| geneid | 3912 |
|---|---|
| ensemblid | ENSG00000091136.15 |
| hgncid | 6486 |
| symbol | LAMB1 |
| name | laminin subunit beta 1 |
| refseq_nuc | NM_002291.3 |
| refseq_prot | NP_002282.2 |
| ensembl_nuc | ENST00000222399.11 |
| ensembl_prot | ENSP00000222399.6 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 107923799 |
| end | 108003161 |
| strand | - |
| ver | v1.2 |
| region | chr7:107923799-108003161 |
| region5000 | chr7:107918799-108008161 |
| regionname0 | LAMB1_chr7_107923799_108003161 |
| regionname5000 | LAMB1_chr7_107918799_108008161 |
| 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 | 0/1 | 1786 | 212 | 49 | 36 | 99 | 6 | 21 | 70 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002 | 1/0 | 1786 | 72 | 17 | 16 | 21 | 7 | 10 | 19 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0003 | 0/0 | 1786 | 30 | 1 | 6 | 23 | 0 | 0 | 19 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0004 | 0/0 | 1786 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0005 | 0/0 | 1786 | 5 | 3 | 1 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0006 | 0/0 | 1786 | 4 | 1 | 1 | 0 | 0 | 2 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0007 | 0/0 | 1786 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0008 | 0/0 | 1786 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0009 | 0/0 | 1786 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0010 | 0/0 | 1786 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0011 | 0/0 | 1786 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0012 | 0/0 | 1786 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0013 | 0/0 | 1786 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0014 | 0/0 | 1786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0015 | 0/0 | 1786 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0016 | 0/0 | 1786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0017 | 0/0 | 1786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0018 | 0/0 | 1786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0019 | 0/0 | 1786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0020 | 0/0 | 1786 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0021 | 0/0 | 1786 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0022 | 0/0 | 1786 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0023 | 0/0 | 1786 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0024 | 0/0 | 1786 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0025 | 0/0 | 1786 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0026 | 0/0 | 1786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0027 | 0/0 | 1786 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0028 | 0/0 | 1786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0029 | 0/0 | 1786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0030 | 0/0 | 1786 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| 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 | 5361 | 83 | 7 | 18 | 45 | 4 | 9 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0002 | 0/1 | 5361 | 50 | 3 | 12 | 30 | 1 | 3 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0003 | 1/0 | 5361 | 44 | 7 | 7 | 18 | 5 | 6 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0004 | 0/0 | 5361 | 24 | 1 | 4 | 19 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0005 | 0/0 | 5361 | 17 | 6 | 1 | 9 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0006 | 0/0 | 5361 | 14 | 6 | 1 | 2 | 0 | 5 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0007 | 0/0 | 5361 | 11 | 11 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0008 | 0/0 | 5361 | 9 | 1 | 3 | 2 | 1 | 2 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0009 | 0/0 | 5361 | 8 | 1 | 3 | 4 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0010 | 0/0 | 5361 | 6 | 3 | 2 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0011 | 0/0 | 5361 | 4 | 1 | 1 | 0 | 0 | 2 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0012 | 0/0 | 5361 | 4 | 2 | 1 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0013 | 0/0 | 5361 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0014 | 0/0 | 5361 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0015 | 0/0 | 5361 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0016 | 0/0 | 5361 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0017 | 0/0 | 5361 | 3 | 0 | 0 | 3 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0018 | 0/0 | 5361 | 3 | 0 | 0 | 2 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0019 | 0/0 | 5361 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0020 | 0/0 | 5361 | 2 | 0 | 0 | 2 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0021 | 0/0 | 5361 | 2 | 0 | 1 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0022 | 0/0 | 5361 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0023 | 0/0 | 5361 | 2 | 0 | 2 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0024 | 0/0 | 5361 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0025 | 0/0 | 5361 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0026 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0027 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0028 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0029 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0030 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0031 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0032 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0033 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0034 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0035 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0036 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0037 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0038 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0039 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0040 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0041 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0042 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0043 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0044 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0045 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0046 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0047 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0048 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0049 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0050 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0051 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0052 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0053 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0054 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0055 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0056 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0057 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0058 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0059 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0060 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0061 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0062 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0063 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0064 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0065 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0066 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0067 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0068 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0069 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0070 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0071 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0072 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0073 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0074 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0075 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0076 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0077 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0078 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0079 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0080 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0081 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0082 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| c0083 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 0/1 | 290 | 266 | 78 | 38 | 126 | 6 | 17 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| t0002 | 1/0 | 290 | 93 | 14 | 27 | 24 | 8 | 19 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| t0003 | 0/0 | 290 | 4 | 4 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| t0004 | 0/0 | 290 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0023 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| 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 | 5361 | 83 | 7 | 18 | 45 | 4 | 9 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0002 | 0/1 | 5361 | 50 | 3 | 12 | 30 | 1 | 3 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0005 | 0/0 | 5361 | 17 | 6 | 1 | 9 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0006 | 0/0 | 5361 | 14 | 6 | 1 | 2 | 0 | 5 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0007 | 0/0 | 5361 | 11 | 11 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0009 | 0/0 | 5361 | 8 | 1 | 3 | 4 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0014 | 0/0 | 5361 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0017 | 0/0 | 5361 | 3 | 0 | 0 | 3 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0018 | 0/0 | 5361 | 3 | 0 | 0 | 2 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0022 | 0/0 | 5361 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0027 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0028 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0029 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0032 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0035 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0042 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0043 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0044 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0045 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0056 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0058 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0059 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0063 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0072 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0073 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0077 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0078 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0083 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0003 | 1/0 | 5361 | 44 | 7 | 7 | 18 | 5 | 6 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0008 | 0/0 | 5361 | 9 | 1 | 3 | 2 | 1 | 2 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0010 | 0/0 | 5361 | 6 | 3 | 2 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0013 | 0/0 | 5361 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0019 | 0/0 | 5361 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0021 | 0/0 | 5361 | 2 | 0 | 1 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0026 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0039 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0052 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0053 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0054 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0081 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0003c0004 | 0/0 | 5361 | 24 | 1 | 4 | 19 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0003c0020 | 0/0 | 5361 | 2 | 0 | 0 | 2 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0003c0038 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0003c0049 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0003c0050 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0003c0079 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0004c0015 | 0/0 | 5361 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0004c0016 | 0/0 | 5361 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0004c0066 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0004c0067 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0004c0068 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0004c0069 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0005c0012 | 0/0 | 5361 | 4 | 2 | 1 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0005c0065 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0006c0011 | 0/0 | 5361 | 4 | 1 | 1 | 0 | 0 | 2 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0007c0024 | 0/0 | 5361 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0007c0031 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0008c0023 | 0/0 | 5361 | 2 | 0 | 2 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0008c0080 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0009c0070 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0009c0071 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0010c0062 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0010c0082 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0011c0025 | 0/0 | 5361 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0012c0075 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0013c0064 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0014c0036 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0015c0037 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0016c0048 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0017c0076 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0018c0047 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0019c0033 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0020c0057 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0021c0055 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0022c0030 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0023c0041 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0024c0040 | 0/0 | 5361 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0025c0051 | 0/0 | 5361 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0026c0060 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0027c0061 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0028c0034 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0029c0046 | 0/0 | 5361 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0030c0074 | 0/0 | 5361 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 0/0 | 5650 | 70 | 7 | 9 | 44 | 2 | 8 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0001t0002 | 0/0 | 5650 | 13 | 0 | 9 | 1 | 2 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0002t0001 | 0/1 | 5650 | 50 | 3 | 12 | 30 | 1 | 3 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0005t0001 | 0/0 | 5650 | 17 | 6 | 1 | 9 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0006t0001 | 0/0 | 5650 | 9 | 6 | 0 | 1 | 0 | 2 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0006t0002 | 0/0 | 5650 | 5 | 0 | 1 | 1 | 0 | 3 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0007t0001 | 0/0 | 5650 | 9 | 9 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0007t0003 | 0/0 | 5650 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0009t0001 | 0/0 | 5650 | 8 | 1 | 3 | 4 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0014t0001 | 0/0 | 5650 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0014t0003 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0017t0001 | 0/0 | 5650 | 3 | 0 | 0 | 3 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0018t0001 | 0/0 | 5650 | 2 | 0 | 0 | 2 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0018t0002 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0022t0001 | 0/0 | 5650 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0027t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0028t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0029t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0032t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0035t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0042t0001 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0043t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0044t0002 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0045t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0056t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0058t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0059t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0063t0001 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0072t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0073t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0077t0001 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0078t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0001c0083t0002 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0003t0001 | 0/0 | 5650 | 5 | 2 | 1 | 1 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0003t0002 | 1/0 | 5650 | 39 | 5 | 6 | 17 | 4 | 6 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0008t0002 | 0/0 | 5650 | 9 | 1 | 3 | 2 | 1 | 2 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0010t0001 | 0/0 | 5650 | 6 | 3 | 2 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0013t0001 | 0/0 | 5650 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0019t0002 | 0/0 | 5650 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0021t0002 | 0/0 | 5650 | 2 | 0 | 1 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0026t0002 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0039t0002 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0052t0002 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0053t0002 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0054t0001 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0002c0081t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0003c0004t0001 | 0/0 | 5650 | 23 | 1 | 4 | 18 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0003c0004t0002 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0003c0020t0001 | 0/0 | 5650 | 2 | 0 | 0 | 2 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0003c0038t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0003c0049t0001 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0003c0050t0002 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0003c0079t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0004c0015t0001 | 0/0 | 5650 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0004c0015t0002 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0004c0016t0001 | 0/0 | 5650 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0004c0066t0004 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0004c0067t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0004c0068t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0004c0069t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0005c0012t0002 | 0/0 | 5650 | 4 | 2 | 1 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0005c0065t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0006c0011t0002 | 0/0 | 5650 | 4 | 1 | 1 | 0 | 0 | 2 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0007c0024t0001 | 0/0 | 5650 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0007c0031t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0008c0023t0001 | 0/0 | 5650 | 2 | 0 | 2 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0008c0080t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0009c0070t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0009c0071t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0010c0062t0002 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0010c0082t0002 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0011c0025t0001 | 0/0 | 5650 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0012c0075t0001 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0013c0064t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0014c0036t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0015c0037t0002 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0016c0048t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0017c0076t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0018c0047t0003 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0019c0033t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0020c0057t0002 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0021c0055t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0022c0030t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0023c0041t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0024c0040t0001 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0025c0051t0001 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0026c0060t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0027c0061t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0028c0034t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0029c0046t0002 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| a0030c0074t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | copy fasta | chr7 | 107918799 | 108008161 |
| actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0005t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0005t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0005t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0005t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0005t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0005t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0005t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0005t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0005t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0005t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0005t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0005t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0005t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0005t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0005t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0006t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0006t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0006t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0006t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0006t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0006t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0006t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0006t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0006t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0006t0002g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0006t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0006t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0006t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0006t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0007t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0007t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0007t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0007t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0007t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0007t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0007t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0007t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0007t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0007t0003g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0007t0003g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0009t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0009t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0009t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0009t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0009t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0009t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0009t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0009t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0014t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0014t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0014t0003g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0017t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0017t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0017t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0018t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0018t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0018t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0022t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0022t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0027t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0028t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0029t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0032t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0035t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0042t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0043t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0044t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0045t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0056t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0058t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0059t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0063t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0072t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0073t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0077t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0078t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0001c0083t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0023 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0003t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0008t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0008t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0008t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0008t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0008t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0008t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0008t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0008t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0008t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0010t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0010t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0010t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0010t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0010t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0010t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0013t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0013t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0013t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0019t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0019t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0021t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0021t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0026t0002g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0039t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0052t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0053t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0054t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0002c0081t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0004t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0020t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0020t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0038t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0049t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0050t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0003c0079t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0004c0015t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0004c0015t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0004c0015t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0004c0016t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0004c0016t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0004c0016t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0004c0066t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0004c0067t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0004c0068t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0004c0069t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0005c0012t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0005c0012t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0005c0012t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0005c0012t0002g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0005c0065t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0006c0011t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0006c0011t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0006c0011t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0006c0011t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0007c0024t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0007c0024t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0007c0031t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0008c0023t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0008c0023t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0008c0080t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0009c0070t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0009c0071t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0010c0062t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0010c0082t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0011c0025t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0011c0025t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0012c0075t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0013c0064t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0014c0036t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0015c0037t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0016c0048t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0017c0076t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0018c0047t0003g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0019c0033t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0020c0057t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0021c0055t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0022c0030t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0023c0041t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0024c0040t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0025c0051t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0026c0060t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0027c0061t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0028c0034t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0029c0046t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| a0030c0074t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00099 | hp1 | a0002 | c0003 | t0001 | g0284 | EUR | GBR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00099 | hp2 | a0002 | c0003 | t0002 | g0258 | EUR | GBR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00140 | hp1 | a0002 | c0003 | t0002 | g0161 | EUR | GBR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00140 | hp2 | a0001 | c0002 | t0001 | g0049 | EUR | GBR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00323 | hp1 | a0002 | c0010 | t0001 | g0155 | EUR | FIN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00408 | hp1 | a0001 | c0009 | t0001 | g0280 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00408 | hp2 | a0001 | c0005 | t0001 | g0101 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00423 | hp1 | a0001 | c0006 | t0001 | g0251 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00423 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00438 | hp1 | a0003 | c0004 | t0001 | g0081 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00438 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00558 | hp1 | a0001 | c0002 | t0001 | g0344 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00558 | hp2 | a0001 | c0001 | t0001 | g0213 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00609 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00609 | hp2 | a0001 | c0005 | t0001 | g0129 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00621 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00621 | hp2 | a0001 | c0073 | t0001 | g0256 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00639 | hp1 | a0003 | c0004 | t0001 | g0148 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00639 | hp2 | a0002 | c0010 | t0001 | g0227 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00642 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00642 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00673 | hp1 | a0002 | c0003 | t0002 | g0121 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00673 | hp2 | a0001 | c0002 | t0001 | g0215 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00733 | hp1 | a0002 | c0003 | t0002 | g0013 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00733 | hp2 | a0001 | c0006 | t0002 | g0116 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00735 | hp1 | a0001 | c0009 | t0001 | g0018 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00735 | hp2 | a0002 | c0008 | t0002 | g0273 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00738 | hp1 | a0002 | c0026 | t0002 | g0352 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00738 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00741 | hp1 | a0003 | c0004 | t0001 | g0171 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG00741 | hp2 | a0006 | c0011 | t0002 | g0060 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01069 | hp1 | a0002 | c0003 | t0002 | g0010 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01069 | hp2 | a0008 | c0023 | t0001 | g0051 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01070 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01070 | hp2 | a0002 | c0021 | t0002 | g0066 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01081 | hp1 | a0002 | c0003 | t0001 | g0165 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01081 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01099 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01099 | hp2 | a0002 | c0054 | t0001 | g0181 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01106 | hp1 | a0012 | c0075 | t0001 | g0043 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01106 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01109 | hp1 | a0002 | c0003 | t0002 | g0017 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01109 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01168 | hp1 | a0002 | c0008 | t0002 | g0272 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01168 | hp2 | a0001 | c0002 | t0001 | g0057 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01175 | hp1 | a0001 | c0083 | t0002 | g0074 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01175 | hp2 | a0001 | c0005 | t0001 | g0059 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01192 | hp1 | a0001 | c0002 | t0001 | g0211 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01192 | hp2 | a0010 | c0062 | t0002 | g0293 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01243 | hp1 | a0005 | c0012 | t0002 | g0353 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01243 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01255 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01255 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01256 | hp1 | a0003 | c0049 | t0001 | g0056 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01256 | hp2 | a0002 | c0003 | t0002 | g0045 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01257 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01257 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01258 | hp1 | a0002 | c0003 | t0002 | g0046 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01258 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01261 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01261 | hp2 | a0003 | c0004 | t0001 | g0214 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01346 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01346 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01361 | hp1 | a0003 | c0050 | t0002 | g0146 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01433 | hp1 | a0004 | c0066 | t0004 | g0021 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01433 | hp2 | a0008 | c0023 | t0001 | g0053 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01515 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01515 | hp2 | a0001 | c0042 | t0001 | g0112 | EUR | IBS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01517 | hp1 | a0002 | c0003 | t0002 | g0288 | EUR | IBS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01517 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01884 | hp1 | a0008 | c0080 | t0001 | g0276 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01884 | hp2 | a0002 | c0010 | t0001 | g0044 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01891 | hp1 | a0001 | c0007 | t0001 | g0130 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01891 | hp2 | a0001 | c0014 | t0003 | g0360 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01928 | hp1 | a0001 | c0002 | t0001 | g0265 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01928 | hp2 | a0002 | c0053 | t0002 | g0145 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01943 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01943 | hp2 | a0002 | c0010 | t0001 | g0162 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01952 | hp1 | a0024 | c0040 | t0001 | g0241 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01952 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01975 | hp1 | a0002 | c0008 | t0002 | g0268 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01975 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01981 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01981 | hp2 | a0001 | c0002 | t0001 | g0240 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01993 | hp1 | a0001 | c0009 | t0001 | g0281 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG01993 | hp2 | a0002 | c0003 | t0002 | g0242 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02004 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02004 | hp2 | a0001 | c0002 | t0001 | g0144 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02015 | hp1 | a0001 | c0009 | t0001 | g0282 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02015 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02027 | hp1 | a0001 | c0002 | t0001 | g0217 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02027 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02055 | hp1 | a0001 | c0007 | t0003 | g0361 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02055 | hp2 | a0001 | c0005 | t0001 | g0351 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02056 | hp1 | a0003 | c0004 | t0001 | g0164 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02056 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02080 | hp1 | a0005 | c0012 | t0002 | g0323 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02080 | hp2 | a0001 | c0005 | t0001 | g0244 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02083 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02129 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02129 | hp2 | a0001 | c0006 | t0002 | g0235 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02132 | hp2 | a0002 | c0003 | t0002 | g0315 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02135 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02135 | hp2 | a0001 | c0005 | t0001 | g0326 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02145 | hp1 | a0002 | c0003 | t0002 | g0092 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02145 | hp2 | a0001 | c0005 | t0001 | g0150 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02148 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02148 | hp2 | a0003 | c0004 | t0001 | g0238 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02155 | hp1 | a0023 | c0041 | t0001 | g0322 | EAS | CDX | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CDX | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02165 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02165 | hp2 | a0021 | c0055 | t0001 | g0243 | EAS | CDX | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02257 | hp1 | a0001 | c0002 | t0001 | g0237 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02257 | hp2 | a0005 | c0012 | t0002 | g0135 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02258 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02258 | hp2 | a0001 | c0006 | t0001 | g0341 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02280 | hp1 | a0001 | c0043 | t0001 | g0127 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02280 | hp2 | a0002 | c0013 | t0001 | g0030 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02293 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02293 | hp2 | a0001 | c0009 | t0001 | g0270 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02451 | hp1 | a0001 | c0007 | t0001 | g0343 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02451 | hp2 | a0001 | c0009 | t0001 | g0271 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02523 | hp2 | a0001 | c0009 | t0001 | g0194 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02572 | hp1 | a0001 | c0007 | t0003 | g0362 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02572 | hp2 | a0001 | c0078 | t0001 | g0024 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02615 | hp1 | a0011 | c0025 | t0001 | g0340 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02615 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02622 | hp1 | a0001 | c0035 | t0001 | g0037 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02622 | hp2 | a0001 | c0007 | t0001 | g0009 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02630 | hp1 | a0002 | c0003 | t0002 | g0347 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02630 | hp2 | a0001 | c0032 | t0001 | g0028 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02647 | hp1 | a0004 | c0015 | t0001 | g0138 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02647 | hp2 | a0004 | c0067 | t0001 | g0137 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02698 | hp1 | a0010 | c0082 | t0002 | g0204 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02698 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02717 | hp1 | a0001 | c0002 | t0001 | g0337 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02717 | hp2 | a0001 | c0007 | t0001 | g0124 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02723 | hp1 | a0026 | c0060 | t0001 | g0036 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02723 | hp2 | a0007 | c0031 | t0001 | g0072 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02735 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02735 | hp2 | a0002 | c0039 | t0002 | g0203 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02738 | hp1 | a0025 | c0051 | t0001 | g0253 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02738 | hp2 | a0002 | c0003 | t0002 | g0054 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02809 | hp1 | a0009 | c0070 | t0001 | g0348 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02809 | hp2 | a0016 | c0048 | t0001 | g0027 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02818 | hp1 | a0002 | c0003 | t0002 | g0075 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02818 | hp2 | a0004 | c0069 | t0001 | g0134 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02886 | hp1 | a0014 | c0036 | t0001 | g0068 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02886 | hp2 | a0007 | c0024 | t0001 | g0184 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02895 | hp1 | a0004 | c0015 | t0002 | g0008 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02895 | hp2 | a0002 | c0003 | t0002 | g0339 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02896 | hp1 | a0001 | c0006 | t0001 | g0356 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02896 | hp2 | a0028 | c0034 | t0001 | g0031 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02897 | hp1 | a0002 | c0003 | t0002 | g0338 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02897 | hp2 | a0001 | c0006 | t0001 | g0358 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02922 | hp1 | a0029 | c0046 | t0002 | g0333 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02922 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02965 | hp1 | a0001 | c0059 | t0001 | g0041 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02965 | hp2 | a0001 | c0007 | t0001 | g0319 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02970 | hp1 | a0001 | c0022 | t0001 | g0029 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02970 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02976 | hp1 | a0002 | c0003 | t0001 | g0071 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02976 | hp2 | a0004 | c0016 | t0001 | g0354 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03017 | hp1 | a0001 | c0006 | t0001 | g0133 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03017 | hp2 | a0002 | c0003 | t0002 | g0233 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03041 | hp1 | a0002 | c0010 | t0001 | g0180 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03041 | hp2 | a0005 | c0012 | t0002 | g0136 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03098 | hp1 | a0002 | c0010 | t0001 | g0334 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03098 | hp2 | a0001 | c0002 | t0001 | g0247 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03130 | hp1 | a0007 | c0024 | t0001 | g0032 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03130 | hp2 | a0005 | c0065 | t0001 | g0147 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03139 | hp1 | a0001 | c0014 | t0001 | g0336 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03139 | hp2 | a0002 | c0019 | t0002 | g0308 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03209 | hp1 | a0001 | c0028 | t0001 | g0350 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03209 | hp2 | a0001 | c0007 | t0001 | g0126 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03225 | hp1 | a0009 | c0071 | t0001 | g0067 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03225 | hp2 | a0001 | c0072 | t0001 | g0025 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03239 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03239 | hp2 | a0006 | c0011 | t0002 | g0259 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03486 | hp1 | a0019 | c0033 | t0001 | g0040 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03486 | hp2 | a0004 | c0068 | t0001 | g0139 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03490 | hp2 | a0001 | c0006 | t0002 | g0224 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03491 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03491 | hp2 | a0001 | c0002 | t0001 | g0310 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03492 | hp2 | a0001 | c0002 | t0001 | g0298 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03516 | hp1 | a0001 | c0045 | t0001 | g0038 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03516 | hp2 | a0002 | c0019 | t0002 | g0304 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03540 | hp1 | a0001 | c0007 | t0001 | g0115 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03540 | hp2 | a0001 | c0005 | t0001 | g0035 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03579 | hp1 | a0001 | c0044 | t0002 | g0345 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03579 | hp2 | a0001 | c0022 | t0001 | g0039 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03654 | hp1 | a0001 | c0006 | t0002 | g0327 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03654 | hp2 | a0002 | c0008 | t0002 | g0156 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03669 | hp1 | a0001 | c0006 | t0002 | g0185 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03669 | hp2 | a0002 | c0003 | t0002 | g0176 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03710 | hp1 | a0002 | c0003 | t0002 | g0168 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03710 | hp2 | a0002 | c0003 | t0002 | g0175 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03831 | hp1 | a0006 | c0011 | t0002 | g0330 | SAS | BEB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03831 | hp2 | a0002 | c0052 | t0002 | g0160 | SAS | BEB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03834 | hp1 | a0015 | c0037 | t0002 | g0232 | SAS | BEB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03834 | hp2 | a0001 | c0018 | t0002 | g0269 | SAS | BEB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG04115 | hp1 | a0001 | c0077 | t0001 | g0275 | SAS | STU | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG04115 | hp2 | a0001 | c0006 | t0001 | g0193 | SAS | STU | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG04184 | hp1 | a0001 | c0005 | t0001 | g0248 | SAS | BEB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG04184 | hp2 | a0001 | c0063 | t0001 | g0324 | SAS | BEB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG04199 | hp1 | a0002 | c0003 | t0002 | g0285 | SAS | STU | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG04199 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | STU | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG04204 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | STU | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG04204 | hp2 | a0001 | c0002 | t0001 | g0297 | SAS | STU | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG04228 | hp1 | a0002 | c0008 | t0002 | g0274 | SAS | STU | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG04228 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | STU | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18522 | hp1 | a0001 | c0006 | t0001 | g0254 | AFR | YRI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18522 | hp2 | a0002 | c0013 | t0001 | g0069 | AFR | YRI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18612 | hp1 | a0003 | c0004 | t0001 | g0080 | EAS | CHB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18612 | hp2 | a0003 | c0004 | t0001 | g0229 | EAS | CHB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18906 | hp1 | a0002 | c0008 | t0002 | g0006 | AFR | YRI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18906 | hp2 | a0001 | c0027 | t0001 | g0349 | AFR | YRI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18939 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18939 | hp2 | a0003 | c0004 | t0001 | g0082 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18942 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18942 | hp2 | a0002 | c0003 | t0002 | g0163 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18944 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18944 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18945 | hp1 | a0003 | c0020 | t0001 | g0195 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18945 | hp2 | a0002 | c0003 | t0002 | g0113 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18946 | hp1 | a0001 | c0002 | t0001 | g0117 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18946 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18948 | hp1 | a0002 | c0003 | t0002 | g0264 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18949 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18949 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18952 | hp1 | a0022 | c0030 | t0001 | g0312 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18952 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18953 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18953 | hp2 | a0003 | c0004 | t0001 | g0158 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18954 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18954 | hp2 | a0001 | c0005 | t0001 | g0096 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18960 | hp1 | a0002 | c0003 | t0002 | g0120 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18960 | hp2 | a0003 | c0004 | t0001 | g0252 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18962 | hp1 | a0002 | c0003 | t0002 | g0076 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18962 | hp2 | a0027 | c0061 | t0001 | g0123 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18966 | hp1 | a0001 | c0017 | t0001 | g0093 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18966 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18967 | hp1 | a0003 | c0004 | t0001 | g0084 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18967 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18969 | hp1 | a0002 | c0003 | t0001 | g0291 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18969 | hp2 | a0001 | c0002 | t0001 | g0328 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18971 | hp1 | a0001 | c0029 | t0001 | g0311 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18971 | hp2 | a0003 | c0004 | t0001 | g0318 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18975 | hp1 | a0001 | c0009 | t0001 | g0283 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18977 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18977 | hp2 | a0002 | c0008 | t0002 | g0279 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18981 | hp1 | a0003 | c0004 | t0001 | g0191 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18981 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18982 | hp1 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18982 | hp2 | a0003 | c0004 | t0001 | g0230 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18984 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18984 | hp2 | a0003 | c0004 | t0001 | g0317 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18985 | hp1 | a0001 | c0017 | t0001 | g0257 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18985 | hp2 | a0002 | c0003 | t0002 | g0142 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18988 | hp1 | a0002 | c0003 | t0002 | g0198 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18988 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18989 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18990 | hp1 | a0013 | c0064 | t0001 | g0255 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18993 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18993 | hp2 | a0002 | c0003 | t0002 | g0208 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18994 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18994 | hp2 | a0002 | c0021 | t0002 | g0108 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18995 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18995 | hp2 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18998 | hp1 | a0002 | c0003 | t0002 | g0301 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA18998 | hp2 | a0003 | c0004 | t0002 | g0154 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19001 | hp1 | a0003 | c0004 | t0001 | g0250 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19001 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19003 | hp1 | a0001 | c0005 | t0001 | g0114 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19003 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19007 | hp1 | a0003 | c0020 | t0001 | g0187 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19007 | hp2 | a0001 | c0058 | t0001 | g0143 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19009 | hp1 | a0003 | c0004 | t0001 | g0086 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19009 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19010 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19010 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19011 | hp2 | a0001 | c0002 | t0001 | g0209 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19012 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19012 | hp2 | a0001 | c0005 | t0001 | g0329 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19030 | hp1 | a0018 | c0047 | t0003 | g0359 | AFR | LWK | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19030 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | LWK | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19043 | hp1 | a0001 | c0006 | t0001 | g0042 | AFR | LWK | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19043 | hp2 | a0004 | c0015 | t0001 | g0140 | AFR | LWK | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19055 | hp1 | a0003 | c0004 | t0001 | g0079 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19055 | hp2 | a0001 | c0018 | t0001 | g0178 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19056 | hp1 | a0001 | c0005 | t0001 | g0190 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19056 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19057 | hp1 | a0001 | c0002 | t0001 | g0122 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19057 | hp2 | a0002 | c0003 | t0002 | g0220 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19058 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19058 | hp2 | a0030 | c0074 | t0001 | g0200 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19060 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19060 | hp2 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19062 | hp1 | a0003 | c0038 | t0001 | g0231 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19062 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19065 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19065 | hp2 | a0001 | c0018 | t0001 | g0277 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19066 | hp1 | a0003 | c0004 | t0001 | g0157 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19066 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19068 | hp1 | a0002 | c0003 | t0002 | g0212 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19068 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19070 | hp1 | a0001 | c0017 | t0001 | g0095 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19070 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19076 | hp2 | a0002 | c0008 | t0002 | g0278 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19080 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19080 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19081 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19081 | hp2 | a0002 | c0003 | t0002 | g0099 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19082 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19082 | hp2 | a0003 | c0004 | t0001 | g0225 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19084 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19085 | hp1 | a0003 | c0004 | t0001 | g0236 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19085 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19087 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19088 | hp1 | a0001 | c0056 | t0001 | g0088 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19088 | hp2 | a0001 | c0005 | t0001 | g0219 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19090 | hp1 | a0002 | c0003 | t0002 | g0182 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19090 | hp2 | a0003 | c0079 | t0001 | g0179 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19091 | hp1 | a0002 | c0003 | t0002 | g0159 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19091 | hp2 | a0002 | c0003 | t0002 | g0169 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19240 | hp1 | a0004 | c0016 | t0001 | g0332 | AFR | YRI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA19240 | hp2 | a0001 | c0005 | t0001 | g0119 | AFR | YRI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA20129 | hp1 | a0017 | c0076 | t0001 | g0005 | AFR | ASW | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA20129 | hp2 | a0002 | c0013 | t0001 | g0034 | AFR | ASW | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA20752 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA20752 | hp2 | a0002 | c0008 | t0002 | g0098 | EUR | TSI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA20805 | hp1 | a0002 | c0003 | t0002 | g0166 | EUR | TSI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA20805 | hp2 | a0020 | c0057 | t0002 | g0090 | EUR | TSI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02109 | hp1 | a0011 | c0025 | t0001 | g0141 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02109 | hp2 | a0001 | c0005 | t0001 | g0357 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02486 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02559 | hp1 | a0004 | c0016 | t0001 | g0355 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG02559 | hp2 | a0001 | c0007 | t0001 | g0007 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03471 | hp1 | a0002 | c0081 | t0001 | g0020 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG03471 | hp2 | a0001 | c0007 | t0001 | g0125 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG06807 | hp1 | a0001 | c0014 | t0001 | g0346 | AFR | USA | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| HG06807 | hp2 | a0006 | c0011 | t0002 | g0058 | AFR | USA | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA20300 | hp1 | a0003 | c0004 | t0001 | g0206 | AFR | USA | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA20300 | hp2 | a0002 | c0003 | t0001 | g0070 | AFR | USA | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA21309 | hp1 | a0001 | c0006 | t0001 | g0128 | AFR | LWK | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| NA21309 | hp2 | a0001 | c0005 | t0001 | g0026 | AFR | LWK | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0052 | REF | REF | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| homoSapiens_grch38 | hp1 | a0002 | c0003 | t0002 | g0023 | REF | REF | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:107929427
|
T | G | 1 | a0025 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.4730A>C | p.Glu1577Ala | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 30/34 | 4867/5650 | 4730/5361 | 1577/1786 | chr7 | 107929427 | ||
| chr7:107929517
|
A | G | 2 | a0006a0020 | 5 | HG00741.hp2 HG03239.hp2 HG03831.hp1 others(2): Show |
missense_variant | MODERATE | c.4640T>C | p.Ile1547Thr | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 30/34 | 4777/5650 | 4640/5361 | 1547/1786 | chr7 | 107929517 | ||
| chr7:107937131
|
G | T | 1 | a0021 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.3908C>A | p.Ala1303Asp | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/34 | 4045/5650 | 3908/5361 | 1303/1786 | chr7 | 107937131 | ||
| chr7:107940100
|
C | A | 2 | a0014a0016 | 2 | HG02809.hp2 HG02886.hp1 |
missense_variant | MODERATE | c.3650G>T | p.Arg1217Leu | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/34 | 3787/5650 | 3650/5361 | 1217/1786 | chr7 | 107940100 | ||
| chr7:107940127
|
T | C | 1 | a0022 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.3623A>G | p.Lys1208Arg | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/34 | 3760/5650 | 3623/5361 | 1208/1786 | chr7 | 107940127 | ||
| chr7:107952179
|
C | T | 2 | a0023a0030 | 2 | HG02155.hp1 NA19058.hp2 |
missense_variant | MODERATE | c.3124G>A | p.Gly1042Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/34 | 3261/5650 | 3124/5361 | 1042/1786 | chr7 | 107952179 | ||
| chr7:107953544
|
T | C | 25 | a0001a0003a0004others(22): Show | 280 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(277): Show |
missense_variant | MODERATE | c.3065A>G | p.Gln1022Arg | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/34 | 3202/5650 | 3065/5361 | 1022/1786 | chr7 | 107953544 | ||
| chr7:107953689
|
G | C | 1 | a0007 | 3 | HG02723.hp2 HG02886.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.2920C>G | p.Gln974Glu | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/34 | 3057/5650 | 2920/5361 | 974/1786 | chr7 | 107953689 | ||
| chr7:107953740
|
C | T | 1 | a0008 | 3 | HG01069.hp2 HG01433.hp2 HG01884.hp1 |
missense_variant | MODERATE | c.2869G>A | p.Asp957Asn | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/34 | 3006/5650 | 2869/5361 | 957/1786 | chr7 | 107953740 | ||
| chr7:107955551
|
C | T | 1 | a0024 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.2770G>A | p.Asp924Asn | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/34 | 2907/5650 | 2770/5361 | 924/1786 | chr7 | 107955551 | ||
| chr7:107959361
|
C | T | 2 | a0003a0025 | 31 | HG00438.hp1 HG00639.hp1 HG00741.hp1 others(28): Show |
missense_variant | MODERATE | c.2578G>A | p.Gly860Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/34 | 2715/5650 | 2578/5361 | 860/1786 | chr7 | 107959361 | ||
| chr7:107959382
|
G | A | 1 | a0026 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.2557C>T | p.Arg853Trp | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/34 | 2694/5650 | 2557/5361 | 853/1786 | chr7 | 107959382 | ||
| chr7:107959394
|
G | A | 1 | a0027 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.2545C>T | p.Arg849Trp | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/34 | 2682/5650 | 2545/5361 | 849/1786 | chr7 | 107959394 | ||
| chr7:107959397
|
C | G | 1 | a0028 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.2542G>C | p.Ala848Pro | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/34 | 2679/5650 | 2542/5361 | 848/1786 | chr7 | 107959397 | ||
| chr7:107959738
|
T | C | 1 | a0029 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.2411A>G | p.Asn804Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 19/34 | 2548/5650 | 2411/5361 | 804/1786 | chr7 | 107959738 | ||
| chr7:107959766
|
G | C | 1 | a0010 | 2 | HG01192.hp2 HG02698.hp1 |
missense_variant | MODERATE | c.2383C>G | p.Arg795Gly | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 19/34 | 2520/5650 | 2383/5361 | 795/1786 | chr7 | 107959766 | ||
| chr7:107960646
|
C | G | 1 | a0019 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.2113G>C | p.Val705Leu | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 18/34 | 2250/5650 | 2113/5361 | 705/1786 | chr7 | 107960646 | ||
| chr7:107961219
|
G | A | 1 | a0018 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.2096C>T | p.Thr699Met | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 17/34 | 2233/5650 | 2096/5361 | 699/1786 | chr7 | 107961219 | ||
| chr7:107961306
|
A | G | 4 | a0011a0014a0016others(1): Show | 5 | HG02109.hp1 HG02615.hp1 HG02809.hp2 others(2): Show |
missense_variant | MODERATE | c.2009T>C | p.Val670Ala | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 17/34 | 2146/5650 | 2009/5361 | 670/1786 | chr7 | 107961306 | ||
| chr7:107962996
|
A | G | 1 | a0015 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1766T>C | p.Val589Ala | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/34 | 1903/5650 | 1766/5361 | 589/1786 | chr7 | 107962996 | ||
| chr7:107973066
|
C | G | 1 | a0014 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.1488G>C | p.Glu496Asp | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/34 | 1625/5650 | 1488/5361 | 496/1786 | chr7 | 107973066 | ||
| chr7:107975021
|
G | A | 1 | a0013 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.1447C>T | p.Arg483Cys | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/34 | 1584/5650 | 1447/5361 | 483/1786 | chr7 | 107975021 | ||
| chr7:107975743
|
G | A | 3 | a0004a0005a0011 | 17 | HG01243.hp1 HG01433.hp1 HG02080.hp1 others(14): Show |
missense_variant | MODERATE | c.1135C>T | p.Pro379Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 10/34 | 1272/5650 | 1135/5361 | 379/1786 | chr7 | 107975743 | ||
| chr7:107978116
|
G | A | 1 | a0009 | 2 | HG02809.hp1 HG03225.hp1 |
missense_variant | MODERATE | c.931C>T | p.Leu311Phe | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/34 | 1068/5650 | 931/5361 | 311/1786 | chr7 | 107978116 | ||
| chr7:107986288
|
C | A | 1 | a0030 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.499G>T | p.Ala167Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 6/34 | 636/5650 | 499/5361 | 167/1786 | chr7 | 107986288 | ||
| chr7:107986311
|
G | C | 1 | a0012 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.476C>G | p.Thr159Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 6/34 | 613/5650 | 476/5361 | 159/1786 | chr7 | 107986311 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:107924065
|
G | A | 1 | a0001c0058 | 1 | NA19007.hp2 | synonymous_variant | LOW | c.5247C>T | p.Asp1749Asp | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 34/34 | 5384/5650 | 5247/5361 | 1749/1786 | chr7 | 107924065 | ||
| chr7:107926300
|
G | A | 1 | a0002c0054 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.4947C>T | p.Ser1649Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/34 | 5084/5650 | 4947/5361 | 1649/1786 | chr7 | 107926300 | ||
| chr7:107926318
|
G | A | 3 | a0001c0022a0001c0078a0004c0067 | 4 | HG02572.hp2 HG02647.hp2 HG02970.hp1 others(1): Show |
synonymous_variant | LOW | c.4929C>T | p.Asn1643Asn | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/34 | 5066/5650 | 4929/5361 | 1643/1786 | chr7 | 107926318 | ||
| chr7:107926357
|
A | G | 1 | a0004c0069 | 1 | HG02818.hp2 | splice_region_variant&synonymous_variant | LOW | c.4890T>C | p.Ile1630Ile | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/34 | 5027/5650 | 4890/5361 | 1630/1786 | chr7 | 107926357 | ||
| chr7:107929072
|
A | G | 44 | a0001c0002a0001c0005a0001c0007others(41): Show | 160 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(157): Show |
synonymous_variant | LOW | c.4879T>C | p.Leu1627Leu | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/34 | 5016/5650 | 4879/5361 | 1627/1786 | chr7 | 107929072 | ||
| chr7:107929572
|
A | G | 1 | a0001c0056 | 1 | NA19088.hp1 | synonymous_variant | LOW | c.4585T>C | p.Leu1529Leu | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 30/34 | 4722/5650 | 4585/5361 | 1529/1786 | chr7 | 107929572 | ||
| chr7:107932285
|
C | A | 1 | a0001c0045 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.4281G>T | p.Gly1427Gly | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 28/34 | 4418/5650 | 4281/5361 | 1427/1786 | chr7 | 107932285 | ||
| chr7:107932330
|
G | A | 3 | a0009c0070a0011c0025a0017c0076 | 4 | HG02109.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.4236C>T | p.Gly1412Gly | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 28/34 | 4373/5650 | 4236/5361 | 1412/1786 | chr7 | 107932330 | ||
| chr7:107932345
|
G | A | 1 | a0007c0024 | 2 | HG02886.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.4221C>T | p.Ser1407Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 28/34 | 4358/5650 | 4221/5361 | 1407/1786 | chr7 | 107932345 | ||
| chr7:107935421
|
G | A | 1 | a0001c0042 | 1 | HG01515.hp2 | synonymous_variant | LOW | c.4182C>T | p.Ala1394Ala | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/34 | 4319/5650 | 4182/5361 | 1394/1786 | chr7 | 107935421 | ||
| chr7:107940045
|
C | T | 1 | a0002c0053 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.3705G>A | p.Ala1235Ala | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/34 | 3842/5650 | 3705/5361 | 1235/1786 | chr7 | 107940045 | ||
| chr7:107940120
|
A | G | 1 | a0003c0049 | 1 | HG01256.hp1 | synonymous_variant | LOW | c.3630T>C | p.Ser1210Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/34 | 3767/5650 | 3630/5361 | 1210/1786 | chr7 | 107940120 | ||
| chr7:107940282
|
A | C | 1 | a0002c0052 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.3468T>G | p.Gly1156Gly | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/34 | 3605/5650 | 3468/5361 | 1156/1786 | chr7 | 107940282 | ||
| chr7:107940303
|
G | A | 1 | a0004c0066 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.3447C>T | p.Gly1149Gly | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/34 | 3584/5650 | 3447/5361 | 1149/1786 | chr7 | 107940303 | ||
| chr7:107951275
|
G | A | 12 | a0001c0014a0001c0027a0001c0035others(9): Show | 16 | HG01891.hp2 HG02280.hp1 HG02559.hp1 others(13): Show |
synonymous_variant | LOW | c.3342C>T | p.Cys1114Cys | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/34 | 3479/5650 | 3342/5361 | 1114/1786 | chr7 | 107951275 | ||
| chr7:107952162
|
G | A | 3 | a0001c0007a0001c0028a0001c0032 | 13 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(10): Show |
synonymous_variant | LOW | c.3141C>T | p.Cys1047Cys | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/34 | 3278/5650 | 3141/5361 | 1047/1786 | chr7 | 107952162 | ||
| chr7:107953597
|
C | T | 1 | a0004c0069 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.3012G>A | p.Thr1004Thr | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/34 | 3149/5650 | 3012/5361 | 1004/1786 | chr7 | 107953597 | ||
| chr7:107960509
|
C | T | 1 | a0009c0070 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.2250G>A | p.Pro750Pro | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 18/34 | 2387/5650 | 2250/5361 | 750/1786 | chr7 | 107960509 | ||
| chr7:107961275
|
C | T | 1 | a0001c0032 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.2040G>A | p.Val680Val | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 17/34 | 2177/5650 | 2040/5361 | 680/1786 | chr7 | 107961275 | ||
| chr7:107962917
|
G | A | 1 | a0001c0063 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.1845C>T | p.Arg615Arg | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/34 | 1982/5650 | 1845/5361 | 615/1786 | chr7 | 107962917 | ||
| chr7:107962986
|
A | C | 33 | a0001c0002a0001c0006a0001c0007others(30): Show | 118 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(115): Show |
synonymous_variant | LOW | c.1776T>G | p.Pro592Pro | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/34 | 1913/5650 | 1776/5361 | 592/1786 | chr7 | 107962986 | ||
| chr7:107964657
|
G | A | 2 | a0004c0069a0009c0071 | 2 | HG02818.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.1593C>T | p.Cys531Cys | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/34 | 1730/5650 | 1593/5361 | 531/1786 | chr7 | 107964657 | ||
| chr7:107964678
|
C | T | 3 | a0002c0039a0003c0038a0015c0037 | 3 | HG02735.hp2 HG03834.hp1 NA19062.hp1 |
