Search by Genic region
Multiple Alignments (by aa haplotype frequency)
Multiple Alignments (by aa haplotype similarity)
| geneid | 22798 |
|---|---|
| ensemblid | ENSG00000091128.13 |
| hgncid | 6491 |
| symbol | LAMB4 |
| name | laminin subunit beta 4 |
| refseq_nuc | NM_007356.3 |
| refseq_prot | NP_031382.2 |
| ensembl_nuc | ENST00000388781.8 |
| ensembl_prot | ENSP00000373433.3 |
| mane_status | MANE Select |
| chr | chr7 |
| start | 108023553 |
| end | 108130361 |
| strand | - |
| ver | v1.2 |
| region | chr7:108023553-108130361 |
| region5000 | chr7:108018553-108135361 |
| regionname0 | LAMB4_chr7_108023553_108130361 |
| regionname5000 | LAMB4_chr7_108018553_108135361 |
| ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001 | 1/1 | 1761 | 149 | 18 | 32 | 74 | 8 | 15 | 53 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0002 | 0/0 | 1761 | 30 | 0 | 2 | 22 | 1 | 5 | 20 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0003 | 0/0 | 1761 | 12 | 10 | 2 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0004 | 0/0 | 1761 | 9 | 1 | 0 | 7 | 0 | 1 | 6 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0005 | 0/0 | 1761 | 8 | 3 | 1 | 4 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0006 | 0/0 | 1761 | 8 | 8 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0007 | 0/0 | 1761 | 7 | 7 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0008 | 0/0 | 1761 | 6 | 6 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0009 | 0/0 | 1761 | 5 | 2 | 1 | 2 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0010 | 0/0 | 1761 | 4 | 4 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0011 | 0/0 | 1761 | 4 | 1 | 1 | 0 | 0 | 2 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0012 | 0/0 | 1761 | 4 | 3 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0013 | 0/0 | 1761 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0014 | 0/0 | 1761 | 3 | 0 | 1 | 1 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0015 | 0/0 | 1761 | 3 | 0 | 3 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0016 | 0/0 | 1761 | 3 | 2 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0017 | 0/0 | 1761 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0018 | 0/0 | 1761 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0019 | 0/0 | 1761 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0020 | 0/0 | 1761 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0021 | 0/0 | 1761 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0022 | 0/0 | 1761 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0023 | 0/0 | 1761 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0024 | 0/0 | 1761 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0025 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0026 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0027 | 0/0 | 1761 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0028 | 0/0 | 1761 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0029 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0030 | 0/0 | 1761 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0031 | 0/0 | 1761 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0032 | 0/0 | 1761 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0033 | 0/0 | 1761 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0034 | 0/0 | 1761 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0035 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0036 | 0/0 | 1761 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0037 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0038 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0039 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0040 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0041 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0042 | 0/0 | 1761 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| c0001 | 1/0 | 5286 | 76 | 10 | 17 | 39 | 5 | 4 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0002 | 0/1 | 5286 | 61 | 5 | 14 | 28 | 3 | 10 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0003 | 0/0 | 5286 | 19 | 0 | 2 | 14 | 0 | 3 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0004 | 0/0 | 5286 | 12 | 10 | 2 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0005 | 0/0 | 5286 | 7 | 1 | 0 | 6 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0006 | 0/0 | 5286 | 6 | 0 | 0 | 5 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0007 | 0/0 | 5286 | 6 | 0 | 0 | 6 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0008 | 0/0 | 5286 | 6 | 2 | 1 | 3 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0009 | 0/0 | 5286 | 5 | 2 | 1 | 2 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0010 | 0/0 | 5286 | 4 | 4 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0011 | 0/0 | 5286 | 4 | 4 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0012 | 0/0 | 5286 | 4 | 0 | 0 | 1 | 1 | 2 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0013 | 0/0 | 5286 | 4 | 4 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0014 | 0/0 | 5286 | 4 | 1 | 1 | 0 | 0 | 2 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0015 | 0/0 | 5286 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0016 | 0/0 | 5286 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0017 | 0/0 | 5286 | 3 | 0 | 3 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0018 | 0/0 | 5286 | 2 | 1 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0019 | 0/0 | 5286 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0020 | 0/0 | 5286 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0021 | 0/0 | 5286 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0022 | 0/0 | 5286 | 2 | 1 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0023 | 0/0 | 5286 | 2 | 1 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0024 | 0/0 | 5286 | 2 | 1 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0025 | 0/0 | 5286 | 2 | 0 | 1 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0026 | 0/0 | 5286 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0027 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0028 | 0/0 | 5286 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0029 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0030 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0031 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0032 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0033 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0034 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0035 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0036 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0037 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0038 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0039 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0040 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0041 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0042 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0043 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0044 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0045 | 0/0 | 5286 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0046 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0047 | 0/0 | 5286 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0048 | 0/0 | 5286 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0049 | 0/0 | 5286 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0050 | 0/0 | 5286 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0051 | 0/0 | 5286 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0052 | 0/0 | 5286 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0053 | 0/0 | 5286 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0054 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0055 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0056 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0057 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0058 | 0/0 | 5286 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0059 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0060 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0061 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0062 | 0/0 | 5286 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0063 | 0/0 | 5286 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0064 | 0/0 | 5286 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0065 | 0/0 | 5286 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0066 | 0/0 | 5286 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0067 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0068 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0069 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0070 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0071 | 0/0 | 5286 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0072 | 0/0 | 5286 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| c0073 | 0/0 | 5286 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| t0001 | 1/1 | 576 | 190 | 33 | 41 | 83 | 9 | 22 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| t0002 | 0/0 | 576 | 68 | 55 | 6 | 6 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| t0003 | 0/0 | 576 | 32 | 1 | 1 | 24 | 0 | 6 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| t0004 | 0/0 | 576 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| t0005 | 0/0 | 576 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| 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 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0278 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001 | 1/0 | 5286 | 76 | 10 | 17 | 39 | 5 | 4 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0002 | 0/1 | 5286 | 61 | 5 | 14 | 28 | 3 | 10 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0006 | 0/0 | 5286 | 6 | 0 | 0 | 5 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0052 | 0/0 | 5286 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0054 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0060 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0063 | 0/0 | 5286 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0066 | 0/0 | 5286 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0070 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0002c0003 | 0/0 | 5286 | 19 | 0 | 2 | 14 | 0 | 3 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0002c0007 | 0/0 | 5286 | 6 | 0 | 0 | 6 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0002c0012 | 0/0 | 5286 | 4 | 0 | 0 | 1 | 1 | 2 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0002c0049 | 0/0 | 5286 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0003c0004 | 0/0 | 5286 | 12 | 10 | 2 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0004c0005 | 0/0 | 5286 | 7 | 1 | 0 | 6 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0004c0071 | 0/0 | 5286 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0004c0072 | 0/0 | 5286 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0005c0008 | 0/0 | 5286 | 6 | 2 | 1 | 3 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0005c0023 | 0/0 | 5286 | 2 | 1 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0006c0010 | 0/0 | 5286 | 4 | 4 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0006c0016 | 0/0 | 5286 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0006c0027 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0007c0011 | 0/0 | 5286 | 4 | 4 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0007c0019 | 0/0 | 5286 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0007c0037 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0008c0015 | 0/0 | 5286 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0008c0038 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0008c0039 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0008c0044 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0009c0009 | 0/0 | 5286 | 5 | 2 | 1 | 2 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0010c0013 | 0/0 | 5286 | 4 | 4 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0011c0014 | 0/0 | 5286 | 4 | 1 | 1 | 0 | 0 | 2 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0012c0022 | 0/0 | 5286 | 2 | 1 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0012c0059 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0012c0069 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0013c0026 | 0/0 | 5286 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0013c0068 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0014c0025 | 0/0 | 5286 | 2 | 0 | 1 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0014c0058 | 0/0 | 5286 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0015c0017 | 0/0 | 5286 | 3 | 0 | 3 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0016c0055 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0016c0061 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0016c0062 | 0/0 | 5286 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0017c0030 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0017c0041 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0017c0043 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0018c0024 | 0/0 | 5286 | 2 | 1 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0019c0020 | 0/0 | 5286 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0020c0021 | 0/0 | 5286 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0021c0028 | 0/0 | 5286 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0021c0040 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0022c0029 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0022c0034 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0023c0018 | 0/0 | 5286 | 2 | 1 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0024c0047 | 0/0 | 5286 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0025c0057 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0026c0056 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0027c0065 | 0/0 | 5286 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0028c0064 | 0/0 | 5286 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0029c0067 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0030c0048 | 0/0 | 5286 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0031c0053 | 0/0 | 5286 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0032c0050 | 0/0 | 5286 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0033c0051 | 0/0 | 5286 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0034c0073 | 0/0 | 5286 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0035c0046 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0036c0045 | 0/0 | 5286 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0037c0042 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0038c0036 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0039c0032 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0040c0031 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0041c0033 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0042c0035 | 0/0 | 5286 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001 | 1/0 | 5861 | 68 | 8 | 17 | 33 | 5 | 4 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0001t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0001t0003 | 0/0 | 5861 | 7 | 1 | 0 | 6 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0002t0001 | 0/1 | 5861 | 47 | 4 | 13 | 19 | 3 | 7 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0002t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0002t0003 | 0/0 | 5861 | 13 | 0 | 1 | 9 | 0 | 3 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0006t0001 | 0/0 | 5861 | 3 | 0 | 0 | 3 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0006t0003 | 0/0 | 5861 | 2 | 0 | 0 | 1 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0006t0005 | 0/0 | 5861 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0052t0003 | 0/0 | 5861 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0054t0001 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0060t0004 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0063t0001 | 0/0 | 5861 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0066t0001 | 0/0 | 5861 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0001c0070t0001 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0002c0003t0001 | 0/0 | 5861 | 18 | 0 | 2 | 13 | 0 | 3 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0002c0003t0003 | 0/0 | 5861 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0002c0007t0001 | 0/0 | 5861 | 6 | 0 | 0 | 6 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0002c0012t0001 | 0/0 | 5861 | 4 | 0 | 0 | 1 | 1 | 2 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0002c0049t0001 | 0/0 | 5861 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0003c0004t0002 | 0/0 | 5861 | 12 | 10 | 2 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0004c0005t0001 | 0/0 | 5861 | 2 | 1 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0004c0005t0003 | 0/0 | 5861 | 5 | 0 | 0 | 5 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0004c0071t0001 | 0/0 | 5861 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0004c0072t0003 | 0/0 | 5861 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0005c0008t0002 | 0/0 | 5861 | 6 | 2 | 1 | 3 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0005c0023t0002 | 0/0 | 5861 | 2 | 1 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0006c0010t0001 | 0/0 | 5861 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0006c0010t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0006c0016t0001 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0006c0016t0002 | 0/0 | 5861 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0006c0027t0001 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0007c0011t0001 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0007c0011t0002 | 0/0 | 5861 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0007c0019t0002 | 0/0 | 5861 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0007c0037t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0008c0015t0002 | 0/0 | 5861 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0008c0038t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0008c0039t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0008c0044t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0009c0009t0001 | 0/0 | 5861 | 5 | 2 | 1 | 2 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0010c0013t0002 | 0/0 | 5861 | 4 | 4 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0011c0014t0001 | 0/0 | 5861 | 4 | 1 | 1 | 0 | 0 | 2 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0012c0022t0002 | 0/0 | 5861 | 2 | 1 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0012c0059t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0012c0069t0001 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0013c0026t0002 | 0/0 | 5861 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0013c0068t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0014c0025t0001 | 0/0 | 5861 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0014c0025t0002 | 0/0 | 5861 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0014c0058t0002 | 0/0 | 5861 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0015c0017t0001 | 0/0 | 5861 | 3 | 0 | 3 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0016c0055t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0016c0061t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0016c0062t0001 | 0/0 | 5861 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0017c0030t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0017c0041t0001 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0017c0043t0001 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0018c0024t0001 | 0/0 | 5861 | 2 | 1 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0019c0020t0001 | 0/0 | 5861 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0020c0021t0002 | 0/0 | 5861 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0021c0028t0002 | 0/0 | 5861 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0021c0040t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0022c0029t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0022c0034t0001 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0023c0018t0002 | 0/0 | 5861 | 2 | 1 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0024c0047t0001 | 0/0 | 5861 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0025c0057t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0026c0056t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0027c0065t0001 | 0/0 | 5861 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0028c0064t0002 | 0/0 | 5861 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0029c0067t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0030c0048t0001 | 0/0 | 5861 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0031c0053t0001 | 0/0 | 5861 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0032c0050t0001 | 0/0 | 5861 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0033c0051t0001 | 0/0 | 5861 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0034c0073t0003 | 0/0 | 5861 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0035c0046t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0036c0045t0003 | 0/0 | 5861 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0037c0042t0001 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0038c0036t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0039c0032t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0040c0031t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0041c0033t0001 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| a0042c0035t0002 | 0/0 | 5861 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | copy fasta | chr7 | 108018553 | 108135361 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| a0001c0001t0001g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0206 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0278 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0002g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0003g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0003g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0003g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0003g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0003g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0001t0003g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0009 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0018 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0021 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0052 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0067 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0002g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0003g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0003g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0003g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0003g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0003g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0003g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0003g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0003g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0002t0003g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0006t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0006t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0006t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0006t0003g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0006t0003g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0006t0005g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0052t0003g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0054t0001g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0060t0004g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0063t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0066t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0001c0070t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0001g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0001g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0003t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0007t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0007t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0007t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0007t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0007t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0007t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0012t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0012t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0012t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0012t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0002c0049t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0003c0004t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0003c0004t0002g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0003c0004t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0003c0004t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0003c0004t0002g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0003c0004t0002g0225 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0003c0004t0002g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0003c0004t0002g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0003c0004t0002g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0003c0004t0002g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0003c0004t0002g0269 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0003c0004t0002g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0004c0005t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0004c0005t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0004c0005t0003g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0004c0005t0003g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0004c0005t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0004c0005t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0004c0005t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0004c0071t0001g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0004c0072t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0005c0008t0002g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0005c0008t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0005c0008t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0005c0008t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0005c0008t0002g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0005c0008t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0005c0023t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0005c0023t0002g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0006c0010t0001g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0006c0010t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0006c0010t0001g0291 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0006c0010t0002g0290 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0006c0016t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0006c0016t0002g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0006c0016t0002g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0006c0027t0001g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0007c0011t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0007c0011t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0007c0011t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0007c0011t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0007c0019t0002g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0007c0019t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0007c0037t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0008c0015t0002g0001 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0008c0015t0002g0002 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0008c0015t0002g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0008c0038t0002g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0008c0039t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0008c0044t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0009c0009t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0009c0009t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0009c0009t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0009c0009t0001g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0009c0009t0001g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0010c0013t0002g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0010c0013t0002g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0010c0013t0002g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0010c0013t0002g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0011c0014t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0011c0014t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0011c0014t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0011c0014t0001g0242 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0012c0022t0002g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0012c0022t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0012c0059t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0012c0069t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0013c0026t0002g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0013c0026t0002g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0013c0068t0002g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0014c0025t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0014c0025t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0014c0058t0002g0057 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0015c0017t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0015c0017t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0015c0017t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0016c0055t0002g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0016c0061t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0016c0062t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0017c0030t0002g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0017c0041t0001g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0017c0043t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0018c0024t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0018c0024t0001g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0019c0020t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0019c0020t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0020c0021t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0020c0021t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0021c0028t0002g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0021c0040t0002g0004 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0022c0029t0002g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0022c0034t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0023c0018t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0023c0018t0002g0285 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0024c0047t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0025c0057t0002g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0026c0056t0002g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0027c0065t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0028c0064t0002g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0029c0067t0002g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0030c0048t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0031c0053t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0032c0050t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0033c0051t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0034c0073t0003g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0035c0046t0002g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0036c0045t0003g0251 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0037c0042t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0038c0036t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0039c0032t0002g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0040c0031t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0041c0033t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| a0042c0035t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|
