| geneid | 8994 |
|---|---|
| ensemblid | ENSG00000144791.10 |
| hgncid | 6612 |
| symbol | LIMD1 |
| name | LIM domain containing 1 |
| refseq_nuc | NM_014240.3 |
| refseq_prot | NP_055055.1 |
| ensembl_nuc | ENST00000273317.5 |
| ensembl_prot | ENSP00000273317.4 |
| mane_status | MANE Select |
| chr | chr3 |
| start | 45594751 |
| end | 45686341 |
| strand | + |
| ver | v1.2 |
| region | chr3:45594751-45686341 |
| region5000 | chr3:45589751-45691341 |
| regionname0 | LIMD1_chr3_45594751_45686341 |
| regionname5000 | LIMD1_chr3_45589751_45691341 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 676 | 351 | 87 | 73 | 145 | 14 | 30 | 107 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0002 | 0/0 | 676 | 2 | 0 | 0 | 2 | 0 | 0 | 2 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0003 | 0/0 | 676 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0004 | 0/0 | 676 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0005 | 0/0 | 676 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0006 | 0/0 | 676 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0007 | 0/0 | 676 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 0/0 | 2031 | 249 | 50 | 42 | 126 | 10 | 21 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| c0002 | 1/1 | 2031 | 83 | 26 | 26 | 16 | 4 | 9 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| c0003 | 0/0 | 2031 | 6 | 4 | 2 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| c0004 | 0/0 | 2031 | 4 | 1 | 3 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| c0005 | 0/0 | 2031 | 4 | 4 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| c0006 | 0/0 | 2031 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| c0007 | 0/0 | 2031 | 2 | 2 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| c0008 | 0/0 | 2031 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| c0009 | 0/0 | 2031 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| c0010 | 0/0 | 2031 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| c0011 | 0/0 | 2031 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| c0012 | 0/0 | 2031 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| c0013 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| c0014 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/0 | 9375 | 39 | 3 | 7 | 25 | 0 | 4 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0002 | 0/0 | 9388 | 12 | 0 | 0 | 11 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0003 | 0/0 | 9386 | 12 | 1 | 2 | 8 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0004 | 0/0 | 9375 | 10 | 0 | 0 | 10 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0005 | 0/0 | 9377 | 8 | 1 | 1 | 4 | 0 | 2 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0006 | 0/0 | 9388 | 7 | 0 | 1 | 5 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0007 | 0/0 | 9353 | 7 | 0 | 3 | 4 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0008 | 0/0 | 9381 | 5 | 0 | 3 | 1 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0009 | 0/0 | 9385 | 5 | 5 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0010 | 0/0 | 9367 | 5 | 0 | 0 | 5 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0011 | 0/0 | 9394 | 4 | 4 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0012 | 0/0 | 9379 | 4 | 0 | 0 | 2 | 0 | 2 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0013 | 0/0 | 9388 | 4 | 0 | 0 | 4 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0014 | 0/0 | 9390 | 3 | 0 | 3 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0015 | 0/0 | 9435 | 3 | 0 | 0 | 3 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0016 | 0/0 | 9386 | 3 | 0 | 1 | 0 | 2 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0017 | 0/0 | 9382 | 3 | 0 | 3 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0018 | 0/0 | 9366 | 3 | 0 | 0 | 2 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0019 | 0/0 | 9443 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0020 | 0/0 | 9420 | 2 | 1 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0021 | 0/0 | 9414 | 2 | 2 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0022 | 0/0 | 9412 | 2 | 0 | 2 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0023 | 0/0 | 9415 | 2 | 2 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0024 | 0/0 | 9399 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0025 | 0/0 | 9408 | 2 | 1 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0026 | 0/0 | 9395 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0027 | 0/0 | 9407 | 2 | 0 | 1 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0028 | 0/0 | 9404 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0029 | 0/0 | 9400 | 2 | 0 | 2 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0030 | 0/0 | 9402 | 2 | 0 | 1 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0031 | 0/0 | 9402 | 2 | 0 | 2 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0032 | 0/0 | 9400 | 2 | 2 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0033 | 0/0 | 9400 | 2 | 0 | 1 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0034 | 0/0 | 9398 | 2 | 0 | 0 | 0 | 2 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0035 | 0/0 | 9399 | 2 | 2 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0036 | 0/0 | 9396 | 2 | 0 | 1 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0037 | 0/0 | 9392 | 2 | 0 | 1 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0038 | 0/0 | 9438 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0039 | 0/0 | 9387 | 2 | 2 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0040 | 0/0 | 9438 | 2 | 0 | 0 | 1 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0041 | 0/0 | 9436 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0042 | 0/0 | 9434 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0043 | 0/0 | 9388 | 2 | 0 | 2 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0044 | 0/0 | 9389 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0045 | 0/0 | 9375 | 2 | 0 | 2 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0046 | 0/0 | 9388 | 2 | 2 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0047 | 0/0 | 9373 | 2 | 0 | 1 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0048 | 0/0 | 9382 | 2 | 2 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0049 | 0/0 | 9370 | 2 | 0 | 0 | 0 | 2 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0050 | 0/0 | 9355 | 2 | 0 | 1 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0051 | 0/0 | 9464 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0052 | 0/0 | 9464 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0053 | 0/0 | 9456 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0054 | 0/0 | 9454 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0055 | 0/0 | 9449 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0056 | 0/0 | 9441 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0057 | 0/0 | 9437 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0058 | 0/0 | 9434 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0059 | 0/0 | 9432 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0060 | 0/0 | 9432 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0061 | 0/0 | 9432 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0062 | 0/0 | 9432 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0063 | 0/0 | 9428 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0064 | 0/0 | 9428 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0065 | 0/0 | 9428 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0066 | 0/0 | 9426 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0067 | 0/0 | 9422 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0068 | 0/0 | 9426 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0069 | 0/0 | 9399 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0070 | 0/0 | 9424 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0071 | 0/0 | 9425 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0072 | 0/0 | 9422 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0073 | 0/0 | 9418 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0074 | 0/0 | 9421 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0075 | 0/0 | 9420 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0076 | 0/0 | 9421 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0077 | 0/0 | 9419 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0078 | 0/0 | 9418 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0079 | 0/0 | 9416 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0080 | 0/1 | 9418 | 1 | 0 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0081 | 0/0 | 9419 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0082 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0083 | 0/0 | 9414 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0084 | 0/0 | 9414 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0085 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0086 | 0/0 | 9417 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0087 | 0/0 | 9414 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0088 | 0/0 | 9410 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0089 | 0/0 | 9401 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0090 | 0/0 | 9401 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0091 | 0/0 | 9410 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0092 | 0/0 | 9412 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0093 | 0/0 | 9413 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0094 | 1/0 | 9412 | 1 | 0 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0095 | 0/0 | 9410 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0096 | 0/0 | 9410 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0097 | 0/0 | 9413 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0098 | 0/0 | 9410 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0099 | 0/0 | 9410 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0100 | 0/0 | 9410 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0101 | 0/0 | 9411 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0102 | 0/0 | 9406 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0103 | 0/0 | 9408 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0104 | 0/0 | 9397 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0105 | 0/0 | 9397 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0106 | 0/0 | 9411 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0107 | 0/0 | 9408 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0108 | 0/0 | 9404 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0109 | 0/0 | 9406 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0110 | 0/0 | 9406 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0111 | 0/0 | 9409 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0112 | 0/0 | 9406 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0113 | 0/0 | 9393 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0114 | 0/0 | 9404 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0115 | 0/0 | 9391 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0116 | 0/0 | 9402 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0117 | 0/0 | 9403 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0118 | 0/0 | 9421 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0119 | 0/0 | 9396 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0120 | 0/0 | 9387 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0121 | 0/0 | 9398 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0122 | 0/0 | 9485 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0123 | 0/0 | 9448 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0124 | 0/0 | 9398 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0125 | 0/0 | 9398 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0126 | 0/0 | 9385 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0127 | 0/0 | 9398 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0128 | 0/0 | 9489 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0129 | 0/0 | 9440 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0130 | 0/0 | 9392 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0131 | 0/0 | 9383 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0132 | 0/0 | 9396 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0133 | 0/0 | 9392 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0134 | 0/0 | 9450 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0135 | 0/0 | 9383 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0136 | 0/0 | 9394 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0137 | 0/0 | 9395 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0138 | 0/0 | 9490 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0139 | 0/0 | 9483 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0140 | 0/0 | 9436 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0141 | 0/0 | 9393 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0142 | 0/0 | 9390 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0143 | 0/0 | 9432 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0144 | 0/0 | 9392 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0145 | 0/0 | 9390 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0146 | 0/0 | 9379 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0147 | 0/0 | 9379 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0148 | 0/0 | 9390 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0149 | 0/0 | 9442 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0150 | 0/0 | 9440 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0151 | 0/0 | 9438 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0152 | 0/0 | 9434 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0153 | 0/0 | 9432 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0154 | 0/0 | 9418 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0155 | 0/0 | 9393 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0156 | 0/0 | 9390 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0157 | 0/0 | 9390 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0158 | 0/0 | 9390 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0159 | 0/0 | 9400 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0160 | 0/0 | 9390 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0161 | 0/0 | 9377 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0162 | 0/0 | 9377 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0163 | 0/0 | 9377 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0164 | 0/0 | 9440 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0165 | 0/0 | 9437 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0166 | 0/0 | 9437 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0167 | 0/0 | 9435 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0168 | 0/0 | 9422 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0169 | 0/0 | 9433 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0170 | 0/0 | 9432 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0171 | 0/0 | 9388 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0172 | 0/0 | 9375 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0173 | 0/0 | 9388 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0174 | 0/0 | 9389 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0175 | 0/0 | 9389 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0176 | 0/0 | 9388 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0177 | 0/0 | 9386 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0178 | 0/0 | 9388 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0179 | 0/0 | 9389 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0180 | 0/0 | 9375 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0181 | 0/0 | 9375 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0182 | 0/0 | 9375 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0183 | 0/0 | 9375 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0184 | 0/0 | 9375 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0185 | 0/0 | 9374 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0186 | 0/0 | 9375 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0187 | 0/0 | 9375 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0188 | 0/0 | 9386 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0189 | 0/0 | 9385 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0190 | 0/0 | 9375 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0191 | 0/0 | 9435 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0192 | 0/0 | 9433 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0193 | 0/0 | 9431 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0194 | 0/0 | 9386 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0195 | 0/0 | 9387 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0196 | 0/0 | 9386 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0197 | 0/0 | 9384 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0198 | 0/0 | 9382 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0199 | 0/0 | 9368 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0200 | 0/0 | 9366 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0201 | 0/0 | 9353 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0202 | 0/0 | 9353 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0203 | 0/0 | 9378 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0204 | 0/0 | 9458 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0205 | 0/0 | 9454 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0206 | 0/0 | 9452 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| t0207 | 0/0 | 9448 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0006 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| g0355 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 0/0 | 2031 | 249 | 50 | 42 | 126 | 10 | 21 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002 | 1/1 | 2031 | 83 | 26 | 26 | 16 | 4 | 9 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0003 | 0/0 | 2031 | 6 | 4 | 2 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0004 | 0/0 | 2031 | 4 | 1 | 3 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0005 | 0/0 | 2031 | 4 | 4 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0007 | 0/0 | 2031 | 2 | 2 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0008 | 0/0 | 2031 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0014 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0002c0006 | 0/0 | 2031 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0003c0010 | 0/0 | 2031 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0004c0011 | 0/0 | 2031 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0005c0012 | 0/0 | 2031 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0006c0013 | 0/0 | 2031 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0007c0009 | 0/0 | 2031 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 11405 | 38 | 3 | 7 | 24 | 0 | 4 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0002 | 0/0 | 11418 | 11 | 0 | 0 | 10 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0003 | 0/0 | 11416 | 12 | 1 | 2 | 8 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0004 | 0/0 | 11405 | 9 | 0 | 0 | 9 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0005 | 0/0 | 11407 | 8 | 1 | 1 | 4 | 0 | 2 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0006 | 0/0 | 11418 | 7 | 0 | 1 | 5 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0007 | 0/0 | 11383 | 7 | 0 | 3 | 4 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0008 | 0/0 | 11411 | 4 | 0 | 3 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0009 | 0/0 | 11415 | 5 | 5 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0010 | 0/0 | 11397 | 5 | 0 | 0 | 5 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0012 | 0/0 | 11409 | 4 | 0 | 0 | 2 | 0 | 2 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0013 | 0/0 | 11418 | 4 | 0 | 0 | 4 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0014 | 0/0 | 11420 | 3 | 0 | 3 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0015 | 0/0 | 11465 | 3 | 0 | 0 | 3 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0016 | 0/0 | 11416 | 3 | 0 | 1 | 0 | 2 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0017 | 0/0 | 11412 | 2 | 0 | 2 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0018 | 0/0 | 11396 | 3 | 0 | 0 | 2 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0019 | 0/0 | 11473 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0023 | 0/0 | 11445 | 2 | 2 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0032 | 0/0 | 11430 | 2 | 2 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0037 | 0/0 | 11422 | 2 | 0 | 1 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0038 | 0/0 | 11468 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0039 | 0/0 | 11417 | 2 | 2 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0040 | 0/0 | 11468 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0041 | 0/0 | 11466 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0042 | 0/0 | 11464 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0043 | 0/0 | 11418 | 2 | 0 | 2 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0044 | 0/0 | 11419 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0045 | 0/0 | 11405 | 2 | 0 | 2 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0046 | 0/0 | 11418 | 2 | 2 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0047 | 0/0 | 11403 | 2 | 0 | 1 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0048 | 0/0 | 11412 | 2 | 2 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0049 | 0/0 | 11400 | 2 | 0 | 0 | 0 | 2 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0050 | 0/0 | 11385 | 2 | 0 | 1 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0053 | 0/0 | 11486 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0056 | 0/0 | 11471 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0057 | 0/0 | 11467 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0058 | 0/0 | 11464 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0064 | 0/0 | 11458 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0068 | 0/0 | 11456 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0069 | 0/0 | 11429 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0074 | 0/0 | 11451 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0075 | 0/0 | 11450 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0076 | 0/0 | 11451 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0078 | 0/0 | 11448 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0081 | 0/0 | 11449 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0082 | 0/0 | 11447 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0083 | 0/0 | 11444 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0084 | 0/0 | 11444 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0085 | 0/0 | 11447 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0086 | 0/0 | 11447 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0091 | 0/0 | 11440 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0096 | 0/0 | 11440 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0097 | 0/0 | 11443 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0106 | 0/0 | 11441 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0109 | 0/0 | 11436 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0111 | 0/0 | 11439 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0116 | 0/0 | 11432 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0123 | 0/0 | 11478 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0129 | 0/0 | 11470 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0134 | 0/0 | 11480 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0135 | 0/0 | 11413 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0140 | 0/0 | 11466 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0143 | 0/0 | 11462 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0144 | 0/0 | 11422 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0145 | 0/0 | 11420 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0147 | 0/0 | 11409 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0148 | 0/0 | 11420 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0149 | 0/0 | 11472 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0150 | 0/0 | 11470 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0151 | 0/0 | 11468 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0152 | 0/0 | 11464 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0153 | 0/0 | 11462 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0154 | 0/0 | 11448 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0155 | 0/0 | 11423 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0156 | 0/0 | 11420 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0157 | 0/0 | 11420 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0158 | 0/0 | 11420 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0159 | 0/0 | 11430 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0160 | 0/0 | 11420 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0161 | 0/0 | 11407 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0162 | 0/0 | 11407 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0163 | 0/0 | 11407 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0164 | 0/0 | 11470 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0165 | 0/0 | 11467 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0166 | 0/0 | 11467 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0167 | 0/0 | 11465 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0168 | 0/0 | 11452 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0169 | 0/0 | 11463 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0170 | 0/0 | 11462 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0171 | 0/0 | 11418 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0172 | 0/0 | 11405 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0173 | 0/0 | 11418 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0174 | 0/0 | 11419 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0175 | 0/0 | 11419 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0176 | 0/0 | 11418 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0177 | 0/0 | 11416 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0178 | 0/0 | 11418 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0180 | 0/0 | 11405 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0181 | 0/0 | 11405 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0182 | 0/0 | 11405 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0183 | 0/0 | 11405 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0184 | 0/0 | 11405 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0185 | 0/0 | 11404 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0186 | 0/0 | 11405 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0187 | 0/0 | 11405 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0188 | 0/0 | 11416 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0189 | 0/0 | 11415 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0190 | 0/0 | 11405 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0191 | 0/0 | 11465 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0192 | 0/0 | 11463 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0193 | 0/0 | 11461 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0194 | 0/0 | 11416 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0195 | 0/0 | 11417 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0196 | 0/0 | 11416 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0197 | 0/0 | 11414 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0198 | 0/0 | 11412 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0199 | 0/0 | 11398 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0200 | 0/0 | 11396 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0201 | 0/0 | 11383 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0202 | 0/0 | 11383 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0001t0203 | 0/0 | 11408 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0011 | 0/0 | 11424 | 4 | 4 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0020 | 0/0 | 11450 | 2 | 1 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0021 | 0/0 | 11444 | 2 | 2 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0024 | 0/0 | 11429 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0025 | 0/0 | 11438 | 2 | 1 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0026 | 0/0 | 11425 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0027 | 0/0 | 11437 | 2 | 0 | 1 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0028 | 0/0 | 11434 | 2 | 0 | 0 | 2 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0029 | 0/0 | 11430 | 2 | 0 | 2 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0030 | 0/0 | 11432 | 2 | 0 | 1 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0031 | 0/0 | 11432 | 2 | 0 | 2 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0033 | 0/0 | 11430 | 2 | 0 | 1 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0034 | 0/0 | 11428 | 2 | 0 | 0 | 0 | 2 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0035 | 0/0 | 11429 | 2 | 2 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0036 | 0/0 | 11426 | 2 | 0 | 1 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0051 | 0/0 | 11494 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0052 | 0/0 | 11494 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0054 | 0/0 | 11484 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0055 | 0/0 | 11479 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0059 | 0/0 | 11462 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0060 | 0/0 | 11462 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0061 | 0/0 | 11462 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0062 | 0/0 | 11462 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0063 | 0/0 | 11458 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0065 | 0/0 | 11458 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0066 | 0/0 | 11456 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0067 | 0/0 | 11452 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0070 | 0/0 | 11454 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0071 | 0/0 | 11455 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0072 | 0/0 | 11452 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0073 | 0/0 | 11448 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0077 | 0/0 | 11449 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0080 | 0/1 | 11448 | 1 | 0 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0087 | 0/0 | 11444 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0088 | 0/0 | 11440 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0089 | 0/0 | 11431 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0090 | 0/0 | 11431 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0092 | 0/0 | 11442 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0093 | 0/0 | 11443 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0094 | 1/0 | 11442 | 1 | 0 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0098 | 0/0 | 11440 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0099 | 0/0 | 11440 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0100 | 0/0 | 11440 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0101 | 0/0 | 11441 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0102 | 0/0 | 11436 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0104 | 0/0 | 11427 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0107 | 0/0 | 11438 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0108 | 0/0 | 11434 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0110 | 0/0 | 11436 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0112 | 0/0 | 11436 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0113 | 0/0 | 11423 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0114 | 0/0 | 11434 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0115 | 0/0 | 11421 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0117 | 0/0 | 11433 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0119 | 0/0 | 11426 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0120 | 0/0 | 11417 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0124 | 0/0 | 11428 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0125 | 0/0 | 11428 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0126 | 0/0 | 11415 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0127 | 0/0 | 11428 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0130 | 0/0 | 11422 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0131 | 0/0 | 11413 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0132 | 0/0 | 11426 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0136 | 0/0 | 11424 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0206 | 0/0 | 11482 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0002t0207 | 0/0 | 11478 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0003t0103 | 0/0 | 11438 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0003t0121 | 0/0 | 11428 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0003t0133 | 0/0 | 11422 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0003t0137 | 0/0 | 11425 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0003t0141 | 0/0 | 11423 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0003t0142 | 0/0 | 11420 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0004t0022 | 0/0 | 11442 | 2 | 0 | 2 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0004t0079 | 0/0 | 11446 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0004t0118 | 0/0 | 11451 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0005t0122 | 0/0 | 11515 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0005t0128 | 0/0 | 11519 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0005t0138 | 0/0 | 11520 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0005t0139 | 0/0 | 11513 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0007t0204 | 0/0 | 11488 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0007t0205 | 0/0 | 11484 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0008t0002 | 0/0 | 11418 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0008t0004 | 0/0 | 11405 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0001c0014t0001 | 0/0 | 11405 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0002c0006t0008 | 0/0 | 11411 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0002c0006t0146 | 0/0 | 11409 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0003c0010t0105 | 0/0 | 11427 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0004c0011t0017 | 0/0 | 11412 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0005c0012t0040 | 0/0 | 11468 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0006c0013t0179 | 0/0 | 11419 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| a0007c0009t0095 | 0/0 | 11440 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | copy fasta | chr3 | 45589751 | 45691341 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0183 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0002g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0002g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0002g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0002g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0002g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0002g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0002g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0002g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0002g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0002g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0002g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0003g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0003g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0003g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0003g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0003g0249 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0003g0250 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0004g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0004g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0004g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0004g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0004g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0004g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0004g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0005g0005 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0005g0166 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0005g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0005g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0005g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0005g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0005g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0006g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0006g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0006g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0006g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0006g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0006g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0006g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0007g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0007g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0007g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0007g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0007g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0007g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0007g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0008g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0008g0200 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0008g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0008g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0009g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0009g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0009g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0009g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0009g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0010g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0010g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0010g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0010g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0010g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0012g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0012g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0012g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0012g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0013g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0013g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0013g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0013g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0014g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0014g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0014g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0015g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0015g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0015g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0016g0001 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0016g0108 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0017g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0017g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0018g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0018g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0018g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0019g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0019g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0023g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0023g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0032g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0032g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0037g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0037g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0038g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0038g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0039g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0039g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0040g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0041g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0041g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0042g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0042g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0043g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0043g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0044g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0044g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0045g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0045g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0046g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0046g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0047g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0047g0226 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0048g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0048g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0049g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0049g0088 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0050g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0050g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0053g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0056g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0057g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0058g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0064g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0068g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0069g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0074g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0075g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0076g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0078g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0081g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0082g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0083g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0084g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0085g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0086g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0091g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0096g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0097g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0106g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0109g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0111g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0116g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0123g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0129g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0134g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0135g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0140g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0143g0265 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0144g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0145g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0147g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0148g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0149g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0150g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0151g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0152g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0153g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0154g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0155g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0156g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0157g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0158g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0159g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0160g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0161g0208 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0162g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0163g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0164g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0165g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0166g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0167g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0168g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0169g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0170g0282 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0171g0193 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0172g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0173g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0174g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0175g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0176g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0177g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0178g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0180g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0181g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0182g0212 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0183g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0184g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0185g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0186g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0187g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0188g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0189g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0190g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0191g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0192g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0193g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0194g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0195g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0196g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0197g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0198g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0199g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0200g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0201g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0202g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0001t0203g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0011g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0011g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0011g0292 