synonymous_variant | LOW | c.1572G>A | p.Ala524Ala | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/34 | 1709/5650 | 1572/5361 | 524/1786 | chr7 | 107964678 | ||
| chr7:107975061
|
C | T | 18 | a0001c0009a0001c0018a0001c0029others(15): Show | 35 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
synonymous_variant | LOW | c.1407G>A | p.Gly469Gly | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/34 | 1544/5650 | 1407/5361 | 469/1786 | chr7 | 107975061 | ||
| chr7:107975741
|
C | T | 3 | a0001c0027a0001c0028a0002c0019 | 4 | HG03139.hp2 HG03209.hp1 HG03516.hp2 others(1): Show |
synonymous_variant | LOW | c.1137G>A | p.Pro379Pro | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 10/34 | 1274/5650 | 1137/5361 | 379/1786 | chr7 | 107975741 | ||
| chr7:107978156
|
G | A | 1 | a0001c0072 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.891C>T | p.His297His | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/34 | 1028/5650 | 891/5361 | 297/1786 | chr7 | 107978156 | ||
| chr7:107980633
|
T | C | 2 | a0001c0017a0001c0073 | 4 | HG00621.hp2 NA18966.hp1 NA18985.hp1 others(1): Show |
synonymous_variant | LOW | c.855A>G | p.Gly285Gly | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/34 | 992/5650 | 855/5361 | 285/1786 | chr7 | 107980633 | ||
| chr7:107986319
|
A | G | 1 | a0002c0026 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.468T>C | p.Phe156Phe | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 6/34 | 605/5650 | 468/5361 | 156/1786 | chr7 | 107986319 | ||
| chr7:107986325
|
G | A | 11 | a0001c0009a0001c0018a0001c0077others(8): Show | 28 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(25): Show |
synonymous_variant | LOW | c.462C>T | p.Ser154Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 6/34 | 599/5650 | 462/5361 | 154/1786 | chr7 | 107986325 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:107923866
|
T | C | 1 | a0004c0066t0004 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*85A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 34/34 | 85 | chr7 | 107923866 | |||||
| chr7:107923921
|
T | G | 68 | a0001c0001t0001a0001c0002t0001a0001c0005t0001others(65): Show | 271 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(268): Show |
3_prime_UTR_variant | MODIFIER | c.*30A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 34/34 | 30 | chr7 | 107923921 | |||||
| chr7:108002907
|
G | A | 3 | a0001c0007t0003a0001c0014t0003a0018c0047t0003 | 4 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-22C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/34 | 22 | chr7 | 108002907 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:107924094
|
G | A | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(267): Show | 271 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(268): Show |
splice_region_variant&intron_variant | LOW | c.5225-7C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 33/33 | chr7 | 107924094 | ||||||
| chr7:107924097
|
G | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(267): Show | 271 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.5225-10C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 33/33 | chr7 | 107924097 | ||||||
| chr7:107924525
|
T | G | 1 | a0001c0001t0001g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.5065-136A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107924525 | ||||||
| chr7:107924538
|
A | G | 13 | a0001c0005t0001g0357a0001c0007t0001g0007a0001c0007t0001g0009others(10): Show | 13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.5065-149T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107924538 | ||||||
| chr7:107924562
|
A | C | 222 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(219): Show | 223 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.5065-173T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107924562 | ||||||
| chr7:107924580
|
T | G | 7 | a0001c0001t0001g0012a0001c0001t0001g0151a0001c0001t0001g0335others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.5065-191A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107924580 | ||||||
| chr7:107924649
|
T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0260 | 2 | HG00438.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.5065-260A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107924649 | ||||||
| chr7:107924667
|
A | C | 1 | a0001c0002t0001g0286 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.5065-278T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107924667 | ||||||
| chr7:107924693
|
C | T | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(267): Show | 271 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.5065-304G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107924693 | ||||||
| chr7:107924998
|
T | C | 2 | a0001c0005t0001g0119a0002c0081t0001g0020 | 2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5065-609A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107924998 | ||||||
| chr7:107925138
|
A | T | 4 | a0001c0022t0001g0029a0001c0022t0001g0039a0001c0078t0001g0024others(1): Show | 4 | HG02572.hp2 HG02647.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.5065-749T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107925138 | ||||||
| chr7:107925270
|
G | A | 2 | a0001c0006t0001g0042a0001c0006t0001g0128 | 2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.5065-881C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107925270 | ||||||
| chr7:107925380
|
T | C | 13 | a0001c0005t0001g0357a0001c0007t0001g0007a0001c0007t0001g0009others(10): Show | 13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.5064+803A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107925380 | ||||||
| chr7:107925436
|
A | C | 31 | a0001c0001t0001g0012a0001c0001t0001g0151a0001c0001t0001g0335others(28): Show | 31 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.5064+747T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107925436 | ||||||
| chr7:107925542
|
A | G | 10 | a0001c0002t0001g0306a0001c0005t0001g0129a0003c0004t0001g0084others(7): Show | 10 | HG00609.hp2 NA18612.hp2 NA18967.hp1 others(7): Show |
intron_variant | MODIFIER | c.5064+641T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107925542 | ||||||
| chr7:107925558
|
C | T | 1 | a0001c0028t0001g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5064+625G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107925558 | ||||||
| chr7:107925898
|
T | TA | 12 | a0001c0001t0001g0299a0001c0005t0001g0026a0001c0005t0001g0351others(9): Show | 12 | HG02055.hp2 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.5064+284dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107925898 | ||||||
| chr7:107925898
|
T | TAA | 263 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(260): Show | 265 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(262): Show |
intron_variant | MODIFIER | c.5064+283_5064+284d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107925898 | ||||||
| chr7:107925985
|
A | G | 276 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(273): Show | 277 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.5064+198T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107925985 | ||||||
| chr7:107926043
|
G | T | 276 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(273): Show | 277 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.5064+140C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107926043 | ||||||
| chr7:107926044
|
G | A | 1 | a0001c0001t0001g0170 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5064+139C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107926044 | ||||||
| chr7:107926367
|
C | T | 3 | a0001c0005t0001g0026a0001c0005t0001g0351a0004c0069t0001g0134 | 3 | HG02055.hp2 HG02818.hp2 NA21309.hp2 |
splice_region_variant&intron_variant | LOW | c.4888-8G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107926367 | ||||||
| chr7:107926641
|
T | C | 30 | a0001c0001t0001g0012a0001c0001t0001g0151a0001c0001t0001g0335others(27): Show | 30 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.4888-282A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107926641 | ||||||
| chr7:107926761
|
T | C | 26 | a0001c0001t0001g0012a0001c0001t0001g0151a0001c0001t0001g0335others(23): Show | 26 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.4888-402A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107926761 | ||||||
| chr7:107926844
|
G | A | 1 | a0001c0001t0001g0300 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.4888-485C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107926844 | ||||||
| chr7:107926994
|
T | C | 1 | a0001c0006t0002g0327 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4888-635A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107926994 | ||||||
| chr7:107927028
|
A | G | 31 | a0001c0001t0001g0012a0001c0001t0001g0151a0001c0001t0001g0335others(28): Show | 31 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.4888-669T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107927028 | ||||||
| chr7:107927349
|
T | C | 30 | a0001c0001t0001g0012a0001c0001t0001g0151a0001c0001t0001g0335others(27): Show | 30 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.4888-990A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107927349 | ||||||
| chr7:107927414
|
TTCAG | T | 83 | a0001c0002t0001g0014a0001c0002t0001g0049a0001c0002t0001g0052others(80): Show | 83 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(80): Show |
intron_variant | MODIFIER | c.4888-1059_4888-105 others(8): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107927414 | ||||||
| chr7:107927571
|
A | T | 1 | a0003c0004t0001g0080 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4888-1212T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107927571 | ||||||
| chr7:107927599
|
C | G | 7 | a0001c0001t0001g0012a0001c0001t0001g0151a0001c0001t0001g0335others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4888-1240G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107927599 | ||||||
| chr7:107927703
|
C | G | 1 | a0001c0001t0001g0325 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4888-1344G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107927703 | ||||||
| chr7:107927742
|
A | AT | 29 | a0001c0001t0001g0012a0001c0001t0001g0151a0001c0001t0001g0335others(26): Show | 29 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.4887+1321dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107927742 | ||||||
| chr7:107927967
|
G | A | 2 | a0007c0024t0001g0032a0007c0024t0001g0184 | 2 | HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4887+1097C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107927967 | ||||||
| chr7:107928064
|
G | A | 29 | a0001c0001t0001g0012a0001c0001t0001g0151a0001c0001t0001g0335others(26): Show | 29 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.4887+1000C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928064 | ||||||
| chr7:107928094
|
A | T | 1 | a0003c0004t0001g0250 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.4887+970T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928094 | ||||||
| chr7:107928154
|
G | A | 308 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(305): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(306): Show |
intron_variant | MODIFIER | c.4887+910C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928154 | ||||||
| chr7:107928218
|
T | C | 275 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(272): Show | 276 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.4887+846A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928218 | ||||||
| chr7:107928365
|
T | A | 9 | a0001c0005t0001g0026a0001c0005t0001g0351a0001c0007t0001g0319others(6): Show | 9 | HG02055.hp2 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.4887+699A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928365 | ||||||
| chr7:107928488
|
A | G | 9 | a0001c0001t0001g0085a0001c0001t0001g0188a0001c0001t0001g0189others(6): Show | 9 | HG02132.hp1 HG02523.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.4887+576T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928488 | ||||||
| chr7:107928501
|
CT | C | 19 | a0001c0002t0001g0247a0001c0005t0001g0026a0001c0005t0001g0351others(16): Show | 19 | HG01433.hp1 HG02055.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.4887+562delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928501 | ||||||
| chr7:107928683
|
G | T | 4 | a0001c0005t0001g0101a0001c0005t0001g0190a0001c0005t0001g0219others(1): Show | 4 | HG00408.hp2 HG02080.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.4887+381C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928683 | ||||||
| chr7:107928744
|
C | T | 1 | a0002c0003t0002g0168 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4887+320G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928744 | ||||||
| chr7:107928789
|
G | A | 18 | a0001c0002t0001g0247a0001c0005t0001g0026a0001c0005t0001g0351others(15): Show | 18 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.4887+275C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928789 | ||||||
| chr7:107928826
|
T | G | 1 | a0001c0002t0001g0197 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.4887+238A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928826 | ||||||
| chr7:107928865
|
TGAA | T | 18 | a0001c0002t0001g0247a0001c0005t0001g0026a0001c0005t0001g0351others(15): Show | 18 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.4887+196_4887+198d others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928865 | ||||||
| chr7:107928969
|
T | A | 19 | a0001c0005t0001g0119a0001c0005t0001g0357a0001c0007t0001g0007others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.4887+95A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928969 | ||||||
| chr7:107929253
|
A | T | 13 | a0001c0005t0001g0357a0001c0007t0001g0007a0001c0007t0001g0009others(10): Show | 13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.4746-48T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 30/33 | chr7 | 107929253 | ||||||
| chr7:107929748
|
T | A | 20 | a0001c0005t0001g0357a0001c0007t0001g0007a0001c0007t0001g0009others(17): Show | 20 | HG01433.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.4538-129A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107929748 | ||||||
| chr7:107929974
|
A | G | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4538-355T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107929974 | ||||||
| chr7:107930074
|
C | T | 3 | a0011c0025t0001g0141a0011c0025t0001g0340a0017c0076t0001g0005 | 3 | HG02109.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4538-455G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107930074 | ||||||
| chr7:107930232
|
G | A | 8 | a0001c0002t0001g0337a0001c0005t0001g0026a0001c0005t0001g0351others(5): Show | 8 | HG02055.hp2 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.4538-613C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107930232 | ||||||
| chr7:107930482
|
T | C | 283 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(280): Show | 285 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(282): Show |
intron_variant | MODIFIER | c.4538-863A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107930482 | ||||||
| chr7:107930620
|
A | G | 2 | a0001c0007t0001g0009a0001c0007t0001g0115 | 2 | HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4537+736T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107930620 | ||||||
| chr7:107930805
|
A | G | 19 | a0001c0005t0001g0119a0001c0005t0001g0357a0001c0007t0001g0007others(16): Show | 19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.4537+551T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107930805 | ||||||
| chr7:107930813
|
C | G | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4537+543G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107930813 | ||||||
| chr7:107930943
|
A | G | 9 | a0003c0004t0001g0079a0003c0004t0001g0080a0003c0004t0001g0081others(6): Show | 9 | HG00438.hp1 NA18612.hp1 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.4537+413T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107930943 | ||||||
| chr7:107931000
|
A | G | 1 | a0002c0008t0002g0268 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4537+356T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107931000 | ||||||
| chr7:107931094
|
C | T | 1 | a0001c0001t0001g0221 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4537+262G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107931094 | ||||||
| chr7:107931096
|
C | T | 2 | a0002c0003t0002g0013a0002c0008t0002g0098 | 2 | HG00733.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.4537+260G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107931096 | ||||||
| chr7:107931170
|
G | A | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4537+186C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107931170 | ||||||
| chr7:107931517
|
A | G | 1 | a0002c0003t0002g0076 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4393-17T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 28/33 | chr7 | 107931517 | ||||||
| chr7:107931703
|
A | G | 7 | a0001c0001t0001g0012a0001c0001t0001g0151a0001c0001t0001g0335others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4393-203T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 28/33 | chr7 | 107931703 | ||||||
| chr7:107932140
|
A | G | 2 | a0007c0024t0001g0032a0007c0024t0001g0184 | 2 | HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4392+34T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 28/33 | chr7 | 107932140 | ||||||
| chr7:107932547
|
G | A | 6 | a0001c0001t0001g0109a0001c0001t0001g0216a0001c0001t0001g0218others(3): Show | 6 | HG02135.hp1 NA18946.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.4189-170C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107932547 | ||||||
| chr7:107932728
|
G | A | 1 | a0001c0001t0001g0262 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4189-351C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107932728 | ||||||
| chr7:107932731
|
T | TA | 28 | a0001c0002t0001g0247a0001c0005t0001g0026a0001c0005t0001g0119others(25): Show | 28 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.4189-355dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107932731 | ||||||
| chr7:107932742
|
C | G | 28 | a0001c0002t0001g0247a0001c0005t0001g0026a0001c0005t0001g0119others(25): Show | 28 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.4189-365G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107932742 | ||||||
| chr7:107932765
|
C | A | 27 | a0001c0002t0001g0247a0001c0005t0001g0026a0001c0005t0001g0119others(24): Show | 27 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.4189-388G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107932765 | ||||||
| chr7:107932799
|
T | C | 2 | a0003c0004t0001g0082a0003c0004t0001g0317 | 2 | NA18939.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.4189-422A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107932799 | ||||||
| chr7:107932809
|
T | G | 275 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(272): Show | 277 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(274): Show |
intron_variant | MODIFIER | c.4189-432A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107932809 | ||||||
| chr7:107932823
|
C | A | 253 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(250): Show | 255 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(252): Show |
intron_variant | MODIFIER | c.4189-446G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107932823 | ||||||
| chr7:107932902
|
C | G | 2 | a0002c0003t0002g0159a0002c0003t0002g0212 | 2 | NA19068.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.4189-525G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107932902 | ||||||
| chr7:107933009
|
C | G | 1 | a0001c0001t0001g0226 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4189-632G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933009 | ||||||
| chr7:107933062
|
C | G | 4 | a0009c0070t0001g0348a0011c0025t0001g0141a0011c0025t0001g0340others(1): Show | 4 | HG02109.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4189-685G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933062 | ||||||
| chr7:107933297
|
T | G | 1 | a0001c0002t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4189-920A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933297 | ||||||
| chr7:107933303
|
A | G | 2 | a0014c0036t0001g0068a0016c0048t0001g0027 | 2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.4189-926T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933303 | ||||||
| chr7:107933516
|
T | G | 27 | a0001c0002t0001g0247a0001c0005t0001g0026a0001c0005t0001g0119others(24): Show | 27 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.4189-1139A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933516 | ||||||
| chr7:107933593
|
G | C | 17 | a0001c0002t0001g0247a0001c0005t0001g0119a0001c0022t0001g0029others(14): Show | 17 | HG01243.hp1 HG02280.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.4189-1216C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933593 | ||||||
| chr7:107933603
|
G | GA | 13 | a0001c0002t0001g0337a0001c0005t0001g0026a0001c0005t0001g0351others(10): Show | 13 | HG02055.hp2 HG02109.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.4189-1227dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933603 | ||||||
| chr7:107933603
|
G | GAA | 16 | a0001c0002t0001g0247a0001c0005t0001g0119a0001c0022t0001g0029others(13): Show | 16 | HG01243.hp1 HG02280.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.4189-1228_4189-122 others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933603 | ||||||
| chr7:107933615
|
C | A | 26 | a0001c0002t0001g0247a0001c0005t0001g0026a0001c0005t0001g0119others(23): Show | 26 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.4189-1238G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933615 | ||||||
| chr7:107933683
|
A | G | 143 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(140): Show | 144 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.4189-1306T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933683 | ||||||
| chr7:107933692
|
C | T | 9 | a0001c0001t0002g0192a0002c0003t0002g0099a0002c0003t0002g0113others(6): Show | 9 | HG01993.hp2 NA18945.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.4189-1315G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933692 | ||||||
| chr7:107933830
|
A | G | 1 | a0002c0081t0001g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4189-1453T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933830 | ||||||
| chr7:107933843
|
G | C | 2 | a0001c0005t0001g0026a0001c0005t0001g0351 | 2 | HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.4189-1466C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933843 | ||||||
| chr7:107933859
|
C | T | 1 | a0002c0081t0001g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4189-1482G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933859 | ||||||
| chr7:107933861
|
C | T | 1 | a0001c0001t0002g0061 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4189-1484G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933861 | ||||||
| chr7:107933901
|
G | A | 3 | a0001c0002t0001g0247a0001c0027t0001g0349a0001c0043t0001g0127 | 3 | HG02280.hp1 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4188+1514C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933901 | ||||||
| chr7:107933913
|
G | A | 2 | a0001c0078t0001g0024a0004c0067t0001g0137 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.4188+1502C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933913 | ||||||
| chr7:107933937
|
A | G | 1 | a0001c0002t0001g0331 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.4188+1478T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933937 | ||||||
| chr7:107933954
|
G | A | 1 | a0004c0066t0004g0021 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4188+1461C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933954 | ||||||
| chr7:107933982
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(138): Show | 142 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.4188+1433T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933982 | ||||||
| chr7:107933986
|
AT | A | 8 | a0001c0006t0001g0133a0002c0003t0002g0347a0002c0013t0001g0030others(5): Show | 8 | HG01243.hp1 HG02280.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.4188+1428delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933986 | ||||||
| chr7:107934050
|
T | C | 1 | a0002c0010t0001g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4188+1365A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934050 | ||||||
| chr7:107934339
|
G | A | 102 | a0001c0002t0001g0014a0001c0002t0001g0049a0001c0002t0001g0052others(99): Show | 102 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.4188+1076C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934339 | ||||||
| chr7:107934390
|
C | T | 2 | a0001c0001t0001g0087a0001c0001t0001g0316 | 2 | NA18977.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.4188+1025G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934390 | ||||||
| chr7:107934433
|
A | G | 1 | a0004c0015t0002g0008 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4188+982T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934433 | ||||||
| chr7:107934659
|
C | T | 1 | a0002c0010t0001g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4188+756G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934659 | ||||||
| chr7:107934717
|
C | T | 146 | a0001c0002t0001g0014a0001c0002t0001g0049a0001c0002t0001g0052others(143): Show | 146 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.4188+698G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934717 | ||||||
| chr7:107934835
|
G | A | 3 | a0001c0005t0001g0035a0001c0005t0001g0150a0004c0068t0001g0139 | 3 | HG02145.hp2 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4188+580C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934835 | ||||||
| chr7:107934902
|
T | TA | 6 | a0001c0001t0002g0002a0001c0001t0002g0061a0002c0003t0002g0159others(3): Show | 7 | HG01261.hp1 HG01515.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.4188+512dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934902 | ||||||
| chr7:107934902
|
TA | T | 28 | a0001c0002t0001g0247a0001c0005t0001g0026a0001c0005t0001g0119others(25): Show | 28 | HG01891.hp1 HG01993.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.4188+512delT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934902 | ||||||
| chr7:107934902
|
TAA | T | 14 | a0001c0001t0001g0033a0001c0001t0001g0342a0001c0002t0001g0337others(11): Show | 14 | HG01433.hp1 HG02109.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.4188+511_4188+512d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934902 | ||||||
| chr7:107934902
|
TAAA | T | 223 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(220): Show | 224 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(221): Show |
intron_variant | MODIFIER | c.4188+510_4188+512d others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934902 | ||||||
| chr7:107934903
|
A | T | 4 | a0001c0022t0001g0029a0001c0022t0001g0039a0001c0078t0001g0024others(1): Show | 4 | HG02572.hp2 HG02647.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.4188+512T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934903 | ||||||
| chr7:107935067
|
T | A | 1 | a0001c0002t0001g0118 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.4188+348A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935067 | ||||||
| chr7:107935112
|
G | A | 104 | a0001c0002t0001g0014a0001c0002t0001g0049a0001c0002t0001g0052others(101): Show | 104 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.4188+303C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935112 | ||||||
| chr7:107935113
|
G | A | 20 | a0001c0002t0001g0247a0001c0005t0001g0026a0001c0005t0001g0119others(17): Show | 20 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.4188+302C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935113 | ||||||
| chr7:107935148
|
G | A | 20 | a0001c0002t0001g0247a0001c0005t0001g0026a0001c0005t0001g0119others(17): Show | 20 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.4188+267C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935148 | ||||||
| chr7:107935282
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0245 | 2 | NA18944.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.4188+133A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935282 | ||||||
| chr7:107935342
|
TCTTTG | T | 4 | a0002c0010t0001g0334a0007c0024t0001g0032a0007c0024t0001g0184others(1): Show | 4 | HG02723.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.4188+68_4188+72del others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935342 | ||||||
| chr7:107935343
|
CTTTGTTT others(7): Show |
C | 13 | a0001c0005t0001g0357a0001c0007t0001g0007a0001c0007t0001g0009others(10): Show | 13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.4188+58_4188+71del others(14): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935343 | ||||||
| chr7:107935347
|
G | GT | 41 | a0001c0001t0001g0012a0001c0001t0001g0073a0001c0001t0001g0151others(38): Show | 41 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.4188+67dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935347 | ||||||
| chr7:107935347
|
G | GTT | 6 | a0001c0002t0001g0337a0001c0035t0001g0037a0002c0003t0001g0070others(3): Show | 6 | HG01361.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.4188+66_4188+67dup others(2): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935347 | ||||||
| chr7:107935347
|
G | GTTTTTTT others(3): Show |
1 | a0001c0005t0001g0351 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4188+58_4188+67dup others(10): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935347 | ||||||
| chr7:107935347
|
G | GTTTTTTT others(7): Show |
2 | a0001c0007t0001g0319a0009c0071t0001g0067 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4188+54_4188+67dup others(14): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935347 | ||||||
| chr7:107935347
|
G | GTTTTTTT others(11): Show |
1 | a0001c0032t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4188+50_4188+67dup others(18): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935347 | ||||||
| chr7:107935347
|
GTTTT | G | 11 | a0001c0002t0001g0247a0001c0022t0001g0029a0001c0027t0001g0349others(8): Show | 11 | HG02280.hp1 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.4188+64_4188+67del others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935347 | ||||||
| chr7:107935347
|
GTTTTTTT others(6): Show |
G | 103 | a0001c0001t0001g0263a0001c0002t0001g0014a0001c0002t0001g0049others(100): Show | 103 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.4188+55_4188+67del others(13): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935347 | ||||||
| chr7:107935348
|
T | G | 4 | a0002c0010t0001g0334a0007c0024t0001g0032a0007c0024t0001g0184others(1): Show | 4 | HG02723.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.4188+67A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935348 | ||||||
| chr7:107935350
|
T | G | 1 | a0004c0066t0004g0021 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4188+65A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935350 | ||||||
| chr7:107935352
|
T | TC | 4 | a0001c0001t0001g0100a0001c0001t0001g0111a0001c0001t0001g0226others(1): Show | 4 | HG02698.hp2 HG02735.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.4188+62_4188+63ins others(1): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935352 | ||||||
| chr7:107935353
|
T | G | 1 | a0001c0005t0001g0119 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4188+62A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935353 | ||||||
| chr7:107935354
|
T | G | 12 | a0001c0002t0001g0247a0001c0027t0001g0349a0001c0043t0001g0127others(9): Show | 12 | HG02280.hp1 HG02280.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.4188+61A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935354 | ||||||
| chr7:107935356
|
T | G | 4 | a0001c0001t0001g0100a0001c0001t0001g0111a0001c0001t0001g0226others(1): Show | 4 | HG02698.hp2 HG02735.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.4188+59A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935356 | ||||||
| chr7:107935357
|
T | G | 9 | a0001c0002t0001g0247a0001c0027t0001g0349a0001c0043t0001g0127others(6): Show | 9 | HG01433.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.4188+58A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935357 | ||||||
| chr7:107935358
|
T | G | 3 | a0001c0006t0001g0133a0001c0006t0001g0193a0001c0077t0001g0275 | 3 | HG03017.hp1 HG04115.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.4188+57A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935358 | ||||||
| chr7:107935704
|
C | T | 4 | a0001c0044t0002g0345a0002c0019t0002g0308a0002c0026t0002g0352others(1): Show | 4 | HG00738.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3947-48G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107935704 | ||||||
| chr7:107935848
|
G | A | 2 | a0001c0007t0001g0319a0009c0071t0001g0067 | 2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3947-192C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107935848 | ||||||
| chr7:107935908
|
T | C | 2 | a0001c0001t0001g0172a0001c0001t0001g0260 | 2 | HG00438.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.3947-252A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107935908 | ||||||
| chr7:107935910
|
T | C | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3947-254A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107935910 | ||||||
| chr7:107936001
|
G | C | 1 | a0009c0070t0001g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3947-345C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936001 | ||||||
| chr7:107936045
|
G | A | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3947-389C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936045 | ||||||
| chr7:107936375
|
T | A | 2 | a0001c0001t0001g0083a0001c0001t0001g0300 | 2 | NA19010.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.3946+718A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936375 | ||||||
| chr7:107936419
|
A | G | 5 | a0006c0011t0002g0058a0006c0011t0002g0060a0006c0011t0002g0259others(2): Show | 5 | HG00741.hp2 HG03239.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.3946+674T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936419 | ||||||
| chr7:107936460
|
A | G | 1 | a0001c0001t0001g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3946+633T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936460 | ||||||
| chr7:107936637
|
T | G | 1 | a0001c0001t0002g0003 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3946+456A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936637 | ||||||
| chr7:107936661
|
A | T | 1 | a0001c0001t0002g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3946+432T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936661 | ||||||
| chr7:107936817
|
G | A | 1 | a0001c0059t0001g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3946+276C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936817 | ||||||
| chr7:107936822
|
GA | G | 242 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(239): Show | 243 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(240): Show |
intron_variant | MODIFIER | c.3946+270delT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936822 | ||||||
| chr7:107936836
|
C | T | 5 | a0002c0013t0001g0030a0002c0013t0001g0034a0002c0013t0001g0069others(2): Show | 5 | HG02280.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3946+257G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936836 | ||||||
| chr7:107936905
|
G | A | 1 | a0003c0004t0001g0229 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3946+188C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936905 | ||||||
| chr7:107936921
|
T | C | 1 | a0025c0051t0001g0253 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3946+172A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936921 | ||||||
| chr7:107936945
|
T | G | 123 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(120): Show | 124 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.3946+148A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936945 | ||||||
| chr7:107937003
|
CT | C | 109 | a0001c0001t0001g0249a0001c0002t0001g0014a0001c0002t0001g0049others(106): Show | 109 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.3946+89delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107937003 | ||||||
| chr7:107937011
|
T | C | 103 | a0001c0001t0001g0249a0001c0002t0001g0014a0001c0002t0001g0049others(100): Show | 103 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.3946+82A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107937011 | ||||||
| chr7:107937049
|
G | A | 5 | a0001c0002t0001g0077a0001c0002t0001g0078a0001c0002t0001g0122others(2): Show | 5 | NA18966.hp2 NA18989.hp1 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.3946+44C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107937049 | ||||||
| chr7:107937560
|