| HG00140 | hp1 | a0001 | c0002 | t0001 | g0021 | EUR | GBR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG00140 | hp2 | a0001 | c0001 | t0001 | g0220 | EUR | GBR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG00280 | hp1 | a0001 | c0001 | t0001 | g0250 | EUR | FIN | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG00280 | hp2 | a0014 | c0058 | t0002 | g0057 | EUR | FIN | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG00323 | hp1 | a0002 | c0012 | t0001 | g0159 | EUR | FIN | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG00323 | hp2 | a0001 | c0001 | t0001 | g0150 | EUR | FIN | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG00423 | hp1 | a0001 | c0001 | t0001 | g0168 | EAS | CHS | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG00423 | hp2 | a0005 | c0023 | t0002 | g0027 | EAS | CHS | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG00544 | hp1 | a0009 | c0009 | t0001 | g0228 | EAS | CHS | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG00544 | hp2 | a0001 | c0002 | t0001 | g0033 | EAS | CHS | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG00558 | hp1 | a0001 | c0001 | t0001 | g0258 | EAS | CHS | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG00558 | hp2 | a0001 | c0002 | t0001 | g0063 | EAS | CHS | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG00621 | hp1 | a0001 | c0006 | t0005 | g0292 | EAS | CHS | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG00621 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | CHS | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG00738 | hp1 | a0003 | c0004 | t0002 | g0007 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG00738 | hp2 | a0001 | c0002 | t0001 | g0050 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG00741 | hp1 | a0021 | c0028 | t0002 | g0092 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG00741 | hp2 | a0001 | c0002 | t0001 | g0024 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01069 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01069 | hp2 | a0001 | c0002 | t0001 | g0081 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01074 | hp1 | a0001 | c0001 | t0001 | g0254 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01074 | hp2 | a0023 | c0018 | t0002 | g0285 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01099 | hp1 | a0001 | c0001 | t0001 | g0240 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01099 | hp2 | a0001 | c0002 | t0001 | g0045 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01106 | hp1 | a0024 | c0047 | t0001 | g0165 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01106 | hp2 | a0001 | c0002 | t0001 | g0051 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01167 | hp1 | a0001 | c0001 | t0001 | g0190 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01167 | hp2 | a0001 | c0002 | t0001 | g0047 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01169 | hp1 | a0001 | c0002 | t0001 | g0080 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01169 | hp2 | a0001 | c0001 | t0001 | g0191 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01175 | hp1 | a0001 | c0063 | t0001 | g0270 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01175 | hp2 | a0001 | c0002 | t0001 | g0016 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01243 | hp1 | a0001 | c0002 | t0003 | g0022 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01243 | hp2 | a0012 | c0022 | t0002 | g0279 | AMR | PUR | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01255 | hp1 | a0001 | c0002 | t0001 | g0067 | AMR | CLM | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01255 | hp2 | a0001 | c0001 | t0001 | g0201 | AMR | CLM | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01256 | hp1 | a0001 | c0002 | t0001 | g0055 | AMR | CLM | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01256 | hp2 | a0002 | c0003 | t0001 | g0141 | AMR | CLM | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01258 | hp1 | a0002 | c0003 | t0001 | g0138 | AMR | CLM | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01258 | hp2 | a0001 | c0001 | t0001 | g0169 | AMR | CLM | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01261 | hp1 | a0015 | c0017 | t0001 | g0070 | AMR | CLM | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01261 | hp2 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01346 | hp1 | a0005 | c0008 | t0002 | g0223 | AMR | CLM | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01346 | hp2 | a0015 | c0017 | t0001 | g0071 | AMR | CLM | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01361 | hp1 | a0001 | c0001 | t0001 | g0206 | AMR | CLM | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01361 | hp2 | a0001 | c0002 | t0001 | g0025 | AMR | CLM | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01433 | hp1 | a0001 | c0001 | t0001 | g0253 | AMR | CLM | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01433 | hp2 | a0018 | c0024 | t0001 | g0109 | AMR | CLM | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01496 | hp1 | a0003 | c0004 | t0002 | g0225 | AMR | CLM | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01496 | hp2 | a0001 | c0002 | t0001 | g0061 | AMR | CLM | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01515 | hp1 | a0001 | c0002 | t0001 | g0059 | EUR | IBS | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01515 | hp2 | a0001 | c0001 | t0001 | g0249 | EUR | IBS | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01516 | hp1 | a0001 | c0002 | t0001 | g0066 | EUR | IBS | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01516 | hp2 | a0001 | c0001 | t0001 | g0192 | EUR | IBS | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01884 | hp1 | a0001 | c0002 | t0001 | g0020 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01884 | hp2 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01943 | hp1 | a0001 | c0001 | t0001 | g0041 | AMR | PEL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01943 | hp2 | a0009 | c0009 | t0001 | g0010 | AMR | PEL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01975 | hp1 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01975 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PEL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01978 | hp1 | a0015 | c0017 | t0001 | g0011 | AMR | PEL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01978 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PEL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01981 | hp1 | a0001 | c0002 | t0001 | g0065 | AMR | PEL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG01981 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PEL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02040 | hp1 | a0001 | c0001 | t0003 | g0015 | EAS | KHV | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02040 | hp2 | a0005 | c0008 | t0002 | g0187 | EAS | KHV | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02055 | hp1 | a0005 | c0008 | t0002 | g0110 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02055 | hp2 | a0008 | c0015 | t0002 | g0087 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02056 | hp1 | a0002 | c0003 | t0001 | g0143 | EAS | KHV | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02056 | hp2 | a0027 | c0065 | t0001 | g0277 | EAS | KHV | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02080 | hp1 | a0001 | c0052 | t0003 | g0072 | EAS | KHV | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02080 | hp2 | a0001 | c0002 | t0001 | g0238 | EAS | KHV | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02083 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02083 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | KHV | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02129 | hp1 | a0005 | c0008 | t0002 | g0274 | EAS | KHV | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02129 | hp2 | a0001 | c0002 | t0001 | g0036 | EAS | KHV | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02132 | hp1 | a0001 | c0001 | t0001 | g0273 | EAS | KHV | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02132 | hp2 | a0001 | c0002 | t0001 | g0056 | EAS | KHV | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02145 | hp1 | a0006 | c0016 | t0001 | g0083 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02145 | hp2 | a0001 | c0002 | t0001 | g0026 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02148 | hp1 | a0014 | c0025 | t0001 | g0118 | AMR | PEL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02148 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02155 | hp1 | a0001 | c0002 | t0003 | g0031 | EAS | CDX | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02155 | hp2 | a0001 | c0001 | t0001 | g0261 | EAS | CDX | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02165 | hp1 | a0014 | c0025 | t0002 | g0233 | EAS | CDX | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02165 | hp2 | a0002 | c0003 | t0001 | g0137 | EAS | CDX | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02257 | hp1 | a0001 | c0001 | t0001 | g0044 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02257 | hp2 | a0010 | c0013 | t0002 | g0221 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02258 | hp1 | a0008 | c0039 | t0002 | g0147 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02258 | hp2 | a0003 | c0004 | t0002 | g0269 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02280 | hp1 | a0001 | c0001 | t0001 | g0106 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02280 | hp2 | a0008 | c0038 | t0002 | g0152 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02293 | hp1 | a0011 | c0014 | t0001 | g0224 | AMR | PEL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02293 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PEL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02451 | hp1 | a0001 | c0001 | t0003 | g0247 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02451 | hp2 | a0012 | c0069 | t0001 | g0158 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02523 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | KHV | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02523 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02572 | hp1 | a0038 | c0036 | t0002 | g0089 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02572 | hp2 | a0001 | c0070 | t0001 | g0246 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02615 | hp1 | a0008 | c0015 | t0002 | g0002 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02615 | hp2 | a0019 | c0020 | t0001 | g0088 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02622 | hp1 | a0003 | c0004 | t0002 | g0189 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02622 | hp2 | a0008 | c0044 | t0002 | g0091 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02647 | hp1 | a0010 | c0013 | t0002 | g0161 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02647 | hp2 | a0005 | c0023 | t0002 | g0215 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02683 | hp1 | a0001 | c0002 | t0003 | g0046 | SAS | PJL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02683 | hp2 | a0011 | c0014 | t0001 | g0242 | SAS | PJL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02717 | hp1 | a0008 | c0015 | t0002 | g0001 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02717 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02723 | hp1 | a0001 | c0054 | t0001 | g0146 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02723 | hp2 | a0012 | c0059 | t0002 | g0222 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02735 | hp1 | a0001 | c0002 | t0001 | g0069 | SAS | PJL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02735 | hp2 | a0002 | c0012 | t0001 | g0207 | SAS | PJL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02738 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02738 | hp2 | a0001 | c0002 | t0001 | g0008 | SAS | PJL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02809 | hp1 | a0006 | c0027 | t0001 | g0085 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02809 | hp2 | a0017 | c0043 | t0001 | g0084 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02818 | hp1 | a0017 | c0041 | t0001 | g0003 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02818 | hp2 | a0023 | c0018 | t0002 | g0095 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02886 | hp1 | a0037 | c0042 | t0001 | g0151 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02886 | hp2 | a0035 | c0046 | t0002 | g0211 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02895 | hp1 | a0003 | c0004 | t0002 | g0218 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02895 | hp2 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02896 | hp1 | a0007 | c0019 | t0002 | g0096 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02896 | hp2 | a0013 | c0026 | t0002 | g0153 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02897 | hp1 | a0013 | c0026 | t0002 | g0154 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02897 | hp2 | a0001 | c0001 | t0001 | g0210 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02922 | hp1 | a0040 | c0031 | t0002 | g0006 | AFR | ESN | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02922 | hp2 | a0022 | c0034 | t0001 | g0103 | AFR | ESN | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02965 | hp1 | a0007 | c0037 | t0002 | g0093 | AFR | ESN | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02965 | hp2 | a0006 | c0016 | t0002 | g0086 | AFR | ESN | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02970 | hp1 | a0009 | c0009 | t0001 | g0267 | AFR | ESN | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02970 | hp2 | a0007 | c0011 | t0002 | g0102 | AFR | ESN | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03017 | hp1 | a0001 | c0001 | t0001 | g0219 | SAS | PJL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03017 | hp2 | a0001 | c0002 | t0003 | g0078 | SAS | PJL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03041 | hp1 | a0007 | c0011 | t0002 | g0157 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03041 | hp2 | a0001 | c0002 | t0001 | g0060 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03098 | hp1 | a0042 | c0035 | t0002 | g0094 | AFR | MSL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03098 | hp2 | a0006 | c0010 | t0001 | g0288 | AFR | MSL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03130 | hp1 | a0006 | c0010 | t0002 | g0290 | AFR | ESN | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03130 | hp2 | a0001 | c0001 | t0002 | g0208 | AFR | ESN | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03139 | hp1 | a0020 | c0021 | t0002 | g0098 | AFR | ESN | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03139 | hp2 | a0003 | c0004 | t0002 | g0231 | AFR | ESN | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03195 | hp1 | a0006 | c0010 | t0001 | g0289 | AFR | ESN | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03195 | hp2 | a0005 | c0008 | t0002 | g0105 | AFR | ESN | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03209 | hp1 | a0001 | c0001 | t0001 | g0107 | AFR | MSL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03209 | hp2 | a0012 | c0022 | t0002 | g0148 | AFR | MSL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03225 | hp1 | a0001 | c0060 | t0004 | g0216 | AFR | MSL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03225 | hp2 | a0009 | c0009 | t0001 | g0266 | AFR | MSL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03239 | hp1 | a0001 | c0002 | t0001 | g0049 | SAS | PJL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03239 | hp2 | a0002 | c0003 | t0001 | g0182 | SAS | PJL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03486 | hp1 | a0007 | c0019 | t0002 | g0005 | AFR | MSL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03486 | hp2 | a0026 | c0056 | t0002 | g0232 | AFR | MSL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03490 | hp1 | a0001 | c0006 | t0003 | g0139 | SAS | PJL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03490 | hp2 | a0011 | c0014 | t0001 | g0117 | SAS | PJL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03516 | hp1 | a0003 | c0004 | t0002 | g0175 | AFR | ESN | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03516 | hp2 | a0041 | c0033 | t0001 | g0090 | AFR | ESN | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03540 | hp1 | a0010 | c0013 | t0002 | g0173 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03540 | hp2 | a0019 | c0020 | t0001 | g0097 | AFR | GWD | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03579 | hp1 | a0003 | c0004 | t0002 | g0281 | AFR | MSL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03579 | hp2 | a0016 | c0061 | t0002 | g0155 | AFR | MSL | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03688 | hp1 | a0004 | c0071 | t0001 | g0239 | SAS | STU | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03688 | hp2 | a0001 | c0002 | t0001 | g0009 | SAS | STU | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03831 | hp1 | a0036 | c0045 | t0003 | g0251 | SAS | BEB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03831 | hp2 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03834 | hp1 | a0001 | c0002 | t0001 | g0077 | SAS | BEB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03834 | hp2 | a0002 | c0012 | t0001 | g0248 | SAS | BEB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03927 | hp1 | a0002 | c0003 | t0001 | g0111 | SAS | BEB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03927 | hp2 | a0001 | c0002 | t0001 | g0076 | SAS | BEB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03942 | hp1 | a0001 | c0002 | t0001 | g0017 | SAS | BEB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG03942 | hp2 | a0034 | c0073 | t0003 | g0212 | SAS | BEB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG04115 | hp1 | a0016 | c0062 | t0001 | g0160 | SAS | STU | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG04115 | hp2 | a0030 | c0048 | t0001 | g0123 | SAS | STU | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG04184 | hp1 | a0002 | c0003 | t0001 | g0135 | SAS | BEB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG04184 | hp2 | a0001 | c0002 | t0003 | g0058 | SAS | BEB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG04204 | hp1 | a0031 | c0053 | t0001 | g0074 | SAS | STU | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG04204 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | STU | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18522 | hp1 | a0006 | c0010 | t0001 | g0291 | AFR | YRI | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18522 | hp2 | a0007 | c0011 | t0001 | g0100 | AFR | YRI | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18612 | hp1 | a0001 | c0002 | t0001 | g0079 | EAS | CHB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18612 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | CHB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18747 | hp1 | a0004 | c0005 | t0003 | g0236 | EAS | CHB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18747 | hp2 | a0001 | c0001 | t0001 | g0259 | EAS | CHB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18906 | hp1 | a0013 | c0068 | t0002 | g0227 | AFR | YRI | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18906 | hp2 | a0021 | c0040 | t0002 | g0004 | AFR | YRI | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18942 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18942 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18945 | hp1 | a0004 | c0005 | t0003 | g0235 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18945 | hp2 | a0002 | c0007 | t0001 | g0127 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18948 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18948 | hp2 | a0001 | c0001 | t0001 | g0237 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18949 | hp1 | a0001 | c0001 | t0003 | g0174 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18949 | hp2 | a0002 | c0003 | t0001 | g0132 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18950 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18950 | hp2 | a0001 | c0002 | t0003 | g0162 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18957 | hp1 | a0001 | c0002 | t0001 | g0037 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18957 | hp2 | a0002 | c0003 | t0001 | g0126 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18962 | hp1 | a0001 | c0002 | t0001 | g0029 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18962 | hp2 | a0001 | c0001 | t0001 | g0276 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18963 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18963 | hp2 | a0002 | c0003 | t0001 | g0122 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18968 | hp1 | a0001 | c0006 | t0001 | g0144 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18968 | hp2 | a0009 | c0009 | t0001 | g0229 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18970 | hp1 | a0002 | c0007 | t0001 | g0128 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18970 | hp2 | a0001 | c0001 | t0003 | g0186 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18971 | hp1 | a0001 | c0001 | t0003 | g0185 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18971 | hp2 | a0002 | c0003 | t0001 | g0120 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18972 | hp1 | a0001 | c0002 | t0001 | g0064 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18972 | hp2 | a0028 | c0064 | t0002 | g0283 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18975 | hp1 | a0002 | c0007 | t0001 | g0125 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18975 | hp2 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18980 | hp1 | a0001 | c0002 | t0001 | g0032 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18980 | hp2 | a0004 | c0072 | t0003 | g0245 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18981 | hp1 | a0002 | c0012 | t0001 | g0196 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18981 | hp2 | a0002 | c0003 | t0001 | g0112 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18982 | hp1 | a0001 | c0006 | t0001 | g0142 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18982 | hp2 | a0005 | c0008 | t0002 | g0271 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18983 | hp1 | a0002 | c0003 | t0001 | g0129 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18983 | hp2 | a0001 | c0002 | t0003 | g0073 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18985 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18985 | hp2 | a0004 | c0005 | t0003 | g0179 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18986 | hp1 | a0004 | c0005 | t0003 | g0184 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18986 | hp2 | a0032 | c0050 | t0001 | g0134 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18989 | hp1 | a0001 | c0002 | t0001 | g0075 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18989 | hp2 | a0002 | c0049 | t0001 | g0204 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18990 | hp1 | a0002 | c0003 | t0001 | g0131 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18990 | hp2 | a0001 | c0002 | t0001 | g0183 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18993 | hp1 | a0033 | c0051 | t0001 | g0205 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18993 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18994 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA18994 | hp2 | a0002 | c0007 | t0001 | g0124 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19000 | hp1 | a0001 | c0002 | t0001 | g0019 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19000 | hp2 | a0001 | c0001 | t0001 | g0282 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19001 | hp1 | a0002 | c0003 | t0001 | g0082 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19001 | hp2 | a0001 | c0002 | t0001 | g0170 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19002 | hp1 | a0002 | c0003 | t0001 | g0114 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19002 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19003 | hp1 | a0001 | c0002 | t0001 | g0062 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19003 | hp2 | a0001 | c0001 | t0003 | g0181 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19004 | hp1 | a0001 | c0001 | t0001 | g0230 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19004 | hp2 | a0004 | c0005 | t0001 | g0116 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19005 | hp1 | a0001 | c0002 | t0001 | g0028 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19005 | hp2 | a0001 | c0002 | t0003 | g0048 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19007 | hp1 | a0002 | c0003 | t0001 | g0133 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19007 | hp2 | a0001 | c0002 | t0001 | g0043 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19009 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19009 | hp2 | a0002 | c0007 | t0001 | g0136 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19010 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19010 | hp2 | a0001 | c0002 | t0001 | g0018 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19011 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19011 | hp2 | a0001 | c0002 | t0003 | g0053 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19030 | hp1 | a0006 | c0016 | t0002 | g0101 | AFR | LWK | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19030 | hp2 | a0020 | c0021 | t0002 | g0099 | AFR | LWK | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19043 | hp1 | a0011 | c0014 | t0001 | g0214 | AFR | LWK | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19043 | hp2 | a0007 | c0011 | t0002 | g0156 | AFR | LWK | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19060 | hp1 | a0004 | c0005 | t0003 | g0180 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19060 | hp2 | a0001 | c0006 | t0003 | g0121 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19076 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19076 | hp2 | a0001 | c0002 | t0001 | g0035 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19083 | hp1 | a0001 | c0002 | t0003 | g0023 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19083 | hp2 | a0002 | c0003 | t0001 | g0113 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19084 | hp1 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19084 | hp2 | a0001 | c0002 | t0003 | g0054 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19085 | hp1 | a0001 | c0066 | t0001 | g0012 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19085 | hp2 | a0002 | c0003 | t0003 | g0130 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19087 | hp1 | a0001 | c0001 | t0003 | g0255 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19087 | hp2 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19088 | hp1 | a0001 | c0006 | t0001 | g0145 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19088 | hp2 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19090 | hp1 | a0001 | c0002 | t0003 | g0176 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19090 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19091 | hp1 | a0002 | c0007 | t0001 | g0140 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19091 | hp2 | a0001 | c0002 | t0003 | g0034 | EAS | JPT | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19240 | hp1 | a0022 | c0029 | t0002 | g0284 | AFR | YRI | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA19240 | hp2 | a0003 | c0004 | t0002 | g0268 | AFR | YRI | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA20129 | hp1 | a0003 | c0004 | t0002 | g0243 | AFR | ASW | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA20129 | hp2 | a0016 | c0055 | t0002 | g0213 | AFR | ASW | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02109 | hp1 | a0025 | c0057 | t0002 | g0280 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02109 | hp2 | a0010 | c0013 | t0002 | g0171 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02486 | hp1 | a0003 | c0004 | t0002 | g0244 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02486 | hp2 | a0017 | c0030 | t0002 | g0286 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02559 | hp1 | a0029 | c0067 | t0002 | g0257 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG02559 | hp2 | a0003 | c0004 | t0002 | g0217 | AFR | ACB | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG06807 | hp1 | a0001 | c0001 | t0001 | g0104 | AFR | USA | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| HG06807 | hp2 | a0004 | c0005 | t0001 | g0178 | AFR | USA | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA20300 | hp1 | a0001 | c0002 | t0001 | g0068 | AFR | USA | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA20300 | hp2 | a0018 | c0024 | t0001 | g0108 | AFR | USA | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA21309 | hp1 | a0001 | c0002 | t0002 | g0149 | AFR | LWK | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| NA21309 | hp2 | a0039 | c0032 | t0002 | g0287 | AFR | LWK | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| homoSapiens_chm13v2 | hp1 | a0001 | c0002 | t0001 | g0052 | REF | REF | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0278 | REF | REF | LAMB4_chr7_108018553_108135361 | LAMB4 | chr7 | 108018553 | 108135361 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:108030962
|
C | G | 10 | a0003a0005a0014others(7): Show | 32 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(29): Show |
missense_variant | MODERATE | c.4836G>C | p.Arg1612Ser | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 32/34 | 4925/5861 | 4836/5286 | 1612/1761 | chr7 | 108030962 | ||
| chr7:108037476
|
G | A | 1 | a0027 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.4591C>T | p.Leu1531Phe | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/34 | 4680/5861 | 4591/5286 | 1531/1761 | chr7 | 108037476 | ||
| chr7:108037539
|
G | A | 19 | a0003a0005a0007others(16): Show | 62 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(59): Show |
missense_variant | MODERATE | c.4528C>T | p.His1510Tyr | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/34 | 4617/5861 | 4528/5286 | 1510/1761 | chr7 | 108037539 | ||
| chr7:108037559
|
G | A | 1 | a0034 | 1 | HG03942.hp2 | missense_variant | MODERATE | c.4508C>T | p.Ala1503Val | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/34 | 4597/5861 | 4508/5286 | 1503/1761 | chr7 | 108037559 | ||
| chr7:108043829
|
C | A | 4 | a0022a0026a0029others(1): Show | 5 | HG02559.hp1 HG02922.hp2 HG03098.hp1 others(2): Show |
missense_variant | MODERATE | c.4394G>T | p.Gly1465Val | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/34 | 4483/5861 | 4394/5286 | 1465/1761 | chr7 | 108043829 | ||
| chr7:108049399
|
G | T | 16 | a0003a0007a0008others(13): Show | 52 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
missense_variant | MODERATE | c.4049C>A | p.Thr1350Asn | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 27/34 | 4138/5861 | 4049/5286 | 1350/1761 | chr7 | 108049399 | ||
| chr7:108055656
|
A | C | 1 | a0015 | 3 | HG01261.hp1 HG01346.hp2 HG01978.hp1 |
missense_variant | MODERATE | c.3731T>G | p.Val1244Gly | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/34 | 3820/5861 | 3731/5286 | 1244/1761 | chr7 | 108055656 | ||
| chr7:108055855
|
A | G | 1 | a0030 | 1 | HG04115.hp2 | missense_variant | MODERATE | c.3532T>C | p.Cys1178Arg | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/34 | 3621/5861 | 3532/5286 | 1178/1761 | chr7 | 108055855 | ||
| chr7:108065840
|
T | C | 1 | a0025 | 1 | HG02109.hp1 | missense_variant | MODERATE | c.2758A>G | p.Asn920Asp | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 21/34 | 2847/5861 | 2758/5286 | 920/1761 | chr7 | 108065840 | ||
