp1 | a0001 | c0001 | t0036 | g0043 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18990 | hp1 | a0001 | c0001 | t0067 | g0185 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18990 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18993 | hp1 | a0001 | c0001 | t0002 | g0059 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18993 | hp2 | a0001 | c0001 | t0003 | g0167 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18995 | hp1 | a0001 | c0001 | t0017 | g0052 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18995 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18997 | hp1 | a0001 | c0001 | t0008 | g0033 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18997 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18999 | hp1 | a0002 | c0002 | t0004 | g0012 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA18999 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19000 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19005 | hp1 | a0001 | c0001 | t0035 | g0151 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19005 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19006 | hp1 | a0001 | c0001 | t0073 | g0144 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19006 | hp2 | a0007 | c0005 | t0002 | g0068 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19007 | hp1 | a0001 | c0001 | t0002 | g0203 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19007 | hp2 | a0001 | c0001 | t0085 | g0080 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19009 | hp1 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19009 | hp2 | a0001 | c0001 | t0017 | g0052 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19010 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19012 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19012 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19030 | hp1 | a0003 | c0003 | t0012 | g0009 | AFR | LWK | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19030 | hp2 | a0001 | c0001 | t0016 | g0022 | AFR | LWK | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19043 | hp1 | a0001 | c0001 | t0016 | g0130 | AFR | LWK | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19043 | hp2 | a0001 | c0001 | t0014 | g0082 | AFR | LWK | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19057 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19059 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19059 | hp2 | a0001 | c0001 | t0010 | g0055 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19060 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19065 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19065 | hp2 | a0001 | c0001 | t0036 | g0043 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19066 | hp1 | a0001 | c0001 | t0001 | g0170 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19066 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19067 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19067 | hp2 | a0001 | c0001 | t0002 | g0051 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19068 | hp1 | a0001 | c0001 | t0037 | g0060 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19068 | hp2 | a0001 | c0001 | t0009 | g0011 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19070 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19070 | hp2 | a0001 | c0001 | t0006 | g0014 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19072 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19072 | hp2 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19074 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19074 | hp2 | a0002 | c0002 | t0004 | g0012 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19077 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19077 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19083 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19083 | hp2 | a0002 | c0002 | t0004 | g0017 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19084 | hp2 | a0001 | c0001 | t0009 | g0153 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19086 | hp1 | a0001 | c0001 | t0003 | g0010 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19086 | hp2 | a0002 | c0002 | t0039 | g0061 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19087 | hp1 | a0001 | c0001 | t0065 | g0216 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19087 | hp2 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19088 | hp1 | a0002 | c0002 | t0004 | g0012 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19090 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19091 | hp1 | a0001 | c0001 | t0093 | g0152 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19091 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19240 | hp1 | a0001 | c0001 | t0013 | g0113 | AFR | YRI | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA19240 | hp2 | a0001 | c0001 | t0007 | g0008 | AFR | YRI | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA20129 | hp1 | a0001 | c0001 | t0018 | g0072 | AFR | ASW | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA20129 | hp2 | a0001 | c0001 | t0013 | g0104 | AFR | ASW | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA20805 | hp1 | a0001 | c0001 | t0002 | g0225 | EUR | TSI | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA20805 | hp2 | a0001 | c0001 | t0005 | g0006 | EUR | TSI | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA20905 | hp1 | a0001 | c0001 | t0003 | g0019 | SAS | GIH | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA20905 | hp2 | a0001 | c0001 | t0002 | g0201 | SAS | GIH | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01123 | hp1 | a0001 | c0001 | t0011 | g0018 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG01123 | hp2 | a0001 | c0001 | t0001 | g0139 | AMR | CLM | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02109 | hp1 | a0001 | c0001 | t0014 | g0028 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02109 | hp2 | a0001 | c0001 | t0010 | g0199 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02486 | hp1 | a0001 | c0001 | t0077 | g0161 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02486 | hp2 | a0001 | c0001 | t0005 | g0094 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02559 | hp1 | a0001 | c0001 | t0015 | g0015 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG02559 | hp2 | a0001 | c0001 | t0002 | g0025 | AFR | ACB | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03471 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG03471 | hp2 | a0001 | c0001 | t0091 | g0150 | AFR | MSL | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG06807 | hp1 | a0001 | c0001 | t0007 | g0008 | AFR | USA | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| HG06807 | hp2 | a0001 | c0001 | t0005 | g0096 | AFR | USA | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA20300 | hp1 | a0001 | c0001 | t0002 | g0057 | AFR | USA | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA20300 | hp2 | a0001 | c0001 | t0022 | g0020 | AFR | USA | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA21309 | hp1 | a0001 | c0001 | t0020 | g0172 | AFR | LWK | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| NA21309 | hp2 | a0001 | c0001 | t0001 | g0039 | AFR | LWK | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| homoSapiens | chm13v2 | a0001 | c0001 | t0046 | g0071 | REF | REF | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| homoSapiens | grch38p0 | a0001 | c0001 | t0016 | g0168 | REF | REF | C13orf46_chr13_113948705_113979076 | C13orf46 | chr13 | 113948705 | 113979076 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113964985 | C | T | 1 | a0006 | 1 | HG02071.hp1 | missense_variant | MODERATE | c.514G>A | p.Asp172Asn | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/7 | 593/3786 | 514/639 | 172/212 | chr13 | 113964985 | |||
| chr13:113968621 | C | T | 1 | a0002 | 13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
missense_variant | MODERATE | c.382G>A | p.Ala128Thr | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 3/7 | 461/3786 | 382/639 | 128/212 | chr13 | 113968621 | |||
| chr13:113968627 | C | T | 1 | a0005 | 1 | HG01978.hp1 | missense_variant | MODERATE | c.376G>A | p.Glu126Lys | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 3/7 | 455/3786 | 376/639 | 126/212 | chr13 | 113968627 | |||
| chr13:113973867 | C | CCCAGACT others(29): Show |
1 | a0007 | 1 | NA19006.hp2 | conservative_inframe_insertion | MODERATE | c.130_131insAGGAGGCC others(28): Show |
p.Leu43_Gly44insGluG others(32): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/7 | 209/3786 | 130/639 | 44/212 | chr13 | 113973867 | |||
| chr13:113973898 | C | G | 1 | a0003 | 6 | HG01496.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
missense_variant | MODERATE | c.100G>C | p.Ala34Pro | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/7 | 179/3786 | 100/639 | 34/212 | chr13 | 113973898 | |||
| chr13:113973961 | G | A | 1 | a0004 | 2 | HG01952.hp1 HG02717.hp2 |
missense_variant | MODERATE | c.37C>T | p.Arg13Trp | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/7 | 116/3786 | 37/639 | 13/212 | chr13 | 113973961 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113964962 | C | T | 1 | a0001c0008 | 1 | NA18940.hp1 | synonymous_variant | LOW | c.537G>A | p.Pro179Pro | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/7 | 616/3786 | 537/639 | 179/212 | chr13 | 113964962 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113953718 | C | T | 1 | a0001c0001t0030 | 2 | HG02040.hp1 HG02132.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3055G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 3055 | chr13 | 113953718 | ||||||
| chr13:113953769 | G | A | 2 | a0001c0001t0059 a0001c0001t0076 |
2 | HG02145.hp1 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3004C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 3004 | chr13 | 113953769 | ||||||
| chr13:113953778 | C | A | 6 | a0001c0001t0013 a0001c0001t0053 a0001c0001t0054 others(3): Show |
11 | HG01109.hp1 HG02257.hp2 HG02622.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2995G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 2995 | chr13 | 113953778 | ||||||
| chr13:113953800 | C | T | 1 | a0001c0001t0051 | 1 | HG01256.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2973G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 2973 | chr13 | 113953800 | ||||||
| chr13:113953878 | G | A | 3 | a0001c0001t0065 a0002c0002t0004 a0002c0002t0039 |
13 | HG01993.hp1 HG02004.hp2 HG02273.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2895C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 2895 | chr13 | 113953878 | ||||||
| chr13:113953911 | A | G | 1 | a0001c0001t0070 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2862T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 2862 | chr13 | 113953911 | ||||||
| chr13:113953987 | G | A | 4 | a0001c0001t0011 a0001c0001t0043 a0001c0001t0050 others(1): Show |
10 | HG00642.hp2 HG00741.hp2 HG01081.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2786C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 2786 | chr13 | 113953987 | ||||||
| chr13:113954020 | G | T | 52 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0011 others(49): Show |
200 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(197): Show |
3_prime_UTR_variant | MODIFIER | c.*2753C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 2753 | chr13 | 113954020 | ||||||
| chr13:113954117 | G | A | 6 | a0001c0001t0005 a0001c0001t0015 a0001c0001t0021 others(3): Show |
23 | HG00738.hp2 HG01069.hp1 HG01070.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2656C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 2656 | chr13 | 113954117 | ||||||
| chr13:113954158 | A | G | 93 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(90): Show |
395 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(392): Show |
3_prime_UTR_variant | MODIFIER | c.*2615T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 2615 | chr13 | 113954158 | ||||||
| chr13:113954180 | C | T | 1 | a0001c0001t0081 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2593G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 2593 | chr13 | 113954180 | ||||||
| chr13:113954228 | G | A | 3 | a0001c0001t0023 a0001c0001t0067 a0004c0004t0023 |
4 | HG01928.hp1 HG01952.hp1 HG02300.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2545C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 2545 | chr13 | 113954228 | ||||||
| chr13:113954320 | G | A | 1 | a0001c0001t0083 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2453C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 2453 | chr13 | 113954320 | ||||||
| chr13:113954403 | G | A | 1 | a0001c0001t0068 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2370C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 2370 | chr13 | 113954403 | ||||||
| chr13:113954505 | C | T | 1 | a0001c0001t0080 | 1 | HG02698.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2268G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 2268 | chr13 | 113954505 | ||||||
| chr13:113954542 | C | T | 2 | a0001c0001t0064 a0001c0001t0079 |
2 | HG02083.hp1 HG03239.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2231G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 2231 | chr13 | 113954542 | ||||||
| chr13:113954672 | G | A | 1 | a0001c0001t0015 | 6 | HG01069.hp1 HG01071.hp1 HG02258.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2101C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 2101 | chr13 | 113954672 | ||||||
| chr13:113954811 | C | CGAGGAGC others(13): Show |
1 | a0001c0001t0073 | 1 | NA19006.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1942_*1961dupATCT others(16): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1961 | chr13 | 113954811 | ||||||
| chr13:113954811 | CGAGGAGC others(13): Show |
C | 1 | a0001c0001t0091 | 1 | HG03471.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1942_*1961delATCT others(16): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1942 | chr13 | 113954811 | ||||||
| chr13:113954823 | GGTGGAGA others(21): Show |
G | 29 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0003 others(26): Show |
134 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(131): Show |
3_prime_UTR_variant | MODIFIER | c.*1922_*1949delATCT others(24): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1922 | chr13 | 113954823 | ||||||
| chr13:113954842 | C | T | 2 | a0001c0001t0034 a0001c0001t0089 |
3 | HG00735.hp1 HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1931G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1931 | chr13 | 113954842 | ||||||
| chr13:113954843 | G | C | 2 | a0001c0001t0034 a0001c0001t0089 |
3 | HG00735.hp1 HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1930C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1930 | chr13 | 113954843 | ||||||
| chr13:113954848 | A | G | 2 | a0001c0001t0034 a0001c0001t0089 |
3 | HG00735.hp1 HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1925T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1925 | chr13 | 113954848 | ||||||
| chr13:113954851 | T | G | 2 | a0001c0001t0034 a0001c0001t0089 |
3 | HG00735.hp1 HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1922A>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1922 | chr13 | 113954851 | ||||||
| chr13:113954863 | C | G | 2 | a0001c0001t0034 a0001c0001t0089 |
3 | HG00735.hp1 HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1910G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1910 | chr13 | 113954863 | ||||||
| chr13:113954865 | T | C | 2 | a0001c0001t0034 a0001c0001t0089 |
3 | HG00735.hp1 HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1908A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1908 | chr13 | 113954865 | ||||||
| chr13:113954866 | G | A | 2 | a0001c0001t0034 a0001c0001t0089 |
3 | HG00735.hp1 HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1907C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1907 | chr13 | 113954866 | ||||||
| chr13:113954868 | G | A | 2 | a0001c0001t0034 a0001c0001t0089 |
3 | HG00735.hp1 HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1905C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1905 | chr13 | 113954868 | ||||||
| chr13:113954871 | G | C | 2 | a0001c0001t0034 a0001c0001t0089 |
3 | HG00735.hp1 HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1902C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1902 | chr13 | 113954871 | ||||||
| chr13:113954886 | A | G | 2 | a0001c0001t0034 a0001c0001t0089 |
3 | HG00735.hp1 HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1887T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1887 | chr13 | 113954886 | ||||||
| chr13:113954886 | AGAGACGA others(1035): Show |
A | 1 | a0001c0001t0088 | 1 | HG02965.hp2 | 3_prime_UTR_variant | MODIFIER | c.*845_*1886del | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 845 | chr13 | 113954886 | ||||||
| chr13:113954891 | C | CGAG | 2 | a0001c0001t0034 a0001c0001t0089 |
3 | HG00735.hp1 HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1879_*1881dupCTC | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1881 | chr13 | 113954891 | ||||||
| chr13:113954891 | C | CGAGGAGC others(16): Show |
1 | a0001c0001t0085 | 1 | NA19007.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1859_*1881dupCTCG others(19): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1881 | chr13 | 113954891 | ||||||