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0011g0293 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0020g0309 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0020g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0021g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0021g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0024g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0024g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0025g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0025g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0026g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0026g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0027g0299 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0027g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0028g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0028g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0029g0029 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0029g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0030g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0030g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0031g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0031g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0033g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0033g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0034g0345 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0034g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0035g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0035g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0036g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0036g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0051g0306 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0052g0307 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0054g0330 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0055g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0059g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0060g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0061g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0062g0317 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0063g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0065g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0066g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0067g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0070g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0071g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0072g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0073g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0077g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0080g0355 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0087g0335 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0088g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0089g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0090g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0092g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0093g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0094g0006 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0098g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0099g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0100g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0101g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0102g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0104g0302 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0107g0334 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0108g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0110g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0112g0304 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0113g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0114g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0115g0003 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0117g0337 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0119g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0120g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0124g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0125g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0126g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0127g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0130g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0131g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0132g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0136g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0206g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0002t0207g0312 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0003t0103g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0003t0121g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0003t0133g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0003t0137g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0003t0141g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0003t0142g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0004t0022g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0004t0022g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0004t0079g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0004t0118g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0005t0122g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0005t0128g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0005t0138g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0005t0139g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0007t0204g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0007t0205g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0008t0002g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0008t0004g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0001c0014t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0002c0006t0008g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0002c0006t0146g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0003c0010t0105g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0004c0011t0017g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0005c0012t0040g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0006c0013t0179g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| a0007c0009t0095g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0001 | c0002 | t0034 | g0345 | EUR | GBR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00099 | hp2 | a0001 | c0001 | t0047 | g0226 | EUR | GBR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00140 | hp1 | a0001 | c0002 | t0098 | g0325 | EUR | GBR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00140 | hp2 | a0001 | c0001 | t0016 | g0001 | EUR | GBR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00323 | hp1 | a0001 | c0001 | t0016 | g0108 | EUR | FIN | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00323 | hp2 | a0001 | c0001 | t0171 | g0193 | EUR | FIN | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00423 | hp1 | a0001 | c0001 | t0038 | g0264 | EAS | CHS | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00423 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00438 | hp1 | a0001 | c0001 | t0183 | g0168 | EAS | CHS | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00438 | hp2 | a0001 | c0001 | t0192 | g0290 | EAS | CHS | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00558 | hp1 | a0001 | c0001 | t0042 | g0278 | EAS | CHS | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00558 | hp2 | a0001 | c0001 | t0004 | g0235 | EAS | CHS | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00597 | hp1 | a0001 | c0001 | t0166 | g0263 | EAS | CHS | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00597 | hp2 | a0001 | c0001 | t0186 | g0215 | EAS | CHS | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00609 | hp1 | a0001 | c0001 | t0002 | g0092 | EAS | CHS | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00609 | hp2 | a0001 | c0001 | t0040 | g0269 | EAS | CHS | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00621 | hp1 | a0001 | c0001 | t0006 | g0101 | EAS | CHS | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00621 | hp2 | a0001 | c0001 | t0004 | g0184 | EAS | CHS | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00639 | hp1 | a0001 | c0001 | t0008 | g0232 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00639 | hp2 | a0001 | c0002 | t0136 | g0324 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00673 | hp1 | a0001 | c0002 | t0066 | g0305 | EAS | CHS | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00673 | hp2 | a0001 | c0001 | t0001 | g0227 | EAS | CHS | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00733 | hp1 | a0001 | c0002 | t0071 | g0313 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00733 | hp2 | a0001 | c0001 | t0045 | g0253 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00735 | hp1 | a0001 | c0002 | t0117 | g0337 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00735 | hp2 | a0001 | c0001 | t0014 | g0039 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00738 | hp1 | a0001 | c0002 | t0052 | g0307 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG00738 | hp2 | a0001 | c0001 | t0037 | g0211 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01069 | hp1 | a0001 | c0001 | t0047 | g0182 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01069 | hp2 | a0001 | c0002 | t0112 | g0304 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01070 | hp1 | a0001 | c0001 | t0008 | g0185 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01070 | hp2 | a0001 | c0002 | t0206 | g0310 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01074 | hp1 | a0001 | c0001 | t0008 | g0200 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01074 | hp2 | a0001 | c0001 | t0109 | g0145 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01081 | hp1 | a0001 | c0002 | t0054 | g0330 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01081 | hp2 | a0001 | c0001 | t0017 | g0081 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01106 | hp1 | a0001 | c0002 | t0065 | g0341 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01106 | hp2 | a0001 | c0001 | t0045 | g0214 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01109 | hp1 | a0001 | c0001 | t0091 | g0125 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01109 | hp2 | a0001 | c0004 | t0022 | g0349 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01167 | hp1 | a0001 | c0003 | t0103 | g0124 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01167 | hp2 | a0001 | c0002 | t0029 | g0030 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01168 | hp1 | a0001 | c0002 | t0031 | g0332 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01168 | hp2 | a0001 | c0004 | t0079 | g0352 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01169 | hp1 | a0001 | c0002 | t0029 | g0029 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01169 | hp2 | a0001 | c0002 | t0031 | g0333 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01175 | hp1 | a0001 | c0002 | t0207 | g0312 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01175 | hp2 | a0001 | c0002 | t0025 | g0338 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01192 | hp1 | a0001 | c0001 | t0001 | g0252 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01192 | hp2 | a0001 | c0002 | t0125 | g0353 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01243 | hp1 | a0001 | c0001 | t0116 | g0146 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01243 | hp2 | a0001 | c0003 | t0121 | g0152 | AMR | PUR | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01255 | hp1 | a0001 | c0001 | t0176 | g0103 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01255 | hp2 | a0001 | c0002 | t0030 | g0326 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0161 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01257 | hp2 | a0001 | c0002 | t0027 | g0336 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01258 | hp1 | a0001 | c0001 | t0043 | g0104 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01261 | hp1 | a0001 | c0002 | t0033 | g0347 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01261 | hp2 | a0001 | c0001 | t0203 | g0254 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01346 | hp1 | a0001 | c0001 | t0187 | g0178 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01346 | hp2 | a0001 | c0002 | t0036 | g0346 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01358 | hp1 | a0001 | c0001 | t0003 | g0250 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01358 | hp2 | a0001 | c0001 | t0001 | g0179 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01361 | hp1 | a0001 | c0002 | t0104 | g0302 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01361 | hp2 | a0001 | c0002 | t0101 | g0300 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01433 | hp1 | a0001 | c0001 | t0156 | g0118 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01433 | hp2 | a0001 | c0004 | t0022 | g0350 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01496 | hp1 | a0001 | c0001 | t0014 | g0035 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01496 | hp2 | a0001 | c0001 | t0006 | g0189 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01516 | hp1 | a0001 | c0002 | t0027 | g0299 | EUR | IBS | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01516 | hp2 | a0001 | c0001 | t0049 | g0088 | EUR | IBS | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01517 | hp1 | a0001 | c0001 | t0008 | g0236 | EUR | IBS | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01517 | hp2 | a0001 | c0001 | t0049 | g0084 | EUR | IBS | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01891 | hp1 | a0001 | c0001 | t0053 | g0139 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01891 | hp2 | a0001 | c0001 | t0023 | g0149 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01928 | hp1 | a0001 | c0001 | t0001 | g0183 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01928 | hp2 | a0001 | c0001 | t0043 | g0040 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01934 | hp1 | a0001 | c0001 | t0014 | g0038 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01934 | hp2 | a0001 | c0001 | t0174 | g0248 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01943 | hp1 | a0001 | c0001 | t0003 | g0249 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01943 | hp2 | a0001 | c0002 | t0059 | g0327 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01952 | hp1 | a0001 | c0001 | t0007 | g0061 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01952 | hp2 | a0001 | c0001 | t0016 | g0001 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01975 | hp1 | a0001 | c0001 | t0159 | g0036 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01975 | hp2 | a0001 | c0001 | t0007 | g0063 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01978 | hp1 | a0001 | c0001 | t0001 | g0228 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01978 | hp2 | a0001 | c0002 | t0060 | g0316 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01993 | hp1 | a0001 | c0001 | t0050 | g0060 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01993 | hp2 | a0001 | c0001 | t0145 | g0082 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0230 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02004 | hp2 | a0001 | c0001 | t0017 | g0089 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02015 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02015 | hp2 | a0001 | c0001 | t0057 | g0257 | EAS | KHV | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02055 | hp1 | a0001 | c0001 | t0076 | g0132 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02055 | hp2 | a0001 | c0001 | t0003 | g0090 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02056 | hp1 | a0001 | c0001 | t0010 | g0050 | EAS | KHV | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | KHV | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02074 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | KHV | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02074 | hp2 | a0001 | c0001 | t0150 | g0285 | EAS | KHV | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02080 | hp1 | a0001 | c0001 | t0004 | g0188 | EAS | KHV | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02080 | hp2 | a0001 | c0001 | t0006 | g0251 | EAS | KHV | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02083 | hp1 | a0001 | c0001 | t0147 | g0175 | EAS | KHV | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02083 | hp2 | a0001 | c0001 | t0003 | g0077 | EAS | KHV | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02129 | hp1 | a0001 | c0001 | t0042 | g0279 | EAS | KHV | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02129 | hp2 | a0001 | c0001 | t0002 | g0093 | EAS | KHV | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02132 | hp1 | a0001 | c0001 | t0038 | g0286 | EAS | KHV | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02132 | hp2 | a0001 | c0001 | t0005 | g0219 | EAS | KHV | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02135 | hp1 | a0001 | c0001 | t0004 | g0199 | EAS | KHV | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02135 | hp2 | a0001 | c0001 | t0191 | g0289 | EAS | KHV | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02145 | hp1 | a0001 | c0002 | t0020 | g0340 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02145 | hp2 | a0001 | c0002 | t0131 | g0027 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02148 | hp1 | a0001 | c0001 | t0007 | g0062 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02148 | hp2 | a0001 | c0002 | t0099 | g0322 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02155 | hp1 | a0001 | c0001 | t0149 | g0048 | EAS | CDX | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0207 | EAS | CDX | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02165 | hp1 | a0001 | c0002 | t0033 | g0315 | EAS | CDX | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02165 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | CDX | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02257 | hp1 | a0001 | c0002 | t0092 | g0318 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02257 | hp2 | a0001 | c0002 | t0108 | g0014 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0173 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02258 | hp2 | a0001 | c0002 | t0093 | g0123 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02273 | hp1 | a0001 | c0001 | t0005 | g0170 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02273 | hp2 | a0001 | c0001 | t0180 | g0229 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02280 | hp1 | a0001 | c0001 | t0081 | g0151 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02280 | hp2 | a0001 | c0002 | t0011 | g0292 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02300 | hp1 | a0001 | c0002 | t0087 | g0335 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02300 | hp2 | a0001 | c0002 | t0130 | g0031 | AMR | PEL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02451 | hp1 | a0001 | c0001 | t0096 | g0138 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02451 | hp2 | a0001 | c0005 | t0139 | g0156 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02523 | hp1 | a0001 | c0001 | t0019 | g0284 | EAS | KHV | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02523 | hp2 | a0001 | c0001 | t0012 | g0204 | EAS | KHV | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02615 | hp1 | a0001 | c0004 | t0118 | g0351 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02615 | hp2 | a0001 | c0003 | t0141 | g0153 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02622 | hp1 | a0001 | c0001 | t0001 | g0198 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02622 | hp2 | a0001 | c0002 | t0025 | g0321 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02630 | hp1 | a0001 | c0001 | t0068 | g0128 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02630 | hp2 | a0001 | c0001 | t0048 | g0119 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02647 | hp1 | a0001 | c0002 | t0132 | g0032 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02647 | hp2 | a0001 | c0001 | t0082 | g0137 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02683 | hp1 | a0001 | c0002 | t0070 | g0308 | SAS | PJL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02683 | hp2 | a0001 | c0001 | t0001 | g0242 | SAS | PJL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02717 | hp1 | a0001 | c0002 | t0102 | g0007 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02717 | hp2 | a0001 | c0001 | t0074 | g0135 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02735 | hp1 | a0001 | c0001 | t0002 | g0080 | SAS | PJL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02735 | hp2 | a0001 | c0001 | t0153 | g0270 | SAS | PJL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02738 | hp1 | a0001 | c0001 | t0005 | g0005 | SAS | PJL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02738 | hp2 | a0001 | c0002 | t0107 | g0334 | SAS | PJL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02809 | hp1 | a0001 | c0001 | t0189 | g0024 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02809 | hp2 | a0001 | c0002 | t0067 | g0008 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02818 | hp1 | a0001 | c0001 | t0009 | g0015 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02818 | hp2 | a0001 | c0001 | t0198 | g0121 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02886 | hp1 | a0001 | c0001 | t0123 | g0266 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02886 | hp2 | a0001 | c0007 | t0204 | g0002 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02895 | hp1 | a0001 | c0002 | t0035 | g0044 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02895 | hp2 | a0001 | c0001 | t0009 | g0018 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02897 | hp1 | a0001 | c0002 | t0021 | g0012 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02897 | hp2 | a0001 | c0002 | t0035 | g0043 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02965 | hp1 | a0001 | c0001 | t0032 | g0144 | AFR | ESN | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02965 | hp2 | a0001 | c0001 | t0058 | g0147 | AFR | ESN | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02970 | hp1 | a0001 | c0002 | t0120 | g0028 | AFR | ESN | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02970 | hp2 | a0007 | c0009 | t0095 | g0354 | AFR | ESN | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02976 | hp1 | a0001 | c0001 | t0086 | g0131 | AFR | ESN | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02976 | hp2 | a0001 | c0001 | t0097 | g0268 | AFR | ESN | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03017 | hp1 | a0001 | c0001 | t0003 | g0224 | SAS | PJL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03017 | hp2 | a0005 | c0012 | t0040 | g0271 | SAS | PJL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03041 | hp1 | a0001 | c0003 | t0133 | g0158 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03041 | hp2 | a0001 | c0001 | t0085 | g0148 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03098 | hp1 | a0001 | c0001 | t0148 | g0026 | AFR | MSL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03098 | hp2 | a0001 | c0001 | t0084 | g0141 | AFR | MSL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03130 | hp1 | a0001 | c0001 | t0140 | g0267 | AFR | ESN | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03130 | hp2 | a0001 | c0001 | t0078 | g0129 | AFR | ESN | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03139 | hp1 | a0001 | c0002 | t0088 | g0009 | AFR | ESN | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03139 | hp2 | a0001 | c0007 | t0205 | g0002 | AFR | ESN | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03195 | hp1 | a0001 | c0001 | t0032 | g0143 | AFR | ESN | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03195 | hp2 | a0001 | c0001 | t0129 | g0288 | AFR | ESN | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03209 | hp1 | a0001 | c0001 | t0048 | g0120 | AFR | MSL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03209 | hp2 | a0001 | c0003 | t0142 | g0157 | AFR | MSL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03225 | hp1 | a0001 | c0001 | t0111 | g0133 | AFR | MSL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03225 | hp2 | a0001 | c0001 | t0009 | g0021 | AFR | MSL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03453 | hp1 | a0001 | c0001 | t0106 | g0126 | AFR | MSL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03453 | hp2 | a0001 | c0002 | t0011 | g0293 | AFR | MSL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03486 | hp1 | a0001 | c0001 | t0046 | g0019 | AFR | MSL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03486 | hp2 | a0001 | c0005 | t0138 | g0159 | AFR | MSL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03490 | hp1 | a0001 | c0001 | t0197 | g0114 | SAS | PJL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03490 | hp2 | a0001 | c0001 | t0001 | g0221 | SAS | PJL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03491 | hp1 | a0001 | c0001 | t0181 | g0220 | SAS | PJL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03491 | hp2 | a0001 | c0002 | t0020 | g0309 | SAS | PJL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03516 | hp1 | a0001 | c0001 | t0005 | g0222 | AFR | ESN | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03516 | hp2 | a0001 | c0005 | t0122 | g0155 | AFR | ESN | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03540 | hp1 | a0001 | c0002 | t0119 | g0033 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03540 | hp2 | a0001 | c0002 | t0110 | g0342 | AFR | GWD | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03579 | hp1 | a0001 | c0003 | t0137 | g0154 | AFR | MSL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03579 | hp2 | a0001 | c0001 | t0001 | g0223 | AFR | MSL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03669 | hp1 | a0003 | c0010 | t0105 | g0339 | SAS | PJL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03669 | hp2 | a0001 | c0002 | t0030 | g0319 | SAS | PJL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03688 | hp1 | a0001 | c0002 | t0036 | g0320 | SAS | STU | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03688 | hp2 | a0001 | c0001 | t0001 | g0177 | SAS | STU | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03704 | hp1 | a0001 | c0002 | t0072 | g0301 | SAS | PJL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03704 | hp2 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03710 | hp1 | a0001 | c0002 | t0062 | g0317 | SAS | PJL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03710 | hp2 | a0001 | c0001 | t0012 | g0127 | SAS | PJL | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03831 | hp1 | a0001 | c0002 | t0126 | g0297 | SAS | BEB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03831 | hp2 | a0001 | c0001 | t0170 | g0282 | SAS | BEB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03834 | hp1 | a0001 | c0001 | t0006 | g0075 | SAS | BEB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03834 | hp2 | a0001 | c0001 | t0005 | g0166 | SAS | BEB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03927 | hp1 | a0001 | c0002 | t0051 | g0306 | SAS | BEB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03927 | hp2 | a0001 | c0001 | t0190 | g0174 | SAS | BEB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03942 | hp1 | a0001 | c0001 | t0184 | g0234 | SAS | BEB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG03942 | hp2 | a0001 | c0001 | t0012 | g0004 | SAS | BEB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG04184 | hp1 | a0001 | c0001 | t0161 | g0208 | SAS | BEB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG04184 | hp2 | a0001 | c0001 | t0157 | g0247 | SAS | BEB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG04199 | hp1 | a0001 | c0001 | t0018 | g0055 | SAS | STU | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG04199 | hp2 | a0001 | c0001 | t0037 | g0213 | SAS | STU | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18522 | hp1 | a0001 | c0001 | t0039 | g0016 | AFR | YRI | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18522 | hp2 | a0001 | c0001 | t0083 | g0140 | AFR | YRI | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18747 | hp1 | a0001 | c0001 | t0185 | g0100 | EAS | CHB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18747 | hp2 | a0001 | c0001 | t0196 | g0165 | EAS | CHB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18906 | hp1 | a0001 | c0001 | t0155 | g0023 | AFR | YRI | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18906 | hp2 | a0001 | c0001 | t0023 | g0150 | AFR | YRI | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18940 | hp1 | a0001 | c0001 | t0041 | g0272 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18940 | hp2 | a0001 | c0001 | t0002 | g0116 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18941 | hp1 | a0001 | c0001 | t0010 | g0053 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18941 | hp2 | a0001 | c0008 | t0004 | g0091 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18943 | hp1 | a0001 | c0001 | t0004 | g0233 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18943 | hp2 | a0001 | c0001 | t0002 | g0096 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18944 | hp1 | a0001 | c0001 | t0199 | g0072 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18944 | hp2 | a0001 | c0002 | t0026 | g0298 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18945 | hp1 | a0001 | c0001 | t0134 | g0277 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18945 | hp2 | a0001 | c0002 | t0024 | g0296 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18946 | hp1 | a0001 | c0001 | t0173 | g0244 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18946 | hp2 | a0001 | c0002 | t0115 | g0003 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18947 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18947 | hp2 | a0001 | c0001 | t0044 | g0098 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18951 | hp1 | a0001 | c0001 | t0001 | g0162 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18951 | hp2 | a0001 | c0001 | t0167 | g0275 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18952 | hp1 | a0001 | c0001 | t0004 | g0187 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18952 | hp2 | a0001 | c0001 | t0152 | g0049 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18953 | hp1 | a0001 | c0001 | t0002 | g0111 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18953 | hp2 | a0001 | c0001 | t0010 | g0052 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18954 | hp1 | a0001 | c0001 | t0188 | g0076 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18954 | hp2 | a0001 | c0001 | t0007 | g0059 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18956 | hp1 | a0001 | c0001 | t0162 | g0164 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18956 | hp2 | a0001 | c0001 | t0160 | g0099 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18957 | hp1 | a0001 | c0001 | t0013 | g0068 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18957 | hp2 | a0001 | c0001 | t0201 | g0056 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18959 | hp1 | a0001 | c0001 | t0200 | g0071 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18959 | hp2 | a0001 | c0001 | t0168 | g0273 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18960 | hp1 | a0001 | c0001 | t0164 | g0274 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18960 | hp2 | a0001 | c0001 | t0005 | g0172 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18962 | hp1 | a0001 | c0001 | t0002 | g0106 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18962 | hp2 | a0001 | c0001 | t0056 | g0047 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18963 | hp1 | a0001 | c0001 | t0163 | g0191 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18963 | hp2 | a0001 | c0001 | t0010 | g0066 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18964 | hp1 | a0001 | c0001 | t0202 | g0203 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18964 | hp2 | a0001 | c0001 | t0003 | g0112 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18966 | hp1 | a0001 | c0008 | t0002 | g0107 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18966 | hp2 | a0001 | c0002 | t0089 | g0343 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18967 | hp1 | a0001 | c0001 | t0002 | g0105 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18970 | hp1 | a0001 | c0002 | t0100 | g0323 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18970 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18973 | hp1 | a0001 | c0002 | t0026 | g0003 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18973 | hp2 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18977 | hp1 | a0002 | c0006 | t0146 | g0163 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18977 | hp2 | a0001 | c0001 | t0002 | g0097 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18978 | hp1 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18978 | hp2 | a0001 | c0001 | t0002 | g0102 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18981 | hp1 | a0001 | c0001 | t0004 | g0167 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18981 | hp2 | a0001 | c0001 | t0050 | g0064 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18982 | hp1 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18982 | hp2 | a0001 | c0001 | t0003 | g0078 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18983 | hp1 | a0001 | c0014 | t0001 | g0169 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18983 | hp2 | a0001 | c0002 | t0028 | g0328 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18988 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18988 | hp2 | a0001 | c0001 | t0003 | g0087 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18991 | hp1 | a0001 | c0001 | t0005 | g0237 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18991 | hp2 | a0006 | c0013 | t0179 | g0095 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18992 | hp1 | a0001 | c0001 | t0004 | g0216 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18992 | hp2 | a0001 | c0001 | t0003 | g0115 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18993 | hp2 | a0001 | c0001 | t0006 | g0073 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18994 | hp1 | a0001 | c0001 | t0193 | g0281 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18994 | hp2 | a0001 | c0001 | t0003 | g0042 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18995 | hp1 | a0001 | c0001 | t0013 | g0067 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18995 | hp2 | a0001 | c0001 | t0041 | g0276 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18997 | hp1 | a0001 | c0001 | t0135 | g0210 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18997 | hp2 | a0001 | c0001 | t0019 | g0287 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18998 | hp1 | a0001 | c0001 | t0001 | g0238 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA18998 | hp2 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19000 | hp1 | a0001 | c0002 | t0055 | g0331 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19005 | hp1 | a0001 | c0002 | t0028 | g0329 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19005 | hp2 | a0001 | c0001 | t0007 | g0046 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19007 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19007 | hp2 | a0001 | c0001 | t0169 | g0258 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19009 | hp1 | a0001 | c0001 | t0012 | g0240 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19009 | hp2 | a0001 | c0001 | t0175 | g0245 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19010 | hp1 | a0001 | c0001 | t0015 | g0261 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19012 | hp1 | a0001 | c0002 | t0090 | g0295 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19012 | hp2 | a0001 | c0001 | t0018 | g0054 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19030 | hp1 | a0001 | c0002 | t0127 | g0122 | AFR | LWK | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19030 | hp2 | a0001 | c0001 | t0064 | g0259 | AFR | LWK | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19043 | hp1 | a0001 | c0001 | t0009 | g0025 | AFR | LWK | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19043 | hp2 | a0001 | c0002 | t0011 | g0034 | AFR | LWK | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19054 | hp1 | a0001 | c0001 | t0151 | g0283 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19054 | hp2 | a0001 | c0001 | t0004 | g0218 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19057 | hp1 | a0001 | c0001 | t0015 | g0262 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19057 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19062 | hp1 | a0001 | c0001 | t0006 | g0085 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19062 | hp2 | a0001 | c0001 | t0007 | g0058 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19063 | hp1 | a0001 | c0002 | t0024 | g0294 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19063 | hp2 | a0001 | c0001 | t0010 | g0051 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19065 | hp1 | a0001 | c0001 | t0165 | g0280 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19065 | hp2 | a0001 | c0001 | t0007 | g0065 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19068 | hp1 | a0001 | c0001 | t0003 | g0074 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0171 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19077 | hp1 | a0001 | c0002 | t0113 | g0344 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19077 | hp2 | a0001 | c0001 | t0006 | g0113 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19078 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19078 | hp2 | a0001 | c0001 | t0015 | g0260 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19079 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19079 | hp2 | a0001 | c0001 | t0013 | g0070 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19084 | hp1 | a0001 | c0002 | t0114 | g0314 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19084 | hp2 | a0001 | c0001 | t0177 | g0083 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19085 | hp1 | a0001 | c0001 | t0002 | g0110 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19085 | hp2 | a0001 | c0001 | t0005 | g0192 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19087 | hp1 | a0001 | c0001 | t0013 | g0069 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19087 | hp2 | a0001 | c0001 | t0154 | g0256 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19090 | hp1 | a0001 | c0002 | t0063 | g0303 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19090 | hp2 | a0001 | c0001 | t0044 | g0243 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19091 | hp1 | a0002 | c0006 | t0008 | g0231 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19091 | hp2 | a0001 | c0001 | t0018 | g0057 | EAS | JPT | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19240 | hp1 | a0001 | c0001 | t0046 | g0017 | AFR | YRI | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA19240 | hp2 | a0001 | c0001 | t0069 | g0134 | AFR | YRI | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA20129 | hp1 | a0001 | c0002 | t0021 | g0011 | AFR | ASW | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA20129 | hp2 | a0001 | c0005 | t0128 | g0160 | AFR | ASW | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA20752 | hp1 | a0001 | c0001 | t0182 | g0212 | EUR | TSI | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA20752 | hp2 | a0001 | c0002 | t0034 | g0348 | EUR | TSI | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA20805 | hp1 | a0001 | c0001 | t0143 | g0265 | EUR | TSI | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA20805 | hp2 | a0001 | c0001 | t0194 | g0246 | EUR | TSI | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01123 | hp1 | a0004 | c0011 | t0017 | g0109 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG01123 | hp2 | a0001 | c0001 | t0158 | g0037 | AMR | CLM | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02109 | hp1 | a0001 | c0002 | t0061 | g0311 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02109 | hp2 | a0001 | c0002 | t0011 | g0291 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02486 | hp1 | a0001 | c0001 | t0195 | g0136 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02486 | hp2 | a0001 | c0002 | t0124 | g0041 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02559 | hp1 | a0001 | c0001 | t0178 | g0086 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG02559 | hp2 | a0001 | c0001 | t0009 | g0022 | AFR | ACB | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG06807 | hp1 | a0001 | c0001 | t0172 | g0239 | AFR | USA | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| HG06807 | hp2 | a0001 | c0002 | t0077 | g0010 | AFR | USA | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA20300 | hp1 | a0001 | c0001 | t0039 | g0020 | AFR | USA | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA20300 | hp2 | a0001 | c0002 | t0073 | g0013 | AFR | USA | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA21309 | hp1 | a0001 | c0001 | t0075 | g0130 | AFR | LWK | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| NA21309 | hp2 | a0001 | c0001 | t0144 | g0117 | AFR | LWK | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0080 | g0355 | REF | REF | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| homoSapiens_grch38 | hp1 | a0001 | c0002 | t0094 | g0006 | REF | REF | LIMD1_chr3_45589751_45691341 | LIMD1 | chr3 | 45589751 | 45691341 |
| chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:45595204
|
G | A | 1 | a0007 | 1 | HG02970.hp2 | missense_variant | MODERATE | c.325G>A | p.Ala109Thr | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 454/11442 | 325/2031 | 109/676 | chr3 | 45595204 | ||
| chr3:45595520
|
G | A | 1 | a0003 | 1 | HG03669.hp1 | missense_variant | MODERATE | c.641G>A | p.Ser214Asn | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 770/11442 | 641/2031 | 214/676 | chr3 | 45595520 | ||
| chr3:45595738
|
G | C | 1 | a0004 | 1 | HG01123.hp1 | missense_variant | MODERATE | c.859G>C | p.Val287Leu | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 988/11442 | 859/2031 | 287/676 | chr3 | 45595738 | ||
| chr3:45596122
|
G | A | 1 | a0002 | 2 | NA18977.hp1 NA19091.hp1 |
missense_variant | MODERATE | c.1243G>A | p.Gly415Arg | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 1372/11442 | 1243/2031 | 415/676 | chr3 | 45596122 | ||
| chr3:45596263
|
G | T | 1 | a0006 | 1 | NA18991.hp2 | missense_variant | MODERATE | c.1384G>T | p.Ala462Ser | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 1513/11442 | 1384/2031 | 462/676 | chr3 | 45596263 | ||
| chr3:45673494
|
C | G | 1 | a0005 | 1 | HG03017.hp2 | missense_variant | MODERATE | c.1813C>G | p.Leu605Val | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 6/8 | 1942/11442 | 1813/2031 | 605/676 | chr3 | 45673494 |
| chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:45595617
|
T | C | 1 | a0001c0004 | 4 | HG01109.hp2 HG01168.hp2 HG01433.hp2 others(1): Show |
synonymous_variant | LOW | c.738T>C | p.Gly246Gly | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 867/11442 | 738/2031 | 246/676 | chr3 | 45595617 | ||
| chr3:45595659
|
A | G | 1 | a0001c0014 | 1 | NA18983.hp1 | synonymous_variant | LOW | c.780A>G | p.Thr260Thr | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 909/11442 | 780/2031 | 260/676 | chr3 | 45595659 | ||
| chr3:45595761
|
C | T | 8 | a0001c0001a0001c0007a0001c0008others(5): Show | 259 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(256): Show |
synonymous_variant | LOW | c.882C>T | p.Thr294Thr | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 1011/11442 | 882/2031 | 294/676 | chr3 | 45595761 | ||
| chr3:45595878
|
C | T | 1 | a0001c0005 | 4 | HG02451.hp2 HG03486.hp2 HG03516.hp2 others(1): Show |
synonymous_variant | LOW | c.999C>T | p.Pro333Pro | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 1128/11442 | 999/2031 | 333/676 | chr3 | 45595878 | ||
| chr3:45595947
|
T | C | 10 | a0001c0001a0001c0003a0001c0005others(7): Show | 269 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(266): Show |
synonymous_variant | LOW | c.1068T>C | p.Gly356Gly | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 1197/11442 | 1068/2031 | 356/676 | chr3 | 45595947 | ||
| chr3:45595948
|
C | T | 1 | a0001c0008 | 2 | NA18941.hp2 NA18966.hp1 |
synonymous_variant | LOW | c.1069C>T | p.Leu357Leu | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 1198/11442 | 1069/2031 | 357/676 | chr3 | 45595948 | ||
| chr3:45596139
|
C | T | 1 | a0001c0007 | 2 | HG02886.hp2 HG03139.hp2 |
synonymous_variant | LOW | c.1260C>T | p.Asp420Asp | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 1389/11442 | 1260/2031 | 420/676 | chr3 | 45596139 |
| chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:45594751
|
C | G | 2 | a0001c0007t0204a0001c0007t0205 | 2 | HG02886.hp2 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-129C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 129 | chr3 | 45594751 | |||||
| chr3:45594751
|
C | T | 2 | a0001c0002t0206a0001c0002t0207 | 2 | HG01070.hp2 HG01175.hp1 |
5_prime_UTR_variant | MODIFIER | c.-129C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 129 | chr3 | 45594751 | |||||
| chr3:45594776
|
TCAACACA others(14): Show |
T | 1 | a0001c0001t0203 | 1 | HG01261.hp2 | 5_prime_UTR_variant | MODIFIER | c.-101_-81delACACACA others(14): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 81 | INFO_REALIGN_3_PRIME | chr3 | 45594776 | ||||
| chr3:45594778
|
A | AAC | 7 | a0001c0001t0023a0001c0001t0086a0001c0002t0087others(4): Show | 9 | HG01109.hp2 HG01433.hp2 HG01891.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-37_-36dupAC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 35 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