G | A | 18 | a0001c0002t0001g0337a0001c0005t0001g0357a0001c0007t0001g0007others(15): Show | 18 | HG01433.hp1 HG01891.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.3762-283C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107937560 | ||||||
| chr7:107937649
|
A | G | 2 | a0001c0002t0001g0196a0001c0002t0001g0209 | 2 | NA19011.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.3762-372T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107937649 | ||||||
| chr7:107937791
|
A | G | 1 | a0001c0001t0001g0249 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3762-514T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107937791 | ||||||
| chr7:107937806
|
G | A | 4 | a0001c0001t0001g0151a0002c0003t0001g0070a0002c0003t0001g0071others(1): Show | 4 | HG02970.hp2 HG02976.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.3762-529C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107937806 | ||||||
| chr7:107937877
|
TAAG | T | 18 | a0001c0002t0001g0239a0003c0004t0001g0082a0003c0004t0001g0084others(15): Show | 18 | HG00741.hp1 HG01256.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.3762-603_3762-601d others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107937877 | ||||||
| chr7:107937954
|
C | T | 4 | a0001c0001t0001g0100a0001c0001t0001g0111a0001c0001t0001g0226others(1): Show | 4 | HG02698.hp2 HG02735.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.3762-677G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107937954 | ||||||
| chr7:107937970
|
A | G | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3762-693T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107937970 | ||||||
| chr7:107938088
|
G | C | 1 | a0001c0002t0001g0240 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3762-811C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107938088 | ||||||
| chr7:107938096
|
C | T | 4 | a0001c0044t0002g0345a0002c0019t0002g0308a0002c0026t0002g0352others(1): Show | 4 | HG00738.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3762-819G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107938096 | ||||||
| chr7:107938416
|
AT | A | 105 | a0001c0002t0001g0014a0001c0002t0001g0049a0001c0002t0001g0052others(102): Show | 105 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(102): Show |
intron_variant | MODIFIER | c.3762-1140delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107938416 | ||||||
| chr7:107938460
|
G | A | 2 | a0007c0024t0001g0032a0007c0024t0001g0184 | 2 | HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3762-1183C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107938460 | ||||||
| chr7:107938499
|
T | C | 6 | a0001c0002t0001g0337a0009c0070t0001g0348a0011c0025t0001g0141others(3): Show | 6 | HG02109.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3762-1222A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107938499 | ||||||
| chr7:107938508
|
A | G | 1 | a0001c0017t0001g0257 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3762-1231T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107938508 | ||||||
| chr7:107938587
|
G | A | 1 | a0001c0001t0001g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3762-1310C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107938587 | ||||||
| chr7:107938747
|
C | T | 1 | a0001c0005t0001g0114 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3761+1242G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107938747 | ||||||
| chr7:107938939
|
T | G | 1 | a0007c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3761+1050A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107938939 | ||||||
| chr7:107939158
|
A | G | 253 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(250): Show | 254 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.3761+831T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939158 | ||||||
| chr7:107939158
|
A | T | 1 | a0001c0018t0001g0178 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3761+831T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939158 | ||||||
| chr7:107939186
|
T | C | 1 | a0001c0009t0001g0283 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3761+803A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939186 | ||||||
| chr7:107939200
|
G | A | 3 | a0001c0002t0001g0197a0001c0002t0001g0215a0001c0009t0001g0283 | 3 | HG00673.hp2 NA18975.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.3761+789C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939200 | ||||||
| chr7:107939206
|
C | G | 9 | a0001c0005t0001g0026a0001c0005t0001g0351a0001c0022t0001g0029others(6): Show | 9 | HG02055.hp2 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3761+783G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939206 | ||||||
| chr7:107939226
|
G | A | 1 | a0004c0066t0004g0021 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3761+763C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939226 | ||||||
| chr7:107939229
|
A | T | 252 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(249): Show | 253 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.3761+760T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939229 | ||||||
| chr7:107939311
|
C | CA | 44 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0087others(41): Show | 44 | HG00423.hp2 HG00558.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.3761+677dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939311 | ||||||
| chr7:107939428
|
G | A | 3 | a0001c0001t0002g0192a0002c0003t0002g0182a0002c0008t0002g0278 | 3 | NA18994.hp1 NA19076.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.3761+561C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939428 | ||||||
| chr7:107939438
|
A | G | 13 | a0001c0005t0001g0357a0001c0007t0001g0007a0001c0007t0001g0009others(10): Show | 13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.3761+551T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939438 | ||||||
| chr7:107939503
|
A | T | 1 | a0001c0002t0001g0064 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3761+486T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939503 | ||||||
| chr7:107939532
|
T | C | 1 | a0029c0046t0002g0333 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3761+457A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939532 | ||||||
| chr7:107939614
|
G | A | 1 | a0001c0059t0001g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3761+375C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939614 | ||||||
| chr7:107939658
|
C | T | 5 | a0002c0013t0001g0030a0002c0013t0001g0034a0002c0013t0001g0069others(2): Show | 5 | HG02280.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3761+331G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939658 | ||||||
| chr7:107940394
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(264): Show | 269 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.3392-36T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107940394 | ||||||
| chr7:107940589
|
T | C | 1 | a0001c0002t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3392-231A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107940589 | ||||||
| chr7:107940590
|
A | G | 267 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(264): Show | 269 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.3392-232T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107940590 | ||||||
| chr7:107940650
|
A | G | 1 | a0029c0046t0002g0333 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3392-292T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107940650 | ||||||
| chr7:107940660
|
T | A | 1 | a0004c0066t0004g0021 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3392-302A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107940660 | ||||||
| chr7:107940670
|
C | G | 270 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(267): Show | 272 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(269): Show |
intron_variant | MODIFIER | c.3392-312G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107940670 | ||||||
| chr7:107940836
|
A | G | 1 | a0026c0060t0001g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3392-478T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107940836 | ||||||
| chr7:107940840
|
A | G | 1 | a0001c0007t0001g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3392-482T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107940840 | ||||||
| chr7:107940901
|
T | C | 267 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(264): Show | 269 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.3392-543A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107940901 | ||||||
| chr7:107941024
|
A | G | 1 | a0008c0023t0001g0053 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3392-666T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941024 | ||||||
| chr7:107941049
|
G | A | 4 | a0009c0070t0001g0348a0011c0025t0001g0141a0011c0025t0001g0340others(1): Show | 4 | HG02109.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3392-691C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941049 | ||||||
| chr7:107941134
|
C | T | 262 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(259): Show | 264 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.3392-776G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941134 | ||||||
| chr7:107941246
|
G | A | 1 | a0001c0005t0001g0248 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3392-888C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941246 | ||||||
| chr7:107941491
|
A | G | 268 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(265): Show | 269 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(266): Show |
intron_variant | MODIFIER | c.3392-1133T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941491 | ||||||
| chr7:107941539
|
T | A | 1 | a0004c0068t0001g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3392-1181A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941539 | ||||||
| chr7:107941653
|
G | A | 1 | a0001c0006t0002g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3392-1295C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941653 | ||||||
| chr7:107941655
|
AT | A | 248 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(245): Show | 249 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.3392-1298delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941655 | ||||||
| chr7:107941816
|
A | G | 1 | a0003c0004t0001g0250 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3392-1458T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941816 | ||||||
| chr7:107941819
|
C | T | 1 | a0001c0028t0001g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3392-1461G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941819 | ||||||
| chr7:107941822
|
C | CT | 12 | a0001c0001t0002g0019a0001c0001t0002g0089a0001c0001t0002g0177others(9): Show | 12 | HG01243.hp2 HG01346.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.3392-1465dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941822 | ||||||
| chr7:107941822
|
CT | C | 30 | a0001c0001t0002g0003a0001c0001t0002g0047a0001c0001t0002g0267others(27): Show | 30 | HG00099.hp2 HG00140.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.3392-1465delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941822 | ||||||
| chr7:107941822
|
CTT | C | 8 | a0001c0005t0001g0026a0001c0045t0001g0038a0002c0003t0002g0010others(5): Show | 8 | HG01069.hp1 HG02818.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.3392-1466_3392-146 others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941822 | ||||||
| chr7:107941822
|
CTTTTTT | C | 7 | a0001c0001t0001g0292a0001c0007t0001g0009a0001c0007t0001g0130others(4): Show | 7 | HG01891.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3392-1470_3392-146 others(10): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941822 | ||||||
| chr7:107941822
|
CTTTTTTT | C | 30 | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0170others(27): Show | 30 | HG02027.hp2 HG02055.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.3392-1471_3392-146 others(11): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941822 | ||||||
| chr7:107941822
|
CTTTTTTT others(1): Show |
C | 94 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0015others(91): Show | 95 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.3392-1472_3392-146 others(12): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941822 | ||||||
| chr7:107941822
|
CTTTTTTT others(2): Show |
C | 25 | a0001c0001t0001g0063a0001c0001t0001g0085a0001c0001t0001g0111others(22): Show | 25 | HG00558.hp2 HG00621.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.3392-1473_3392-146 others(13): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941822 | ||||||
| chr7:107941822
|
CTTTTTTT others(3): Show |
C | 94 | a0001c0002t0001g0014a0001c0002t0001g0049a0001c0002t0001g0052others(91): Show | 94 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(91): Show |
intron_variant | MODIFIER | c.3392-1474_3392-146 others(14): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941822 | ||||||
| chr7:107941822
|
CTTTTTTT others(4): Show |
C | 3 | a0001c0005t0001g0150a0001c0042t0001g0112a0009c0070t0001g0348 | 3 | HG01515.hp2 HG02145.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3392-1475_3392-146 others(15): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941822 | ||||||
| chr7:107941878
|
T | C | 127 | a0001c0001t0001g0249a0001c0002t0001g0014a0001c0002t0001g0049others(124): Show | 127 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.3392-1520A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941878 | ||||||
| chr7:107942001
|
C | T | 1 | a0002c0008t0002g0278 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3392-1643G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942001 | ||||||
| chr7:107942001
|
CTT | C | 252 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(249): Show | 253 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.3392-1645_3392-164 others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942001 | ||||||
| chr7:107942106
|
C | T | 1 | a0001c0002t0001g0297 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3392-1748G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942106 | ||||||
| chr7:107942176
|
G | A | 1 | a0001c0002t0001g0106 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3392-1818C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942176 | ||||||
| chr7:107942182
|
G | T | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3392-1824C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942182 | ||||||
| chr7:107942233
|
G | A | 17 | a0001c0005t0001g0357a0001c0007t0001g0007a0001c0007t0001g0009others(14): Show | 17 | HG01433.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.3392-1875C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942233 | ||||||
| chr7:107942277
|
A | G | 4 | a0009c0070t0001g0348a0011c0025t0001g0141a0011c0025t0001g0340others(1): Show | 4 | HG02109.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3392-1919T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942277 | ||||||
| chr7:107942280
|
G | T | 2 | a0002c0003t0002g0347a0005c0012t0002g0353 | 2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.3392-1922C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942280 | ||||||
| chr7:107942282
|
G | A | 1 | a0001c0001t0001g0063 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3392-1924C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942282 | ||||||
| chr7:107942335
|
T | C | 1 | a0001c0072t0001g0025 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3392-1977A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942335 | ||||||
| chr7:107942355
|
G | T | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3392-1997C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942355 | ||||||
| chr7:107942497
|
G | C | 16 | a0001c0005t0001g0357a0001c0007t0001g0007a0001c0007t0001g0009others(13): Show | 16 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.3392-2139C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942497 | ||||||
| chr7:107942726
|
T | C | 1 | a0001c0002t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3392-2368A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942726 | ||||||
| chr7:107942740
|
A | G | 121 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(118): Show | 122 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.3392-2382T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942740 | ||||||
| chr7:107942796
|
G | A | 109 | a0001c0002t0001g0014a0001c0002t0001g0049a0001c0002t0001g0052others(106): Show | 109 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(106): Show |
intron_variant | MODIFIER | c.3392-2438C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942796 | ||||||
| chr7:107943063
|
G | T | 1 | a0022c0030t0001g0312 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3392-2705C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943063 | ||||||
| chr7:107943073
|
G | A | 1 | a0001c0002t0001g0202 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3392-2715C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943073 | ||||||
| chr7:107943132
|
C | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(115): Show | 119 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.3392-2774G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943132 | ||||||
| chr7:107943181
|
G | A | 249 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(246): Show | 250 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(247): Show |
intron_variant | MODIFIER | c.3392-2823C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943181 | ||||||
| chr7:107943246
|
G | A | 1 | a0001c0005t0001g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3392-2888C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943246 | ||||||
| chr7:107943310
|
G | T | 1 | a0001c0001t0002g0061 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3392-2952C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943310 | ||||||
| chr7:107943456
|
A | T | 118 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(115): Show | 119 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.3392-3098T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943456 | ||||||
| chr7:107943634
|
C | T | 2 | a0001c0001t0001g0083a0001c0001t0001g0300 | 2 | NA19010.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.3392-3276G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943634 | ||||||
| chr7:107943716
|
G | A | 2 | a0007c0024t0001g0032a0007c0024t0001g0184 | 2 | HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3392-3358C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943716 | ||||||
| chr7:107943829
|
C | G | 2 | a0001c0078t0001g0024a0004c0067t0001g0137 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3392-3471G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943829 | ||||||
| chr7:107943876
|
G | A | 1 | a0007c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3392-3518C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943876 | ||||||
| chr7:107943944
|
CG | C | 3 | a0007c0024t0001g0032a0007c0024t0001g0184a0007c0031t0001g0072 | 3 | HG02723.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3392-3587delC | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943944 | ||||||
| chr7:107944087
|
A | G | 1 | a0001c0002t0001g0217 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3392-3729T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107944087 | ||||||
| chr7:107944144
|
A | C | 1 | a0001c0001t0001g0170 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3392-3786T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107944144 | ||||||
| chr7:107944335
|
G | T | 246 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(243): Show | 247 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(244): Show |
intron_variant | MODIFIER | c.3392-3977C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107944335 | ||||||
| chr7:107944401
|
C | T | 2 | a0001c0005t0001g0026a0001c0005t0001g0351 | 2 | HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3392-4043G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107944401 | ||||||
| chr7:107944452
|
T | C | 1 | a0001c0002t0001g0065 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3392-4094A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107944452 | ||||||
| chr7:107944480
|
A | C | 1 | a0002c0010t0001g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3392-4122T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107944480 | ||||||
| chr7:107944705
|
AC | A | 61 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0015others(58): Show | 62 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.3392-4348delG | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107944705 | ||||||
| chr7:107944925
|
G | A | 20 | a0001c0005t0001g0114a0001c0005t0001g0129a0001c0005t0001g0326others(17): Show | 20 | HG00609.hp2 HG00741.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.3392-4567C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107944925 | ||||||
| chr7:107945028
|
C | T | 236 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(233): Show | 237 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.3392-4670G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945028 | ||||||
| chr7:107945041
|
G | T | 20 | a0001c0005t0001g0114a0001c0005t0001g0129a0001c0005t0001g0326others(17): Show | 20 | HG00609.hp2 HG00741.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.3392-4683C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945041 | ||||||
| chr7:107945076
|
T | A | 1 | a0029c0046t0002g0333 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3392-4718A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945076 | ||||||
| chr7:107945083
|
T | C | 1 | a0001c0001t0002g0267 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3392-4725A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945083 | ||||||
| chr7:107945098
|
G | A | 1 | a0003c0004t0001g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3392-4740C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945098 | ||||||
| chr7:107945181
|
A | G | 2 | a0001c0027t0001g0349a0001c0043t0001g0127 | 2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3392-4823T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945181 | ||||||
| chr7:107945399
|
C | T | 112 | a0001c0001t0002g0061a0001c0002t0001g0014a0001c0002t0001g0049others(109): Show | 112 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.3392-5041G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945399 | ||||||
| chr7:107945475
|
C | A | 1 | a0001c0002t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3392-5117G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945475 | ||||||
| chr7:107945809
|
C | T | 108 | a0001c0001t0002g0061a0001c0002t0001g0014a0001c0002t0001g0049others(105): Show | 108 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(105): Show |
intron_variant | MODIFIER | c.3391+5417G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945809 | ||||||
| chr7:107945910
|
T | G | 1 | a0001c0002t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3391+5316A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945910 | ||||||
| chr7:107946026
|
T | C | 26 | a0001c0001t0001g0012a0001c0001t0001g0335a0001c0002t0001g0247others(23): Show | 26 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.3391+5200A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946026 | ||||||
| chr7:107946073
|
A | C | 259 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(256): Show | 261 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.3391+5153T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946073 | ||||||
| chr7:107946139
|
C | T | 2 | a0001c0006t0001g0042a0001c0006t0001g0128 | 2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3391+5087G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946139 | ||||||
| chr7:107946309
|
T | C | 7 | a0001c0001t0001g0102a0001c0001t0001g0186a0001c0001t0001g0234others(4): Show | 7 | HG02056.hp2 HG02165.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.3391+4917A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946309 | ||||||
| chr7:107946526
|
A | C | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3391+4700T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946526 | ||||||
| chr7:107946530
|
A | G | 1 | a0001c0005t0001g0059 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3391+4696T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946530 | ||||||
| chr7:107946563
|
C | T | 2 | a0002c0003t0001g0291a0007c0031t0001g0072 | 2 | HG02723.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.3391+4663G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946563 | ||||||
| chr7:107946583
|
C | T | 14 | a0001c0005t0001g0357a0001c0007t0001g0007a0001c0007t0001g0009others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.3391+4643G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946583 | ||||||
| chr7:107946589
|
C | T | 1 | a0001c0002t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3391+4637G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946589 | ||||||
| chr7:107946640
|
T | C | 1 | a0001c0044t0002g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3391+4586A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946640 | ||||||
| chr7:107946660
|
A | G | 17 | a0001c0001t0001g0012a0001c0001t0001g0335a0001c0014t0001g0336others(14): Show | 17 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.3391+4566T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946660 | ||||||
| chr7:107946930
|
G | C | 1 | a0004c0066t0004g0021 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3391+4296C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946930 | ||||||
| chr7:107947072
|
G | A | 1 | a0001c0002t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3391+4154C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947072 | ||||||
| chr7:107947124
|
C | T | 3 | a0001c0001t0002g0047a0001c0001t0002g0152a0001c0001t0002g0153 | 3 | HG00738.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3391+4102G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947124 | ||||||
| chr7:107947422
|
T | C | 1 | a0001c0002t0001g0247 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3391+3804A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947422 | ||||||
| chr7:107947434
|
A | G | 8 | a0001c0002t0001g0247a0001c0005t0001g0026a0001c0005t0001g0351others(5): Show | 8 | HG02055.hp2 HG02723.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.3391+3792T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947434 | ||||||
| chr7:107947941
|
C | T | 1 | a0001c0002t0001g0065 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3391+3285G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947941 | ||||||
| chr7:107947972
|
ATCT | A | 3 | a0002c0003t0002g0176a0002c0003t0002g0258a0002c0003t0002g0288 | 3 | HG00099.hp2 HG01517.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.3391+3251_3391+325 others(7): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947972 | ||||||
| chr7:107947983
|
C | CT | 14 | a0001c0001t0001g0063a0001c0001t0001g0085a0001c0001t0001g0100others(11): Show | 15 | HG01070.hp1 HG01168.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.3391+3242dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947983 | ||||||
| chr7:107947983
|
C | CTT | 222 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(219): Show | 223 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(220): Show |
intron_variant | MODIFIER | c.3391+3241_3391+324 others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947983 | ||||||
| chr7:107947983
|
C | CTTT | 11 | a0001c0001t0001g0303a0001c0001t0001g0321a0001c0002t0001g0118others(8): Show | 11 | HG01433.hp1 HG02109.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.3391+3240_3391+324 others(7): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947983 | ||||||
| chr7:107947983
|
C | CTTTT | 9 | a0001c0002t0001g0247a0001c0005t0001g0026a0001c0005t0001g0351others(6): Show | 9 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3391+3239_3391+324 others(8): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947983 | ||||||
| chr7:107947983
|
C | CTTTTT | 8 | a0001c0007t0001g0007a0001c0007t0001g0124a0001c0007t0001g0125others(5): Show | 8 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.3391+3238_3391+324 others(9): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947983 | ||||||
| chr7:107947983
|
C | T | 4 | a0001c0002t0001g0297a0007c0024t0001g0032a0007c0024t0001g0184others(1): Show | 4 | HG02723.hp2 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.3391+3243G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947983 | ||||||
| chr7:107947983
|
CT | C | 14 | a0001c0014t0001g0336a0001c0014t0001g0346a0001c0027t0001g0349others(11): Show | 14 | HG02280.hp1 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.3391+3242delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947983 | ||||||
| chr7:107948135
|
C | T | 1 | a0001c0006t0001g0193 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3391+3091G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948135 | ||||||
| chr7:107948150
|
T | C | 1 | a0001c0001t0001g0249 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3391+3076A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948150 | ||||||
| chr7:107948159
|
G | A | 168 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(165): Show | 169 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.3391+3067C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948159 | ||||||
| chr7:107948282
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3391+2944G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948282 | ||||||
| chr7:107948388
|
A | G | 1 | a0001c0001t0001g0261 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.3391+2838T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948388 | ||||||
| chr7:107948488
|
G | A | 4 | a0001c0027t0001g0349a0001c0043t0001g0127a0001c0078t0001g0024others(1): Show | 4 | HG02280.hp1 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3391+2738C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948488 | ||||||
| chr7:107948690
|
G | A | 1 | a0001c0059t0001g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3391+2536C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948690 | ||||||
| chr7:107948732
|
A | T | 14 | a0001c0014t0001g0336a0001c0014t0001g0346a0001c0014t0003g0360others(11): Show | 14 | HG01891.hp2 HG02280.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.3391+2494T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948732 | ||||||
| chr7:107948781
|
C | G | 1 | a0007c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3391+2445G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948781 | ||||||
| chr7:107948821
|
G | A | 1 | a0001c0002t0001g0049 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3391+2405C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948821 | ||||||
| chr7:107949054
|
C | T | 12 | a0001c0007t0001g0007a0001c0007t0001g0009a0001c0007t0001g0115others(9): Show | 12 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3391+2172G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107949054 | ||||||
| chr7:107949061
|
A | G | 1 | a0001c0006t0002g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3391+2165T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107949061 | ||||||
| chr7:107949116
|
T | C | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3391+2110A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107949116 | ||||||
| chr7:107949205
|
G | A | 1 | a0004c0067t0001g0137 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3391+2021C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107949205 | ||||||
| chr7:107949471
|
T | TTTAACAG others(30): Show |
1 | a0002c0008t0002g0278 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3391+1718_3391+175 others(41): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107949471 | ||||||
| chr7:107949799
|
A | C | 1 | a0001c0002t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3391+1427T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107949799 | ||||||
| chr7:107949889
|
A | G | 13 | a0001c0007t0001g0007a0001c0007t0001g0009a0001c0007t0001g0115others(10): Show | 13 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.3391+1337T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107949889 | ||||||
| chr7:107949952
|
C | T | 98 | a0001c0001t0002g0061a0001c0002t0001g0014a0001c0002t0001g0049others(95): Show | 98 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.3391+1274G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107949952 | ||||||
| chr7:107950003
|
G | A | 4 | a0009c0070t0001g0348a0011c0025t0001g0141a0011c0025t0001g0340others(1): Show | 4 | HG02109.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3391+1223C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950003 | ||||||
| chr7:107950018
|
T | A | 98 | a0001c0001t0002g0061a0001c0002t0001g0014a0001c0002t0001g0049others(95): Show | 98 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.3391+1208A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950018 | ||||||
| chr7:107950067
|
T | C | 2 | a0001c0001t0001g0001a0001c0001t0001g0004 | 3 | HG03490.hp1 HG03492.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.3391+1159A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950067 | ||||||
| chr7:107950111
|
C | T | 32 | a0001c0002t0001g0337a0001c0005t0001g0357a0001c0007t0001g0007others(29): Show | 32 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.3391+1115G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950111 | ||||||
| chr7:107950229
|
C | CA | 9 | a0001c0001t0001g0085a0001c0001t0001g0216a0001c0001t0001g0218others(6): Show | 9 | HG02723.hp2 HG02886.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.3391+996dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950229 | ||||||
| chr7:107950293
|
G | C | 272 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(269): Show | 274 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(271): Show |
intron_variant | MODIFIER | c.3391+933C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950293 | ||||||
| chr7:107950386
|
A | G | 13 | a0001c0007t0001g0007a0001c0007t0001g0009a0001c0007t0001g0115others(10): Show | 13 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.3391+840T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950386 | ||||||
| chr7:107950494
|
G | T | 25 | a0001c0014t0001g0336a0001c0014t0001g0346a0001c0014t0003g0360others(22): Show | 25 | HG01433.hp1 HG01891.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.3391+732C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950494 | ||||||
| chr7:107950523
|
G | T | 1 | a0002c0008t0002g0278 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3391+703C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950523 | ||||||
| chr7:107950524
|
T | G | 1 | a0002c0008t0002g0278 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3391+702A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950524 | ||||||
| chr7:107950776
|
T | A | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3391+450A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950776 | ||||||
| chr7:107950923
|
G | GGT | 21 | a0001c0002t0001g0110a0001c0002t0001g0202a0001c0002t0001g0211others(18): Show | 21 | HG00323.hp1 HG01192.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.3391+301_3391+302d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | ||||||
| chr7:107950923
|
G | GGTGT | 62 | a0001c0001t0002g0002a0001c0001t0002g0047a0001c0002t0001g0049others(59): Show | 63 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.3391+299_3391+302d others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | ||||||
| chr7:107950923
|
G | GGTGTGT | 9 | a0001c0002t0001g0196a0001c0005t0001g0248a0001c0009t0001g0283others(6): Show | 9 | HG01361.hp1 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.3391+297_3391+302d others(8): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | ||||||
| chr7:107950923
|
G | GGTGTGTG others(1): Show |
7 | a0001c0001t0002g0152a0001c0001t0002g0153a0001c0042t0001g0112others(4): Show | 7 | HG00741.hp1 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3391+295_3391+302d others(10): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | ||||||
| chr7:107950923
|
GGT | G | 84 | a0001c0001t0002g0050a0001c0001t0002g0267a0001c0005t0001g0357others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(81): Show |
intron_variant | MODIFIER | c.3391+301_3391+302d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | ||||||
| chr7:107950923
|
GGTGT | G | 5 | a0002c0013t0001g0030a0002c0013t0001g0069a0005c0012t0002g0353others(2): Show | 5 | HG01243.hp1 HG02280.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3391+299_3391+302d others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | ||||||
| chr7:107950923
|
GGTGTGT | G | 10 | a0001c0002t0001g0337a0001c0005t0001g0026a0001c0005t0001g0351others(7): Show | 10 | HG02055.hp2 HG02165.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.3391+297_3391+302d others(8): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | ||||||