| chr13:113954905 | C | T | 3 | a0001c0001t0029 a0001c0001t0049 a0001c0001t0078 |
4 | HG00639.hp2 HG03098.hp1 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1868G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1868 | chr13 | 113954905 | ||||||
| chr13:113954921 | C | G | 2 | a0001c0001t0034 a0001c0001t0089 |
3 | HG00735.hp1 HG01070.hp1 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1852G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1852 | chr13 | 113954921 | ||||||
| chr13:113954921 | CATCTGGC others(16): Show |
C | 3 | a0001c0001t0022 a0001c0001t0075 a0001c0001t0084 |
5 | HG02451.hp1 HG02630.hp2 HG03516.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1829_*1851delCCTC others(19): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1829 | chr13 | 113954921 | ||||||
| chr13:113954957 | C | T | 26 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0017 others(23): Show |
127 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
3_prime_UTR_variant | MODIFIER | c.*1816G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1816 | chr13 | 113954957 | ||||||
| chr13:113954964 | GAGGATCT others(39): Show |
G | 1 | a0001c0001t0069 | 1 | HG03669.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1763_*1808delACTC others(42): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1763 | chr13 | 113954964 | ||||||
| chr13:113954980 | C | CGAGGAGG others(16): Show |
4 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0053 others(1): Show |
12 | HG01109.hp1 HG01891.hp1 HG02622.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1770_*1792dupCTCT others(19): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1792 | chr13 | 113954980 | ||||||
| chr13:113954980 | C | T | 2 | a0001c0001t0025 a0001c0001t0045 |
3 | HG01069.hp2 HG01515.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1793G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1793 | chr13 | 113954980 | ||||||
| chr13:113954987 | GAGGATCT others(16): Show |
G | 22 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0017 others(19): Show |
122 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(119): Show |
3_prime_UTR_variant | MODIFIER | c.*1763_*1785delACTC others(19): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1763 | chr13 | 113954987 | ||||||
| chr13:113954998 | A | G | 7 | a0001c0001t0011 a0001c0001t0018 a0001c0001t0025 others(4): Show |
17 | HG00642.hp2 HG00741.hp1 HG01069.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1775T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1775 | chr13 | 113954998 | ||||||
| chr13:113954998 | AGAGAGGA others(16): Show |
A | 3 | a0001c0001t0002 a0001c0001t0009 a0001c0001t0080 |
3 | HG00423.hp2 HG02698.hp1 NA18612.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1752_*1774delCGCC others(19): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1752 | chr13 | 113954998 | ||||||
| chr13:113955003 | G | C | 2 | a0001c0001t0025 a0001c0001t0045 |
3 | HG01069.hp2 HG01515.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1770C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1770 | chr13 | 113955003 | ||||||
| chr13:113955010 | T | G | 16 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(13): Show |
34 | HG01069.hp2 HG01109.hp1 HG01515.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*1763A>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1763 | chr13 | 113955010 | ||||||
| chr13:113955021 | G | A | 1 | a0002c0002t0039 | 1 | NA19086.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1752C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1752 | chr13 | 113955021 | ||||||
| chr13:113955044 | G | A | 1 | a0001c0001t0025 | 2 | HG01515.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1729C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1729 | chr13 | 113955044 | ||||||
| chr13:113955051 | A | G | 1 | a0001c0001t0063 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1722T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1722 | chr13 | 113955051 | ||||||
| chr13:113955063 | C | T | 1 | a0001c0001t0061 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1710G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1710 | chr13 | 113955063 | ||||||
| chr13:113955123 | TGGAGACG others(259): Show |
T | 1 | a0001c0001t0077 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1384_*1649del | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1384 | chr13 | 113955123 | ||||||
| chr13:113955140 | C | T | 3 | a0002c0002t0004 a0002c0002t0038 a0002c0002t0039 |
13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1633G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1633 | chr13 | 113955140 | ||||||
| chr13:113955141 | G | A | 1 | a0001c0001t0001 | 1 | NA18939.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1632C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1632 | chr13 | 113955141 | ||||||
| chr13:113955149 | TGAGGAGC others(13): Show |
T | 4 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0055 others(1): Show |
4 | HG02257.hp2 HG03486.hp1 HG03579.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1604_*1623delCTCT others(16): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1604 | chr13 | 113955149 | ||||||
| chr13:113955173 | G | C | 26 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0017 others(23): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1600C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1600 | chr13 | 113955173 | ||||||
| chr13:113955181 | G | T | 1 | a0001c0001t0001 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1592C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1592 | chr13 | 113955181 | ||||||
| chr13:113955201 | C | T | 26 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0017 others(23): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1572G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1572 | chr13 | 113955201 | ||||||
| chr13:113955229 | C | T | 5 | a0001c0001t0011 a0001c0001t0018 a0001c0001t0050 others(2): Show |
14 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1544G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1544 | chr13 | 113955229 | ||||||
| chr13:113955256 | CATCTGGC others(789): Show |
C | 4 | a0001c0001t0020 a0001c0001t0034 a0001c0001t0089 others(1): Show |
8 | HG00735.hp1 HG01070.hp1 HG01071.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*721_*1516del | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 721 | chr13 | 113955256 | ||||||
| chr13:113955273 | G | T | 1 | a0001c0001t0001 | 1 | HG00408.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1500C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1500 | chr13 | 113955273 | ||||||
| chr13:113955287 | G | A | 7 | a0001c0001t0011 a0001c0001t0018 a0001c0001t0029 others(4): Show |
17 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1486C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1486 | chr13 | 113955287 | ||||||
| chr13:113955313 | G | GAGT | 26 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0017 others(23): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*1457_*1459dupACT | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1459 | chr13 | 113955313 | ||||||
| chr13:113955336 | G | T | 7 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0055 others(4): Show |
9 | HG02257.hp1 HG02257.hp2 HG02258.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1437C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1437 | chr13 | 113955336 | ||||||
| chr13:113955369 | C | T | 2 | a0001c0001t0029 a0001c0001t0049 |
3 | HG00639.hp2 HG03098.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1404G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1404 | chr13 | 113955369 | ||||||
| chr13:113955381 | G | A | 1 | a0001c0001t0017 | 1 | NA18995.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1392C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1392 | chr13 | 113955381 | ||||||
| chr13:113955386 | C | T | 7 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0027 others(4): Show |
19 | HG00738.hp2 HG01070.hp2 HG01168.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1387G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1387 | chr13 | 113955386 | ||||||
| chr13:113955390 | G | A | 7 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0027 others(4): Show |
19 | HG00738.hp2 HG01070.hp2 HG01168.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*1383C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1383 | chr13 | 113955390 | ||||||
| chr13:113955392 | AGACGAGG others(13): Show |
A | 2 | a0001c0001t0008 a0001c0001t0085 |
9 | HG01993.hp2 HG02080.hp1 HG02083.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1361_*1380delACCG others(16): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1361 | chr13 | 113955392 | ||||||
| chr13:113955406 | C | T | 1 | a0001c0001t0076 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1367G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1367 | chr13 | 113955406 | ||||||
| chr13:113955415 | C | T | 3 | a0001c0001t0056 a0001c0001t0057 a0001c0001t0071 |
3 | HG03669.hp1 HG03704.hp1 HG04115.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1358G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1358 | chr13 | 113955415 | ||||||
| chr13:113955435 | T | C | 33 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0010 others(30): Show |
147 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(144): Show |
3_prime_UTR_variant | MODIFIER | c.*1338A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1338 | chr13 | 113955435 | ||||||
| chr13:113955447 | G | A | 1 | a0001c0001t0009 | 8 | HG00544.hp2 HG02165.hp2 HG02523.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1326C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1326 | chr13 | 113955447 | ||||||
| chr13:113955486 | T | C | 10 | a0001c0001t0011 a0001c0001t0018 a0001c0001t0029 others(7): Show |
30 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*1287A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1287 | chr13 | 113955486 | ||||||
| chr13:113955514 | C | T | 1 | a0001c0001t0062 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1259G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1259 | chr13 | 113955514 | ||||||
| chr13:113955529 | CGGAGACG others(13): Show |
C | 1 | a0001c0001t0026 | 2 | HG01358.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1224_*1243delACGA others(16): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1224 | chr13 | 113955529 | ||||||
| chr13:113955535 | C | CGAGGAGC others(13): Show |
1 | a0001c0001t0003 | 6 | HG00558.hp2 HG00609.hp2 HG02155.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1218_*1237dupCTCT others(16): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1237 | chr13 | 113955535 | ||||||
| chr13:113955535 | C | T | 1 | a0001c0001t0005 | 8 | HG00738.hp2 HG01070.hp2 HG01255.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1238G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1238 | chr13 | 113955535 | ||||||
| chr13:113955535 | CGAGGAGC others(13): Show |
C | 10 | a0001c0001t0017 a0001c0001t0021 a0001c0001t0037 others(7): Show |
20 | HG00423.hp1 HG00642.hp2 HG00741.hp2 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1218_*1237delCTCT others(16): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1218 | chr13 | 113955535 | ||||||
| chr13:113955555 | G | T | 1 | a0001c0001t0026 | 2 | HG01358.hp2 HG04184.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1218C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1218 | chr13 | 113955555 | ||||||
| chr13:113955556 | G | A | 1 | a0001c0001t0086 | 1 | HG02572.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1217C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1217 | chr13 | 113955556 | ||||||
| chr13:113955563 | ATCTCGTG others(56): Show |
A | 1 | a0001c0001t0047 | 1 | HG04204.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1147_*1209delCACT others(59): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1147 | chr13 | 113955563 | ||||||
| chr13:113955574 | A | C | 46 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(43): Show |
191 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*1199T>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1199 | chr13 | 113955574 | ||||||
| chr13:113955583 | ATCTCGTG others(36): Show |
A | 46 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(43): Show |
191 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(188): Show |
3_prime_UTR_variant | MODIFIER | c.*1147_*1189delCACT others(39): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1147 | chr13 | 113955583 | ||||||
| chr13:113955585 | C | T | 1 | a0001c0001t0075 | 1 | HG02451.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1188G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1188 | chr13 | 113955585 | ||||||
| chr13:113955602 | C | A | 1 | a0001c0001t0001 | 1 | HG01074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1171G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1171 | chr13 | 113955602 | ||||||
| chr13:113955633 | G | A | 48 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(45): Show |
193 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(190): Show |
3_prime_UTR_variant | MODIFIER | c.*1140C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1140 | chr13 | 113955633 | ||||||
| chr13:113955638 | C | T | 1 | a0001c0001t0033 | 2 | HG01243.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1135G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1135 | chr13 | 113955638 | ||||||
| chr13:113955639 | GAGGAGTA others(16): Show |
G | 14 | a0001c0001t0003 a0001c0001t0017 a0001c0001t0021 others(11): Show |
37 | HG00423.hp1 HG00558.hp2 HG00609.hp2 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*1111_*1133delTGTC others(19): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1111 | chr13 | 113955639 | ||||||
| chr13:113955656 | A | G | 43 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(40): Show |
178 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(175): Show |
3_prime_UTR_variant | MODIFIER | c.*1117T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1117 | chr13 | 113955656 | ||||||
| chr13:113955662 | A | G | 79 | a0001c0001t0001 a0001c0001t0002 a0001c0001t0005 others(76): Show |
363 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(360): Show |
3_prime_UTR_variant | MODIFIER | c.*1111T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1111 | chr13 | 113955662 | ||||||
| chr13:113955673 | T | C | 1 | a0001c0001t0070 | 1 | HG02074.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1100A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1100 | chr13 | 113955673 | ||||||
| chr13:113955682 | G | C | 2 | a0001c0001t0041 a0001c0001t0048 |
2 | HG03041.hp2 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1091C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1091 | chr13 | 113955682 | ||||||
| chr13:113955711 | G | T | 1 | a0003c0003t0012 | 6 | HG01496.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1062C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1062 | chr13 | 113955711 | ||||||
| chr13:113955725 | A | G | 1 | a0001c0001t0092 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1048T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1048 | chr13 | 113955725 | ||||||
| chr13:113955753 | GGAGGAGC others(13): Show |
G | 1 | a0001c0001t0032 | 2 | HG03491.hp2 HG04184.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1000_*1019delGTCT others(16): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1000 | chr13 | 113955753 | ||||||
| chr13:113955762 | T | G | 1 | a0001c0001t0001 | 1 | HG03017.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1011A>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1011 | chr13 | 113955762 | ||||||
| chr13:113955762 | TCCGGCGG others(13): Show |
T | 12 | a0001c0001t0001 a0001c0001t0005 a0001c0001t0006 others(9): Show |
28 | HG00597.hp2 HG00738.hp2 HG01070.hp2 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*991_*1010delCTGCT others(15): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 991 | chr13 | 113955762 | ||||||
| chr13:113955765 | G | A | 3 | a0001c0001t0013 a0001c0001t0053 a0001c0001t0077 |
5 | HG01109.hp1 HG02486.hp1 HG02622.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1008C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1008 | chr13 | 113955765 | ||||||
| chr13:113955767 | C | T | 1 | a0001c0001t0001 | 1 | NA18522.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1006G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 1006 | chr13 | 113955767 | ||||||
| chr13:113955777 | G | A | 36 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0011 others(33): Show |
158 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
3_prime_UTR_variant | MODIFIER | c.*996C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 996 | chr13 | 113955777 | ||||||
| chr13:113955784 | C | T | 2 | a0001c0001t0029 a0001c0001t0049 |
3 | HG00639.hp2 HG03098.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*989G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 989 | chr13 | 113955784 | ||||||
| chr13:113955808 | G | A | 35 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0011 others(32): Show |
157 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(154): Show |