| chr7:108066450
|
T | C | 3 | a0002a0032a0033 | 32 | HG00323.hp1 HG01256.hp2 HG01258.hp1 others(29): Show |
missense_variant | MODERATE | c.2597A>G | p.Asn866Ser | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 20/34 | 2686/5861 | 2597/5286 | 866/1761 | chr7 | 108066450 | ||
| chr7:108066454
|
A | G | 1 | a0031 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.2593T>C | p.Cys865Arg | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 20/34 | 2682/5861 | 2593/5286 | 865/1761 | chr7 | 108066454 | ||
| chr7:108078219
|
G | A | 1 | a0032 | 1 | NA18986.hp2 | missense_variant | MODERATE | c.1985C>T | p.Ala662Val | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 16/34 | 2074/5861 | 1985/5286 | 662/1761 | chr7 | 108078219 | ||
| chr7:108078316
|
A | T | 1 | a0040 | 1 | HG02922.hp1 | missense_variant&splice_region_variant | MODERATE | c.1888T>A | p.Ser630Thr | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 16/34 | 1977/5861 | 1888/5286 | 630/1761 | chr7 | 108078316 | ||
| chr7:108079717
|
C | A | 13 | a0003a0006a0007others(10): Show | 52 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(49): Show |
missense_variant | MODERATE | c.1771G>T | p.Val591Phe | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 15/34 | 1860/5861 | 1771/5286 | 591/1761 | chr7 | 108079717 | ||
| chr7:108091639
|
C | A | 1 | a0033 | 1 | NA18993.hp1 | missense_variant | MODERATE | c.1688G>T | p.Gly563Val | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/34 | 1777/5861 | 1688/5286 | 563/1761 | chr7 | 108091639 | ||
| chr7:108095277
|
T | A | 1 | a0019 | 2 | HG02615.hp2 HG03540.hp2 |
missense_variant | MODERATE | c.1421A>T | p.Gln474Leu | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/34 | 1510/5861 | 1421/5286 | 474/1761 | chr7 | 108095277 | ||
| chr7:108105845
|
C | T | 1 | a0024 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.842G>A | p.Arg281Gln | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/34 | 931/5861 | 842/5286 | 281/1761 | chr7 | 108105845 | ||
| chr7:108105987
|
G | A | 2 | a0004a0034 | 10 | HG03688.hp1 HG03942.hp2 HG06807.hp2 others(7): Show |
missense_variant | MODERATE | c.700C>T | p.His234Tyr | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/34 | 789/5861 | 700/5286 | 234/1761 | chr7 | 108105987 | ||
| chr7:108106530
|
G | T | 1 | a0035 | 1 | HG02886.hp2 | missense_variant | MODERATE | c.634C>A | p.Pro212Thr | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 7/34 | 723/5861 | 634/5286 | 212/1761 | chr7 | 108106530 | ||
| chr7:108109223
|
C | G | 1 | a0036 | 1 | HG03831.hp1 | missense_variant | MODERATE | c.350G>C | p.Arg117Thr | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 5/34 | 439/5861 | 350/5286 | 117/1761 | chr7 | 108109223 | ||
| chr7:108116065
|
A | G | 15 | a0006a0007a0008others(12): Show | 40 | HG00741.hp1 HG01074.hp2 HG02055.hp2 others(37): Show |
missense_variant | MODERATE | c.131T>C | p.Met44Thr | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/34 | 220/5861 | 131/5286 | 44/1761 | chr7 | 108116065 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:108034346
|
C | T | 1 | a0016c0061 | 1 | HG03579.hp2 | splice_region_variant&synonymous_variant | LOW | c.4680G>A | p.Glu1560Glu | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/34 | 4769/5861 | 4680/5286 | 1560/1761 | chr7 | 108034346 | ||
| chr7:108037549
|
C | A | 2 | a0001c0066a0002c0007 | 7 | NA18945.hp2 NA18970.hp1 NA18975.hp1 others(4): Show |
synonymous_variant | LOW | c.4518G>T | p.Val1506Val | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/34 | 4607/5861 | 4518/5286 | 1506/1761 | chr7 | 108037549 | ||
| chr7:108043843
|
C | T | 1 | a0016c0061 | 1 | HG03579.hp2 | synonymous_variant | LOW | c.4380G>A | p.Leu1460Leu | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/34 | 4469/5861 | 4380/5286 | 1460/1761 | chr7 | 108043843 | ||
| chr7:108052236
|
A | G | 1 | a0001c0063 | 1 | HG01175.hp1 | synonymous_variant | LOW | c.3777T>C | p.Asn1259Asn | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 26/34 | 3866/5861 | 3777/5286 | 1259/1761 | chr7 | 108052236 | ||
| chr7:108055844
|
C | T | 33 | a0001c0054a0001c0060a0001c0070others(30): Show | 59 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(56): Show |
synonymous_variant | LOW | c.3543G>A | p.Gln1181Gln | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/34 | 3632/5861 | 3543/5286 | 1181/1761 | chr7 | 108055844 | ||
| chr7:108055900
|
G | T | 4 | a0001c0054a0001c0060a0001c0070others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
synonymous_variant | LOW | c.3487C>A | p.Arg1163Arg | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/34 | 3576/5861 | 3487/5286 | 1163/1761 | chr7 | 108055900 | ||
| chr7:108055907
|
G | A | 2 | a0007c0037a0008c0039 | 2 | HG02258.hp1 HG02965.hp1 |
synonymous_variant | LOW | c.3480C>T | p.Arg1160Arg | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/34 | 3569/5861 | 3480/5286 | 1160/1761 | chr7 | 108055907 | ||
| chr7:108065763
|
C | T | 2 | a0008c0044a0012c0069 | 2 | HG02451.hp2 HG02622.hp2 |
splice_region_variant&synonymous_variant | LOW | c.2835G>A | p.Thr945Thr | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 21/34 | 2924/5861 | 2835/5286 | 945/1761 | chr7 | 108065763 | ||
| chr7:108068146
|
G | A | 1 | a0002c0049 | 1 | NA18989.hp2 | synonymous_variant | LOW | c.2316C>T | p.His772His | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 19/34 | 2405/5861 | 2316/5286 | 772/1761 | chr7 | 108068146 | ||
| chr7:108079727
|
A | G | 1 | a0021c0028 | 1 | HG00741.hp1 | synonymous_variant | LOW | c.1761T>C | p.Pro587Pro | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 15/34 | 1850/5861 | 1761/5286 | 587/1761 | chr7 | 108079727 | ||
| chr7:108079775
|
C | T | 4 | a0008c0038a0008c0039a0017c0043others(1): Show | 4 | HG02258.hp1 HG02280.hp2 HG02809.hp2 others(1): Show |
synonymous_variant | LOW | c.1713G>A | p.Thr571Thr | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 15/34 | 1802/5861 | 1713/5286 | 571/1761 | chr7 | 108079775 | ||
| chr7:108079781
|
C | T | 1 | a0004c0072 | 1 | NA18980.hp2 | synonymous_variant | LOW | c.1707G>A | p.Ser569Ser | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 15/34 | 1796/5861 | 1707/5286 | 569/1761 | chr7 | 108079781 | ||
| chr7:108092381
|
C | T | 6 | a0007c0037a0012c0059a0022c0034others(3): Show | 6 | HG02572.hp1 HG02723.hp2 HG02922.hp2 others(3): Show |
synonymous_variant | LOW | c.1506G>A | p.Gly502Gly | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 13/34 | 1595/5861 | 1506/5286 | 502/1761 | chr7 | 108092381 | ||
| chr7:108098437
|
G | A | 20 | a0001c0002a0001c0052a0001c0054others(17): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
synonymous_variant | LOW | c.1326C>T | p.Tyr442Tyr | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/34 | 1415/5861 | 1326/5286 | 442/1761 | chr7 | 108098437 | ||
| chr7:108098503
|
G | A | 19 | a0001c0002a0001c0054a0005c0023others(16): Show | 89 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(86): Show |
synonymous_variant | LOW | c.1260C>T | p.Ala420Ala | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/34 | 1349/5861 | 1260/5286 | 420/1761 | chr7 | 108098503 | ||
| chr7:108103135
|
C | T | 1 | a0004c0071 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.1089G>A | p.Gln363Gln | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/34 | 1178/5861 | 1089/5286 | 363/1761 | chr7 | 108103135 | ||
| chr7:108103219
|
A | G | 20 | a0001c0002a0001c0052a0001c0054others(17): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
synonymous_variant | LOW | c.1005T>C | p.Asn335Asn | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/34 | 1094/5861 | 1005/5286 | 335/1761 | chr7 | 108103219 | ||
| chr7:108104584
|
A | G | 12 | a0001c0006a0001c0070a0002c0003others(9): Show | 40 | HG00621.hp1 HG01256.hp2 HG01258.hp1 others(37): Show |
synonymous_variant | LOW | c.906T>C | p.Asp302Asp | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 9/34 | 995/5861 | 906/5286 | 302/1761 | chr7 | 108104584 | ||
| chr7:108105868
|
T | C | 4 | a0001c0070a0008c0044a0012c0069others(1): Show | 4 | HG02451.hp2 HG02572.hp2 HG02622.hp2 others(1): Show |
synonymous_variant | LOW | c.819A>G | p.Glu273Glu | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/34 | 908/5861 | 819/5286 | 273/1761 | chr7 | 108105868 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:108023556
|
T | C | 1 | a0001c0060t0004 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*483A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 34/34 | 483 | chr7 | 108023556 | |||||
| chr7:108023764
|
A | C | 38 | a0001c0001t0002a0001c0002t0002a0003c0004t0002others(35): Show | 68 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*275T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 34/34 | 275 | chr7 | 108023764 | |||||
| chr7:108023797
|
G | T | 10 | a0001c0001t0003a0001c0002t0003a0001c0006t0003others(7): Show | 33 | HG00621.hp1 HG01243.hp1 HG02040.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*242C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 34/34 | 242 | chr7 | 108023797 | |||||
| chr7:108023984
|
G | A | 38 | a0001c0001t0002a0001c0002t0002a0003c0004t0002others(35): Show | 68 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*55C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 34/34 | 55 | chr7 | 108023984 | |||||
| chr7:108024001
|
C | T | 38 | a0001c0001t0002a0001c0002t0002a0003c0004t0002others(35): Show | 68 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*38G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 34/34 | 38 | chr7 | 108024001 | |||||
| chr7:108130314
|
G | A | 1 | a0001c0006t0005 | 1 | HG00621.hp1 | 5_prime_UTR_variant | MODIFIER | c.-42C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/34 | 7150 | chr7 | 108130314 | |||||
| chr7:108130315
|
G | A | 1 | a0001c0006t0005 | 1 | HG00621.hp1 | 5_prime_UTR_variant | MODIFIER | c.-43C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/34 | 7151 | chr7 | 108130315 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| chr7:108024214
|
A | G | 68 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(65): Show | 68 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.5147-36T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108024214 | ||||||
| chr7:108024342
|
G | T | 44 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(41): Show | 44 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.5147-164C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108024342 | ||||||
| chr7:108024499
|
G | C | 2 | a0008c0015t0002g0001a0008c0015t0002g0002 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.5147-321C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108024499 | ||||||
| chr7:108024533
|
C | G | 2 | a0012c0069t0001g0158a0022c0034t0001g0103 | 2 | HG02451.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.5147-355G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108024533 | ||||||
| chr7:108024595
|
C | T | 1 | a0002c0003t0001g0082 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.5147-417G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108024595 | ||||||
| chr7:108024679
|
G | A | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5147-501C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108024679 | ||||||
| chr7:108024714
|
G | GATCC | 12 | a0006c0016t0002g0101a0007c0037t0002g0093a0008c0015t0002g0001others(9): Show | 12 | HG02258.hp1 HG02615.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.5147-540_5147-537d others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108024714 | ||||||
| chr7:108024714
|
G | GATCCATC others(5): Show |
29 | a0001c0002t0002g0149a0003c0004t0002g0007a0003c0004t0002g0175others(26): Show | 29 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(26): Show |
intron_variant | MODIFIER | c.5147-548_5147-537d others(14): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108024714 | ||||||
| chr7:108024714
|
G | GATCCATC others(9): Show |
22 | a0001c0001t0002g0208a0003c0004t0002g0189a0003c0004t0002g0218others(19): Show | 22 | HG00741.hp1 HG01074.hp2 HG01346.hp1 others(19): Show |
intron_variant | MODIFIER | c.5147-552_5147-537d others(18): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108024714 | ||||||
| chr7:108024714
|
G | GATCCATC others(13): Show |
1 | a0007c0011t0002g0102 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.5147-556_5147-537d others(22): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108024714 | ||||||
| chr7:108024714
|
G | GATCCATC others(17): Show |
1 | a0008c0015t0002g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5147-560_5147-537d others(26): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108024714 | ||||||
| chr7:108024714
|
G | GATCCATC others(21): Show |
2 | a0022c0029t0002g0284a0029c0067t0002g0257 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5147-564_5147-537d others(30): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108024714 | ||||||
| chr7:108024739
|
A | ATCCATCC others(13): Show |
1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5147-562_5147-561i others(22): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108024739 | ||||||
| chr7:108024742
|
C | T | 1 | a0002c0003t0001g0112 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.5147-564G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108024742 | ||||||
| chr7:108024843
|
T | C | 70 | a0001c0001t0002g0208a0001c0002t0002g0149a0001c0070t0001g0246others(67): Show | 70 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.5147-665A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108024843 | ||||||
| chr7:108024923
|
A | G | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5147-745T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108024923 | ||||||
| chr7:108024956
|
G | A | 68 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(65): Show | 68 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.5147-778C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108024956 | ||||||
| chr7:108025015
|
C | T | 68 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(65): Show | 68 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.5147-837G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025015 | ||||||
| chr7:108025321
|
T | C | 68 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(65): Show | 68 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.5147-1143A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025321 | ||||||
| chr7:108025340
|
G | A | 4 | a0001c0002t0001g0026a0001c0002t0001g0065a0001c0002t0001g0067others(1): Show | 4 | HG01255.hp1 HG01981.hp1 HG02145.hp2 others(1): Show |
intron_variant | MODIFIER | c.5147-1162C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025340 | ||||||
| chr7:108025379
|
T | TTC | 33 | a0001c0001t0002g0208a0003c0004t0002g0007a0003c0004t0002g0175others(30): Show | 33 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.5147-1202_5147-120 others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025379 | ||||||
| chr7:108025379
|
T | TTCTTTC | 15 | a0003c0004t0002g0189a0003c0004t0002g0218a0003c0004t0002g0281others(12): Show | 15 | HG01074.hp2 HG02055.hp2 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.5147-1202_5147-120 others(10): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025379 | ||||||
| chr7:108025381
|
T | C | 19 | a0001c0002t0002g0149a0003c0004t0002g0217a0003c0004t0002g0225others(16): Show | 19 | HG00423.hp2 HG01496.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.5147-1203A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025381 | ||||||
| chr7:108025383
|
C | T | 19 | a0001c0002t0002g0149a0003c0004t0002g0217a0003c0004t0002g0225others(16): Show | 19 | HG00423.hp2 HG01496.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.5147-1205G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025383 | ||||||
| chr7:108025384
|
T | TTTC | 32 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(29): Show | 32 | HG00738.hp1 HG01074.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.5147-1207_5147-120 others(7): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025384 | ||||||
| chr7:108025385
|
T | C | 19 | a0001c0002t0002g0149a0003c0004t0002g0217a0003c0004t0002g0225others(16): Show | 19 | HG00423.hp2 HG01496.hp1 HG02040.hp2 others(16): Show |
intron_variant | MODIFIER | c.5147-1207A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025385 | ||||||
| chr7:108025385
|
T | TTC | 16 | a0001c0001t0002g0208a0003c0004t0002g0268a0005c0008t0002g0223others(13): Show | 16 | HG00280.hp2 HG00741.hp1 HG01346.hp1 others(13): Show |
intron_variant | MODIFIER | c.5147-1208_5147-120 others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025385 | ||||||
| chr7:108025388
|
C | CTT | 33 | a0001c0001t0001g0030a0001c0001t0001g0150a0001c0001t0001g0169others(30): Show | 33 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(30): Show |
intron_variant | MODIFIER | c.5147-1212_5147-121 others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025388 | ||||||
| chr7:108025388
|
C | T | 36 | a0001c0001t0002g0208a0001c0002t0002g0149a0002c0003t0001g0082others(33): Show | 36 | HG00280.hp2 HG00423.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.5147-1210G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025388 | ||||||
| chr7:108025389
|
T | C | 36 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0217others(33): Show | 36 | HG00280.hp2 HG00423.hp2 HG00741.hp1 others(33): Show |
intron_variant | MODIFIER | c.5147-1211A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025389 | ||||||
| chr7:108025389
|
T | TTTC | 32 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(29): Show | 32 | HG00738.hp1 HG01074.hp2 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.5147-1212_5147-121 others(7): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025389 | ||||||
| chr7:108025389
|
T | TTTCTTTC others(20): Show |
2 | a0001c0070t0001g0246a0017c0043t0001g0084 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.5147-1212_5147-121 others(31): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025389 | ||||||
| chr7:108025389
|
T | TTTTC | 45 | a0001c0001t0001g0014a0001c0001t0001g0177a0001c0001t0001g0209others(42): Show | 45 | HG01069.hp1 HG01074.hp1 HG01433.hp1 others(42): Show |
intron_variant | MODIFIER | c.5147-1215_5147-121 others(8): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025389 | ||||||
| chr7:108025389
|
T | TTTTCTTT others(1): Show |
4 | a0002c0003t0001g0131a0006c0010t0001g0288a0016c0062t0001g0160others(1): Show | 4 | HG02886.hp1 HG03098.hp2 HG04115.hp1 others(1): Show |
intron_variant | MODIFIER | c.5147-1219_5147-121 others(12): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025389 | ||||||
| chr7:108025389
|
T | TTTTCTTT others(9): Show |
1 | a0002c0012t0001g0207 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.5147-1227_5147-121 others(20): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025389 | ||||||
| chr7:108025389
|
TTTTC | T | 41 | a0001c0001t0001g0013a0001c0001t0001g0038a0001c0001t0001g0104others(38): Show | 41 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(38): Show |
intron_variant | MODIFIER | c.5147-1215_5147-121 others(8): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025389 | ||||||
| chr7:108025408
|
T | TC | 49 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(46): Show | 49 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(46): Show |
intron_variant | MODIFIER | c.5147-1231dupG | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025408 | ||||||
| chr7:108025414
|
T | C | 1 | a0020c0021t0002g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.5147-1236A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025414 | ||||||
| chr7:108025417
|
C | CT | 18 | a0003c0004t0002g0217a0003c0004t0002g0225a0005c0008t0002g0105others(15): Show | 18 | HG00423.hp2 HG01496.hp1 HG02040.hp2 others(15): Show |
intron_variant | MODIFIER | c.5147-1240dupA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025417 | ||||||
| chr7:108025420
|
C | T | 1 | a0019c0020t0001g0088 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5147-1242G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025420 | ||||||
| chr7:108025421
|
T | C | 1 | a0019c0020t0001g0088 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.5147-1243A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025421 | ||||||
| chr7:108025423
|
T | TC | 9 | a0003c0004t0002g0217a0003c0004t0002g0225a0005c0008t0002g0187others(6): Show | 9 | HG01496.hp1 HG02040.hp2 HG02129.hp1 others(6): Show |
intron_variant | MODIFIER | c.5147-1246dupG | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025423 | ||||||
| chr7:108025427
|
T | TC | 6 | a0005c0008t0002g0105a0005c0023t0002g0027a0008c0039t0002g0147others(3): Show | 6 | HG00423.hp2 HG02165.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.5147-1250dupG | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025427 | ||||||
| chr7:108025432
|
C | CCTTTCTT others(74): Show |
2 | a0007c0019t0002g0005a0023c0018t0002g0095 | 2 | HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.5147-1255_5147-125 others(85): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025432 | ||||||
| chr7:108025432
|
C | CCTTTCTT others(70): Show |
1 | a0038c0036t0002g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.5147-1255_5147-125 others(81): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025432 | ||||||
| chr7:108025433
|
T | C | 3 | a0007c0019t0002g0005a0023c0018t0002g0095a0038c0036t0002g0089 | 3 | HG02572.hp1 HG02818.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.5147-1255A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTCTTTCT others(69): Show |
1 | a0010c0013t0002g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.5147-1256_5147-125 others(80): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTCTTTCT others(65): Show |
8 | a0003c0004t0002g0217a0003c0004t0002g0225a0005c0008t0002g0187others(5): Show | 8 | HG01496.hp1 HG02040.hp2 HG02129.hp1 others(5): Show |
intron_variant | MODIFIER | c.5147-1256_5147-125 others(76): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTTCTTCT others(73): Show |
1 | a0008c0039t0002g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.5147-1256_5147-125 others(84): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTTCTTCT others(64): Show |
1 | a0012c0059t0002g0222 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5147-1256_5147-125 others(75): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTTCTTCT others(69): Show |
4 | a0005c0008t0002g0105a0005c0023t0002g0027a0014c0025t0002g0233others(1): Show | 4 | HG00423.hp2 HG02165.hp1 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.5147-1256_5147-125 others(80): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTTCTTTC others(106): Show |
2 | a0006c0016t0002g0086a0020c0021t0002g0098 | 2 | HG02965.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.5147-1256_5147-125 others(117): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTTCTTTC others(102): Show |
1 | a0001c0002t0002g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.5147-1256_5147-125 others(113): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTTCTTTC others(90): Show |
1 | a0008c0015t0002g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.5147-1256_5147-125 others(101): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTTCTTTC others(82): Show |
2 | a0022c0029t0002g0284a0029c0067t0002g0257 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.5147-1256_5147-125 others(93): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTTCTTTC others(78): Show |
6 | a0001c0001t0002g0208a0006c0010t0002g0290a0007c0011t0002g0102others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.5147-1256_5147-125 others(89): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTTCTTTC others(70): Show |
1 | a0013c0068t0002g0227 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.5147-1256_5147-125 others(81): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTTCTTTC others(66): Show |
1 | a0006c0016t0002g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5147-1256_5147-125 others(77): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTTCTTTC others(57): Show |
1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5147-1256_5147-125 others(68): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTTCTTTC others(58): Show |
4 | a0007c0011t0002g0156a0007c0037t0002g0093a0010c0013t0002g0221others(1): Show | 4 | HG02257.hp2 HG02965.hp1 NA19030.hp2 others(1): Show |
intron_variant | MODIFIER | c.5147-1256_5147-125 others(69): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTTCTTTC others(49): Show |
1 | a0007c0019t0002g0096 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.5147-1256_5147-125 others(60): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTTCTTTC others(54): Show |
7 | a0007c0011t0002g0157a0008c0015t0002g0001a0008c0015t0002g0002others(4): Show | 7 | HG01243.hp2 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.5147-1256_5147-125 others(65): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTTCTTTC others(50): Show |
20 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(17): Show | 20 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.5147-1256_5147-125 others(61): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTTCTTTC others(46): Show |
1 | a0003c0004t0002g0231 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.5147-1256_5147-125 others(57): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025433
|
T | TTTCTTTC others(46): Show |
2 | a0013c0026t0002g0153a0013c0026t0002g0154 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.5147-1256_5147-125 others(57): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025433 | ||||||
| chr7:108025437
|
T | C | 68 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(65): Show | 68 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.5147-1259A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025437 | ||||||
| chr7:108025444
|
T | C | 68 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(65): Show | 68 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.5147-1266A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025444 | ||||||
| chr7:108025616
|
T | C | 1 | a0012c0059t0002g0222 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.5147-1438A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025616 | ||||||
| chr7:108025744
|
G | A | 1 | a0001c0002t0001g0067 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.5147-1566C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025744 | ||||||
| chr7:108025745
|
G | T | 68 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(65): Show | 68 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.5147-1567C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025745 | ||||||
| chr7:108025797
|
G | T | 6 | a0001c0001t0002g0208a0006c0010t0002g0290a0007c0011t0002g0102others(3): Show | 6 | HG02280.hp2 HG02486.hp2 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.5147-1619C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025797 | ||||||
| chr7:108025824
|
C | A | 68 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(65): Show | 68 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.5147-1646G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025824 | ||||||
| chr7:108025875
|
G | A | 2 | a0001c0070t0001g0246a0017c0043t0001g0084 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.5147-1697C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025875 | ||||||
| chr7:108025896
|
C | A | 68 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(65): Show | 68 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.5147-1718G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025896 | ||||||
| chr7:108025921
|
C | T | 68 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(65): Show | 68 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.5147-1743G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108025921 | ||||||
| chr7:108026022
|
G | C | 1 | a0002c0003t0001g0120 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.5147-1844C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108026022 | ||||||
| chr7:108026025
|
G | T | 1 | a0001c0002t0003g0031 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.5147-1847C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108026025 | ||||||
| chr7:108026193
|
G | A | 1 | a0006c0016t0002g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.5147-2015C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108026193 | ||||||
| chr7:108026230
|
C | G | 66 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(63): Show | 66 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.5147-2052G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108026230 | ||||||
| chr7:108026248
|
A | G | 2 | a0001c0070t0001g0246a0017c0043t0001g0084 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.5147-2070T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108026248 | ||||||
| chr7:108026257
|
G | C | 6 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0172others(3): Show | 6 | HG02280.hp1 HG02717.hp2 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.5147-2079C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108026257 | ||||||
| chr7:108026285
|
A | G | 68 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(65): Show | 68 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.5147-2107T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108026285 | ||||||
| chr7:108026321
|
G | A | 1 | a0001c0001t0001g0198 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.5147-2143C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108026321 | ||||||
| chr7:108026412
|
A | G | 68 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(65): Show | 68 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.5147-2234T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108026412 | ||||||
| chr7:108026415
|
G | A | 68 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(65): Show | 68 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.5147-2237C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108026415 | ||||||
| chr7:108026419
|
C | T | 68 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(65): Show | 68 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.5147-2241G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108026419 | ||||||
| chr7:108026439
|
C | T | 1 | a0041c0033t0001g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.5147-2261G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108026439 | ||||||
| chr7:108026481
|
T | G | 68 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(65): Show | 68 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(65): Show |
intron_variant | MODIFIER | c.5147-2303A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108026481 | ||||||
| chr7:108026746
|
C | T | 2 | a0001c0070t0001g0246a0017c0043t0001g0084 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.5146+2297G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108026746 | ||||||
| chr7:108026825
|
C | A | 12 | a0006c0016t0002g0101a0007c0037t0002g0093a0008c0015t0002g0001others(9): Show | 12 | HG02258.hp1 HG02615.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.5146+2218G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108026825 | ||||||
| chr7:108027052
|
G | T | 71 | a0001c0001t0002g0208a0001c0002t0002g0149a0001c0070t0001g0246others(68): Show | 71 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(68): Show |
intron_variant | MODIFIER | c.5146+1991C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108027052 | ||||||
| chr7:108027399
|
C | T | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5146+1644G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108027399 | ||||||
| chr7:108027557
|