A | AACAC | 4 | a0001c0001t0082a0001c0001t0083a0001c0001t0084others(1): Show | 4 | HG02647.hp2 HG03041.hp2 HG03098.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-39_-36dupACAC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 35 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
A | AACACAC | 7 | a0001c0001t0076a0001c0001t0078a0001c0001t0081others(4): Show | 8 | HG01168.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-41_-36dupACACAC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 35 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
A | AACACACA others(1): Show |
3 | a0001c0001t0074a0001c0001t0075a0001c0002t0020 | 4 | HG02145.hp1 HG02717.hp2 HG03491.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-43_-36dupACACACAC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 35 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
A | AACACACA others(3): Show |
1 | a0001c0002t0073 | 1 | NA20300.hp2 | 5_prime_UTR_variant | MODIFIER | c.-45_-36dupACACACAC others(2): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 35 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
A | AACACACA others(5): Show |
3 | a0001c0002t0070a0001c0002t0071a0001c0002t0072 | 3 | HG00733.hp1 HG02683.hp1 HG03704.hp1 |
5_prime_UTR_variant | MODIFIER | c.-47_-36dupACACACAC others(4): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 35 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
A | AACACACA others(7): Show |
4 | a0001c0001t0068a0001c0001t0069a0001c0002t0066others(1): Show | 4 | HG00673.hp1 HG02630.hp1 HG02809.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-49_-36dupACACACAC others(6): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 35 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
A | AACACACA others(9): Show |
3 | a0001c0001t0064a0001c0002t0063a0001c0002t0065 | 3 | HG01106.hp1 NA19030.hp2 NA19090.hp1 |
5_prime_UTR_variant | MODIFIER | c.-51_-36dupACACACAC others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 35 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
A | AACACACA others(13): Show |
4 | a0001c0002t0059a0001c0002t0060a0001c0002t0061others(1): Show | 4 | HG01943.hp2 HG01978.hp2 HG02109.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-55_-36dupACACACAC others(12): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 35 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
A | AACACACA others(17): Show |
2 | a0001c0001t0057a0001c0001t0058 | 2 | HG02015.hp2 HG02965.hp2 |
5_prime_UTR_variant | MODIFIER | c.-59_-36dupACACACAC others(16): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 35 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
A | AACACACA others(21): Show |
1 | a0001c0001t0056 | 1 | NA18962.hp2 | 5_prime_UTR_variant | MODIFIER | c.-63_-36dupACACACAC others(20): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 35 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
A | AACACACA others(23): Show |
1 | a0001c0001t0019 | 2 | HG02523.hp1 NA18997.hp2 |
5_prime_UTR_variant | MODIFIER | c.-65_-36dupACACACAC others(22): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 35 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
A | AACACACA others(29): Show |
2 | a0001c0002t0055a0001c0002t0207 | 2 | HG01175.hp1 NA19000.hp1 |
5_prime_UTR_variant | MODIFIER | c.-71_-36dupACACACAC others(28): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 35 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
A | AACACACA others(33): Show |
1 | a0001c0002t0206 | 1 | HG01070.hp2 | 5_prime_UTR_variant | MODIFIER | c.-75_-36dupACACACAC others(32): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 35 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
A | AACACACA others(35): Show |
2 | a0001c0002t0054a0001c0007t0205 | 2 | HG01081.hp1 HG03139.hp2 |
5_prime_UTR_variant | MODIFIER | c.-77_-36dupACACACAC others(34): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 35 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
A | AACACACA others(39): Show |
2 | a0001c0001t0053a0001c0007t0204 | 2 | HG01891.hp1 HG02886.hp2 |
5_prime_UTR_variant | MODIFIER | c.-81_-36dupACACACAC others(38): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 35 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
A | AACACACA others(45): Show |
2 | a0001c0002t0051a0001c0002t0052 | 2 | HG00738.hp1 HG03927.hp1 |
5_prime_UTR_variant | MODIFIER | c.-87_-36dupACACACAC others(44): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 35 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
AAC | A | 8 | a0001c0002t0098a0001c0002t0099a0001c0002t0100others(5): Show | 8 | HG00140.hp1 HG01167.hp1 HG01361.hp1 others(5): Show |
5_prime_UTR_variant | MODIFIER | c.-37_-36delAC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 36 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
AACAC | A | 7 | a0001c0001t0106a0001c0001t0109a0001c0002t0025others(4): Show | 9 | HG01074.hp2 HG01175.hp2 HG02257.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-39_-36delACAC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 36 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
AACACAC | A | 4 | a0001c0001t0111a0001c0002t0027a0001c0002t0112others(1): Show | 5 | HG01069.hp2 HG01257.hp2 HG01516.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-41_-36delACACAC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 36 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
AACACACA others(1): Show |
A | 5 | a0001c0001t0116a0001c0002t0028a0001c0002t0029others(2): Show | 7 | HG01167.hp2 HG01169.hp1 HG01243.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-43_-36delACACACAC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 36 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
AACACACA others(3): Show |
A | 4 | a0001c0001t0032a0001c0002t0030a0001c0002t0031others(1): Show | 7 | HG00735.hp1 HG01168.hp1 HG01169.hp2 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-45_-36delACACACAC others(2): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 36 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
AACACACA others(5): Show |
A | 4 | a0001c0002t0033a0001c0002t0119a0001c0002t0120others(1): Show | 5 | HG01243.hp2 HG01261.hp1 HG02165.hp1 others(2): Show |
5_prime_UTR_variant | MODIFIER | c.-47_-36delACACACAC others(4): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 36 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
AACACACA others(7): Show |
A | 6 | a0001c0002t0011a0001c0002t0034a0001c0002t0124others(3): Show | 10 | HG00099.hp1 HG01192.hp2 HG02109.hp2 others(7): Show |
5_prime_UTR_variant | MODIFIER | c.-49_-36delACACACAC others(6): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 36 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
AACACACA others(9): Show |
A | 7 | a0001c0001t0135a0001c0002t0035a0001c0002t0036others(4): Show | 9 | HG01346.hp2 HG02145.hp2 HG02300.hp2 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-51_-36delACACACAC others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 36 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
AACACACA others(11): Show |
A | 4 | a0001c0001t0008a0001c0002t0136a0001c0003t0137others(1): Show | 7 | HG00639.hp1 HG00639.hp2 HG01070.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-53_-36delACACACAC others(10): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 36 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
AACACACA others(13): Show |
A | 9 | a0001c0001t0012a0001c0001t0037a0001c0001t0144others(6): Show | 13 | HG00738.hp2 HG01993.hp2 HG02083.hp1 others(10): Show |
5_prime_UTR_variant | MODIFIER | c.-55_-36delACACACAC others(12): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 36 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
AACACACA others(15): Show |
A | 13 | a0001c0001t0005a0001c0001t0006a0001c0001t0014others(10): Show | 29 | HG00621.hp1 HG00735.hp2 HG01123.hp2 others(26): Show |
5_prime_UTR_variant | MODIFIER | c.-57_-36delACACACAC others(14): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 36 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
AACACACA others(17): Show |
A | 33 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(30): Show | 110 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(107): Show |
5_prime_UTR_variant | MODIFIER | c.-59_-36delACACACAC others(16): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 36 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
AACACACA others(19): Show |
A | 6 | a0001c0001t0016a0001c0001t0047a0001c0001t0194others(3): Show | 9 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-61_-36delACACACAC others(18): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 36 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
AACACACA others(21): Show |
A | 4 | a0001c0001t0017a0001c0001t0048a0001c0001t0198others(1): Show | 6 | HG01081.hp2 HG01123.hp1 HG02004.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-63_-36delACACACAC others(20): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 36 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
AACACACA others(35): Show |
A | 1 | a0001c0001t0049 | 2 | HG01516.hp2 HG01517.hp2 |
5_prime_UTR_variant | MODIFIER | c.-77_-36delACACACAC others(34): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 36 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
AACACACA others(37): Show |
A | 2 | a0001c0001t0050a0001c0001t0199 | 3 | HG01993.hp1 NA18944.hp1 NA18981.hp2 |
5_prime_UTR_variant | MODIFIER | c.-79_-36delACACACAC others(36): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 36 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594778
|
AACACACA others(39): Show |
A | 6 | a0001c0001t0007a0001c0001t0010a0001c0001t0018others(3): Show | 18 | HG01952.hp1 HG01975.hp2 HG02056.hp1 others(15): Show |
5_prime_UTR_variant | MODIFIER | c.-81_-36delACACACAC others(38): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 36 | INFO_REALIGN_3_PRIME | chr3 | 45594778 | ||||
| chr3:45594788
|
C | CACACACA others(68): Show |
1 | a0001c0005t0138 | 1 | HG03486.hp2 | 5_prime_UTR_variant | MODIFIER | c.-54_-53insGGCACCTG others(67): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 53 | INFO_REALIGN_3_PRIME | chr3 | 45594788 | ||||
| chr3:45594789
|
A | ACACACAC others(30): Show |
1 | a0001c0001t0134 | 1 | NA18945.hp1 | 5_prime_UTR_variant | MODIFIER | c.-90_-54dupCACACACA others(29): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 53 | INFO_REALIGN_3_PRIME | chr3 | 45594789 | ||||
| chr3:45594790
|
C | CACACACA others(70): Show |
1 | a0001c0005t0128 | 1 | NA20129.hp2 | 5_prime_UTR_variant | MODIFIER | c.-50_-49insGGCACCTG others(69): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 49 | INFO_REALIGN_3_PRIME | chr3 | 45594790 | ||||
| chr3:45594790
|
C | CACACACA others(66): Show |
1 | a0001c0005t0139 | 1 | HG02451.hp2 | 5_prime_UTR_variant | MODIFIER | c.-54_-53insGGCACCTG others(65): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 53 | INFO_REALIGN_3_PRIME | chr3 | 45594790 | ||||
| chr3:45594791
|
A | ACACACAC others(20): Show |
2 | a0001c0001t0164a0001c0001t0165 | 2 | NA18960.hp1 NA19065.hp1 |
5_prime_UTR_variant | MODIFIER | c.-88_-62dupCACACACA others(19): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 61 | INFO_REALIGN_3_PRIME | chr3 | 45594791 | ||||
| chr3:45594791
|
A | ACACACAC others(22): Show |
1 | a0001c0001t0149 | 1 | HG02155.hp1 | 5_prime_UTR_variant | MODIFIER | c.-88_-60dupCACACACA others(21): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 59 | INFO_REALIGN_3_PRIME | chr3 | 45594791 | ||||
| chr3:45594793
|
A | ACACACAC others(16): Show |
1 | a0001c0001t0191 | 1 | HG02135.hp2 | 5_prime_UTR_variant | MODIFIER | c.-86_-64dupCACACACA others(15): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 63 | INFO_REALIGN_3_PRIME | chr3 | 45594793 | ||||
| chr3:45594793
|
A | ACACACAC others(18): Show |
4 | a0001c0001t0040a0001c0001t0166a0001c0001t0167others(1): Show | 4 | HG00597.hp1 HG00609.hp2 HG03017.hp2 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-86_-62dupCACACACA others(17): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 61 | INFO_REALIGN_3_PRIME | chr3 | 45594793 | ||||
| chr3:45594793
|
A | ACACACAC others(20): Show |
1 | a0001c0001t0150 | 1 | HG02074.hp2 | 5_prime_UTR_variant | MODIFIER | c.-86_-60dupCACACACA others(19): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 59 | INFO_REALIGN_3_PRIME | chr3 | 45594793 | ||||
| chr3:45594794
|
C | CACACACA others(68): Show |
1 | a0001c0005t0122 | 1 | HG03516.hp2 | 5_prime_UTR_variant | MODIFIER | c.-48_-47insGGCACCTG others(67): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 47 | INFO_REALIGN_3_PRIME | chr3 | 45594794 | ||||
| chr3:45594795
|
A | ACACACAC others(14): Show |
1 | a0001c0001t0192 | 1 | HG00438.hp2 | 5_prime_UTR_variant | MODIFIER | c.-84_-64dupCACACACA others(13): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 63 | INFO_REALIGN_3_PRIME | chr3 | 45594795 | ||||
| chr3:45594795
|
A | ACACACAC others(16): Show |
3 | a0001c0001t0015a0001c0001t0041a0001c0001t0168 | 6 | NA18940.hp1 NA18959.hp2 NA18995.hp2 others(3): Show |
5_prime_UTR_variant | MODIFIER | c.-84_-62dupCACACACA others(15): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 61 | INFO_REALIGN_3_PRIME | chr3 | 45594795 | ||||
| chr3:45594795
|
A | ACACACAC others(18): Show |
2 | a0001c0001t0038a0001c0001t0151 | 3 | HG00423.hp1 HG02132.hp1 NA19054.hp1 |
5_prime_UTR_variant | MODIFIER | c.-84_-60dupCACACACA others(17): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 59 | INFO_REALIGN_3_PRIME | chr3 | 45594795 | ||||
| chr3:45594795
|
A | ACACACAC others(28): Show |
1 | a0001c0001t0123 | 1 | HG02886.hp1 | 5_prime_UTR_variant | MODIFIER | c.-84_-50dupCACACACA others(27): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 49 | INFO_REALIGN_3_PRIME | chr3 | 45594795 | ||||
| chr3:45594797
|
A | ACACACAC others(12): Show |
1 | a0001c0001t0193 | 1 | NA18994.hp1 | 5_prime_UTR_variant | MODIFIER | c.-82_-64dupCACACACA others(11): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 63 | INFO_REALIGN_3_PRIME | chr3 | 45594797 | ||||
| chr3:45594797
|
A | ACACACAC others(14): Show |
2 | a0001c0001t0042a0001c0001t0169 | 3 | HG00558.hp1 HG02129.hp1 NA19007.hp2 |
5_prime_UTR_variant | MODIFIER | c.-82_-62dupCACACACA others(13): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 61 | INFO_REALIGN_3_PRIME | chr3 | 45594797 | ||||
| chr3:45594799
|
A | ACACACAC others(12): Show |
1 | a0001c0001t0170 | 1 | HG03831.hp2 | 5_prime_UTR_variant | MODIFIER | c.-80_-62dupCACACACA others(11): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 61 | INFO_REALIGN_3_PRIME | chr3 | 45594799 | ||||
| chr3:45594799
|
A | ACACACAC others(14): Show |
1 | a0001c0001t0152 | 1 | NA18952.hp2 | 5_prime_UTR_variant | MODIFIER | c.-80_-60dupCACACACA others(13): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 59 | INFO_REALIGN_3_PRIME | chr3 | 45594799 | ||||
| chr3:45594801
|
A | ACACACAC others(12): Show |
2 | a0001c0001t0153a0001c0001t0154 | 2 | HG02735.hp2 NA19087.hp2 |
5_prime_UTR_variant | MODIFIER | c.-78_-60dupCACACACA others(11): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 59 | INFO_REALIGN_3_PRIME | chr3 | 45594801 | ||||
| chr3:45594801
|
A | ACACACAC others(16): Show |
1 | a0001c0001t0140 | 1 | HG03130.hp1 | 5_prime_UTR_variant | MODIFIER | c.-78_-56dupCACACACA others(15): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 55 | INFO_REALIGN_3_PRIME | chr3 | 45594801 | ||||
| chr3:45594801
|
A | ACACACAC others(20): Show |
1 | a0001c0001t0129 | 1 | HG03195.hp2 | 5_prime_UTR_variant | MODIFIER | c.-78_-52dupCACACACA others(19): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 51 | INFO_REALIGN_3_PRIME | chr3 | 45594801 | ||||
| chr3:45594803
|
A | ACACACAC others(12): Show |
1 | a0001c0001t0143 | 1 | NA20805.hp1 | 5_prime_UTR_variant | MODIFIER | c.-76_-58dupCACACACA others(11): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 57 | INFO_REALIGN_3_PRIME | chr3 | 45594803 | ||||
| chr3:45594821
|
A | ACACACAC others(4): Show |
1 | a0001c0004t0118 | 1 | HG02615.hp1 | 5_prime_UTR_variant | MODIFIER | c.-58_-48dupCACACACA others(3): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 47 | INFO_REALIGN_3_PRIME | chr3 | 45594821 | ||||
| chr3:45594843
|
A | G | 69 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(66): Show | 175 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(172): Show |
5_prime_UTR_variant | MODIFIER | c.-37A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 37 | chr3 | 45594843 | |||||
| chr3:45594845
|
G | A | 1 | a0001c0001t0091 | 1 | HG01109.hp1 | 5_prime_UTR_variant | MODIFIER | c.-35G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/8 | 35 | chr3 | 45594845 | |||||
| chr3:45677110
|
G | A | 11 | a0001c0001t0049a0001c0001t0076a0001c0001t0086others(8): Show | 13 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*51G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 51 | chr3 | 45677110 | |||||
| chr3:45677191
|
G | T | 1 | a0001c0001t0190 | 1 | HG03927.hp2 | 3_prime_UTR_variant | MODIFIER | c.*132G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 132 | chr3 | 45677191 | |||||
| chr3:45677240
|
C | T | 1 | a0001c0001t0069 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*181C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 181 | chr3 | 45677240 | |||||
| chr3:45677274
|
A | ATTT | 6 | a0001c0001t0023a0001c0001t0081a0001c0001t0085others(3): Show | 7 | HG01891.hp2 HG02280.hp1 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*217_*219dupTTT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 220 | INFO_REALIGN_3_PRIME | chr3 | 45677274 | ||||
| chr3:45677573
|
A | G | 31 | a0001c0001t0009a0001c0001t0023a0001c0001t0032others(28): Show | 40 | HG01074.hp2 HG01109.hp1 HG01243.hp1 others(37): Show |
3_prime_UTR_variant | MODIFIER | c.*514A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 514 | chr3 | 45677573 | |||||
| chr3:45677694
|
C | T | 2 | a0001c0001t0084a0001c0001t0096 | 2 | HG02451.hp1 HG03098.hp2 |
3_prime_UTR_variant | MODIFIER | c.*635C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 635 | chr3 | 45677694 | |||||
| chr3:45677717
|
T | C | 41 | a0001c0001t0014a0001c0001t0043a0001c0001t0064others(38): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(49): Show |
3_prime_UTR_variant | MODIFIER | c.*658T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 658 | chr3 | 45677717 | |||||
| chr3:45677762
|
G | A | 1 | a0001c0001t0172 | 1 | HG06807.hp1 | 3_prime_UTR_variant | MODIFIER | c.*703G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 703 | chr3 | 45677762 | |||||
| chr3:45677781
|
T | A | 11 | a0001c0001t0049a0001c0001t0076a0001c0001t0086others(8): Show | 13 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*722T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 722 | chr3 | 45677781 | |||||
| chr3:45677896
|
C | T | 1 | a0001c0001t0143 | 1 | NA20805.hp1 | 3_prime_UTR_variant | MODIFIER | c.*837C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 837 | chr3 | 45677896 | |||||
| chr3:45677985
|
C | G | 1 | a0001c0001t0091 | 1 | HG01109.hp1 | 3_prime_UTR_variant | MODIFIER | c.*926C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 926 | chr3 | 45677985 | |||||
| chr3:45678023
|
A | G | 1 | a0001c0001t0188 | 1 | NA18954.hp1 | 3_prime_UTR_variant | MODIFIER | c.*964A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 964 | chr3 | 45678023 | |||||
| chr3:45678069
|
G | A | 37 | a0001c0001t0010a0001c0001t0019a0001c0001t0038others(34): Show | 47 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*1010G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 1010 | chr3 | 45678069 | |||||
| chr3:45678153
|
G | T | 11 | a0001c0001t0049a0001c0001t0076a0001c0001t0086others(8): Show | 13 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1094G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 1094 | chr3 | 45678153 | |||||
| chr3:45678333
|
GCCCAACT others(6): Show |
G | 44 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(41): Show | 113 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
3_prime_UTR_variant | MODIFIER | c.*1275_*1287delCCCA others(9): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 1275 | chr3 | 45678333 | |||||
| chr3:45678914
|
C | G | 1 | a0001c0001t0187 | 1 | HG01346.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1855C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 1855 | chr3 | 45678914 | |||||
| chr3:45678950
|
C | T | 11 | a0001c0001t0049a0001c0001t0076a0001c0001t0086others(8): Show | 13 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1891C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 1891 | chr3 | 45678950 | |||||
| chr3:45678951
|
G | A | 1 | a0001c0002t0102 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1892G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 1892 | chr3 | 45678951 | |||||
| chr3:45679024
|
G | A | 1 | a0001c0001t0151 | 1 | NA19054.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1965G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 1965 | chr3 | 45679024 | |||||
| chr3:45679217
|
G | A | 2 | a0001c0001t0046a0001c0002t0132 | 3 | HG02647.hp1 HG03486.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2158G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 2158 | chr3 | 45679217 | |||||
| chr3:45679307
|
C | A | 11 | a0001c0002t0011a0001c0002t0021a0001c0002t0029others(8): Show | 16 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*2248C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 2248 | chr3 | 45679307 | |||||
| chr3:45679490
|
G | A | 7 | a0001c0001t0015a0001c0001t0018a0001c0001t0166others(4): Show | 11 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2431G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 2431 | chr3 | 45679490 | |||||
| chr3:45679523
|
A | G | 1 | a0001c0001t0045 | 2 | HG00733.hp2 HG01106.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2464A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 2464 | chr3 | 45679523 | |||||
| chr3:45679553
|
A | C | 1 | a0001c0002t0035 | 2 | HG02895.hp1 HG02897.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2494A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 2494 | chr3 | 45679553 | |||||
| chr3:45679619
|
G | A | 3 | a0001c0001t0143a0001c0001t0153a0001c0001t0170 | 3 | HG02735.hp2 HG03831.hp2 NA20805.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2560G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 2560 | chr3 | 45679619 | |||||
| chr3:45679693
|
G | A | 7 | a0001c0001t0076a0001c0001t0086a0001c0001t0106others(4): Show | 8 | HG02055.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2634G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 2634 | chr3 | 45679693 | |||||
| chr3:45679810
|
G | A | 1 | a0001c0001t0069 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2751G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 2751 | chr3 | 45679810 | |||||
| chr3:45679903
|
G | A | 1 | a0001c0001t0180 | 1 | HG02273.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2844G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 2844 | chr3 | 45679903 | |||||
| chr3:45680005
|
G | A | 2 | a0001c0007t0204a0001c0007t0205 | 2 | HG02886.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2946G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 2946 | chr3 | 45680005 | |||||
| chr3:45680166
|
C | T | 1 | a0001c0001t0186 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3107C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 3107 | chr3 | 45680166 | |||||
| chr3:45680187
|
G | A | 11 | a0001c0001t0049a0001c0001t0076a0001c0001t0086others(8): Show | 13 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3128G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 3128 | chr3 | 45680187 | |||||
| chr3:45680324
|
T | C | 17 | a0001c0001t0015a0001c0001t0018a0001c0001t0049others(14): Show | 23 | HG00438.hp2 HG00597.hp1 HG01433.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3265T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 3265 | chr3 | 45680324 | |||||
| chr3:45680506
|
G | A | 1 | a0001c0002t0059 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3447G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 3447 | chr3 | 45680506 | |||||
| chr3:45680568
|
C | T | 11 | a0001c0001t0049a0001c0001t0076a0001c0001t0086others(8): Show | 13 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3509C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 3509 | chr3 | 45680568 | |||||
| chr3:45680609
|
C | A | 1 | a0001c0001t0176 | 1 | HG01255.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3550C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 3550 | chr3 | 45680609 | |||||
| chr3:45680618
|
A | AT | 37 | a0001c0001t0010a0001c0001t0019a0001c0001t0038others(34): Show | 47 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(44): Show |
3_prime_UTR_variant | MODIFIER | c.*3568dupT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 3569 | INFO_REALIGN_3_PRIME | chr3 | 45680618 | ||||
| chr3:45680694
|
T | C | 11 | a0001c0001t0049a0001c0001t0076a0001c0001t0086others(8): Show | 13 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*3635T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 3635 | chr3 | 45680694 | |||||
| chr3:45680711
|
AGTGGCTC others(21): Show |
A | 1 | a0001c0001t0069 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3661_*3688delTGCC others(24): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 3661 | INFO_REALIGN_3_PRIME | chr3 | 45680711 | ||||
| chr3:45680781
|
C | T | 2 | a0001c0001t0049a0001c0001t0156 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3722C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 3722 | chr3 | 45680781 | |||||
| chr3:45680805
|
G | A | 1 | a0001c0001t0069 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3746G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 3746 | chr3 | 45680805 | |||||
| chr3:45680878
|
C | T | 1 | a0003c0010t0105 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3819C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 3819 | chr3 | 45680878 | |||||
| chr3:45680934
|
T | G | 1 | a0001c0002t0098 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3875T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 3875 | chr3 | 45680934 | |||||
| chr3:45681009
|
C | CAAA | 7 | a0001c0001t0076a0001c0001t0086a0001c0001t0106others(4): Show | 8 | HG02055.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*3964_*3966dupAAA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 3967 | INFO_REALIGN_3_PRIME | chr3 | 45681009 | ||||
| chr3:45681009
|
CA | C | 13 | a0001c0001t0185a0001c0002t0011a0001c0002t0021others(10): Show | 18 | HG01069.hp2 HG01167.hp2 HG01169.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*3966delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 3966 | INFO_REALIGN_3_PRIME | chr3 | 45681009 | ||||
| chr3:45681127
|
C | T | 1 | a0001c0001t0069 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4068C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 4068 | chr3 | 45681127 | |||||
| chr3:45681162
|
C | G | 7 | a0001c0001t0015a0001c0001t0018a0001c0001t0166others(4): Show | 11 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4103C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 4103 | chr3 | 45681162 | |||||
| chr3:45681473
|
A | G | 1 | a0001c0001t0147 | 1 | HG02083.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4414A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 4414 | chr3 | 45681473 | |||||
| chr3:45681599
|
C | G | 10 | a0001c0001t0049a0001c0001t0076a0001c0001t0086others(7): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*4540C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 4540 | chr3 | 45681599 | |||||
| chr3:45681672
|
G | C | 1 | a0001c0001t0181 | 1 | HG03491.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4613G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 4613 | chr3 | 45681672 | |||||
| chr3:45681786
|
G | A | 1 | a0001c0002t0028 | 2 | NA18983.hp2 NA19005.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4727G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 4727 | chr3 | 45681786 | |||||
| chr3:45681786
|
G | C | 2 | a0001c0007t0204a0001c0007t0205 | 2 | HG02886.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4727G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 4727 | chr3 | 45681786 | |||||
| chr3:45681942
|
T | C | 23 | a0001c0001t0157a0001c0001t0171a0001c0001t0199others(20): Show | 29 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*4883T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 4883 | chr3 | 45681942 | |||||
| chr3:45681974
|
C | T | 2 | a0001c0001t0184a0003c0010t0105 | 2 | HG03669.hp1 HG03942.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4915C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 4915 | chr3 | 45681974 | |||||
| chr3:45682283
|
G | A | 4 | a0001c0001t0082a0001c0001t0140a0001c0003t0137others(1): Show | 4 | HG02615.hp2 HG02647.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5224G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 5224 | chr3 | 45682283 | |||||
| chr3:45682395
|
T | C | 1 | a0001c0001t0069 | 1 | NA19240.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5336T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 5336 | chr3 | 45682395 | |||||
| chr3:45682398
|
C | G | 97 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(94): Show | 188 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(185): Show |
3_prime_UTR_variant | MODIFIER | c.*5339C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 5339 | chr3 | 45682398 | |||||
| chr3:45682789
|
A | G | 2 | a0001c0002t0110a0007c0009t0095 | 2 | HG02970.hp2 HG03540.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5730A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 5730 | chr3 | 45682789 | |||||
| chr3:45682792
|
C | T | 7 | a0001c0001t0015a0001c0001t0018a0001c0001t0166others(4): Show | 11 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*5733C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 5733 | chr3 | 45682792 | |||||
| chr3:45682924
|
G | A | 1 | a0001c0002t0051 | 1 | HG03927.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5865G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 5865 | chr3 | 45682924 | |||||
| chr3:45683055
|
T | C | 45 | a0001c0001t0013a0001c0001t0014a0001c0001t0043others(42): Show | 60 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(57): Show |
3_prime_UTR_variant | MODIFIER | c.*5996T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 5996 | chr3 | 45683055 | |||||
| chr3:45683081
|
G | A | 6 | a0001c0001t0023a0001c0001t0081a0001c0001t0085others(3): Show | 7 | HG01891.hp2 HG02280.hp1 HG02886.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6022G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 6022 | chr3 | 45683081 | |||||
| chr3:45683118
|
C | T | 171 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(168): Show | 284 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(281): Show |
3_prime_UTR_variant | MODIFIER | c.*6059C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 6059 | chr3 | 45683118 | |||||
| chr3:45683342
|
A | G | 1 | a0001c0001t0163 | 1 | NA18963.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6283A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 6283 | chr3 | 45683342 | |||||
| chr3:45683404
|
A | G | 9 | a0001c0001t0004a0001c0001t0135a0001c0001t0154others(6): Show | 18 | HG00558.hp2 HG00621.hp2 HG02080.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*6345A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 6345 | chr3 | 45683404 | |||||
| chr3:45683415
|
T | A | 1 | a0001c0001t0177 | 1 | NA19084.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6356T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 6356 | chr3 | 45683415 | |||||
| chr3:45683539
|
G | T | 191 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(188): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*6480G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 6480 | chr3 | 45683539 | |||||
| chr3:45683585
|
T | A | 2 | a0001c0001t0046a0001c0002t0132 | 3 | HG02647.hp1 HG03486.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6526T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 6526 | chr3 | 45683585 | |||||
| chr3:45683749
|
G | C | 1 | a0001c0001t0178 | 1 | HG02559.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6690G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 6690 | chr3 | 45683749 | |||||
| chr3:45683777
|
T | C | 1 | a0001c0002t0125 | 1 | HG01192.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6718T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 6718 | chr3 | 45683777 | |||||
| chr3:45683779
|
G | A | 2 | a0001c0001t0175a0001c0002t0055 | 2 | NA19000.hp1 NA19009.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6720G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 6720 | chr3 | 45683779 | |||||
| chr3:45683800
|
G | C | 2 | a0001c0001t0049a0001c0001t0156 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6741G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 6741 | chr3 | 45683800 | |||||
| chr3:45683803
|
G | A | 4 | a0001c0001t0082a0001c0001t0140a0001c0003t0137others(1): Show | 4 | HG02615.hp2 HG02647.hp2 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*6744G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 6744 | chr3 | 45683803 | |||||
| chr3:45683884
|
A | G | 7 | a0001c0001t0015a0001c0001t0018a0001c0001t0166others(4): Show | 11 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*6825A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 6825 | chr3 | 45683884 | |||||
| chr3:45683888
|
G | A | 1 | a0001c0001t0161 | 1 | HG04184.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6829G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 6829 | chr3 | 45683888 | |||||
| chr3:45684080
|
CAG | C | 39 | a0001c0001t0003a0001c0001t0006a0001c0001t0017others(36): Show | 61 | HG00621.hp1 HG01074.hp2 HG01081.hp2 others(58): Show |
3_prime_UTR_variant | MODIFIER | c.*7024_*7025delAG | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 7024 | INFO_REALIGN_3_PRIME | chr3 | 45684080 | ||||
| chr3:45684281
|
T | C | 212 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(209): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
3_prime_UTR_variant | MODIFIER | c.*7222T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 7222 | chr3 | 45684281 | |||||
| chr3:45684291
|
C | G | 190 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(187): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
3_prime_UTR_variant | MODIFIER | c.*7232C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 7232 | chr3 | 45684291 | |||||
| chr3:45684334
|
G | A | 9 | a0001c0001t0013a0001c0001t0193a0001c0002t0028others(6): Show | 13 | HG01081.hp1 HG01943.hp2 HG01978.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*7275G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 7275 | chr3 | 45684334 | |||||
| chr3:45684406
|
A | G | 1 | a0001c0001t0186 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7347A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 7347 | chr3 | 45684406 | |||||
| chr3:45684584
|
G | A | 7 | a0001c0001t0015a0001c0001t0018a0001c0001t0166others(4): Show | 11 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7525G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 7525 | chr3 | 45684584 | |||||
| chr3:45684587
|
G | A | 1 | a0001c0001t0158 | 1 | HG01123.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7528G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 7528 | chr3 | 45684587 | |||||
| chr3:45684603
|
T | C | 14 | a0001c0001t0009a0001c0001t0039a0001c0001t0189others(11): Show | 24 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*7544T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 7544 | chr3 | 45684603 | |||||
| chr3:45684789
|
G | GGGAGGCG others(3): Show |
1 | a0001c0001t0159 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7731_*7740dupGGAG others(6): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 7741 | INFO_REALIGN_3_PRIME | chr3 | 45684789 | ||||
| chr3:45684795
|
C | T | 1 | a0001c0003t0121 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7736C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 7736 | chr3 | 45684795 | |||||
| chr3:45684834
|
A | C | 1 | a0001c0003t0137 | 1 | HG03579.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7775A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 7775 | chr3 | 45684834 | |||||
| chr3:45685056
|
GATT | G | 14 | a0001c0001t0009a0001c0001t0039a0001c0001t0189others(11): Show | 24 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*8001_*8003delATT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 8001 | INFO_REALIGN_3_PRIME | chr3 | 45685056 | ||||
| chr3:45685106
|
T | C | 14 | a0001c0001t0009a0001c0001t0039a0001c0001t0189others(11): Show | 24 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*8047T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 8047 | chr3 | 45685106 | |||||
| chr3:45685209
|
C | G | 1 | a0001c0001t0186 | 1 | HG00597.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8150C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 8150 | chr3 | 45685209 | |||||
| chr3:45685425
|
G | A | 1 | a0001c0003t0121 | 1 | HG01243.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8366G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 8366 | chr3 | 45685425 | |||||
| chr3:45685460
|
A | G | 1 | a0001c0001t0189 | 1 | HG02809.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8401A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 8401 | chr3 | 45685460 | |||||
| chr3:45685608
|
G | A | 191 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(188): Show | 323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
3_prime_UTR_variant | MODIFIER | c.*8549G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 8549 | chr3 | 45685608 | |||||
| chr3:45685903
|
A | G | 2 | a0001c0001t0049a0001c0001t0156 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
3_prime_UTR_variant | MODIFIER | c.*8844A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 8844 | chr3 | 45685903 | |||||
| chr3:45686112
|
A | T | 1 | a0001c0001t0159 | 1 | HG01975.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9053A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 9053 | chr3 | 45686112 | |||||
| chr3:45686159
|
C | T | 2 | a0001c0001t0058a0001c0001t0116 | 2 | HG01243.hp1 HG02965.hp2 |
3_prime_UTR_variant | MODIFIER | c.*9100C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 9100 | chr3 | 45686159 | |||||
| chr3:45686220
|
C | T | 4 | a0001c0002t0110a0001c0003t0121a0001c0003t0142others(1): Show | 4 | HG01243.hp2 HG02970.hp2 HG03209.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*9161C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 9161 | chr3 | 45686220 | |||||
| chr3:45686269
|
A | G | 202 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(199): Show | 336 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
3_prime_UTR_variant | MODIFIER | c.*9210A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 9210 | chr3 | 45686269 | |||||
| chr3:45686270
|
G | T | 1 | a0001c0001t0183 | 1 | HG00438.hp1 | 3_prime_UTR_variant | MODIFIER | c.*9211G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 8/8 | 9211 | chr3 | 45686270 |
| chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr3:45596338
|
A | G | 64 | a0001c0002t0020g0309a0001c0002t0020g0340a0001c0002t0024g0294others(61): Show | 64 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(61): Show |
intron_variant | MODIFIER | c.1408+51A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45596338 | ||||||
| chr3:45596660
|
C | G | 3 | a0001c0002t0011g0291a0001c0002t0011g0292a0001c0002t0011g0293 | 3 | HG02109.hp2 HG02280.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.1408+373C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45596660 | ||||||
| chr3:45596666
|
C | T | 35 | a0001c0001t0015g0260a0001c0001t0015g0261a0001c0001t0015g0262others(32): Show | 35 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(32): Show |
intron_variant | MODIFIER | c.1408+379C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45596666 | ||||||
| chr3:45596714
|
G | T | 1 | a0001c0001t0001g0255 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1408+427G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45596714 | ||||||
| chr3:45596763
|
C | T | 95 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0171others(92): Show | 95 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(92): Show |
intron_variant | MODIFIER | c.1408+476C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45596763 | ||||||
| chr3:45596863
|
C | CT | 123 | a0001c0001t0001g0171a0001c0001t0001g0173a0001c0001t0001g0176others(120): Show | 123 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(120): Show |
intron_variant | MODIFIER | c.1408+592dupT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45596863 | |||||
| chr3:45596863
|
C | CTTT | 9 | a0001c0003t0121g0152a0001c0003t0133g0158a0001c0003t0137g0154others(6): Show | 9 | HG01243.hp2 HG02451.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.1408+590_1408+592d others(5): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45596863 | |||||
| chr3:45597028
|
A | AT | 230 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(227): Show | 231 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.1408+753dupT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45597028 | |||||
| chr3:45597028
|
A | ATT | 9 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0032g0143others(6): Show | 9 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(6): Show |
intron_variant | MODIFIER | c.1408+752_1408+753d others(4): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45597028 | |||||
| chr3:45597041
|
A | T | 1 | a0001c0001t0203g0254 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1408+754A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45597041 | ||||||
| chr3:45597046
|
G | T | 1 | a0001c0002t0125g0353 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1408+759G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45597046 | ||||||
| chr3:45597051
|
A | G | 1 | a0001c0001t0045g0253 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1408+764A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45597051 | ||||||
| chr3:45597140
|
G | T | 1 | a0001c0001t0001g0252 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.1408+853G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45597140 | ||||||
| chr3:45597179
|
G | T | 1 | a0001c0002t0127g0122 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1408+892G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45597179 | ||||||
| chr3:45597467
|
T | C | 2 | a0001c0007t0204g0002a0001c0007t0205g0002 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1408+1180T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45597467 | ||||||
| chr3:45597503
|
A | C | 4 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0081g0151others(1): Show | 4 | HG01891.hp2 HG02280.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1408+1216A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45597503 | ||||||
| chr3:45597868
|
G | A | 2 | a0001c0007t0204g0002a0001c0007t0205g0002 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1408+1581G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45597868 | ||||||
| chr3:45597960
|
T | A | 104 | a0001c0001t0001g0045a0001c0001t0001g0161a0001c0001t0001g0162others(101): Show | 104 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1408+1673T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45597960 | ||||||
| chr3:45597989
|
A | G | 4 | a0001c0001t0048g0119a0001c0001t0048g0120a0001c0001t0156g0118others(1): Show | 4 | HG01433.hp1 HG02630.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1408+1702A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45597989 | ||||||
| chr3:45598336
|
A | C | 2 | a0001c0002t0035g0043a0001c0002t0035g0044 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1408+2049A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45598336 | ||||||
| chr3:45598466
|
G | A | 1 | a0001c0001t0057g0257 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1408+2179G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45598466 | ||||||
| chr3:45598657
|
GAGAGAAT others(6): Show |
G | 1 | a0001c0003t0121g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1408+2377_1408+238 others(17): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45598657 | |||||
| chr3:45598735
|
A | C | 66 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(63): Show | 67 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1408+2448A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45598735 | ||||||
| chr3:45598889
|
T | C | 1 | a0001c0001t0032g0143 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1408+2602T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45598889 | ||||||
| chr3:45599004
|
G | A | 1 | a0001c0001t0162g0164 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1408+2717G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45599004 | ||||||
| chr3:45599022
|
G | C | 40 | a0001c0001t0015g0260a0001c0001t0015g0261a0001c0001t0015g0262others(37): Show | 40 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(37): Show |
intron_variant | MODIFIER | c.1408+2735G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45599022 | ||||||
| chr3:45599138
|
T | C | 3 | a0001c0002t0027g0299a0001c0002t0072g0301a0001c0002t0101g0300 | 3 | HG01361.hp2 HG01516.hp1 HG03704.hp1 |
intron_variant | MODIFIER | c.1408+2851T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45599138 | ||||||
| chr3:45599147
|
T | G | 1 | a0001c0003t0121g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1408+2860T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45599147 | ||||||
| chr3:45599191
|
A | G | 23 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0032g0143others(20): Show | 23 | HG01074.hp2 HG01243.hp1 HG01243.hp2 others(20): Show |
intron_variant | MODIFIER | c.1408+2904A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45599191 | ||||||
| chr3:45599221
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1408+2934A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45599221 | ||||||
| chr3:45599240
|
G | A | 65 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(62): Show | 66 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1408+2953G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45599240 | ||||||