3_prime_UTR_variant | MODIFIER | c.*965C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 965 | chr13 | 113955808 | ||||||
| chr13:113955827 | T | C | 2 | a0001c0001t0024 a0001c0001t0087 |
4 | HG01256.hp1 HG01258.hp1 HG01346.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*946A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 946 | chr13 | 113955827 | ||||||
| chr13:113955870 | AGAG | A | 1 | a0001c0001t0014 | 6 | HG02109.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*900_*902delCTC | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 900 | chr13 | 113955870 | ||||||
| chr13:113955885 | G | A | 2 | a0001c0001t0036 a0001c0001t0093 |
3 | NA18989.hp1 NA19065.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*888C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 888 | chr13 | 113955885 | ||||||
| chr13:113955908 | A | G | 26 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0017 others(23): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*865T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 865 | chr13 | 113955908 | ||||||
| chr13:113955940 | C | G | 7 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0027 others(4): Show |
19 | HG00738.hp2 HG01070.hp2 HG01168.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*833G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 833 | chr13 | 113955940 | ||||||
| chr13:113955963 | C | G | 5 | a0001c0001t0011 a0001c0001t0018 a0001c0001t0050 others(2): Show |
14 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*810G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 810 | chr13 | 113955963 | ||||||
| chr13:113955970 | C | T | 26 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0017 others(23): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*803G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 803 | chr13 | 113955970 | ||||||
| chr13:113955976 | C | CGAGGAGT others(16): Show |
3 | a0002c0002t0004 a0002c0002t0038 a0002c0002t0039 |
13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*796_*797insCTCTCC others(17): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 796 | chr13 | 113955976 | ||||||
| chr13:113955993 | C | T | 1 | a0001c0001t0054 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*780G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 780 | chr13 | 113955993 | ||||||
| chr13:113955994 | A | G | 66 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0005 others(63): Show |
271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*779T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 779 | chr13 | 113955994 | ||||||
| chr13:113956016 | C | T | 2 | a0001c0001t0029 a0001c0001t0049 |
3 | HG00639.hp2 HG03098.hp1 HG03209.hp2 |
3_prime_UTR_variant | MODIFIER | c.*757G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 757 | chr13 | 113956016 | ||||||
| chr13:113956039 | C | T | 7 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0027 others(4): Show |
19 | HG00738.hp2 HG01070.hp2 HG01168.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*734G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 734 | chr13 | 113956039 | ||||||
| chr13:113956040 | A | G | 56 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(53): Show |
212 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(209): Show |
3_prime_UTR_variant | MODIFIER | c.*733T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 733 | chr13 | 113956040 | ||||||
| chr13:113956082 | C | T | 7 | a0001c0001t0005 a0001c0001t0026 a0001c0001t0027 others(4): Show |
19 | HG00738.hp2 HG01070.hp2 HG01168.hp2 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*691G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 691 | chr13 | 113956082 | ||||||
| chr13:113956098 | T | G | 1 | a0001c0001t0092 | 1 | HG03225.hp2 | 3_prime_UTR_variant | MODIFIER | c.*675A>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 675 | chr13 | 113956098 | ||||||
| chr13:113956117 | G | T | 26 | a0001c0001t0002 a0001c0001t0010 a0001c0001t0017 others(23): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
3_prime_UTR_variant | MODIFIER | c.*656C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 656 | chr13 | 113956117 | ||||||
| chr13:113956151 | C | T | 1 | a0001c0001t0053 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*622G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 622 | chr13 | 113956151 | ||||||
| chr13:113956153 | A | G | 13 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(10): Show |
30 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*620T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 620 | chr13 | 113956153 | ||||||
| chr13:113956166 | TCCGGCGG others(33): Show |
T | 1 | a0001c0001t0076 | 1 | HG02145.hp1 | 3_prime_UTR_variant | MODIFIER | c.*567_*606delGTGCTC others(34): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 567 | chr13 | 113956166 | ||||||
| chr13:113956178 | A | G | 58 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(55): Show |
214 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*595T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 595 | chr13 | 113956178 | ||||||
| chr13:113956250 | G | A | 3 | a0002c0002t0004 a0002c0002t0038 a0002c0002t0039 |
13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*523C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 523 | chr13 | 113956250 | ||||||
| chr13:113956252 | C | A | 1 | a0001c0001t0071 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*521G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 521 | chr13 | 113956252 | ||||||
| chr13:113956263 | A | G | 58 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(55): Show |
214 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(211): Show |
3_prime_UTR_variant | MODIFIER | c.*510T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 510 | chr13 | 113956263 | ||||||
| chr13:113956283 | G | A | 1 | a0001c0001t0072 | 1 | NA18943.hp1 | 3_prime_UTR_variant | MODIFIER | c.*490C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 490 | chr13 | 113956283 | ||||||
| chr13:113956304 | CATCTGGT others(16): Show |
C | 2 | a0001c0001t0073 a0001c0001t0074 |
2 | NA18962.hp2 NA19006.hp1 |
3_prime_UTR_variant | MODIFIER | c.*446_*468delACTACT others(17): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 446 | chr13 | 113956304 | ||||||
| chr13:113956327 | TATCTGGT others(33): Show |
T | 13 | a0001c0001t0007 a0001c0001t0013 a0001c0001t0014 others(10): Show |
30 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(27): Show |
3_prime_UTR_variant | MODIFIER | c.*406_*445delGCTCCT others(34): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 406 | chr13 | 113956327 | ||||||
| chr13:113956337 | A | AGAG | 17 | a0001c0001t0005 a0001c0001t0011 a0001c0001t0018 others(14): Show |
54 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(51): Show |
3_prime_UTR_variant | MODIFIER | c.*433_*435dupCTC | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 435 | chr13 | 113956337 | ||||||
| chr13:113956340 | GGAGTAGT others(10): Show |
G | 1 | a0001c0001t0041 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*416_*432delTCCACC others(11): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 416 | chr13 | 113956340 | ||||||
| chr13:113956341 | G | GAGT | 19 | a0001c0001t0002 a0001c0001t0030 a0001c0001t0031 others(16): Show |
109 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(106): Show |
3_prime_UTR_variant | MODIFIER | c.*429_*431dupACT | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 431 | chr13 | 113956341 | ||||||
| chr13:113956344 | TAGTATCT others(13): Show |
T | 9 | a0001c0001t0001 a0001c0001t0003 a0001c0001t0019 others(6): Show |
38 | HG00609.hp1 HG00673.hp1 HG01123.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*409_*428delCCTCCT others(14): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 409 | chr13 | 113956344 | ||||||
| chr13:113956347 | T | C | 1 | a0001c0001t0077 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*426A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 426 | chr13 | 113956347 | ||||||
| chr13:113956347 | TATCTGGT others(10): Show |
T | 9 | a0001c0001t0010 a0001c0001t0017 a0001c0001t0021 others(6): Show |
21 | HG00423.hp1 HG00741.hp2 HG01069.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*409_*425delCCTCCT others(11): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 409 | chr13 | 113956347 | ||||||
| chr13:113956347 | TATCTGGT others(13): Show |
T | 17 | a0001c0001t0002 a0001c0001t0030 a0001c0001t0031 others(14): Show |
107 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(104): Show |
3_prime_UTR_variant | MODIFIER | c.*406_*425delGCTCCT others(14): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 406 | chr13 | 113956347 | ||||||
| chr13:113956364 | G | T | 3 | a0001c0001t0041 a0001c0001t0073 a0001c0001t0074 |
3 | HG03041.hp2 NA18962.hp2 NA19006.hp1 |
3_prime_UTR_variant | MODIFIER | c.*409C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 409 | chr13 | 113956364 | ||||||
| chr13:113956367 | C | T | 10 | a0001c0001t0010 a0001c0001t0017 a0001c0001t0021 others(7): Show |
22 | HG00423.hp1 HG00741.hp2 HG01069.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*406G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 406 | chr13 | 113956367 | ||||||
| chr13:113956547 | A | G | 57 | a0001c0001t0002 a0001c0001t0005 a0001c0001t0007 others(54): Show |
213 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*226T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 226 | chr13 | 113956547 | ||||||
| chr13:113956574 | G | A | 1 | a0001c0001t0035 | 2 | HG02572.hp1 NA19005.hp1 |
3_prime_UTR_variant | MODIFIER | c.*199C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 199 | chr13 | 113956574 | ||||||
| chr13:113956725 | C | T | 1 | a0001c0001t0040 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*48G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 48 | chr13 | 113956725 | ||||||
| chr13:113956767 | G | A | 2 | a0001c0001t0036 a0001c0001t0093 |
3 | NA18989.hp1 NA19065.hp2 NA19091.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 7/7 | 6 | chr13 | 113956767 | ||||||
| chr13:113974045 | C | T | 4 | a0001c0001t0037 a0002c0002t0004 a0002c0002t0038 others(1): Show |
14 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(11): Show |
5_prime_UTR_variant | MODIFIER | c.-48G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/7 | 48 | chr13 | 113974045 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr13:113956921 | C | T | 71 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(68): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.573-82G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113956921 | |||||||
| chr13:113957093 | G | A | 71 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(68): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.573-254C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957093 | |||||||
| chr13:113957206 | T | C | 1 | a0001c0001t0005g0094 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.573-367A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957206 | |||||||
| chr13:113957262 | C | T | 1 | a0001c0001t0070g0196 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.573-423G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957262 | |||||||
| chr13:113957281 | C | T | 1 | a0001c0001t0001g0038 | 2 | HG03710.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.573-442G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957281 | |||||||
| chr13:113957393 | C | CGCACTCT others(574): Show |
2 | a0001c0001t0001g0016 a0001c0001t0001g0132 |
5 | HG00735.hp2 HG00738.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.573-1135_573-555du others(582): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957393 | |||||||
| chr13:113957393 | C | T | 8 | a0002c0002t0004g0012 a0002c0002t0004g0017 a0002c0002t0004g0062 others(5): Show |
13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.573-554G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957393 | |||||||
| chr13:113957407 | A | G | 1 | a0001c0001t0054g0111 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.573-568T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957407 | |||||||
| chr13:113957454 | G | C | 1 | a0001c0001t0002g0230 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.573-615C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957454 | |||||||
| chr13:113957471 | G | A | 1 | a0001c0001t0017g0207 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.573-632C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957471 | |||||||
| chr13:113957510 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.573-671A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957510 | |||||||
| chr13:113957620 | A | G | 1 | a0001c0001t0002g0203 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.573-781T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957620 | |||||||
| chr13:113957650 | C | A | 1 | a0001c0001t0061g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.573-811G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957650 | |||||||
| chr13:113957656 | T | C | 8 | a0002c0002t0004g0012 a0002c0002t0004g0017 a0002c0002t0004g0062 others(5): Show |
13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.573-817A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957656 | |||||||
| chr13:113957688 | TCCA | T | 2 | a0003c0003t0012g0009 a0003c0003t0012g0067 |
6 | HG01496.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.573-852_573-850del others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957688 | |||||||
| chr13:113957706 | C | T | 1 | a0001c0001t0075g0235 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.573-867G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957706 | |||||||
| chr13:113957762 | G | A | 71 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(68): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.573-923C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957762 | |||||||
| chr13:113957776 | C | T | 2 | a0001c0001t0002g0059 a0001c0001t0002g0229 |
3 | NA18949.hp2 NA18957.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.573-937G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957776 | |||||||
| chr13:113957844 | C | T | 14 | a0001c0001t0001g0114 a0001c0001t0011g0018 a0001c0001t0011g0026 others(11): Show |
18 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.573-1005G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957844 | |||||||
| chr13:113957874 | C | A | 1 | a0001c0001t0002g0054 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.573-1035G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957874 | |||||||
| chr13:113957884 | C | A | 1 | a0001c0001t0001g0164 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.573-1045G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957884 | |||||||
| chr13:113957892 | C | A | 4 | a0001c0001t0002g0024 a0001c0001t0002g0209 a0001c0001t0063g0208 others(1): Show |
6 | HG00642.hp1 HG01361.hp2 HG01978.hp1 others(3): Show |
intron_variant | MODIFIER | c.573-1053G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957892 | |||||||
| chr13:113957909 | C | T | 2 | a0001c0001t0018g0070 a0001c0001t0018g0072 |
2 | HG00741.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.573-1070G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957909 | |||||||
| chr13:113957920 | C | A | 1 | a0001c0001t0002g0201 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.573-1081G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957920 | |||||||
| chr13:113957965 | G | T | 2 | a0001c0001t0009g0143 a0001c0001t0009g0154 |
2 | HG02165.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.573-1126C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957965 | |||||||
| chr13:113957983 | C | T | 1 | a0001c0001t0077g0161 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.573-1144G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957983 | |||||||
| chr13:113957984 | C | A | 1 | a0001c0001t0077g0161 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.573-1145G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113957984 | |||||||
| chr13:113958040 | C | T | 1 | a0001c0001t0001g0085 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.573-1201G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958040 | |||||||
| chr13:113958051 | G | A | 12 | a0001c0001t0005g0006 a0001c0001t0005g0091 a0001c0001t0005g0094 others(9): Show |
19 | HG00738.hp2 HG01070.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.573-1212C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958051 | |||||||
| chr13:113958057 | C | CG | 70 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(67): Show |
127 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.573-1219dupC | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958057 | |||||||
| chr13:113958057 | C | T | 2 | a0001c0001t0029g0050 a0001c0001t0049g0176 |
3 | HG00639.hp2 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.573-1218G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958057 | |||||||
| chr13:113958087 | C | T | 1 | a0001c0001t0037g0060 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.573-1248G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958087 | |||||||
| chr13:113958088 | C | A | 2 | a0001c0001t0002g0231 a0001c0001t0068g0218 |
2 | HG01346.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.573-1249G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958088 | |||||||