C | T | 72 | a0001c0001t0002g0208a0001c0002t0002g0149a0001c0070t0001g0246others(69): Show | 72 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.5146+1486G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108027557 | ||||||
| chr7:108027859
|
C | T | 1 | a0002c0003t0001g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.5146+1184G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108027859 | ||||||
| chr7:108027869
|
G | A | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.5146+1174C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108027869 | ||||||
| chr7:108027920
|
T | C | 3 | a0001c0002t0001g0060a0001c0002t0001g0061a0001c0002t0001g0081 | 3 | HG01069.hp2 HG01496.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.5146+1123A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108027920 | ||||||
| chr7:108027939
|
C | T | 1 | a0001c0006t0003g0121 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.5146+1104G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108027939 | ||||||
| chr7:108027990
|
G | A | 1 | a0001c0002t0001g0025 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.5146+1053C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108027990 | ||||||
| chr7:108028047
|
G | A | 1 | a0001c0002t0003g0048 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.5146+996C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108028047 | ||||||
| chr7:108028048
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.5146+995A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108028048 | ||||||
| chr7:108028093
|
T | C | 3 | a0001c0002t0001g0009a0001c0002t0001g0077a0002c0003t0001g0111 | 3 | HG03688.hp2 HG03834.hp1 HG03927.hp1 |
intron_variant | MODIFIER | c.5146+950A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108028093 | ||||||
| chr7:108028109
|
T | A | 13 | a0006c0016t0002g0101a0007c0037t0002g0093a0008c0015t0002g0001others(10): Show | 13 | HG02258.hp1 HG02615.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.5146+934A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108028109 | ||||||
| chr7:108028317
|
T | C | 2 | a0002c0003t0001g0138a0002c0003t0001g0141 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.5146+726A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108028317 | ||||||
| chr7:108028472
|
A | AT | 44 | a0001c0001t0001g0040a0001c0001t0001g0115a0001c0001t0001g0119others(41): Show | 44 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(41): Show |
intron_variant | MODIFIER | c.5146+570dupA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108028472 | ||||||
| chr7:108028472
|
A | ATT | 6 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0282others(3): Show | 6 | HG01261.hp2 HG02145.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.5146+569_5146+570d others(4): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108028472 | ||||||
| chr7:108028472
|
AT | A | 16 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0237others(13): Show | 16 | HG01069.hp2 HG01256.hp2 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.5146+570delA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108028472 | ||||||
| chr7:108028500
|
G | T | 2 | a0001c0006t0001g0142a0032c0050t0001g0134 | 2 | NA18982.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.5146+543C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108028500 | ||||||
| chr7:108028501
|
G | C | 2 | a0001c0006t0001g0142a0032c0050t0001g0134 | 2 | NA18982.hp1 NA18986.hp2 |
intron_variant | MODIFIER | c.5146+542C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108028501 | ||||||
| chr7:108028567
|
C | T | 1 | a0001c0002t0001g0238 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.5146+476G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108028567 | ||||||
| chr7:108028633
|
C | A | 1 | a0003c0004t0002g0268 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.5146+410G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108028633 | ||||||
| chr7:108028634
|
G | T | 8 | a0006c0016t0002g0101a0012c0022t0002g0148a0012c0059t0002g0222others(5): Show | 8 | HG02723.hp2 HG02896.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.5146+409C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 33/33 | chr7 | 108028634 | ||||||
| chr7:108029217
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4993-21T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 32/33 | chr7 | 108029217 | ||||||
| chr7:108029361
|
T | C | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.4993-165A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 32/33 | chr7 | 108029361 | ||||||
| chr7:108029473
|
G | C | 4 | a0001c0001t0001g0038a0015c0017t0001g0011a0015c0017t0001g0070others(1): Show | 4 | HG01261.hp1 HG01346.hp2 HG01978.hp1 others(1): Show |
intron_variant | MODIFIER | c.4993-277C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 32/33 | chr7 | 108029473 | ||||||
| chr7:108029630
|
G | T | 1 | a0004c0005t0001g0116 | 1 | NA19004.hp2 | intron_variant | MODIFIER | c.4993-434C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 32/33 | chr7 | 108029630 | ||||||
| chr7:108029734
|
T | A | 2 | a0001c0070t0001g0246a0017c0043t0001g0084 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4993-538A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 32/33 | chr7 | 108029734 | ||||||
| chr7:108029849
|
G | C | 89 | a0001c0001t0001g0013a0001c0001t0001g0038a0001c0001t0001g0104others(86): Show | 89 | HG00323.hp1 HG00423.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.4993-653C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 32/33 | chr7 | 108029849 | ||||||
| chr7:108029901
|
T | C | 72 | a0001c0001t0002g0208a0001c0002t0002g0149a0001c0070t0001g0246others(69): Show | 72 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.4993-705A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 32/33 | chr7 | 108029901 | ||||||
| chr7:108030118
|
C | CA | 10 | a0001c0001t0001g0202a0002c0007t0001g0124a0005c0008t0002g0271others(7): Show | 10 | HG00280.hp2 HG00544.hp1 HG02129.hp1 others(7): Show |
intron_variant | MODIFIER | c.4992+687dupT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 32/33 | chr7 | 108030118 | ||||||
| chr7:108030120
|
A | C | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0002t0001g0036 | 3 | HG01167.hp1 HG01169.hp2 HG02129.hp2 |
intron_variant | MODIFIER | c.4992+686T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 32/33 | chr7 | 108030120 | ||||||
| chr7:108030432
|
G | T | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4992+374C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 32/33 | chr7 | 108030432 | ||||||
| chr7:108030434
|
T | C | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4992+372A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 32/33 | chr7 | 108030434 | ||||||
| chr7:108030657
|
G | A | 65 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0150others(62): Show | 65 | HG00280.hp1 HG00323.hp2 HG00558.hp1 others(62): Show |
intron_variant | MODIFIER | c.4992+149C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 32/33 | chr7 | 108030657 | ||||||
| chr7:108030687
|
G | C | 1 | a0001c0001t0001g0044 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.4992+119C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 32/33 | chr7 | 108030687 | ||||||
| chr7:108030786
|
G | T | 12 | a0001c0001t0002g0208a0001c0002t0002g0149a0006c0010t0002g0290others(9): Show | 12 | HG02055.hp2 HG02280.hp2 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.4992+20C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 32/33 | chr7 | 108030786 | ||||||
| chr7:108031041
|
C | T | 2 | a0022c0029t0002g0284a0029c0067t0002g0257 | 2 | HG02559.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.4819-62G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108031041 | ||||||
| chr7:108031185
|
C | T | 72 | a0001c0001t0002g0208a0001c0002t0002g0149a0001c0070t0001g0246others(69): Show | 72 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.4819-206G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108031185 | ||||||
| chr7:108031195
|
A | G | 2 | a0001c0070t0001g0246a0017c0043t0001g0084 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4819-216T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108031195 | ||||||
| chr7:108031293
|
G | A | 2 | a0001c0070t0001g0246a0017c0043t0001g0084 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4819-314C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108031293 | ||||||
| chr7:108031340
|
AAAAAAAA others(1): Show |
A | 43 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(40): Show | 43 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.4819-369_4819-362d others(10): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108031340 | ||||||
| chr7:108031369
|
GA | G | 51 | a0001c0001t0001g0188a0001c0001t0001g0234a0001c0001t0001g0249others(48): Show | 51 | HG00621.hp1 HG01106.hp1 HG01243.hp1 others(48): Show |
intron_variant | MODIFIER | c.4819-391delT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108031369 | ||||||
| chr7:108031478
|
C | A | 2 | a0001c0070t0001g0246a0017c0043t0001g0084 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4819-499G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108031478 | ||||||
| chr7:108031540
|
A | C | 1 | a0011c0014t0001g0242 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4819-561T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108031540 | ||||||
| chr7:108031541
|
C | T | 2 | a0001c0070t0001g0246a0017c0043t0001g0084 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4819-562G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108031541 | ||||||
| chr7:108031680
|
G | T | 1 | a0001c0002t0001g0008 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.4819-701C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108031680 | ||||||
| chr7:108031754
|
A | T | 45 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(42): Show | 45 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.4819-775T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108031754 | ||||||
| chr7:108031867
|
T | C | 2 | a0001c0070t0001g0246a0017c0043t0001g0084 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4819-888A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108031867 | ||||||
| chr7:108032005
|
C | A | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4819-1026G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032005 | ||||||
| chr7:108032020
|
G | A | 1 | a0009c0009t0001g0010 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.4819-1041C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032020 | ||||||
| chr7:108032095
|
A | G | 1 | a0001c0006t0003g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4819-1116T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032095 | ||||||
| chr7:108032097
|
A | C | 2 | a0009c0009t0001g0266a0009c0009t0001g0267 | 2 | HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.4819-1118T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032097 | ||||||
| chr7:108032196
|
T | C | 70 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(67): Show | 70 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.4819-1217A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032196 | ||||||
| chr7:108032221
|
C | T | 2 | a0004c0005t0003g0235a0004c0005t0003g0236 | 2 | NA18747.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.4819-1242G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032221 | ||||||
| chr7:108032261
|
G | A | 6 | a0001c0002t0002g0149a0006c0016t0002g0086a0008c0015t0002g0087others(3): Show | 6 | HG02055.hp2 HG02559.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.4819-1282C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032261 | ||||||
| chr7:108032397
|
TA | T | 103 | a0001c0001t0001g0014a0001c0001t0001g0272a0001c0001t0002g0208others(100): Show | 103 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(100): Show |
intron_variant | MODIFIER | c.4819-1419delT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032397 | ||||||
| chr7:108032410
|
T | C | 4 | a0001c0002t0003g0023a0001c0002t0003g0053a0001c0002t0003g0054others(1): Show | 4 | NA18983.hp2 NA19011.hp2 NA19083.hp1 others(1): Show |
intron_variant | MODIFIER | c.4819-1431A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032410 | ||||||
| chr7:108032439
|
C | T | 1 | a0005c0008t0002g0271 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.4819-1460G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032439 | ||||||
| chr7:108032442
|
C | G | 10 | a0006c0016t0002g0101a0008c0015t0002g0001a0008c0015t0002g0002others(7): Show | 10 | HG02615.hp1 HG02717.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.4819-1463G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032442 | ||||||
| chr7:108032450
|
A | C | 1 | a0041c0033t0001g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4819-1471T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032450 | ||||||
| chr7:108032488
|
G | T | 1 | a0006c0027t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.4819-1509C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032488 | ||||||
| chr7:108032633
|
T | C | 70 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(67): Show | 70 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(67): Show |
intron_variant | MODIFIER | c.4818+1575A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032633 | ||||||
| chr7:108032686
|
G | C | 1 | a0014c0058t0002g0057 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.4818+1522C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032686 | ||||||
| chr7:108032695
|
C | CGT | 17 | a0001c0001t0001g0030a0001c0001t0001g0042a0001c0001t0001g0044others(14): Show | 17 | HG00544.hp1 HG01099.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.4818+1511_4818+151 others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032695 | ||||||
| chr7:108032695
|
C | CGTGT | 26 | a0001c0001t0001g0014a0001c0001t0001g0272a0001c0002t0001g0052others(23): Show | 26 | HG01516.hp1 HG01981.hp2 HG02165.hp2 others(23): Show |
intron_variant | MODIFIER | c.4818+1509_4818+151 others(8): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032695 | ||||||
| chr7:108032695
|
C | CGTGTGT | 6 | a0002c0003t0001g0082a0002c0003t0001g0129a0002c0003t0001g0138others(3): Show | 6 | HG01256.hp2 HG01258.hp1 HG03834.hp2 others(3): Show |
intron_variant | MODIFIER | c.4818+1507_4818+151 others(10): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032695 | ||||||
| chr7:108032695
|
CGT | C | 39 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0172others(36): Show | 39 | HG00738.hp1 HG00741.hp1 HG01074.hp2 others(36): Show |
intron_variant | MODIFIER | c.4818+1511_4818+151 others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032695 | ||||||
| chr7:108032695
|
CGTGT | C | 19 | a0001c0001t0002g0208a0006c0010t0002g0290a0006c0016t0002g0101others(16): Show | 19 | HG02280.hp2 HG02486.hp2 HG02615.hp1 others(16): Show |
intron_variant | MODIFIER | c.4818+1509_4818+151 others(8): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032695 | ||||||
| chr7:108032695
|
CGTGTGT | C | 7 | a0001c0002t0002g0149a0006c0016t0002g0086a0008c0015t0002g0087others(4): Show | 7 | HG02055.hp2 HG02559.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.4818+1507_4818+151 others(10): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032695 | ||||||
| chr7:108032697
|
T | C | 1 | a0001c0001t0001g0038 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.4818+1511A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032697 | ||||||
| chr7:108032879
|
C | T | 12 | a0006c0016t0002g0101a0007c0037t0002g0093a0008c0015t0002g0001others(9): Show | 12 | HG02258.hp1 HG02615.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.4818+1329G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108032879 | ||||||
| chr7:108033184
|
C | T | 69 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(66): Show | 69 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.4818+1024G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108033184 | ||||||
| chr7:108033265
|
T | C | 45 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(42): Show | 45 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.4818+943A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108033265 | ||||||
| chr7:108033346
|
A | G | 1 | a0001c0002t0001g0068 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.4818+862T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108033346 | ||||||
| chr7:108033480
|
G | A | 1 | a0001c0001t0001g0203 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.4818+728C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108033480 | ||||||
| chr7:108033541
|
T | C | 144 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0150others(141): Show | 144 | HG00280.hp1 HG00280.hp2 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.4818+667A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108033541 | ||||||
| chr7:108033591
|
T | C | 12 | a0007c0037t0002g0093a0008c0015t0002g0001a0008c0015t0002g0002others(9): Show | 12 | HG02258.hp1 HG02615.hp1 HG02717.hp1 others(9): Show |
intron_variant | MODIFIER | c.4818+617A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108033591 | ||||||
| chr7:108033637
|
C | G | 2 | a0001c0070t0001g0246a0017c0043t0001g0084 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4818+571G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108033637 | ||||||
| chr7:108033657
|
C | A | 2 | a0001c0070t0001g0246a0017c0043t0001g0084 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4818+551G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108033657 | ||||||
| chr7:108033735
|
A | AT | 8 | a0001c0001t0001g0193a0001c0001t0001g0202a0001c0002t0001g0019others(5): Show | 8 | HG02080.hp1 HG02145.hp2 HG03579.hp2 others(5): Show |
intron_variant | MODIFIER | c.4818+472dupA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108033735 | ||||||
| chr7:108033735
|
AT | A | 20 | a0001c0001t0001g0190a0001c0001t0001g0206a0001c0001t0001g0240others(17): Show | 20 | HG00323.hp1 HG00558.hp1 HG01074.hp1 others(17): Show |
intron_variant | MODIFIER | c.4818+472delA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108033735 | ||||||
| chr7:108033735
|
ATT | A | 57 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(54): Show | 57 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(54): Show |
intron_variant | MODIFIER | c.4818+471_4818+472d others(4): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108033735 | ||||||
| chr7:108033860
|
A | T | 45 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(42): Show | 45 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.4818+348T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108033860 | ||||||
| chr7:108033910
|
C | G | 1 | a0001c0002t0001g0170 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.4818+298G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108033910 | ||||||
| chr7:108034111
|
A | T | 5 | a0005c0008t0002g0187a0005c0008t0002g0271a0005c0008t0002g0274others(2): Show | 5 | HG00423.hp2 HG02040.hp2 HG02129.hp1 others(2): Show |
intron_variant | MODIFIER | c.4818+97T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108034111 | ||||||
| chr7:108034115
|
G | A | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4818+93C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 31/33 | chr7 | 108034115 | ||||||
| chr7:108034510
|
T | C | 3 | a0001c0001t0001g0104a0009c0009t0001g0228a0009c0009t0001g0229 | 3 | HG00544.hp1 HG06807.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.4680-164A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108034510 | ||||||
| chr7:108034531
|
A | T | 1 | a0021c0028t0002g0092 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4680-185T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108034531 | ||||||
| chr7:108034548
|
C | T | 2 | a0001c0070t0001g0246a0017c0043t0001g0084 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4680-202G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108034548 | ||||||
| chr7:108034652
|
C | T | 2 | a0003c0004t0002g0268a0003c0004t0002g0269 | 2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.4680-306G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108034652 | ||||||
| chr7:108034778
|
T | C | 261 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0030others(258): Show | 261 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(258): Show |
intron_variant | MODIFIER | c.4680-432A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108034778 | ||||||
| chr7:108034787
|
T | G | 1 | a0004c0005t0003g0236 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.4680-441A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108034787 | ||||||
| chr7:108035214
|
T | C | 11 | a0001c0001t0001g0039a0001c0001t0001g0040a0001c0001t0001g0041others(8): Show | 11 | HG00558.hp2 HG01943.hp1 HG01975.hp1 others(8): Show |
intron_variant | MODIFIER | c.4680-868A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035214 | ||||||
| chr7:108035256
|
G | A | 2 | a0001c0001t0001g0169a0001c0001t0001g0250 | 2 | HG00280.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.4680-910C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035256 | ||||||
| chr7:108035408
|
G | C | 13 | a0007c0037t0002g0093a0008c0015t0002g0001a0008c0015t0002g0002others(10): Show | 13 | HG02055.hp2 HG02258.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.4680-1062C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035408 | ||||||
| chr7:108035546
|
G | GA | 171 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0030others(168): Show | 171 | HG00280.hp1 HG00323.hp1 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.4680-1201dupT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035546 | ||||||
| chr7:108035546
|
GA | G | 43 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(40): Show | 43 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.4680-1201delT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035546 | ||||||
| chr7:108035604
|
CA | C | 206 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0030others(203): Show | 206 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(203): Show |
intron_variant | MODIFIER | c.4680-1259delT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035604 | ||||||
| chr7:108035604
|
CAA | C | 51 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0115others(48): Show | 51 | HG00558.hp1 HG00621.hp1 HG01106.hp1 others(48): Show |
intron_variant | MODIFIER | c.4680-1260_4680-125 others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035604 | ||||||
| chr7:108035605
|
A | C | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4680-1259T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035605 | ||||||
| chr7:108035621
|
A | G | 3 | a0001c0001t0002g0208a0016c0055t0002g0213a0017c0030t0002g0286 | 3 | HG02486.hp2 HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4680-1275T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035621 | ||||||
| chr7:108035622
|
A | G | 1 | a0001c0060t0004g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4680-1276T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035622 | ||||||
| chr7:108035622
|
AG | A | 3 | a0001c0001t0002g0208a0016c0055t0002g0213a0017c0030t0002g0286 | 3 | HG02486.hp2 HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4680-1277delC | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035622 | ||||||
| chr7:108035623
|
G | A | 1 | a0001c0060t0004g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4680-1277C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035623 | ||||||
| chr7:108035633
|
C | T | 69 | a0001c0001t0002g0208a0001c0002t0002g0149a0001c0070t0001g0246others(66): Show | 69 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.4680-1287G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035633 | ||||||
| chr7:108035667
|
A | G | 1 | a0002c0003t0001g0135 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4680-1321T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035667 | ||||||
| chr7:108035669
|
C | G | 2 | a0001c0002t0001g0019a0001c0002t0001g0183 | 2 | NA18990.hp2 NA19000.hp1 |
intron_variant | MODIFIER | c.4680-1323G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035669 | ||||||
| chr7:108035855
|
CT | C | 62 | a0001c0001t0001g0190a0001c0001t0002g0208a0001c0002t0002g0149others(59): Show | 62 | HG00280.hp2 HG00423.hp2 HG00741.hp1 others(59): Show |
intron_variant | MODIFIER | c.4680-1510delA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035855 | ||||||
| chr7:108035855
|
CTT | C | 8 | a0003c0004t0002g0007a0003c0004t0002g0189a0003c0004t0002g0217others(5): Show | 8 | HG00738.hp1 HG01496.hp1 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.4680-1511_4680-151 others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035855 | ||||||
| chr7:108035927
|
C | T | 4 | a0001c0002t0001g0033a0001c0002t0001g0035a0001c0002t0001g0037others(1): Show | 4 | HG00544.hp2 NA18957.hp1 NA19001.hp2 others(1): Show |
intron_variant | MODIFIER | c.4679+1461G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035927 | ||||||
| chr7:108035941
|
C | T | 3 | a0001c0001t0002g0208a0016c0055t0002g0213a0017c0030t0002g0286 | 3 | HG02486.hp2 HG03130.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.4679+1447G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108035941 | ||||||
| chr7:108036018
|
C | T | 1 | a0001c0002t0001g0017 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.4679+1370G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036018 | ||||||
| chr7:108036019
|
G | A | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4679+1369C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036019 | ||||||
| chr7:108036026
|
T | G | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4679+1362A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036026 | ||||||
| chr7:108036046
|
C | T | 1 | a0001c0002t0001g0019 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.4679+1342G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036046 | ||||||
| chr7:108036194
|
A | AT | 17 | a0001c0002t0002g0149a0007c0037t0002g0093a0008c0015t0002g0001others(14): Show | 17 | HG02055.hp2 HG02258.hp1 HG02559.hp1 others(14): Show |
intron_variant | MODIFIER | c.4679+1193dupA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036194 | ||||||
| chr7:108036194
|
A | ATT | 48 | a0001c0001t0002g0208a0003c0004t0002g0007a0003c0004t0002g0175others(45): Show | 48 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.4679+1192_4679+119 others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036194 | ||||||
| chr7:108036219
|
C | T | 67 | a0001c0001t0002g0208a0001c0002t0002g0149a0003c0004t0002g0007others(64): Show | 67 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(64): Show |
intron_variant | MODIFIER | c.4679+1169G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036219 | ||||||
| chr7:108036223
|
T | C | 69 | a0001c0001t0002g0208a0001c0002t0002g0149a0001c0070t0001g0246others(66): Show | 69 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.4679+1165A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036223 | ||||||
| chr7:108036314
|
A | C | 1 | a0002c0012t0001g0248 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4679+1074T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036314 | ||||||
| chr7:108036350
|
G | A | 2 | a0008c0015t0002g0001a0008c0015t0002g0002 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.4679+1038C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036350 | ||||||
| chr7:108036380
|
G | A | 1 | a0001c0002t0003g0078 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.4679+1008C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036380 | ||||||
| chr7:108036407
|
C | T | 1 | a0001c0002t0001g0076 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.4679+981G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036407 | ||||||
| chr7:108036418
|
C | G | 1 | a0001c0001t0001g0164 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4679+970G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036418 | ||||||
| chr7:108036477
|
C | T | 1 | a0001c0001t0003g0181 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.4679+911G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036477 | ||||||
| chr7:108036491
|
T | A | 1 | a0001c0060t0004g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4679+897A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036491 | ||||||
| chr7:108036531
|
T | G | 3 | a0008c0015t0002g0087a0008c0039t0002g0147a0020c0021t0002g0099 | 3 | HG02055.hp2 HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4679+857A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036531 | ||||||
| chr7:108036586
|
G | A | 2 | a0002c0003t0003g0130a0004c0005t0003g0184 | 2 | NA18986.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.4679+802C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036586 | ||||||
| chr7:108036652
|
T | C | 1 | a0009c0009t0001g0267 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.4679+736A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036652 | ||||||
| chr7:108036667
|
G | A | 1 | a0002c0012t0001g0159 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4679+721C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036667 | ||||||
| chr7:108036825
|
T | C | 1 | a0001c0006t0003g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.4679+563A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036825 | ||||||
| chr7:108036925
|
T | A | 69 | a0001c0001t0002g0208a0001c0002t0002g0149a0001c0070t0001g0246others(66): Show | 69 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(66): Show |
intron_variant | MODIFIER | c.4679+463A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108036925 | ||||||
| chr7:108037040
|
A | T | 1 | a0001c0001t0001g0261 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.4679+348T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108037040 | ||||||
| chr7:108037089
|
G | A | 229 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0030others(226): Show | 229 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.4679+299C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108037089 | ||||||
| chr7:108037111
|
G | T | 229 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0030others(226): Show | 229 | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.4679+277C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108037111 | ||||||
| chr7:108037144
|
T | C | 2 | a0001c0070t0001g0246a0017c0043t0001g0084 | 2 | HG02572.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.4679+244A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108037144 | ||||||
| chr7:108037213
|
G | A | 1 | a0020c0021t0002g0098 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4679+175C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108037213 | ||||||
| chr7:108037229
|
C | T | 47 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(44): Show | 47 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.4679+159G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 30/33 | chr7 | 108037229 | ||||||
| chr7:108038021
|
A | G | 10 | a0008c0015t0002g0001a0008c0015t0002g0002a0012c0022t0002g0148others(7): Show | 10 | HG02615.hp1 HG02717.hp1 HG02723.hp2 others(7): Show |
intron_variant | MODIFIER | c.4472-426T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108038021 | ||||||
| chr7:108038039
|
A | G | 3 | a0001c0054t0001g0146a0019c0020t0001g0088a0019c0020t0001g0097 | 3 | HG02615.hp2 HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.4472-444T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108038039 | ||||||
| chr7:108038316
|
T | C | 8 | a0001c0002t0001g0016a0001c0002t0001g0024a0001c0002t0001g0049others(5): Show | 8 | HG00738.hp2 HG00741.hp2 HG01106.hp2 others(5): Show |
intron_variant | MODIFIER | c.4472-721A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108038316 | ||||||
| chr7:108038427
|
C | T | 1 | a0001c0001t0003g0247 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4472-832G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108038427 | ||||||
| chr7:108038522
|