| chr3:45599334
|
C | CT | 324 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(321): Show | 325 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(322): Show |
intron_variant | MODIFIER | c.1408+3047_1408+304 others(5): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45599334 | ||||||
| chr3:45599421
|
C | T | 2 | a0001c0007t0204g0002a0001c0007t0205g0002 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1408+3134C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45599421 | ||||||
| chr3:45599428
|
T | C | 113 | a0001c0001t0001g0045a0001c0001t0001g0161a0001c0001t0001g0162others(110): Show | 113 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1408+3141T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45599428 | ||||||
| chr3:45599461
|
G | A | 4 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0081g0151others(1): Show | 4 | HG01891.hp2 HG02280.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1408+3174G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45599461 | ||||||
| chr3:45599526
|
A | G | 4 | a0001c0002t0033g0347a0001c0002t0034g0345a0001c0002t0034g0348others(1): Show | 4 | HG00099.hp1 HG01261.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1408+3239A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45599526 | ||||||
| chr3:45599628
|
C | T | 1 | a0001c0001t0196g0165 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1408+3341C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45599628 | ||||||
| chr3:45599738
|
G | A | 5 | a0001c0001t0003g0042a0001c0001t0013g0067a0001c0001t0013g0068others(2): Show | 5 | NA18957.hp1 NA18994.hp2 NA18995.hp1 others(2): Show |
intron_variant | MODIFIER | c.1408+3451G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45599738 | ||||||
| chr3:45599929
|
G | A | 1 | a0001c0001t0091g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1408+3642G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45599929 | ||||||
| chr3:45599942
|
G | A | 2 | a0001c0007t0204g0002a0001c0007t0205g0002 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1408+3655G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45599942 | ||||||
| chr3:45599943
|
CA | C | 63 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(60): Show | 63 | HG00423.hp1 HG00558.hp1 HG00597.hp1 others(60): Show |
intron_variant | MODIFIER | c.1408+3657delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45599943 | ||||||
| chr3:45600044
|
G | C | 2 | a0001c0005t0122g0155a0001c0005t0139g0156 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1408+3757G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45600044 | ||||||
| chr3:45600046
|
T | C | 1 | a0001c0001t0086g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1408+3759T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45600046 | ||||||
| chr3:45600062
|
T | C | 1 | a0001c0001t0005g0166 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1408+3775T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45600062 | ||||||
| chr3:45600207
|
A | C | 5 | a0001c0001t0074g0135a0001c0001t0082g0137a0001c0001t0195g0136others(2): Show | 5 | HG02486.hp1 HG02647.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408+3920A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45600207 | ||||||
| chr3:45600314
|
T | A | 57 | a0001c0001t0010g0050a0001c0001t0014g0035a0001c0001t0014g0038others(54): Show | 57 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1408+4027T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45600314 | ||||||
| chr3:45600334
|
T | C | 1 | a0001c0001t0064g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1408+4047T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45600334 | ||||||
| chr3:45600524
|
T | C | 17 | a0001c0001t0010g0051a0001c0001t0010g0052a0001c0001t0010g0053others(14): Show | 17 | HG00423.hp1 HG00438.hp2 HG00597.hp1 others(14): Show |
intron_variant | MODIFIER | c.1408+4237T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45600524 | ||||||
| chr3:45600526
|
C | T | 1 | a0001c0001t0018g0057 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1408+4239C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45600526 | ||||||
| chr3:45600689
|
C | A | 68 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(65): Show | 68 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(65): Show |
intron_variant | MODIFIER | c.1408+4402C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45600689 | ||||||
| chr3:45600731
|
C | G | 65 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(62): Show | 66 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1408+4444C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45600731 | ||||||
| chr3:45600767
|
A | C | 1 | a0001c0005t0128g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1408+4480A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45600767 | ||||||
| chr3:45600781
|
A | C | 1 | a0001c0002t0113g0344 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.1408+4494A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45600781 | ||||||
| chr3:45600907
|
C | A | 2 | a0001c0001t0074g0135a0001c0001t0195g0136 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1408+4620C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45600907 | ||||||
| chr3:45601233
|
C | G | 1 | a0001c0001t0129g0288 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1408+4946C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45601233 | ||||||
| chr3:45601523
|
C | T | 1 | a0001c0001t0144g0117 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1408+5236C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45601523 | ||||||
| chr3:45601671
|
G | C | 2 | a0001c0001t0074g0135a0001c0001t0195g0136 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1408+5384G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45601671 | ||||||
| chr3:45601708
|
G | A | 1 | a0001c0001t0143g0265 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1408+5421G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45601708 | ||||||
| chr3:45601873
|
G | A | 2 | a0001c0001t0005g0166a0001c0001t0203g0254 | 2 | HG01261.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1408+5586G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45601873 | ||||||
| chr3:45601943
|
C | CT | 16 | a0001c0001t0001g0241a0001c0001t0002g0116a0001c0001t0003g0115others(13): Show | 16 | HG00438.hp2 HG01168.hp2 HG01891.hp1 others(13): Show |
intron_variant | MODIFIER | c.1408+5673dupT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45601943 | |||||
| chr3:45601943
|
CT | C | 6 | a0001c0001t0004g0167a0001c0001t0048g0119a0001c0001t0048g0120others(3): Show | 6 | HG00438.hp1 HG02451.hp2 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1408+5673delT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45601943 | |||||
| chr3:45601950
|
T | A | 58 | a0001c0001t0010g0050a0001c0001t0014g0035a0001c0001t0014g0038others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(55): Show |
intron_variant | MODIFIER | c.1408+5663T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45601950 | ||||||
| chr3:45602031
|
C | T | 5 | a0001c0001t0053g0139a0001c0001t0083g0140a0001c0001t0084g0141others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408+5744C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45602031 | ||||||
| chr3:45602047
|
A | G | 3 | a0001c0001t0001g0238a0001c0001t0005g0237a0001c0001t0175g0245 | 3 | NA18991.hp1 NA18998.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1408+5760A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45602047 | ||||||
| chr3:45602067
|
C | T | 1 | a0001c0001t0197g0114 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1408+5780C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45602067 | ||||||
| chr3:45602088
|
G | A | 1 | a0001c0014t0001g0169 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.1408+5801G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45602088 | ||||||
| chr3:45602156
|
G | C | 57 | a0001c0001t0005g0170a0001c0001t0010g0050a0001c0001t0014g0035others(54): Show | 57 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(54): Show |
intron_variant | MODIFIER | c.1408+5869G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45602156 | ||||||
| chr3:45602191
|
A | G | 27 | a0001c0001t0019g0284a0001c0001t0019g0287a0001c0001t0038g0264others(24): Show | 27 | HG00423.hp1 HG00558.hp1 HG02015.hp2 others(24): Show |
intron_variant | MODIFIER | c.1408+5904A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45602191 | ||||||
| chr3:45602232
|
G | A | 1 | a0001c0001t0038g0264 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1408+5945G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45602232 | ||||||
| chr3:45602557
|
A | AC | 66 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(63): Show | 67 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1408+6276dupC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45602557 | |||||
| chr3:45602654
|
T | C | 4 | a0001c0001t0069g0134a0001c0001t0076g0132a0001c0001t0086g0131others(1): Show | 4 | HG02055.hp1 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1408+6367T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45602654 | ||||||
| chr3:45602691
|
G | A | 63 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(60): Show | 64 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1408+6404G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45602691 | ||||||
| chr3:45602718
|
T | TGTACCA | 118 | a0001c0001t0001g0045a0001c0001t0001g0161a0001c0001t0001g0162others(115): Show | 118 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(115): Show |
intron_variant | MODIFIER | c.1408+6436_1408+643 others(10): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45602718 | |||||
| chr3:45602740
|
A | G | 1 | a0001c0005t0128g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1408+6453A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45602740 | ||||||
| chr3:45602753
|
C | T | 2 | a0001c0007t0204g0002a0001c0007t0205g0002 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1408+6466C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45602753 | ||||||
| chr3:45602799
|
G | A | 14 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(11): Show | 14 | HG02486.hp1 HG02559.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.1408+6512G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45602799 | ||||||
| chr3:45602817
|
T | C | 2 | a0001c0002t0029g0029a0001c0002t0029g0030 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1408+6530T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45602817 | ||||||
| chr3:45602835
|
CT | C | 9 | a0001c0001t0001g0171a0001c0001t0014g0035a0001c0001t0069g0134others(6): Show | 9 | HG01496.hp1 HG02055.hp1 HG02897.hp2 others(6): Show |
intron_variant | MODIFIER | c.1408+6565delT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45602835 | |||||
| chr3:45602925
|
C | T | 3 | a0001c0001t0008g0236a0001c0001t0009g0025a0001c0001t0189g0024 | 3 | HG01517.hp1 HG02809.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.1408+6638C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45602925 | ||||||
| chr3:45602933
|
C | T | 12 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(9): Show | 12 | HG02559.hp2 HG02809.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1408+6646C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45602933 | ||||||
| chr3:45603038
|
G | A | 1 | a0001c0001t0006g0073 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1408+6751G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45603038 | ||||||
| chr3:45603088
|
G | A | 66 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(63): Show | 67 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1408+6801G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45603088 | ||||||
| chr3:45603088
|
G | T | 10 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0032g0143others(7): Show | 10 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1408+6801G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45603088 | ||||||
| chr3:45603175
|
T | C | 1 | a0001c0001t0106g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1408+6888T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45603175 | ||||||
| chr3:45603250
|
G | A | 2 | a0001c0007t0204g0002a0001c0007t0205g0002 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1408+6963G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45603250 | ||||||
| chr3:45603357
|
C | G | 12 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(9): Show | 12 | HG02559.hp2 HG02809.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1408+7070C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45603357 | ||||||
| chr3:45603434
|
T | TCA | 25 | a0001c0001t0007g0058a0001c0001t0007g0059a0001c0001t0007g0061others(22): Show | 25 | HG00438.hp2 HG00597.hp1 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.1408+7147_1408+714 others(6): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45603434 | ||||||
| chr3:45603443
|
G | A | 2 | a0001c0002t0035g0043a0001c0002t0035g0044 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1408+7156G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45603443 | ||||||
| chr3:45603446
|
A | C | 5 | a0001c0001t0053g0139a0001c0001t0083g0140a0001c0001t0084g0141others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408+7159A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45603446 | ||||||
| chr3:45603587
|
A | C | 1 | a0001c0001t0097g0268 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1408+7300A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45603587 | ||||||
| chr3:45603590
|
C | T | 102 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(99): Show | 103 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1408+7303C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45603590 | ||||||
| chr3:45603650
|
G | A | 1 | a0001c0001t0001g0255 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.1408+7363G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45603650 | ||||||
| chr3:45603926
|
A | G | 3 | a0001c0002t0026g0003a0001c0002t0026g0298a0001c0002t0115g0003 | 3 | NA18944.hp2 NA18946.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1408+7639A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45603926 | ||||||
| chr3:45603994
|
CA | C | 102 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(99): Show | 103 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1408+7709delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45603994 | |||||
| chr3:45604205
|
C | T | 2 | a0001c0001t0048g0119a0001c0001t0048g0120 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1408+7918C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45604205 | ||||||
| chr3:45604434
|
C | A | 12 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(9): Show | 12 | HG02559.hp2 HG02809.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1408+8147C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45604434 | ||||||
| chr3:45604593
|
G | A | 4 | a0001c0001t0069g0134a0001c0001t0076g0132a0001c0001t0086g0131others(1): Show | 4 | HG02055.hp1 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1408+8306G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45604593 | ||||||
| chr3:45604675
|
A | C | 3 | a0001c0001t0097g0268a0001c0001t0123g0266a0001c0001t0129g0288 | 3 | HG02886.hp1 HG02976.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1408+8388A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45604675 | ||||||
| chr3:45604678
|
G | A | 1 | a0001c0001t0003g0074 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.1408+8391G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45604678 | ||||||
| chr3:45604715
|
C | T | 1 | a0001c0001t0004g0235 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.1408+8428C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45604715 | ||||||
| chr3:45604718
|
A | G | 1 | a0001c0001t0184g0234 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1408+8431A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45604718 | ||||||
| chr3:45604761
|
C | T | 1 | a0001c0001t0006g0251 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1408+8474C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45604761 | ||||||
| chr3:45604762
|
G | A | 1 | a0001c0001t0096g0138 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1408+8475G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45604762 | ||||||
| chr3:45604810
|
C | T | 12 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(9): Show | 12 | HG02559.hp2 HG02809.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1408+8523C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45604810 | ||||||
| chr3:45604935
|
C | T | 1 | a0001c0002t0127g0122 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1408+8648C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45604935 | ||||||
| chr3:45604976
|
A | G | 32 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(29): Show | 32 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.1408+8689A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45604976 | ||||||
| chr3:45604991
|
C | T | 2 | a0001c0001t0074g0135a0001c0001t0195g0136 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1408+8704C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45604991 | ||||||
| chr3:45605387
|
T | C | 243 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(240): Show | 244 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(241): Show |
intron_variant | MODIFIER | c.1408+9100T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45605387 | ||||||
| chr3:45605523
|
A | G | 2 | a0001c0002t0027g0336a0001c0002t0117g0337 | 2 | HG00735.hp1 HG01257.hp2 |
intron_variant | MODIFIER | c.1408+9236A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45605523 | ||||||
| chr3:45605554
|
ATTC | A | 97 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(94): Show | 98 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(95): Show |
intron_variant | MODIFIER | c.1408+9270_1408+927 others(7): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45605554 | |||||
| chr3:45605680
|
T | C | 1 | a0001c0001t0005g0172 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1408+9393T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45605680 | ||||||
| chr3:45605731
|
C | T | 32 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(29): Show | 32 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.1408+9444C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45605731 | ||||||
| chr3:45605795
|
G | A | 5 | a0001c0001t0053g0139a0001c0001t0083g0140a0001c0001t0084g0141others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408+9508G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45605795 | ||||||
| chr3:45606031
|
T | A | 151 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(148): Show | 152 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(149): Show |
intron_variant | MODIFIER | c.1408+9744T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45606031 | ||||||
| chr3:45606162
|
C | T | 50 | a0001c0001t0007g0058a0001c0001t0007g0059a0001c0001t0007g0061others(47): Show | 50 | HG00438.hp2 HG00597.hp1 HG01074.hp2 others(47): Show |
intron_variant | MODIFIER | c.1408+9875C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45606162 | ||||||
| chr3:45606238
|
G | A | 1 | a0001c0001t0001g0173 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1408+9951G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45606238 | ||||||
| chr3:45606282
|
C | T | 1 | a0001c0001t0064g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1408+9995C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45606282 | ||||||
| chr3:45606284
|
C | T | 2 | a0001c0007t0204g0002a0001c0007t0205g0002 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1408+9997C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45606284 | ||||||
| chr3:45606523
|
C | T | 99 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(96): Show | 100 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1408+10236C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45606523 | ||||||
| chr3:45606524
|
C | G | 185 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(182): Show | 186 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(183): Show |
intron_variant | MODIFIER | c.1408+10237C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45606524 | ||||||
| chr3:45606577
|
C | T | 1 | a0001c0001t0155g0023 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1408+10290C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45606577 | ||||||
| chr3:45606661
|
C | T | 186 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(183): Show | 187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1408+10374C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45606661 | ||||||
| chr3:45606775
|
C | T | 14 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(11): Show | 14 | HG02486.hp1 HG02559.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.1408+10488C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45606775 | ||||||
| chr3:45606826
|
G | A | 1 | a0001c0001t0010g0051 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.1408+10539G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45606826 | ||||||
| chr3:45606886
|
G | C | 186 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(183): Show | 187 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(184): Show |
intron_variant | MODIFIER | c.1408+10599G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45606886 | ||||||
| chr3:45606983
|
G | A | 12 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(9): Show | 12 | HG02559.hp2 HG02809.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1408+10696G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45606983 | ||||||
| chr3:45607110
|
A | T | 1 | a0001c0001t0064g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1408+10823A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45607110 | ||||||
| chr3:45607178
|
C | T | 10 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0032g0143others(7): Show | 10 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1408+10891C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45607178 | ||||||
| chr3:45607274
|
A | G | 61 | a0001c0001t0010g0050a0001c0001t0014g0035a0001c0001t0014g0038others(58): Show | 61 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.1408+10987A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45607274 | ||||||
| chr3:45607287
|
A | G | 6 | a0001c0001t0019g0284a0001c0001t0019g0287a0001c0001t0038g0264others(3): Show | 6 | HG00423.hp1 HG02074.hp2 HG02132.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408+11000A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45607287 | ||||||
| chr3:45607305
|
G | T | 192 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(189): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1408+11018G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45607305 | ||||||
| chr3:45607434
|
G | C | 114 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(111): Show | 115 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.1408+11147G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45607434 | ||||||
| chr3:45607477
|
C | T | 1 | a0001c0001t0156g0118 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1408+11190C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45607477 | ||||||
| chr3:45607594
|
G | A | 14 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(11): Show | 14 | HG02486.hp1 HG02559.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.1408+11307G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45607594 | ||||||
| chr3:45607608
|
G | C | 2 | a0001c0001t0040g0269a0005c0012t0040g0271 | 2 | HG00609.hp2 HG03017.hp2 |
intron_variant | MODIFIER | c.1408+11321G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45607608 | ||||||
| chr3:45607610
|
A | G | 1 | a0001c0003t0103g0124 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1408+11323A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45607610 | ||||||
| chr3:45607613
|
G | A | 337 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(334): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1408+11326G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45607613 | ||||||
| chr3:45607653
|
G | T | 1 | a0001c0001t0156g0118 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1408+11366G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45607653 | ||||||
| chr3:45607673
|
G | A | 333 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(330): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1408+11386G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45607673 | ||||||
| chr3:45607686
|
C | CT | 192 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(189): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1408+11401dupT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45607686 | |||||
| chr3:45607826
|
A | G | 192 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(189): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1408+11539A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45607826 | ||||||
| chr3:45607863
|
T | C | 10 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0032g0143others(7): Show | 10 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1408+11576T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45607863 | ||||||
| chr3:45607925
|
T | C | 192 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(189): Show | 193 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(190): Show |
intron_variant | MODIFIER | c.1408+11638T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45607925 | ||||||
| chr3:45607962
|
C | T | 1 | a0001c0001t0004g0233 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.1408+11675C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45607962 | ||||||
| chr3:45608049
|
G | A | 1 | a0001c0005t0128g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1408+11762G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45608049 | ||||||
| chr3:45608364
|
C | T | 2 | a0001c0002t0029g0029a0001c0002t0029g0030 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1408+12077C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45608364 | ||||||
| chr3:45608372
|
G | A | 115 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(112): Show | 116 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(113): Show |
intron_variant | MODIFIER | c.1408+12085G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45608372 | ||||||
| chr3:45608381
|
C | T | 2 | a0001c0007t0204g0002a0001c0007t0205g0002 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1408+12094C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45608381 | ||||||
| chr3:45608417
|
G | A | 1 | a0001c0001t0156g0118 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1408+12130G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45608417 | ||||||
| chr3:45608455
|
C | T | 2 | a0001c0001t0156g0118a0001c0002t0124g0041 | 2 | HG01433.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1408+12168C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45608455 | ||||||
| chr3:45608456
|
G | A | 1 | a0001c0001t0190g0174 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1408+12169G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45608456 | ||||||
| chr3:45608551
|
G | T | 1 | a0001c0001t0197g0114 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1408+12264G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45608551 | ||||||
| chr3:45608754
|
T | C | 187 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(184): Show | 188 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1408+12467T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45608754 | ||||||
| chr3:45608820
|
A | G | 14 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(11): Show | 14 | HG02486.hp1 HG02559.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.1408+12533A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45608820 | ||||||
| chr3:45608826
|
C | A | 115 | a0001c0001t0001g0045a0001c0001t0001g0161a0001c0001t0001g0162others(112): Show | 115 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(112): Show |
intron_variant | MODIFIER | c.1408+12539C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45608826 | ||||||
| chr3:45608833
|
C | T | 1 | a0001c0001t0157g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1408+12546C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45608833 | ||||||
| chr3:45608839
|
C | CA | 134 | a0001c0001t0001g0045a0001c0001t0001g0161a0001c0001t0001g0162others(131): Show | 134 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(131): Show |
intron_variant | MODIFIER | c.1408+12571dupA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45608839 | |||||
| chr3:45608839
|
C | CAA | 7 | a0001c0001t0003g0112a0001c0001t0013g0068a0001c0001t0015g0260others(4): Show | 7 | HG03041.hp1 HG03209.hp2 HG03831.hp2 others(4): Show |
intron_variant | MODIFIER | c.1408+12570_1408+12 others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45608839 | |||||
| chr3:45608839
|
C | CAAA | 93 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(90): Show | 94 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(91): Show |
intron_variant | MODIFIER | c.1408+12569_1408+12 others(9): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45608839 | |||||
| chr3:45608839
|
C | CAAAA | 17 | a0001c0001t0003g0142a0001c0001t0006g0073a0001c0001t0009g0015others(14): Show | 17 | HG02559.hp2 HG02809.hp1 HG02818.hp1 others(14): Show |
intron_variant | MODIFIER | c.1408+12568_1408+12 others(10): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45608839 | |||||
| chr3:45608839
|
CA | C | 74 | a0001c0001t0010g0050a0001c0001t0014g0035a0001c0001t0014g0038others(71): Show | 74 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(71): Show |
intron_variant | MODIFIER | c.1408+12571delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45608839 | |||||
| chr3:45608888
|
C | G | 100 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(97): Show | 101 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1408+12601C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45608888 | ||||||
| chr3:45609539
|
G | A | 10 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0032g0143others(7): Show | 10 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1408+13252G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45609539 | ||||||
| chr3:45609822
|
GT | G | 5 | a0001c0001t0053g0139a0001c0001t0083g0140a0001c0001t0084g0141others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408+13540delT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45609822 | |||||
| chr3:45609963
|
G | A | 1 | a0001c0001t0006g0075 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1408+13676G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45609963 | ||||||
| chr3:45610027
|
A | G | 1 | a0001c0001t0007g0046 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1408+13740A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45610027 | ||||||
| chr3:45610060
|
C | T | 11 | a0001c0001t0002g0111a0001c0001t0023g0149a0001c0001t0023g0150others(8): Show | 11 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(8): Show |
intron_variant | MODIFIER | c.1408+13773C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45610060 | ||||||
| chr3:45610064
|
C | T | 3 | a0001c0001t0068g0128a0001c0001t0075g0130a0001c0001t0078g0129 | 3 | HG02630.hp1 HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1408+13777C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45610064 | ||||||
| chr3:45610065
|
G | T | 12 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(9): Show | 12 | HG02559.hp2 HG02809.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1408+13778G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45610065 | ||||||
| chr3:45610210
|
T | G | 1 | a0001c0001t0006g0251 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1408+13923T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45610210 | ||||||
| chr3:45610222
|
C | G | 3 | a0001c0001t0001g0228a0001c0001t0001g0230a0001c0001t0180g0229 | 3 | HG01978.hp1 HG02004.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1408+13935C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45610222 | ||||||
| chr3:45610343
|
C | A | 14 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(11): Show | 14 | HG02486.hp1 HG02559.hp2 HG02717.hp2 others(11): Show |
intron_variant | MODIFIER | c.1408+14056C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45610343 | ||||||
| chr3:45610396
|
C | G | 1 | a0001c0001t0002g0110 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1408+14109C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45610396 | ||||||
| chr3:45610403
|
G | T | 63 | a0001c0001t0010g0050a0001c0001t0014g0035a0001c0001t0014g0038others(60): Show | 63 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(60): Show |
intron_variant | MODIFIER | c.1408+14116G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45610403 | ||||||
| chr3:45610424
|
G | A | 1 | a0001c0002t0124g0041 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1408+14137G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45610424 | ||||||
| chr3:45610554
|
G | A | 66 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(63): Show | 67 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1408+14267G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45610554 | ||||||
| chr3:45610563
|
G | T | 100 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(97): Show | 101 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1408+14276G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45610563 | ||||||
| chr3:45610669
|
G | A | 101 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(98): Show | 102 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.1408+14382G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45610669 | ||||||
| chr3:45610783
|
C | T | 99 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(96): Show | 100 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(97): Show |
intron_variant | MODIFIER | c.1408+14496C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45610783 | ||||||
| chr3:45610901
|
A | G | 100 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(97): Show | 101 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1408+14614A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45610901 | ||||||
| chr3:45610952
|
A | C | 10 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0032g0143others(7): Show | 10 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1408+14665A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45610952 | ||||||
| chr3:45611140
|
G | A | 2 | a0001c0001t0074g0135a0001c0001t0195g0136 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1408+14853G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45611140 | ||||||
| chr3:45611169
|
G | A | 2 | a0001c0005t0122g0155a0001c0005t0139g0156 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1408+14882G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45611169 | ||||||
| chr3:45611242
|
A | G | 100 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(97): Show | 101 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1408+14955A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45611242 | ||||||
| chr3:45611347
|
A | G | 12 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(9): Show | 12 | HG02559.hp2 HG02809.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1408+15060A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45611347 | ||||||
| chr3:45611454
|
G | A | 1 | a0001c0001t0014g0035 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1408+15167G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45611454 | ||||||
| chr3:45611482
|
T | C | 1 | a0001c0003t0142g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1408+15195T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45611482 | ||||||
| chr3:45611723
|
TCTGAGGC others(14): Show |
T | 25 | a0001c0001t0007g0058a0001c0001t0007g0059a0001c0001t0007g0061others(22): Show | 25 | HG00438.hp2 HG00597.hp1 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.1408+15446_1408+15 others(27): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45611723 | |||||
| chr3:45611762
|
G | A | 1 | a0001c0002t0025g0338 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1408+15475G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45611762 | ||||||
| chr3:45611784
|
G | T | 1 | a0001c0002t0011g0034 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1408+15497G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45611784 | ||||||
| chr3:45611791
|
G | A | 100 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(97): Show | 101 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1408+15504G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45611791 | ||||||
| chr3:45611892
|
T | C | 88 | a0001c0001t0007g0058a0001c0001t0007g0059a0001c0001t0007g0061others(85): Show | 88 | HG00099.hp1 HG00140.hp1 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.1408+15605T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45611892 | ||||||
| chr3:45611917
|
T | C | 5 | a0001c0001t0053g0139a0001c0001t0083g0140a0001c0001t0084g0141others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408+15630T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45611917 | ||||||
| chr3:45611944
|
G | A | 159 | a0001c0001t0001g0045a0001c0001t0001g0161a0001c0001t0001g0162others(156): Show | 159 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(156): Show |
intron_variant | MODIFIER | c.1408+15657G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45611944 | ||||||
| chr3:45611981
|
C | T | 2 | a0001c0007t0204g0002a0001c0007t0205g0002 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1408+15694C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45611981 | ||||||
| chr3:45612022
|
G | A | 1 | a0007c0009t0095g0354 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1408+15735G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45612022 | ||||||
| chr3:45612070
|
G | GCGCTCT | 53 | a0001c0001t0010g0050a0001c0001t0014g0035a0001c0001t0014g0038others(50): Show | 53 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(50): Show |
intron_variant | MODIFIER | c.1408+15784_1408+15 others(12): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45612070 | |||||
| chr3:45612070
|
G | GCGCTCTC others(1): Show |
5 | a0001c0002t0020g0309a0001c0002t0051g0306a0001c0002t0052g0307others(2): Show | 5 | HG00738.hp1 HG01167.hp1 HG02683.hp1 others(2): Show |
intron_variant | MODIFIER | c.1408+15784_1408+15 others(14): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45612070 | |||||
| chr3:45612070
|
G | GCGCTCTC others(3): Show |
1 | a0001c0002t0066g0305 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1408+15784_1408+15 others(16): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45612070 | |||||
| chr3:45612070
|
G | GCT | 42 | a0001c0001t0001g0161a0001c0001t0001g0176a0001c0001t0001g0177others(39): Show | 42 | HG00558.hp1 HG00609.hp2 HG01069.hp1 others(39): Show |
intron_variant | MODIFIER | c.1408+15812_1408+15 others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45612070 | |||||
| chr3:45612070
|
G | GCTCTCT | 10 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0032g0143others(7): Show | 10 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1408+15808_1408+15 others(12): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45612070 | |||||
| chr3:45612070
|
G | T | 3 | a0001c0001t0005g0166a0001c0001t0203g0254a0001c0005t0128g0160 | 3 | HG01261.hp2 HG03834.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1408+15783G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45612070 | ||||||
| chr3:45612070
|
GCT | G | 76 | a0001c0001t0001g0094a0001c0001t0001g0227a0001c0001t0002g0080others(73): Show | 77 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(74): Show |
intron_variant | MODIFIER | c.1408+15812_1408+15 others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45612070 | |||||
| chr3:45612072
|
T | G | 12 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(9): Show | 12 | HG02559.hp2 HG02809.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1408+15785T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45612072 | ||||||
| chr3:45612085
|
C | T | 34 | a0001c0001t0007g0058a0001c0001t0007g0059a0001c0001t0007g0061others(31): Show | 34 | HG00438.hp2 HG00597.hp1 HG01891.hp1 others(31): Show |
intron_variant | MODIFIER | c.1408+15798C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45612085 | ||||||
| chr3:45612241
|
T | C | 3 | a0001c0003t0121g0152a0001c0003t0133g0158a0001c0003t0142g0157 | 3 | HG01243.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1408+15954T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45612241 | ||||||
| chr3:45612299
|
G | T | 1 | a0001c0002t0117g0337 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1408+16012G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45612299 | ||||||
| chr3:45612492
|
C | T | 2 | a0001c0001t0074g0135a0001c0001t0195g0136 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1408+16205C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45612492 | ||||||
| chr3:45612515
|
TAGG | T | 100 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(97): Show | 101 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.1408+16234_1408+16 others(9): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45612515 | |||||
| chr3:45612866
|
C | T | 60 | a0001c0001t0010g0050a0001c0001t0014g0035a0001c0001t0014g0038others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1408+16579C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45612866 | ||||||
| chr3:45612950
|
G | A | 3 | a0001c0003t0121g0152a0001c0003t0133g0158a0001c0003t0142g0157 | 3 | HG01243.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1408+16663G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45612950 | ||||||
| chr3:45612961
|
C | T | 1 | a0001c0002t0119g0033 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1408+16674C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45612961 | ||||||
| chr3:45613077
|
G | GC | 4 | a0001c0001t0016g0001a0001c0001t0016g0108a0001c0002t0080g0355others(1): Show | 5 | HG00140.hp2 HG00323.hp1 HG01123.hp1 others(2): Show |
intron_variant | MODIFIER | c.1408+16795dupC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45613077 | |||||
| chr3:45613169
|
T | G | 1 | a0001c0001t0002g0080 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1408+16882T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45613169 | ||||||
| chr3:45613172
|
C | G | 337 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(334): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.1408+16885C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45613172 | ||||||
| chr3:45613228
|
A | G | 6 | a0001c0002t0011g0034a0001c0002t0011g0291a0001c0002t0011g0292others(3): Show | 6 | HG02109.hp2 HG02280.hp2 HG02300.hp2 others(3): Show |
intron_variant | MODIFIER | c.1408+16941A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45613228 | ||||||
| chr3:45613260
|
G | A | 333 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(330): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1408+16973G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45613260 | ||||||
| chr3:45613580
|
G | GT | 72 | a0001c0001t0001g0173a0001c0001t0001g0221a0001c0001t0001g0223others(69): Show | 72 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(69): Show |
intron_variant | MODIFIER | c.1408+17308dupT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45613580 | |||||
| chr3:45614051
|
C | T | 2 | a0001c0007t0204g0002a0001c0007t0205g0002 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1408+17764C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45614051 | ||||||
| chr3:45614285
|
T | C | 1 | a0001c0001t0006g0113 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1408+17998T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45614285 | ||||||
| chr3:45614409
|
T | TA | 32 | a0001c0001t0007g0058a0001c0001t0007g0059a0001c0001t0007g0061others(29): Show | 32 | HG00438.hp2 HG00597.hp1 HG01081.hp2 others(29): Show |
intron_variant | MODIFIER | c.1408+18140dupA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45614409 | |||||
| chr3:45614409
|
TA | T | 6 | a0001c0001t0002g0106a0001c0001t0111g0133a0001c0001t0162g0164others(3): Show | 6 | HG01168.hp2 HG02451.hp2 HG03225.hp1 others(3): Show |
intron_variant | MODIFIER | c.1408+18140delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45614409 | |||||
| chr3:45614456
|
C | T | 1 | a0001c0001t0017g0081 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1408+18169C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45614456 | ||||||
| chr3:45614568
|
A | C | 200 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(197): Show | 201 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(198): Show |
intron_variant | MODIFIER | c.1408+18281A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45614568 | ||||||
| chr3:45614671
|
C | T | 28 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(25): Show | 28 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(25): Show |
intron_variant | MODIFIER | c.1408+18384C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45614671 | ||||||
| chr3:45614768
|
G | GT | 173 | a0001c0001t0003g0042a0001c0001t0003g0074a0001c0001t0003g0077others(170): Show | 174 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1408+18496dupT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45614768 | |||||
| chr3:45614768
|
G | GTT | 135 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(132): Show | 135 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.1408+18495_1408+18 others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45614768 | |||||
| chr3:45614768
|
G | GTTT | 17 | a0001c0001t0001g0171a0001c0001t0001g0181a0001c0001t0001g0183others(14): Show | 17 | HG00438.hp1 HG01069.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.1408+18494_1408+18 others(9): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45614768 | |||||
| chr3:45614787
|
G | A | 60 | a0001c0001t0010g0050a0001c0001t0014g0035a0001c0001t0014g0038others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1408+18500G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45614787 | ||||||
| chr3:45614858
|
G | C | 321 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(318): Show | 322 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(319): Show |