| chr13:113958150 | C | T | 1 | a0001c0001t0064g0202 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.573-1311G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958150 | |||||||
| chr13:113958151 | G | A | 12 | a0001c0001t0005g0006 a0001c0001t0005g0091 a0001c0001t0005g0094 others(9): Show |
19 | HG00738.hp2 HG01070.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.573-1312C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958151 | |||||||
| chr13:113958179 | CTGCACCC others(41): Show |
C | 2 | a0001c0001t0001g0137 a0001c0001t0035g0166 |
2 | HG02572.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.573-1388_573-1341d others(50): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958179 | |||||||
| chr13:113958209 | G | A | 1 | a0003c0003t0012g0009 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.573-1370C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958209 | |||||||
| chr13:113958223 | C | T | 1 | a0001c0001t0002g0024 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.573-1384G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958223 | |||||||
| chr13:113958507 | C | T | 2 | a0003c0003t0012g0009 a0003c0003t0012g0067 |
6 | HG01496.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.573-1668G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958507 | |||||||
| chr13:113958548 | G | A | 23 | a0001c0001t0007g0008 a0001c0001t0007g0105 a0001c0001t0007g0174 others(20): Show |
30 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.573-1709C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958548 | |||||||
| chr13:113958630 | G | A | 1 | a0001c0001t0009g0153 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.573-1791C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958630 | |||||||
| chr13:113958654 | C | T | 2 | a0001c0001t0007g0008 a0001c0001t0013g0110 |
7 | HG01891.hp1 HG02886.hp1 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.573-1815G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958654 | |||||||
| chr13:113958740 | C | A | 1 | a0001c0001t0005g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.573-1901G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958740 | |||||||
| chr13:113958742 | T | C | 1 | a0001c0001t0005g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.573-1903A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958742 | |||||||
| chr13:113958744 | G | A | 1 | a0001c0001t0005g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.573-1905C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958744 | |||||||
| chr13:113958745 | T | TAACACCA others(22): Show |
1 | a0001c0001t0005g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.573-1907_573-1906i others(31): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958745 | |||||||
| chr13:113958746 | G | C | 1 | a0001c0001t0005g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.573-1907C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958746 | |||||||
| chr13:113958750 | A | G | 1 | a0002c0002t0004g0062 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.573-1911T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958750 | |||||||
| chr13:113958751 | T | A | 1 | a0001c0001t0005g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.573-1912A>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958751 | |||||||
| chr13:113958752 | G | A | 1 | a0001c0001t0005g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.573-1913C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958752 | |||||||
| chr13:113958803 | G | T | 1 | a0002c0002t0004g0063 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.573-1964C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958803 | |||||||
| chr13:113958997 | G | C | 1 | a0001c0001t0005g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.573-2158C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958997 | |||||||
| chr13:113958999 | C | A | 1 | a0001c0001t0005g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.573-2160G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113958999 | |||||||
| chr13:113959000 | A | G | 1 | a0001c0001t0005g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.573-2161T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113959000 | |||||||
| chr13:113959011 | CTCATGCT others(27): Show |
C | 1 | a0001c0001t0005g0095 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.573-2206_573-2173d others(36): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113959011 | |||||||
| chr13:113959034 | TG | T | 11 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(8): Show |
14 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.573-2196delC | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113959034 | |||||||
| chr13:113959261 | G | A | 1 | a0001c0001t0009g0154 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.573-2422C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113959261 | |||||||
| chr13:113959309 | T | C | 5 | a0001c0001t0014g0028 a0001c0001t0014g0081 a0001c0001t0014g0082 others(2): Show |
6 | HG02109.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.573-2470A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113959309 | |||||||
| chr13:113959392 | G | T | 2 | a0001c0001t0029g0050 a0001c0001t0049g0176 |
3 | HG00639.hp2 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.573-2553C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113959392 | |||||||
| chr13:113959434 | T | C | 1 | a0001c0001t0006g0155 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.573-2595A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113959434 | |||||||
| chr13:113959464 | C | T | 1 | a0001c0001t0002g0215 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.573-2625G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113959464 | |||||||
| chr13:113959605 | C | T | 1 | a0001c0001t0001g0115 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.573-2766G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113959605 | |||||||
| chr13:113959627 | T | C | 1 | a0002c0002t0038g0065 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.573-2788A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113959627 | |||||||
| chr13:113959650 | G | T | 3 | a0001c0001t0001g0049 a0001c0001t0001g0179 a0001c0001t0079g0171 |
4 | HG00140.hp2 HG01168.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.573-2811C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113959650 | |||||||
| chr13:113959751 | T | C | 23 | a0001c0001t0007g0008 a0001c0001t0007g0105 a0001c0001t0007g0174 others(20): Show |
30 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.573-2912A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113959751 | |||||||
| chr13:113959754 | G | A | 1 | a0001c0001t0001g0027 | 2 | HG03688.hp2 HG03704.hp2 |
intron_variant | MODIFIER | c.573-2915C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113959754 | |||||||
| chr13:113959841 | A | C | 3 | a0001c0001t0056g0175 a0001c0001t0057g0107 a0001c0001t0071g0108 |
3 | HG03669.hp1 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.573-3002T>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113959841 | |||||||
| chr13:113959919 | G | A | 1 | a0001c0001t0002g0211 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.573-3080C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113959919 | |||||||
| chr13:113960009 | T | C | 1 | a0001c0001t0001g0156 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.573-3170A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113960009 | |||||||
| chr13:113960024 | A | G | 130 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(127): Show |
214 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.573-3185T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113960024 | |||||||
| chr13:113960104 | A | C | 23 | a0001c0001t0007g0008 a0001c0001t0007g0105 a0001c0001t0007g0174 others(20): Show |
30 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.573-3265T>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113960104 | |||||||
| chr13:113960168 | A | G | 1 | a0001c0001t0003g0142 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.573-3329T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113960168 | |||||||
| chr13:113960234 | C | T | 1 | a0001c0001t0011g0076 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.573-3395G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113960234 | |||||||
| chr13:113960255 | C | CA | 130 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(127): Show |
214 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.573-3417dupT | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113960255 | |||||||
| chr13:113960427 | T | A | 11 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(8): Show |
14 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.573-3588A>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113960427 | |||||||
| chr13:113960428 | C | T | 11 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(8): Show |
14 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.573-3589G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113960428 | |||||||
| chr13:113960430 | C | T | 11 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(8): Show |
14 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.573-3591G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113960430 | |||||||
| chr13:113960517 | T | C | 1 | a0001c0001t0002g0184 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.573-3678A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113960517 | |||||||
| chr13:113960789 | T | G | 71 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(68): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.573-3950A>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113960789 | |||||||
| chr13:113960794 | G | A | 1 | a0001c0001t0081g0120 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.573-3955C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113960794 | |||||||
| chr13:113960796 | C | T | 4 | a0002c0002t0004g0012 a0002c0002t0004g0017 a0002c0002t0004g0066 others(1): Show |
9 | HG03834.hp1 NA18947.hp1 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.573-3957G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113960796 | |||||||
| chr13:113960887 | T | C | 1 | a0001c0001t0010g0232 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.572+4040A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113960887 | |||||||
| chr13:113960983 | A | C | 5 | a0001c0001t0005g0091 a0001c0001t0005g0096 a0001c0001t0027g0030 others(2): Show |
7 | HG01168.hp2 HG01169.hp2 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.572+3944T>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113960983 | |||||||
| chr13:113961091 | G | A | 2 | a0001c0001t0001g0157 a0001c0001t0006g0044 |
3 | HG00099.hp2 HG01257.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.572+3836C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113961091 | |||||||
| chr13:113961297 | TTAATA | T | 2 | a0001c0001t0029g0050 a0001c0001t0049g0176 |
3 | HG00639.hp2 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.572+3625_572+3629d others(7): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113961297 | |||||||
| chr13:113961327 | T | C | 11 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(8): Show |
14 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.572+3600A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113961327 | |||||||
| chr13:113961341 | C | T | 233 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(230): Show |
408 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(405): Show |
intron_variant | MODIFIER | c.572+3586G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113961341 | |||||||
| chr13:113961360 | T | C | 1 | a0001c0001t0001g0086 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.572+3567A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113961360 | |||||||
| chr13:113961426 | C | T | 1 | a0001c0001t0002g0057 | 2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.572+3501G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113961426 | |||||||
| chr13:113961472 | A | AGAAAATA others(310): Show |
1 | a0001c0001t0002g0229 | 1 | NA18949.hp2 | intron_variant | MODIFIER | c.572+3454_572+3455i others(319): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113961472 | |||||||
| chr13:113961472 | A | AGAAATAA others(310): Show |
1 | a0001c0001t0044g0212 | 1 | NA18965.hp2 | intron_variant | MODIFIER | c.572+3454_572+3455i others(319): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113961472 | |||||||
| chr13:113961472 | A | AGAAATAA others(309): Show |
1 | a0001c0001t0002g0057 | 2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.572+3454_572+3455i others(318): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113961472 | |||||||
| chr13:113961472 | A | AGAAATAA others(309): Show |
1 | a0007c0005t0002g0068 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.572+3454_572+3455i others(318): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113961472 | |||||||
| chr13:113961472 | A | AGAAATAA others(310): Show |
43 | a0001c0001t0002g0002 a0001c0001t0002g0005 a0001c0001t0002g0025 others(40): Show |
75 | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
intron_variant | MODIFIER | c.572+3454_572+3455i others(319): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113961472 | |||||||
| chr13:113961472 | A | AGAAATAA others(311): Show |
23 | a0001c0001t0002g0003 a0001c0001t0002g0023 a0001c0001t0002g0024 others(20): Show |
46 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(43): Show |
intron_variant | MODIFIER | c.572+3454_572+3455i others(320): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113961472 | |||||||
| chr13:113961472 | A | AGAAATAA others(312): Show |
1 | a0001c0001t0002g0051 | 2 | HG01261.hp2 NA19067.hp2 |
intron_variant | MODIFIER | c.572+3454_572+3455i others(321): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113961472 | |||||||
| chr13:113961553 | T | C | 1 | a0001c0001t0079g0171 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.572+3374A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113961553 | |||||||
| chr13:113961624 | G | C | 71 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(68): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.572+3303C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113961624 | |||||||
| chr13:113961672 | A | C | 1 | a0001c0001t0001g0037 | 2 | HG00099.hp1 HG00323.hp2 |
intron_variant | MODIFIER | c.572+3255T>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113961672 | |||||||
| chr13:113961746 | G | T | 2 | a0003c0003t0012g0009 a0003c0003t0012g0067 |
6 | HG01496.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.572+3181C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113961746 | |||||||
| chr13:113961853 | A | G | 93 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(90): Show |
159 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.572+3074T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113961853 | |||||||
| chr13:113962006 | C | T | 2 | a0001c0001t0002g0023 a0001c0001t0002g0186 |
4 | HG00280.hp1 HG01192.hp1 HG01884.hp2 others(1): Show |
intron_variant | MODIFIER | c.572+2921G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113962006 | |||||||
| chr13:113962057 | G | A | 23 | a0001c0001t0007g0008 a0001c0001t0007g0105 a0001c0001t0007g0174 others(20): Show |
30 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.572+2870C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113962057 | |||||||
| chr13:113962123 | G | A | 1 | a0001c0001t0001g0079 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.572+2804C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113962123 | |||||||
| chr13:113962134 | T | C | 3 | a0001c0001t0001g0029 a0001c0001t0001g0085 a0001c0001t0001g0086 |
4 | NA18949.hp1 NA18951.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.572+2793A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113962134 | |||||||
| chr13:113962141 | C | T | 1 | a0001c0001t0033g0141 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.572+2786G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113962141 | |||||||
| chr13:113962161 | C | T | 1 | a0001c0001t0014g0082 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.572+2766G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113962161 | |||||||
| chr13:113962222 | C | T | 71 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(68): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.572+2705G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113962222 | |||||||
| chr13:113962330 | T | C | 3 | a0001c0001t0020g0048 a0001c0001t0020g0158 a0001c0001t0020g0172 |
4 | HG02615.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.572+2597A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113962330 | |||||||
| chr13:113962334 | G | A | 71 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(68): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.572+2593C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113962334 | |||||||
| chr13:113962397 | C | G | 1 | a0001c0001t0001g0114 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.572+2530G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113962397 | |||||||
| chr13:113962446 | A | G | 3 | a0001c0001t0029g0050 a0001c0001t0049g0176 a0001c0001t0075g0235 |