A | T | 1 | a0004c0005t0003g0179 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.4472-927T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108038522 | ||||||
| chr7:108038532
|
T | G | 113 | a0001c0001t0001g0030a0001c0001t0001g0115a0001c0001t0001g0150others(110): Show | 113 | HG00140.hp1 HG00280.hp1 HG00280.hp2 others(110): Show |
intron_variant | MODIFIER | c.4472-937A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108038532 | ||||||
| chr7:108038750
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.4472-1155G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108038750 | ||||||
| chr7:108038770
|
G | T | 3 | a0001c0054t0001g0146a0001c0070t0001g0246a0017c0043t0001g0084 | 3 | HG02572.hp2 HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.4472-1175C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108038770 | ||||||
| chr7:108038783
|
T | C | 1 | a0001c0002t0002g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4472-1188A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108038783 | ||||||
| chr7:108038798
|
T | A | 1 | a0001c0060t0004g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.4472-1203A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108038798 | ||||||
| chr7:108038882
|
G | C | 4 | a0001c0001t0001g0115a0001c0001t0001g0194a0001c0001t0001g0195others(1): Show | 4 | HG02080.hp2 NA18942.hp2 NA18963.hp1 others(1): Show |
intron_variant | MODIFIER | c.4472-1287C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108038882 | ||||||
| chr7:108038935
|
C | T | 73 | a0001c0001t0002g0208a0001c0002t0001g0019a0001c0002t0001g0183others(70): Show | 73 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.4472-1340G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108038935 | ||||||
| chr7:108039360
|
TTCTG | T | 7 | a0001c0001t0001g0167a0001c0001t0001g0241a0001c0001t0001g0273others(4): Show | 7 | HG02056.hp2 HG02132.hp1 NA18962.hp1 others(4): Show |
intron_variant | MODIFIER | c.4472-1769_4472-176 others(8): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108039360 | ||||||
| chr7:108039402
|
G | A | 2 | a0001c0060t0004g0216a0016c0061t0002g0155 | 2 | HG03225.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.4472-1807C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108039402 | ||||||
| chr7:108039470
|
C | CT | 52 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(49): Show | 52 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(49): Show |
intron_variant | MODIFIER | c.4472-1876dupA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108039470 | ||||||
| chr7:108039470
|
CT | C | 73 | a0001c0001t0002g0208a0001c0002t0001g0019a0001c0002t0001g0183others(70): Show | 73 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(70): Show |
intron_variant | MODIFIER | c.4472-1876delA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108039470 | ||||||
| chr7:108039507
|
C | T | 2 | a0008c0015t0002g0001a0008c0015t0002g0002 | 2 | HG02615.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.4472-1912G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108039507 | ||||||
| chr7:108039557
|
C | T | 4 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.4472-1962G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108039557 | ||||||
| chr7:108039711
|
C | T | 1 | a0001c0001t0001g0282 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.4472-2116G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108039711 | ||||||
| chr7:108039878
|
C | T | 1 | a0001c0001t0001g0260 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4472-2283G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108039878 | ||||||
| chr7:108039879
|
A | T | 1 | a0001c0001t0001g0260 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.4472-2284T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108039879 | ||||||
| chr7:108040032
|
A | G | 1 | a0013c0068t0002g0227 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4472-2437T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108040032 | ||||||
| chr7:108040214
|
G | T | 1 | a0004c0005t0003g0179 | 1 | NA18985.hp2 | intron_variant | MODIFIER | c.4472-2619C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108040214 | ||||||
| chr7:108040236
|
A | C | 3 | a0007c0037t0002g0093a0008c0039t0002g0147a0020c0021t0002g0099 | 3 | HG02258.hp1 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4472-2641T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108040236 | ||||||
| chr7:108040311
|
A | G | 40 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0002t0001g0019others(37): Show | 40 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.4472-2716T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108040311 | ||||||
| chr7:108040441
|
C | T | 4 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.4472-2846G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108040441 | ||||||
| chr7:108040488
|
C | T | 1 | a0041c0033t0001g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4472-2893G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108040488 | ||||||
| chr7:108040549
|
T | C | 1 | a0021c0040t0002g0004 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.4472-2954A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108040549 | ||||||
| chr7:108040751
|
A | T | 1 | a0006c0016t0002g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.4471+3001T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108040751 | ||||||
| chr7:108040831
|
A | G | 1 | a0007c0037t0002g0093 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4471+2921T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108040831 | ||||||
| chr7:108040856
|
A | G | 1 | a0001c0001t0001g0115 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.4471+2896T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108040856 | ||||||
| chr7:108040878
|
A | C | 1 | a0040c0031t0002g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.4471+2874T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108040878 | ||||||
| chr7:108041027
|
C | T | 3 | a0001c0001t0001g0276a0001c0006t0001g0144a0001c0006t0001g0145 | 3 | NA18962.hp2 NA18968.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.4471+2725G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108041027 | ||||||
| chr7:108041163
|
C | G | 4 | a0001c0001t0002g0208a0008c0015t0002g0087a0016c0055t0002g0213others(1): Show | 4 | HG02055.hp2 HG02486.hp2 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.4471+2589G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108041163 | ||||||
| chr7:108041172
|
A | T | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4471+2580T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108041172 | ||||||
| chr7:108041543
|
C | T | 1 | a0001c0002t0002g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4471+2209G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108041543 | ||||||
| chr7:108041584
|
A | G | 38 | a0001c0002t0001g0019a0001c0002t0001g0183a0001c0002t0003g0162others(35): Show | 38 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.4471+2168T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108041584 | ||||||
| chr7:108041660
|
C | T | 1 | a0021c0028t0002g0092 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.4471+2092G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108041660 | ||||||
| chr7:108041665
|
G | A | 1 | a0008c0015t0002g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4471+2087C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108041665 | ||||||
| chr7:108041676
|
T | C | 1 | a0007c0037t0002g0093 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4471+2076A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108041676 | ||||||
| chr7:108041700
|
C | T | 1 | a0004c0072t0003g0245 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.4471+2052G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108041700 | ||||||
| chr7:108041743
|
G | A | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4471+2009C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108041743 | ||||||
| chr7:108041758
|
G | A | 4 | a0001c0002t0001g0019a0001c0002t0001g0183a0001c0002t0003g0162others(1): Show | 4 | HG04115.hp1 NA18950.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.4471+1994C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108041758 | ||||||
| chr7:108041867
|
C | T | 5 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(2): Show | 5 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.4471+1885G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108041867 | ||||||
| chr7:108041890
|
T | C | 2 | a0001c0001t0001g0042a0001c0001t0001g0044 | 2 | HG01261.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.4471+1862A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108041890 | ||||||
| chr7:108041921
|
C | A | 75 | a0001c0001t0002g0208a0001c0002t0001g0019a0001c0002t0001g0183others(72): Show | 75 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.4471+1831G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108041921 | ||||||
| chr7:108042096
|
C | A | 1 | a0013c0068t0002g0227 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4471+1656G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042096 | ||||||
| chr7:108042229
|
T | C | 33 | a0001c0001t0001g0014a0001c0001t0003g0255a0001c0002t0001g0052others(30): Show | 33 | HG01256.hp2 HG01258.hp1 HG01516.hp1 others(30): Show |
intron_variant | MODIFIER | c.4471+1523A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042229 | ||||||
| chr7:108042260
|
T | C | 1 | a0001c0001t0001g0275 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.4471+1492A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042260 | ||||||
| chr7:108042283
|
G | A | 2 | a0001c0001t0001g0192a0001c0001t0001g0201 | 2 | HG01255.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.4471+1469C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042283 | ||||||
| chr7:108042324
|
C | A | 9 | a0003c0004t0002g0225a0007c0011t0002g0156a0007c0011t0002g0157others(6): Show | 9 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(6): Show |
intron_variant | MODIFIER | c.4471+1428G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042324 | ||||||
| chr7:108042646
|
T | C | 1 | a0029c0067t0002g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4471+1106A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042646 | ||||||
| chr7:108042655
|
C | T | 39 | a0001c0002t0001g0019a0001c0002t0001g0183a0001c0002t0003g0162others(36): Show | 39 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.4471+1097G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042655 | ||||||
| chr7:108042701
|
C | T | 1 | a0032c0050t0001g0134 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.4471+1051G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042701 | ||||||
| chr7:108042714
|
T | C | 75 | a0001c0001t0002g0208a0001c0002t0001g0019a0001c0002t0001g0183others(72): Show | 75 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(72): Show |
intron_variant | MODIFIER | c.4471+1038A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042714 | ||||||
| chr7:108042785
|
C | G | 2 | a0001c0054t0001g0146a0017c0043t0001g0084 | 2 | HG02723.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.4471+967G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042785 | ||||||
| chr7:108042925
|
C | CTCAA | 5 | a0003c0004t0002g0231a0003c0004t0002g0268a0003c0004t0002g0269others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.4471+826_4471+827i others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042925 | ||||||
| chr7:108042927
|
C | CAA | 33 | a0001c0002t0001g0019a0003c0004t0002g0007a0003c0004t0002g0175others(30): Show | 33 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(30): Show |
intron_variant | MODIFIER | c.4471+824_4471+825i others(4): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042927 | ||||||
| chr7:108042928
|
T | A | 2 | a0001c0002t0001g0183a0001c0002t0003g0162 | 2 | NA18950.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.4471+824A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042928 | ||||||
| chr7:108042929
|
C | A | 2 | a0001c0002t0001g0183a0001c0002t0003g0162 | 2 | NA18950.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.4471+823G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042929 | ||||||
| chr7:108042931
|
C | CTGTG | 20 | a0003c0004t0002g0007a0003c0004t0002g0189a0003c0004t0002g0217others(17): Show | 20 | HG00423.hp2 HG00738.hp1 HG00741.hp1 others(17): Show |
intron_variant | MODIFIER | c.4471+820_4471+821i others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042931 | ||||||
| chr7:108042931
|
C | CTGTGTG | 8 | a0003c0004t0002g0175a0007c0019t0002g0005a0009c0009t0001g0266others(5): Show | 8 | HG00280.hp2 HG02148.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.4471+820_4471+821i others(8): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042931 | ||||||
| chr7:108042931
|
C | CTGTGTGT others(7): Show |
1 | a0038c0036t0002g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.4471+820_4471+821i others(16): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042931 | ||||||
| chr7:108042931
|
C | G | 5 | a0003c0004t0002g0231a0003c0004t0002g0268a0003c0004t0002g0269others(2): Show | 5 | HG01243.hp2 HG02258.hp2 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.4471+821G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042931 | ||||||
| chr7:108042932
|
A | T | 40 | a0001c0002t0001g0019a0001c0002t0001g0183a0001c0002t0003g0162others(37): Show | 40 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.4471+820T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042932 | ||||||
| chr7:108042933
|
A | C | 2 | a0001c0002t0001g0183a0001c0002t0003g0162 | 2 | NA18950.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.4471+819T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042933 | ||||||
| chr7:108042933
|
A | G | 38 | a0001c0002t0001g0019a0003c0004t0002g0007a0003c0004t0002g0175others(35): Show | 38 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.4471+819T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042933 | ||||||
| chr7:108042935
|
C | G | 40 | a0001c0002t0001g0019a0001c0002t0001g0183a0001c0002t0003g0162others(37): Show | 40 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.4471+817G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042935 | ||||||
| chr7:108042937
|
C | CTG | 57 | a0001c0001t0001g0044a0001c0001t0001g0104a0001c0001t0001g0115others(54): Show | 57 | HG00140.hp1 HG00423.hp1 HG00621.hp1 others(54): Show |
intron_variant | MODIFIER | c.4471+813_4471+814d others(4): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042937 | ||||||
| chr7:108042937
|
C | CTGTG | 8 | a0001c0001t0001g0042a0001c0001t0001g0282a0001c0002t0001g0024others(5): Show | 8 | HG00323.hp1 HG00741.hp2 HG01243.hp1 others(5): Show |
intron_variant | MODIFIER | c.4471+811_4471+814d others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042937 | ||||||
| chr7:108042937
|
C | CTGTGTG | 6 | a0001c0002t0001g0025a0003c0004t0002g0225a0007c0011t0002g0157others(3): Show | 6 | HG01361.hp2 HG01496.hp1 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.4471+809_4471+814d others(8): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042937 | ||||||
| chr7:108042937
|
C | CTGTGTGT others(1): Show |
13 | a0001c0001t0002g0208a0007c0011t0001g0100a0007c0011t0002g0102others(10): Show | 13 | HG02280.hp2 HG02486.hp2 HG02559.hp1 others(10): Show |
intron_variant | MODIFIER | c.4471+807_4471+814d others(10): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042937 | ||||||
| chr7:108042937
|
C | CTGTGTGT others(3): Show |
7 | a0002c0003t0001g0135a0008c0015t0002g0001a0008c0044t0002g0091others(4): Show | 7 | HG02622.hp2 HG02647.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.4471+805_4471+814d others(12): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042937 | ||||||
| chr7:108042937
|
C | CTGTGTGT others(5): Show |
1 | a0012c0059t0002g0222 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.4471+803_4471+814d others(14): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042937 | ||||||
| chr7:108042937
|
C | CTGTGTGT others(7): Show |
2 | a0013c0026t0002g0153a0013c0026t0002g0154 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4471+801_4471+814d others(16): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042937 | ||||||
| chr7:108042937
|
C | CTGTGTGT others(9): Show |
1 | a0007c0037t0002g0093 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.4471+799_4471+814d others(18): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042937 | ||||||
| chr7:108042937
|
C | G | 43 | a0001c0001t0001g0199a0001c0002t0001g0019a0001c0002t0001g0183others(40): Show | 43 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.4471+815G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042937 | ||||||
| chr7:108042937
|
CTG | C | 6 | a0001c0001t0001g0030a0001c0001t0001g0177a0001c0002t0001g0060others(3): Show | 6 | HG01069.hp1 HG03041.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.4471+813_4471+814d others(4): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042937 | ||||||
| chr7:108042937
|
CTGTG | C | 8 | a0001c0001t0001g0150a0001c0001t0001g0190a0001c0001t0001g0191others(5): Show | 8 | HG00280.hp1 HG00323.hp2 HG01069.hp2 others(5): Show |
intron_variant | MODIFIER | c.4471+811_4471+814d others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042937 | ||||||
| chr7:108042937
|
CTGTGTGT others(5): Show |
C | 1 | a0001c0002t0002g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.4471+803_4471+814d others(14): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042937 | ||||||
| chr7:108042937
|
CTGTGTGT others(7): Show |
C | 1 | a0017c0043t0001g0084 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4471+801_4471+814d others(16): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042937 | ||||||
| chr7:108042953
|
G | C | 1 | a0017c0043t0001g0084 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4471+799C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042953 | ||||||
| chr7:108042979
|
A | G | 2 | a0001c0001t0003g0015a0001c0006t0003g0121 | 2 | HG02040.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.4471+773T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108042979 | ||||||
| chr7:108043197
|
T | A | 13 | a0007c0011t0002g0102a0008c0015t0002g0001a0008c0015t0002g0002others(10): Show | 13 | HG02280.hp2 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.4471+555A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043197 | ||||||
| chr7:108043353
|
C | A | 3 | a0007c0037t0002g0093a0008c0039t0002g0147a0020c0021t0002g0099 | 3 | HG02258.hp1 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4471+399G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043353 | ||||||
| chr7:108043525
|
A | C | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4471+227T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043525 | ||||||
| chr7:108043538
|
CTATGATG others(136): Show |
C | 119 | a0001c0001t0001g0014a0001c0001t0002g0208a0001c0001t0003g0255others(116): Show | 119 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(116): Show |
intron_variant | MODIFIER | c.4471+71_4471+213de others(1): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043538 | ||||||
| chr7:108043545
|
GTTTTTTT others(1): Show |
G | 9 | a0001c0001t0001g0042a0001c0001t0001g0044a0001c0001t0001g0119others(6): Show | 9 | HG01261.hp2 HG02145.hp2 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.4471+199_4471+206d others(10): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043545 | ||||||
| chr7:108043545
|
GTTTTTTT others(3): Show |
G | 11 | a0001c0001t0001g0210a0001c0001t0003g0174a0001c0001t0003g0247others(8): Show | 11 | HG01106.hp1 HG01243.hp1 HG02451.hp1 others(8): Show |
intron_variant | MODIFIER | c.4471+197_4471+206d others(12): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043545 | ||||||
| chr7:108043545
|
GTTTTTTT others(4): Show |
G | 6 | a0001c0001t0001g0188a0001c0002t0001g0009a0001c0002t0003g0046others(3): Show | 6 | HG01975.hp2 HG02683.hp1 HG03490.hp1 others(3): Show |
intron_variant | MODIFIER | c.4471+196_4471+206d others(13): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043545 | ||||||
| chr7:108043545
|
GTTTTTTT others(5): Show |
G | 5 | a0001c0001t0001g0249a0001c0001t0003g0186a0001c0002t0001g0059others(2): Show | 5 | HG01515.hp1 HG01515.hp2 HG02886.hp1 others(2): Show |
intron_variant | MODIFIER | c.4471+195_4471+206d others(14): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043545 | ||||||
| chr7:108043545
|
GTTTTTTT others(6): Show |
G | 8 | a0001c0001t0001g0167a0001c0001t0001g0202a0001c0001t0001g0275others(5): Show | 8 | HG01978.hp1 HG02056.hp2 HG03927.hp1 others(5): Show |
intron_variant | MODIFIER | c.4471+194_4471+206d others(15): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043545 | ||||||
| chr7:108043545
|
GTTTTTTT others(7): Show |
G | 13 | a0001c0001t0001g0104a0001c0001t0001g0164a0001c0001t0001g0203others(10): Show | 13 | HG00544.hp1 HG01099.hp1 HG01346.hp2 others(10): Show |
intron_variant | MODIFIER | c.4471+193_4471+206d others(16): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043545 | ||||||
| chr7:108043545
|
GTTTTTTT others(8): Show |
G | 16 | a0001c0001t0001g0013a0001c0001t0001g0168a0001c0001t0001g0252others(13): Show | 16 | HG00323.hp1 HG00423.hp1 HG01069.hp2 others(13): Show |
intron_variant | MODIFIER | c.4471+192_4471+206d others(17): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043545 | ||||||
| chr7:108043545
|
GTTTTTTT others(9): Show |
G | 5 | a0001c0001t0001g0190a0001c0001t0001g0237a0001c0001t0001g0250others(2): Show | 5 | HG00280.hp1 HG01167.hp1 HG02080.hp1 others(2): Show |
intron_variant | MODIFIER | c.4471+191_4471+206d others(18): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043545 | ||||||
| chr7:108043545
|
GTTTTTTT others(10): Show |
G | 7 | a0001c0001t0001g0169a0001c0001t0001g0191a0001c0001t0001g0197others(4): Show | 7 | HG01169.hp2 HG01258.hp2 HG02523.hp1 others(4): Show |
intron_variant | MODIFIER | c.4471+190_4471+206d others(19): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043545 | ||||||
| chr7:108043545
|
GTTTTTTT others(11): Show |
G | 9 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0150others(6): Show | 9 | HG00323.hp2 HG01255.hp2 HG01496.hp2 others(6): Show |
intron_variant | MODIFIER | c.4471+189_4471+206d others(20): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043545 | ||||||
| chr7:108043545
|
GTTTTTTT others(12): Show |
G | 5 | a0006c0016t0001g0083a0006c0016t0002g0101a0011c0014t0001g0214others(2): Show | 5 | HG02145.hp1 HG02818.hp1 HG04204.hp1 others(2): Show |
intron_variant | MODIFIER | c.4471+188_4471+206d others(21): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043545 | ||||||
| chr7:108043545
|
GTTTTTTT others(17): Show |
G | 1 | a0034c0073t0003g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4471+183_4471+206d others(26): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043545 | ||||||
| chr7:108043545
|
GTTTTTTT others(24): Show |
G | 1 | a0011c0014t0001g0242 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4471+176_4471+206d others(33): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043545 | ||||||
| chr7:108043545
|
GTTTTTTT others(26): Show |
G | 4 | a0001c0001t0001g0193a0001c0001t0001g0262a0001c0002t0001g0008others(1): Show | 4 | HG02080.hp2 HG02738.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.4471+174_4471+206d others(35): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043545 | ||||||
| chr7:108043545
|
GTTTTTTT others(27): Show |
G | 41 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(38): Show | 41 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(38): Show |
intron_variant | MODIFIER | c.4471+173_4471+206d others(36): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043545 | ||||||
| chr7:108043545
|
GTTTTTTT others(28): Show |
G | 3 | a0001c0001t0001g0030a0001c0001t0001g0256a0001c0001t0001g0260 | 3 | NA18950.hp1 NA18985.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.4471+172_4471+206d others(37): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043545 | ||||||
| chr7:108043545
|
GTTTTTTT others(29): Show |
G | 3 | a0001c0002t0001g0065a0001c0002t0001g0067a0001c0002t0001g0068 | 3 | HG01255.hp1 HG01981.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.4471+171_4471+206d others(38): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043545 | ||||||
| chr7:108043562
|
T | G | 1 | a0006c0010t0002g0290 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4471+190A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043562 | ||||||
| chr7:108043571
|
T | G | 3 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254 | 3 | HG01074.hp1 HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.4471+181A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043571 | ||||||
| chr7:108043734
|
T | C | 2 | a0004c0005t0003g0235a0004c0005t0003g0236 | 2 | NA18747.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.4471+18A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 29/33 | chr7 | 108043734 | ||||||
| chr7:108043921
|
G | A | 4 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.4327-25C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108043921 | ||||||
| chr7:108043948
|
T | G | 36 | a0001c0001t0002g0208a0001c0054t0001g0146a0001c0060t0004g0216others(33): Show | 36 | HG01496.hp1 HG02055.hp2 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.4327-52A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108043948 | ||||||
| chr7:108043979
|
G | A | 1 | a0013c0068t0002g0227 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4327-83C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108043979 | ||||||
| chr7:108044141
|
C | T | 4 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.4327-245G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108044141 | ||||||
| chr7:108044167
|
C | G | 4 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.4327-271G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108044167 | ||||||
| chr7:108044260
|
G | A | 30 | a0001c0001t0002g0208a0003c0004t0002g0225a0007c0011t0001g0100others(27): Show | 30 | HG01496.hp1 HG02055.hp2 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.4327-364C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108044260 | ||||||
| chr7:108044461
|
T | C | 30 | a0001c0001t0002g0208a0003c0004t0002g0225a0007c0011t0001g0100others(27): Show | 30 | HG01496.hp1 HG02055.hp2 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.4327-565A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108044461 | ||||||
| chr7:108044808
|
C | G | 2 | a0004c0005t0003g0235a0004c0005t0003g0236 | 2 | NA18747.hp1 NA18945.hp1 |
intron_variant | MODIFIER | c.4327-912G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108044808 | ||||||
| chr7:108044955
|
C | CA | 72 | a0001c0001t0001g0014a0001c0001t0001g0030a0001c0001t0001g0275others(69): Show | 72 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(69): Show |
intron_variant | MODIFIER | c.4327-1060dupT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108044955 | ||||||
| chr7:108044973
|
AAG | A | 7 | a0003c0004t0002g0225a0007c0011t0001g0100a0007c0011t0002g0156others(4): Show | 7 | HG01496.hp1 HG02257.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.4327-1079_4327-107 others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108044973 | ||||||
| chr7:108044974
|
AG | A | 22 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(19): Show | 22 | HG02055.hp2 HG02109.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.4327-1079delC | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108044974 | ||||||
| chr7:108044975
|
G | A | 44 | a0001c0001t0002g0208a0001c0002t0001g0019a0001c0002t0001g0183others(41): Show | 44 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.4327-1079C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108044975 | ||||||
| chr7:108044994
|
GA | G | 39 | a0001c0002t0001g0019a0001c0002t0001g0183a0001c0002t0003g0162others(36): Show | 39 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.4327-1099delT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108044994 | ||||||
| chr7:108045140
|
T | TC | 30 | a0001c0001t0002g0208a0003c0004t0002g0225a0007c0011t0001g0100others(27): Show | 30 | HG01496.hp1 HG02055.hp2 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.4327-1245dupG | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108045140 | ||||||
| chr7:108045398
|
T | A | 1 | a0029c0067t0002g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.4327-1502A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108045398 | ||||||
| chr7:108045439
|
C | T | 1 | a0001c0001t0003g0181 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.4327-1543G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108045439 | ||||||
| chr7:108045450
|
A | G | 94 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(91): Show | 94 | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(91): Show |
intron_variant | MODIFIER | c.4327-1554T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108045450 | ||||||
| chr7:108045495
|
G | A | 30 | a0001c0001t0002g0208a0003c0004t0002g0225a0007c0011t0001g0100others(27): Show | 30 | HG01496.hp1 HG02055.hp2 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.4327-1599C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108045495 | ||||||
| chr7:108045595
|
A | G | 2 | a0001c0001t0001g0030a0001c0001t0001g0256 | 2 | NA18950.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.4327-1699T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108045595 | ||||||
| chr7:108045723
|
C | G | 39 | a0001c0002t0001g0019a0001c0002t0001g0183a0001c0002t0003g0162others(36): Show | 39 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.4327-1827G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108045723 | ||||||
| chr7:108045740
|
T | C | 4 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.4327-1844A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108045740 | ||||||
| chr7:108045782
|
A | G | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4327-1886T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108045782 | ||||||
| chr7:108046229
|
T | C | 2 | a0001c0002t0001g0063a0013c0068t0002g0227 | 2 | HG00558.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.4326+1679A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108046229 | ||||||
| chr7:108046236
|
A | AT | 7 | a0001c0001t0001g0164a0001c0002t0001g0017a0001c0002t0003g0053others(4): Show | 7 | HG02055.hp1 HG02145.hp1 HG02738.hp1 others(4): Show |
intron_variant | MODIFIER | c.4326+1671dupA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108046236 | ||||||
| chr7:108046236
|
AT | A | 6 | a0001c0001t0001g0163a0001c0002t0001g0076a0001c0002t0002g0149others(3): Show | 6 | HG02965.hp2 HG03688.hp1 HG03831.hp2 others(3): Show |
intron_variant | MODIFIER | c.4326+1671delA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108046236 | ||||||
| chr7:108046236
|
ATT | A | 9 | a0001c0001t0002g0208a0001c0054t0001g0146a0001c0060t0004g0216others(6): Show | 9 | HG02055.hp2 HG02486.hp2 HG02572.hp2 others(6): Show |
intron_variant | MODIFIER | c.4326+1670_4326+167 others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108046236 | ||||||
| chr7:108046236
|
ATTT | A | 26 | a0003c0004t0002g0225a0007c0011t0002g0102a0007c0011t0002g0156others(23): Show | 26 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(23): Show |
intron_variant | MODIFIER | c.4326+1669_4326+167 others(7): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108046236 | ||||||
| chr7:108046236
|
ATTTT | A | 40 | a0001c0002t0001g0019a0001c0002t0001g0183a0001c0002t0003g0162others(37): Show | 40 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.4326+1668_4326+167 others(8): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108046236 | ||||||
| chr7:108046298
|
C | A | 1 | a0001c0001t0001g0272 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.4326+1610G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108046298 | ||||||