intron_variant | MODIFIER | c.1408+18571G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45614858 | ||||||
| chr3:45615070
|
A | G | 60 | a0001c0001t0010g0050a0001c0001t0014g0035a0001c0001t0014g0038others(57): Show | 60 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(57): Show |
intron_variant | MODIFIER | c.1408+18783A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45615070 | ||||||
| chr3:45615092
|
A | C | 1 | a0001c0001t0186g0215 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1408+18805A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45615092 | ||||||
| chr3:45615110
|
A | G | 25 | a0001c0001t0007g0058a0001c0001t0007g0059a0001c0001t0007g0061others(22): Show | 25 | HG00438.hp2 HG00597.hp1 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.1408+18823A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45615110 | ||||||
| chr3:45615231
|
G | A | 66 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(63): Show | 67 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1408+18944G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45615231 | ||||||
| chr3:45615303
|
G | C | 34 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(31): Show | 34 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1408+19016G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45615303 | ||||||
| chr3:45615337
|
C | A | 2 | a0001c0001t0074g0135a0001c0001t0195g0136 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1408+19050C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45615337 | ||||||
| chr3:45615698
|
G | A | 1 | a0001c0005t0128g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1408+19411G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45615698 | ||||||
| chr3:45615823
|
C | T | 112 | a0001c0001t0001g0045a0001c0001t0001g0161a0001c0001t0001g0162others(109): Show | 112 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(109): Show |
intron_variant | MODIFIER | c.1408+19536C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45615823 | ||||||
| chr3:45615860
|
G | A | 1 | a0001c0001t0156g0118 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1408+19573G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45615860 | ||||||
| chr3:45615885
|
C | T | 5 | a0001c0001t0053g0139a0001c0001t0083g0140a0001c0001t0084g0141others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1408+19598C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45615885 | ||||||
| chr3:45615886
|
G | A | 1 | a0001c0001t0003g0090 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1408+19599G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45615886 | ||||||
| chr3:45615944
|
T | C | 12 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(9): Show | 12 | HG02559.hp2 HG02809.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1408+19657T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45615944 | ||||||
| chr3:45615971
|
A | G | 1 | a0001c0002t0124g0041 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1408+19684A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45615971 | ||||||
| chr3:45616350
|
ATTGTTAG others(7): Show |
A | 4 | a0001c0001t0007g0058a0001c0001t0007g0059a0001c0002t0089g0343others(1): Show | 4 | NA18954.hp2 NA18966.hp2 NA19062.hp2 others(1): Show |
intron_variant | MODIFIER | c.1409-19797_1409-19 others(20): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45616350 | |||||
| chr3:45616363
|
T | G | 21 | a0001c0001t0007g0061a0001c0001t0007g0062a0001c0001t0007g0063others(18): Show | 21 | HG00438.hp2 HG00597.hp1 HG01952.hp1 others(18): Show |
intron_variant | MODIFIER | c.1409-19787T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45616363 | ||||||
| chr3:45616457
|
G | T | 33 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(30): Show | 33 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1409-19693G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45616457 | ||||||
| chr3:45616482
|
C | T | 5 | a0001c0001t0032g0143a0001c0001t0032g0144a0001c0001t0109g0145others(2): Show | 5 | HG01074.hp2 HG01243.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409-19668C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45616482 | ||||||
| chr3:45616587
|
TC | T | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1409-19558delC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45616587 | |||||
| chr3:45616601
|
G | C | 3 | a0001c0003t0121g0152a0001c0003t0133g0158a0001c0003t0142g0157 | 3 | HG01243.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1409-19549G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45616601 | ||||||
| chr3:45616800
|
G | T | 2 | a0001c0007t0204g0002a0001c0007t0205g0002 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1409-19350G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45616800 | ||||||
| chr3:45616837
|
C | T | 33 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(30): Show | 33 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1409-19313C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45616837 | ||||||
| chr3:45616980
|
G | A | 4 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0081g0151others(1): Show | 4 | HG01891.hp2 HG02280.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1409-19170G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45616980 | ||||||
| chr3:45617034
|
A | AT | 150 | a0001c0001t0001g0045a0001c0001t0001g0161a0001c0001t0001g0162others(147): Show | 150 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(147): Show |
intron_variant | MODIFIER | c.1409-19099dupT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45617034 | |||||
| chr3:45617034
|
A | ATT | 14 | a0001c0001t0001g0241a0001c0001t0005g0005a0001c0001t0018g0055others(11): Show | 14 | HG00733.hp2 HG00738.hp2 HG01106.hp2 others(11): Show |
intron_variant | MODIFIER | c.1409-19100_1409-19 others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45617034 | |||||
| chr3:45617592
|
A | G | 1 | a0001c0001t0005g0005 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.1409-18558A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45617592 | ||||||
| chr3:45617616
|
C | G | 333 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(330): Show | 334 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(331): Show |
intron_variant | MODIFIER | c.1409-18534C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45617616 | ||||||
| chr3:45617762
|
A | T | 1 | a0001c0001t0007g0065 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.1409-18388A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45617762 | ||||||
| chr3:45617798
|
C | G | 1 | a0001c0001t0162g0164 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.1409-18352C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45617798 | ||||||
| chr3:45617864
|
T | C | 124 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(121): Show | 125 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(122): Show |
intron_variant | MODIFIER | c.1409-18286T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45617864 | ||||||
| chr3:45618049
|
G | T | 2 | a0001c0007t0204g0002a0001c0007t0205g0002 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1409-18101G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45618049 | ||||||
| chr3:45618196
|
G | A | 1 | a0001c0001t0145g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1409-17954G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45618196 | ||||||
| chr3:45618257
|
C | T | 1 | a0001c0002t0124g0041 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1409-17893C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45618257 | ||||||
| chr3:45618581
|
A | G | 5 | a0001c0001t0053g0139a0001c0001t0083g0140a0001c0001t0084g0141others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409-17569A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45618581 | ||||||
| chr3:45618626
|
A | G | 2 | a0001c0007t0204g0002a0001c0007t0205g0002 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1409-17524A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45618626 | ||||||
| chr3:45618795
|
T | G | 11 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(8): Show | 11 | HG02559.hp2 HG02809.hp1 HG02818.hp1 others(8): Show |
intron_variant | MODIFIER | c.1409-17355T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45618795 | ||||||
| chr3:45618983
|
G | A | 1 | a0001c0001t0058g0147 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1409-17167G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45618983 | ||||||
| chr3:45619081
|
G | A | 1 | a0001c0001t0010g0066 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1409-17069G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45619081 | ||||||
| chr3:45619246
|
C | T | 2 | a0001c0007t0204g0002a0001c0007t0205g0002 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1409-16904C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45619246 | ||||||
| chr3:45619295
|
C | T | 33 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(30): Show | 33 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1409-16855C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45619295 | ||||||
| chr3:45619531
|
G | C | 3 | a0001c0001t0068g0128a0001c0001t0075g0130a0001c0001t0078g0129 | 3 | HG02630.hp1 HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1409-16619G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45619531 | ||||||
| chr3:45619685
|
A | G | 2 | a0001c0001t0074g0135a0001c0001t0195g0136 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1409-16465A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45619685 | ||||||
| chr3:45619730
|
C | T | 12 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0032g0143others(9): Show | 12 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1409-16420C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45619730 | ||||||
| chr3:45619828
|
G | C | 1 | a0001c0001t0200g0071 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1409-16322G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45619828 | ||||||
| chr3:45619828
|
G | GC | 49 | a0001c0001t0001g0161a0001c0001t0001g0179a0001c0001t0001g0180others(46): Show | 49 | HG00621.hp1 HG00735.hp1 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.1409-16311dupC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45619828 | |||||
| chr3:45619828
|
G | GCC | 27 | a0001c0001t0001g0241a0001c0001t0001g0252a0001c0001t0007g0059others(24): Show | 27 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(24): Show |
intron_variant | MODIFIER | c.1409-16312_1409-16 others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45619828 | |||||
| chr3:45619828
|
GC | G | 86 | a0001c0001t0001g0094a0001c0001t0001g0186a0001c0001t0001g0217others(83): Show | 86 | HG00099.hp2 HG00323.hp1 HG00423.hp1 others(83): Show |
intron_variant | MODIFIER | c.1409-16311delC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45619828 | |||||
| chr3:45619828
|
GCC | G | 28 | a0001c0001t0003g0074a0001c0001t0009g0015a0001c0001t0009g0018others(25): Show | 28 | HG00558.hp1 HG01891.hp1 HG02155.hp1 others(25): Show |
intron_variant | MODIFIER | c.1409-16312_1409-16 others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45619828 | |||||
| chr3:45619833
|
C | G | 2 | a0001c0007t0204g0002a0001c0007t0205g0002 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1409-16317C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45619833 | ||||||
| chr3:45619839
|
C | A | 2 | a0001c0001t0004g0184a0001c0002t0124g0041 | 2 | HG00621.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.1409-16311C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45619839 | ||||||
| chr3:45619945
|
C | G | 6 | a0001c0001t0068g0128a0001c0001t0075g0130a0001c0001t0078g0129others(3): Show | 6 | HG01109.hp1 HG02630.hp1 HG03130.hp2 others(3): Show |
intron_variant | MODIFIER | c.1409-16205C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45619945 | ||||||
| chr3:45620033
|
G | A | 4 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0081g0151others(1): Show | 4 | HG01891.hp2 HG02280.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1409-16117G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45620033 | ||||||
| chr3:45620373
|
C | T | 5 | a0001c0001t0053g0139a0001c0001t0083g0140a0001c0001t0084g0141others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409-15777C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45620373 | ||||||
| chr3:45620404
|
A | G | 1 | a0001c0002t0124g0041 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1409-15746A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45620404 | ||||||
| chr3:45620410
|
T | C | 32 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(29): Show | 32 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.1409-15740T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45620410 | ||||||
| chr3:45620454
|
A | G | 1 | a0001c0001t0012g0127 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1409-15696A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45620454 | ||||||
| chr3:45620624
|
T | C | 294 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(291): Show | 295 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(292): Show |
intron_variant | MODIFIER | c.1409-15526T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45620624 | ||||||
| chr3:45620643
|
C | T | 5 | a0001c0001t0053g0139a0001c0001t0083g0140a0001c0001t0084g0141others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409-15507C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45620643 | ||||||
| chr3:45620719
|
ACT | A | 25 | a0001c0001t0007g0058a0001c0001t0007g0059a0001c0001t0007g0061others(22): Show | 25 | HG00438.hp2 HG00597.hp1 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.1409-15428_1409-15 others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45620719 | |||||
| chr3:45620820
|
G | A | 1 | a0001c0008t0004g0091 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1409-15330G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45620820 | ||||||
| chr3:45620954
|
A | G | 1 | a0001c0001t0008g0232 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.1409-15196A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45620954 | ||||||
| chr3:45621117
|
T | C | 1 | a0001c0001t0064g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1409-15033T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45621117 | ||||||
| chr3:45621158
|
C | T | 65 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(62): Show | 66 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1409-14992C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45621158 | ||||||
| chr3:45621169
|
G | A | 8 | a0001c0001t0004g0167a0001c0001t0004g0184a0001c0001t0004g0187others(5): Show | 8 | HG00621.hp2 HG02080.hp1 NA18952.hp1 others(5): Show |
intron_variant | MODIFIER | c.1409-14981G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45621169 | ||||||
| chr3:45621284
|
C | T | 33 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(30): Show | 33 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1409-14866C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45621284 | ||||||
| chr3:45621328
|
C | T | 4 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0081g0151others(1): Show | 4 | HG01891.hp2 HG02280.hp1 HG03041.hp2 others(1): Show |
intron_variant | MODIFIER | c.1409-14822C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45621328 | ||||||
| chr3:45621337
|
C | T | 1 | a0001c0001t0049g0084 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1409-14813C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45621337 | ||||||
| chr3:45621338
|
T | C | 1 | a0001c0001t0049g0084 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1409-14812T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45621338 | ||||||
| chr3:45621339
|
C | T | 1 | a0001c0001t0049g0084 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.1409-14811C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45621339 | ||||||
| chr3:45621369
|
A | G | 1 | a0001c0001t0009g0025 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1409-14781A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45621369 | ||||||
| chr3:45621663
|
C | T | 33 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(30): Show | 33 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1409-14487C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45621663 | ||||||
| chr3:45621700
|
T | C | 353 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(350): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1409-14450T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45621700 | ||||||
| chr3:45621804
|
C | T | 1 | a0001c0001t0193g0281 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1409-14346C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45621804 | ||||||
| chr3:45621833
|
A | G | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1409-14317A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45621833 | ||||||
| chr3:45621847
|
A | G | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1409-14303A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45621847 | ||||||
| chr3:45621849
|
A | G | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1409-14301A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45621849 | ||||||
| chr3:45621861
|
G | A | 2 | a0001c0007t0204g0002a0001c0007t0205g0002 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1409-14289G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45621861 | ||||||
| chr3:45621880
|
T | C | 1 | a0001c0001t0006g0189 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1409-14270T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45621880 | ||||||
| chr3:45621909
|
A | G | 12 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0032g0143others(9): Show | 12 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1409-14241A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45621909 | ||||||
| chr3:45622005
|
G | A | 1 | a0001c0001t0153g0270 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1409-14145G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45622005 | ||||||
| chr3:45622061
|
C | CA | 64 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0001g0241others(61): Show | 65 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1409-14074dupA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45622061 | |||||
| chr3:45622115
|
A | G | 33 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(30): Show | 33 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1409-14035A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45622115 | ||||||
| chr3:45622133
|
A | G | 1 | a0001c0001t0001g0225 | 1 | NA19078.hp1 | intron_variant | MODIFIER | c.1409-14017A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45622133 | ||||||
| chr3:45622152
|
A | T | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1409-13998A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45622152 | ||||||
| chr3:45622207
|
G | C | 10 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0032g0143others(7): Show | 10 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1409-13943G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45622207 | ||||||
| chr3:45622416
|
T | A | 1 | a0001c0001t0002g0105 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1409-13734T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45622416 | ||||||
| chr3:45622421
|
A | G | 1 | a0001c0001t0002g0105 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1409-13729A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45622421 | ||||||
| chr3:45622424
|
T | G | 3 | a0001c0001t0002g0105a0001c0007t0204g0002a0001c0007t0205g0002 | 3 | HG02886.hp2 HG03139.hp2 NA18967.hp1 |
intron_variant | MODIFIER | c.1409-13726T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45622424 | ||||||
| chr3:45622426
|
C | T | 1 | a0001c0001t0002g0105 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1409-13724C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45622426 | ||||||
| chr3:45622432
|
A | T | 1 | a0001c0001t0002g0105 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1409-13718A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45622432 | ||||||
| chr3:45622438
|
T | C | 2 | a0001c0005t0122g0155a0001c0005t0139g0156 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1409-13712T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45622438 | ||||||
| chr3:45622668
|
A | AT | 12 | a0001c0001t0001g0241a0001c0001t0002g0105a0001c0001t0004g0216others(9): Show | 12 | HG00597.hp1 HG02486.hp2 HG02738.hp1 others(9): Show |
intron_variant | MODIFIER | c.1409-13463dupT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45622668 | |||||
| chr3:45622668
|
AT | A | 14 | a0001c0001t0001g0255a0001c0001t0007g0059a0001c0001t0008g0185others(11): Show | 14 | HG01069.hp2 HG01070.hp1 HG01167.hp1 others(11): Show |
intron_variant | MODIFIER | c.1409-13463delT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45622668 | |||||
| chr3:45622688
|
A | T | 1 | a0001c0001t0002g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1409-13462A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45622688 | ||||||
| chr3:45622879
|
G | A | 1 | a0001c0001t0007g0059 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1409-13271G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45622879 | ||||||
| chr3:45623193
|
A | T | 25 | a0001c0001t0007g0058a0001c0001t0007g0059a0001c0001t0007g0061others(22): Show | 25 | HG00438.hp2 HG00597.hp1 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.1409-12957A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45623193 | ||||||
| chr3:45623207
|
T | A | 165 | a0001c0001t0001g0045a0001c0001t0001g0161a0001c0001t0001g0162others(162): Show | 165 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(162): Show |
intron_variant | MODIFIER | c.1409-12943T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45623207 | ||||||
| chr3:45623243
|
G | A | 2 | a0001c0001t0001g0190a0001c0002t0066g0305 | 2 | HG00673.hp1 NA18973.hp2 |
intron_variant | MODIFIER | c.1409-12907G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45623243 | ||||||
| chr3:45623355
|
G | A | 19 | a0001c0002t0011g0034a0001c0002t0011g0291a0001c0002t0011g0292others(16): Show | 19 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.1409-12795G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45623355 | ||||||
| chr3:45623380
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1409-12770G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45623380 | ||||||
| chr3:45623562
|
T | A | 1 | a0001c0008t0002g0107 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1409-12588T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45623562 | ||||||
| chr3:45623611
|
A | T | 25 | a0001c0001t0007g0058a0001c0001t0007g0059a0001c0001t0007g0061others(22): Show | 25 | HG00438.hp2 HG00597.hp1 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.1409-12539A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45623611 | ||||||
| chr3:45623702
|
G | A | 295 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(292): Show | 296 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(293): Show |
intron_variant | MODIFIER | c.1409-12448G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45623702 | ||||||
| chr3:45623846
|
C | T | 2 | a0001c0001t0074g0135a0001c0001t0195g0136 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1409-12304C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45623846 | ||||||
| chr3:45623985
|
G | C | 1 | a0001c0001t0005g0172 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1409-12165G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45623985 | ||||||
| chr3:45624445
|
C | T | 6 | a0001c0001t0032g0143a0001c0001t0032g0144a0001c0001t0058g0147others(3): Show | 6 | HG01074.hp2 HG01243.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1409-11705C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45624445 | ||||||
| chr3:45624483
|
G | A | 1 | a0001c0002t0024g0296 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1409-11667G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45624483 | ||||||
| chr3:45624516
|
G | A | 12 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(9): Show | 12 | HG02559.hp2 HG02809.hp1 HG02818.hp1 others(9): Show |
intron_variant | MODIFIER | c.1409-11634G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45624516 | ||||||
| chr3:45624538
|
C | T | 1 | a0001c0001t0166g0263 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1409-11612C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45624538 | ||||||
| chr3:45624564
|
T | G | 25 | a0001c0001t0007g0058a0001c0001t0007g0059a0001c0001t0007g0061others(22): Show | 25 | HG00438.hp2 HG00597.hp1 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.1409-11586T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45624564 | ||||||
| chr3:45624738
|
CA | C | 28 | a0001c0001t0007g0058a0001c0001t0007g0059a0001c0001t0007g0061others(25): Show | 28 | HG00438.hp2 HG00597.hp1 HG01952.hp1 others(25): Show |
intron_variant | MODIFIER | c.1409-11403delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45624738 | |||||
| chr3:45624881
|
C | CT | 10 | a0001c0001t0001g0161a0001c0001t0001g0180a0001c0001t0004g0216others(7): Show | 10 | HG01243.hp2 HG01257.hp1 HG01258.hp2 others(7): Show |
intron_variant | MODIFIER | c.1409-11252dupT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45624881 | |||||
| chr3:45624881
|
CT | C | 102 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(99): Show | 103 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(100): Show |
intron_variant | MODIFIER | c.1409-11252delT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45624881 | |||||
| chr3:45625008
|
T | C | 33 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(30): Show | 33 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1409-11142T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45625008 | ||||||
| chr3:45625080
|
T | TATGTTAA others(4): Show |
2 | a0001c0001t0032g0143a0001c0001t0109g0145 | 2 | HG01074.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1409-11070_1409-11 others(17): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45625080 | ||||||
| chr3:45625083
|
T | G | 2 | a0001c0001t0032g0143a0001c0001t0109g0145 | 2 | HG01074.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1409-11067T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45625083 | ||||||
| chr3:45625085
|
A | C | 2 | a0001c0001t0032g0143a0001c0001t0109g0145 | 2 | HG01074.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1409-11065A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45625085 | ||||||
| chr3:45625086
|
G | C | 25 | a0001c0001t0007g0058a0001c0001t0007g0059a0001c0001t0007g0061others(22): Show | 25 | HG00438.hp2 HG00597.hp1 HG01952.hp1 others(22): Show |
intron_variant | MODIFIER | c.1409-11064G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45625086 | ||||||
| chr3:45625895
|
T | C | 131 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(128): Show | 132 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(129): Show |
intron_variant | MODIFIER | c.1409-10255T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45625895 | ||||||
| chr3:45626025
|
G | C | 3 | a0001c0003t0121g0152a0001c0003t0133g0158a0001c0003t0142g0157 | 3 | HG01243.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1409-10125G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45626025 | ||||||
| chr3:45626073
|
T | C | 1 | a0001c0001t0003g0090 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1409-10077T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45626073 | ||||||
| chr3:45626169
|
G | T | 7 | a0001c0002t0028g0328a0001c0002t0028g0329a0001c0002t0054g0330others(4): Show | 7 | HG01081.hp1 HG01943.hp2 HG01978.hp2 others(4): Show |
intron_variant | MODIFIER | c.1409-9981G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45626169 | ||||||
| chr3:45626321
|
A | G | 1 | a0001c0001t0185g0100 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.1409-9829A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45626321 | ||||||
| chr3:45626497
|
G | A | 113 | a0001c0001t0001g0045a0001c0001t0001g0161a0001c0001t0001g0162others(110): Show | 113 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1409-9653G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45626497 | ||||||
| chr3:45626840
|
T | A | 12 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0032g0143others(9): Show | 12 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1409-9310T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45626840 | ||||||
| chr3:45626893
|
CA | C | 291 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(288): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(289): Show |
intron_variant | MODIFIER | c.1409-9243delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45626893 | |||||
| chr3:45627016
|
T | G | 2 | a0001c0002t0031g0332a0001c0002t0031g0333 | 2 | HG01168.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1409-9134T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627016 | ||||||
| chr3:45627037
|
C | G | 1 | a0001c0002t0034g0348 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1409-9113C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627037 | ||||||
| chr3:45627058
|
G | A | 1 | a0001c0001t0074g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1409-9092G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627058 | ||||||
| chr3:45627083
|
C | T | 32 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(29): Show | 32 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(29): Show |
intron_variant | MODIFIER | c.1409-9067C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627083 | ||||||
| chr3:45627144
|
G | A | 1 | a0001c0001t0045g0253 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1409-9006G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627144 | ||||||
| chr3:45627234
|
A | C | 1 | a0001c0002t0127g0122 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1409-8916A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627234 | ||||||
| chr3:45627237
|
A | T | 65 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(62): Show | 66 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1409-8913A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627237 | ||||||
| chr3:45627292
|
C | T | 18 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(15): Show | 18 | HG00609.hp1 HG01255.hp1 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.1409-8858C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627292 | ||||||
| chr3:45627367
|
C | T | 1 | a0001c0002t0011g0034 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1409-8783C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627367 | ||||||
| chr3:45627381
|
T | C | 23 | a0001c0001t0048g0119a0001c0001t0048g0120a0001c0002t0011g0034others(20): Show | 23 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1409-8769T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627381 | ||||||
| chr3:45627403
|
T | C | 1 | a0001c0001t0199g0072 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1409-8747T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627403 | ||||||
| chr3:45627485
|
G | A | 23 | a0001c0001t0048g0119a0001c0001t0048g0120a0001c0002t0011g0034others(20): Show | 23 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1409-8665G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627485 | ||||||
| chr3:45627611
|
C | G | 34 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(31): Show | 34 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1409-8539C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627611 | ||||||
| chr3:45627706
|
C | CA | 142 | a0001c0001t0001g0045a0001c0001t0001g0161a0001c0001t0001g0162others(139): Show | 142 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(139): Show |
intron_variant | MODIFIER | c.1409-8425dupA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45627706 | |||||
| chr3:45627706
|
C | CAA | 16 | a0001c0001t0005g0005a0001c0001t0023g0149a0001c0001t0023g0150others(13): Show | 16 | HG01074.hp2 HG01261.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.1409-8426_1409-842 others(6): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45627706 | |||||
| chr3:45627732
|
G | T | 5 | a0001c0001t0053g0139a0001c0001t0083g0140a0001c0001t0084g0141others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409-8418G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627732 | ||||||
| chr3:45627774
|
G | A | 1 | a0001c0001t0064g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1409-8376G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627774 | ||||||
| chr3:45627929
|
A | T | 34 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(31): Show | 34 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1409-8221A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627929 | ||||||
| chr3:45627938
|
G | T | 2 | a0001c0002t0029g0029a0001c0002t0029g0030 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.1409-8212G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627938 | ||||||
| chr3:45627987
|
G | T | 1 | a0001c0001t0156g0118 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1409-8163G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627987 | ||||||
| chr3:45627992
|
A | G | 5 | a0001c0001t0001g0162a0001c0001t0001g0171a0001c0001t0001g0206others(2): Show | 5 | HG02155.hp2 NA18951.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409-8158A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45627992 | ||||||
| chr3:45628007
|
C | CAAAAAA | 148 | a0001c0001t0001g0045a0001c0001t0001g0161a0001c0001t0001g0162others(145): Show | 148 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(145): Show |
intron_variant | MODIFIER | c.1409-8136_1409-813 others(10): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45628007 | |||||
| chr3:45628007
|
C | CAAAAAAA | 72 | a0001c0001t0001g0225a0001c0001t0005g0005a0001c0001t0007g0058others(69): Show | 72 | HG00423.hp1 HG00438.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.1409-8137_1409-813 others(11): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45628007 | |||||
| chr3:45628007
|
C | CAAAAAAA others(1): Show |
7 | a0001c0001t0053g0139a0001c0001t0083g0140a0001c0001t0084g0141others(4): Show | 7 | HG01891.hp1 HG02451.hp1 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.1409-8138_1409-813 others(12): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45628007 | |||||
| chr3:45628015
|
A | AAAAAAG | 64 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(61): Show | 65 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(62): Show |
intron_variant | MODIFIER | c.1409-8131_1409-813 others(10): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45628015 | |||||
| chr3:45628133
|
C | G | 5 | a0001c0001t0053g0139a0001c0001t0083g0140a0001c0001t0084g0141others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409-8017C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45628133 | ||||||
| chr3:45628387
|
C | T | 29 | a0001c0001t0157g0247a0001c0001t0199g0072a0001c0001t0200g0071others(26): Show | 29 | HG00099.hp1 HG00140.hp1 HG00639.hp2 others(26): Show |
intron_variant | MODIFIER | c.1409-7763C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45628387 | ||||||
| chr3:45628430
|
T | G | 1 | a0001c0001t0143g0265 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.1409-7720T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45628430 | ||||||
| chr3:45628474
|
A | G | 3 | a0001c0002t0031g0332a0001c0002t0031g0333a0001c0002t0107g0334 | 3 | HG01168.hp1 HG01169.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1409-7676A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45628474 | ||||||
| chr3:45628593
|
G | A | 39 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(36): Show | 39 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1409-7557G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45628593 | ||||||
| chr3:45628675
|
G | T | 1 | a0001c0001t0195g0136 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1409-7475G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45628675 | ||||||
| chr3:45628705
|
T | C | 10 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0032g0143others(7): Show | 10 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1409-7445T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45628705 | ||||||
| chr3:45628768
|
C | T | 1 | a0001c0002t0132g0032 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1409-7382C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45628768 | ||||||
| chr3:45628791
|
C | G | 2 | a0001c0001t0048g0119a0001c0001t0048g0120 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1409-7359C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45628791 | ||||||
| chr3:45628986
|
C | T | 5 | a0001c0001t0053g0139a0001c0001t0083g0140a0001c0001t0084g0141others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409-7164C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45628986 | ||||||
| chr3:45629021
|
C | T | 34 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(31): Show | 34 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1409-7129C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45629021 | ||||||
| chr3:45629129
|
C | T | 1 | a0001c0001t0003g0142 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.1409-7021C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45629129 | ||||||
| chr3:45629152
|
G | A | 1 | a0001c0005t0128g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1409-6998G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45629152 | ||||||
| chr3:45629224
|
C | T | 116 | a0001c0001t0001g0045a0001c0001t0001g0161a0001c0001t0001g0162others(113): Show | 116 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(113): Show |
intron_variant | MODIFIER | c.1409-6926C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45629224 | ||||||
| chr3:45629370
|
G | A | 1 | a0001c0002t0124g0041 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1409-6780G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45629370 | ||||||
| chr3:45629412
|
C | CA | 161 | a0001c0001t0001g0045a0001c0001t0001g0161a0001c0001t0001g0162others(158): Show | 161 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.1409-6720dupA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45629412 | |||||
| chr3:45629426
|
A | AAAG | 33 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(30): Show | 33 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1409-6722_1409-672 others(7): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45629426 | |||||
| chr3:45629426
|
A | AG | 7 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0068g0128others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1409-6724_1409-672 others(5): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45629426 | ||||||
| chr3:45629601
|
T | G | 34 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(31): Show | 34 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1409-6549T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45629601 | ||||||
| chr3:45629686
|
G | A | 1 | a0001c0001t0193g0281 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1409-6464G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45629686 | ||||||
| chr3:45629712
|
C | T | 65 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(62): Show | 66 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1409-6438C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45629712 | ||||||
| chr3:45629741
|
C | T | 1 | a0001c0001t0005g0172 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1409-6409C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45629741 | ||||||
| chr3:45629768
|
G | A | 5 | a0001c0001t0053g0139a0001c0001t0083g0140a0001c0001t0084g0141others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409-6382G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45629768 | ||||||
| chr3:45629775
|
C | G | 1 | a0001c0001t0004g0188 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1409-6375C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45629775 | ||||||
| chr3:45629775
|
C | T | 163 | a0001c0001t0001g0045a0001c0001t0001g0161a0001c0001t0001g0162others(160): Show | 163 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(160): Show |
intron_variant | MODIFIER | c.1409-6375C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45629775 | ||||||
| chr3:45629909
|
C | T | 290 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(287): Show | 291 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.1409-6241C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45629909 | ||||||
| chr3:45630041
|
T | G | 1 | a0001c0003t0133g0158 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.1409-6109T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45630041 | ||||||
| chr3:45630051
|
A | C | 1 | a0001c0001t0001g0079 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1409-6099A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45630051 | ||||||
| chr3:45630141
|
CAT | C | 23 | a0001c0001t0048g0119a0001c0001t0048g0120a0001c0002t0011g0034others(20): Show | 23 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(20): Show |
intron_variant | MODIFIER | c.1409-6008_1409-600 others(6): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45630141 | ||||||
| chr3:45630162
|
TC | T | 256 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(253): Show | 257 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(254): Show |
intron_variant | MODIFIER | c.1409-5986delC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45630162 | |||||
| chr3:45630227
|
A | G | 1 | a0001c0001t0046g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1409-5923A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45630227 | ||||||
| chr3:45630350
|
G | T | 1 | a0001c0001t0013g0068 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.1409-5800G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45630350 | ||||||
| chr3:45630470
|
A | G | 1 | a0002c0006t0146g0163 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1409-5680A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45630470 | ||||||
| chr3:45630717
|
G | T | 7 | a0001c0001t0010g0050a0001c0002t0027g0299a0001c0002t0027g0336others(4): Show | 7 | HG00735.hp1 HG01257.hp2 HG01361.hp2 others(4): Show |
intron_variant | MODIFIER | c.1409-5433G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45630717 | ||||||
| chr3:45630718
|
G | A | 65 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(62): Show | 66 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1409-5432G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45630718 | ||||||
| chr3:45630727
|
G | T | 2 | a0001c0001t0074g0135a0001c0001t0195g0136 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1409-5423G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45630727 | ||||||
| chr3:45630732
|
T | A | 34 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(31): Show | 34 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(31): Show |
intron_variant | MODIFIER | c.1409-5418T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45630732 | ||||||
| chr3:45631133
|
G | A | 1 | a0001c0001t0158g0037 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1409-5017G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45631133 | ||||||
| chr3:45631263
|
T | A | 2 | a0001c0002t0071g0313a0001c0002t0112g0304 | 2 | HG00733.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1409-4887T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45631263 | ||||||
| chr3:45631300
|
C | CA | 24 | a0001c0001t0008g0232a0001c0001t0048g0119a0001c0001t0048g0120others(21): Show | 24 | HG00639.hp1 HG01167.hp2 HG01169.hp1 others(21): Show |
intron_variant | MODIFIER | c.1409-4840dupA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45631300 | |||||
| chr3:45631311
|
C | G | 2 | a0001c0005t0122g0155a0001c0005t0139g0156 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1409-4839C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45631311 | ||||||
| chr3:45631341
|
G | A | 1 | a0001c0001t0005g0192 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1409-4809G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45631341 | ||||||
| chr3:45631379
|
G | T | 290 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(287): Show | 291 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.1409-4771G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45631379 | ||||||
| chr3:45631433
|
C | T | 12 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0032g0143others(9): Show | 12 | HG01074.hp2 HG01243.hp1 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.1409-4717C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45631433 | ||||||
| chr3:45631460
|
C | T | 33 | a0001c0001t0010g0066a0001c0001t0019g0284a0001c0001t0019g0287others(30): Show | 33 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(30): Show |
intron_variant | MODIFIER | c.1409-4690C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45631460 | ||||||
| chr3:45631526
|
T | G | 113 | a0001c0001t0001g0045a0001c0001t0001g0161a0001c0001t0001g0162others(110): Show | 113 | HG00099.hp2 HG00323.hp2 HG00423.hp2 others(110): Show |
intron_variant | MODIFIER | c.1409-4624T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45631526 | ||||||
| chr3:45631570
|
G | A | 255 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(252): Show | 256 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(253): Show |
intron_variant | MODIFIER | c.1409-4580G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45631570 | ||||||
| chr3:45631598
|
C | T | 65 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(62): Show | 66 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1409-4552C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45631598 | ||||||
| chr3:45631610
|
G | A | 5 | a0001c0001t0053g0139a0001c0001t0083g0140a0001c0001t0084g0141others(2): Show | 5 | HG01891.hp1 HG02451.hp1 HG03098.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409-4540G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45631610 | ||||||
| chr3:45631641
|
C | G | 353 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(350): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1409-4509C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45631641 | ||||||
| chr3:45631694
|
G | A | 1 | a0001c0001t0008g0236 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1409-4456G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45631694 | ||||||
| chr3:45631821
|