4 | HG00639.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.572+2481T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113962446 | |||||||
| chr13:113962454 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.572+2473G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113962454 | |||||||
| chr13:113962495 | C | T | 71 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(68): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.572+2432G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113962495 | |||||||
| chr13:113962539 | T | C | 2 | a0001c0001t0001g0045 a0001c0001t0001g0162 |
3 | NA18954.hp2 NA19067.hp1 NA19072.hp2 |
intron_variant | MODIFIER | c.572+2388A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113962539 | |||||||
| chr13:113962552 | T | C | 71 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(68): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.572+2375A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113962552 | |||||||
| chr13:113962665 | C | T | 1 | a0001c0001t0006g0140 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.572+2262G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113962665 | |||||||
| chr13:113962928 | G | A | 5 | a0001c0001t0014g0028 a0001c0001t0014g0081 a0001c0001t0014g0082 others(2): Show |
6 | HG02109.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.572+1999C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113962928 | |||||||
| chr13:113963069 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.572+1858G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963069 | |||||||
| chr13:113963084 | A | G | 1 | a0001c0001t0002g0233 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.572+1843T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963084 | |||||||
| chr13:113963123 | G | A | 1 | a0001c0001t0005g0096 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.572+1804C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963123 | |||||||
| chr13:113963132 | T | C | 71 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(68): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.572+1795A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963132 | |||||||
| chr13:113963155 | A | G | 1 | a0001c0001t0030g0180 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.572+1772T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963155 | |||||||
| chr13:113963177 | G | C | 130 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(127): Show |
214 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.572+1750C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963177 | |||||||
| chr13:113963196 | CGTCCTCA others(30): Show |
C | 1 | a0001c0001t0092g0099 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.572+1694_572+1730d others(39): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963196 | |||||||
| chr13:113963208 | T | TGCCCCTG others(12): Show |
1 | a0001c0001t0002g0222 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.572+1700_572+1718d others(21): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963208 | |||||||
| chr13:113963227 | GGCCCCTG others(11): Show |
G | 3 | a0001c0001t0011g0026 a0001c0001t0011g0076 a0001c0001t0051g0077 |
4 | HG01256.hp2 HG01496.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.572+1682_572+1699d others(20): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963227 | |||||||
| chr13:113963229 | C | CCCCTGTC others(11): Show |
4 | a0001c0001t0002g0005 a0001c0001t0002g0217 a0001c0008t0002g0198 others(1): Show |
9 | HG01975.hp2 HG03239.hp1 NA18940.hp1 others(6): Show |
intron_variant | MODIFIER | c.572+1697_572+1698i others(20): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963229 | |||||||
| chr13:113963247 | C | A | 3 | a0001c0001t0002g0213 a0001c0001t0002g0214 a0001c0001t0010g0055 |
4 | HG02165.hp1 NA18944.hp1 NA18974.hp1 others(1): Show |
intron_variant | MODIFIER | c.572+1680G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963247 | |||||||
| chr13:113963247 | C | G | 68 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(65): Show |
124 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(121): Show |
intron_variant | MODIFIER | c.572+1680G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963247 | |||||||
| chr13:113963265 | G | C | 1 | a0001c0001t0001g0121 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.572+1662C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963265 | |||||||
| chr13:113963265 | GCCCTGTC others(12): Show |
G | 1 | a0001c0001t0001g0139 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.572+1643_572+1661d others(21): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963265 | |||||||
| chr13:113963279 | C | T | 3 | a0001c0001t0002g0215 a0001c0001t0068g0218 a0001c0001t0070g0196 |
3 | HG01099.hp2 HG01346.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.572+1648G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963279 | |||||||
| chr13:113963281 | CG | C | 3 | a0001c0001t0002g0215 a0001c0001t0068g0218 a0001c0001t0070g0196 |
3 | HG01099.hp2 HG01346.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.572+1645delC | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963281 | |||||||
| chr13:113963283 | G | A | 3 | a0001c0001t0002g0215 a0001c0001t0068g0218 a0001c0001t0070g0196 |
3 | HG01099.hp2 HG01346.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.572+1644C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963283 | |||||||
| chr13:113963298 | T | C | 3 | a0001c0001t0002g0215 a0001c0001t0068g0218 a0001c0001t0070g0196 |
3 | HG01099.hp2 HG01346.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.572+1629A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963298 | |||||||
| chr13:113963302 | C | G | 3 | a0001c0001t0002g0215 a0001c0001t0068g0218 a0001c0001t0070g0196 |
3 | HG01099.hp2 HG01346.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.572+1625G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963302 | |||||||
| chr13:113963305 | CT | C | 3 | a0001c0001t0002g0215 a0001c0001t0068g0218 a0001c0001t0070g0196 |
3 | HG01099.hp2 HG01346.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.572+1621delA | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963305 | |||||||
| chr13:113963319 | G | A | 68 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(65): Show |
125 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.572+1608C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963319 | |||||||
| chr13:113963320 | GTC | G | 63 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(60): Show |
117 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.572+1605_572+1606d others(4): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963320 | |||||||
| chr13:113963320 | GTCCCTGT others(46): Show |
G | 5 | a0001c0001t0002g0025 a0001c0001t0010g0232 a0001c0001t0021g0056 others(2): Show |
8 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.572+1554_572+1606d others(55): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963320 | |||||||
| chr13:113963321 | T | C | 62 | a0001c0001t0002g0215 a0001c0001t0005g0006 a0001c0001t0005g0091 others(59): Show |
89 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(86): Show |
intron_variant | MODIFIER | c.572+1606A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963321 | |||||||
| chr13:113963325 | T | C | 63 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(60): Show |
117 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.572+1602A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963325 | |||||||
| chr13:113963336 | C | T | 63 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(60): Show |
117 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.572+1591G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963336 | |||||||
| chr13:113963337 | T | C | 63 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(60): Show |
117 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.572+1590A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963337 | |||||||
| chr13:113963338 | C | G | 63 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(60): Show |
117 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.572+1589G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963338 | |||||||
| chr13:113963338 | C | T | 1 | a0001c0001t0074g0125 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.572+1589G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963338 | |||||||
| chr13:113963341 | CCCGTCCT others(9): Show |
C | 3 | a0001c0001t0002g0215 a0001c0001t0068g0218 a0001c0001t0070g0196 |
3 | HG01099.hp2 HG01346.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.572+1570_572+1585d others(18): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963341 | |||||||
| chr13:113963343 | C | CT | 63 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(60): Show |
117 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.572+1583_572+1584i others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963343 | |||||||
| chr13:113963343 | C | T | 1 | a0001c0001t0001g0086 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.572+1584G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963343 | |||||||
| chr13:113963351 | G | GC | 63 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(60): Show |
117 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.572+1575dupG | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963351 | |||||||
| chr13:113963357 | G | C | 63 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(60): Show |
117 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.572+1570C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963357 | |||||||
| chr13:113963359 | CCGTCCTC others(7): Show |
C | 1 | a0002c0002t0004g0017 | 3 | NA18947.hp1 NA18971.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.572+1554_572+1567d others(16): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963359 | |||||||
| chr13:113963360 | C | CCT | 58 | a0001c0001t0005g0006 a0001c0001t0005g0091 a0001c0001t0005g0094 others(55): Show |
83 | HG00639.hp2 HG00642.hp2 HG00738.hp2 others(80): Show |
intron_variant | MODIFIER | c.572+1566_572+1567i others(4): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963360 | |||||||
| chr13:113963360 | C | CT | 63 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(60): Show |
117 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(114): Show |
intron_variant | MODIFIER | c.572+1566_572+1567i others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963360 | |||||||
| chr13:113963360 | C | T | 3 | a0001c0001t0002g0215 a0001c0001t0068g0218 a0001c0001t0070g0196 |
3 | HG01099.hp2 HG01346.hp1 HG02074.hp1 |
intron_variant | MODIFIER | c.572+1567G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963360 | |||||||
| chr13:113963376 | C | T | 1 | a0002c0002t0004g0017 | 3 | NA18947.hp1 NA18971.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.572+1551G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963376 | |||||||
| chr13:113963388 | C | CG | 5 | a0001c0001t0002g0025 a0001c0001t0010g0232 a0001c0001t0021g0056 others(2): Show |
8 | HG02451.hp2 HG02559.hp2 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.572+1538dupC | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963388 | |||||||
| chr13:113963389 | G | T | 1 | a0002c0002t0004g0017 | 3 | NA18947.hp1 NA18971.hp1 NA19083.hp2 |
intron_variant | MODIFIER | c.572+1538C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963389 | |||||||
| chr13:113963407 | G | A | 12 | a0001c0001t0005g0006 a0001c0001t0005g0091 a0001c0001t0005g0094 others(9): Show |
19 | HG00738.hp2 HG01070.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.572+1520C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963407 | |||||||
| chr13:113963454 | T | TC | 22 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(19): Show |
31 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.572+1472dupG | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963454 | |||||||
| chr13:113963465 | CCT | C | 11 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(8): Show |
14 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.572+1460_572+1461d others(4): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963465 | |||||||
| chr13:113963467 | TGTCCTCA others(10): Show |
T | 1 | a0001c0001t0002g0002 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.572+1443_572+1459d others(19): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963467 | |||||||
| chr13:113963480 | A | G | 1 | a0001c0001t0053g0112 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.572+1447T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963480 | |||||||
| chr13:113963484 | CGTCCTCA others(12): Show |
C | 1 | a0004c0004t0001g0236 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.572+1424_572+1442d others(21): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963484 | |||||||
| chr13:113963497 | GGCCCCTG others(11): Show |
G | 1 | a0001c0001t0018g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.572+1412_572+1429d others(20): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963497 | |||||||
| chr13:113963537 | CCT | C | 71 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(68): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.572+1388_572+1389d others(4): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963537 | |||||||
| chr13:113963568 | C | G | 1 | a0001c0001t0002g0223 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.572+1359G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963568 | |||||||
| chr13:113963647 | G | A | 3 | a0001c0001t0011g0026 a0001c0001t0011g0076 a0001c0001t0051g0077 |
4 | HG01256.hp2 HG01496.hp1 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.572+1280C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963647 | |||||||
| chr13:113963660 | C | CA | 4 | a0001c0001t0002g0005 a0001c0001t0002g0217 a0001c0008t0002g0198 others(1): Show |
10 | HG01975.hp2 HG03239.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.572+1266_572+1267i others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963660 | |||||||
| chr13:113963661 | T | C | 4 | a0001c0001t0002g0005 a0001c0001t0002g0217 a0001c0008t0002g0198 others(1): Show |
10 | HG01975.hp2 HG03239.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.572+1266A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963661 | |||||||
| chr13:113963662 | T | G | 4 | a0001c0001t0002g0005 a0001c0001t0002g0217 a0001c0008t0002g0198 others(1): Show |
10 | HG01975.hp2 HG03239.hp1 NA18612.hp1 others(7): Show |
intron_variant | MODIFIER | c.572+1265A>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963662 | |||||||
| chr13:113963662 | T | TGCCCCTG others(12): Show |
67 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0023 others(64): Show |
118 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(115): Show |
intron_variant | MODIFIER | c.572+1246_572+1264d others(21): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963662 | |||||||
| chr13:113963662 | TGCCCCTG others(12): Show |
T | 1 | a0001c0001t0003g0138 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.572+1246_572+1264d others(21): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963662 | |||||||
| chr13:113963786 | C | T | 1 | a0001c0001t0020g0172 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.572+1141G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963786 | |||||||
| chr13:113963815 | C | T | 1 | a0001c0001t0011g0078 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.572+1112G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963815 | |||||||
| chr13:113963880 | C | A | 1 | a0001c0001t0077g0161 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.572+1047G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963880 | |||||||
| chr13:113963881 | G | A | 8 | a0002c0002t0004g0012 a0002c0002t0004g0017 a0002c0002t0004g0062 others(5): Show |
13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.572+1046C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963881 | |||||||
| chr13:113963917 | C | T | 1 | a0001c0001t0002g0223 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.572+1010G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963917 | |||||||
| chr13:113963919 | C | T | 9 | a0001c0001t0020g0048 a0002c0002t0004g0012 a0002c0002t0004g0017 others(6): Show |
15 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.572+1008G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963919 | |||||||
| chr13:113963955 | A | G | 3 | a0001c0001t0056g0175 a0001c0001t0057g0107 a0001c0001t0071g0108 |
3 | HG03669.hp1 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.572+972T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113963955 | |||||||
| chr13:113964070 | C | T | 6 | a0001c0001t0007g0008 a0001c0001t0013g0034 a0001c0001t0013g0110 others(3): Show |
12 | HG01109.hp1 HG01891.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.572+857G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113964070 | |||||||
| chr13:113964213 | T | C | 1 | a0001c0001t0065g0216 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.572+714A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113964213 | |||||||
| chr13:113964318 | A | G | 8 | a0002c0002t0004g0012 a0002c0002t0004g0017 a0002c0002t0004g0062 others(5): Show |