| chr7:108046482
|
T | C | 13 | a0007c0011t0002g0102a0008c0015t0002g0001a0008c0015t0002g0002others(10): Show | 13 | HG02280.hp2 HG02559.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.4326+1426A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108046482 | ||||||
| chr7:108046517
|
A | G | 1 | a0013c0068t0002g0227 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.4326+1391T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108046517 | ||||||
| chr7:108046630
|
A | G | 11 | a0001c0001t0001g0030a0001c0001t0001g0256a0001c0001t0001g0258others(8): Show | 11 | HG00558.hp1 HG02132.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.4326+1278T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108046630 | ||||||
| chr7:108046785
|
C | A | 1 | a0007c0011t0001g0100 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.4326+1123G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108046785 | ||||||
| chr7:108046826
|
C | T | 10 | a0001c0002t0001g0069a0003c0004t0002g0225a0007c0011t0002g0156others(7): Show | 10 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(7): Show |
intron_variant | MODIFIER | c.4326+1082G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108046826 | ||||||
| chr7:108046938
|
T | G | 1 | a0002c0012t0001g0159 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4326+970A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108046938 | ||||||
| chr7:108047131
|
T | C | 1 | a0005c0008t0002g0271 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.4326+777A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108047131 | ||||||
| chr7:108047228
|
T | C | 35 | a0001c0002t0001g0019a0001c0002t0001g0183a0001c0002t0003g0162others(32): Show | 35 | HG00280.hp2 HG00423.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.4326+680A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108047228 | ||||||
| chr7:108047303
|
C | T | 4 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.4326+605G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108047303 | ||||||
| chr7:108047340
|
A | T | 1 | a0002c0012t0001g0159 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.4326+568T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108047340 | ||||||
| chr7:108047384
|
A | G | 6 | a0001c0002t0001g0019a0001c0002t0001g0183a0001c0002t0003g0162others(3): Show | 6 | HG01243.hp2 HG02886.hp2 HG04115.hp1 others(3): Show |
intron_variant | MODIFIER | c.4326+524T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108047384 | ||||||
| chr7:108047389
|
A | G | 2 | a0001c0001t0001g0166a0001c0001t0001g0199 | 2 | HG00621.hp2 HG02523.hp2 |
intron_variant | MODIFIER | c.4326+519T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108047389 | ||||||
| chr7:108047402
|
C | A | 1 | a0041c0033t0001g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.4326+506G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108047402 | ||||||
| chr7:108047544
|
G | T | 1 | a0002c0003t0001g0120 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.4326+364C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108047544 | ||||||
| chr7:108047604
|
G | A | 2 | a0008c0039t0002g0147a0020c0021t0002g0099 | 2 | HG02258.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.4326+304C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108047604 | ||||||
| chr7:108047668
|
T | C | 60 | a0001c0001t0002g0208a0001c0054t0001g0146a0001c0060t0004g0216others(57): Show | 60 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.4326+240A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 28/33 | chr7 | 108047668 | ||||||
| chr7:108048158
|
C | CT | 45 | a0001c0001t0001g0014a0001c0001t0001g0044a0001c0001t0001g0203others(42): Show | 45 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.4123-48dupA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 27/33 | chr7 | 108048158 | ||||||
| chr7:108048158
|
C | CTT | 17 | a0003c0004t0002g0189a0003c0004t0002g0244a0005c0008t0002g0274others(14): Show | 17 | HG01243.hp2 HG02129.hp1 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4123-49_4123-48dup others(2): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 27/33 | chr7 | 108048158 | ||||||
| chr7:108048240
|
C | T | 4 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.4123-129G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 27/33 | chr7 | 108048240 | ||||||
| chr7:108048386
|
A | G | 57 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(54): Show | 57 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(54): Show |
intron_variant | MODIFIER | c.4123-275T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 27/33 | chr7 | 108048386 | ||||||
| chr7:108048452
|
C | G | 1 | a0027c0065t0001g0277 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4123-341G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 27/33 | chr7 | 108048452 | ||||||
| chr7:108048495
|
A | G | 17 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(14): Show | 17 | HG00544.hp1 HG00738.hp1 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.4123-384T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 27/33 | chr7 | 108048495 | ||||||
| chr7:108048660
|
T | C | 1 | a0003c0004t0002g0007 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.4123-549A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 27/33 | chr7 | 108048660 | ||||||
| chr7:108048669
|
A | C | 7 | a0003c0004t0002g0225a0007c0011t0002g0156a0007c0011t0002g0157others(4): Show | 7 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.4123-558T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 27/33 | chr7 | 108048669 | ||||||
| chr7:108048699
|
T | G | 3 | a0001c0001t0003g0247a0001c0002t0003g0022a0001c0002t0003g0046 | 3 | HG01243.hp1 HG02451.hp1 HG02683.hp1 |
intron_variant | MODIFIER | c.4123-588A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 27/33 | chr7 | 108048699 | ||||||
| chr7:108048716
|
T | TG | 107 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0001g0275others(104): Show | 107 | HG00323.hp1 HG00544.hp1 HG00738.hp1 others(104): Show |
intron_variant | MODIFIER | c.4123-606dupC | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 27/33 | chr7 | 108048716 | ||||||
| chr7:108048842
|
G | A | 43 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(40): Show | 43 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(40): Show |
intron_variant | MODIFIER | c.4122+484C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 27/33 | chr7 | 108048842 | ||||||
| chr7:108048850
|
C | A | 1 | a0011c0014t0001g0242 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.4122+476G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 27/33 | chr7 | 108048850 | ||||||
| chr7:108048893
|
G | A | 1 | a0034c0073t0003g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.4122+433C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 27/33 | chr7 | 108048893 | ||||||
| chr7:108049289
|
C | A | 1 | a0017c0043t0001g0084 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.4122+37G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 27/33 | chr7 | 108049289 | ||||||
| chr7:108049536
|
G | A | 4 | a0001c0001t0001g0197a0001c0001t0001g0198a0001c0001t0001g0237others(1): Show | 4 | NA18942.hp1 NA18948.hp2 NA19002.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.3917-5C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 26/33 | chr7 | 108049536 | ||||||
| chr7:108049855
|
A | T | 1 | a0007c0019t0002g0096 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.3917-324T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 26/33 | chr7 | 108049855 | ||||||
| chr7:108049980
|
G | A | 3 | a0001c0001t0001g0262a0001c0001t0001g0265a0001c0002t0001g0018 | 3 | HG02083.hp2 NA19010.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.3917-449C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 26/33 | chr7 | 108049980 | ||||||
| chr7:108050030
|
G | A | 1 | a0006c0010t0001g0291 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.3917-499C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 26/33 | chr7 | 108050030 | ||||||
| chr7:108050050
|
T | C | 4 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.3917-519A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 26/33 | chr7 | 108050050 | ||||||
| chr7:108050559
|
A | G | 1 | a0002c0012t0001g0248 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.3917-1028T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 26/33 | chr7 | 108050559 | ||||||
| chr7:108050700
|
C | A | 3 | a0009c0009t0001g0266a0009c0009t0001g0267a0012c0069t0001g0158 | 3 | HG02451.hp2 HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.3917-1169G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 26/33 | chr7 | 108050700 | ||||||
| chr7:108050772
|
A | T | 1 | a0001c0002t0001g0025 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3917-1241T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 26/33 | chr7 | 108050772 | ||||||
| chr7:108050900
|
G | A | 1 | a0001c0002t0001g0008 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.3916+1197C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 26/33 | chr7 | 108050900 | ||||||
| chr7:108051445
|
A | T | 6 | a0005c0023t0002g0215a0023c0018t0002g0095a0023c0018t0002g0285others(3): Show | 6 | HG01074.hp2 HG02109.hp1 HG02559.hp1 others(3): Show |
intron_variant | MODIFIER | c.3916+652T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 26/33 | chr7 | 108051445 | ||||||
| chr7:108051537
|
C | T | 1 | a0041c0033t0001g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3916+560G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 26/33 | chr7 | 108051537 | ||||||
| chr7:108051660
|
C | T | 6 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(3): Show | 6 | HG00741.hp1 HG02055.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.3916+437G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 26/33 | chr7 | 108051660 | ||||||
| chr7:108051710
|
T | A | 1 | a0008c0039t0002g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3916+387A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 26/33 | chr7 | 108051710 | ||||||
| chr7:108051741
|
C | T | 24 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(21): Show | 24 | HG00544.hp1 HG00738.hp1 HG01243.hp2 others(21): Show |
intron_variant | MODIFIER | c.3916+356G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 26/33 | chr7 | 108051741 | ||||||
| chr7:108051966
|
A | G | 19 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(16): Show | 19 | HG00741.hp1 HG02055.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.3916+131T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 26/33 | chr7 | 108051966 | ||||||
| chr7:108052609
|
GC | G | 3 | a0003c0004t0002g0243a0003c0004t0002g0244a0021c0040t0002g0004 | 3 | HG02486.hp1 NA18906.hp2 NA20129.hp1 |
intron_variant | MODIFIER | c.3756-353delG | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108052609 | ||||||
| chr7:108052705
|
CT | C | 3 | a0015c0017t0001g0011a0015c0017t0001g0070a0015c0017t0001g0071 | 3 | HG01261.hp1 HG01346.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.3756-449delA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108052705 | ||||||
| chr7:108052786
|
C | T | 1 | a0009c0009t0001g0267 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3756-529G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108052786 | ||||||
| chr7:108052992
|
G | A | 6 | a0001c0001t0001g0200a0001c0002t0003g0023a0001c0002t0003g0048others(3): Show | 6 | NA18948.hp1 NA18983.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.3756-735C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108052992 | ||||||
| chr7:108053010
|
T | C | 53 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(50): Show | 53 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.3756-753A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108053010 | ||||||
| chr7:108053018
|
C | T | 1 | a0012c0059t0002g0222 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3756-761G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108053018 | ||||||
| chr7:108053033
|
T | C | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3756-776A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108053033 | ||||||
| chr7:108053234
|
G | C | 1 | a0013c0068t0002g0227 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3756-977C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108053234 | ||||||
| chr7:108053262
|
G | A | 1 | a0002c0007t0001g0140 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.3756-1005C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108053262 | ||||||
| chr7:108053295
|
G | A | 53 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(50): Show | 53 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(50): Show |
intron_variant | MODIFIER | c.3756-1038C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108053295 | ||||||
| chr7:108053382
|
A | T | 1 | a0001c0002t0001g0049 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3756-1125T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108053382 | ||||||
| chr7:108053465
|
G | A | 1 | a0040c0031t0002g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3756-1208C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108053465 | ||||||
| chr7:108053693
|
T | C | 7 | a0003c0004t0002g0225a0007c0011t0002g0156a0007c0011t0002g0157others(4): Show | 7 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.3756-1436A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108053693 | ||||||
| chr7:108054007
|
G | A | 2 | a0001c0002t0001g0032a0001c0002t0003g0034 | 2 | NA18980.hp1 NA19091.hp2 |
intron_variant | MODIFIER | c.3755+1625C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108054007 | ||||||
| chr7:108054014
|
A | G | 11 | a0007c0011t0002g0102a0008c0015t0002g0001a0008c0015t0002g0002others(8): Show | 11 | HG02280.hp2 HG02615.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.3755+1618T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108054014 | ||||||
| chr7:108054059
|
A | G | 4 | a0008c0044t0002g0091a0009c0009t0001g0266a0009c0009t0001g0267others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3755+1573T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108054059 | ||||||
| chr7:108054160
|
A | G | 1 | a0008c0039t0002g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3755+1472T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108054160 | ||||||
| chr7:108054303
|
T | G | 4 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.3755+1329A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108054303 | ||||||
| chr7:108054323
|
C | T | 21 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(18): Show | 21 | HG00544.hp1 HG00738.hp1 HG01243.hp2 others(18): Show |
intron_variant | MODIFIER | c.3755+1309G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108054323 | ||||||
| chr7:108054441
|
G | T | 2 | a0002c0003t0001g0138a0002c0003t0001g0141 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.3755+1191C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108054441 | ||||||
| chr7:108054748
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3755+884A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108054748 | ||||||
| chr7:108054927
|
G | T | 1 | a0001c0001t0001g0230 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3755+705C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108054927 | ||||||
| chr7:108055040
|
C | T | 1 | a0001c0002t0003g0058 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.3755+592G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108055040 | ||||||
| chr7:108055187
|
G | GT | 44 | a0001c0001t0001g0013a0001c0001t0001g0202a0001c0001t0001g0234others(41): Show | 44 | HG00323.hp1 HG00741.hp2 HG01256.hp2 others(41): Show |
intron_variant | MODIFIER | c.3755+444dupA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108055187 | ||||||
| chr7:108055187
|
GT | G | 7 | a0001c0001t0001g0249a0001c0002t0001g0055a0001c0002t0001g0059others(4): Show | 7 | HG01256.hp1 HG01515.hp1 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.3755+444delA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108055187 | ||||||
| chr7:108055187
|
GTTT | G | 52 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(49): Show | 52 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.3755+442_3755+444d others(5): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108055187 | ||||||
| chr7:108055195
|
T | G | 1 | a0041c0033t0001g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3755+437A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108055195 | ||||||
| chr7:108055218
|
C | G | 2 | a0007c0037t0002g0093a0008c0039t0002g0147 | 2 | HG02258.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.3755+414G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108055218 | ||||||
| chr7:108055273
|
G | A | 1 | a0002c0012t0001g0159 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.3755+359C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108055273 | ||||||
| chr7:108055360
|
T | C | 1 | a0013c0068t0002g0227 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3755+272A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108055360 | ||||||
| chr7:108055533
|
T | C | 1 | a0042c0035t0002g0094 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.3755+99A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108055533 | ||||||
| chr7:108055556
|
C | T | 1 | a0001c0002t0001g0018 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.3755+76G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 25/33 | chr7 | 108055556 | ||||||
| chr7:108056078
|
T | A | 1 | a0001c0002t0001g0016 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3380-71A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 24/33 | chr7 | 108056078 | ||||||
| chr7:108056209
|
A | G | 2 | a0001c0001t0001g0194a0001c0001t0001g0195 | 2 | NA18942.hp2 NA18963.hp1 |
intron_variant | MODIFIER | c.3380-202T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 24/33 | chr7 | 108056209 | ||||||
| chr7:108056349
|
C | T | 4 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.3380-342G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 24/33 | chr7 | 108056349 | ||||||
| chr7:108056463
|
C | T | 4 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.3380-456G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 24/33 | chr7 | 108056463 | ||||||
| chr7:108056486
|
G | C | 1 | a0020c0021t0002g0099 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3380-479C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 24/33 | chr7 | 108056486 | ||||||
| chr7:108056681
|
C | G | 6 | a0001c0001t0001g0200a0001c0002t0003g0023a0001c0002t0003g0048others(3): Show | 6 | NA18948.hp1 NA18983.hp2 NA19005.hp2 others(3): Show |
intron_variant | MODIFIER | c.3380-674G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 24/33 | chr7 | 108056681 | ||||||
| chr7:108056971
|
C | CA | 25 | a0001c0001t0001g0014a0001c0001t0001g0169a0001c0001t0001g0198others(22): Show | 25 | HG01175.hp2 HG01243.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.3379+860dupT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 24/33 | chr7 | 108056971 | ||||||
| chr7:108057098
|
A | T | 4 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.3379+734T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 24/33 | chr7 | 108057098 | ||||||
| chr7:108057200
|
G | T | 1 | a0007c0037t0002g0093 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3379+632C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 24/33 | chr7 | 108057200 | ||||||
| chr7:108057271
|
C | T | 90 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(87): Show | 90 | HG00140.hp1 HG00280.hp1 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.3379+561G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 24/33 | chr7 | 108057271 | ||||||
| chr7:108057272
|
G | A | 1 | a0005c0008t0002g0223 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3379+560C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 24/33 | chr7 | 108057272 | ||||||
| chr7:108057327
|
G | A | 1 | a0007c0037t0002g0093 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3379+505C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 24/33 | chr7 | 108057327 | ||||||
| chr7:108057339
|
A | G | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3379+493T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 24/33 | chr7 | 108057339 | ||||||
| chr7:108057462
|
G | A | 1 | a0034c0073t0003g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.3379+370C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 24/33 | chr7 | 108057462 | ||||||
| chr7:108057535
|
T | G | 4 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.3379+297A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 24/33 | chr7 | 108057535 | ||||||
| chr7:108057565
|
T | G | 1 | a0001c0001t0001g0230 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.3379+267A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 24/33 | chr7 | 108057565 | ||||||
| chr7:108057583
|
T | A | 2 | a0005c0008t0002g0271a0014c0025t0002g0233 | 2 | HG02165.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.3379+249A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 24/33 | chr7 | 108057583 | ||||||
| chr7:108057776
|
C | A | 4 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.3379+56G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 24/33 | chr7 | 108057776 | ||||||
| chr7:108057932
|
T | C | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | splice_region_variant&intron_variant | LOW | c.3283-4A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108057932 | ||||||
| chr7:108058044
|
G | A | 1 | a0013c0068t0002g0227 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.3283-116C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108058044 | ||||||
| chr7:108058128
|
G | C | 1 | a0022c0034t0001g0103 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.3283-200C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108058128 | ||||||
| chr7:108058167
|
C | T | 52 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(49): Show | 52 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.3283-239G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108058167 | ||||||
| chr7:108058327
|
A | G | 52 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(49): Show | 52 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(49): Show |
intron_variant | MODIFIER | c.3283-399T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108058327 | ||||||
| chr7:108058486
|
G | A | 1 | a0041c0033t0001g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3283-558C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108058486 | ||||||
| chr7:108058534
|
A | T | 1 | a0007c0037t0002g0093 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3283-606T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108058534 | ||||||
| chr7:108058678
|
C | T | 1 | a0022c0029t0002g0284 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3283-750G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108058678 | ||||||
| chr7:108058819
|
G | A | 5 | a0001c0002t0001g0026a0001c0002t0001g0045a0001c0002t0001g0065others(2): Show | 5 | HG01099.hp2 HG01255.hp1 HG01981.hp1 others(2): Show |
intron_variant | MODIFIER | c.3283-891C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108058819 | ||||||
| chr7:108058820
|
C | A | 1 | a0019c0020t0001g0088 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.3283-892G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108058820 | ||||||
| chr7:108058944
|
C | T | 2 | a0001c0001t0001g0193a0004c0071t0001g0239 | 2 | HG03688.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.3283-1016G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108058944 | ||||||
| chr7:108059097
|
C | CT | 42 | a0001c0001t0001g0014a0001c0001t0001g0039a0001c0001t0001g0163others(39): Show | 42 | HG00558.hp1 HG01069.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.3283-1170dupA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108059097 | ||||||
| chr7:108059097
|
CT | C | 16 | a0001c0001t0001g0040a0001c0001t0001g0191a0001c0001t0001g0195others(13): Show | 16 | HG00741.hp1 HG01074.hp2 HG01169.hp2 others(13): Show |
intron_variant | MODIFIER | c.3283-1170delA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108059097 | ||||||
| chr7:108059097
|
CTT | C | 7 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.3283-1171_3283-117 others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108059097 | ||||||
| chr7:108059097
|
CTTT | C | 17 | a0003c0004t0002g0225a0007c0011t0002g0102a0007c0011t0002g0156others(14): Show | 17 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(14): Show |
intron_variant | MODIFIER | c.3283-1172_3283-117 others(7): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108059097 | ||||||
| chr7:108059097
|
CTTTTTTT others(4): Show |
C | 25 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(22): Show | 25 | HG00544.hp1 HG00738.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.3283-1180_3283-117 others(15): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108059097 | ||||||
| chr7:108059130
|
G | A | 1 | a0038c0036t0002g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.3283-1202C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108059130 | ||||||
| chr7:108059262
|
T | C | 15 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(12): Show | 15 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.3283-1334A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108059262 | ||||||
| chr7:108059317
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3283-1389A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108059317 | ||||||
| chr7:108059690
|
C | T | 7 | a0003c0004t0002g0225a0007c0011t0002g0156a0007c0011t0002g0157others(4): Show | 7 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.3283-1762G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108059690 | ||||||
| chr7:108059715
|
T | TG | 15 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(12): Show | 15 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.3283-1788dupC | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108059715 | ||||||
| chr7:108059761
|
T | TG | 15 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(12): Show | 15 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.3283-1834dupC | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108059761 | ||||||
| chr7:108059852
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.3283-1924G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108059852 | ||||||
| chr7:108059947
|
A | C | 4 | a0011c0014t0001g0224a0011c0014t0001g0242a0014c0025t0001g0118others(1): Show | 4 | HG00280.hp2 HG02148.hp1 HG02293.hp1 others(1): Show |
intron_variant | MODIFIER | c.3283-2019T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108059947 | ||||||
| chr7:108059980
|
T | C | 15 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(12): Show | 15 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.3283-2052A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108059980 | ||||||
| chr7:108060099
|
G | A | 25 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(22): Show | 25 | HG00544.hp1 HG00738.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.3283-2171C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108060099 | ||||||
| chr7:108060227
|
T | C | 1 | a0001c0001t0001g0169 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.3283-2299A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108060227 | ||||||
| chr7:108060302
|
G | T | 15 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(12): Show | 15 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.3283-2374C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108060302 | ||||||
| chr7:108060448
|
G | A | 10 | a0007c0011t0002g0102a0008c0015t0002g0001a0008c0015t0002g0002others(7): Show | 10 | HG02280.hp2 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.3282+2326C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108060448 | ||||||
| chr7:108060462
|
T | C | 1 | a0012c0059t0002g0222 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3282+2312A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108060462 | ||||||
| chr7:108060563
|
G | A | 1 | a0001c0001t0001g0219 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.3282+2211C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108060563 | ||||||
| chr7:108060728
|
T | A | 1 | a0014c0025t0001g0118 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.3282+2046A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108060728 | ||||||
| chr7:108060783
|
G | A | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.3282+1991C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108060783 | ||||||
| chr7:108060950
|
T | C | 2 | a0020c0021t0002g0098a0020c0021t0002g0099 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3282+1824A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108060950 | ||||||
| chr7:108061027
|
G | A | 15 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(12): Show | 15 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.3282+1747C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108061027 | ||||||
| chr7:108061134
|
T | G | 15 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(12): Show | 15 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.3282+1640A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108061134 | ||||||
| chr7:108061254
|
AG | A | 4 | a0008c0044t0002g0091a0009c0009t0001g0266a0009c0009t0001g0267others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3282+1519delC | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108061254 | ||||||
| chr7:108061275
|
G | A | 2 | a0020c0021t0002g0098a0020c0021t0002g0099 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.3282+1499C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108061275 | ||||||
| chr7:108061291
|
A | G | 1 | a0041c0033t0001g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3282+1483T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108061291 | ||||||
| chr7:108061467
|
C | T | 15 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(12): Show | 15 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.3282+1307G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108061467 | ||||||
| chr7:108061468
|
G | A | 2 | a0003c0004t0002g0217a0003c0004t0002g0218 | 2 | HG02559.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.3282+1306C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108061468 | ||||||
| chr7:108061571
|
T | C | 6 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(3): Show | 6 | HG00741.hp1 HG02055.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.3282+1203A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108061571 | ||||||
| chr7:108061641
|
A | G | 1 | a0001c0060t0004g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3282+1133T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108061641 | ||||||
| chr7:108061646
|
G | A | 1 | a0041c0033t0001g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.3282+1128C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108061646 | ||||||
| chr7:108061653
|
C | T | 16 | a0001c0001t0001g0167a0001c0054t0001g0146a0001c0060t0004g0216others(13): Show | 16 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(13): Show |
intron_variant | MODIFIER | c.3282+1121G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108061653 | ||||||
| chr7:108061739
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3282+1035G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108061739 | ||||||
| chr7:108061739
|
CA | C | 65 | a0001c0001t0001g0013a0001c0001t0001g0106a0001c0001t0001g0209others(62): Show | 65 | HG00323.hp1 HG01256.hp2 HG01258.hp1 others(62): Show |
intron_variant | MODIFIER | c.3282+1034delT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108061739 | ||||||
| chr7:108061739
|
CAA | C | 41 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(38): Show | 41 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(38): Show |