| chr7:107950923
|
GGTGTGTG others(1): Show |
G | 7 | a0001c0001t0001g0015a0001c0001t0001g0316a0001c0001t0002g0192others(4): Show | 7 | HG00323.hp2 HG00408.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3391+295_3391+302d others(10): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | ||||||
| chr7:107950923
|
GGTGTGTG others(3): Show |
G | 120 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(117): Show | 121 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.3391+293_3391+302d others(12): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | ||||||
| chr7:107950923
|
GGTGTGTG others(11): Show |
G | 1 | a0001c0002t0001g0331 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3391+285_3391+302d others(20): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | ||||||
| chr7:107950971
|
C | A | 4 | a0002c0003t0002g0166a0002c0008t0002g0272a0002c0010t0001g0155others(1): Show | 4 | HG00323.hp1 HG01070.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.3391+255G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950971 | ||||||
| chr7:107951126
|
G | A | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3391+100C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107951126 | ||||||
| chr7:107951205
|
G | A | 1 | a0001c0014t0001g0346 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3391+21C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107951205 | ||||||
| chr7:107951207
|
G | A | 3 | a0001c0002t0001g0247a0001c0022t0001g0029a0001c0022t0001g0039 | 3 | HG02970.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3391+19C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107951207 | ||||||
| chr7:107951381
|
CT | C | 4 | a0001c0001t0002g0047a0001c0001t0002g0152a0001c0001t0002g0153others(1): Show | 4 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3295-60delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951381 | ||||||
| chr7:107951469
|
A | G | 106 | a0001c0001t0002g0002a0001c0001t0002g0047a0001c0001t0002g0050others(103): Show | 107 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.3295-147T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951469 | ||||||
| chr7:107951471
|
C | T | 6 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0010t0001g0334others(3): Show | 6 | HG00738.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3295-149G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951471 | ||||||
| chr7:107951622
|
C | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0342 | 2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3295-300G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951622 | ||||||
| chr7:107951662
|
C | CA | 124 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(121): Show | 125 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.3295-341dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951662 | ||||||
| chr7:107951680
|
T | C | 2 | a0001c0005t0001g0119a0009c0071t0001g0067 | 2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3294+329A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951680 | ||||||
| chr7:107951753
|
A | G | 23 | a0001c0002t0001g0306a0001c0005t0001g0114a0001c0005t0001g0129others(20): Show | 23 | HG00609.hp2 HG00741.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.3294+256T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951753 | ||||||
| chr7:107951900
|
C | T | 1 | a0001c0001t0001g0213 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3294+109G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951900 | ||||||
| chr7:107951946
|
C | A | 1 | a0007c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3294+63G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951946 | ||||||
| chr7:107951958
|
G | A | 160 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(157): Show | 161 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.3294+51C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951958 | ||||||
| chr7:107952337
|
G | A | 7 | a0002c0003t0002g0076a0002c0003t0002g0169a0002c0003t0002g0198others(4): Show | 7 | NA18962.hp1 NA18988.hp1 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.3080-114C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107952337 | ||||||
| chr7:107952400
|
C | T | 2 | a0001c0005t0001g0119a0009c0071t0001g0067 | 2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3080-177G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107952400 | ||||||
| chr7:107952437
|
A | G | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3080-214T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107952437 | ||||||
| chr7:107952512
|
A | C | 35 | a0001c0001t0001g0183a0001c0002t0001g0247a0001c0007t0001g0007others(32): Show | 35 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.3080-289T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107952512 | ||||||
| chr7:107952526
|
T | A | 1 | a0001c0059t0001g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3080-303A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107952526 | ||||||
| chr7:107952835
|
G | A | 16 | a0001c0014t0001g0336a0001c0014t0001g0346a0001c0014t0003g0360others(13): Show | 16 | HG01891.hp2 HG02280.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.3080-612C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107952835 | ||||||
| chr7:107952906
|
A | G | 2 | a0001c0001t0001g0173a0001c0001t0001g0321 | 2 | NA19076.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.3079+624T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107952906 | ||||||
| chr7:107952997
|
A | C | 1 | a0002c0003t0002g0264 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3079+533T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107952997 | ||||||
| chr7:107953128
|
G | A | 1 | a0001c0059t0001g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3079+402C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953128 | ||||||
| chr7:107953152
|
T | A | 1 | a0001c0018t0001g0277 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3079+378A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953152 | ||||||
| chr7:107953162
|
A | T | 1 | a0001c0018t0001g0277 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3079+368T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953162 | ||||||
| chr7:107953167
|
A | G | 1 | a0001c0018t0001g0277 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3079+363T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953167 | ||||||
| chr7:107953169
|
C | T | 1 | a0001c0018t0001g0277 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3079+361G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953169 | ||||||
| chr7:107953174
|
T | A | 1 | a0001c0018t0001g0277 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3079+356A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953174 | ||||||
| chr7:107953193
|
T | C | 1 | a0001c0018t0001g0277 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3079+337A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953193 | ||||||
| chr7:107953200
|
T | C | 1 | a0004c0066t0004g0021 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3079+330A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953200 | ||||||
| chr7:107953202
|
C | CAAAAAAT others(238): Show |
1 | a0001c0018t0001g0277 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3079+327_3079+328i others(247): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953202 | ||||||
| chr7:107953295
|
T | C | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3079+235A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953295 | ||||||
| chr7:107953359
|
TA | T | 264 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(261): Show | 265 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(262): Show |
intron_variant | MODIFIER | c.3079+170delT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953359 | ||||||
| chr7:107953425
|
A | C | 1 | a0001c0001t0001g0205 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.3079+105T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953425 | ||||||
| chr7:107953816
|
A | C | 1 | a0009c0071t0001g0067 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2855-62T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107953816 | ||||||
| chr7:107954060
|
C | T | 1 | a0001c0005t0001g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2855-306G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954060 | ||||||
| chr7:107954104
|
G | A | 96 | a0001c0001t0002g0050a0001c0001t0002g0061a0001c0002t0001g0014others(93): Show | 96 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(93): Show |
intron_variant | MODIFIER | c.2855-350C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954104 | ||||||
| chr7:107954166
|
T | G | 6 | a0002c0003t0002g0347a0002c0013t0001g0030a0002c0013t0001g0034others(3): Show | 6 | HG01243.hp1 HG02280.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2855-412A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954166 | ||||||
| chr7:107954272
|
A | G | 20 | a0001c0002t0001g0306a0001c0005t0001g0129a0003c0004t0001g0082others(17): Show | 20 | HG00609.hp2 HG00741.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.2855-518T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954272 | ||||||
| chr7:107954331
|
AT | A | 102 | a0001c0001t0001g0213a0001c0001t0002g0050a0001c0002t0001g0014others(99): Show | 102 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(99): Show |
intron_variant | MODIFIER | c.2855-578delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954331 | ||||||
| chr7:107954332
|
T | A | 3 | a0001c0001t0002g0061a0001c0005t0001g0059a0001c0059t0001g0041 | 3 | HG01175.hp2 HG01261.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2855-578A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954332 | ||||||
| chr7:107954556
|
C | T | 1 | a0001c0006t0002g0235 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2855-802G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954556 | ||||||
| chr7:107954638
|
C | T | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2854+829G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954638 | ||||||
| chr7:107954683
|
C | A | 1 | a0003c0004t0001g0086 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2854+784G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954683 | ||||||
| chr7:107954707
|
C | T | 3 | a0007c0024t0001g0032a0007c0024t0001g0184a0007c0031t0001g0072 | 3 | HG02723.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2854+760G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954707 | ||||||
| chr7:107954881
|
A | T | 16 | a0001c0001t0001g0183a0001c0014t0001g0336a0001c0014t0001g0346others(13): Show | 16 | HG01891.hp2 HG02280.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2854+586T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954881 | ||||||
| chr7:107954939
|
C | A | 1 | a0007c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2854+528G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954939 | ||||||
| chr7:107954939
|
C | T | 3 | a0002c0003t0002g0175a0002c0039t0002g0203a0015c0037t0002g0232 | 3 | HG02735.hp2 HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2854+528G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954939 | ||||||
| chr7:107954945
|
C | T | 262 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(259): Show | 263 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(260): Show |
intron_variant | MODIFIER | c.2854+522G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954945 | ||||||
| chr7:107954952
|
TG | T | 35 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0087others(32): Show | 35 | HG00558.hp2 HG00621.hp1 HG02083.hp2 others(32): Show |
intron_variant | MODIFIER | c.2854+514delC | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954952 | ||||||
| chr7:107955144
|
T | G | 14 | a0001c0006t0001g0042a0001c0006t0001g0128a0001c0007t0001g0007others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2854+323A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107955144 | ||||||
| chr7:107955167
|
G | C | 2 | a0001c0002t0001g0117a0001c0002t0001g0118 | 2 | NA18946.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.2854+300C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107955167 | ||||||
| chr7:107955287
|
A | G | 4 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0294others(1): Show | 4 | HG01109.hp2 HG01255.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.2854+180T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107955287 | ||||||
| chr7:107955371
|
A | T | 1 | a0002c0003t0002g0159 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2854+96T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107955371 | ||||||
| chr7:107955447
|
A | C | 4 | a0009c0070t0001g0348a0011c0025t0001g0141a0011c0025t0001g0340others(1): Show | 4 | HG02109.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2854+20T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107955447 | ||||||
| chr7:107955648
|
G | A | 1 | a0001c0002t0001g0331 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2691-18C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107955648 | ||||||
| chr7:107955898
|
G | GT | 140 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(137): Show | 141 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.2691-269dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107955898 | ||||||
| chr7:107955902
|
T | G | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2691-272A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107955902 | ||||||
| chr7:107955927
|
G | A | 2 | a0010c0062t0002g0293a0010c0082t0002g0204 | 2 | HG01192.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2691-297C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107955927 | ||||||
| chr7:107955928
|
C | T | 1 | a0001c0002t0001g0199 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2691-298G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107955928 | ||||||
| chr7:107955975
|
G | A | 15 | a0001c0014t0001g0336a0001c0014t0001g0346a0001c0014t0003g0360others(12): Show | 15 | HG01891.hp2 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2691-345C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107955975 | ||||||
| chr7:107956056
|
C | G | 14 | a0001c0006t0001g0042a0001c0006t0001g0128a0001c0007t0001g0007others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2691-426G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107956056 | ||||||
| chr7:107956281
|
C | T | 2 | a0001c0027t0001g0349a0001c0043t0001g0127 | 2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2691-651G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107956281 | ||||||
| chr7:107956459
|
G | A | 1 | a0003c0004t0001g0250 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2691-829C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107956459 | ||||||
| chr7:107956664
|
T | C | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2691-1034A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107956664 | ||||||
| chr7:107956811
|
G | A | 2 | a0001c0005t0001g0026a0001c0005t0001g0351 | 2 | HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2691-1181C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107956811 | ||||||
| chr7:107956829
|
T | C | 2 | a0004c0015t0002g0008a0004c0069t0001g0134 | 2 | HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2691-1199A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107956829 | ||||||
| chr7:107956930
|
G | A | 14 | a0001c0006t0001g0042a0001c0006t0001g0128a0001c0007t0001g0007others(11): Show | 14 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2691-1300C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107956930 | ||||||
| chr7:107956931
|
C | T | 6 | a0001c0006t0001g0254a0001c0006t0001g0341a0001c0006t0001g0356others(3): Show | 6 | HG01433.hp1 HG02258.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2691-1301G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107956931 | ||||||
| chr7:107957045
|
A | G | 8 | a0001c0001t0002g0050a0001c0002t0001g0052a0001c0006t0001g0133others(5): Show | 8 | HG00408.hp1 HG00642.hp1 HG00735.hp1 others(5): Show |
intron_variant | MODIFIER | c.2691-1415T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957045 | ||||||
| chr7:107957058
|
G | A | 15 | a0001c0014t0001g0346a0001c0027t0001g0349a0001c0035t0001g0037others(12): Show | 15 | HG02280.hp1 HG02559.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2691-1428C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957058 | ||||||
| chr7:107957116
|
G | A | 3 | a0001c0001t0002g0047a0001c0001t0002g0152a0001c0001t0002g0153 | 3 | HG00738.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2691-1486C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957116 | ||||||
| chr7:107957118
|
G | A | 1 | a0004c0015t0002g0008 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2691-1488C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957118 | ||||||
| chr7:107957345
|
C | T | 1 | a0002c0053t0002g0145 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2691-1715G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957345 | ||||||
| chr7:107957506
|
C | G | 83 | a0001c0001t0002g0002a0001c0001t0002g0047a0001c0001t0002g0050others(80): Show | 84 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.2690+1743G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957506 | ||||||
| chr7:107957529
|
C | T | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2690+1720G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957529 | ||||||
| chr7:107957544
|
G | A | 2 | a0001c0001t0001g0033a0001c0001t0001g0342 | 2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2690+1705C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957544 | ||||||
| chr7:107957555
|
A | G | 4 | a0001c0022t0001g0039a0011c0025t0001g0141a0011c0025t0001g0340others(1): Show | 4 | HG02109.hp1 HG02615.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2690+1694T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957555 | ||||||
| chr7:107957833
|
A | G | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2690+1416T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957833 | ||||||
| chr7:107957858
|
A | C | 1 | a0001c0005t0001g0119 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2690+1391T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957858 | ||||||
| chr7:107958336
|
G | C | 1 | a0002c0003t0002g0168 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2690+913C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107958336 | ||||||
| chr7:107958348
|
A | G | 1 | a0001c0007t0001g0343 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2690+901T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107958348 | ||||||
| chr7:107958644
|
G | A | 20 | a0001c0002t0001g0337a0001c0014t0001g0336a0001c0014t0001g0346others(17): Show | 20 | HG01243.hp1 HG01891.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.2690+605C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107958644 | ||||||
| chr7:107958691
|
T | G | 1 | a0001c0002t0001g0302 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2690+558A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107958691 | ||||||
| chr7:107958837
|
A | C | 1 | a0001c0001t0002g0003 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2690+412T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107958837 | ||||||
| chr7:107958948
|
G | C | 1 | a0003c0049t0001g0056 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2690+301C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107958948 | ||||||
| chr7:107959001
|
G | A | 1 | a0002c0010t0001g0227 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2690+248C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107959001 | ||||||
| chr7:107959038
|
G | C | 1 | a0001c0005t0001g0248 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2690+211C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107959038 | ||||||
| chr7:107959502
|
G | A | 1 | a0001c0072t0001g0025 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2459-22C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 19/33 | chr7 | 107959502 | ||||||
| chr7:107960113
|
C | T | 117 | a0001c0001t0002g0050a0001c0002t0001g0014a0001c0002t0001g0049others(114): Show | 117 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(114): Show |
intron_variant | MODIFIER | c.2315-279G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 18/33 | chr7 | 107960113 | ||||||
| chr7:107960142
|
G | A | 2 | a0010c0062t0002g0293a0010c0082t0002g0204 | 2 | HG01192.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2314+303C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 18/33 | chr7 | 107960142 | ||||||
| chr7:107960688
|
G | T | 1 | a0009c0070t0001g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2110-39C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 17/33 | chr7 | 107960688 | ||||||
| chr7:107961078
|
T | C | 88 | a0001c0001t0002g0002a0001c0001t0002g0047a0001c0001t0002g0050others(85): Show | 89 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(86): Show |
intron_variant | MODIFIER | c.2109+128A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 17/33 | chr7 | 107961078 | ||||||
| chr7:107961091
|
G | T | 4 | a0001c0001t0002g0002a0001c0001t0002g0047a0001c0001t0002g0152others(1): Show | 5 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2109+115C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 17/33 | chr7 | 107961091 | ||||||
| chr7:107961138
|
C | G | 1 | a0009c0070t0001g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2109+68G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 17/33 | chr7 | 107961138 | ||||||
| chr7:107961402
|
C | G | 1 | a0002c0008t0002g0273 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1986-73G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 16/33 | chr7 | 107961402 | ||||||
| chr7:107961537
|
C | T | 3 | a0011c0025t0001g0141a0011c0025t0001g0340a0017c0076t0001g0005 | 3 | HG02109.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1985+12G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 16/33 | chr7 | 107961537 | ||||||
| chr7:107961781
|
C | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0342 | 2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1858-105G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107961781 | ||||||
| chr7:107961853
|
C | T | 1 | a0001c0002t0001g0222 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1858-177G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107961853 | ||||||
| chr7:107961869
|
C | G | 22 | a0001c0006t0001g0042a0001c0006t0001g0128a0001c0006t0001g0254others(19): Show | 22 | HG01433.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1858-193G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107961869 | ||||||
| chr7:107962061
|
T | G | 1 | a0021c0055t0001g0243 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1858-385A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962061 | ||||||
| chr7:107962083
|
C | T | 1 | a0030c0074t0001g0200 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1858-407G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962083 | ||||||
| chr7:107962179
|
C | T | 43 | a0001c0005t0001g0026a0001c0005t0001g0351a0001c0014t0001g0336others(40): Show | 43 | HG00099.hp1 HG00099.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.1858-503G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962179 | ||||||
| chr7:107962216
|
C | T | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1858-540G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962216 | ||||||
| chr7:107962359
|
C | T | 7 | a0001c0035t0001g0037a0002c0003t0001g0070a0002c0003t0001g0071others(4): Show | 7 | HG00738.hp1 HG02622.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1857+546G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962359 | ||||||
| chr7:107962387
|
G | C | 2 | a0007c0024t0001g0032a0007c0024t0001g0184 | 2 | HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1857+518C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962387 | ||||||
| chr7:107962416
|
GA | G | 11 | a0001c0002t0001g0337a0001c0014t0003g0360a0001c0027t0001g0349others(8): Show | 11 | HG01891.hp2 HG02572.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1857+488delT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962416 | ||||||
| chr7:107962512
|
A | G | 23 | a0001c0006t0001g0042a0001c0006t0001g0128a0001c0006t0001g0254others(20): Show | 23 | HG01433.hp1 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1857+393T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962512 | ||||||
| chr7:107962582
|
C | T | 3 | a0001c0027t0001g0349a0001c0078t0001g0024a0004c0067t0001g0137 | 3 | HG02572.hp2 HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1857+323G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962582 | ||||||
| chr7:107962664
|
A | G | 1 | a0004c0016t0001g0354 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1857+241T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962664 | ||||||
| chr7:107962697
|
G | C | 1 | a0001c0006t0001g0341 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1857+208C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962697 | ||||||
| chr7:107962700
|
C | G | 6 | a0001c0002t0001g0103a0001c0002t0001g0104a0001c0002t0001g0105others(3): Show | 6 | HG00642.hp2 HG00733.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1857+205G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962700 | ||||||
| chr7:107962707
|
CA | C | 80 | a0001c0001t0001g0111a0001c0001t0001g0228a0001c0002t0001g0014others(77): Show | 80 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.1857+197delT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962707 | ||||||
| chr7:107962707
|
CAA | C | 65 | a0001c0001t0001g0048a0001c0002t0001g0117a0001c0002t0001g0247others(62): Show | 65 | HG00639.hp1 HG01070.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1857+196_1857+197d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962707 | ||||||
| chr7:107962722
|
A | G | 3 | a0001c0001t0001g0001a0001c0001t0001g0004a0002c0003t0002g0092 | 4 | HG02145.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1857+183T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962722 | ||||||
| chr7:107962810
|
A | G | 2 | a0001c0001t0001g0173a0001c0001t0001g0321 | 2 | NA19076.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1857+95T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962810 | ||||||
| chr7:107962837
|
T | G | 20 | a0001c0001t0001g0048a0001c0005t0001g0119a0001c0005t0001g0129others(17): Show | 20 | HG00609.hp2 HG00639.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1857+68A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962837 | ||||||
| chr7:107962848
|
A | G | 5 | a0001c0002t0001g0247a0001c0005t0001g0357a0001c0022t0001g0029others(2): Show | 5 | HG02109.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1857+57T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962848 | ||||||
| chr7:107963222
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1699-159A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107963222 | ||||||
| chr7:107963303
|
G | C | 1 | a0003c0004t0001g0236 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1699-240C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107963303 | ||||||
| chr7:107963639
|
C | T | 5 | a0001c0006t0001g0254a0001c0006t0001g0341a0001c0006t0001g0356others(2): Show | 5 | HG02258.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1699-576G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107963639 | ||||||
| chr7:107963721
|
A | C | 1 | a0002c0008t0002g0273 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1699-658T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107963721 | ||||||
| chr7:107963817
|
C | T | 6 | a0001c0002t0001g0222a0001c0002t0001g0266a0001c0002t0001g0295others(3): Show | 6 | HG02622.hp2 NA18944.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1698+735G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107963817 | ||||||
| chr7:107963818
|
G | A | 2 | a0001c0078t0001g0024a0004c0067t0001g0137 | 2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1698+734C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107963818 | ||||||
| chr7:107963869
|
C | T | 7 | a0001c0001t0001g0011a0001c0001t0001g0016a0001c0001t0001g0033others(4): Show | 7 | HG00642.hp1 HG01109.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1698+683G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107963869 | ||||||
| chr7:107963870
|
G | A | 1 | a0002c0008t0002g0273 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1698+682C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107963870 | ||||||
| chr7:107964028
|
C | T | 3 | a0001c0006t0002g0224a0007c0024t0001g0184a0028c0034t0001g0031 | 3 | HG02886.hp2 HG02896.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1698+524G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107964028 | ||||||
| chr7:107964050
|
T | C | 21 | a0001c0014t0001g0336a0001c0044t0002g0345a0002c0003t0001g0284others(18): Show | 21 | HG00099.hp1 HG00099.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.1698+502A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107964050 | ||||||
| chr7:107964097
|
C | T | 1 | a0001c0006t0002g0327 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1698+455G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107964097 | ||||||
| chr7:107964098
|
G | A | 1 | a0001c0002t0001g0223 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1698+454C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107964098 | ||||||
| chr7:107964373
|
T | G | 243 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0015others(240): Show | 243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1698+179A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107964373 | ||||||
| chr7:107964476
|
G | A | 1 | a0001c0017t0001g0257 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1698+76C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107964476 | ||||||
| chr7:107964741
|
C | T | 1 | a0001c0001t0001g0111 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1563-54G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107964741 | ||||||
| chr7:107964836
|
AG | A | 8 | a0001c0001t0001g0083a0001c0002t0001g0077a0001c0002t0001g0110others(5): Show | 8 | NA18967.hp1 NA18982.hp1 NA18985.hp1 others(5): Show |
intron_variant | MODIFIER | c.1563-150delC | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107964836 | ||||||
| chr7:107964837
|
G | A | 60 | a0001c0001t0001g0087a0001c0001t0001g0188a0001c0001t0001g0189others(57): Show | 60 | HG00140.hp2 HG00408.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1563-150C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107964837 | ||||||
| chr7:107964859
|
A | T | 14 | a0001c0001t0001g0033a0001c0001t0001g0303a0001c0001t0001g0342others(11): Show | 14 | HG01433.hp1 HG02109.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1563-172T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107964859 | ||||||
| chr7:107964867
|
G | A | 16 | a0001c0001t0001g0033a0001c0001t0001g0342a0001c0006t0001g0128others(13): Show | 16 | HG00738.hp1 HG01433.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1563-180C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107964867 | ||||||
| chr7:107964964
|
A | G | 6 | a0001c0007t0001g0115a0001c0022t0001g0029a0001c0022t0001g0039others(3): Show | 6 | HG02572.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1563-277T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107964964 | ||||||
| chr7:107964967
|
C | T | 300 | a0001c0001t0001g0004a0001c0001t0001g0011a0001c0001t0001g0015others(297): Show | 301 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(298): Show |
intron_variant | MODIFIER | c.1563-280G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107964967 | ||||||
| chr7:107965080
|
G | A | 1 | a0001c0005t0001g0059 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1563-393C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965080 | ||||||
| chr7:107965088
|
G | A | 5 | a0001c0006t0001g0341a0001c0027t0001g0349a0001c0078t0001g0024others(2): Show | 5 | HG02258.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1563-401C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965088 | ||||||
| chr7:107965108
|
C | T | 1 | a0001c0032t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1563-421G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965108 | ||||||
| chr7:107965111
|
A | G | 1 | a0002c0010t0001g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1563-424T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965111 | ||||||
| chr7:107965161
|
A | G | 1 | a0001c0072t0001g0025 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1563-474T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965161 | ||||||
| chr7:107965232
|
A | G | 13 | a0001c0001t0001g0335a0001c0001t0001g0342a0001c0006t0001g0341others(10): Show | 13 | HG01243.hp1 HG01433.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1563-545T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965232 | ||||||
| chr7:107965233
|
C | A | 1 | a0001c0035t0001g0037 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1563-546G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965233 | ||||||
| chr7:107965264
|
C | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0172a0001c0001t0001g0260others(4): Show | 7 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(4): Show |
intron_variant | MODIFIER | c.1563-577G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965264 | ||||||
| chr7:107965299
|
G | T | 3 | a0004c0016t0001g0354a0004c0016t0001g0355a0005c0012t0002g0353 | 3 | HG01243.hp1 HG02559.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1563-612C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965299 | ||||||
| chr7:107965367
|
G | A | 1 | a0002c0008t0002g0274 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1563-680C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965367 | ||||||
| chr7:107965486
|
C | G | 157 | a0001c0001t0001g0012a0001c0001t0001g0015a0001c0001t0001g0033others(154): Show | 157 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1563-799G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965486 | ||||||
| chr7:107965503
|
C | T | 1 | a0001c0001t0002g0019 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1563-816G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965503 | ||||||
| chr7:107965516
|
T | C | 14 | a0001c0001t0001g0033a0001c0007t0003g0361a0002c0013t0001g0034others(11): Show | 14 | HG02055.hp1 HG02109.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1563-829A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965516 | ||||||
| chr7:107965520
|
G | T | 3 | a0001c0002t0001g0286a0001c0002t0001g0298a0001c0002t0001g0310 | 3 | HG03491.hp2 HG03492.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1563-833C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965520 | ||||||
| chr7:107965521
|
G | A | 3 | a0001c0002t0001g0286a0001c0002t0001g0298a0001c0002t0001g0310 | 3 | HG03491.hp2 HG03492.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1563-834C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965521 | ||||||
| chr7:107965562
|
A | G | 1 | a0002c0008t0002g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1563-875T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965562 | ||||||
| chr7:107965602
|
G | A | 1 | a0002c0010t0001g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1563-915C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965602 | ||||||
| chr7:107965603
|
T | C | 2 | a0001c0001t0001g0262a0001c0001t0001g0263 | 2 | HG02027.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.1563-916A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965603 | ||||||
| chr7:107965714
|
G | T | 2 | a0001c0005t0001g0035a0026c0060t0001g0036 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1563-1027C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965714 | ||||||
| chr7:107965759
|
A | C | 2 | a0001c0006t0002g0235a0003c0004t0001g0230 | 2 | HG02129.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1563-1072T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965759 | ||||||
| chr7:107965782
|
C | T | 2 | a0001c0005t0001g0035a0026c0060t0001g0036 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1563-1095G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965782 | ||||||
| chr7:107965828
|
G | A | 2 | a0004c0015t0002g0008a0011c0025t0001g0141 | 2 | HG02109.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1563-1141C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965828 | ||||||
| chr7:107965831
|
G | C | 7 | a0001c0001t0001g0201a0001c0001t0001g0205a0001c0001t0001g0216others(4): Show | 7 | HG00673.hp2 HG02129.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1563-1144C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965831 | ||||||
| chr7:107966102
|
T | C | 1 | a0001c0006t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1563-1415A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966102 | ||||||
| chr7:107966139
|
C | T | 3 | a0001c0032t0001g0028a0001c0072t0001g0025a0001c0078t0001g0024 | 3 | HG02572.hp2 HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1563-1452G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966139 | ||||||