13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.572+609T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113964318 | |||||||
| chr13:113964431 | C | T | 71 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(68): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.572+496G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113964431 | |||||||
| chr13:113964525 | T | C | 71 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(68): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.572+402A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113964525 | |||||||
| chr13:113964652 | C | T | 5 | a0001c0001t0001g0039 a0001c0001t0001g0137 a0001c0001t0003g0126 others(2): Show |
6 | HG00733.hp2 HG02572.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.572+275G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113964652 | |||||||
| chr13:113964804 | A | AGGGGGGA others(29): Show |
1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.572+87_572+122dupG others(35): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 6/6 | chr13 | 113964804 | |||||||
| chr13:113965237 | A | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(161): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.505-243T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965237 | |||||||
| chr13:113965309 | C | T | 1 | a0001c0001t0002g0223 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.505-315G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965309 | |||||||
| chr13:113965517 | G | A | 4 | a0001c0001t0007g0174 a0001c0001t0013g0101 a0001c0001t0058g0100 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-523C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965517 | |||||||
| chr13:113965527 | ATGATTAT others(30): Show |
A | 1 | a0001c0001t0003g0136 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.505-570_505-534del others(37): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965527 | |||||||
| chr13:113965561 | C | T | 1 | a0001c0001t0053g0112 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.505-567G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965561 | |||||||
| chr13:113965563 | ATGGTGAT others(17): Show |
A | 8 | a0002c0002t0004g0012 a0002c0002t0004g0017 a0002c0002t0004g0062 others(5): Show |
13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.505-593_505-570del others(24): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965563 | |||||||
| chr13:113965626 | A | G | 22 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(19): Show |
31 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(28): Show |
intron_variant | MODIFIER | c.505-632T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965626 | |||||||
| chr13:113965669 | TAATGGTG others(20): Show |
T | 1 | a0001c0001t0002g0184 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.505-702_505-676del others(27): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965669 | |||||||
| chr13:113965677 | ATGG | A | 14 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(11): Show |
18 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(15): Show |
intron_variant | MODIFIER | c.505-686_505-684del others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965677 | |||||||
| chr13:113965680 | GTGA | G | 3 | a0001c0001t0001g0036 a0001c0001t0067g0185 a0004c0004t0001g0236 |
4 | HG02145.hp2 HG02717.hp2 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.505-689_505-687del others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965680 | |||||||
| chr13:113965716 | ATGG | A | 6 | a0001c0001t0013g0113 a0001c0001t0014g0028 a0001c0001t0014g0081 others(3): Show |
7 | HG02109.hp1 HG02630.hp1 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.505-725_505-723del others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965716 | |||||||
| chr13:113965746 | G | GTGA | 155 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(152): Show |
274 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(271): Show |
intron_variant | MODIFIER | c.505-755_505-753dup others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965746 | |||||||
| chr13:113965746 | G | GTGATGAT others(32): Show |
1 | a0001c0001t0003g0136 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.505-753_505-752ins others(39): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965746 | |||||||
| chr13:113965749 | ATGATGGT others(5): Show |
A | 2 | a0001c0001t0029g0050 a0001c0001t0049g0176 |
3 | HG00639.hp2 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.505-767_505-756del others(12): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965749 | |||||||
| chr13:113965752 | ATGG | A | 4 | a0001c0001t0001g0039 a0001c0001t0003g0126 a0001c0001t0019g0129 others(1): Show |
5 | HG00733.hp2 HG02451.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.505-761_505-759del others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965752 | |||||||
| chr13:113965758 | A | ATGG | 153 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(150): Show |
270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.505-767_505-765dup others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965758 | |||||||
| chr13:113965764 | A | G | 4 | a0001c0001t0014g0028 a0001c0001t0014g0081 a0001c0001t0014g0082 others(1): Show |
5 | HG02109.hp1 HG02630.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.505-770T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965764 | |||||||
| chr13:113965767 | A | G | 5 | a0001c0001t0001g0039 a0001c0001t0003g0126 a0001c0001t0014g0083 others(2): Show |
6 | HG00733.hp2 HG02451.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-773T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965767 | |||||||
| chr13:113965768 | T | C | 1 | a0001c0001t0003g0122 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.505-774A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965768 | |||||||
| chr13:113965770 | G | A | 5 | a0001c0001t0001g0159 a0001c0001t0014g0028 a0001c0001t0014g0081 others(2): Show |
6 | HG02109.hp1 HG02630.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.505-776C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965770 | |||||||
| chr13:113965773 | A | G | 4 | a0001c0001t0014g0028 a0001c0001t0014g0081 a0001c0001t0014g0082 others(1): Show |
5 | HG02109.hp1 HG02630.hp1 HG03130.hp1 others(2): Show |
intron_variant | MODIFIER | c.505-779T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965773 | |||||||
| chr13:113965776 | G | A | 8 | a0001c0001t0001g0039 a0001c0001t0003g0126 a0001c0001t0014g0028 others(5): Show |
10 | HG00733.hp2 HG02109.hp1 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.505-782C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965776 | |||||||
| chr13:113965779 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0003g0126 a0001c0001t0019g0129 |
4 | HG00733.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-785T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965779 | |||||||
| chr13:113965779 | ATGATGGT others(11): Show |
A | 3 | a0001c0001t0029g0050 a0001c0001t0049g0176 a0001c0001t0075g0235 |
4 | HG00639.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.505-803_505-786del others(18): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965779 | |||||||
| chr13:113965782 | ATGGTAAT others(8): Show |
A | 3 | a0001c0001t0001g0039 a0001c0001t0003g0126 a0001c0001t0019g0129 |
4 | HG00733.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-803_505-789del others(15): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965782 | |||||||
| chr13:113965796 | G | C | 12 | a0001c0001t0005g0006 a0001c0001t0005g0091 a0001c0001t0005g0094 others(9): Show |
19 | HG00738.hp2 HG01070.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.505-802C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965796 | |||||||
| chr13:113965810 | T | C | 3 | a0001c0001t0056g0175 a0001c0001t0057g0107 a0001c0001t0071g0108 |
3 | HG03669.hp1 HG03704.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.505-816A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965810 | |||||||
| chr13:113965821 | A | C | 1 | a0001c0001t0077g0161 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.505-827T>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965821 | |||||||
| chr13:113965839 | G | GTGA | 141 | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0016 others(138): Show |
239 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
intron_variant | MODIFIER | c.505-848_505-846dup others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965839 | |||||||
| chr13:113965842 | ATGATGGT others(8): Show |
A | 22 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0035 others(19): Show |
44 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.505-863_505-849del others(15): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965842 | |||||||
| chr13:113965848 | G | A | 1 | a0001c0001t0061g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.505-854C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965848 | |||||||
| chr13:113965851 | A | G | 1 | a0001c0001t0061g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.505-857T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965851 | |||||||
| chr13:113965854 | G | A | 1 | a0001c0001t0061g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.505-860C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965854 | |||||||
| chr13:113965875 | A | G | 22 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0035 others(19): Show |
44 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.505-881T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965875 | |||||||
| chr13:113965880 | GGTGGTA | G | 22 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0035 others(19): Show |
44 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(41): Show |
intron_variant | MODIFIER | c.505-892_505-887del others(6): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965880 | |||||||
| chr13:113965922 | A | AATG | 154 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(151): Show |
268 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(265): Show |
intron_variant | MODIFIER | c.505-931_505-929dup others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965922 | |||||||
| chr13:113965931 | GATT | G | 8 | a0002c0002t0004g0012 a0002c0002t0004g0017 a0002c0002t0004g0062 others(5): Show |
13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.505-940_505-938del others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965931 | |||||||
| chr13:113965940 | G | T | 8 | a0002c0002t0004g0012 a0002c0002t0004g0017 a0002c0002t0004g0062 others(5): Show |
13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.505-946C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965940 | |||||||
| chr13:113965941 | G | A | 8 | a0002c0002t0004g0012 a0002c0002t0004g0017 a0002c0002t0004g0062 others(5): Show |
13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.505-947C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965941 | |||||||
| chr13:113965947 | A | G | 8 | a0002c0002t0004g0012 a0002c0002t0004g0017 a0002c0002t0004g0062 others(5): Show |
13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.505-953T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965947 | |||||||
| chr13:113965951 | T | C | 2 | a0001c0001t0001g0160 a0001c0001t0002g0217 |
2 | NA18973.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.505-957A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965951 | |||||||
| chr13:113965953 | G | A | 8 | a0002c0002t0004g0012 a0002c0002t0004g0017 a0002c0002t0004g0062 others(5): Show |
13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.505-959C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965953 | |||||||
| chr13:113965964 | TATA | T | 11 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(8): Show |
14 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.505-973_505-971del others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965964 | |||||||
| chr13:113965994 | AGTGGTGA others(11): Show |
A | 2 | a0001c0001t0002g0003 a0001c0001t0065g0216 |
4 | HG00423.hp2 HG00544.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.505-1018_505-1001d others(20): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113965994 | |||||||
| chr13:113966067 | ATGG | A | 11 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(8): Show |
14 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.505-1076_505-1074d others(5): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966067 | |||||||
| chr13:113966099 | GTGA | G | 8 | a0002c0002t0004g0012 a0002c0002t0004g0017 a0002c0002t0004g0062 others(5): Show |
13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.505-1108_505-1106d others(5): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966099 | |||||||
| chr13:113966102 | ATGATGAT others(5): Show |
A | 2 | a0001c0001t0001g0040 a0001c0001t0001g0163 |
3 | NA18957.hp1 NA18964.hp2 NA19060.hp1 |
intron_variant | MODIFIER | c.505-1120_505-1109d others(14): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966102 | |||||||
| chr13:113966105 | ATGATGAT others(2): Show |
A | 103 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(100): Show |
195 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(192): Show |
intron_variant | MODIFIER | c.505-1120_505-1112d others(11): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966105 | |||||||
| chr13:113966132 | A | C | 3 | a0001c0001t0029g0050 a0001c0001t0049g0176 a0001c0001t0075g0235 |
4 | HG00639.hp2 HG02451.hp1 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.505-1138T>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966132 | |||||||
| chr13:113966154 | C | T | 1 | a0001c0001t0001g0036 | 2 | HG02145.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.505-1160G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966154 | |||||||
| chr13:113966177 | A | G | 1 | a0001c0001t0001g0040 | 2 | NA18957.hp1 NA19060.hp1 |
intron_variant | MODIFIER | c.504+1164T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966177 | |||||||
| chr13:113966183 | A | G | 1 | a0001c0001t0006g0134 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.504+1158T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966183 | |||||||
| chr13:113966184 | T | C | 1 | a0001c0001t0006g0134 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.504+1157A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966184 | |||||||
| chr13:113966184 | T | TGGC | 161 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(158): Show |
280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.504+1156_504+1157i others(5): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966184 | |||||||
| chr13:113966252 | GTGA | G | 5 | a0001c0001t0015g0133 a0002c0002t0004g0062 a0002c0002t0004g0063 others(2): Show |
5 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(2): Show |
intron_variant | MODIFIER | c.504+1086_504+1088d others(5): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966252 | |||||||
| chr13:113966303 | GTGA | G | 2 | a0001c0001t0001g0016 a0001c0001t0001g0132 |
5 | HG00735.hp2 HG00738.hp1 HG01106.hp1 others(2): Show |
intron_variant | MODIFIER | c.504+1035_504+1037d others(5): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966303 | |||||||
| chr13:113966351 | C | T | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+990G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966351 | |||||||
| chr13:113966353 | GTGA | G | 11 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(8): Show |
14 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.504+985_504+987del others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966353 | |||||||
| chr13:113966368 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0003g0126 a0001c0001t0019g0129 |
4 | HG00733.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.504+973T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966368 | |||||||
| chr13:113966371 | GTGA | G | 12 | a0001c0001t0005g0006 a0001c0001t0005g0091 a0001c0001t0005g0094 others(9): Show |
19 | HG00738.hp2 HG01070.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.504+967_504+969del others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966371 | |||||||
| chr13:113966383 | A | G | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+958T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966383 | |||||||
| chr13:113966386 | G | A | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+955C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966386 | |||||||
| chr13:113966397 | A | G | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+944T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966397 | |||||||
| chr13:113966404 | GTGA | G | 19 | a0001c0001t0001g0114 a0001c0001t0007g0008 a0001c0001t0007g0105 others(16): Show |
25 | HG01109.hp1 HG01891.hp1 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.504+934_504+936del others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966404 | |||||||
| chr13:113966426 | A | G | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+915T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966426 | |||||||
| chr13:113966459 | G | T | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+882C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966459 | |||||||
| chr13:113966469 | A | G | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+872T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966469 | |||||||