intron_variant | MODIFIER | c.3282+1033_3282+103 others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108061739 | ||||||
| chr7:108061742
|
A | G | 1 | a0006c0027t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3282+1032T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108061742 | ||||||
| chr7:108062033
|
C | T | 15 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(12): Show | 15 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.3282+741G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108062033 | ||||||
| chr7:108062222
|
A | G | 2 | a0009c0009t0001g0228a0009c0009t0001g0229 | 2 | HG00544.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.3282+552T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108062222 | ||||||
| chr7:108062311
|
G | A | 15 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(12): Show | 15 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(12): Show |
intron_variant | MODIFIER | c.3282+463C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108062311 | ||||||
| chr7:108062336
|
A | G | 17 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(14): Show | 17 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(14): Show |
intron_variant | MODIFIER | c.3282+438T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108062336 | ||||||
| chr7:108062432
|
C | A | 108 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(105): Show | 108 | HG00323.hp1 HG00544.hp1 HG00738.hp1 others(105): Show |
intron_variant | MODIFIER | c.3282+342G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108062432 | ||||||
| chr7:108062563
|
G | A | 7 | a0001c0002t0001g0016a0001c0002t0001g0024a0001c0002t0001g0049others(4): Show | 7 | HG00738.hp2 HG00741.hp2 HG01106.hp2 others(4): Show |
intron_variant | MODIFIER | c.3282+211C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108062563 | ||||||
| chr7:108062571
|
CG | C | 10 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(7): Show | 10 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.3282+202delC | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108062571 | ||||||
| chr7:108062607
|
G | T | 1 | a0001c0001t0001g0041 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3282+167C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108062607 | ||||||
| chr7:108062611
|
T | C | 5 | a0007c0011t0002g0102a0008c0015t0002g0001a0008c0015t0002g0002others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.3282+163A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108062611 | ||||||
| chr7:108062692
|
G | T | 6 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(3): Show | 6 | HG00741.hp1 HG02055.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.3282+82C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 23/33 | chr7 | 108062692 | ||||||
| chr7:108063100
|
G | T | 1 | a0001c0001t0003g0185 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.3062-106C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 22/33 | chr7 | 108063100 | ||||||
| chr7:108063125
|
A | T | 1 | a0001c0001t0001g0014 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3062-131T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 22/33 | chr7 | 108063125 | ||||||
| chr7:108063150
|
T | A | 9 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(6): Show | 9 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.3062-156A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 22/33 | chr7 | 108063150 | ||||||
| chr7:108063220
|
G | A | 1 | a0001c0001t0001g0206 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.3062-226C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 22/33 | chr7 | 108063220 | ||||||
| chr7:108063281
|
A | C | 1 | a0021c0028t0002g0092 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.3062-287T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 22/33 | chr7 | 108063281 | ||||||
| chr7:108063295
|
C | G | 3 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246 | 3 | HG02572.hp2 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.3062-301G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 22/33 | chr7 | 108063295 | ||||||
| chr7:108063666
|
C | T | 1 | a0017c0030t0002g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.3061+95G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 22/33 | chr7 | 108063666 | ||||||
| chr7:108063667
|
T | A | 10 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(7): Show | 10 | HG02280.hp2 HG02572.hp2 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.3061+94A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 22/33 | chr7 | 108063667 | ||||||
| chr7:108063687
|
T | C | 1 | a0003c0004t0002g0225 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.3061+74A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 22/33 | chr7 | 108063687 | ||||||
| chr7:108063754
|
G | C | 7 | a0003c0004t0002g0225a0007c0011t0002g0156a0007c0011t0002g0157others(4): Show | 7 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.3061+7C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 22/33 | chr7 | 108063754 | ||||||
| chr7:108064203
|
G | A | 7 | a0007c0011t0002g0102a0008c0015t0002g0001a0008c0015t0002g0002others(4): Show | 7 | HG02280.hp2 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2837-218C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 21/33 | chr7 | 108064203 | ||||||
| chr7:108064243
|
T | C | 65 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(62): Show | 65 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(62): Show |
intron_variant | MODIFIER | c.2837-258A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 21/33 | chr7 | 108064243 | ||||||
| chr7:108064409
|
C | T | 7 | a0007c0011t0002g0102a0008c0015t0002g0001a0008c0015t0002g0002others(4): Show | 7 | HG02280.hp2 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.2837-424G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 21/33 | chr7 | 108064409 | ||||||
| chr7:108064411
|
A | C | 1 | a0001c0002t0001g0017 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2837-426T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 21/33 | chr7 | 108064411 | ||||||
| chr7:108064700
|
C | G | 1 | a0028c0064t0002g0283 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2837-715G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 21/33 | chr7 | 108064700 | ||||||
| chr7:108064785
|
T | C | 5 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(2): Show | 5 | HG00741.hp1 HG02055.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2837-800A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 21/33 | chr7 | 108064785 | ||||||
| chr7:108064893
|
CT | C | 71 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(68): Show | 71 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(68): Show |
intron_variant | MODIFIER | c.2836+868delA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 21/33 | chr7 | 108064893 | ||||||
| chr7:108065150
|
C | A | 48 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(45): Show | 48 | HG00140.hp1 HG00544.hp2 HG00558.hp2 others(45): Show |
intron_variant | MODIFIER | c.2836+612G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 21/33 | chr7 | 108065150 | ||||||
| chr7:108065248
|
G | A | 55 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(52): Show | 55 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.2836+514C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 21/33 | chr7 | 108065248 | ||||||
| chr7:108065323
|
GA | G | 55 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(52): Show | 55 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(52): Show |
intron_variant | MODIFIER | c.2836+438delT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 21/33 | chr7 | 108065323 | ||||||
| chr7:108065332
|
T | G | 2 | a0001c0001t0001g0190a0001c0001t0001g0191 | 2 | HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.2836+430A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 21/33 | chr7 | 108065332 | ||||||
| chr7:108065467
|
G | A | 3 | a0001c0001t0001g0262a0001c0001t0001g0265a0001c0002t0001g0018 | 3 | HG02083.hp2 NA19010.hp2 NA19090.hp2 |
intron_variant | MODIFIER | c.2836+295C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 21/33 | chr7 | 108065467 | ||||||
| chr7:108065467
|
G | T | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2836+295C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 21/33 | chr7 | 108065467 | ||||||
| chr7:108065591
|
G | A | 3 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246 | 3 | HG02572.hp2 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2836+171C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 21/33 | chr7 | 108065591 | ||||||
| chr7:108065646
|
T | C | 6 | a0001c0002t0001g0056a0001c0006t0005g0292a0004c0005t0003g0179others(3): Show | 6 | HG00621.hp1 HG02132.hp2 NA18980.hp2 others(3): Show |
intron_variant | MODIFIER | c.2836+116A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 21/33 | chr7 | 108065646 | ||||||
| chr7:108065944
|
A | G | 3 | a0007c0011t0002g0102a0008c0038t0002g0152a0012c0022t0002g0148 | 3 | HG02280.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2679-25T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 20/33 | chr7 | 108065944 | ||||||
| chr7:108066053
|
AAACGACT others(12): Show |
A | 7 | a0003c0004t0002g0225a0007c0011t0002g0156a0007c0011t0002g0157others(4): Show | 7 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2679-153_2679-135d others(21): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 20/33 | chr7 | 108066053 | ||||||
| chr7:108066074
|
T | C | 7 | a0003c0004t0002g0225a0007c0011t0002g0156a0007c0011t0002g0157others(4): Show | 7 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2679-155A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 20/33 | chr7 | 108066074 | ||||||
| chr7:108066087
|
C | T | 4 | a0001c0001t0001g0188a0001c0002t0001g0019a0001c0002t0001g0183others(1): Show | 4 | HG01975.hp2 NA18950.hp2 NA18990.hp2 others(1): Show |
intron_variant | MODIFIER | c.2679-168G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 20/33 | chr7 | 108066087 | ||||||
| chr7:108066108
|
T | C | 1 | a0001c0002t0001g0079 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2679-189A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 20/33 | chr7 | 108066108 | ||||||
| chr7:108066147
|
T | C | 1 | a0002c0003t0001g0111 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2678+222A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 20/33 | chr7 | 108066147 | ||||||
| chr7:108066264
|
C | A | 1 | a0001c0001t0001g0197 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.2678+105G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 20/33 | chr7 | 108066264 | ||||||
| chr7:108066695
|
C | A | 3 | a0001c0001t0001g0252a0001c0001t0001g0253a0001c0001t0001g0254 | 3 | HG01074.hp1 HG01433.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.2447-95G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 19/33 | chr7 | 108066695 | ||||||
| chr7:108066743
|
T | C | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2447-143A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 19/33 | chr7 | 108066743 | ||||||
| chr7:108066907
|
A | C | 3 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246 | 3 | HG02572.hp2 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2447-307T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 19/33 | chr7 | 108066907 | ||||||
| chr7:108067046
|
G | A | 1 | a0003c0004t0002g0225 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2447-446C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 19/33 | chr7 | 108067046 | ||||||
| chr7:108067113
|
T | C | 1 | a0008c0039t0002g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2447-513A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 19/33 | chr7 | 108067113 | ||||||
| chr7:108067352
|
T | C | 1 | a0008c0039t0002g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2446+664A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 19/33 | chr7 | 108067352 | ||||||
| chr7:108067459
|
G | A | 1 | a0001c0002t0001g0043 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.2446+557C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 19/33 | chr7 | 108067459 | ||||||
| chr7:108067535
|
G | C | 1 | a0006c0027t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2446+481C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 19/33 | chr7 | 108067535 | ||||||
| chr7:108067716
|
C | T | 5 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(2): Show | 5 | HG00741.hp1 HG02055.hp2 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2446+300G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 19/33 | chr7 | 108067716 | ||||||
| chr7:108067928
|
C | T | 37 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(34): Show | 37 | HG00544.hp1 HG00738.hp1 HG00741.hp1 others(34): Show |
intron_variant | MODIFIER | c.2446+88G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 19/33 | chr7 | 108067928 | ||||||
| chr7:108068453
|
A | G | 3 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246 | 3 | HG02572.hp2 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2303-294T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 18/33 | chr7 | 108068453 | ||||||
| chr7:108068516
|
A | G | 1 | a0034c0073t0003g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.2303-357T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 18/33 | chr7 | 108068516 | ||||||
| chr7:108068520
|
C | CTTTA | 66 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(63): Show | 66 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.2303-365_2303-362d others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 18/33 | chr7 | 108068520 | ||||||
| chr7:108068652
|
G | T | 1 | a0006c0016t0002g0086 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.2303-493C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 18/33 | chr7 | 108068652 | ||||||
| chr7:108068680
|
T | TTTTG | 7 | a0001c0002t0001g0037a0002c0003t0001g0132a0002c0003t0001g0133others(4): Show | 7 | HG02293.hp1 HG02683.hp2 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.2303-525_2303-522d others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 18/33 | chr7 | 108068680 | ||||||
| chr7:108068982
|
G | C | 33 | a0001c0006t0005g0292a0002c0003t0001g0082a0002c0003t0001g0111others(30): Show | 33 | HG00323.hp1 HG00621.hp1 HG01256.hp2 others(30): Show |
intron_variant | MODIFIER | c.2302+726C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 18/33 | chr7 | 108068982 | ||||||
| chr7:108069043
|
C | T | 2 | a0009c0009t0001g0228a0009c0009t0001g0229 | 2 | HG00544.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.2302+665G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 18/33 | chr7 | 108069043 | ||||||
| chr7:108069083
|
C | T | 10 | a0003c0004t0002g0217a0006c0016t0002g0086a0009c0009t0001g0228others(7): Show | 10 | HG00280.hp2 HG00544.hp1 HG01243.hp2 others(7): Show |
intron_variant | MODIFIER | c.2302+625G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 18/33 | chr7 | 108069083 | ||||||
| chr7:108069101
|
C | T | 5 | a0007c0011t0002g0102a0008c0015t0002g0001a0008c0015t0002g0002others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2302+607G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 18/33 | chr7 | 108069101 | ||||||
| chr7:108069184
|
T | G | 1 | a0008c0039t0002g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2302+524A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 18/33 | chr7 | 108069184 | ||||||
| chr7:108069284
|
G | A | 1 | a0007c0011t0002g0157 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2302+424C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 18/33 | chr7 | 108069284 | ||||||
| chr7:108069368
|
A | G | 2 | a0020c0021t0002g0098a0020c0021t0002g0099 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2302+340T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 18/33 | chr7 | 108069368 | ||||||
| chr7:108069470
|
A | G | 1 | a0024c0047t0001g0165 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.2302+238T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 18/33 | chr7 | 108069470 | ||||||
| chr7:108069494
|
C | A | 3 | a0007c0011t0002g0102a0008c0038t0002g0152a0012c0022t0002g0148 | 3 | HG02280.hp2 HG02970.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.2302+214G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 18/33 | chr7 | 108069494 | ||||||
| chr7:108069615
|
G | A | 2 | a0013c0026t0002g0153a0013c0026t0002g0154 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.2302+93C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 18/33 | chr7 | 108069615 | ||||||
| chr7:108069678
|
C | T | 40 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(37): Show | 40 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2302+30G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 18/33 | chr7 | 108069678 | ||||||
| chr7:108070058
|
T | G | 2 | a0017c0043t0001g0084a0041c0033t0001g0090 | 2 | HG02809.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.2125-173A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108070058 | ||||||
| chr7:108070119
|
T | C | 8 | a0007c0011t0001g0100a0007c0037t0002g0093a0008c0039t0002g0147others(5): Show | 8 | HG00741.hp1 HG02258.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2125-234A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108070119 | ||||||
| chr7:108070154
|
T | G | 32 | a0001c0001t0001g0013a0001c0001t0001g0119a0001c0001t0001g0150others(29): Show | 32 | HG00323.hp2 HG00423.hp1 HG01074.hp1 others(29): Show |
intron_variant | MODIFIER | c.2125-269A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108070154 | ||||||
| chr7:108070172
|
CA | C | 3 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246 | 3 | HG02572.hp2 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2125-288delT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108070172 | ||||||
| chr7:108070265
|
T | C | 1 | a0007c0011t0001g0100 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2125-380A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108070265 | ||||||
| chr7:108070567
|
C | G | 1 | a0007c0037t0002g0093 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.2125-682G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108070567 | ||||||
| chr7:108070624
|
T | C | 1 | a0010c0013t0002g0171 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2125-739A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108070624 | ||||||
| chr7:108070782
|
A | G | 4 | a0007c0011t0001g0100a0007c0037t0002g0093a0009c0009t0001g0266others(1): Show | 4 | HG02965.hp1 HG02970.hp1 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.2125-897T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108070782 | ||||||
| chr7:108070831
|
T | C | 1 | a0008c0039t0002g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2125-946A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108070831 | ||||||
| chr7:108070841
|
C | T | 1 | a0001c0001t0001g0206 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.2125-956G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108070841 | ||||||
| chr7:108070880
|
G | A | 1 | a0023c0018t0002g0285 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.2125-995C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108070880 | ||||||
| chr7:108070906
|
C | G | 2 | a0001c0001t0001g0192a0001c0001t0001g0201 | 2 | HG01255.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.2125-1021G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108070906 | ||||||
| chr7:108070982
|
C | T | 2 | a0005c0023t0002g0215a0026c0056t0002g0232 | 2 | HG02647.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2125-1097G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108070982 | ||||||
| chr7:108071020
|
G | A | 39 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(36): Show | 39 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.2125-1135C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108071020 | ||||||
| chr7:108071121
|
G | C | 5 | a0007c0011t0002g0102a0008c0015t0002g0001a0008c0015t0002g0002others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2125-1236C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108071121 | ||||||
| chr7:108071126
|
CA | C | 39 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(36): Show | 39 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.2125-1242delT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108071126 | ||||||
| chr7:108071161
|
C | T | 5 | a0007c0011t0002g0102a0008c0015t0002g0001a0008c0015t0002g0002others(2): Show | 5 | HG02280.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.2125-1276G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108071161 | ||||||
| chr7:108071178
|
C | T | 1 | a0001c0001t0001g0201 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2125-1293G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108071178 | ||||||
| chr7:108071248
|
C | T | 4 | a0001c0001t0001g0177a0001c0001t0001g0206a0001c0001t0001g0219others(1): Show | 4 | HG01069.hp1 HG01361.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.2125-1363G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108071248 | ||||||
| chr7:108071346
|
CA | C | 25 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(22): Show | 25 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.2125-1462delT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108071346 | ||||||
| chr7:108071347
|
A | C | 22 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(19): Show | 22 | HG01433.hp2 HG01496.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.2125-1462T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108071347 | ||||||
| chr7:108071354
|
T | C | 25 | a0003c0004t0002g0007a0003c0004t0002g0175a0003c0004t0002g0189others(22): Show | 25 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(22): Show |
intron_variant | MODIFIER | c.2125-1469A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108071354 | ||||||
| chr7:108071362
|
C | A | 2 | a0001c0006t0001g0144a0001c0006t0001g0145 | 2 | NA18968.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.2125-1477G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108071362 | ||||||
| chr7:108071601
|
G | A | 4 | a0012c0059t0002g0222a0022c0029t0002g0284a0022c0034t0001g0103others(1): Show | 4 | HG02723.hp2 HG02922.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.2125-1716C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108071601 | ||||||
| chr7:108071629
|
T | C | 47 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(44): Show | 47 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(44): Show |
intron_variant | MODIFIER | c.2125-1744A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108071629 | ||||||
| chr7:108071663
|
A | G | 1 | a0021c0028t0002g0092 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.2125-1778T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108071663 | ||||||
| chr7:108071796
|
C | G | 1 | a0017c0043t0001g0084 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2125-1911G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108071796 | ||||||
| chr7:108071934
|
CT | C | 40 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(37): Show | 40 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2125-2050delA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108071934 | ||||||
| chr7:108072311
|
T | C | 48 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(45): Show | 48 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.2125-2426A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108072311 | ||||||
| chr7:108072657
|
C | G | 48 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(45): Show | 48 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.2125-2772G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108072657 | ||||||
| chr7:108072659
|
C | T | 2 | a0020c0021t0002g0098a0020c0021t0002g0099 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2125-2774G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108072659 | ||||||
| chr7:108072694
|
G | A | 10 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(7): Show | 10 | HG01433.hp2 HG02055.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.2125-2809C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108072694 | ||||||
| chr7:108072704
|
T | C | 48 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(45): Show | 48 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.2125-2819A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108072704 | ||||||
| chr7:108072714
|
G | A | 40 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(37): Show | 40 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2125-2829C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108072714 | ||||||
| chr7:108072816
|
G | A | 4 | a0008c0039t0002g0147a0020c0021t0002g0098a0020c0021t0002g0099others(1): Show | 4 | HG00741.hp1 HG02258.hp1 HG03139.hp1 others(1): Show |
intron_variant | MODIFIER | c.2125-2931C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108072816 | ||||||
| chr7:108072829
|
C | T | 40 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(37): Show | 40 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2125-2944G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108072829 | ||||||
| chr7:108072836
|
C | T | 40 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(37): Show | 40 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.2125-2951G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108072836 | ||||||
| chr7:108072870
|
A | G | 48 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(45): Show | 48 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.2125-2985T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108072870 | ||||||
| chr7:108072946
|
T | C | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2125-3061A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108072946 | ||||||
| chr7:108073098
|
A | G | 65 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(62): Show | 65 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.2125-3213T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108073098 | ||||||
| chr7:108073146
|
C | T | 1 | a0011c0014t0001g0214 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.2125-3261G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108073146 | ||||||
| chr7:108073257
|
C | T | 2 | a0001c0001t0003g0174a0001c0001t0003g0181 | 2 | NA18949.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.2125-3372G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108073257 | ||||||
| chr7:108073573
|
G | C | 39 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(36): Show | 39 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.2124+3371C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108073573 | ||||||
| chr7:108073607
|
A | C | 41 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(38): Show | 41 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.2124+3337T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108073607 | ||||||
| chr7:108073762
|
C | T | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2124+3182G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108073762 | ||||||
| chr7:108073810
|
C | T | 7 | a0003c0004t0002g0225a0007c0011t0002g0156a0007c0011t0002g0157others(4): Show | 7 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2124+3134G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108073810 | ||||||
| chr7:108073963
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.2124+2981C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108073963 | ||||||
| chr7:108073985
|
T | C | 3 | a0001c0002t0001g0009a0001c0002t0001g0076a0001c0002t0001g0077 | 3 | HG03688.hp2 HG03834.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.2124+2959A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108073985 | ||||||
| chr7:108074574
|
G | T | 2 | a0020c0021t0002g0098a0020c0021t0002g0099 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2124+2370C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108074574 | ||||||
| chr7:108074716
|
C | G | 15 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(12): Show | 15 | HG01433.hp2 HG02055.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2124+2228G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108074716 | ||||||
| chr7:108074728
|
C | A | 17 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(14): Show | 17 | HG01433.hp2 HG02055.hp1 HG02055.hp2 others(14): Show |
intron_variant | MODIFIER | c.2124+2216G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108074728 | ||||||
| chr7:108074941
|
T | C | 3 | a0006c0016t0002g0101a0013c0026t0002g0153a0013c0026t0002g0154 | 3 | HG02896.hp2 HG02897.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.2124+2003A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108074941 | ||||||
| chr7:108075212
|
C | T | 3 | a0002c0003t0001g0122a0002c0049t0001g0204a0033c0051t0001g0205 | 3 | NA18963.hp2 NA18989.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.2124+1732G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108075212 | ||||||
| chr7:108075213
|
G | A | 58 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(55): Show | 58 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.2124+1731C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108075213 | ||||||
| chr7:108075280
|
T | A | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2124+1664A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108075280 | ||||||
| chr7:108075420
|
A | G | 2 | a0001c0001t0001g0167a0001c0001t0001g0241 | 2 | NA18975.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.2124+1524T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108075420 | ||||||
| chr7:108075437
|
T | C | 1 | a0001c0002t0003g0078 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2124+1507A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108075437 | ||||||
| chr7:108075460
|
G | A | 28 | a0001c0001t0001g0013a0001c0001t0001g0119a0001c0001t0001g0150others(25): Show | 28 | HG00323.hp2 HG00423.hp1 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.2124+1484C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108075460 | ||||||
| chr7:108075684
|
G | A | 2 | a0001c0001t0001g0263a0001c0001t0003g0185 | 2 | HG02083.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.2124+1260C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108075684 | ||||||
| chr7:108075829
|
G | A | 3 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246 | 3 | HG02572.hp2 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2124+1115C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108075829 | ||||||
| chr7:108075839
|
A | C | 3 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246 | 3 | HG02572.hp2 HG02723.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.2124+1105T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108075839 | ||||||
| chr7:108075855
|
G | A | 1 | a0001c0001t0003g0015 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.2124+1089C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108075855 | ||||||
| chr7:108075954
|
G | A | 1 | a0010c0013t0002g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.2124+990C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108075954 | ||||||
| chr7:108076068
|
T | A | 2 | a0020c0021t0002g0098a0020c0021t0002g0099 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2124+876A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108076068 | ||||||
| chr7:108076218
|
T | C | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2124+726A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108076218 | ||||||
| chr7:108076262
|
A | C | 59 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(56): Show | 59 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(56): Show |
intron_variant | MODIFIER | c.2124+682T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108076262 | ||||||
| chr7:108076322
|