| chr7:107966189
|
G | C | 28 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(25): Show | 28 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1563-1502C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966189 | ||||||
| chr7:107966235
|
G | T | 1 | a0001c0007t0003g0362 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1563-1548C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966235 | ||||||
| chr7:107966250
|
G | A | 3 | a0001c0035t0001g0037a0019c0033t0001g0040a0028c0034t0001g0031 | 3 | HG02622.hp1 HG02896.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1563-1563C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966250 | ||||||
| chr7:107966286
|
C | T | 1 | a0002c0010t0001g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1563-1599G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966286 | ||||||
| chr7:107966296
|
C | T | 1 | a0001c0005t0001g0150 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1563-1609G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966296 | ||||||
| chr7:107966373
|
G | A | 14 | a0001c0001t0001g0033a0002c0013t0001g0034a0002c0019t0002g0308others(11): Show | 14 | HG02109.hp1 HG02257.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1563-1686C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966373 | ||||||
| chr7:107966402
|
G | T | 2 | a0001c0005t0001g0035a0026c0060t0001g0036 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1563-1715C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966402 | ||||||
| chr7:107966501
|
G | A | 3 | a0002c0003t0002g0045a0002c0003t0002g0046a0006c0011t0002g0259 | 3 | HG01256.hp2 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1563-1814C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966501 | ||||||
| chr7:107966772
|
G | A | 1 | a0001c0032t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1563-2085C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966772 | ||||||
| chr7:107967078
|
T | C | 1 | a0001c0002t0001g0240 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1563-2391A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967078 | ||||||
| chr7:107967108
|
A | G | 1 | a0001c0005t0001g0219 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1563-2421T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967108 | ||||||
| chr7:107967127
|
G | C | 1 | a0001c0002t0001g0297 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1563-2440C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967127 | ||||||
| chr7:107967281
|
T | G | 1 | a0001c0001t0002g0002 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1563-2594A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967281 | ||||||
| chr7:107967311
|
C | T | 1 | a0001c0001t0001g0342 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1563-2624G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967311 | ||||||
| chr7:107967312
|
G | A | 1 | a0007c0024t0001g0184 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1563-2625C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967312 | ||||||
| chr7:107967367
|
A | T | 1 | a0002c0003t0002g0013 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1563-2680T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967367 | ||||||
| chr7:107967429
|
T | G | 1 | a0006c0011t0002g0330 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1563-2742A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967429 | ||||||
| chr7:107967444
|
TTTCA | T | 5 | a0001c0001t0001g0226a0001c0001t0001g0287a0001c0006t0001g0133others(2): Show | 5 | HG01361.hp1 HG02698.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1563-2761_1563-275 others(8): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967444 | ||||||
| chr7:107967457
|
C | T | 74 | a0001c0001t0001g0011a0001c0001t0001g0022a0001c0001t0001g0062others(71): Show | 75 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.1563-2770G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967457 | ||||||
| chr7:107967476
|
C | T | 1 | a0001c0032t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1563-2789G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967476 | ||||||
| chr7:107967503
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1563-2816C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967503 | ||||||
| chr7:107967525
|
T | C | 32 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(29): Show | 32 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1563-2838A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967525 | ||||||
| chr7:107967649
|
C | T | 6 | a0001c0001t0001g0012a0001c0002t0001g0247a0001c0006t0001g0254others(3): Show | 6 | HG02080.hp1 HG02258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1563-2962G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967649 | ||||||
| chr7:107967740
|
T | C | 1 | a0029c0046t0002g0333 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1563-3053A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967740 | ||||||
| chr7:107967890
|
T | A | 1 | a0001c0006t0002g0327 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1563-3203A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967890 | ||||||
| chr7:107967919
|
T | C | 126 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(123): Show | 128 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(125): Show |
intron_variant | MODIFIER | c.1563-3232A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967919 | ||||||
| chr7:107968093
|
G | C | 1 | a0001c0006t0002g0235 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1563-3406C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107968093 | ||||||
| chr7:107968386
|
G | A | 2 | a0001c0005t0001g0035a0026c0060t0001g0036 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1563-3699C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107968386 | ||||||
| chr7:107968437
|
G | A | 33 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(30): Show | 33 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1563-3750C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107968437 | ||||||
| chr7:107968494
|
T | C | 1 | a0001c0014t0001g0346 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1563-3807A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107968494 | ||||||
| chr7:107968594
|
G | C | 32 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(29): Show | 32 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1563-3907C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107968594 | ||||||
| chr7:107968613
|
T | C | 1 | a0001c0001t0002g0019 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1563-3926A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107968613 | ||||||
| chr7:107968681
|
G | A | 2 | a0001c0005t0001g0035a0026c0060t0001g0036 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1563-3994C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107968681 | ||||||
| chr7:107968846
|
G | C | 2 | a0001c0072t0001g0025a0001c0078t0001g0024 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1562+4146C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107968846 | ||||||
| chr7:107969026
|
C | T | 1 | a0001c0032t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1562+3966G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969026 | ||||||
| chr7:107969061
|
A | G | 33 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(30): Show | 33 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1562+3931T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969061 | ||||||
| chr7:107969287
|
C | CA | 57 | a0001c0001t0001g0011a0001c0001t0001g0048a0001c0001t0001g0091others(54): Show | 57 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.1562+3704dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969287 | ||||||
| chr7:107969287
|
CA | C | 38 | a0001c0002t0001g0077a0001c0002t0001g0078a0001c0002t0001g0132others(35): Show | 38 | HG00438.hp1 HG01243.hp1 HG01256.hp2 others(35): Show |
intron_variant | MODIFIER | c.1562+3704delT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969287 | ||||||
| chr7:107969428
|
T | TA | 33 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(30): Show | 33 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1562+3563dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969428 | ||||||
| chr7:107969465
|
C | T | 1 | a0007c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1562+3527G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969465 | ||||||
| chr7:107969466
|
G | A | 2 | a0001c0005t0001g0035a0026c0060t0001g0036 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1562+3526C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969466 | ||||||
| chr7:107969596
|
A | G | 2 | a0001c0072t0001g0025a0001c0078t0001g0024 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1562+3396T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969596 | ||||||
| chr7:107969708
|
G | C | 3 | a0001c0014t0001g0346a0001c0022t0001g0029a0002c0013t0001g0030 | 3 | HG02280.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1562+3284C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969708 | ||||||
| chr7:107969716
|
C | T | 110 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(107): Show | 112 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(109): Show |
intron_variant | MODIFIER | c.1562+3276G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969716 | ||||||
| chr7:107970094
|
A | G | 5 | a0001c0001t0001g0012a0001c0001t0001g0342a0001c0002t0001g0247others(2): Show | 5 | HG02258.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1562+2898T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970094 | ||||||
| chr7:107970106
|
C | T | 2 | a0001c0072t0001g0025a0001c0078t0001g0024 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1562+2886G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970106 | ||||||
| chr7:107970170
|
G | A | 1 | a0001c0002t0001g0202 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1562+2822C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970170 | ||||||
| chr7:107970230
|
T | C | 2 | a0001c0072t0001g0025a0001c0078t0001g0024 | 2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1562+2762A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970230 | ||||||
| chr7:107970433
|
A | G | 4 | a0001c0001t0002g0177a0002c0003t0002g0045a0002c0003t0002g0046others(1): Show | 4 | HG01256.hp2 HG01258.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1562+2559T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970433 | ||||||
| chr7:107970450
|
C | G | 2 | a0001c0005t0001g0035a0026c0060t0001g0036 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1562+2542G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970450 | ||||||
| chr7:107970488
|
C | CA | 18 | a0001c0002t0001g0196a0001c0002t0001g0328a0001c0005t0001g0035others(15): Show | 18 | HG00738.hp1 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1562+2503dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970488 | ||||||
| chr7:107970504
|
A | AG | 6 | a0001c0022t0001g0039a0001c0056t0001g0088a0002c0003t0002g0220others(3): Show | 6 | HG02895.hp2 HG02897.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1562+2487_1562+248 others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970504 | ||||||
| chr7:107970505
|
A | AAG | 50 | a0001c0001t0001g0303a0001c0001t0001g0321a0001c0009t0001g0018others(47): Show | 50 | HG00735.hp1 HG00735.hp2 HG01168.hp1 others(47): Show |
intron_variant | MODIFIER | c.1562+2486_1562+248 others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970505 | ||||||
| chr7:107970505
|
A | AG | 158 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0073others(155): Show | 158 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1562+2486dupC | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970505 | ||||||
| chr7:107970505
|
A | G | 8 | a0001c0022t0001g0039a0001c0028t0001g0350a0001c0056t0001g0088others(5): Show | 8 | HG02895.hp2 HG02897.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.1562+2487T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970505 | ||||||
| chr7:107970506
|
G | T | 1 | a0001c0007t0001g0007 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1562+2486C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970506 | ||||||
| chr7:107970733
|
AT | A | 35 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(32): Show | 35 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1562+2258delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970733 | ||||||
| chr7:107970736
|
T | A | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1562+2256A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970736 | ||||||
| chr7:107970815
|
T | A | 1 | a0001c0006t0002g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1562+2177A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970815 | ||||||
| chr7:107970869
|
A | G | 2 | a0002c0003t0002g0301a0003c0004t0002g0154 | 2 | NA18998.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1562+2123T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970869 | ||||||
| chr7:107970980
|
C | T | 2 | a0001c0005t0001g0035a0026c0060t0001g0036 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1562+2012G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970980 | ||||||
| chr7:107970983
|
C | T | 6 | a0001c0002t0001g0057a0001c0005t0001g0059a0002c0021t0002g0066others(3): Show | 6 | HG00741.hp2 HG01070.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1562+2009G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970983 | ||||||
| chr7:107971024
|
G | A | 3 | a0001c0014t0003g0360a0001c0044t0002g0345a0018c0047t0003g0359 | 3 | HG01891.hp2 HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1562+1968C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971024 | ||||||
| chr7:107971049
|
A | G | 9 | a0001c0001t0001g0083a0001c0001t0001g0085a0001c0001t0001g0087others(6): Show | 9 | NA18954.hp1 NA18967.hp1 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.1562+1943T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971049 | ||||||
| chr7:107971095
|
T | G | 1 | a0001c0058t0001g0143 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1562+1897A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971095 | ||||||
| chr7:107971205
|
G | T | 33 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(30): Show | 33 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1562+1787C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971205 | ||||||
| chr7:107971260
|
T | C | 1 | a0001c0006t0001g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1562+1732A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971260 | ||||||
| chr7:107971418
|
G | T | 1 | a0012c0075t0001g0043 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1562+1574C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971418 | ||||||
| chr7:107971602
|
T | C | 1 | a0001c0005t0001g0326 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1562+1390A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971602 | ||||||
| chr7:107971673
|
T | G | 1 | a0002c0010t0001g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1562+1319A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971673 | ||||||
| chr7:107971688
|
C | T | 1 | a0001c0032t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1562+1304G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971688 | ||||||
| chr7:107971704
|
T | C | 1 | a0001c0006t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1562+1288A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971704 | ||||||
| chr7:107971757
|
G | A | 2 | a0001c0005t0001g0219a0001c0005t0001g0244 | 2 | HG02080.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1562+1235C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971757 | ||||||
| chr7:107971877
|
G | T | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1562+1115C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971877 | ||||||
| chr7:107971900
|
C | A | 33 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(30): Show | 33 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1562+1092G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971900 | ||||||
| chr7:107972128
|
G | A | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1562+864C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972128 | ||||||
| chr7:107972171
|
A | G | 17 | a0004c0015t0001g0138a0004c0015t0001g0140a0004c0015t0002g0008others(14): Show | 17 | HG01243.hp1 HG01433.hp1 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.1562+821T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972171 | ||||||
| chr7:107972184
|
A | G | 164 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0073others(161): Show | 164 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.1562+808T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972184 | ||||||
| chr7:107972258
|
G | C | 2 | a0001c0001t0001g0173a0001c0001t0001g0174 | 2 | NA19084.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1562+734C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972258 | ||||||
| chr7:107972339
|
C | T | 28 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(25): Show | 28 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1562+653G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972339 | ||||||
| chr7:107972372
|
A | G | 1 | a0001c0005t0001g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1562+620T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972372 | ||||||
| chr7:107972391
|
A | G | 5 | a0001c0014t0003g0360a0001c0044t0002g0345a0002c0003t0002g0347others(2): Show | 5 | HG00738.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1562+601T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972391 | ||||||
| chr7:107972402
|
G | T | 1 | a0008c0023t0001g0051 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1562+590C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972402 | ||||||
| chr7:107972539
|
T | C | 1 | a0029c0046t0002g0333 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1562+453A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972539 | ||||||
| chr7:107972587
|
C | CA | 20 | a0001c0001t0001g0289a0001c0007t0001g0319a0001c0032t0001g0028others(17): Show | 20 | HG01243.hp1 HG01433.hp1 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.1562+404dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972587 | ||||||
| chr7:107972587
|
CA | C | 164 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0073others(161): Show | 164 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.1562+404delT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972587 | ||||||
| chr7:107972719
|
A | G | 12 | a0001c0006t0001g0042a0001c0007t0001g0009a0001c0014t0001g0346others(9): Show | 12 | HG00738.hp1 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1562+273T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972719 | ||||||
| chr7:107972762
|
T | C | 172 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0073others(169): Show | 172 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.1562+230A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972762 | ||||||
| chr7:107972934
|
G | A | 240 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0048others(237): Show | 240 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1562+58C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972934 | ||||||
| chr7:107972941
|
A | C | 1 | a0001c0028t0001g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1562+51T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972941 | ||||||
| chr7:107973273
|
A | G | 1 | a0001c0002t0001g0328 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1483-202T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973273 | ||||||
| chr7:107973360
|
T | C | 1 | a0001c0007t0003g0362 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1483-289A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973360 | ||||||
| chr7:107973452
|
A | C | 1 | a0001c0005t0001g0248 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1483-381T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973452 | ||||||
| chr7:107973462
|
T | C | 2 | a0001c0001t0002g0192a0002c0003t0002g0159 | 2 | NA18994.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1483-391A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973462 | ||||||
| chr7:107973505
|
G | A | 2 | a0001c0001t0001g0188a0001c0001t0001g0189 | 2 | NA18939.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1483-434C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973505 | ||||||
| chr7:107973509
|
C | T | 1 | a0001c0002t0001g0222 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1483-438G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973509 | ||||||
| chr7:107973558
|
A | G | 28 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(25): Show | 28 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1483-487T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973558 | ||||||
| chr7:107973851
|
G | A | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1483-780C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973851 | ||||||
| chr7:107973925
|
T | G | 200 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0073others(197): Show | 200 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1483-854A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973925 | ||||||
| chr7:107973961
|
T | C | 17 | a0004c0015t0001g0138a0004c0015t0001g0140a0004c0015t0002g0008others(14): Show | 17 | HG01243.hp1 HG01433.hp1 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.1483-890A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973961 | ||||||
| chr7:107974042
|
A | C | 1 | a0001c0009t0001g0194 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1482+944T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974042 | ||||||
| chr7:107974118
|
A | G | 266 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(263): Show | 267 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.1482+868T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974118 | ||||||
| chr7:107974224
|
T | A | 35 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(32): Show | 35 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1482+762A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974224 | ||||||
| chr7:107974357
|
G | GT | 30 | a0001c0005t0001g0035a0001c0006t0001g0042a0001c0007t0001g0009others(27): Show | 30 | HG00323.hp1 HG01243.hp1 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.1482+628dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974357 | ||||||
| chr7:107974357
|
GT | G | 6 | a0001c0032t0001g0028a0002c0003t0002g0045a0002c0003t0002g0046others(3): Show | 6 | HG01256.hp2 HG01258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1482+628delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974357 | ||||||
| chr7:107974485
|
T | C | 193 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0073others(190): Show | 193 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.1482+501A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974485 | ||||||
| chr7:107974576
|
A | G | 2 | a0001c0007t0001g0319a0001c0022t0001g0039 | 2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1482+410T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974576 | ||||||
| chr7:107974579
|
G | A | 249 | a0001c0001t0001g0012a0001c0001t0001g0033a0001c0001t0001g0048others(246): Show | 249 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.1482+407C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974579 | ||||||
| chr7:107974760
|
T | A | 3 | a0001c0014t0001g0346a0001c0022t0001g0029a0002c0013t0001g0030 | 3 | HG02280.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1482+226A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974760 | ||||||
| chr7:107974817
|
A | G | 5 | a0001c0001t0001g0131a0001c0001t0001g0201a0001c0002t0001g0286others(2): Show | 5 | HG02129.hp1 HG02293.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1482+169T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974817 | ||||||
| chr7:107974829
|
C | T | 35 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(32): Show | 35 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1482+157G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974829 | ||||||
| chr7:107974889
|
G | T | 15 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0173others(12): Show | 15 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.1482+97C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974889 | ||||||
| chr7:107975116
|
G | A | 1 | a0002c0010t0001g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1370-18C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 11/33 | chr7 | 107975116 | ||||||
| chr7:107975550
|
C | T | 1 | a0003c0079t0001g0179 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1190-137G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 10/33 | chr7 | 107975550 | ||||||
| chr7:107975566
|
C | G | 35 | a0001c0006t0001g0042a0001c0009t0001g0018a0001c0009t0001g0194others(32): Show | 35 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1189+123G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 10/33 | chr7 | 107975566 | ||||||
| chr7:107975604
|
C | A | 28 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(25): Show | 28 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1189+85G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 10/33 | chr7 | 107975604 | ||||||
| chr7:107975623
|
T | C | 35 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(32): Show | 35 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1189+66A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 10/33 | chr7 | 107975623 | ||||||
| chr7:107975633
|
G | A | 35 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(32): Show | 35 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1189+56C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 10/33 | chr7 | 107975633 | ||||||
| chr7:107975920
|
T | C | 2 | a0001c0035t0001g0037a0028c0034t0001g0031 | 2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1001-43A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107975920 | ||||||
| chr7:107975958
|
A | G | 1 | a0001c0002t0001g0122 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1001-81T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107975958 | ||||||
| chr7:107976130
|
A | T | 1 | a0001c0017t0001g0093 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1001-253T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976130 | ||||||
| chr7:107976177
|
C | G | 1 | a0001c0001t0002g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1001-300G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976177 | ||||||
| chr7:107976245
|
A | G | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1001-368T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976245 | ||||||
| chr7:107976317
|
G | A | 18 | a0001c0007t0001g0319a0004c0015t0001g0138a0004c0015t0001g0140others(15): Show | 18 | HG01243.hp1 HG01433.hp1 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.1001-440C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976317 | ||||||
| chr7:107976329
|
G | C | 1 | a0012c0075t0001g0043 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1001-452C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976329 | ||||||
| chr7:107976347
|
G | A | 21 | a0001c0001t0001g0048a0001c0001t0002g0047a0001c0007t0001g0009others(18): Show | 21 | HG00738.hp2 HG01106.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1001-470C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976347 | ||||||
| chr7:107976372
|
C | T | 1 | a0001c0005t0001g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1001-495G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976372 | ||||||
| chr7:107976440
|
C | T | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1001-563G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976440 | ||||||
| chr7:107976500
|
G | A | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1001-623C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976500 | ||||||
| chr7:107976544
|
C | T | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1001-667G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976544 | ||||||
| chr7:107976645
|
T | C | 1 | a0011c0025t0001g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1001-768A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976645 | ||||||
| chr7:107976655
|
T | A | 5 | a0001c0002t0001g0196a0001c0002t0001g0199a0002c0003t0002g0076others(2): Show | 5 | NA18962.hp1 NA18988.hp1 NA19058.hp2 others(2): Show |
intron_variant | MODIFIER | c.1001-778A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976655 | ||||||
| chr7:107976703
|
A | G | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG02523.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1001-826T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976703 | ||||||
| chr7:107976759
|
C | A | 27 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(24): Show | 27 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1001-882G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976759 | ||||||
| chr7:107976778
|
G | A | 1 | a0001c0032t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1001-901C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976778 | ||||||
| chr7:107976838
|
T | C | 1 | a0001c0007t0001g0009 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1001-961A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976838 | ||||||
| chr7:107976854
|
CCTCTCCT others(63): Show |
C | 26 | a0001c0001t0001g0048a0001c0001t0002g0047a0001c0007t0001g0009others(23): Show | 26 | HG00738.hp1 HG00738.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.1001-1047_1001-978 others(73): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976854 | ||||||
| chr7:107976856
|
TCTCCTTC others(19): Show |
T | 2 | a0001c0035t0001g0037a0028c0034t0001g0031 | 2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1001-1005_1001-980 others(29): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976856 | ||||||
| chr7:107976856
|
TCTCCTTC others(85): Show |
T | 30 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(27): Show | 30 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1001-1071_1001-980 others(95): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976856 | ||||||
| chr7:107976861
|
T | C | 1 | a0002c0003t0002g0013 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1001-984A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976861 | ||||||
| chr7:107976861
|
T | TTCCTTCC others(11): Show |
124 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(121): Show | 125 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(122): Show |
intron_variant | MODIFIER | c.1001-985_1001-984i others(20): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976861 | ||||||
| chr7:107976861
|
T | TTCCTTCC others(33): Show |
3 | a0001c0002t0001g0122a0001c0007t0001g0007a0027c0061t0001g0123 | 3 | HG02559.hp2 NA18962.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1001-985_1001-984i others(42): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976861 | ||||||
| chr7:107976881
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(132): Show | 136 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(133): Show |
intron_variant | MODIFIER | c.1001-1004A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976881 | ||||||
| chr7:107976882
|
G | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(135): Show | 139 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.1001-1005C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976882 | ||||||
| chr7:107976887
|
T | G | 9 | a0001c0006t0001g0042a0001c0014t0001g0346a0001c0022t0001g0029others(6): Show | 9 | HG02280.hp2 HG02970.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1001-1010A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976887 | ||||||
| chr7:107976903
|
T | C | 10 | a0001c0002t0001g0122a0001c0006t0001g0042a0001c0014t0001g0346others(7): Show | 10 | HG02280.hp2 HG02622.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1001-1026A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976903 | ||||||
| chr7:107976904
|
G | C | 131 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(128): Show | 132 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(129): Show |
intron_variant | MODIFIER | c.1001-1027C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976904 | ||||||
| chr7:107976904
|
G | GCTCCTTC others(59): Show |
1 | a0001c0002t0001g0217 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1001-1028_1001-102 others(70): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976904 | ||||||
| chr7:107976924
|
T | TCTCTCCT others(77): Show |
5 | a0001c0001t0001g0012a0001c0001t0001g0342a0001c0006t0001g0341others(2): Show | 5 | HG02258.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1001-1048_1001-104 others(88): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976924 | ||||||
| chr7:107976926
|
T | C | 6 | a0001c0002t0001g0122a0001c0002t0001g0217a0001c0007t0001g0007others(3): Show | 6 | HG02027.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1001-1049A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976926 | ||||||
| chr7:107976926
|
T | TCTCCTTC others(15): Show |
4 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0003t0002g0288others(1): Show | 4 | HG01517.hp1 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-1071_1001-105 others(26): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976926 | ||||||
| chr7:107976926
|
T | TCTCCTTC others(37): Show |
161 | a0001c0001t0001g0033a0001c0001t0001g0073a0001c0001t0001g0083others(158): Show | 162 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1000+1077_1001-105 others(48): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976926 | ||||||
| chr7:107976926
|
T | TCTCCTTC others(59): Show |
2 | a0001c0001t0001g0151a0029c0046t0002g0333 | 2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1001-1050_1001-104 others(70): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976926 | ||||||
| chr7:107976926
|
T | TCTCCTTC others(279): Show |
1 | a0001c0001t0001g0313 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1001-1050_1001-104 others(290): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976926 | ||||||
| chr7:107976947
|
C | T | 5 | a0001c0014t0003g0360a0001c0044t0002g0345a0002c0003t0002g0347others(2): Show | 5 | HG00738.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001-1070G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976947 | ||||||
| chr7:107976948
|
C | CCTCCTTC others(11): Show |
3 | a0001c0002t0001g0122a0002c0003t0002g0013a0027c0061t0001g0123 | 3 | HG00733.hp1 NA18962.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1000+1081_1001-107 others(22): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976948 | ||||||
| chr7:107976948
|
C | CCTCCTTC others(33): Show |
5 | a0003c0004t0001g0079a0003c0004t0001g0080a0003c0004t0001g0157others(2): Show | 5 | NA18612.hp1 NA18953.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+1059_1001-107 others(44): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976948 | ||||||
| chr7:107976948
|
C | CCTCCTTC others(55): Show |
71 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0015others(68): Show | 72 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1001-1072_1001-107 others(66): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976948 | ||||||
| chr7:107976948
|
C | CCTCCTTC others(77): Show |
1 | a0003c0004t0001g0082 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1001-1072_1001-107 others(88): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976948 | ||||||
| chr7:107976948
|
C | CCTCCTTC others(121): Show |
1 | a0001c0001t0001g0294 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1001-1072_1001-107 others(132): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976948 | ||||||
| chr7:107976948
|
C | T | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1001-1071G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976948 | ||||||
| chr7:107976969
|
C | T | 1 | a0002c0010t0001g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1000+1078G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976969 | ||||||
| chr7:107976970
|
C | CCTCCTTC others(681): Show |
5 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0002g0061others(2): Show | 5 | HG01070.hp1 HG01255.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+1076_1000+107 others(692): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976970 | ||||||
| chr7:107976970
|
C | T | 5 | a0001c0006t0001g0042a0001c0014t0001g0346a0001c0022t0001g0029others(2): Show | 5 | HG02280.hp2 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+1077G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976970 | ||||||
| chr7:107976990
|
T | TCTCTCCT others(554): Show |
1 | a0002c0010t0001g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1000+1056_1000+105 others(565): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976990 | ||||||
| chr7:107976990
|
TTC | T | 5 | a0001c0006t0001g0042a0001c0014t0001g0346a0001c0022t0001g0029others(2): Show | 5 | HG02280.hp2 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+1055_1000+105 others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976990 | ||||||