G | A | 1 | a0001c0001t0002g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1409-4329G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45631821 | ||||||
| chr3:45631956
|
T | C | 1 | a0001c0001t0192g0290 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.1409-4194T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45631956 | ||||||
| chr3:45632332
|
C | T | 1 | a0001c0002t0021g0012 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1409-3818C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45632332 | ||||||
| chr3:45632335
|
A | G | 1 | a0001c0001t0012g0240 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1409-3815A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45632335 | ||||||
| chr3:45632339
|
A | T | 15 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(12): Show | 15 | HG02559.hp2 HG02809.hp1 HG02818.hp1 others(12): Show |
intron_variant | MODIFIER | c.1409-3811A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45632339 | ||||||
| chr3:45632485
|
C | G | 18 | a0001c0002t0011g0034a0001c0002t0011g0291a0001c0002t0011g0292others(15): Show | 18 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1409-3665C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45632485 | ||||||
| chr3:45632497
|
A | G | 39 | a0001c0001t0010g0050a0001c0001t0010g0066a0001c0001t0019g0284others(36): Show | 39 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1409-3653A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45632497 | ||||||
| chr3:45632783
|
T | G | 19 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(16): Show | 19 | HG01891.hp2 HG02280.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.1409-3367T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45632783 | ||||||
| chr3:45632867
|
A | G | 2 | a0001c0001t0187g0178a0001c0002t0104g0302 | 2 | HG01346.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.1409-3283A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45632867 | ||||||
| chr3:45632895
|
C | T | 39 | a0001c0001t0010g0050a0001c0001t0010g0066a0001c0001t0019g0284others(36): Show | 39 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1409-3255C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45632895 | ||||||
| chr3:45632983
|
G | A | 2 | a0001c0001t0048g0119a0001c0001t0048g0120 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1409-3167G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45632983 | ||||||
| chr3:45633129
|
G | C | 1 | a0001c0001t0184g0234 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1409-3021G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45633129 | ||||||
| chr3:45633175
|
T | A | 1 | a0001c0001t0006g0085 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1409-2975T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45633175 | ||||||
| chr3:45633196
|
C | T | 1 | a0001c0001t0166g0263 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1409-2954C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45633196 | ||||||
| chr3:45633247
|
G | A | 43 | a0001c0001t0010g0050a0001c0001t0010g0066a0001c0001t0019g0284others(40): Show | 43 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(40): Show |
intron_variant | MODIFIER | c.1409-2903G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45633247 | ||||||
| chr3:45633280
|
G | A | 18 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(15): Show | 18 | HG00609.hp1 HG01255.hp1 HG02129.hp2 others(15): Show |
intron_variant | MODIFIER | c.1409-2870G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45633280 | ||||||
| chr3:45633339
|
A | G | 4 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(1): Show | 4 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1409-2811A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45633339 | ||||||
| chr3:45633416
|
A | G | 39 | a0001c0001t0010g0050a0001c0001t0010g0066a0001c0001t0019g0284others(36): Show | 39 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1409-2734A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45633416 | ||||||
| chr3:45633559
|
C | T | 304 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(301): Show | 305 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.1409-2591C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45633559 | ||||||
| chr3:45633869
|
T | C | 1 | a0001c0005t0138g0159 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1409-2281T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45633869 | ||||||
| chr3:45633918
|
G | T | 18 | a0001c0002t0011g0034a0001c0002t0011g0291a0001c0002t0011g0292others(15): Show | 18 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(15): Show |
intron_variant | MODIFIER | c.1409-2232G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45633918 | ||||||
| chr3:45633934
|
A | G | 4 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(1): Show | 4 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.1409-2216A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45633934 | ||||||
| chr3:45634140
|
A | G | 14 | a0001c0001t0010g0051a0001c0001t0010g0052a0001c0001t0010g0053others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.1409-2010A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45634140 | ||||||
| chr3:45634189
|
A | G | 3 | a0001c0001t0001g0202a0001c0001t0012g0204a0001c0001t0202g0203 | 3 | HG02074.hp1 HG02523.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1409-1961A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45634189 | ||||||
| chr3:45634855
|
C | T | 2 | a0001c0001t0005g0166a0001c0001t0203g0254 | 2 | HG01261.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1409-1295C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45634855 | ||||||
| chr3:45634983
|
A | G | 1 | a0001c0002t0051g0306 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1409-1167A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45634983 | ||||||
| chr3:45635247
|
T | TTC | 3 | a0001c0002t0031g0332a0001c0002t0031g0333a0001c0002t0107g0334 | 3 | HG01168.hp1 HG01169.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1409-888_1409-887d others(4): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45635247 | |||||
| chr3:45635267
|
G | A | 39 | a0001c0001t0010g0050a0001c0001t0010g0066a0001c0001t0019g0284others(36): Show | 39 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1409-883G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45635267 | ||||||
| chr3:45635404
|
AG | A | 10 | a0001c0001t0032g0143a0001c0001t0032g0144a0001c0001t0053g0139others(7): Show | 10 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1409-742delG | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45635404 | |||||
| chr3:45635409
|
C | T | 10 | a0001c0001t0032g0143a0001c0001t0032g0144a0001c0001t0053g0139others(7): Show | 10 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1409-741C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45635409 | ||||||
| chr3:45635451
|
G | T | 1 | a0001c0002t0071g0313 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1409-699G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45635451 | ||||||
| chr3:45635466
|
C | G | 1 | a0001c0001t0193g0281 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.1409-684C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45635466 | ||||||
| chr3:45635655
|
T | C | 5 | a0001c0001t0032g0143a0001c0001t0032g0144a0001c0001t0109g0145others(2): Show | 5 | HG01074.hp2 HG01243.hp1 HG02818.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409-495T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45635655 | ||||||
| chr3:45635668
|
C | T | 3 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1409-482C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45635668 | ||||||
| chr3:45635673
|
G | A | 1 | a0001c0001t0064g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1409-477G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45635673 | ||||||
| chr3:45635732
|
C | CA | 21 | a0001c0001t0001g0201a0001c0001t0004g0167a0001c0001t0009g0015others(18): Show | 21 | HG01123.hp2 HG01891.hp1 HG01928.hp2 others(18): Show |
intron_variant | MODIFIER | c.1409-390dupA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45635732 | |||||
| chr3:45635732
|
C | CAA | 19 | a0001c0001t0001g0161a0001c0001t0001g0177a0001c0001t0001g0255others(16): Show | 19 | HG01069.hp1 HG01243.hp2 HG01257.hp1 others(16): Show |
intron_variant | MODIFIER | c.1409-391_1409-390d others(4): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45635732 | |||||
| chr3:45635732
|
C | CAAA | 72 | a0001c0001t0001g0045a0001c0001t0001g0162a0001c0001t0001g0171others(69): Show | 72 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.1409-392_1409-390d others(5): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45635732 | |||||
| chr3:45635732
|
C | CAAAA | 28 | a0001c0001t0001g0183a0001c0001t0001g0194a0001c0001t0001g0195others(25): Show | 28 | HG00423.hp2 HG00597.hp2 HG00621.hp2 others(25): Show |
intron_variant | MODIFIER | c.1409-393_1409-390d others(6): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45635732 | |||||
| chr3:45635732
|
CA | C | 14 | a0001c0001t0018g0057a0001c0001t0032g0143a0001c0001t0032g0144others(11): Show | 14 | HG00597.hp1 HG01074.hp2 HG01243.hp1 others(11): Show |
intron_variant | MODIFIER | c.1409-390delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45635732 | |||||
| chr3:45635732
|
CAA | C | 12 | a0001c0001t0010g0051a0001c0001t0010g0052a0001c0001t0010g0053others(9): Show | 12 | HG00438.hp2 HG02135.hp2 HG04199.hp1 others(9): Show |
intron_variant | MODIFIER | c.1409-391_1409-390d others(4): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45635732 | |||||
| chr3:45635732
|
CAAAAAA | C | 37 | a0001c0001t0010g0050a0001c0001t0010g0066a0001c0001t0019g0284others(34): Show | 37 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(34): Show |
intron_variant | MODIFIER | c.1409-395_1409-390d others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45635732 | |||||
| chr3:45635732
|
CAAAAAAA others(4): Show |
C | 1 | a0006c0013t0179g0095 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1409-400_1409-390d others(13): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45635732 | |||||
| chr3:45635732
|
CAAAAAAA others(5): Show |
C | 67 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(64): Show | 68 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.1409-401_1409-390d others(14): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45635732 | |||||
| chr3:45635732
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0197g0114 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.1409-402_1409-390d others(15): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr3 | 45635732 | |||||
| chr3:45635906
|
G | A | 117 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0002g0080others(114): Show | 118 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.1409-244G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45635906 | ||||||
| chr3:45635988
|
G | C | 5 | a0001c0001t0001g0162a0001c0001t0001g0171a0001c0001t0001g0201others(2): Show | 5 | HG02015.hp1 NA18951.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.1409-162G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45635988 | ||||||
| chr3:45635991
|
G | A | 1 | a0001c0001t0007g0058 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1409-159G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45635991 | ||||||
| chr3:45636052
|
T | A | 1 | a0001c0001t0007g0058 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1409-98T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45636052 | ||||||
| chr3:45636071
|
G | A | 4 | a0001c0001t0048g0119a0001c0001t0048g0120a0001c0005t0122g0155others(1): Show | 4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1409-79G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45636071 | ||||||
| chr3:45636072
|
C | A | 4 | a0001c0001t0048g0119a0001c0001t0048g0120a0001c0005t0122g0155others(1): Show | 4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1409-78C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45636072 | ||||||
| chr3:45636080
|
A | G | 4 | a0001c0004t0022g0349a0001c0004t0022g0350a0001c0004t0079g0352others(1): Show | 4 | HG01109.hp2 HG01168.hp2 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.1409-70A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45636080 | ||||||
| chr3:45636145
|
G | T | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
splice_region_variant&intron_variant | LOW | c.1409-5G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45636145 | ||||||
| chr3:45636146
|
C | G | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
splice_region_variant&intron_variant | LOW | c.1409-4C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45636146 | ||||||
| chr3:45636147
|
A | C | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
splice_region_variant&intron_variant | LOW | c.1409-3A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 1/7 | chr3 | 45636147 | ||||||
| chr3:45636290
|
G | A | 67 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(64): Show | 68 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.1510+39G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45636290 | ||||||
| chr3:45636323
|
G | GAGA | 111 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(108): Show | 112 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.1510+73_1510+75dup others(3): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45636323 | |||||
| chr3:45636437
|
G | A | 5 | a0001c0001t0069g0134a0001c0001t0076g0132a0001c0001t0086g0131others(2): Show | 5 | HG02055.hp1 HG02976.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.1510+186G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45636437 | ||||||
| chr3:45636470
|
A | G | 42 | a0001c0001t0010g0050a0001c0001t0010g0066a0001c0001t0019g0284others(39): Show | 42 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(39): Show |
intron_variant | MODIFIER | c.1510+219A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45636470 | ||||||
| chr3:45636499
|
G | T | 1 | a0001c0001t0007g0058 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1510+248G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45636499 | ||||||
| chr3:45636509
|
A | T | 2 | a0001c0001t0039g0016a0001c0001t0039g0020 | 2 | NA18522.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.1510+258A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45636509 | ||||||
| chr3:45636538
|
A | T | 2 | a0001c0002t0110g0342a0007c0009t0095g0354 | 2 | HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1510+287A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45636538 | ||||||
| chr3:45636833
|
C | T | 14 | a0001c0001t0010g0051a0001c0001t0010g0052a0001c0001t0010g0053others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.1510+582C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45636833 | ||||||
| chr3:45636936
|
G | C | 1 | a0001c0001t0006g0085 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1510+685G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45636936 | ||||||
| chr3:45637238
|
C | G | 2 | a0001c0001t0074g0135a0001c0001t0195g0136 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1510+987C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45637238 | ||||||
| chr3:45637280
|
T | A | 1 | a0001c0001t0007g0058 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1510+1029T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45637280 | ||||||
| chr3:45637282
|
A | AT | 261 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(258): Show | 262 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(259): Show |
intron_variant | MODIFIER | c.1510+1047dupT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45637282 | |||||
| chr3:45637282
|
A | ATT | 33 | a0001c0001t0001g0195a0001c0001t0010g0051a0001c0001t0010g0053others(30): Show | 33 | HG00423.hp2 HG00438.hp2 HG00597.hp1 others(30): Show |
intron_variant | MODIFIER | c.1510+1046_1510+104 others(6): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45637282 | |||||
| chr3:45637282
|
A | T | 1 | a0001c0001t0007g0058 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1510+1031A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45637282 | ||||||
| chr3:45637282
|
AT | A | 6 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(3): Show | 6 | HG01169.hp2 HG01433.hp1 HG01516.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510+1047delT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45637282 | |||||
| chr3:45637437
|
C | A | 11 | a0001c0001t0046g0017a0001c0001t0046g0019a0001c0002t0011g0034others(8): Show | 11 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.1510+1186C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45637437 | ||||||
| chr3:45637473
|
G | A | 14 | a0001c0001t0010g0051a0001c0001t0010g0052a0001c0001t0010g0053others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.1510+1222G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45637473 | ||||||
| chr3:45637489
|
C | T | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+1238C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45637489 | ||||||
| chr3:45637530
|
C | T | 9 | a0001c0001t0076g0132a0001c0001t0086g0131a0001c0001t0111g0133others(6): Show | 9 | HG01243.hp2 HG02055.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1510+1279C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45637530 | ||||||
| chr3:45637571
|
G | A | 3 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1510+1320G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45637571 | ||||||
| chr3:45637702
|
G | A | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+1451G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45637702 | ||||||
| chr3:45637748
|
AT | A | 110 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(107): Show | 111 | HG00140.hp2 HG00323.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1510+1499delT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45637748 | |||||
| chr3:45637819
|
T | C | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+1568T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45637819 | ||||||
| chr3:45637839
|
G | C | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+1588G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45637839 | ||||||
| chr3:45637844
|
A | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+1593A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45637844 | ||||||
| chr3:45637857
|
G | T | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+1606G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45637857 | ||||||
| chr3:45637877
|
T | C | 3 | a0001c0001t0001g0227a0001c0001t0005g0219a0001c0001t0163g0191 | 3 | HG00673.hp2 HG02132.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.1510+1626T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45637877 | ||||||
| chr3:45637909
|
A | T | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+1658A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45637909 | ||||||
| chr3:45638027
|
A | AAC | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+1776_1510+177 others(6): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45638027 | ||||||
| chr3:45638028
|
C | A | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+1777C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45638028 | ||||||
| chr3:45638033
|
C | CA | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+1783dupA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45638033 | |||||
| chr3:45638065
|
T | TG | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+1815dupG | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45638065 | |||||
| chr3:45638121
|
T | A | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+1870T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45638121 | ||||||
| chr3:45638173
|
C | A | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+1922C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45638173 | ||||||
| chr3:45638178
|
A | T | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+1927A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45638178 | ||||||
| chr3:45638179
|
AC | A | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+1931delC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45638179 | |||||
| chr3:45638185
|
T | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+1934T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45638185 | ||||||
| chr3:45638186
|
A | T | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+1935A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45638186 | ||||||
| chr3:45638274
|
CTTTA | C | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+2036_1510+203 others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45638274 | |||||
| chr3:45638291
|
G | T | 4 | a0001c0001t0076g0132a0001c0001t0086g0131a0001c0001t0111g0133others(1): Show | 4 | HG02055.hp1 HG02976.hp1 HG03225.hp1 others(1): Show |
intron_variant | MODIFIER | c.1510+2040G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45638291 | ||||||
| chr3:45638399
|
A | C | 3 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1510+2148A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45638399 | ||||||
| chr3:45638469
|
G | A | 4 | a0001c0001t0082g0137a0001c0001t0140g0267a0001c0003t0137g0154others(1): Show | 4 | HG02615.hp2 HG02647.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1510+2218G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45638469 | ||||||
| chr3:45638487
|
C | T | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+2236C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45638487 | ||||||
| chr3:45638767
|
T | C | 304 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(301): Show | 305 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.1510+2516T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45638767 | ||||||
| chr3:45639037
|
G | T | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+2786G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45639037 | ||||||
| chr3:45639089
|
T | C | 71 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(68): Show | 72 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1510+2838T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45639089 | ||||||
| chr3:45639200
|
C | T | 11 | a0001c0001t0032g0143a0001c0001t0032g0144a0001c0001t0053g0139others(8): Show | 11 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1510+2949C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45639200 | ||||||
| chr3:45639308
|
G | A | 14 | a0001c0001t0010g0051a0001c0001t0010g0052a0001c0001t0010g0053others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.1510+3057G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45639308 | ||||||
| chr3:45639379
|
C | T | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+3128C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45639379 | ||||||
| chr3:45639414
|
C | G | 4 | a0001c0001t0082g0137a0001c0001t0140g0267a0001c0003t0137g0154others(1): Show | 4 | HG02615.hp2 HG02647.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1510+3163C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45639414 | ||||||
| chr3:45639431
|
A | C | 3 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1510+3180A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45639431 | ||||||
| chr3:45639472
|
A | C | 1 | a0001c0001t0018g0057 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.1510+3221A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45639472 | ||||||
| chr3:45639488
|
G | T | 1 | a0001c0005t0138g0159 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1510+3237G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45639488 | ||||||
| chr3:45639532
|
C | T | 3 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1510+3281C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45639532 | ||||||
| chr3:45639596
|
C | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+3345C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45639596 | ||||||
| chr3:45639597
|
G | A | 4 | a0001c0001t0048g0119a0001c0001t0048g0120a0001c0005t0122g0155others(1): Show | 4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1510+3346G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45639597 | ||||||
| chr3:45639609
|
G | A | 1 | a0001c0001t0006g0251 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.1510+3358G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45639609 | ||||||
| chr3:45639645
|
G | A | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+3394G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45639645 | ||||||
| chr3:45640093
|
T | C | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+3842T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45640093 | ||||||
| chr3:45640200
|
C | T | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+3949C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45640200 | ||||||
| chr3:45640282
|
C | G | 1 | a0001c0005t0128g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1510+4031C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45640282 | ||||||
| chr3:45640416
|
T | TTTG | 4 | a0001c0001t0056g0047a0001c0001t0134g0277a0001c0001t0149g0048others(1): Show | 4 | HG02155.hp1 NA18945.hp1 NA18952.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510+4180_1510+418 others(7): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45640416 | |||||
| chr3:45640419
|
G | T | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+4168G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45640419 | ||||||
| chr3:45640611
|
G | A | 3 | a0001c0001t0001g0238a0001c0001t0005g0237a0001c0001t0175g0245 | 3 | NA18991.hp1 NA18998.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1510+4360G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45640611 | ||||||
| chr3:45640634
|
T | C | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+4383T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45640634 | ||||||
| chr3:45640711
|
T | C | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+4460T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45640711 | ||||||
| chr3:45640722
|
T | G | 304 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(301): Show | 305 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.1510+4471T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45640722 | ||||||
| chr3:45640738
|
T | A | 1 | a0001c0001t0196g0165 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.1510+4487T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45640738 | ||||||
| chr3:45640752
|
T | C | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+4501T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45640752 | ||||||
| chr3:45640761
|
T | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+4510T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45640761 | ||||||
| chr3:45640778
|
A | G | 2 | a0001c0001t0074g0135a0001c0001t0195g0136 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1510+4527A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45640778 | ||||||
| chr3:45640914
|
G | C | 304 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(301): Show | 305 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.1510+4663G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45640914 | ||||||
| chr3:45641048
|
G | A | 1 | a0001c0001t0083g0140 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1510+4797G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45641048 | ||||||
| chr3:45641193
|
G | A | 71 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(68): Show | 72 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1510+4942G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45641193 | ||||||
| chr3:45641194
|
A | AAG | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+4945_1510+494 others(6): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45641194 | |||||
| chr3:45641235
|
T | C | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+4984T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45641235 | ||||||
| chr3:45641405
|
C | T | 71 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(68): Show | 72 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1510+5154C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45641405 | ||||||
| chr3:45641439
|
A | T | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+5188A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45641439 | ||||||
| chr3:45641493
|
A | C | 2 | a0001c0002t0120g0028a0001c0002t0131g0027 | 2 | HG02145.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.1510+5242A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45641493 | ||||||
| chr3:45641498
|
A | T | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+5247A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45641498 | ||||||
| chr3:45641501
|
A | T | 140 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(137): Show | 140 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(137): Show |
intron_variant | MODIFIER | c.1510+5250A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45641501 | ||||||
| chr3:45641536
|
A | G | 3 | a0001c0001t0001g0202a0001c0001t0012g0204a0001c0001t0202g0203 | 3 | HG02074.hp1 HG02523.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1510+5285A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45641536 | ||||||
| chr3:45641615
|
G | A | 349 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(346): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.1510+5364G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45641615 | ||||||
| chr3:45641638
|
A | T | 1 | a0001c0001t0002g0106 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.1510+5387A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45641638 | ||||||
| chr3:45641677
|
G | C | 9 | a0001c0001t0076g0132a0001c0001t0086g0131a0001c0001t0111g0133others(6): Show | 9 | HG01243.hp2 HG02055.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1510+5426G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45641677 | ||||||
| chr3:45641714
|
T | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+5463T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45641714 | ||||||
| chr3:45641832
|
T | C | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+5581T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45641832 | ||||||
| chr3:45641871
|
G | A | 66 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(63): Show | 67 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1510+5620G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45641871 | ||||||
| chr3:45641916
|
T | C | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+5665T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45641916 | ||||||
| chr3:45642189
|
T | C | 40 | a0001c0001t0010g0050a0001c0001t0010g0066a0001c0001t0019g0284others(37): Show | 40 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(37): Show |
intron_variant | MODIFIER | c.1510+5938T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45642189 | ||||||
| chr3:45642330
|
C | A | 1 | a0001c0002t0124g0041 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1510+6079C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45642330 | ||||||
| chr3:45642377
|
A | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+6126A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45642377 | ||||||
| chr3:45642554
|
C | T | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+6303C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45642554 | ||||||
| chr3:45642561
|
G | T | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+6310G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45642561 | ||||||
| chr3:45642567
|
C | T | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+6316C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45642567 | ||||||
| chr3:45642691
|
T | C | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+6440T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45642691 | ||||||
| chr3:45643039
|
A | T | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+6788A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45643039 | ||||||
| chr3:45643156
|
C | T | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+6905C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45643156 | ||||||
| chr3:45643201
|
G | A | 4 | a0001c0001t0048g0119a0001c0001t0048g0120a0001c0005t0122g0155others(1): Show | 4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1510+6950G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45643201 | ||||||
| chr3:45643212
|
G | A | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+6961G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45643212 | ||||||
| chr3:45643298
|
A | C | 1 | a0001c0001t0106g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1510+7047A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45643298 | ||||||
| chr3:45643300
|
T | C | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+7049T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45643300 | ||||||
| chr3:45643414
|
G | A | 1 | a0001c0002t0011g0291 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1510+7163G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45643414 | ||||||
| chr3:45643463
|
C | T | 66 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(63): Show | 67 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1510+7212C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45643463 | ||||||
| chr3:45643480
|
G | A | 1 | a0001c0001t0145g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1510+7229G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45643480 | ||||||
| chr3:45643484
|
CA | C | 6 | a0001c0001t0012g0204a0001c0001t0019g0287a0001c0001t0164g0274others(3): Show | 6 | HG01346.hp1 HG01361.hp1 HG02523.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510+7247delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45643484 | |||||
| chr3:45643584
|
C | G | 1 | a0001c0001t0019g0287 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1510+7333C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45643584 | ||||||
| chr3:45643693
|
C | T | 2 | a0001c0002t0020g0309a0001c0002t0070g0308 | 2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1510+7442C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45643693 | ||||||
| chr3:45643756
|
A | G | 3 | a0001c0001t0068g0128a0001c0001t0075g0130a0001c0001t0078g0129 | 3 | HG02630.hp1 HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1510+7505A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45643756 | ||||||
| chr3:45643758
|
A | G | 1 | a0001c0001t0019g0287 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.1510+7507A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45643758 | ||||||
| chr3:45643788
|
C | T | 14 | a0001c0001t0010g0051a0001c0001t0010g0052a0001c0001t0010g0053others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.1510+7537C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45643788 | ||||||
| chr3:45643795
|
A | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+7544A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45643795 | ||||||
| chr3:45643844
|
A | G | 353 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(350): Show | 354 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(351): Show |
intron_variant | MODIFIER | c.1510+7593A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45643844 | ||||||
| chr3:45643894
|
G | A | 304 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(301): Show | 305 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.1510+7643G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45643894 | ||||||
| chr3:45643902
|
C | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+7651C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45643902 | ||||||
| chr3:45643947
|
GA | G | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+7702delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45643947 | |||||
| chr3:45644012
|
G | C | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+7761G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45644012 | ||||||
| chr3:45644022
|
A | C | 50 | a0001c0001t0010g0050a0001c0001t0010g0066a0001c0001t0019g0284others(47): Show | 50 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1510+7771A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45644022 | ||||||
| chr3:45644023
|
C | T | 304 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(301): Show | 305 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.1510+7772C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45644023 | ||||||
| chr3:45644157
|
G | A | 28 | a0001c0001t0157g0247a0001c0001t0171g0193a0001c0001t0199g0072others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1510+7906G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45644157 | ||||||
| chr3:45644200
|
A | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+7949A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45644200 | ||||||
| chr3:45644233
|
C | T | 3 | a0001c0002t0031g0332a0001c0002t0031g0333a0001c0002t0107g0334 | 3 | HG01168.hp1 HG01169.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1510+7982C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45644233 | ||||||
| chr3:45644256
|
C | A | 50 | a0001c0001t0010g0050a0001c0001t0010g0066a0001c0001t0019g0284others(47): Show | 50 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1510+8005C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45644256 | ||||||
| chr3:45644286
|
T | C | 2 | a0001c0005t0122g0155a0001c0005t0139g0156 | 2 | HG02451.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.1510+8035T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45644286 | ||||||
| chr3:45644347
|
C | A | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+8096C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45644347 | ||||||
| chr3:45644526
|
C | T | 1 | a0001c0005t0128g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1510+8275C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45644526 | ||||||
| chr3:45644553
|
G | A | 1 | a0001c0005t0128g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1510+8302G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45644553 | ||||||
| chr3:45644577
|
A | G | 1 | a0001c0001t0157g0247 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1510+8326A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45644577 | ||||||
| chr3:45644632
|
G | A | 1 | a0001c0001t0161g0208 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1510+8381G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45644632 | ||||||
| chr3:45644786
|
A | AC | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+8536dupC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45644786 | |||||
| chr3:45644978
|
G | A | 1 | a0001c0008t0002g0107 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1510+8727G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45644978 | ||||||
| chr3:45645110
|
A | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+8859A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45645110 | ||||||
| chr3:45645167
|
C | T | 139 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(136): Show | 139 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(136): Show |
intron_variant | MODIFIER | c.1510+8916C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45645167 | ||||||
| chr3:45645338
|
G | T | 1 | a0001c0001t0069g0134 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1510+9087G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45645338 | ||||||
| chr3:45645562
|
G | C | 71 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(68): Show | 72 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1510+9311G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45645562 | ||||||
| chr3:45645562
|
G | T | 233 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(230): Show | 233 | HG00099.hp2 HG00423.hp1 HG00423.hp2 others(230): Show |
intron_variant | MODIFIER | c.1510+9311G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45645562 | ||||||
| chr3:45645591
|
C | T | 1 | a0001c0001t0064g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1510+9340C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45645591 | ||||||
| chr3:45645823
|
A | C | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+9572A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45645823 | ||||||
| chr3:45645870
|
A | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+9619A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45645870 | ||||||
| chr3:45645949
|
G | A | 1 | a0001c0005t0128g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1510+9698G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45645949 | ||||||
| chr3:45645970
|
C | T | 120 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(117): Show | 120 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(117): Show |
intron_variant | MODIFIER | c.1510+9719C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45645970 | ||||||
| chr3:45646029
|
C | CA | 22 | a0001c0001t0001g0202a0001c0001t0004g0233a0001c0001t0005g0166others(19): Show | 22 | HG00597.hp1 HG01074.hp2 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.1510+9796dupA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45646029 | |||||
| chr3:45646029
|
CA | C | 67 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(64): Show | 68 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(65): Show |
intron_variant | MODIFIER | c.1510+9796delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45646029 | |||||
| chr3:45646045
|
A | C | 65 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(62): Show | 66 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1510+9794A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45646045 | ||||||
| chr3:45646081
|
G | A | 304 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(301): Show | 305 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.1510+9830G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45646081 | ||||||
| chr3:45646117
|
A | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+9866A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45646117 | ||||||
| chr3:45646153
|
C | A | 1 | a0001c0001t0178g0086 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1510+9902C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45646153 | ||||||
| chr3:45646225
|
G | C | 1 | a0001c0001t0064g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1510+9974G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45646225 | ||||||
| chr3:45646261
|
G | A | 1 | a0001c0001t0064g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1510+10010G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45646261 | ||||||
| chr3:45646325
|
C | T | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+10074C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45646325 | ||||||
| chr3:45646486
|
C | T | 1 | a0001c0002t0024g0294 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.1510+10235C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45646486 | ||||||
| chr3:45646515
|
A | G | 2 | a0001c0001t0175g0245a0001c0002t0055g0331 | 2 | NA19000.hp1 NA19009.hp2 |
intron_variant | MODIFIER | c.1510+10264A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45646515 | ||||||
| chr3:45646537
|
C | T | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+10286C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45646537 | ||||||
| chr3:45646566
|
G | T | 1 | a0001c0001t0018g0054 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1510+10315G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45646566 | ||||||
| chr3:45646640
|
C | T | 1 | a0001c0001t0084g0141 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1510+10389C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45646640 | ||||||
| chr3:45646691
|
C | CT | 16 | a0001c0001t0002g0105a0001c0001t0005g0005a0001c0001t0010g0051others(13): Show | 16 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(13): Show |
intron_variant | MODIFIER | c.1510+10456dupT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45646691 | |||||
| chr3:45646707
|
T | TG | 39 | a0001c0001t0010g0050a0001c0001t0010g0066a0001c0001t0019g0284others(36): Show | 39 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1510+10457dupG | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45646707 | |||||
| chr3:45646767
|
A | C | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+10516A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45646767 | ||||||
| chr3:45646809
|
C | G | 51 | a0001c0001t0010g0050a0001c0001t0010g0066a0001c0001t0019g0284others(48): Show | 51 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(48): Show |
intron_variant | MODIFIER | c.1510+10558C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45646809 | ||||||
| chr3:45646827
|
T | A | 66 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(63): Show | 67 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(64): Show |
intron_variant | MODIFIER | c.1510+10576T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45646827 | ||||||
| chr3:45646866
|
A | G | 1 | a0001c0005t0128g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1510+10615A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45646866 | ||||||
| chr3:45647269
|
G | A | 1 | a0001c0001t0074g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1510+11018G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45647269 | ||||||
| chr3:45647316
|
C | A | 2 | a0001c0001t0019g0284a0001c0001t0150g0285 | 2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1510+11065C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45647316 | ||||||
| chr3:45647343
|
C | T | 1 | a0001c0001t0074g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1510+11092C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45647343 | ||||||
| chr3:45647394
|
A | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+11143A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45647394 | ||||||
| chr3:45647444
|
C | T | 9 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(6): Show | 9 | HG02559.hp2 HG02809.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.1510+11193C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45647444 | ||||||
| chr3:45647462
|
C | T | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+11211C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45647462 | ||||||
| chr3:45647473
|
A | G | 2 | a0001c0002t0110g0342a0007c0009t0095g0354 | 2 | HG02970.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.1510+11222A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45647473 | ||||||
| chr3:45647541
|