| chr13:113966505 | ATGG | A | 2 | a0003c0003t0012g0009 a0003c0003t0012g0067 |
6 | HG01496.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.504+833_504+835del others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966505 | |||||||
| chr13:113966537 | A | G | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+804T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966537 | |||||||
| chr13:113966540 | A | G | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+801T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966540 | |||||||
| chr13:113966560 | C | A | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+781G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966560 | |||||||
| chr13:113966568 | G | A | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+773C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966568 | |||||||
| chr13:113966581 | T | C | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+760A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966581 | |||||||
| chr13:113966582 | G | T | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+759C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966582 | |||||||
| chr13:113966605 | C | T | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+736G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966605 | |||||||
| chr13:113966606 | A | G | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+735T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966606 | |||||||
| chr13:113966624 | A | G | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+717T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966624 | |||||||
| chr13:113966625 | GTGA | G | 2 | a0001c0001t0001g0036 a0001c0001t0075g0235 |
3 | HG02145.hp2 HG02451.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.504+713_504+715del others(3): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966625 | |||||||
| chr13:113966640 | A | C | 15 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(12): Show |
19 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.504+701T>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966640 | |||||||
| chr13:113966643 | C | G | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+698G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966643 | |||||||
| chr13:113966644 | T | A | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+697A>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966644 | |||||||
| chr13:113966646 | C | G | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+695G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966646 | |||||||
| chr13:113966661 | G | A | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+680C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966661 | |||||||
| chr13:113966664 | G | A | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+677C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966664 | |||||||
| chr13:113966686 | A | G | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+655T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966686 | |||||||
| chr13:113966687 | T | G | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+654A>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966687 | |||||||
| chr13:113966689 | A | G | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+652T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966689 | |||||||
| chr13:113966703 | T | G | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+638A>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966703 | |||||||
| chr13:113966726 | C | A | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+615G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966726 | |||||||
| chr13:113966729 | G | T | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+612C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966729 | |||||||
| chr13:113966732 | G | A | 1 | a0001c0001t0019g0129 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.504+609C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966732 | |||||||
| chr13:113966815 | G | C | 6 | a0001c0001t0007g0008 a0001c0001t0013g0034 a0001c0001t0013g0110 others(3): Show |
12 | HG01109.hp1 HG01891.hp1 HG02622.hp1 others(9): Show |
intron_variant | MODIFIER | c.504+526C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966815 | |||||||
| chr13:113966884 | C | CG | 5 | a0001c0001t0001g0162 a0001c0001t0002g0195 a0001c0001t0002g0222 others(2): Show |
5 | HG00408.hp1 HG00741.hp1 HG01175.hp2 others(2): Show |
intron_variant | MODIFIER | c.504+456dupC | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966884 | |||||||
| chr13:113966927 | G | T | 4 | a0002c0002t0004g0012 a0002c0002t0004g0017 a0002c0002t0004g0066 others(1): Show |
9 | HG03834.hp1 NA18947.hp1 NA18954.hp1 others(6): Show |
intron_variant | MODIFIER | c.504+414C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113966927 | |||||||
| chr13:113967101 | T | A | 1 | a0001c0001t0077g0161 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.504+240A>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113967101 | |||||||
| chr13:113967193 | G | A | 1 | a0001c0001t0002g0217 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.504+148C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113967193 | |||||||
| chr13:113967217 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(161): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.504+124A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113967217 | |||||||
| chr13:113967263 | C | T | 5 | a0001c0001t0014g0028 a0001c0001t0014g0081 a0001c0001t0014g0082 others(2): Show |
6 | HG02109.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.504+78G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113967263 | |||||||
| chr13:113967289 | G | A | 2 | a0001c0001t0002g0231 a0001c0001t0068g0218 |
2 | HG01346.hp1 NA18960.hp1 |
intron_variant | MODIFIER | c.504+52C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 5/6 | chr13 | 113967289 | |||||||
| chr13:113967392 | C | T | 12 | a0001c0001t0005g0006 a0001c0001t0005g0091 a0001c0001t0005g0094 others(9): Show |
19 | HG00738.hp2 HG01070.hp2 HG01168.hp2 others(16): Show |
splice_region_variant&intron_variant | LOW | c.457-4G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113967392 | |||||||
| chr13:113967393 | G | A | 4 | a0001c0001t0001g0045 a0001c0001t0001g0162 a0001c0001t0001g0163 others(1): Show |
5 | NA18954.hp2 NA18964.hp2 NA19000.hp2 others(2): Show |
splice_region_variant&intron_variant | LOW | c.457-5C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113967393 | |||||||
| chr13:113967453 | C | T | 23 | a0001c0001t0007g0008 a0001c0001t0007g0105 a0001c0001t0007g0174 others(20): Show |
30 | HG01109.hp1 HG01891.hp1 HG02109.hp1 others(27): Show |
intron_variant | MODIFIER | c.457-65G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113967453 | |||||||
| chr13:113967491 | C | T | 3 | a0001c0001t0002g0192 a0001c0001t0002g0194 a0001c0001t0062g0193 |
3 | HG01255.hp1 HG01358.hp1 HG01934.hp1 |
intron_variant | MODIFIER | c.457-103G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113967491 | |||||||
| chr13:113967492 | G | A | 2 | a0001c0001t0034g0046 a0001c0001t0089g0165 |
3 | HG00735.hp1 HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.457-104C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113967492 | |||||||
| chr13:113967559 | C | T | 1 | a0001c0001t0001g0131 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.457-171G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113967559 | |||||||
| chr13:113967601 | T | C | 8 | a0002c0002t0004g0012 a0002c0002t0004g0017 a0002c0002t0004g0062 others(5): Show |
13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.457-213A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113967601 | |||||||
| chr13:113967845 | C | A | 11 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(8): Show |
14 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.457-457G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113967845 | |||||||
| chr13:113967872 | C | T | 2 | a0001c0001t0010g0190 a0001c0001t0066g0191 |
2 | HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.457-484G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113967872 | |||||||
| chr13:113967943 | G | A | 1 | a0001c0001t0001g0016 | 4 | HG00738.hp1 HG01106.hp1 HG01167.hp2 others(1): Show |
intron_variant | MODIFIER | c.456+524C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113967943 | |||||||
| chr13:113968015 | G | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(161): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.456+452C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113968015 | |||||||
| chr13:113968037 | C | T | 8 | a0002c0002t0004g0012 a0002c0002t0004g0017 a0002c0002t0004g0062 others(5): Show |
13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.456+430G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113968037 | |||||||
| chr13:113968038 | G | A | 1 | a0003c0003t0012g0067 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.456+429C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113968038 | |||||||
| chr13:113968188 | G | A | 4 | a0001c0001t0013g0034 a0001c0001t0013g0113 a0001c0001t0053g0112 others(1): Show |
5 | HG01109.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.456+279C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113968188 | |||||||
| chr13:113968226 | C | A | 1 | a0001c0001t0010g0219 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.456+241G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113968226 | |||||||
| chr13:113968334 | G | C | 4 | a0001c0001t0013g0034 a0001c0001t0013g0113 a0001c0001t0053g0112 others(1): Show |
5 | HG01109.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.456+133C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113968334 | |||||||
| chr13:113968348 | C | T | 8 | a0002c0002t0004g0012 a0002c0002t0004g0017 a0002c0002t0004g0062 others(5): Show |
13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.456+119G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113968348 | |||||||
| chr13:113968363 | G | A | 13 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(10): Show |
17 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.456+104C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113968363 | |||||||
| chr13:113968403 | G | A | 2 | a0001c0001t0001g0039 a0001c0001t0019g0129 |
3 | HG02895.hp1 HG03486.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.456+64C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113968403 | |||||||
| chr13:113968418 | T | C | 1 | a0001c0001t0035g0166 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.456+49A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113968418 | |||||||
| chr13:113968465 | A | G | 231 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(228): Show |
405 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(402): Show |
splice_donor_variant&intron_variant | HIGH | c.456+2T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 4/6 | chr13 | 113968465 | |||||||
| chr13:113968774 | A | G | 4 | a0001c0001t0007g0174 a0001c0001t0013g0101 a0001c0001t0058g0100 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.243-14T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113968774 | |||||||
| chr13:113968810 | G | A | 11 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(8): Show |
14 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.243-50C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113968810 | |||||||
| chr13:113968830 | T | C | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(161): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.243-70A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113968830 | |||||||
| chr13:113968909 | G | C | 1 | a0001c0001t0071g0108 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.243-149C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113968909 | |||||||
| chr13:113968920 | G | A | 1 | a0001c0001t0003g0167 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.243-160C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113968920 | |||||||
| chr13:113969043 | G | A | 1 | a0001c0001t0061g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.243-283C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969043 | |||||||
| chr13:113969154 | G | A | 21 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(18): Show |
30 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(27): Show |
intron_variant | MODIFIER | c.243-394C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969154 | |||||||
| chr13:113969297 | T | C | 1 | a0001c0001t0061g0109 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.243-537A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969297 | |||||||
| chr13:113969302 | C | T | 1 | a0001c0001t0002g0188 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.243-542G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969302 | |||||||
| chr13:113969311 | T | C | 13 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(10): Show |
17 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.243-551A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969311 | |||||||
| chr13:113969328 | G | A | 1 | a0001c0001t0001g0087 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.243-568C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969328 | |||||||
| chr13:113969452 | C | G | 164 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0013 others(161): Show |
284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
intron_variant | MODIFIER | c.243-692G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969452 | |||||||
| chr13:113969463 | C | T | 1 | a0001c0001t0016g0130 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.243-703G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969463 | |||||||
| chr13:113969500 | G | A | 2 | a0003c0003t0012g0009 a0003c0003t0012g0067 |
6 | HG01496.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.242+671C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969500 | |||||||
| chr13:113969575 | G | A | 1 | a0001c0001t0014g0084 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.242+596C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969575 | |||||||
| chr13:113969712 | C | T | 1 | a0002c0002t0004g0066 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.242+459G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969712 | |||||||
| chr13:113969772 | A | G | 3 | a0001c0001t0001g0039 a0001c0001t0003g0126 a0001c0001t0019g0129 |
4 | HG00733.hp2 HG02895.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+399T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969772 | |||||||
| chr13:113969774 | G | T | 4 | a0001c0001t0007g0174 a0001c0001t0013g0101 a0001c0001t0058g0100 others(1): Show |
4 | HG02257.hp1 HG02258.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.242+397C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969774 | |||||||
| chr13:113969783 | C | T | 1 | a0001c0001t0002g0187 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.242+388G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969783 | |||||||
| chr13:113969789 | G | A | 1 | a0001c0001t0002g0230 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.242+382C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969789 | |||||||
| chr13:113969844 | C | T | 1 | a0001c0001t0001g0173 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.242+327G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969844 | |||||||
| chr13:113969927 | G | C | 1 | a0001c0001t0078g0088 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.242+244C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969927 | |||||||
| chr13:113969931 | C | G | 1 | a0001c0001t0001g0035 | 2 | HG01891.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.242+240G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969931 | |||||||
| chr13:113969967 | A | G | 2 | a0001c0001t0001g0127 a0001c0001t0001g0128 |
2 | HG02293.hp2 HG02698.hp2 |
intron_variant | MODIFIER | c.242+204T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 2/6 | chr13 | 113969967 | |||||||
| chr13:113970397 | C | T | 2 | a0001c0001t0029g0050 a0001c0001t0049g0176 |
3 | HG00639.hp2 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.191-175G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113970397 | |||||||
| chr13:113970430 | A | C | 16 | a0001c0001t0007g0105 a0001c0001t0007g0174 a0001c0001t0013g0101 others(13): Show |
17 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.191-208T>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113970430 | |||||||
| chr13:113970512 | G | A | 3 | a0001c0001t0014g0081 a0001c0001t0014g0082 a0001c0001t0014g0083 |
3 | HG02970.hp2 NA18906.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.191-290C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113970512 | |||||||
| chr13:113970593 | G | A | 1 | a0001c0001t0002g0057 | 2 | HG01243.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.191-371C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113970593 | |||||||
| chr13:113970598 | G | C | 1 | a0001c0001t0018g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.191-376C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113970598 | |||||||
| chr13:113970641 | C | G | 8 | a0002c0002t0004g0012 a0002c0002t0004g0017 a0002c0002t0004g0062 others(5): Show |
13 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(10): Show |