| chr7:107976991
|
T | C | 168 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(165): Show | 169 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(166): Show |
intron_variant | MODIFIER | c.1000+1056A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976991 | ||||||
| chr7:107976992
|
C | T | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1000+1055G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976992 | ||||||
| chr7:107976995
|
C | T | 5 | a0001c0006t0001g0042a0001c0014t0001g0346a0001c0022t0001g0029others(2): Show | 5 | HG02280.hp2 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+1052G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976995 | ||||||
| chr7:107976996
|
C | T | 5 | a0001c0006t0001g0042a0001c0014t0001g0346a0001c0022t0001g0029others(2): Show | 5 | HG02280.hp2 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+1051G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976996 | ||||||
| chr7:107976998
|
T | C | 5 | a0001c0006t0001g0042a0001c0014t0001g0346a0001c0022t0001g0029others(2): Show | 5 | HG02280.hp2 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+1049A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976998 | ||||||
| chr7:107977000
|
C | T | 5 | a0001c0006t0001g0042a0001c0014t0001g0346a0001c0022t0001g0029others(2): Show | 5 | HG02280.hp2 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+1047G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977000 | ||||||
| chr7:107977003
|
C | CCTTTCCT others(13): Show |
1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1000+1043_1000+104 others(24): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977003 | ||||||
| chr7:107977003
|
C | T | 5 | a0001c0006t0001g0042a0001c0014t0001g0346a0001c0022t0001g0029others(2): Show | 5 | HG02280.hp2 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+1044G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977003 | ||||||
| chr7:107977006
|
T | C | 1 | a0001c0042t0001g0112 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1000+1041A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977006 | ||||||
| chr7:107977010
|
T | TTCCTTCC others(48): Show |
1 | a0001c0042t0001g0112 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1000+1036_1000+103 others(59): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977010 | ||||||
| chr7:107977012
|
T | TCCTTCCT others(51): Show |
31 | a0001c0001t0001g0004a0001c0001t0002g0050a0001c0001t0002g0152others(28): Show | 31 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1000+1034_1000+103 others(62): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977012 | ||||||
| chr7:107977012
|
T | TCCTTCCT others(179): Show |
1 | a0002c0054t0001g0181 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1000+1034_1000+103 others(190): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977012 | ||||||
| chr7:107977013
|
C | CCCTCCTT others(15): Show |
1 | a0001c0006t0002g0327 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1000+1033_1000+103 others(26): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977013 | ||||||
| chr7:107977013
|
C | T | 29 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(26): Show | 29 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.1000+1034G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977013 | ||||||
| chr7:107977014
|
T | C | 135 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(132): Show | 136 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1000+1033A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977014 | ||||||
| chr7:107977014
|
T | TCTCCTTC others(37): Show |
6 | a0001c0006t0001g0042a0001c0014t0001g0346a0001c0022t0001g0029others(3): Show | 6 | HG02280.hp2 HG02970.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1000+1032_1000+103 others(48): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977014 | ||||||
| chr7:107977014
|
TCTCCTTC others(15): Show |
T | 2 | a0001c0035t0001g0037a0028c0034t0001g0031 | 2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1000+1011_1000+103 others(26): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977014 | ||||||
| chr7:107977016
|
T | TC | 32 | a0001c0001t0001g0004a0001c0001t0002g0050a0001c0001t0002g0152others(29): Show | 32 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.1000+1030dupG | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977016 | ||||||
| chr7:107977016
|
T | TCCTTCCT others(144): Show |
1 | a0006c0011t0002g0330 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1000+1030_1000+103 others(155): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977016 | ||||||
| chr7:107977036
|
C | T | 30 | a0001c0006t0002g0327a0001c0009t0001g0018a0001c0009t0001g0194others(27): Show | 30 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1000+1011G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977036 | ||||||
| chr7:107977058
|
C | T | 5 | a0001c0014t0003g0360a0001c0044t0002g0345a0002c0003t0002g0347others(2): Show | 5 | HG00738.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+989G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977058 | ||||||
| chr7:107977125
|
T | C | 4 | a0001c0001t0001g0012a0001c0001t0001g0342a0001c0006t0001g0341others(1): Show | 4 | HG02258.hp2 HG02486.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000+922A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977125 | ||||||
| chr7:107977192
|
T | TC | 134 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(131): Show | 135 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1000+854dupG | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977192 | ||||||
| chr7:107977195
|
A | T | 134 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(131): Show | 135 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1000+852T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977195 | ||||||
| chr7:107977196
|
G | A | 134 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(131): Show | 135 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1000+851C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977196 | ||||||
| chr7:107977265
|
G | C | 1 | a0003c0004t0001g0238 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1000+782C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977265 | ||||||
| chr7:107977323
|
G | A | 21 | a0001c0001t0001g0048a0001c0001t0002g0047a0001c0007t0001g0009others(18): Show | 21 | HG00738.hp2 HG01106.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1000+724C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977323 | ||||||
| chr7:107977483
|
G | C | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1000+564C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977483 | ||||||
| chr7:107977562
|
T | G | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1000+485A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977562 | ||||||
| chr7:107977605
|
C | T | 322 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(319): Show | 324 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(321): Show |
intron_variant | MODIFIER | c.1000+442G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977605 | ||||||
| chr7:107977660
|
G | A | 1 | a0001c0005t0001g0129 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1000+387C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977660 | ||||||
| chr7:107977661
|
C | T | 5 | a0001c0014t0003g0360a0001c0044t0002g0345a0002c0003t0002g0347others(2): Show | 5 | HG00738.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+386G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977661 | ||||||
| chr7:107977667
|
T | C | 2 | a0001c0005t0001g0150a0001c0059t0001g0041 | 2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1000+380A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977667 | ||||||
| chr7:107977745
|
A | G | 3 | a0001c0001t0001g0228a0003c0004t0001g0229a0003c0020t0001g0187 | 3 | HG02132.hp1 NA18612.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1000+302T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977745 | ||||||
| chr7:107977758
|
C | CA | 5 | a0001c0001t0001g0307a0001c0002t0001g0239a0001c0007t0001g0130others(2): Show | 5 | HG01891.hp1 HG02738.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1000+288dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977758 | ||||||
| chr7:107977950
|
A | T | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1000+97T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977950 | ||||||
| chr7:107977975
|
A | G | 27 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(24): Show | 27 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1000+72T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977975 | ||||||
| chr7:107978204
|
A | T | 1 | a0001c0001t0001g0022 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.880-37T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978204 | ||||||
| chr7:107978413
|
G | A | 5 | a0001c0014t0003g0360a0001c0044t0002g0345a0002c0003t0002g0347others(2): Show | 5 | HG00738.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-246C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978413 | ||||||
| chr7:107978455
|
T | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.880-288A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978455 | ||||||
| chr7:107978455
|
T | TA | 7 | a0001c0001t0001g0131a0001c0001t0001g0201a0001c0002t0001g0239others(4): Show | 7 | HG02129.hp1 HG02293.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-289dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978455 | ||||||
| chr7:107978455
|
TA | T | 37 | a0001c0001t0001g0012a0001c0001t0001g0048a0001c0001t0001g0111others(34): Show | 37 | HG00140.hp1 HG00738.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.880-289delT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978455 | ||||||
| chr7:107978469
|
AAAACT | A | 7 | a0001c0018t0002g0269a0001c0077t0001g0275a0002c0008t0002g0156others(4): Show | 7 | HG00735.hp2 HG01168.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-307_880-303del others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978469 | ||||||
| chr7:107978549
|
T | A | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.880-382A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978549 | ||||||
| chr7:107978607
|
C | A | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.880-440G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978607 | ||||||
| chr7:107978647
|
G | GT | 120 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(117): Show | 121 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(118): Show |
intron_variant | MODIFIER | c.880-481dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978647 | ||||||
| chr7:107978770
|
T | A | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.880-603A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978770 | ||||||
| chr7:107979002
|
G | A | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.880-835C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979002 | ||||||
| chr7:107979010
|
C | A | 2 | a0001c0001t0001g0073a0002c0039t0002g0203 | 2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.880-843G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979010 | ||||||
| chr7:107979080
|
A | G | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.880-913T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979080 | ||||||
| chr7:107979095
|
G | A | 31 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(28): Show | 31 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.880-928C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979095 | ||||||
| chr7:107979118
|
T | A | 31 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(28): Show | 31 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.880-951A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979118 | ||||||
| chr7:107979121
|
G | C | 6 | a0001c0014t0003g0360a0001c0044t0002g0345a0002c0003t0002g0347others(3): Show | 6 | HG00738.hp1 HG01891.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-954C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979121 | ||||||
| chr7:107979125
|
C | T | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.880-958G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979125 | ||||||
| chr7:107979166
|
T | C | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.880-999A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979166 | ||||||
| chr7:107979196
|
T | TTC | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.880-1031_880-1030d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979196 | ||||||
| chr7:107979485
|
G | C | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.879+1124C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979485 | ||||||
| chr7:107979569
|
A | G | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.879+1040T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979569 | ||||||
| chr7:107979609
|
A | ATACTT | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.879+999_879+1000in others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979609 | ||||||
| chr7:107979664
|
A | G | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.879+945T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979664 | ||||||
| chr7:107979789
|
G | A | 4 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0002t0001g0064others(1): Show | 4 | HG01070.hp1 HG01255.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+820C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979789 | ||||||
| chr7:107979811
|
C | T | 3 | a0001c0001t0001g0012a0001c0001t0001g0342a0001c0006t0001g0341 | 3 | HG02258.hp2 HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.879+798G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979811 | ||||||
| chr7:107979889
|
T | C | 1 | a0001c0001t0001g0102 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.879+720A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979889 | ||||||
| chr7:107979893
|
G | C | 1 | a0002c0003t0002g0166 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.879+716C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979893 | ||||||
| chr7:107980008
|
G | T | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.879+601C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107980008 | ||||||
| chr7:107980027
|
A | G | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.879+582T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107980027 | ||||||
| chr7:107980038
|
C | T | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.879+571G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107980038 | ||||||
| chr7:107980210
|
G | GA | 10 | a0001c0001t0001g0073a0001c0001t0001g0189a0001c0001t0001g0218others(7): Show | 10 | HG00741.hp2 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.879+398dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107980210 | ||||||
| chr7:107980307
|
A | G | 1 | a0028c0034t0001g0031 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.879+302T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107980307 | ||||||
| chr7:107980393
|
C | G | 1 | a0001c0028t0001g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.879+216G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107980393 | ||||||
| chr7:107980410
|
G | A | 1 | a0002c0003t0002g0175 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.879+199C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107980410 | ||||||
| chr7:107980507
|
A | G | 1 | a0001c0002t0001g0328 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.879+102T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107980507 | ||||||
| chr7:107980860
|
GT | G | 41 | a0001c0001t0001g0048a0001c0001t0002g0047a0001c0007t0001g0009others(38): Show | 41 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.677-50delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107980860 | ||||||
| chr7:107980994
|
A | C | 1 | a0001c0001t0001g0221 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.677-183T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107980994 | ||||||
| chr7:107980996
|
G | A | 1 | a0002c0003t0001g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.677-185C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107980996 | ||||||
| chr7:107981148
|
A | C | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.677-337T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981148 | ||||||
| chr7:107981169
|
G | A | 26 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(23): Show | 26 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.677-358C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981169 | ||||||
| chr7:107981175
|
G | A | 17 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0015others(14): Show | 18 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.677-364C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981175 | ||||||
| chr7:107981409
|
T | C | 107 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(104): Show | 108 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(105): Show |
intron_variant | MODIFIER | c.677-598A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981409 | ||||||
| chr7:107981445
|
TA | T | 138 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(135): Show | 139 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.677-635delT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981445 | ||||||
| chr7:107981445
|
TAA | T | 8 | a0001c0001t0001g0151a0001c0002t0001g0077a0001c0002t0001g0104others(5): Show | 8 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.677-636_677-635del others(2): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981445 | ||||||
| chr7:107981446
|
A | T | 2 | a0001c0005t0001g0035a0026c0060t0001g0036 | 2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.677-635T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981446 | ||||||
| chr7:107981535
|
C | T | 1 | a0001c0072t0001g0025 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.677-724G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981535 | ||||||
| chr7:107981605
|
A | C | 1 | a0001c0002t0001g0049 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.677-794T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981605 | ||||||
| chr7:107981705
|
A | G | 181 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(178): Show | 182 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.677-894T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981705 | ||||||
| chr7:107981843
|
G | A | 181 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(178): Show | 182 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.677-1032C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981843 | ||||||
| chr7:107981879
|
C | T | 1 | a0001c0002t0001g0110 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.677-1068G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981879 | ||||||
| chr7:107981970
|
C | T | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.677-1159G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981970 | ||||||
| chr7:107981979
|
G | A | 109 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(106): Show | 110 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(107): Show |
intron_variant | MODIFIER | c.677-1168C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981979 | ||||||
| chr7:107982128
|
T | C | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.677-1317A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107982128 | ||||||
| chr7:107982191
|
G | A | 1 | a0001c0009t0001g0282 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.677-1380C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107982191 | ||||||
| chr7:107982420
|
T | A | 1 | a0001c0001t0002g0002 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.677-1609A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107982420 | ||||||
| chr7:107982553
|
TCTCCTGC others(7): Show |
T | 1 | a0001c0006t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.677-1756_677-1743d others(16): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107982553 | ||||||
| chr7:107982585
|
C | T | 3 | a0001c0001t0001g0048a0001c0001t0002g0047a0001c0007t0001g0009 | 3 | HG00738.hp2 HG01106.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.677-1774G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107982585 | ||||||
| chr7:107982601
|
C | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0342a0001c0006t0001g0341 | 3 | HG02258.hp2 HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.677-1790G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107982601 | ||||||
| chr7:107982666
|
T | C | 3 | a0001c0001t0001g0012a0001c0001t0001g0342a0001c0006t0001g0341 | 3 | HG02258.hp2 HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.677-1855A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107982666 | ||||||
| chr7:107982894
|
T | C | 184 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(181): Show | 185 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.677-2083A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107982894 | ||||||
| chr7:107983006
|
G | C | 2 | a0001c0001t0001g0294a0014c0036t0001g0068 | 2 | HG01257.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.677-2195C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983006 | ||||||
| chr7:107983051
|
T | C | 113 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(110): Show | 114 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(111): Show |
intron_variant | MODIFIER | c.677-2240A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983051 | ||||||
| chr7:107983097
|
A | G | 184 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(181): Show | 185 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.677-2286T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983097 | ||||||
| chr7:107983140
|
T | G | 1 | a0003c0004t0001g0250 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.677-2329A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983140 | ||||||
| chr7:107983145
|
G | A | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.677-2334C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983145 | ||||||
| chr7:107983422
|
A | C | 8 | a0001c0009t0001g0271a0001c0018t0002g0269a0001c0077t0001g0275others(5): Show | 8 | HG00735.hp2 HG01168.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.676+2600T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983422 | ||||||
| chr7:107983427
|
A | G | 1 | a0003c0049t0001g0056 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.676+2595T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983427 | ||||||
| chr7:107983493
|
C | T | 25 | a0001c0001t0001g0094a0001c0001t0001g0097a0001c0001t0001g0167others(22): Show | 26 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.676+2529G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983493 | ||||||
| chr7:107983509
|
G | A | 5 | a0001c0014t0003g0360a0001c0044t0002g0345a0002c0003t0002g0347others(2): Show | 5 | HG00738.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.676+2513C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983509 | ||||||
| chr7:107983547
|
C | CT | 85 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0097others(82): Show | 86 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.676+2474dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983547 | ||||||
| chr7:107983547
|
C | CTT | 16 | a0001c0002t0001g0055a0001c0002t0001g0077a0001c0002t0001g0078others(13): Show | 16 | HG00738.hp1 HG01175.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.676+2473_676+2474d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983547 | ||||||
| chr7:107983547
|
CT | C | 8 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0131others(5): Show | 8 | HG01070.hp1 HG01255.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.676+2474delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983547 | ||||||
| chr7:107983646
|
G | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(179): Show | 183 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.676+2376C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983646 | ||||||
| chr7:107983664
|
C | T | 27 | a0001c0007t0001g0007a0001c0009t0001g0018a0001c0009t0001g0194others(24): Show | 27 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.676+2358G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983664 | ||||||
| chr7:107983674
|
T | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(193): Show | 197 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(194): Show |
intron_variant | MODIFIER | c.676+2348A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983674 | ||||||
| chr7:107983741
|
C | T | 1 | a0001c0063t0001g0324 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.676+2281G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983741 | ||||||
| chr7:107983895
|
G | A | 2 | a0001c0002t0001g0055a0002c0003t0002g0301 | 2 | NA18949.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.676+2127C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983895 | ||||||
| chr7:107983896
|
G | A | 10 | a0001c0001t0001g0048a0001c0001t0002g0047a0001c0006t0001g0193others(7): Show | 10 | HG00738.hp2 HG01106.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.676+2126C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983896 | ||||||
| chr7:107984271
|
CAG | C | 4 | a0001c0001t0001g0091a0001c0002t0001g0240a0002c0003t0002g0242others(1): Show | 4 | HG01952.hp1 HG01981.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.676+1749_676+1750d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107984271 | ||||||
| chr7:107984352
|
G | A | 1 | a0002c0003t0002g0092 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.676+1670C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107984352 | ||||||
| chr7:107984438
|
C | A | 182 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(179): Show | 183 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.676+1584G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107984438 | ||||||
| chr7:107984491
|
G | A | 111 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(108): Show | 112 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(109): Show |
intron_variant | MODIFIER | c.676+1531C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107984491 | ||||||
| chr7:107984553
|
C | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0342a0001c0006t0001g0341 | 3 | HG02258.hp2 HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.676+1469G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107984553 | ||||||
| chr7:107984977
|
C | G | 1 | a0007c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.676+1045G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107984977 | ||||||
| chr7:107985058
|
C | T | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.676+964G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985058 | ||||||
| chr7:107985063
|
T | C | 3 | a0001c0022t0001g0029a0001c0032t0001g0028a0002c0013t0001g0030 | 3 | HG02280.hp2 HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.676+959A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985063 | ||||||
| chr7:107985131
|
A | G | 9 | a0001c0001t0001g0102a0001c0001t0001g0221a0001c0001t0001g0325others(6): Show | 9 | HG00609.hp1 HG02083.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.676+891T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985131 | ||||||
| chr7:107985142
|
G | A | 7 | a0001c0032t0001g0028a0001c0035t0001g0037a0002c0003t0001g0070others(4): Show | 7 | HG02622.hp1 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.676+880C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985142 | ||||||
| chr7:107985362
|
G | A | 33 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(30): Show | 33 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.676+660C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985362 | ||||||
| chr7:107985421
|
C | T | 6 | a0001c0002t0001g0103a0001c0002t0001g0104a0001c0002t0001g0105others(3): Show | 6 | HG00642.hp2 HG01069.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.676+601G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985421 | ||||||
| chr7:107985444
|
G | C | 1 | a0005c0012t0002g0323 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.676+578C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985444 | ||||||
| chr7:107985527
|
G | A | 1 | a0002c0003t0002g0099 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.676+495C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985527 | ||||||
| chr7:107985614
|
A | C | 3 | a0001c0001t0001g0287a0001c0006t0001g0133a0003c0050t0002g0146 | 3 | HG01361.hp1 HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.676+408T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985614 | ||||||
| chr7:107985615
|
G | A | 1 | a0003c0004t0002g0154 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.676+407C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985615 | ||||||
| chr7:107985741
|
C | T | 184 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(181): Show | 185 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.676+281G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985741 | ||||||
| chr7:107985794
|
C | T | 77 | a0001c0001t0001g0073a0001c0001t0001g0091a0001c0001t0001g0102others(74): Show | 77 | HG00438.hp1 HG00609.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.676+228G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985794 | ||||||
| chr7:107986549
|
A | G | 187 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(184): Show | 188 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(185): Show |
intron_variant | MODIFIER | c.424-186T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107986549 | ||||||
| chr7:107986869
|
T | C | 192 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(189): Show | 193 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.424-506A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107986869 | ||||||
| chr7:107986873
|
A | G | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.424-510T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107986873 | ||||||
| chr7:107986957
|
C | T | 1 | a0005c0065t0001g0147 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.424-594G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107986957 | ||||||
| chr7:107987240
|
T | C | 2 | a0001c0006t0001g0356a0001c0006t0001g0358 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.424-877A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987240 | ||||||
| chr7:107987403
|
T | A | 195 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(192): Show | 196 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.424-1040A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987403 | ||||||
| chr7:107987564
|
G | T | 1 | a0003c0020t0001g0195 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.424-1201C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987564 | ||||||
| chr7:107987582
|
C | T | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.424-1219G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987582 | ||||||
| chr7:107987586
|
C | T | 2 | a0001c0001t0001g0342a0001c0006t0001g0341 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.424-1223G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987586 | ||||||
| chr7:107987750
|
C | T | 2 | a0002c0008t0002g0006a0017c0076t0001g0005 | 2 | NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.424-1387G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987750 | ||||||
| chr7:107987766
|
T | C | 198 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(195): Show | 199 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(196): Show |
intron_variant | MODIFIER | c.424-1403A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987766 | ||||||
| chr7:107987794
|
G | A | 2 | a0001c0001t0001g0342a0001c0006t0001g0341 | 2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.424-1431C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987794 | ||||||
| chr7:107987854
|
C | T | 1 | a0001c0005t0001g0219 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.424-1491G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987854 | ||||||
| chr7:107987969
|
G | A | 4 | a0001c0001t0001g0048a0001c0001t0002g0047a0001c0007t0001g0009others(1): Show | 4 | HG00738.hp2 HG01106.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-1606C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987969 | ||||||
| chr7:107988048
|
A | C | 1 | a0001c0078t0001g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.424-1685T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107988048 | ||||||
| chr7:107988126
|
T | A | 1 | a0007c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.424-1763A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107988126 | ||||||
| chr7:107988234
|
C | A | 337 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(334): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.424-1871G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107988234 | ||||||
| chr7:107988348
|
G | A | 27 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(24): Show | 27 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.424-1985C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107988348 | ||||||
| chr7:107988385
|
G | A | 4 | a0001c0001t0001g0048a0001c0001t0002g0047a0001c0007t0001g0009others(1): Show | 4 | HG00738.hp2 HG01106.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-2022C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107988385 | ||||||
| chr7:107988438
|
TCAAA | T | 4 | a0001c0001t0001g0048a0001c0001t0002g0047a0001c0007t0001g0009others(1): Show | 4 | HG00738.hp2 HG01106.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-2079_424-2076d others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107988438 | ||||||
| chr7:107988460
|
G | T | 4 | a0001c0001t0001g0048a0001c0001t0002g0047a0001c0007t0001g0009others(1): Show | 4 | HG00738.hp2 HG01106.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-2097C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107988460 | ||||||
| chr7:107988855
|
T | A | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(138): Show | 142 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(139): Show |
intron_variant | MODIFIER | c.424-2492A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107988855 | ||||||
| chr7:107988932
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.424-2569A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107988932 | ||||||
| chr7:107989004
|
G | A | 1 | a0001c0007t0001g0007 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424-2641C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107989004 | ||||||
| chr7:107989050
|
A | G | 1 | a0001c0059t0001g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.424-2687T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107989050 | ||||||
| chr7:107989092
|
G | C | 1 | a0001c0032t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.424-2729C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107989092 | ||||||
| chr7:107989214
|
C | T | 34 | a0001c0009t0001g0018a0001c0009t0001g0194a0001c0009t0001g0270others(31): Show | 34 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.424-2851G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107989214 | ||||||
| chr7:107989289
|
A | C | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.424-2926T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107989289 | ||||||
| chr7:107989364
|
C | T | 2 | a0001c0001t0001g0073a0002c0039t0002g0203 | 2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.424-3001G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107989364 | ||||||
| chr7:107989378
|
C | T | 1 | a0002c0026t0002g0352 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.424-3015G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107989378 | ||||||
| chr7:107989478
|
T | C | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.424-3115A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107989478 | ||||||
| chr7:107989799
|
G | A | 11 | a0001c0001t0001g0048a0001c0001t0002g0047a0001c0007t0001g0009others(8): Show | 11 | HG00738.hp2 HG01106.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.424-3436C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107989799 | ||||||
| chr7:107990026
|
T | TG | 139 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(136): Show | 140 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(137): Show |
intron_variant | MODIFIER | c.424-3664dupC | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990026 | ||||||
| chr7:107990028
|
T | C | 133 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(130): Show | 134 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.424-3665A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990028 | ||||||
| chr7:107990028
|
T | G | 60 | a0001c0001t0001g0012a0001c0001t0001g0342a0001c0006t0001g0042others(57): Show | 60 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.424-3665A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990028 | ||||||
| chr7:107990037
|
G | T | 67 | a0001c0001t0001g0012a0001c0001t0001g0048a0001c0001t0001g0342others(64): Show | 67 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.424-3674C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990037 | ||||||