C | A | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+11290C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45647541 | ||||||
| chr3:45647638
|
A | T | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+11387A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45647638 | ||||||
| chr3:45647820
|
C | T | 9 | a0001c0001t0076g0132a0001c0001t0086g0131a0001c0001t0111g0133others(6): Show | 9 | HG01243.hp2 HG02055.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1510+11569C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45647820 | ||||||
| chr3:45647900
|
TA | T | 13 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(10): Show | 13 | HG02451.hp2 HG02559.hp2 HG02630.hp2 others(10): Show |
intron_variant | MODIFIER | c.1510+11650delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45647900 | ||||||
| chr3:45647955
|
G | T | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+11704G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45647955 | ||||||
| chr3:45647963
|
C | A | 6 | a0001c0001t0001g0079a0001c0001t0001g0094a0001c0001t0185g0100others(3): Show | 6 | NA18747.hp1 NA18944.hp2 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.1510+11712C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45647963 | ||||||
| chr3:45647968
|
C | T | 1 | a0001c0002t0054g0330 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.1510+11717C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45647968 | ||||||
| chr3:45647981
|
T | G | 71 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(68): Show | 72 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(69): Show |
intron_variant | MODIFIER | c.1510+11730T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45647981 | ||||||
| chr3:45648011
|
C | CTT | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+11760_1510+11 others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45648011 | ||||||
| chr3:45648012
|
C | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+11761C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45648012 | ||||||
| chr3:45648103
|
GA | G | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+11857delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45648103 | |||||
| chr3:45648106
|
A | G | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+11855A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45648106 | ||||||
| chr3:45648356
|
T | C | 1 | a0001c0002t0025g0321 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1510+12105T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45648356 | ||||||
| chr3:45648404
|
A | T | 9 | a0001c0001t0019g0284a0001c0001t0038g0264a0001c0001t0040g0269others(6): Show | 9 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(6): Show |
intron_variant | MODIFIER | c.1510+12153A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45648404 | ||||||
| chr3:45648730
|
C | T | 65 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(62): Show | 66 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1510+12479C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45648730 | ||||||
| chr3:45648794
|
TG | T | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1510+12546delG | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45648794 | |||||
| chr3:45648923
|
T | C | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+12672T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45648923 | ||||||
| chr3:45648954
|
A | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+12703A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45648954 | ||||||
| chr3:45648998
|
C | T | 50 | a0001c0001t0010g0050a0001c0001t0010g0066a0001c0001t0019g0284others(47): Show | 50 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(47): Show |
intron_variant | MODIFIER | c.1510+12747C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45648998 | ||||||
| chr3:45648999
|
A | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+12748A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45648999 | ||||||
| chr3:45649111
|
T | A | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+12860T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649111 | ||||||
| chr3:45649241
|
T | C | 2 | a0001c0001t0074g0135a0001c0001t0195g0136 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1510+12990T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649241 | ||||||
| chr3:45649355
|
G | A | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+13104G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649355 | ||||||
| chr3:45649456
|
C | A | 65 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(62): Show | 66 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1510+13205C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649456 | ||||||
| chr3:45649484
|
A | G | 1 | a0001c0002t0127g0122 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1510+13233A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649484 | ||||||
| chr3:45649490
|
A | T | 1 | a0001c0001t0091g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1510+13239A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649490 | ||||||
| chr3:45649604
|
G | A | 1 | a0001c0001t0168g0273 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1510+13353G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649604 | ||||||
| chr3:45649680
|
CA | C | 14 | a0001c0001t0001g0161a0001c0001t0049g0084a0001c0001t0049g0088others(11): Show | 14 | HG01243.hp2 HG01257.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1510+13442delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45649680 | |||||
| chr3:45649703
|
TGTATAC | T | 10 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(7): Show | 10 | HG02559.hp2 HG02809.hp1 HG02818.hp1 others(7): Show |
intron_variant | MODIFIER | c.1510+13453_1510+13 others(12): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649703 | ||||||
| chr3:45649704
|
G | A | 68 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(65): Show | 69 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(66): Show |
intron_variant | MODIFIER | c.1510+13453G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649704 | ||||||
| chr3:45649707
|
T | C | 63 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(60): Show | 64 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(61): Show |
intron_variant | MODIFIER | c.1510+13456T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649707 | ||||||
| chr3:45649709
|
C | CAT | 77 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(74): Show | 78 | HG00140.hp2 HG00323.hp1 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.1510+13470_1510+13 others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45649709 | |||||
| chr3:45649709
|
C | T | 3 | a0001c0001t0003g0074a0001c0001t0075g0130a0001c0002t0124g0041 | 3 | HG02486.hp2 NA19068.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1510+13458C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649709 | ||||||
| chr3:45649709
|
CATAT | C | 3 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1510+13468_1510+13 others(10): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45649709 | |||||
| chr3:45649715
|
T | C | 14 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(11): Show | 14 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.1510+13464T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649715 | ||||||
| chr3:45649723
|
A | C | 1 | a0001c0001t0017g0089 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.1510+13472A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649723 | ||||||
| chr3:45649723
|
A | T | 9 | a0001c0001t0076g0132a0001c0001t0086g0131a0001c0001t0111g0133others(6): Show | 9 | HG01243.hp2 HG02055.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1510+13472A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649723 | ||||||
| chr3:45649740
|
T | A | 1 | a0001c0001t0075g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1510+13489T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649740 | ||||||
| chr3:45649741
|
T | A | 1 | a0001c0001t0075g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1510+13490T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649741 | ||||||
| chr3:45649749
|
A | G | 1 | a0001c0001t0075g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1510+13498A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649749 | ||||||
| chr3:45649750
|
T | A | 1 | a0001c0001t0075g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1510+13499T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649750 | ||||||
| chr3:45649759
|
T | A | 1 | a0001c0001t0075g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1510+13508T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649759 | ||||||
| chr3:45649762
|
T | A | 1 | a0001c0001t0153g0270 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1510+13511T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649762 | ||||||
| chr3:45649764
|
T | C | 20 | a0001c0001t0046g0017a0001c0001t0046g0019a0001c0002t0011g0034others(17): Show | 20 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1510+13513T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649764 | ||||||
| chr3:45649765
|
A | T | 1 | a0001c0001t0075g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1510+13514A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649765 | ||||||
| chr3:45649770
|
A | T | 1 | a0001c0001t0075g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1510+13519A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649770 | ||||||
| chr3:45649771
|
T | A | 1 | a0001c0001t0075g0130 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1510+13520T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649771 | ||||||
| chr3:45649777
|
A | G | 29 | a0001c0001t0046g0017a0001c0001t0046g0019a0001c0001t0076g0132others(26): Show | 29 | HG01167.hp2 HG01169.hp1 HG01243.hp2 others(26): Show |
intron_variant | MODIFIER | c.1510+13526A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649777 | ||||||
| chr3:45649818
|
A | G | 2 | a0001c0001t0012g0204a0001c0001t0202g0203 | 2 | HG02523.hp2 NA18964.hp1 |
intron_variant | MODIFIER | c.1510+13567A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649818 | ||||||
| chr3:45649840
|
G | GT | 11 | a0001c0001t0032g0143a0001c0001t0032g0144a0001c0001t0053g0139others(8): Show | 11 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1510+13596dupT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45649840 | |||||
| chr3:45649847
|
T | G | 1 | a0002c0006t0146g0163 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1510+13596T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649847 | ||||||
| chr3:45649848
|
G | GT | 211 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(208): Show | 211 | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(208): Show |
intron_variant | MODIFIER | c.1510+13611dupT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45649848 | |||||
| chr3:45649848
|
G | GTT | 15 | a0001c0001t0001g0209a0001c0001t0001g0217a0001c0001t0015g0261others(12): Show | 15 | HG00438.hp1 HG01433.hp1 HG01516.hp2 others(12): Show |
intron_variant | MODIFIER | c.1510+13610_1510+13 others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45649848 | |||||
| chr3:45649848
|
G | T | 12 | a0001c0001t0032g0143a0001c0001t0032g0144a0001c0001t0053g0139others(9): Show | 12 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1510+13597G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649848 | ||||||
| chr3:45649871
|
C | A | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+13620C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649871 | ||||||
| chr3:45649886
|
T | A | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+13635T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45649886 | ||||||
| chr3:45650101
|
C | A | 28 | a0001c0001t0157g0247a0001c0001t0171g0193a0001c0001t0199g0072others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1510+13850C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45650101 | ||||||
| chr3:45650187
|
C | A | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+13936C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45650187 | ||||||
| chr3:45650244
|
T | C | 4 | a0001c0001t0001g0162a0001c0001t0001g0171a0001c0001t0001g0206others(1): Show | 4 | NA18951.hp1 NA19000.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.1510+13993T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45650244 | ||||||
| chr3:45650367
|
G | A | 1 | a0001c0003t0142g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1510+14116G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45650367 | ||||||
| chr3:45650377
|
T | G | 1 | a0001c0002t0024g0296 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.1510+14126T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45650377 | ||||||
| chr3:45650427
|
A | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+14176A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45650427 | ||||||
| chr3:45650438
|
A | C | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+14187A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45650438 | ||||||
| chr3:45650494
|
A | AC | 20 | a0001c0001t0001g0173a0001c0001t0005g0219a0001c0001t0012g0240others(17): Show | 20 | HG00597.hp1 HG00597.hp2 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.1510+14251dupC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45650494 | |||||
| chr3:45650514
|
G | A | 65 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(62): Show | 66 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1510+14263G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45650514 | ||||||
| chr3:45650541
|
C | T | 3 | a0001c0001t0043g0104a0001c0002t0020g0340a0001c0002t0065g0341 | 3 | HG01106.hp1 HG01258.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.1510+14290C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45650541 | ||||||
| chr3:45650584
|
G | A | 2 | a0001c0001t0045g0214a0001c0001t0045g0253 | 2 | HG00733.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1510+14333G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45650584 | ||||||
| chr3:45650660
|
C | T | 14 | a0001c0001t0010g0051a0001c0001t0010g0052a0001c0001t0010g0053others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(11): Show |
intron_variant | MODIFIER | c.1510+14409C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45650660 | ||||||
| chr3:45650709
|
T | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+14458T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45650709 | ||||||
| chr3:45650795
|
A | G | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+14544A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45650795 | ||||||
| chr3:45650806
|
G | A | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+14555G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45650806 | ||||||
| chr3:45650819
|
G | A | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+14568G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45650819 | ||||||
| chr3:45650913
|
G | A | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1510+14662G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45650913 | ||||||
| chr3:45651000
|
T | TGTTTCCT others(312): Show |
1 | a0001c0001t0074g0135 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1511-14635_1511-14 others(325): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45651000 | |||||
| chr3:45651000
|
T | TGTTTCCT others(318): Show |
2 | a0001c0002t0071g0313a0001c0002t0112g0304 | 2 | HG00733.hp1 HG01069.hp2 |
intron_variant | MODIFIER | c.1511-14635_1511-14 others(331): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45651000 | |||||
| chr3:45651000
|
T | TGTTTCCT others(324): Show |
1 | a0001c0001t0096g0138 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1511-14635_1511-14 others(337): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45651000 | |||||
| chr3:45651000
|
T | TGTTTCCT others(325): Show |
1 | a0001c0001t0195g0136 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1511-14635_1511-14 others(338): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45651000 | |||||
| chr3:45651000
|
T | TGTTTCCT others(325): Show |
2 | a0001c0001t0053g0139a0001c0001t0083g0140 | 2 | HG01891.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.1511-14635_1511-14 others(338): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45651000 | |||||
| chr3:45651000
|
T | TGTTTCCT others(326): Show |
2 | a0001c0001t0069g0134a0001c0001t0084g0141 | 2 | HG03098.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1511-14635_1511-14 others(339): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45651000 | |||||
| chr3:45651000
|
T | TGTTTCCT others(329): Show |
8 | a0001c0001t0010g0066a0001c0001t0041g0276a0001c0001t0044g0098others(5): Show | 8 | HG01257.hp2 HG02074.hp2 HG02735.hp2 others(5): Show |
intron_variant | MODIFIER | c.1511-14635_1511-14 others(342): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45651000 | |||||
| chr3:45651000
|
T | TGTTTCCT others(330): Show |
23 | a0001c0001t0019g0284a0001c0001t0019g0287a0001c0001t0038g0264others(20): Show | 23 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1511-14635_1511-14 others(343): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45651000 | |||||
| chr3:45651000
|
T | TGTTTCCT others(330): Show |
1 | a0001c0001t0058g0147 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1511-14635_1511-14 others(343): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45651000 | |||||
| chr3:45651000
|
T | TGTTTCCT others(331): Show |
2 | a0001c0001t0041g0272a0001c0002t0101g0300 | 2 | HG01361.hp2 NA18940.hp1 |
intron_variant | MODIFIER | c.1511-14635_1511-14 others(344): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45651000 | |||||
| chr3:45651000
|
T | TGTTTCCT others(331): Show |
3 | a0001c0001t0032g0143a0001c0001t0032g0144a0001c0001t0109g0145 | 3 | HG01074.hp2 HG02965.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.1511-14635_1511-14 others(344): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45651000 | |||||
| chr3:45651000
|
T | TGTTTCCT others(332): Show |
2 | a0001c0001t0143g0265a0001c0001t0170g0282 | 2 | HG03831.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.1511-14635_1511-14 others(345): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45651000 | |||||
| chr3:45651000
|
T | TGTTTCCT others(332): Show |
1 | a0001c0001t0116g0146 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1511-14635_1511-14 others(345): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45651000 | |||||
| chr3:45651000
|
T | TGTTTCCT others(333): Show |
1 | a0001c0001t0010g0050 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1511-14635_1511-14 others(346): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45651000 | |||||
| chr3:45651000
|
T | TGTTTCCT others(337): Show |
1 | a0001c0001t0198g0121 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1511-14635_1511-14 others(350): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45651000 | |||||
| chr3:45651023
|
G | A | 1 | a0001c0001t0091g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1511-14627G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45651023 | ||||||
| chr3:45651059
|
G | C | 1 | a0001c0004t0079g0352 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1511-14591G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45651059 | ||||||
| chr3:45651170
|
T | G | 1 | a0001c0005t0122g0155 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1511-14480T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45651170 | ||||||
| chr3:45651200
|
T | C | 3 | a0001c0001t0001g0194a0001c0001t0001g0205a0001c0001t0012g0240 | 3 | HG02165.hp2 NA18988.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1511-14450T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45651200 | ||||||
| chr3:45651327
|
CT | C | 119 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(116): Show | 119 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(116): Show |
intron_variant | MODIFIER | c.1511-14320delT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45651327 | |||||
| chr3:45651399
|
G | A | 126 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(123): Show | 126 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1511-14251G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45651399 | ||||||
| chr3:45651409
|
G | A | 304 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(301): Show | 305 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(302): Show |
intron_variant | MODIFIER | c.1511-14241G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45651409 | ||||||
| chr3:45651413
|
G | T | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1511-14237G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45651413 | ||||||
| chr3:45651571
|
C | T | 5 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(2): Show | 5 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(2): Show |
intron_variant | MODIFIER | c.1511-14079C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45651571 | ||||||
| chr3:45651638
|
A | T | 126 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(123): Show | 126 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1511-14012A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45651638 | ||||||
| chr3:45651785
|
A | AC | 9 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(6): Show | 9 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1511-13864dupC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45651785 | |||||
| chr3:45651834
|
G | A | 126 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(123): Show | 126 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1511-13816G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45651834 | ||||||
| chr3:45651839
|
C | T | 1 | a0001c0001t0050g0060 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1511-13811C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45651839 | ||||||
| chr3:45651878
|
T | C | 9 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(6): Show | 9 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1511-13772T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45651878 | ||||||
| chr3:45651884
|
G | A | 9 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(6): Show | 9 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1511-13766G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45651884 | ||||||
| chr3:45651907
|
T | C | 9 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(6): Show | 9 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1511-13743T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45651907 | ||||||
| chr3:45651927
|
C | T | 9 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(6): Show | 9 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1511-13723C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45651927 | ||||||
| chr3:45651927
|
CG | C | 65 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(62): Show | 66 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(63): Show |
intron_variant | MODIFIER | c.1511-13721delG | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45651927 | |||||
| chr3:45652013
|
G | A | 1 | a0001c0005t0128g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1511-13637G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45652013 | ||||||
| chr3:45652029
|
C | T | 1 | a0001c0002t0030g0326 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1511-13621C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45652029 | ||||||
| chr3:45652127
|
A | G | 1 | a0001c0003t0121g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1511-13523A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45652127 | ||||||
| chr3:45652148
|
A | G | 9 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(6): Show | 9 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1511-13502A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45652148 | ||||||
| chr3:45652167
|
T | TA | 9 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(6): Show | 9 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1511-13482dupA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45652167 | |||||
| chr3:45652193
|
C | A | 2 | a0001c0001t0048g0119a0001c0001t0048g0120 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1511-13457C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45652193 | ||||||
| chr3:45652251
|
C | T | 126 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(123): Show | 126 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1511-13399C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45652251 | ||||||
| chr3:45652489
|
T | A | 29 | a0001c0001t0064g0259a0001c0001t0157g0247a0001c0001t0171g0193others(26): Show | 29 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.1511-13161T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45652489 | ||||||
| chr3:45652504
|
T | A | 9 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(6): Show | 9 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1511-13146T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45652504 | ||||||
| chr3:45652565
|
A | C | 1 | a0001c0001t0172g0239 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1511-13085A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45652565 | ||||||
| chr3:45652570
|
T | C | 9 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(6): Show | 9 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1511-13080T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45652570 | ||||||
| chr3:45652626
|
A | G | 1 | a0001c0001t0151g0283 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1511-13024A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45652626 | ||||||
| chr3:45652711
|
G | A | 9 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(6): Show | 9 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(6): Show |
intron_variant | MODIFIER | c.1511-12939G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45652711 | ||||||
| chr3:45652829
|
G | A | 4 | a0001c0001t0048g0119a0001c0001t0048g0120a0001c0005t0122g0155others(1): Show | 4 | HG02451.hp2 HG02630.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1511-12821G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45652829 | ||||||
| chr3:45652867
|
C | T | 126 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(123): Show | 126 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(123): Show |
intron_variant | MODIFIER | c.1511-12783C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45652867 | ||||||
| chr3:45653009
|
G | C | 54 | a0001c0001t0010g0050a0001c0001t0010g0051a0001c0001t0010g0052others(51): Show | 54 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.1511-12641G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45653009 | ||||||
| chr3:45653137
|
T | C | 29 | a0001c0001t0064g0259a0001c0001t0157g0247a0001c0001t0171g0193others(26): Show | 29 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(26): Show |
intron_variant | MODIFIER | c.1511-12513T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45653137 | ||||||
| chr3:45653193
|
C | T | 62 | a0001c0001t0002g0080a0001c0001t0002g0092a0001c0001t0002g0093others(59): Show | 63 | HG00140.hp2 HG00323.hp1 HG00609.hp1 others(60): Show |
intron_variant | MODIFIER | c.1511-12457C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45653193 | ||||||
| chr3:45653365
|
G | A | 33 | a0001c0001t0046g0017a0001c0001t0046g0019a0001c0001t0049g0084others(30): Show | 33 | HG01167.hp2 HG01169.hp1 HG01433.hp1 others(30): Show |
intron_variant | MODIFIER | c.1511-12285G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45653365 | ||||||
| chr3:45653371
|
T | C | 34 | a0001c0001t0046g0017a0001c0001t0046g0019a0001c0001t0049g0084others(31): Show | 34 | HG01167.hp2 HG01169.hp1 HG01433.hp1 others(31): Show |
intron_variant | MODIFIER | c.1511-12279T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45653371 | ||||||
| chr3:45653404
|
C | A | 2 | a0001c0001t0017g0081a0001c0001t0017g0089 | 2 | HG01081.hp2 HG02004.hp2 |
intron_variant | MODIFIER | c.1511-12246C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45653404 | ||||||
| chr3:45653583
|
T | C | 13 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(10): Show | 13 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1511-12067T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45653583 | ||||||
| chr3:45653586
|
A | G | 1 | a0001c0001t0170g0282 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1511-12064A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45653586 | ||||||
| chr3:45653677
|
A | G | 1 | a0001c0005t0128g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1511-11973A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45653677 | ||||||
| chr3:45653680
|
T | C | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-11970T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45653680 | ||||||
| chr3:45653715
|
A | G | 1 | a0001c0001t0153g0270 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1511-11935A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45653715 | ||||||
| chr3:45653831
|
A | G | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-11819A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45653831 | ||||||
| chr3:45653834
|
C | T | 1 | a0001c0001t0145g0082 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1511-11816C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45653834 | ||||||
| chr3:45653888
|
T | C | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-11762T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45653888 | ||||||
| chr3:45653907
|
C | CA | 187 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(184): Show | 188 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(185): Show |
intron_variant | MODIFIER | c.1511-11724dupA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45653907 | |||||
| chr3:45653907
|
C | CAAA | 10 | a0001c0001t0012g0240a0001c0001t0015g0260a0001c0001t0015g0261others(7): Show | 10 | HG00597.hp1 HG02135.hp2 HG04199.hp1 others(7): Show |
intron_variant | MODIFIER | c.1511-11726_1511-11 others(9): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45653907 | |||||
| chr3:45653907
|
CA | C | 21 | a0001c0001t0046g0017a0001c0001t0046g0019a0001c0002t0011g0034others(18): Show | 21 | HG01167.hp2 HG01168.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.1511-11724delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45653907 | |||||
| chr3:45653923
|
A | AG | 10 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0081g0151others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1511-11727_1511-11 others(7): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45653923 | ||||||
| chr3:45653923
|
AAAAGAAA others(3): Show |
A | 1 | a0001c0005t0128g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1511-11723_1511-11 others(16): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45653923 | |||||
| chr3:45653924
|
AAAGAAAA others(2): Show |
A | 11 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(8): Show | 11 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1511-11723_1511-11 others(15): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45653924 | |||||
| chr3:45653933
|
G | GA | 6 | a0001c0001t0003g0042a0001c0001t0013g0067a0001c0001t0013g0068others(3): Show | 6 | NA18957.hp1 NA18994.hp1 NA18994.hp2 others(3): Show |
intron_variant | MODIFIER | c.1511-11705dupA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45653933 | |||||
| chr3:45653933
|
GA | G | 56 | a0001c0001t0010g0050a0001c0001t0010g0051a0001c0001t0010g0052others(53): Show | 56 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(53): Show |
intron_variant | MODIFIER | c.1511-11705delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45653933 | |||||
| chr3:45653934
|
A | G | 11 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(8): Show | 11 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1511-11716A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45653934 | ||||||
| chr3:45653935
|
A | G | 1 | a0001c0005t0128g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1511-11715A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45653935 | ||||||
| chr3:45654034
|
A | G | 1 | a0001c0001t0091g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1511-11616A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45654034 | ||||||
| chr3:45654041
|
A | G | 1 | a0001c0002t0124g0041 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1511-11609A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45654041 | ||||||
| chr3:45654088
|
G | A | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-11562G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45654088 | ||||||
| chr3:45654115
|
C | T | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-11535C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45654115 | ||||||
| chr3:45654173
|
C | G | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-11477C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45654173 | ||||||
| chr3:45654274
|
CAG | C | 11 | a0001c0001t0015g0260a0001c0001t0015g0261a0001c0001t0015g0262others(8): Show | 11 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1511-11375_1511-11 others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45654274 | ||||||
| chr3:45654447
|
T | A | 1 | a0001c0003t0121g0152 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1511-11203T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45654447 | ||||||
| chr3:45654473
|
A | G | 2 | a0001c0001t0048g0119a0001c0001t0048g0120 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1511-11177A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45654473 | ||||||
| chr3:45654605
|
A | G | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1511-11045A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45654605 | ||||||
| chr3:45654615
|
A | G | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1511-11035A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45654615 | ||||||
| chr3:45654619
|
C | G | 356 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(353): Show | 357 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(354): Show |
intron_variant | MODIFIER | c.1511-11031C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45654619 | ||||||
| chr3:45654709
|
G | T | 44 | a0001c0001t0010g0050a0001c0001t0010g0051a0001c0001t0010g0052others(41): Show | 44 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.1511-10941G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45654709 | ||||||
| chr3:45654812
|
C | CA | 36 | a0001c0001t0002g0105a0001c0001t0002g0116a0001c0001t0013g0068others(33): Show | 36 | HG00735.hp2 HG01175.hp2 HG01243.hp2 others(33): Show |
intron_variant | MODIFIER | c.1511-10816dupA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45654812 | |||||
| chr3:45654812
|
C | CAA | 14 | a0001c0001t0009g0015a0001c0001t0009g0021a0001c0001t0009g0022others(11): Show | 14 | HG00438.hp2 HG00597.hp1 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1511-10817_1511-10 others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45654812 | |||||
| chr3:45654812
|
CA | C | 17 | a0001c0001t0046g0017a0001c0001t0046g0019a0001c0002t0011g0034others(14): Show | 17 | HG02257.hp2 HG02258.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1511-10816delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45654812 | |||||
| chr3:45654812
|
CAAAAAAA | C | 18 | a0001c0001t0010g0051a0001c0001t0010g0052a0001c0001t0010g0053others(15): Show | 18 | HG00558.hp1 HG00609.hp2 HG02015.hp2 others(15): Show |
intron_variant | MODIFIER | c.1511-10822_1511-10 others(13): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45654812 | |||||
| chr3:45654828
|
A | AAG | 7 | a0001c0001t0076g0132a0001c0001t0086g0131a0001c0001t0111g0133others(4): Show | 7 | HG02055.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1511-10821_1511-10 others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45654828 | |||||
| chr3:45654829
|
A | G | 113 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(110): Show | 113 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1511-10821A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45654829 | ||||||
| chr3:45654848
|
A | C | 7 | a0001c0001t0076g0132a0001c0001t0086g0131a0001c0001t0111g0133others(4): Show | 7 | HG02055.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1511-10802A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45654848 | ||||||
| chr3:45654851
|
C | T | 10 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0081g0151others(7): Show | 10 | HG01891.hp2 HG02280.hp1 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1511-10799C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45654851 | ||||||
| chr3:45654920
|
A | AT | 60 | a0001c0001t0001g0195a0001c0001t0001g0221a0001c0001t0001g0228others(57): Show | 60 | HG00423.hp2 HG00558.hp2 HG00597.hp2 others(57): Show |
intron_variant | MODIFIER | c.1511-10713dupT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45654920 | |||||
| chr3:45654920
|
AT | A | 48 | a0001c0001t0003g0078a0001c0001t0010g0051a0001c0001t0010g0052others(45): Show | 48 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(45): Show |
intron_variant | MODIFIER | c.1511-10713delT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45654920 | |||||
| chr3:45654920
|
ATT | A | 12 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(9): Show | 12 | HG01243.hp2 HG02559.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1511-10714_1511-10 others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45654920 | |||||
| chr3:45655030
|
C | T | 1 | a0001c0001t0154g0256 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1511-10620C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45655030 | ||||||
| chr3:45655047
|
G | A | 1 | a0001c0002t0099g0322 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1511-10603G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45655047 | ||||||
| chr3:45655069
|
G | A | 116 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(113): Show | 116 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1511-10581G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45655069 | ||||||
| chr3:45655121
|
T | C | 2 | a0001c0001t0048g0119a0001c0001t0048g0120 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1511-10529T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45655121 | ||||||
| chr3:45655206
|
C | T | 55 | a0001c0001t0010g0050a0001c0001t0010g0051a0001c0001t0010g0052others(52): Show | 55 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1511-10444C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45655206 | ||||||
| chr3:45655241
|
C | T | 11 | a0001c0001t0015g0260a0001c0001t0015g0261a0001c0001t0015g0262others(8): Show | 11 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1511-10409C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45655241 | ||||||
| chr3:45655315
|
A | C | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-10335A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45655315 | ||||||
| chr3:45655737
|
G | A | 44 | a0001c0001t0010g0050a0001c0001t0010g0051a0001c0001t0010g0052others(41): Show | 44 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.1511-9913G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45655737 | ||||||
| chr3:45655833
|
A | T | 1 | a0001c0001t0001g0198 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1511-9817A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45655833 | ||||||
| chr3:45655936
|
G | A | 2 | a0001c0001t0074g0135a0001c0001t0195g0136 | 2 | HG02486.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.1511-9714G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45655936 | ||||||
| chr3:45656222
|
ATTG | A | 28 | a0001c0001t0157g0247a0001c0001t0171g0193a0001c0001t0199g0072others(25): Show | 28 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(25): Show |
intron_variant | MODIFIER | c.1511-9425_1511-942 others(7): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45656222 | |||||
| chr3:45656239
|
C | G | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-9411C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45656239 | ||||||
| chr3:45656242
|
T | G | 1 | a0001c0002t0067g0008 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1511-9408T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45656242 | ||||||
| chr3:45656325
|
A | G | 9 | a0001c0001t0194g0246a0001c0002t0020g0309a0001c0002t0052g0307others(6): Show | 9 | HG00738.hp1 HG01070.hp2 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.1511-9325A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45656325 | ||||||
| chr3:45656416
|
A | G | 114 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(111): Show | 114 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.1511-9234A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45656416 | ||||||
| chr3:45656456
|
GA | G | 57 | a0001c0001t0002g0106a0001c0001t0008g0200a0001c0001t0010g0050others(54): Show | 57 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(54): Show |
intron_variant | MODIFIER | c.1511-9180delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45656456 | |||||
| chr3:45656487
|
C | T | 1 | a0001c0001t0069g0134 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.1511-9163C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45656487 | ||||||
| chr3:45656541
|
C | T | 1 | a0001c0005t0128g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1511-9109C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45656541 | ||||||
| chr3:45656611
|
G | A | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-9039G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45656611 | ||||||
| chr3:45656664
|
C | T | 1 | a0001c0005t0128g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1511-8986C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45656664 | ||||||
| chr3:45656680
|
G | T | 1 | a0001c0001t0008g0236 | 1 | HG01517.hp1 | intron_variant | MODIFIER | c.1511-8970G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45656680 | ||||||
| chr3:45656845
|
A | G | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-8805A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45656845 | ||||||
| chr3:45656968
|
C | T | 115 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(112): Show | 115 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1511-8682C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45656968 | ||||||
| chr3:45657017
|
C | G | 1 | a0001c0002t0051g0306 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1511-8633C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45657017 | ||||||
| chr3:45657136
|
C | G | 11 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(8): Show | 11 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1511-8514C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45657136 | ||||||
| chr3:45657524
|
C | CA | 7 | a0001c0001t0001g0228a0001c0001t0002g0105a0001c0001t0004g0188others(4): Show | 7 | HG01109.hp2 HG01978.hp1 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.1511-8106dupA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45657524 | |||||
| chr3:45657524
|
CA | C | 25 | a0001c0001t0006g0189a0001c0001t0023g0149a0001c0001t0023g0150others(22): Show | 25 | HG01074.hp2 HG01243.hp1 HG01496.hp2 others(22): Show |
intron_variant | MODIFIER | c.1511-8106delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45657524 | |||||
| chr3:45657524
|
CAA | C | 84 | a0001c0001t0010g0051a0001c0001t0010g0052a0001c0001t0010g0053others(81): Show | 84 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(81): Show |
intron_variant | MODIFIER | c.1511-8107_1511-810 others(6): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45657524 | |||||
| chr3:45657524
|
CAAAAAAA others(2): Show |
C | 10 | a0001c0001t0010g0050a0001c0001t0044g0098a0001c0001t0175g0245others(7): Show | 10 | HG00733.hp1 HG00735.hp1 HG01069.hp2 others(7): Show |
intron_variant | MODIFIER | c.1511-8114_1511-810 others(13): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45657524 | |||||
| chr3:45657524
|
CAAAAAAA others(4): Show |
C | 3 | a0001c0001t0001g0173a0001c0001t0001g0223a0001c0001t0005g0222 | 3 | HG02258.hp1 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1511-8116_1511-810 others(15): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45657524 | |||||
| chr3:45657539
|
A | G | 1 | a0001c0001t0106g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1511-8111A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45657539 | ||||||
| chr3:45657595
|
G | T | 1 | a0001c0002t0020g0340 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.1511-8055G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45657595 | ||||||
| chr3:45657623
|
A | G | 2 | a0001c0001t0165g0280a0001c0001t0167g0275 | 2 | NA18951.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1511-8027A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45657623 | ||||||
| chr3:45657757
|
C | T | 11 | a0001c0001t0032g0143a0001c0001t0032g0144a0001c0001t0053g0139others(8): Show | 11 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1511-7893C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45657757 | ||||||
| chr3:45657813
|
C | T | 1 | a0001c0001t0006g0101 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1511-7837C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45657813 | ||||||
| chr3:45657890
|
A | G | 11 | a0001c0001t0015g0260a0001c0001t0015g0261a0001c0001t0015g0262others(8): Show | 11 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1511-7760A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45657890 | ||||||
| chr3:45658081
|
G | C | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-7569G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45658081 | ||||||
| chr3:45658307
|
A | G | 1 | a0001c0002t0124g0041 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1511-7343A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45658307 | ||||||
| chr3:45658487
|
T | C | 1 | a0001c0001t0172g0239 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1511-7163T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45658487 | ||||||
| chr3:45658534
|
T | G | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-7116T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45658534 | ||||||
| chr3:45658535
|
C | CT | 42 | a0001c0001t0005g0222a0001c0001t0006g0101a0001c0001t0007g0058others(39): Show | 42 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(39): Show |
intron_variant | MODIFIER | c.1511-7083dupT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45658535 | |||||
| chr3:45658535