intron_variant | MODIFIER | c.191-419G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113970641 | |||||||
| chr13:113970643 | A | C | 73 | a0001c0001t0001g0049 a0001c0001t0001g0179 a0001c0001t0002g0002 others(70): Show |
131 | HG00140.hp2 HG00280.hp1 HG00280.hp2 others(128): Show |
intron_variant | MODIFIER | c.191-421T>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113970643 | |||||||
| chr13:113970661 | C | T | 1 | a0001c0001t0002g0186 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.191-439G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113970661 | |||||||
| chr13:113970747 | C | T | 2 | a0001c0001t0008g0007 a0001c0001t0085g0080 |
7 | HG01993.hp2 HG02080.hp1 HG02083.hp2 others(4): Show |
intron_variant | MODIFIER | c.191-525G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113970747 | |||||||
| chr13:113970791 | G | A | 2 | a0001c0001t0032g0123 a0001c0001t0032g0124 |
2 | HG03491.hp2 HG04184.hp2 |
intron_variant | MODIFIER | c.191-569C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113970791 | |||||||
| chr13:113970798 | T | C | 3 | a0001c0001t0014g0084 a0003c0003t0012g0009 a0003c0003t0012g0067 |
7 | HG01496.hp2 HG02630.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.191-576A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113970798 | |||||||
| chr13:113970852 | C | T | 1 | a0001c0001t0075g0235 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.191-630G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113970852 | |||||||
| chr13:113970857 | C | T | 68 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(65): Show |
125 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(122): Show |
intron_variant | MODIFIER | c.191-635G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113970857 | |||||||
| chr13:113970900 | C | G | 1 | a0007c0005t0002g0068 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.191-678G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113970900 | |||||||
| chr13:113970901 | G | C | 1 | a0007c0005t0002g0068 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.191-679C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113970901 | |||||||
| chr13:113970950 | T | C | 4 | a0001c0001t0013g0034 a0001c0001t0013g0113 a0001c0001t0053g0112 others(1): Show |
5 | HG01109.hp1 HG02622.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.191-728A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113970950 | |||||||
| chr13:113971069 | C | A | 1 | a0001c0001t0034g0046 | 2 | HG01070.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.191-847G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971069 | |||||||
| chr13:113971134 | C | T | 1 | a0001c0001t0067g0185 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.191-912G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971134 | |||||||
| chr13:113971135 | G | A | 1 | a0001c0001t0032g0124 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.191-913C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971135 | |||||||
| chr13:113971194 | A | G | 71 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(68): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.191-972T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971194 | |||||||
| chr13:113971246 | T | C | 1 | a0004c0004t0023g0237 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.191-1024A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971246 | |||||||
| chr13:113971326 | C | T | 1 | a0001c0001t0003g0126 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.191-1104G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971326 | |||||||
| chr13:113971474 | G | A | 1 | a0001c0001t0003g0047 | 2 | HG01928.hp2 HG01943.hp2 |
intron_variant | MODIFIER | c.191-1252C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971474 | |||||||
| chr13:113971527 | G | A | 72 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(69): Show |
129 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(126): Show |
intron_variant | MODIFIER | c.191-1305C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971527 | |||||||
| chr13:113971580 | G | C | 1 | a0001c0001t0075g0235 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.191-1358C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971580 | |||||||
| chr13:113971602 | C | A | 7 | a0001c0001t0002g0058 a0001c0001t0002g0059 a0001c0001t0002g0228 others(4): Show |
9 | HG00423.hp1 HG00597.hp1 NA18942.hp1 others(6): Show |
intron_variant | MODIFIER | c.191-1380G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971602 | |||||||
| chr13:113971619 | C | G | 1 | a0001c0001t0074g0125 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.191-1397G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971619 | |||||||
| chr13:113971630 | C | A | 1 | a0001c0001t0026g0097 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.191-1408G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971630 | |||||||
| chr13:113971658 | G | A | 1 | a0001c0001t0001g0170 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.191-1436C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971658 | |||||||
| chr13:113971664 | C | T | 21 | a0001c0001t0001g0004 a0001c0001t0001g0027 a0001c0001t0001g0035 others(18): Show |
43 | HG00099.hp1 HG00323.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.191-1442G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971664 | |||||||
| chr13:113971724 | G | A | 1 | a0001c0001t0020g0048 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.191-1502C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971724 | |||||||
| chr13:113971788 | A | G | 1 | a0001c0001t0002g0184 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.191-1566T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971788 | |||||||
| chr13:113971797 | C | T | 11 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(8): Show |
14 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.191-1575G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971797 | |||||||
| chr13:113971830 | C | T | 71 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(68): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.191-1608G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971830 | |||||||
| chr13:113971831 | G | A | 1 | a0001c0001t0075g0235 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.191-1609C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971831 | |||||||
| chr13:113971866 | T | C | 3 | a0001c0001t0001g0049 a0001c0001t0001g0179 a0001c0001t0079g0171 |
4 | HG00140.hp2 HG01168.hp1 HG03239.hp2 others(1): Show |
intron_variant | MODIFIER | c.191-1644A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971866 | |||||||
| chr13:113971905 | A | G | 2 | a0001c0001t0029g0050 a0001c0001t0049g0176 |
3 | HG00639.hp2 HG03098.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.191-1683T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113971905 | |||||||
| chr13:113972047 | GGCACCTC others(26): Show |
G | 1 | a0007c0005t0002g0068 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.190+1728_190+1760d others(35): Show |
C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972047 | |||||||
| chr13:113972191 | A | G | 130 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(127): Show |
214 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(211): Show |
intron_variant | MODIFIER | c.190+1617T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972191 | |||||||
| chr13:113972216 | G | A | 1 | a0001c0001t0020g0172 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.190+1592C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972216 | |||||||
| chr13:113972315 | G | C | 1 | a0007c0005t0002g0068 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.190+1493C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972315 | |||||||
| chr13:113972320 | C | G | 1 | a0001c0001t0056g0175 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.190+1488G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972320 | |||||||
| chr13:113972386 | A | G | 1 | a0001c0001t0018g0069 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.190+1422T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972386 | |||||||
| chr13:113972420 | G | A | 71 | a0001c0001t0001g0173 a0001c0001t0002g0002 a0001c0001t0002g0003 others(68): Show |
128 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
intron_variant | MODIFIER | c.190+1388C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972420 | |||||||
| chr13:113972429 | C | T | 5 | a0001c0001t0014g0028 a0001c0001t0014g0081 a0001c0001t0014g0082 others(2): Show |
6 | HG02109.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.190+1379G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972429 | |||||||
| chr13:113972430 | G | A | 1 | a0001c0001t0002g0231 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.190+1378C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972430 | |||||||
| chr13:113972448 | G | A | 1 | a0001c0001t0011g0078 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.190+1360C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972448 | |||||||
| chr13:113972467 | C | T | 4 | a0001c0001t0001g0032 a0001c0001t0008g0007 a0001c0001t0008g0033 others(1): Show |
11 | HG01433.hp2 HG01993.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.190+1341G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972467 | |||||||
| chr13:113972512 | G | T | 1 | a0001c0001t0092g0099 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.190+1296C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972512 | |||||||
| chr13:113972536 | C | A | 1 | a0001c0001t0007g0174 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.190+1272G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972536 | |||||||
| chr13:113972594 | T | A | 69 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(66): Show |
126 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.190+1214A>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972594 | |||||||
| chr13:113972606 | C | T | 69 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(66): Show |
126 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(123): Show |
intron_variant | MODIFIER | c.190+1202G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972606 | |||||||
| chr13:113972626 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.190+1182T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972626 | |||||||
| chr13:113972664 | CA | C | 9 | a0001c0001t0037g0060 a0002c0002t0004g0012 a0002c0002t0004g0017 others(6): Show |
14 | HG01993.hp1 HG02004.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.190+1143delT | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972664 | |||||||
| chr13:113972782 | G | C | 1 | a0001c0001t0056g0175 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.190+1026C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972782 | |||||||
| chr13:113972802 | G | A | 13 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(10): Show |
17 | HG00639.hp2 HG00642.hp2 HG00741.hp1 others(14): Show |
intron_variant | MODIFIER | c.190+1006C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972802 | |||||||
| chr13:113972840 | C | T | 1 | a0001c0001t0045g0183 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.190+968G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972840 | |||||||
| chr13:113972874 | C | G | 12 | a0001c0001t0005g0006 a0001c0001t0005g0091 a0001c0001t0005g0094 others(9): Show |
19 | HG00738.hp2 HG01070.hp2 HG01168.hp2 others(16): Show |
intron_variant | MODIFIER | c.190+934G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972874 | |||||||
| chr13:113972901 | C | T | 3 | a0001c0001t0002g0181 a0001c0001t0030g0180 a0001c0001t0030g0182 |
3 | HG00558.hp1 HG02040.hp1 HG02132.hp1 |
intron_variant | MODIFIER | c.190+907G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972901 | |||||||
| chr13:113972918 | G | C | 1 | a0007c0005t0002g0068 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.190+890C>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972918 | |||||||
| chr13:113972959 | T | C | 2 | a0001c0001t0041g0177 a0001c0001t0048g0178 |
2 | HG03041.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.190+849A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972959 | |||||||
| chr13:113972997 | A | G | 70 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(67): Show |
127 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.190+811T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113972997 | |||||||
| chr13:113973010 | C | T | 2 | a0001c0001t0001g0090 a0001c0001t0076g0089 |
2 | HG02145.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.190+798G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973010 | |||||||
| chr13:113973047 | G | A | 1 | a0001c0001t0001g0179 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.190+761C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973047 | |||||||
| chr13:113973059 | G | A | 1 | a0001c0001t0002g0233 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.190+749C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973059 | |||||||
| chr13:113973112 | A | G | 2 | a0003c0003t0012g0009 a0003c0003t0012g0067 |
6 | HG01496.hp2 HG02809.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.190+696T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973112 | |||||||
| chr13:113973180 | G | A | 1 | a0001c0001t0075g0235 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.190+628C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973180 | |||||||
| chr13:113973224 | T | C | 1 | a0002c0002t0004g0066 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.190+584A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973224 | |||||||
| chr13:113973267 | C | T | 1 | a0001c0001t0014g0081 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.190+541G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973267 | |||||||
| chr13:113973281 | G | A | 70 | a0001c0001t0002g0002 a0001c0001t0002g0003 a0001c0001t0002g0005 others(67): Show |
127 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(124): Show |
intron_variant | MODIFIER | c.190+527C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973281 | |||||||
| chr13:113973331 | C | T | 5 | a0001c0001t0014g0028 a0001c0001t0014g0081 a0001c0001t0014g0082 others(2): Show |
6 | HG02109.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.190+477G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973331 | |||||||
| chr13:113973370 | C | G | 2 | a0001c0001t0001g0087 a0001c0001t0078g0088 |
2 | NA18946.hp1 NA18973.hp1 |
intron_variant | MODIFIER | c.190+438G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973370 | |||||||
| chr13:113973430 | C | T | 5 | a0001c0001t0014g0028 a0001c0001t0014g0081 a0001c0001t0014g0082 others(2): Show |
6 | HG02109.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.190+378G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973430 | |||||||
| chr13:113973436 | A | G | 3 | a0001c0001t0001g0029 a0001c0001t0001g0085 a0001c0001t0001g0086 |
4 | NA18949.hp1 NA18951.hp1 NA19057.hp2 others(1): Show |
intron_variant | MODIFIER | c.190+372T>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973436 | |||||||
| chr13:113973549 | C | T | 5 | a0001c0001t0014g0028 a0001c0001t0014g0081 a0001c0001t0014g0082 others(2): Show |
6 | HG02109.hp1 HG02630.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.190+259G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973549 | |||||||
| chr13:113973629 | C | T | 2 | a0001c0001t0001g0027 a0001c0001t0085g0080 |
3 | HG03688.hp2 HG03704.hp2 NA19007.hp2 |
intron_variant | MODIFIER | c.190+179G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973629 | |||||||
| chr13:113973648 | A | T | 1 | a0007c0005t0002g0068 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.190+160T>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973648 | |||||||
| chr13:113973721 | C | G | 1 | a0007c0005t0002g0068 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.190+87G>C | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973721 | |||||||
| chr13:113973722 | T | C | 1 | a0007c0005t0002g0068 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.190+86A>G | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973722 | |||||||
| chr13:113973723 | G | T | 1 | a0007c0005t0002g0068 | 1 | NA19006.hp2 | intron_variant | MODIFIER | c.190+85C>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973723 | |||||||
| chr13:113973732 | C | A | 1 | a0001c0001t0015g0234 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.190+76G>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973732 | |||||||
| chr13:113973732 | C | T | 2 | a0001c0001t0001g0013 a0001c0001t0001g0079 |
5 | NA18942.hp2 NA18962.hp1 NA18972.hp1 others(2): Show |
intron_variant | MODIFIER | c.190+76G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973732 | |||||||
| chr13:113973774 | G | A | 1 | a0001c0001t0075g0235 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.190+34C>T | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973774 | |||||||
| chr13:113973779 | C | T | 11 | a0001c0001t0011g0018 a0001c0001t0011g0026 a0001c0001t0011g0076 others(8): Show |
14 | HG00642.hp2 HG00741.hp1 HG01081.hp2 others(11): Show |
intron_variant | MODIFIER | c.190+29G>A | C13orf46 | ENSG00000283199.3 | transcript | ENST00000636427.3 | protein_coding | 1/6 | chr13 | 113973779 |