| chr7:107990093
|
C | G | 1 | a0001c0002t0001g0286 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.424-3730G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990093 | ||||||
| chr7:107990151
|
A | G | 1 | a0007c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.424-3788T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990151 | ||||||
| chr7:107990415
|
C | T | 1 | a0001c0005t0001g0101 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.424-4052G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990415 | ||||||
| chr7:107990449
|
G | A | 1 | a0002c0003t0002g0166 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.424-4086C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990449 | ||||||
| chr7:107990535
|
C | T | 1 | a0001c0001t0001g0016 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.424-4172G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990535 | ||||||
| chr7:107990546
|
A | G | 1 | a0002c0010t0001g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.424-4183T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990546 | ||||||
| chr7:107990547
|
AT | A | 18 | a0001c0006t0001g0042a0001c0007t0001g0319a0004c0015t0001g0138others(15): Show | 18 | HG01243.hp1 HG01433.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.424-4185delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990547 | ||||||
| chr7:107990654
|
C | CCA | 21 | a0001c0001t0001g0012a0001c0001t0001g0342a0001c0006t0001g0042others(18): Show | 21 | HG01243.hp1 HG01433.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.423+4231_423+4232d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990654 | ||||||
| chr7:107990709
|
G | C | 1 | a0001c0006t0001g0133 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.423+4178C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990709 | ||||||
| chr7:107990728
|
T | C | 1 | a0003c0004t0001g0318 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.423+4159A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990728 | ||||||
| chr7:107990741
|
C | T | 2 | a0001c0006t0001g0356a0001c0006t0001g0358 | 2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.423+4146G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990741 | ||||||
| chr7:107990898
|
C | T | 1 | a0001c0063t0001g0324 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.423+3989G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990898 | ||||||
| chr7:107990960
|
C | T | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.423+3927G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990960 | ||||||
| chr7:107990982
|
C | T | 1 | a0001c0002t0001g0202 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.423+3905G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990982 | ||||||
| chr7:107991238
|
A | G | 1 | a0002c0010t0001g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.423+3649T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991238 | ||||||
| chr7:107991273
|
T | C | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.423+3614A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991273 | ||||||
| chr7:107991323
|
C | T | 130 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(127): Show | 131 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.423+3564G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991323 | ||||||
| chr7:107991336
|
C | T | 193 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(190): Show | 194 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.423+3551G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991336 | ||||||
| chr7:107991444
|
G | A | 9 | a0001c0001t0001g0048a0001c0001t0002g0047a0001c0007t0001g0009others(6): Show | 9 | HG00738.hp1 HG00738.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.423+3443C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991444 | ||||||
| chr7:107991449
|
T | C | 1 | a0005c0012t0002g0323 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.423+3438A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991449 | ||||||
| chr7:107991462
|
G | C | 6 | a0001c0002t0001g0057a0001c0005t0001g0059a0002c0021t0002g0066others(3): Show | 6 | HG00741.hp2 HG01070.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+3425C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991462 | ||||||
| chr7:107991558
|
T | G | 1 | a0003c0050t0002g0146 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.423+3329A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991558 | ||||||
| chr7:107991584
|
T | G | 1 | a0002c0026t0002g0352 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.423+3303A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991584 | ||||||
| chr7:107991588
|
C | CA | 16 | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0299others(13): Show | 17 | HG01109.hp1 HG01109.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.423+3298dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991588 | ||||||
| chr7:107991639
|
G | A | 1 | a0001c0002t0001g0266 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.423+3248C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991639 | ||||||
| chr7:107991698
|
C | T | 1 | a0009c0071t0001g0067 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.423+3189G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991698 | ||||||
| chr7:107991785
|
G | A | 2 | a0009c0071t0001g0067a0029c0046t0002g0333 | 2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.423+3102C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991785 | ||||||
| chr7:107991786
|
T | C | 1 | a0029c0046t0002g0333 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.423+3101A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991786 | ||||||
| chr7:107991794
|
G | A | 1 | a0001c0072t0001g0025 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.423+3093C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991794 | ||||||
| chr7:107991801
|
G | A | 1 | a0007c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.423+3086C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991801 | ||||||
| chr7:107991905
|
C | CA | 194 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(191): Show | 195 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(192): Show |
intron_variant | MODIFIER | c.423+2981dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991905 | ||||||
| chr7:107991905
|
C | CAA | 10 | a0001c0001t0001g0149a0001c0001t0001g0300a0001c0001t0001g0321others(7): Show | 10 | HG01175.hp1 HG02258.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.423+2980_423+2981d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991905 | ||||||
| chr7:107991905
|
C | CAAA | 6 | a0001c0027t0001g0349a0002c0003t0001g0070a0002c0003t0001g0071others(3): Show | 6 | HG02897.hp1 HG02976.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+2979_423+2981d others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991905 | ||||||
| chr7:107991970
|
T | C | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.423+2917A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991970 | ||||||
| chr7:107992570
|
G | A | 1 | a0011c0025t0001g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.423+2317C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107992570 | ||||||
| chr7:107992623
|
G | A | 2 | a0001c0001t0001g0335a0002c0003t0002g0075 | 2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.423+2264C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107992623 | ||||||
| chr7:107992651
|
T | C | 45 | a0001c0001t0001g0012a0001c0001t0001g0342a0001c0006t0001g0042others(42): Show | 45 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.423+2236A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107992651 | ||||||
| chr7:107992694
|
G | A | 7 | a0001c0027t0001g0349a0001c0028t0001g0350a0002c0003t0001g0070others(4): Show | 7 | HG02976.hp1 HG03139.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.423+2193C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107992694 | ||||||
| chr7:107992726
|
C | T | 14 | a0001c0002t0001g0196a0001c0002t0001g0197a0001c0002t0001g0199others(11): Show | 14 | HG00140.hp1 HG00558.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.423+2161G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107992726 | ||||||
| chr7:107992808
|
T | C | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.423+2079A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107992808 | ||||||
| chr7:107992848
|
T | C | 1 | a0001c0072t0001g0025 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.423+2039A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107992848 | ||||||
| chr7:107992986
|
T | C | 1 | a0029c0046t0002g0333 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.423+1901A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107992986 | ||||||
| chr7:107993072
|
T | C | 171 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0015others(168): Show | 172 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(169): Show |
intron_variant | MODIFIER | c.423+1815A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993072 | ||||||
| chr7:107993203
|
G | A | 3 | a0001c0022t0001g0029a0001c0032t0001g0028a0002c0013t0001g0030 | 3 | HG02280.hp2 HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.423+1684C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993203 | ||||||
| chr7:107993212
|
C | A | 1 | a0001c0002t0001g0302 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.423+1675G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993212 | ||||||
| chr7:107993250
|
C | T | 1 | a0001c0001t0001g0004 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.423+1637G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993250 | ||||||
| chr7:107993278
|
C | T | 1 | a0001c0029t0001g0311 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.423+1609G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993278 | ||||||
| chr7:107993287
|
C | T | 1 | a0003c0020t0001g0195 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.423+1600G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993287 | ||||||
| chr7:107993493
|
G | A | 1 | a0003c0004t0001g0158 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.423+1394C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993493 | ||||||
| chr7:107993511
|
A | G | 9 | a0001c0001t0002g0192a0001c0006t0001g0193a0001c0014t0001g0346others(6): Show | 9 | HG02080.hp1 HG02155.hp1 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.423+1376T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993511 | ||||||
| chr7:107993511
|
A | T | 2 | a0002c0010t0001g0334a0007c0031t0001g0072 | 2 | HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.423+1376T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993511 | ||||||
| chr7:107993801
|
G | C | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.423+1086C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993801 | ||||||
| chr7:107993917
|
C | T | 1 | a0001c0009t0001g0194 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.423+970G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993917 | ||||||
| chr7:107993939
|
T | C | 14 | a0001c0001t0001g0151a0001c0001t0001g0183a0001c0006t0001g0042others(11): Show | 14 | HG02615.hp2 HG02630.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.423+948A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993939 | ||||||
| chr7:107994048
|
C | G | 13 | a0001c0001t0001g0325a0001c0001t0002g0192a0001c0002t0001g0328others(10): Show | 13 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.423+839G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994048 | ||||||
| chr7:107994286
|
T | C | 3 | a0002c0081t0001g0020a0004c0066t0004g0021a0007c0024t0001g0184 | 3 | HG01433.hp1 HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.423+601A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994286 | ||||||
| chr7:107994290
|
A | G | 3 | a0001c0005t0001g0357a0001c0006t0001g0356a0001c0006t0001g0358 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.423+597T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994290 | ||||||
| chr7:107994381
|
C | T | 1 | a0001c0078t0001g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.423+506G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994381 | ||||||
| chr7:107994544
|
G | T | 161 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0015others(158): Show | 162 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.423+343C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994544 | ||||||
| chr7:107994660
|
G | C | 108 | a0001c0001t0001g0048a0001c0001t0001g0062a0001c0001t0001g0063others(105): Show | 108 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.423+227C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994660 | ||||||
| chr7:107994682
|
C | A | 2 | a0002c0010t0001g0155a0003c0004t0001g0148 | 2 | HG00323.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.423+205G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994682 | ||||||
| chr7:107994713
|
T | C | 1 | a0001c0009t0001g0018 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.423+174A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994713 | ||||||
| chr7:107994738
|
G | T | 3 | a0003c0004t0001g0157a0003c0004t0001g0158a0003c0004t0001g0191 | 3 | NA18953.hp2 NA18981.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.423+149C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994738 | ||||||
| chr7:107994806
|
T | C | 1 | a0001c0006t0002g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.423+81A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994806 | ||||||
| chr7:107994859
|
A | G | 1 | a0001c0005t0001g0351 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.423+28T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994859 | ||||||
| chr7:107995027
|
G | C | 12 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0015others(9): Show | 13 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.350-67C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107995027 | ||||||
| chr7:107995396
|
G | A | 3 | a0001c0001t0001g0305a0001c0001t0001g0307a0001c0002t0001g0306 | 3 | NA18989.hp2 NA18990.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.350-436C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107995396 | ||||||
| chr7:107995457
|
C | T | 4 | a0001c0045t0001g0038a0002c0003t0001g0070a0002c0003t0001g0071others(1): Show | 4 | HG02976.hp1 HG03516.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-497G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107995457 | ||||||
| chr7:107995510
|
C | T | 6 | a0001c0014t0001g0346a0001c0027t0001g0349a0001c0028t0001g0350others(3): Show | 6 | HG02630.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-550G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107995510 | ||||||
| chr7:107995548
|
A | G | 6 | a0001c0014t0001g0346a0001c0027t0001g0349a0001c0028t0001g0350others(3): Show | 6 | HG02630.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-588T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107995548 | ||||||
| chr7:107995707
|
G | A | 1 | a0014c0036t0001g0068 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.350-747C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107995707 | ||||||
| chr7:107995972
|
T | C | 1 | a0001c0006t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.350-1012A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107995972 | ||||||
| chr7:107996097
|
AATGTTAG others(1): Show |
A | 11 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(8): Show | 11 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-1145_350-1138d others(10): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996097 | ||||||
| chr7:107996106
|
C | T | 11 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(8): Show | 11 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-1146G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996106 | ||||||
| chr7:107996237
|
A | G | 1 | a0007c0024t0001g0032 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.350-1277T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996237 | ||||||
| chr7:107996294
|
C | CT | 11 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(8): Show | 11 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-1335dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996294 | ||||||
| chr7:107996301
|
T | A | 1 | a0007c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.350-1341A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996301 | ||||||
| chr7:107996351
|
T | C | 11 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(8): Show | 11 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-1391A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996351 | ||||||
| chr7:107996382
|
G | T | 11 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(8): Show | 11 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-1422C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996382 | ||||||
| chr7:107996410
|
G | A | 2 | a0001c0001t0001g0151a0007c0031t0001g0072 | 2 | HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.350-1450C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996410 | ||||||
| chr7:107996457
|
C | T | 1 | a0001c0044t0002g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.350-1497G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996457 | ||||||
| chr7:107996463
|
G | A | 11 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(8): Show | 11 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-1503C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996463 | ||||||
| chr7:107996478
|
G | A | 8 | a0001c0007t0003g0361a0001c0007t0003g0362a0001c0014t0001g0346others(5): Show | 8 | HG02055.hp1 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-1518C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996478 | ||||||
| chr7:107996541
|
C | G | 1 | a0018c0047t0003g0359 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.350-1581G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996541 | ||||||
| chr7:107996718
|
G | A | 4 | a0001c0001t0001g0342a0001c0006t0001g0341a0001c0007t0001g0343others(1): Show | 4 | HG02258.hp2 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+1639C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996718 | ||||||
| chr7:107996832
|
A | T | 11 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(8): Show | 11 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.349+1525T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996832 | ||||||
| chr7:107996930
|
G | A | 11 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(8): Show | 11 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.349+1427C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996930 | ||||||
| chr7:107996936
|
C | T | 1 | a0002c0003t0002g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.349+1421G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996936 | ||||||
| chr7:107996986
|
T | C | 1 | a0007c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.349+1371A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996986 | ||||||
| chr7:107996995
|
G | A | 2 | a0001c0035t0001g0037a0028c0034t0001g0031 | 2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.349+1362C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996995 | ||||||
| chr7:107997157
|
T | C | 1 | a0002c0019t0002g0308 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.349+1200A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997157 | ||||||
| chr7:107997255
|
C | G | 3 | a0001c0005t0001g0357a0001c0006t0001g0356a0001c0006t0001g0358 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.349+1102G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997255 | ||||||
| chr7:107997347
|
C | T | 1 | a0002c0010t0001g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.349+1010G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997347 | ||||||
| chr7:107997352
|
C | G | 182 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(179): Show | 183 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(180): Show |
intron_variant | MODIFIER | c.349+1005G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997352 | ||||||
| chr7:107997428
|
TAAAC | T | 12 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(9): Show | 12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.349+925_349+928del others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997428 | ||||||
| chr7:107997428
|
TAAACAAA others(5): Show |
T | 1 | a0012c0075t0001g0043 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.349+917_349+928del others(12): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997428 | ||||||
| chr7:107997477
|
C | T | 12 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(9): Show | 12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.349+880G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997477 | ||||||
| chr7:107997659
|
G | A | 1 | a0001c0002t0001g0309 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.349+698C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997659 | ||||||
| chr7:107997769
|
A | C | 1 | a0001c0005t0001g0190 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.349+588T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997769 | ||||||
| chr7:107997791
|
T | C | 142 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0062others(139): Show | 142 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.349+566A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997791 | ||||||
| chr7:107997931
|
C | T | 12 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(9): Show | 12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.349+426G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997931 | ||||||
| chr7:107997991
|
C | T | 3 | a0001c0001t0001g0188a0001c0001t0001g0189a0003c0020t0001g0187 | 3 | NA18939.hp1 NA18949.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.349+366G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997991 | ||||||
| chr7:107998016
|
T | A | 1 | a0014c0036t0001g0068 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349+341A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107998016 | ||||||
| chr7:107998292
|
C | G | 5 | a0001c0002t0001g0337a0001c0014t0001g0336a0002c0010t0001g0334others(2): Show | 5 | HG02717.hp1 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+65G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107998292 | ||||||
| chr7:107998628
|
T | C | 3 | a0002c0003t0001g0070a0002c0003t0001g0071a0002c0013t0001g0069 | 3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.214-136A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107998628 | ||||||
| chr7:107998632
|
A | T | 12 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(9): Show | 12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-140T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107998632 | ||||||
| chr7:107998729
|
G | C | 7 | a0001c0002t0001g0337a0001c0014t0001g0336a0002c0003t0002g0338others(4): Show | 7 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-237C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107998729 | ||||||
| chr7:107998901
|
A | G | 12 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(9): Show | 12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-409T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107998901 | ||||||
| chr7:107998935
|
G | A | 1 | a0001c0005t0001g0150 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.214-443C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107998935 | ||||||
| chr7:107999051
|
G | A | 2 | a0001c0007t0003g0361a0001c0007t0003g0362 | 2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.214-559C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999051 | ||||||
| chr7:107999116
|
C | T | 12 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(9): Show | 12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-624G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999116 | ||||||
| chr7:107999146
|
C | A | 1 | a0001c0001t0001g0186 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.214-654G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999146 | ||||||
| chr7:107999147
|
C | T | 2 | a0002c0003t0002g0338a0002c0003t0002g0339 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.214-655G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999147 | ||||||
| chr7:107999182
|
G | C | 12 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(9): Show | 12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-690C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999182 | ||||||
| chr7:107999196
|
A | G | 1 | a0001c0001t0001g0151 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.214-704T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999196 | ||||||
| chr7:107999222
|
C | A | 12 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(9): Show | 12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-730G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999222 | ||||||
| chr7:107999247
|
C | T | 2 | a0001c0001t0001g0011a0002c0003t0002g0010 | 2 | HG01069.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.214-755G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999247 | ||||||
| chr7:107999417
|
T | G | 3 | a0001c0005t0001g0357a0001c0006t0001g0356a0001c0006t0001g0358 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.214-925A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999417 | ||||||
| chr7:107999426
|
A | C | 2 | a0001c0007t0003g0361a0001c0007t0003g0362 | 2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.214-934T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999426 | ||||||
| chr7:107999438
|
C | G | 12 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(9): Show | 12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-946G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999438 | ||||||
| chr7:107999482
|
T | C | 1 | a0001c0001t0002g0019 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.214-990A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999482 | ||||||
| chr7:107999519
|
T | C | 3 | a0001c0005t0001g0357a0001c0006t0001g0356a0001c0006t0001g0358 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.214-1027A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999519 | ||||||
| chr7:107999552
|
A | G | 12 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(9): Show | 12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-1060T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999552 | ||||||
| chr7:107999672
|
A | G | 12 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(9): Show | 12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-1180T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999672 | ||||||
| chr7:107999695
|
C | CCTG | 195 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(192): Show | 196 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.214-1204_214-1203i others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999695 | ||||||
| chr7:107999745
|
A | G | 1 | a0001c0002t0001g0309 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.214-1253T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999745 | ||||||
| chr7:107999763
|
C | CT | 21 | a0001c0001t0001g0033a0001c0001t0001g0073a0001c0002t0001g0337others(18): Show | 21 | HG00738.hp1 HG01175.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.214-1272dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999763 | ||||||
| chr7:107999763
|
C | CTT | 6 | a0001c0005t0001g0026a0001c0022t0001g0029a0001c0032t0001g0028others(3): Show | 6 | HG02280.hp2 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.214-1273_214-1272d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999763 | ||||||
| chr7:107999763
|
C | CTTT | 13 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(10): Show | 13 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.214-1274_214-1272d others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999763 | ||||||
| chr7:107999763
|
CT | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0011a0001c0001t0001g0012others(154): Show | 158 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.214-1272delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999763 | ||||||
| chr7:107999763
|
CTT | C | 7 | a0001c0002t0001g0309a0001c0002t0001g0310a0001c0002t0001g0314others(4): Show | 7 | HG02723.hp2 HG02897.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-1273_214-1272d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999763 | ||||||
| chr7:107999885
|
C | T | 12 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(9): Show | 12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-1393G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999885 | ||||||
| chr7:107999938
|
T | C | 4 | a0001c0002t0001g0337a0001c0014t0001g0336a0002c0003t0002g0338others(1): Show | 4 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-1446A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999938 | ||||||
| chr7:107999962
|
C | T | 2 | a0001c0022t0001g0039a0007c0031t0001g0072 | 2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.214-1470G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999962 | ||||||
| chr7:107999974
|
G | A | 1 | a0014c0036t0001g0068 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.214-1482C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999974 | ||||||
| chr7:108000008
|
G | C | 159 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(156): Show | 160 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.214-1516C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108000008 | ||||||
| chr7:108000072
|
C | A | 1 | a0001c0028t0001g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.213+1486G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108000072 | ||||||
| chr7:108000198
|
C | CA | 177 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(174): Show | 178 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(175): Show |
intron_variant | MODIFIER | c.213+1359dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108000198 | ||||||
| chr7:108000198
|
C | CAA | 8 | a0001c0001t0001g0321a0001c0006t0001g0042a0001c0007t0001g0319others(5): Show | 8 | HG01433.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+1358_213+1359d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108000198 | ||||||
| chr7:108000198
|
C | CAAA | 11 | a0001c0001t0001g0325a0001c0002t0001g0328a0001c0002t0001g0331others(8): Show | 11 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.213+1357_213+1359d others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108000198 | ||||||
| chr7:108000212
|
G | T | 12 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0002t0001g0328others(9): Show | 12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.213+1346C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108000212 | ||||||
| chr7:108000556
|
T | A | 1 | a0001c0001t0001g0022 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.213+1002A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108000556 | ||||||
| chr7:108000700
|
C | T | 25 | a0001c0001t0001g0048a0001c0001t0001g0062a0001c0001t0001g0063others(22): Show | 25 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(22): Show |
intron_variant | MODIFIER | c.213+858G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108000700 | ||||||
| chr7:108001115
|
G | C | 3 | a0001c0005t0001g0357a0001c0006t0001g0356a0001c0006t0001g0358 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.213+443C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108001115 | ||||||
| chr7:108001171
|
C | T | 191 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0011others(188): Show | 192 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.213+387G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108001171 | ||||||
| chr7:108001287
|
G | A | 20 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0001t0001g0335others(17): Show | 20 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.213+271C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108001287 | ||||||
| chr7:108001288
|
C | T | 2 | a0001c0006t0001g0042a0001c0059t0001g0041 | 2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.213+270G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108001288 | ||||||
| chr7:108001326
|
G | A | 1 | a0011c0025t0001g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.213+232C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108001326 | ||||||
| chr7:108001430
|
G | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.213+128C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108001430 | ||||||
| chr7:108001761
|
G | T | 2 | a0001c0014t0003g0360a0018c0047t0003g0359 | 2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.38-28C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108001761 | ||||||
| chr7:108001772
|
G | A | 20 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0001t0001g0335others(17): Show | 20 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.38-39C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108001772 | ||||||
| chr7:108001814
|
G | C | 20 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0001t0001g0335others(17): Show | 20 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.38-81C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108001814 | ||||||
| chr7:108001884
|
G | A | 4 | a0002c0026t0002g0352a0004c0016t0001g0354a0004c0016t0001g0355others(1): Show | 4 | HG00738.hp1 HG01243.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-151C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108001884 | ||||||
| chr7:108001897
|
G | A | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.38-164C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108001897 | ||||||
| chr7:108002117
|
G | C | 20 | a0001c0001t0001g0321a0001c0001t0001g0325a0001c0001t0001g0335others(17): Show | 20 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.38-384C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002117 | ||||||
| chr7:108002142
|
C | CGCGTGCA others(73): Show |
10 | a0001c0007t0003g0361a0001c0007t0003g0362a0001c0014t0001g0346others(7): Show | 10 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.38-489_38-410dupAC others(78): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002142 | ||||||
| chr7:108002169
|
T | A | 3 | a0001c0001t0001g0342a0001c0006t0001g0341a0001c0007t0001g0343 | 3 | HG02258.hp2 HG02451.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.38-436A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002169 | ||||||
| chr7:108002171
|
G | A | 18 | a0001c0001t0001g0033a0001c0005t0001g0026a0001c0005t0001g0035others(15): Show | 18 | HG00738.hp1 HG01243.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.38-438C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002171 | ||||||
| chr7:108002204
|
G | A | 1 | a0001c0002t0001g0344 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.38-471C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002204 | ||||||
| chr7:108002585
|
A | C | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.37+264T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002585 | ||||||
| chr7:108002657
|
G | C | 1 | a0001c0044t0002g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.37+192C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002657 | ||||||
| chr7:108002661
|
C | T | 18 | a0001c0001t0001g0033a0001c0005t0001g0026a0001c0005t0001g0035others(15): Show | 18 | HG00738.hp1 HG01243.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.37+188G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002661 | ||||||
| chr7:108002678
|
C | T | 3 | a0001c0005t0001g0357a0001c0006t0001g0356a0001c0006t0001g0358 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.37+171G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002678 | ||||||
| chr7:108002704
|
G | A | 5 | a0001c0014t0001g0346a0001c0027t0001g0349a0001c0028t0001g0350others(2): Show | 5 | HG02630.hp1 HG02809.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.37+145C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002704 | ||||||
| chr7:108002709
|
G | A | 1 | a0001c0005t0001g0351 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.37+140C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002709 | ||||||
| chr7:108002793
|
T | C | 4 | a0002c0026t0002g0352a0004c0016t0001g0354a0004c0016t0001g0355others(1): Show | 4 | HG00738.hp1 HG01243.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.37+56A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002793 | ||||||
| chr7:108002802
|
C | G | 1 | a0001c0078t0001g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.37+47G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002802 | ||||||
| chr7:108002805
|
T | C | 3 | a0001c0005t0001g0357a0001c0006t0001g0356a0001c0006t0001g0358 | 3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.37+44A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002805 | ||||||
| chr7:108003076
|
T | G | 340 | a0001c0001t0001g0033a0001c0001t0001g0048a0001c0001t0001g0062others(337): Show | 341 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(338): Show |
intron_variant | MODIFIER | c.-87+35A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 1/33 | chr7 | 108003076 |