|
C | CTT | 20 | a0001c0001t0003g0142a0001c0001t0014g0039a0001c0001t0041g0276others(17): Show | 20 | HG00558.hp1 HG00733.hp1 HG00735.hp1 others(17): Show |
intron_variant | MODIFIER | c.1511-7084_1511-708 others(6): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45658535 | |||||
| chr3:45658535
|
C | CTTT | 9 | a0001c0001t0001g0223a0001c0001t0010g0052a0001c0001t0019g0284others(6): Show | 9 | HG01258.hp1 HG01516.hp1 HG02486.hp1 others(6): Show |
intron_variant | MODIFIER | c.1511-7085_1511-708 others(7): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45658535 | |||||
| chr3:45658535
|
CT | C | 136 | a0001c0001t0001g0094a0001c0001t0001g0161a0001c0001t0001g0162others(133): Show | 137 | HG00140.hp2 HG00323.hp1 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1511-7083delT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45658535 | |||||
| chr3:45658535
|
CTT | C | 17 | a0001c0001t0001g0079a0001c0001t0001g0195a0001c0001t0002g0080others(14): Show | 17 | HG00423.hp2 HG01109.hp2 HG01168.hp2 others(14): Show |
intron_variant | MODIFIER | c.1511-7084_1511-708 others(6): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45658535 | |||||
| chr3:45658535
|
CTTT | C | 13 | a0001c0001t0003g0115a0001c0001t0032g0143a0001c0001t0032g0144others(10): Show | 13 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1511-7085_1511-708 others(7): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45658535 | |||||
| chr3:45658535
|
CTTTTTT | C | 6 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118others(3): Show | 6 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1511-7088_1511-708 others(10): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45658535 | |||||
| chr3:45658535
|
CTTTTTTT others(1): Show |
C | 20 | a0001c0001t0046g0017a0001c0001t0046g0019a0001c0002t0011g0034others(17): Show | 20 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1511-7090_1511-708 others(12): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45658535 | |||||
| chr3:45658535
|
CTTTTTTT others(3): Show |
C | 2 | a0001c0007t0204g0002a0001c0007t0205g0002 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1511-7092_1511-708 others(14): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45658535 | |||||
| chr3:45658535
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0010g0050 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1511-7093_1511-708 others(15): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45658535 | |||||
| chr3:45658535
|
CTTTTTTT others(5): Show |
C | 21 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(18): Show | 21 | HG01243.hp2 HG01891.hp2 HG02280.hp1 others(18): Show |
intron_variant | MODIFIER | c.1511-7094_1511-708 others(16): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45658535 | |||||
| chr3:45658535
|
CTTTTTTT others(6): Show |
C | 1 | a0001c0001t0085g0148 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1511-7095_1511-708 others(17): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45658535 | |||||
| chr3:45658535
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0001t0001g0202 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1511-7099_1511-708 others(21): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45658535 | |||||
| chr3:45658593
|
C | T | 3 | a0001c0001t0068g0128a0001c0001t0075g0130a0001c0001t0078g0129 | 3 | HG02630.hp1 HG03130.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1511-7057C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45658593 | ||||||
| chr3:45658633
|
A | G | 266 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(263): Show | 266 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(263): Show |
intron_variant | MODIFIER | c.1511-7017A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45658633 | ||||||
| chr3:45658654
|
C | T | 115 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(112): Show | 115 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1511-6996C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45658654 | ||||||
| chr3:45658678
|
C | T | 3 | a0001c0002t0026g0003a0001c0002t0026g0298a0001c0002t0115g0003 | 3 | NA18944.hp2 NA18946.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1511-6972C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45658678 | ||||||
| chr3:45658823
|
A | G | 293 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1511-6827A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45658823 | ||||||
| chr3:45658825
|
G | T | 11 | a0001c0001t0032g0143a0001c0001t0032g0144a0001c0001t0053g0139others(8): Show | 11 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1511-6825G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45658825 | ||||||
| chr3:45658904
|
G | T | 11 | a0001c0001t0032g0143a0001c0001t0032g0144a0001c0001t0053g0139others(8): Show | 11 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1511-6746G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45658904 | ||||||
| chr3:45658923
|
C | T | 7 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0081g0151others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1511-6727C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45658923 | ||||||
| chr3:45659134
|
G | T | 7 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0081g0151others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1511-6516G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45659134 | ||||||
| chr3:45659150
|
A | G | 1 | a0001c0001t0004g0188 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1511-6500A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45659150 | ||||||
| chr3:45659230
|
A | G | 1 | a0001c0001t0044g0098 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.1511-6420A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45659230 | ||||||
| chr3:45659489
|
G | A | 1 | a0001c0002t0072g0301 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1511-6161G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45659489 | ||||||
| chr3:45659585
|
ACCCCAAA others(16): Show |
A | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-6041_1511-601 others(27): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45659585 | |||||
| chr3:45659702
|
C | A | 1 | a0001c0003t0103g0124 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1511-5948C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45659702 | ||||||
| chr3:45659730
|
C | G | 20 | a0001c0001t0046g0017a0001c0001t0046g0019a0001c0002t0011g0034others(17): Show | 20 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.1511-5920C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45659730 | ||||||
| chr3:45659909
|
A | T | 14 | a0001c0001t0199g0072a0001c0001t0200g0071a0001c0002t0028g0328others(11): Show | 14 | HG00673.hp1 HG01081.hp1 HG01943.hp2 others(11): Show |
intron_variant | MODIFIER | c.1511-5741A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45659909 | ||||||
| chr3:45659963
|
T | C | 293 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1511-5687T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45659963 | ||||||
| chr3:45659981
|
T | G | 1 | a0001c0001t0009g0021 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1511-5669T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45659981 | ||||||
| chr3:45659987
|
T | C | 1 | a0001c0002t0089g0343 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1511-5663T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45659987 | ||||||
| chr3:45660087
|
A | G | 1 | a0001c0005t0128g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1511-5563A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45660087 | ||||||
| chr3:45660260
|
TGAG | T | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-5387_1511-538 others(7): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45660260 | |||||
| chr3:45660304
|
G | A | 2 | a0001c0007t0204g0002a0001c0007t0205g0002 | 2 | HG02886.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1511-5346G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45660304 | ||||||
| chr3:45660320
|
A | C | 55 | a0001c0001t0010g0050a0001c0001t0010g0051a0001c0001t0010g0052others(52): Show | 55 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(52): Show |
intron_variant | MODIFIER | c.1511-5330A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45660320 | ||||||
| chr3:45660345
|
T | G | 11 | a0001c0001t0015g0260a0001c0001t0015g0261a0001c0001t0015g0262others(8): Show | 11 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1511-5305T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45660345 | ||||||
| chr3:45660405
|
C | CT | 50 | a0001c0001t0002g0116a0001c0001t0006g0073a0001c0001t0006g0101others(47): Show | 50 | HG00597.hp2 HG00621.hp1 HG00735.hp1 others(47): Show |
intron_variant | MODIFIER | c.1511-5220dupT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45660405 | |||||
| chr3:45660405
|
C | CTT | 12 | a0001c0001t0023g0150a0001c0001t0032g0143a0001c0001t0081g0151others(9): Show | 12 | HG01109.hp1 HG01243.hp1 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1511-5221_1511-522 others(6): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45660405 | |||||
| chr3:45660405
|
CT | C | 153 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(150): Show | 153 | HG00099.hp2 HG00140.hp1 HG00423.hp2 others(150): Show |
intron_variant | MODIFIER | c.1511-5220delT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45660405 | |||||
| chr3:45660405
|
CTTTTT | C | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-5224_1511-522 others(9): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45660405 | |||||
| chr3:45660430
|
T | C | 3 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1511-5220T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45660430 | ||||||
| chr3:45660439
|
G | A | 1 | a0001c0001t0001g0196 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1511-5211G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45660439 | ||||||
| chr3:45660508
|
C | T | 11 | a0001c0001t0015g0260a0001c0001t0015g0261a0001c0001t0015g0262others(8): Show | 11 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1511-5142C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45660508 | ||||||
| chr3:45660535
|
C | G | 22 | a0001c0001t0014g0035a0001c0001t0014g0038a0001c0001t0014g0039others(19): Show | 22 | HG00735.hp2 HG00738.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1511-5115C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45660535 | ||||||
| chr3:45660563
|
G | A | 1 | a0001c0002t0130g0031 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1511-5087G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45660563 | ||||||
| chr3:45660644
|
G | C | 1 | a0001c0001t0091g0125 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1511-5006G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45660644 | ||||||
| chr3:45660658
|
C | G | 2 | a0001c0001t0005g0166a0001c0001t0203g0254 | 2 | HG01261.hp2 HG03834.hp2 |
intron_variant | MODIFIER | c.1511-4992C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45660658 | ||||||
| chr3:45660696
|
G | A | 22 | a0001c0001t0046g0017a0001c0001t0046g0019a0001c0002t0011g0034others(19): Show | 22 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1511-4954G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45660696 | ||||||
| chr3:45660749
|
C | G | 1 | a0001c0001t0006g0085 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.1511-4901C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45660749 | ||||||
| chr3:45660862
|
A | C | 2 | a0001c0001t0008g0185a0001c0001t0008g0200 | 2 | HG01070.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.1511-4788A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45660862 | ||||||
| chr3:45661221
|
G | A | 1 | a0001c0001t0045g0214 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.1511-4429G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45661221 | ||||||
| chr3:45661611
|
C | G | 1 | a0001c0005t0128g0160 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1511-4039C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45661611 | ||||||
| chr3:45661682
|
C | G | 11 | a0001c0001t0015g0260a0001c0001t0015g0261a0001c0001t0015g0262others(8): Show | 11 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1511-3968C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45661682 | ||||||
| chr3:45661819
|
C | T | 2 | a0001c0001t0019g0284a0001c0001t0150g0285 | 2 | HG02074.hp2 HG02523.hp1 |
intron_variant | MODIFIER | c.1511-3831C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45661819 | ||||||
| chr3:45661820
|
G | A | 7 | a0001c0001t0023g0149a0001c0001t0023g0150a0001c0001t0081g0151others(4): Show | 7 | HG01891.hp2 HG02280.hp1 HG02886.hp1 others(4): Show |
intron_variant | MODIFIER | c.1511-3830G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45661820 | ||||||
| chr3:45662270
|
C | T | 114 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(111): Show | 114 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(111): Show |
intron_variant | MODIFIER | c.1511-3380C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45662270 | ||||||
| chr3:45662275
|
A | AAG | 52 | a0001c0001t0014g0035a0001c0001t0014g0038a0001c0001t0014g0039others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1511-3374_1511-337 others(6): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45662275 | |||||
| chr3:45662276
|
A | AGT | 22 | a0001c0001t0001g0198a0001c0001t0005g0170a0001c0002t0011g0034others(19): Show | 22 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.1511-3350_1511-334 others(6): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45662276 | |||||
| chr3:45662276
|
A | AGTGT | 107 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(104): Show | 107 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.1511-3352_1511-334 others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45662276 | |||||
| chr3:45662276
|
A | AGTGTGT | 8 | a0001c0001t0001g0225a0001c0001t0005g0172a0001c0001t0007g0058others(5): Show | 8 | HG00733.hp2 HG01106.hp2 NA18954.hp2 others(5): Show |
intron_variant | MODIFIER | c.1511-3354_1511-334 others(10): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45662276 | |||||
| chr3:45662276
|
AGT | A | 17 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(14): Show | 17 | HG01243.hp2 HG02559.hp2 HG02615.hp2 others(14): Show |
intron_variant | MODIFIER | c.1511-3350_1511-334 others(6): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45662276 | |||||
| chr3:45662300
|
T | C | 1 | a0001c0001t0002g0092 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.1511-3350T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45662300 | ||||||
| chr3:45662305
|
G | A | 52 | a0001c0001t0014g0035a0001c0001t0014g0038a0001c0001t0014g0039others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1511-3345G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45662305 | ||||||
| chr3:45662665
|
T | C | 1 | a0001c0001t0083g0140 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1511-2985T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45662665 | ||||||
| chr3:45662671
|
T | C | 1 | a0001c0003t0142g0157 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1511-2979T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45662671 | ||||||
| chr3:45662979
|
G | A | 116 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(113): Show | 116 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.1511-2671G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45662979 | ||||||
| chr3:45662983
|
C | CA | 14 | a0001c0001t0009g0022a0001c0001t0012g0240a0001c0001t0049g0084others(11): Show | 14 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(11): Show |
intron_variant | MODIFIER | c.1511-2655dupA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45662983 | |||||
| chr3:45662996
|
C | A | 1 | a0001c0001t0144g0117 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1511-2654C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45662996 | ||||||
| chr3:45663709
|
T | G | 1 | a0001c0001t0180g0229 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.1511-1941T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45663709 | ||||||
| chr3:45663725
|
TTTTAA | T | 8 | a0001c0001t0044g0098a0001c0001t0076g0132a0001c0001t0086g0131others(5): Show | 8 | HG02055.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.1511-1920_1511-191 others(9): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45663725 | |||||
| chr3:45663868
|
A | ATTTT | 11 | a0001c0001t0001g0221a0001c0001t0015g0260a0001c0001t0015g0261others(8): Show | 11 | HG00597.hp1 HG01934.hp2 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1511-1765_1511-176 others(8): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45663868 | |||||
| chr3:45663868
|
A | ATTTTT | 95 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(92): Show | 95 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(92): Show |
intron_variant | MODIFIER | c.1511-1766_1511-176 others(9): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45663868 | |||||
| chr3:45663868
|
A | ATTTTTT | 37 | a0001c0001t0001g0161a0001c0001t0001g0179a0001c0001t0001g0180others(34): Show | 37 | HG00438.hp1 HG01106.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.1511-1767_1511-176 others(10): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45663868 | |||||
| chr3:45663868
|
A | ATTTTTTT others(3): Show |
1 | a0001c0001t0010g0066 | 1 | NA18963.hp2 | intron_variant | MODIFIER | c.1511-1771_1511-176 others(14): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45663868 | |||||
| chr3:45663868
|
A | ATTTTTTT others(9): Show |
4 | a0001c0001t0074g0135a0001c0001t0149g0048a0001c0001t0195g0136others(1): Show | 4 | HG02155.hp1 HG02486.hp1 HG02486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1511-1777_1511-176 others(20): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45663868 | |||||
| chr3:45663868
|
A | ATTTTTTT others(10): Show |
17 | a0001c0001t0010g0051a0001c0001t0010g0052a0001c0001t0010g0053others(14): Show | 17 | HG00558.hp1 HG00609.hp2 HG01074.hp2 others(14): Show |
intron_variant | MODIFIER | c.1511-1778_1511-176 others(21): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45663868 | |||||
| chr3:45663868
|
A | ATTTTTTT others(11): Show |
18 | a0001c0001t0010g0050a0001c0001t0019g0284a0001c0001t0032g0144others(15): Show | 18 | HG00423.hp1 HG00735.hp1 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1511-1779_1511-176 others(22): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45663868 | |||||
| chr3:45663868
|
A | ATTTTTTT others(12): Show |
11 | a0001c0001t0041g0272a0001c0001t0049g0084a0001c0001t0049g0088others(8): Show | 11 | HG00733.hp1 HG01069.hp2 HG01433.hp1 others(8): Show |
intron_variant | MODIFIER | c.1511-1780_1511-176 others(23): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45663868 | |||||
| chr3:45663868
|
A | ATTTTTTT others(13): Show |
1 | a0001c0005t0138g0159 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1511-1781_1511-176 others(24): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45663868 | |||||
| chr3:45663868
|
A | ATTTTTTT others(15): Show |
3 | a0001c0001t0096g0138a0001c0001t0111g0133a0001c0001t0155g0023 | 3 | HG02451.hp1 HG03225.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1511-1762_1511-176 others(26): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45663868 | |||||
| chr3:45663868
|
A | ATTTTTTT others(16): Show |
3 | a0001c0001t0019g0287a0001c0001t0175g0245a0001c0003t0137g0154 | 3 | HG03579.hp1 NA18997.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.1511-1762_1511-176 others(27): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45663868 | |||||
| chr3:45663868
|
A | ATTTTTTT others(17): Show |
1 | a0001c0001t0053g0139 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.1511-1762_1511-176 others(28): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45663868 | |||||
| chr3:45663868
|
A | ATTTTTTT others(18): Show |
1 | a0001c0001t0086g0131 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1511-1762_1511-176 others(29): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45663868 | |||||
| chr3:45663868
|
A | ATTTTTTT others(19): Show |
3 | a0001c0001t0076g0132a0001c0001t0084g0141a0001c0002t0035g0043 | 3 | HG02055.hp1 HG02897.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1511-1762_1511-176 others(30): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45663868 | |||||
| chr3:45663868
|
A | ATTTTTTT others(20): Show |
1 | a0001c0002t0035g0044 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1511-1762_1511-176 others(31): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45663868 | |||||
| chr3:45663868
|
A | ATTTTTTT others(24): Show |
1 | a0001c0002t0055g0331 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.1511-1762_1511-176 others(35): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45663868 | |||||
| chr3:45663868
|
AT | A | 34 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(31): Show | 34 | HG01070.hp2 HG01109.hp1 HG01243.hp2 others(31): Show |
intron_variant | MODIFIER | c.1511-1762delT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr3 | 45663868 | |||||
| chr3:45663917
|
C | T | 1 | a0001c0001t0023g0149 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1511-1733C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45663917 | ||||||
| chr3:45664042
|
T | C | 31 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(28): Show | 31 | HG01109.hp1 HG01243.hp2 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.1511-1608T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45664042 | ||||||
| chr3:45664160
|
T | C | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-1490T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45664160 | ||||||
| chr3:45664202
|
C | G | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-1448C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45664202 | ||||||
| chr3:45664252
|
C | T | 18 | a0001c0001t0015g0260a0001c0001t0015g0261a0001c0001t0015g0262others(15): Show | 18 | HG00438.hp2 HG00597.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.1511-1398C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45664252 | ||||||
| chr3:45664315
|
T | C | 3 | a0001c0003t0121g0152a0001c0003t0133g0158a0001c0003t0142g0157 | 3 | HG01243.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1511-1335T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45664315 | ||||||
| chr3:45664415
|
G | T | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1511-1235G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45664415 | ||||||
| chr3:45664579
|
G | A | 11 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(8): Show | 11 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(8): Show |
intron_variant | MODIFIER | c.1511-1071G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45664579 | ||||||
| chr3:45664613
|
C | T | 1 | a0001c0008t0002g0107 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1511-1037C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45664613 | ||||||
| chr3:45664675
|
C | T | 131 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(128): Show | 131 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(128): Show |
intron_variant | MODIFIER | c.1511-975C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45664675 | ||||||
| chr3:45664702
|
C | T | 22 | a0001c0001t0014g0035a0001c0001t0014g0038a0001c0001t0014g0039others(19): Show | 22 | HG00735.hp2 HG00738.hp1 HG01070.hp2 others(19): Show |
intron_variant | MODIFIER | c.1511-948C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45664702 | ||||||
| chr3:45665105
|
G | A | 1 | a0001c0002t0036g0320 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1511-545G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45665105 | ||||||
| chr3:45665148
|
G | A | 1 | a0001c0002t0124g0041 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1511-502G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45665148 | ||||||
| chr3:45665228
|
A | G | 3 | a0001c0001t0001g0173a0001c0001t0001g0223a0001c0001t0005g0222 | 3 | HG02258.hp1 HG03516.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1511-422A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45665228 | ||||||
| chr3:45665245
|
G | A | 44 | a0001c0001t0010g0050a0001c0001t0010g0051a0001c0001t0010g0052others(41): Show | 44 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.1511-405G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45665245 | ||||||
| chr3:45665487
|
G | A | 3 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0156g0118 | 3 | HG01433.hp1 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.1511-163G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45665487 | ||||||
| chr3:45665547
|
C | T | 4 | a0001c0001t0082g0137a0001c0001t0140g0267a0001c0003t0137g0154others(1): Show | 4 | HG02615.hp2 HG02647.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.1511-103C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45665547 | ||||||
| chr3:45665548
|
G | A | 1 | a0001c0002t0124g0041 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1511-102G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 2/7 | chr3 | 45665548 | ||||||
| chr3:45665827
|
G | A | 11 | a0001c0001t0015g0260a0001c0001t0015g0261a0001c0001t0015g0262others(8): Show | 11 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1578+110G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45665827 | ||||||
| chr3:45665880
|
A | T | 11 | a0001c0001t0032g0143a0001c0001t0032g0144a0001c0001t0053g0139others(8): Show | 11 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1578+163A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45665880 | ||||||
| chr3:45665897
|
T | C | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1578+180T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45665897 | ||||||
| chr3:45665960
|
C | G | 1 | a0001c0001t0064g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1578+243C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45665960 | ||||||
| chr3:45666117
|
A | G | 7 | a0001c0001t0076g0132a0001c0001t0086g0131a0001c0001t0111g0133others(4): Show | 7 | HG02055.hp1 HG02895.hp1 HG02897.hp2 others(4): Show |
intron_variant | MODIFIER | c.1578+400A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45666117 | ||||||
| chr3:45666390
|
C | T | 2 | a0001c0001t0048g0119a0001c0001t0048g0120 | 2 | HG02630.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1578+673C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45666390 | ||||||
| chr3:45666391
|
G | A | 1 | a0001c0001t0186g0215 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1578+674G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45666391 | ||||||
| chr3:45666504
|
A | G | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1578+787A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45666504 | ||||||
| chr3:45666517
|
C | T | 11 | a0001c0001t0015g0260a0001c0001t0015g0261a0001c0001t0015g0262others(8): Show | 11 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1578+800C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45666517 | ||||||
| chr3:45666589
|
A | G | 44 | a0001c0001t0010g0050a0001c0001t0010g0051a0001c0001t0010g0052others(41): Show | 44 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.1578+872A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45666589 | ||||||
| chr3:45666855
|
T | C | 1 | a0001c0002t0124g0041 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1578+1138T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45666855 | ||||||
| chr3:45666988
|
G | A | 1 | a0001c0002t0125g0353 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1578+1271G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45666988 | ||||||
| chr3:45667087
|
A | G | 1 | a0001c0001t0001g0195 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.1579-1207A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45667087 | ||||||
| chr3:45667232
|
G | A | 3 | a0001c0001t0046g0017a0001c0001t0046g0019a0001c0002t0132g0032 | 3 | HG02647.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1579-1062G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45667232 | ||||||
| chr3:45667631
|
G | A | 1 | a0001c0001t0018g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1579-663G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45667631 | ||||||
| chr3:45667635
|
A | G | 1 | a0001c0001t0018g0055 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1579-659A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45667635 | ||||||
| chr3:45667640
|
G | GA | 10 | a0001c0001t0015g0260a0001c0001t0015g0261a0001c0001t0015g0262others(7): Show | 10 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(7): Show |
intron_variant | MODIFIER | c.1579-653dupA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr3 | 45667640 | |||||
| chr3:45667728
|
C | T | 17 | a0001c0002t0011g0034a0001c0002t0011g0291a0001c0002t0011g0292others(14): Show | 17 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(14): Show |
intron_variant | MODIFIER | c.1579-566C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45667728 | ||||||
| chr3:45667813
|
T | C | 1 | a0001c0002t0099g0322 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1579-481T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45667813 | ||||||
| chr3:45667831
|
T | C | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1579-463T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45667831 | ||||||
| chr3:45667836
|
G | A | 1 | a0001c0001t0200g0071 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1579-458G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45667836 | ||||||
| chr3:45668018
|
A | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0225 | 2 | NA18973.hp2 NA19078.hp1 |
intron_variant | MODIFIER | c.1579-276A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 3/7 | chr3 | 45668018 | ||||||
| chr3:45668392
|
A | G | 1 | a0001c0001t0135g0210 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1641+36A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45668392 | ||||||
| chr3:45668476
|
C | T | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1641+120C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45668476 | ||||||
| chr3:45668526
|
G | A | 1 | a0001c0001t0156g0118 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.1641+170G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45668526 | ||||||
| chr3:45668725
|
C | T | 1 | a0001c0001t0001g0209 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1641+369C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45668725 | ||||||
| chr3:45668752
|
CA | C | 280 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(277): Show | 280 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(277): Show |
intron_variant | MODIFIER | c.1641+411delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 45668752 | |||||
| chr3:45668857
|
G | A | 54 | a0001c0001t0010g0050a0001c0001t0010g0051a0001c0001t0010g0052others(51): Show | 54 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(51): Show |
intron_variant | MODIFIER | c.1641+501G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45668857 | ||||||
| chr3:45668871
|
G | A | 2 | a0001c0002t0020g0309a0001c0002t0070g0308 | 2 | HG02683.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1641+515G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45668871 | ||||||
| chr3:45668906
|
G | A | 1 | a0001c0001t0046g0017 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1641+550G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45668906 | ||||||
| chr3:45669364
|
G | A | 1 | a0001c0002t0051g0306 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1641+1008G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45669364 | ||||||
| chr3:45669456
|
A | G | 1 | a0001c0001t0039g0020 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1641+1100A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45669456 | ||||||
| chr3:45669483
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.1641+1127G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45669483 | ||||||
| chr3:45669495
|
G | A | 52 | a0001c0001t0014g0035a0001c0001t0014g0038a0001c0001t0014g0039others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1641+1139G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45669495 | ||||||
| chr3:45669558
|
G | A | 1 | a0001c0001t0106g0126 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1641+1202G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45669558 | ||||||
| chr3:45669606
|
C | T | 3 | a0001c0003t0121g0152a0001c0003t0133g0158a0001c0003t0142g0157 | 3 | HG01243.hp2 HG03041.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1641+1250C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45669606 | ||||||
| chr3:45669875
|
T | C | 293 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1641+1519T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45669875 | ||||||
| chr3:45669877
|
C | G | 113 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(110): Show | 113 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(110): Show |
intron_variant | MODIFIER | c.1641+1521C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45669877 | ||||||
| chr3:45669974
|
G | A | 11 | a0001c0001t0015g0260a0001c0001t0015g0261a0001c0001t0015g0262others(8): Show | 11 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1641+1618G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45669974 | ||||||
| chr3:45669990
|
C | T | 11 | a0001c0001t0032g0143a0001c0001t0032g0144a0001c0001t0053g0139others(8): Show | 11 | HG01074.hp2 HG01243.hp1 HG01891.hp1 others(8): Show |
intron_variant | MODIFIER | c.1641+1634C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45669990 | ||||||
| chr3:45670075
|
G | A | 1 | a0001c0001t0184g0234 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.1641+1719G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45670075 | ||||||
| chr3:45670094
|
C | T | 3 | a0001c0002t0026g0003a0001c0002t0026g0298a0001c0002t0115g0003 | 3 | NA18944.hp2 NA18946.hp2 NA18973.hp1 |
intron_variant | MODIFIER | c.1641+1738C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45670094 | ||||||
| chr3:45670243
|
T | C | 293 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1641+1887T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45670243 | ||||||
| chr3:45670257
|
T | C | 12 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(9): Show | 12 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(9): Show |
intron_variant | MODIFIER | c.1641+1901T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45670257 | ||||||
| chr3:45670398
|
G | GCTT | 44 | a0001c0001t0010g0050a0001c0001t0010g0051a0001c0001t0010g0052others(41): Show | 44 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(41): Show |
intron_variant | MODIFIER | c.1641+2044_1641+204 others(7): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr3 | 45670398 | |||||
| chr3:45670600
|
A | G | 12 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(9): Show | 12 | HG01243.hp2 HG02559.hp2 HG02809.hp1 others(9): Show |
intron_variant | MODIFIER | c.1642-2090A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45670600 | ||||||
| chr3:45670727
|
G | A | 1 | a0001c0001t0166g0263 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.1642-1963G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45670727 | ||||||
| chr3:45670788
|
G | C | 293 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1642-1902G>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45670788 | ||||||
| chr3:45670809
|
C | T | 293 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1642-1881C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45670809 | ||||||
| chr3:45671085
|
A | T | 9 | a0001c0002t0021g0011a0001c0002t0021g0012a0001c0002t0067g0008others(6): Show | 9 | HG02257.hp2 HG02258.hp2 HG02717.hp1 others(6): Show |
intron_variant | MODIFIER | c.1642-1605A>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45671085 | ||||||
| chr3:45671873
|
G | A | 1 | a0001c0001t0064g0259 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1642-817G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45671873 | ||||||
| chr3:45672054
|
C | G | 11 | a0001c0001t0015g0260a0001c0001t0015g0261a0001c0001t0015g0262others(8): Show | 11 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1642-636C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45672054 | ||||||
| chr3:45672290
|
C | T | 1 | a0001c0001t0134g0277 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1642-400C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45672290 | ||||||
| chr3:45672574
|
G | T | 1 | a0001c0001t0170g0282 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1642-116G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 4/7 | chr3 | 45672574 | ||||||
| chr3:45673032
|
G | GA | 17 | a0001c0001t0001g0238a0001c0001t0003g0090a0001c0001t0005g0237others(14): Show | 17 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(14): Show |
intron_variant | MODIFIER | c.1772+224dupA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr3 | 45673032 | |||||
| chr3:45673129
|
T | C | 1 | a0001c0002t0127g0122 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1772+309T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 5/7 | chr3 | 45673129 | ||||||
| chr3:45673240
|
G | T | 1 | a0001c0001t0154g0256 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1773-214G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 5/7 | chr3 | 45673240 | ||||||
| chr3:45673667
|
CT | C | 293 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1824+166delT | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45673667 | |||||
| chr3:45673886
|
C | CA | 6 | a0001c0001t0043g0040a0001c0001t0049g0084a0001c0001t0049g0088others(3): Show | 6 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(3): Show |
intron_variant | MODIFIER | c.1824+393dupA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45673886 | |||||
| chr3:45673897
|
A | C | 1 | a0001c0002t0052g0307 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1824+392A>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 6/7 | chr3 | 45673897 | ||||||
| chr3:45673900
|
C | A | 1 | a0001c0001t0160g0099 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1824+395C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 6/7 | chr3 | 45673900 | ||||||
| chr3:45673993
|
T | C | 13 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(10): Show | 13 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1825-350T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 6/7 | chr3 | 45673993 | ||||||
| chr3:45674006
|
C | A | 7 | a0001c0002t0021g0011a0001c0002t0021g0012a0001c0002t0067g0008others(4): Show | 7 | HG02257.hp2 HG02717.hp1 HG02809.hp2 others(4): Show |
intron_variant | MODIFIER | c.1825-337C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 6/7 | chr3 | 45674006 | ||||||
| chr3:45674019
|
C | T | 1 | a0001c0008t0002g0107 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1825-324C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 6/7 | chr3 | 45674019 | ||||||
| chr3:45674196
|
G | A | 293 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(290): Show | 293 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(290): Show |
intron_variant | MODIFIER | c.1825-147G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 6/7 | chr3 | 45674196 | ||||||
| chr3:45674243
|
AC | A | 13 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(10): Show | 13 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1825-95delC | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr3 | 45674243 | |||||
| chr3:45674268
|
A | G | 1 | a0001c0002t0127g0122 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1825-75A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 6/7 | chr3 | 45674268 | ||||||
| chr3:45674275
|
G | A | 51 | a0001c0001t0014g0035a0001c0001t0014g0038a0001c0001t0014g0039others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(48): Show |
intron_variant | MODIFIER | c.1825-68G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 6/7 | chr3 | 45674275 | ||||||
| chr3:45674277
|
T | C | 27 | a0001c0001t0010g0051a0001c0001t0010g0052a0001c0001t0010g0053others(24): Show | 27 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(24): Show |
intron_variant | MODIFIER | c.1825-66T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 6/7 | chr3 | 45674277 | ||||||
| chr3:45674280
|
A | G | 1 | a0001c0001t0083g0140 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1825-63A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 6/7 | chr3 | 45674280 | ||||||
| chr3:45674555
|
C | T | 2 | a0001c0001t0003g0224a0001c0001t0197g0114 | 2 | HG03017.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.1893+144C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45674555 | ||||||
| chr3:45674716
|
C | G | 13 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(10): Show | 13 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1893+305C>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45674716 | ||||||
| chr3:45674717
|
G | A | 53 | a0001c0001t0010g0050a0001c0001t0010g0051a0001c0001t0010g0052others(50): Show | 53 | HG00423.hp1 HG00558.hp1 HG00609.hp2 others(50): Show |
intron_variant | MODIFIER | c.1893+306G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45674717 | ||||||
| chr3:45675078
|
G | T | 1 | a0001c0001t0151g0283 | 1 | NA19054.hp1 | intron_variant | MODIFIER | c.1893+667G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45675078 | ||||||
| chr3:45675192
|
G | A | 1 | a0001c0002t0124g0041 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1893+781G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45675192 | ||||||
| chr3:45675256
|
G | A | 15 | a0001c0002t0011g0034a0001c0002t0011g0291a0001c0002t0011g0292others(12): Show | 15 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1893+845G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45675256 | ||||||
| chr3:45675299
|
G | A | 1 | a0001c0002t0072g0301 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1893+888G>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45675299 | ||||||
| chr3:45675332
|
C | T | 1 | a0001c0001t0202g0203 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.1893+921C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45675332 | ||||||
| chr3:45675383
|
A | G | 11 | a0001c0001t0015g0260a0001c0001t0015g0261a0001c0001t0015g0262others(8): Show | 11 | HG00438.hp2 HG00597.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.1893+972A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45675383 | ||||||
| chr3:45675436
|
G | T | 1 | a0001c0001t0012g0204 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1893+1025G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45675436 | ||||||
| chr3:45675543
|
C | CTATGAGA others(65): Show |
3 | a0001c0001t0046g0017a0001c0001t0046g0019a0001c0002t0132g0032 | 3 | HG02647.hp1 HG03486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.1893+1201_1894-123 others(76): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 45675543 | |||||
| chr3:45675543
|
CTATGAGA others(65): Show |
C | 52 | a0001c0001t0014g0035a0001c0001t0014g0038a0001c0001t0014g0039others(49): Show | 52 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(49): Show |
intron_variant | MODIFIER | c.1893+1201_1894-123 others(76): Show |
LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 45675543 | |||||
| chr3:45675744
|
T | C | 1 | a0001c0002t0130g0031 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1894-1178T>C | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45675744 | ||||||
| chr3:45675893
|
T | G | 13 | a0001c0001t0049g0084a0001c0001t0049g0088a0001c0001t0076g0132others(10): Show | 13 | HG01433.hp1 HG01516.hp2 HG01517.hp2 others(10): Show |
intron_variant | MODIFIER | c.1894-1029T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45675893 | ||||||
| chr3:45675908
|
C | T | 1 | a0001c0002t0127g0122 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1894-1014C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45675908 | ||||||
| chr3:45675909
|
G | T | 1 | a0001c0001t0006g0101 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.1894-1013G>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45675909 | ||||||
| chr3:45675922
|
C | T | 5 | a0001c0001t0001g0173a0001c0001t0001g0198a0001c0001t0001g0223others(2): Show | 5 | HG02258.hp1 HG02622.hp1 HG03516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1894-1000C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45675922 | ||||||
| chr3:45675978
|
C | T | 15 | a0001c0002t0011g0034a0001c0002t0011g0291a0001c0002t0011g0292others(12): Show | 15 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1894-944C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45675978 | ||||||
| chr3:45676018
|
C | A | 14 | a0001c0001t0009g0015a0001c0001t0009g0018a0001c0001t0009g0021others(11): Show | 14 | HG01243.hp2 HG02559.hp2 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.1894-904C>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45676018 | ||||||
| chr3:45676148
|
A | G | 5 | a0001c0001t0053g0139a0001c0001t0083g0140a0001c0001t0084g0141others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.1894-774A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45676148 | ||||||
| chr3:45676345
|
TA | T | 15 | a0001c0002t0011g0034a0001c0002t0011g0291a0001c0002t0011g0292others(12): Show | 15 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1894-565delA | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr3 | 45676345 | |||||
| chr3:45676373
|
A | G | 4 | a0001c0001t0001g0162a0001c0001t0001g0171a0001c0001t0001g0206others(1): Show | 4 | NA18951.hp1 NA19000.hp2 NA19068.hp2 others(1): Show |
intron_variant | MODIFIER | c.1894-549A>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45676373 | ||||||
| chr3:45676686
|
C | T | 15 | a0001c0002t0011g0034a0001c0002t0011g0291a0001c0002t0011g0292others(12): Show | 15 | HG01167.hp2 HG01169.hp1 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.1894-236C>T | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45676686 | ||||||
| chr3:45676739
|
T | A | 1 | a0001c0001t0002g0116 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1894-183T>A | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45676739 | ||||||
| chr3:45676835
|
T | G | 130 | a0001c0001t0001g0045a0001c0001t0001g0079a0001c0001t0001g0094others(127): Show | 130 | HG00099.hp2 HG00423.hp2 HG00438.hp1 others(127): Show |
intron_variant | MODIFIER | c.1894-87T>G | LIMD1 | ENSG00000144791.10 | transcript | ENST00000273317.5 | protein_coding | 7/7 | chr3 | 45676835 |