T | C | 66 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(63): Show | 66 | HG00280.hp2 HG00544.hp1 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.2124+622A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108076322 | ||||||
| chr7:108076621
|
G | A | 2 | a0020c0021t0002g0098a0020c0021t0002g0099 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2124+323C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108076621 | ||||||
| chr7:108076644
|
T | C | 1 | a0028c0064t0002g0283 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.2124+300A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108076644 | ||||||
| chr7:108076880
|
T | C | 8 | a0003c0004t0002g0225a0007c0011t0002g0156a0007c0011t0002g0157others(5): Show | 8 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2124+64A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 17/33 | chr7 | 108076880 | ||||||
| chr7:108077120
|
C | G | 7 | a0003c0004t0002g0225a0007c0011t0002g0156a0007c0011t0002g0157others(4): Show | 7 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.2004-56G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 16/33 | chr7 | 108077120 | ||||||
| chr7:108077357
|
G | A | 1 | a0001c0002t0001g0064 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.2004-293C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 16/33 | chr7 | 108077357 | ||||||
| chr7:108077487
|
G | A | 1 | a0001c0054t0001g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2004-423C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 16/33 | chr7 | 108077487 | ||||||
| chr7:108077567
|
T | C | 2 | a0008c0044t0002g0091a0012c0069t0001g0158 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.2004-503A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 16/33 | chr7 | 108077567 | ||||||
| chr7:108077693
|
C | CA | 6 | a0001c0001t0001g0260a0003c0004t0002g0007a0003c0004t0002g0243others(3): Show | 6 | HG00738.hp1 HG01943.hp2 HG02486.hp1 others(3): Show |
intron_variant | MODIFIER | c.2003+507dupT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 16/33 | chr7 | 108077693 | ||||||
| chr7:108077818
|
G | A | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2003+383C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 16/33 | chr7 | 108077818 | ||||||
| chr7:108078116
|
C | G | 8 | a0003c0004t0002g0225a0007c0011t0002g0156a0007c0011t0002g0157others(5): Show | 8 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.2003+85G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 16/33 | chr7 | 108078116 | ||||||
| chr7:108078344
|
C | T | 16 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208others(13): Show | 16 | HG01433.hp2 HG02055.hp1 HG02055.hp2 others(13): Show |
intron_variant | MODIFIER | c.1888-28G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 15/33 | chr7 | 108078344 | ||||||
| chr7:108078468
|
G | A | 1 | a0011c0014t0001g0214 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1888-152C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 15/33 | chr7 | 108078468 | ||||||
| chr7:108078497
|
C | A | 8 | a0003c0004t0002g0225a0007c0011t0002g0156a0007c0011t0002g0157others(5): Show | 8 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1888-181G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 15/33 | chr7 | 108078497 | ||||||
| chr7:108078885
|
T | C | 8 | a0003c0004t0002g0225a0007c0011t0002g0156a0007c0011t0002g0157others(5): Show | 8 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1888-569A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 15/33 | chr7 | 108078885 | ||||||
| chr7:108078931
|
G | A | 1 | a0008c0039t0002g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1888-615C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 15/33 | chr7 | 108078931 | ||||||
| chr7:108078955
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208 | 3 | HG02895.hp2 HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.1888-639G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 15/33 | chr7 | 108078955 | ||||||
| chr7:108078990
|
C | G | 4 | a0001c0001t0001g0119a0001c0001t0001g0192a0001c0001t0001g0201others(1): Show | 4 | HG01175.hp1 HG01255.hp2 HG01516.hp2 others(1): Show |
intron_variant | MODIFIER | c.1887+611G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 15/33 | chr7 | 108078990 | ||||||
| chr7:108079019
|
G | C | 7 | a0003c0004t0002g0225a0007c0011t0002g0156a0007c0011t0002g0157others(4): Show | 7 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1887+582C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 15/33 | chr7 | 108079019 | ||||||
| chr7:108079275
|
T | C | 8 | a0003c0004t0002g0225a0007c0011t0002g0156a0007c0011t0002g0157others(5): Show | 8 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1887+326A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 15/33 | chr7 | 108079275 | ||||||
| chr7:108079578
|
A | G | 8 | a0003c0004t0002g0225a0007c0011t0002g0156a0007c0011t0002g0157others(5): Show | 8 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(5): Show |
intron_variant | MODIFIER | c.1887+23T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 15/33 | chr7 | 108079578 | ||||||
| chr7:108079826
|
C | T | 1 | a0001c0063t0001g0270 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1702-40G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108079826 | ||||||
| chr7:108079961
|
T | G | 2 | a0012c0022t0002g0148a0012c0059t0002g0222 | 2 | HG02723.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.1702-175A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108079961 | ||||||
| chr7:108080297
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1702-511A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108080297 | ||||||
| chr7:108080425
|
T | C | 69 | a0001c0006t0001g0142a0001c0006t0001g0144a0001c0006t0001g0145others(66): Show | 69 | HG00323.hp1 HG00621.hp1 HG01074.hp2 others(66): Show |
intron_variant | MODIFIER | c.1702-639A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108080425 | ||||||
| chr7:108080428
|
T | C | 3 | a0006c0016t0002g0101a0007c0011t0001g0100a0007c0011t0002g0102 | 3 | HG02970.hp2 NA18522.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1702-642A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108080428 | ||||||
| chr7:108080676
|
G | A | 221 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0030others(218): Show | 221 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(218): Show |
intron_variant | MODIFIER | c.1702-890C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108080676 | ||||||
| chr7:108080818
|
T | TA | 19 | a0001c0001t0001g0203a0003c0004t0002g0268a0003c0004t0002g0269others(16): Show | 19 | HG01074.hp2 HG02055.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.1702-1033dupT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108080818 | ||||||
| chr7:108080831
|
A | C | 1 | a0011c0014t0001g0214 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1702-1045T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108080831 | ||||||
| chr7:108080832
|
C | A | 17 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(14): Show | 17 | HG01074.hp2 HG02258.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1702-1046G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108080832 | ||||||
| chr7:108080852
|
G | T | 4 | a0001c0054t0001g0146a0001c0060t0004g0216a0001c0070t0001g0246others(1): Show | 4 | HG02572.hp2 HG02723.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1702-1066C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108080852 | ||||||
| chr7:108080938
|
A | G | 11 | a0003c0004t0002g0225a0006c0016t0002g0101a0006c0027t0001g0085others(8): Show | 11 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.1702-1152T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108080938 | ||||||
| chr7:108080957
|
A | G | 2 | a0001c0054t0001g0146a0012c0022t0002g0148 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1702-1171T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108080957 | ||||||
| chr7:108080993
|
G | A | 1 | a0016c0055t0002g0213 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1702-1207C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108080993 | ||||||
| chr7:108080994
|
C | T | 1 | a0001c0002t0003g0048 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.1702-1208G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108080994 | ||||||
| chr7:108081126
|
A | T | 1 | a0040c0031t0002g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1702-1340T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108081126 | ||||||
| chr7:108081302
|
G | A | 70 | a0001c0006t0001g0142a0001c0006t0001g0144a0001c0006t0001g0145others(67): Show | 70 | HG00323.hp1 HG00621.hp1 HG00741.hp1 others(67): Show |
intron_variant | MODIFIER | c.1702-1516C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108081302 | ||||||
| chr7:108081413
|
A | G | 1 | a0002c0012t0001g0248 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1702-1627T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108081413 | ||||||
| chr7:108081426
|
T | C | 7 | a0003c0004t0002g0225a0007c0011t0002g0156a0007c0011t0002g0157others(4): Show | 7 | HG01496.hp1 HG02109.hp2 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.1702-1640A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108081426 | ||||||
| chr7:108081629
|
GTAGA | G | 4 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(1): Show | 4 | HG02258.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1702-1847_1702-184 others(8): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108081629 | ||||||
| chr7:108081704
|
A | G | 161 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(158): Show | 161 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1702-1918T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108081704 | ||||||
| chr7:108081726
|
C | T | 2 | a0001c0002t0001g0050a0001c0002t0001g0051 | 2 | HG00738.hp2 HG01106.hp2 |
intron_variant | MODIFIER | c.1702-1940G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108081726 | ||||||
| chr7:108081759
|
G | C | 2 | a0002c0003t0001g0138a0002c0003t0001g0141 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1702-1973C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108081759 | ||||||
| chr7:108082087
|
T | A | 1 | a0017c0043t0001g0084 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1702-2301A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108082087 | ||||||
| chr7:108082100
|
G | T | 136 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(133): Show | 136 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(133): Show |
intron_variant | MODIFIER | c.1702-2314C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108082100 | ||||||
| chr7:108082137
|
T | A | 4 | a0001c0054t0001g0146a0008c0015t0002g0087a0012c0022t0002g0148others(1): Show | 4 | HG00741.hp1 HG02055.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.1702-2351A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108082137 | ||||||
| chr7:108082200
|
C | T | 153 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(150): Show | 153 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(150): Show |
intron_variant | MODIFIER | c.1702-2414G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108082200 | ||||||
| chr7:108082257
|
A | G | 162 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(159): Show | 162 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1702-2471T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108082257 | ||||||
| chr7:108082329
|
T | TA | 7 | a0001c0001t0001g0169a0001c0060t0004g0216a0001c0070t0001g0246others(4): Show | 7 | HG01258.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.1702-2544dupT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108082329 | ||||||
| chr7:108082329
|
TA | T | 152 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(149): Show | 152 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(149): Show |
intron_variant | MODIFIER | c.1702-2544delT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108082329 | ||||||
| chr7:108082357
|
G | A | 1 | a0001c0002t0001g0024 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1702-2571C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108082357 | ||||||
| chr7:108082413
|
A | G | 1 | a0001c0002t0001g0170 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1702-2627T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108082413 | ||||||
| chr7:108082424
|
T | C | 91 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(88): Show | 91 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1702-2638A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108082424 | ||||||
| chr7:108082427
|
G | C | 2 | a0001c0054t0001g0146a0012c0022t0002g0148 | 2 | HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1702-2641C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108082427 | ||||||
| chr7:108082613
|
C | A | 1 | a0034c0073t0003g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1702-2827G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108082613 | ||||||
| chr7:108082750
|
C | A | 1 | a0001c0001t0001g0226 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1702-2964G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108082750 | ||||||
| chr7:108082778
|
C | T | 1 | a0001c0002t0001g0045 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1702-2992G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108082778 | ||||||
| chr7:108082792
|
T | C | 1 | a0001c0002t0001g0043 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1702-3006A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108082792 | ||||||
| chr7:108082823
|
C | T | 2 | a0008c0015t0002g0087a0021c0028t0002g0092 | 2 | HG00741.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1702-3037G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108082823 | ||||||
| chr7:108083414
|
C | T | 2 | a0002c0003t0001g0138a0002c0003t0001g0141 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.1702-3628G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108083414 | ||||||
| chr7:108083468
|
G | A | 2 | a0001c0060t0004g0216a0001c0070t0001g0246 | 2 | HG02572.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.1702-3682C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108083468 | ||||||
| chr7:108083602
|
G | C | 91 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(88): Show | 91 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1702-3816C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108083602 | ||||||
| chr7:108083604
|
G | T | 1 | a0001c0001t0001g0230 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.1702-3818C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108083604 | ||||||
| chr7:108083764
|
A | G | 1 | a0001c0001t0001g0220 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1702-3978T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108083764 | ||||||
| chr7:108083801
|
C | A | 1 | a0001c0001t0001g0044 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1702-4015G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108083801 | ||||||
| chr7:108083964
|
T | C | 1 | a0001c0002t0001g0170 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1702-4178A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108083964 | ||||||
| chr7:108083996
|
G | A | 23 | a0001c0001t0001g0220a0001c0001t0001g0226a0001c0001t0001g0234others(20): Show | 23 | HG00140.hp2 HG00544.hp1 HG00738.hp1 others(20): Show |
intron_variant | MODIFIER | c.1702-4210C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108083996 | ||||||
| chr7:108084012
|
T | C | 1 | a0018c0024t0001g0108 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1702-4226A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108084012 | ||||||
| chr7:108084203
|
C | T | 1 | a0001c0002t0003g0058 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1702-4417G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108084203 | ||||||
| chr7:108084302
|
C | G | 162 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(159): Show | 162 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1702-4516G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108084302 | ||||||
| chr7:108084413
|
A | G | 1 | a0005c0008t0002g0223 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.1702-4627T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108084413 | ||||||
| chr7:108084535
|
T | G | 1 | a0001c0001t0001g0038 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.1702-4749A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108084535 | ||||||
| chr7:108084555
|
C | T | 1 | a0011c0014t0001g0117 | 1 | HG03490.hp2 | intron_variant | MODIFIER | c.1702-4769G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108084555 | ||||||
| chr7:108084599
|
T | C | 3 | a0001c0001t0001g0030a0001c0001t0001g0256a0001c0001t0001g0260 | 3 | NA18950.hp1 NA18985.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1702-4813A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108084599 | ||||||
| chr7:108084720
|
G | C | 1 | a0008c0015t0002g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1702-4934C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108084720 | ||||||
| chr7:108084725
|
A | G | 1 | a0001c0001t0001g0169 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.1702-4939T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108084725 | ||||||
| chr7:108084784
|
C | CT | 32 | a0001c0001t0001g0163a0001c0001t0001g0206a0001c0001t0001g0220others(29): Show | 32 | HG00140.hp2 HG00544.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.1702-4999dupA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108084784 | ||||||
| chr7:108084784
|
CT | C | 14 | a0001c0001t0001g0030a0001c0001t0001g0210a0001c0002t0001g0021others(11): Show | 14 | HG00140.hp1 HG00738.hp2 HG01255.hp1 others(11): Show |
intron_variant | MODIFIER | c.1702-4999delA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108084784 | ||||||
| chr7:108084784
|
CTT | C | 130 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(127): Show | 130 | HG00280.hp2 HG00323.hp1 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.1702-5000_1702-499 others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108084784 | ||||||
| chr7:108084784
|
CTTT | C | 21 | a0001c0002t0001g0035a0001c0002t0001g0059a0001c0002t0001g0069others(18): Show | 21 | HG00741.hp1 HG01074.hp2 HG01515.hp1 others(18): Show |
intron_variant | MODIFIER | c.1702-5001_1702-499 others(7): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108084784 | ||||||
| chr7:108084994
|
CTCCCAAA others(10): Show |
C | 1 | a0001c0001t0001g0190 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1702-5225_1702-520 others(21): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108084994 | ||||||
| chr7:108085145
|
C | T | 3 | a0001c0001t0001g0190a0001c0001t0001g0191a0001c0001t0001g0250 | 3 | HG00280.hp1 HG01167.hp1 HG01169.hp2 |
intron_variant | MODIFIER | c.1702-5359G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108085145 | ||||||
| chr7:108085147
|
T | C | 1 | a0001c0001t0001g0190 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1702-5361A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108085147 | ||||||
| chr7:108085532
|
T | C | 92 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(89): Show | 92 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1702-5746A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108085532 | ||||||
| chr7:108085569
|
G | A | 161 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(158): Show | 161 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1702-5783C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108085569 | ||||||
| chr7:108085588
|
G | A | 1 | a0009c0009t0001g0010 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.1702-5802C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108085588 | ||||||
| chr7:108085605
|
T | A | 1 | a0001c0001t0001g0190 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1702-5819A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108085605 | ||||||
| chr7:108085707
|
G | A | 1 | a0001c0002t0001g0028 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1701+5919C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108085707 | ||||||
| chr7:108085893
|
G | A | 1 | a0013c0068t0002g0227 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1701+5733C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108085893 | ||||||
| chr7:108085965
|
G | A | 17 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(14): Show | 17 | HG01074.hp2 HG02258.hp2 HG02486.hp2 others(14): Show |
intron_variant | MODIFIER | c.1701+5661C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108085965 | ||||||
| chr7:108086155
|
C | T | 1 | a0005c0008t0002g0271 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.1701+5471G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108086155 | ||||||
| chr7:108086388
|
C | T | 167 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(164): Show | 167 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(164): Show |
intron_variant | MODIFIER | c.1701+5238G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108086388 | ||||||
| chr7:108086429
|
T | C | 1 | a0034c0073t0003g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1701+5197A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108086429 | ||||||
| chr7:108086497
|
G | A | 6 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(3): Show | 6 | HG01074.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1701+5129C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108086497 | ||||||
| chr7:108086759
|
T | C | 36 | a0001c0006t0001g0142a0001c0006t0001g0144a0001c0006t0001g0145others(33): Show | 36 | HG00323.hp1 HG00621.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.1701+4867A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108086759 | ||||||
| chr7:108086780
|
C | G | 1 | a0017c0030t0002g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1701+4846G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108086780 | ||||||
| chr7:108086955
|
G | A | 2 | a0008c0015t0002g0087a0021c0028t0002g0092 | 2 | HG00741.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1701+4671C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108086955 | ||||||
| chr7:108086995
|
T | C | 170 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(167): Show | 170 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(167): Show |
intron_variant | MODIFIER | c.1701+4631A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108086995 | ||||||
| chr7:108087056
|
G | T | 160 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(157): Show | 160 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1701+4570C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108087056 | ||||||
| chr7:108087264
|
C | T | 160 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(157): Show | 160 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(157): Show |
intron_variant | MODIFIER | c.1701+4362G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108087264 | ||||||
| chr7:108087359
|
C | G | 158 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(155): Show | 158 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.1701+4267G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108087359 | ||||||
| chr7:108087494
|
A | T | 1 | a0001c0001t0001g0190 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1701+4132T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108087494 | ||||||
| chr7:108087516
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1701+4110G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108087516 | ||||||
| chr7:108087731
|
A | AC | 161 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(158): Show | 161 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1701+3894_1701+389 others(5): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108087731 | ||||||
| chr7:108087870
|
A | G | 161 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(158): Show | 161 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1701+3756T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108087870 | ||||||
| chr7:108087984
|
A | G | 13 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(10): Show | 13 | HG02258.hp2 HG02615.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1701+3642T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108087984 | ||||||
| chr7:108088067
|
T | C | 148 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(145): Show | 148 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(145): Show |
intron_variant | MODIFIER | c.1701+3559A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108088067 | ||||||
| chr7:108088068
|
G | A | 1 | a0001c0002t0003g0058 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.1701+3558C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108088068 | ||||||
| chr7:108088145
|
A | G | 4 | a0007c0019t0002g0005a0007c0019t0002g0096a0016c0055t0002g0213others(1): Show | 4 | HG02896.hp1 HG02922.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.1701+3481T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108088145 | ||||||
| chr7:108088148
|
C | T | 1 | a0006c0027t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1701+3478G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108088148 | ||||||
| chr7:108088166
|
CT | C | 156 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(153): Show | 156 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(153): Show |
intron_variant | MODIFIER | c.1701+3459delA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108088166 | ||||||
| chr7:108088189
|
G | T | 161 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(158): Show | 161 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1701+3437C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108088189 | ||||||
| chr7:108088516
|
T | C | 1 | a0001c0001t0001g0172 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1701+3110A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108088516 | ||||||
| chr7:108088521
|
C | T | 2 | a0008c0015t0002g0087a0021c0028t0002g0092 | 2 | HG00741.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.1701+3105G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108088521 | ||||||
| chr7:108088593
|
A | G | 1 | a0022c0029t0002g0284 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1701+3033T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108088593 | ||||||
| chr7:108088622
|
G | T | 1 | a0001c0001t0001g0104 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1701+3004C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108088622 | ||||||
| chr7:108088817
|
C | A | 1 | a0001c0001t0001g0190 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1701+2809G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108088817 | ||||||
| chr7:108088846
|
G | A | 1 | a0001c0001t0003g0015 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1701+2780C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108088846 | ||||||
| chr7:108089120
|
A | G | 161 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(158): Show | 161 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1701+2506T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108089120 | ||||||
| chr7:108089195
|
C | T | 1 | a0005c0008t0002g0110 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1701+2431G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108089195 | ||||||
| chr7:108089236
|
T | C | 1 | a0022c0029t0002g0284 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1701+2390A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108089236 | ||||||
| chr7:108089270
|
A | G | 1 | a0001c0001t0001g0197 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1701+2356T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108089270 | ||||||
| chr7:108089369
|
C | T | 10 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(7): Show | 10 | HG02258.hp2 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1701+2257G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108089369 | ||||||
| chr7:108089450
|
T | A | 54 | a0001c0006t0001g0142a0001c0006t0001g0144a0001c0006t0001g0145others(51): Show | 54 | HG00323.hp1 HG00621.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.1701+2176A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108089450 | ||||||
| chr7:108089522
|
T | A | 1 | a0001c0001t0001g0190 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1701+2104A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108089522 | ||||||
| chr7:108089589
|
T | C | 92 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(89): Show | 92 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(89): Show |
intron_variant | MODIFIER | c.1701+2037A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108089589 | ||||||
| chr7:108089639
|
A | C | 1 | a0002c0003t0001g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1701+1987T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108089639 | ||||||
| chr7:108089640
|
C | A | 1 | a0008c0015t0002g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1701+1986G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108089640 | ||||||
| chr7:108089969
|
A | T | 1 | a0008c0038t0002g0152 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1701+1657T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108089969 | ||||||
| chr7:108090175
|
A | T | 1 | a0001c0001t0001g0190 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.1701+1451T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108090175 | ||||||
| chr7:108090205
|
G | A | 91 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(88): Show | 91 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.1701+1421C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108090205 | ||||||
| chr7:108090304
|
C | A | 180 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0030others(177): Show | 180 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(177): Show |
intron_variant | MODIFIER | c.1701+1322G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108090304 | ||||||
| chr7:108090393
|
C | T | 4 | a0001c0001t0001g0177a0001c0001t0001g0206a0001c0001t0001g0219others(1): Show | 4 | HG01069.hp1 HG01361.hp1 HG02622.hp1 others(1): Show |
intron_variant | MODIFIER | c.1701+1233G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108090393 | ||||||
| chr7:108090481
|
T | C | 4 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0066t0001g0012others(1): Show | 4 | HG01981.hp2 HG02040.hp2 HG02293.hp2 others(1): Show |
intron_variant | MODIFIER | c.1701+1145A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108090481 | ||||||
| chr7:108090553
|
C | A | 1 | a0012c0022t0002g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1701+1073G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108090553 | ||||||
| chr7:108090618
|
A | G | 2 | a0001c0002t0002g0149a0023c0018t0002g0095 | 2 | HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1701+1008T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108090618 | ||||||
| chr7:108091090
|
C | T | 1 | a0005c0008t0002g0105 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1701+536G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108091090 | ||||||
| chr7:108091098
|
C | CT | 172 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0030others(169): Show | 172 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(169): Show |
intron_variant | MODIFIER | c.1701+527dupA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 14/33 | chr7 | 108091098 | ||||||
| chr7:108091902
|
T | C | 1 | a0001c0001t0001g0249 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1551-126A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 13/33 | chr7 | 108091902 | ||||||
| chr7:108092016
|
G | T | 1 | a0003c0004t0002g0218 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1551-240C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 13/33 | chr7 | 108092016 | ||||||
| chr7:108092050
|
G | T | 4 | a0006c0016t0001g0083a0011c0014t0001g0214a0013c0026t0002g0153others(1): Show | 4 | HG02145.hp1 HG02896.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.1551-274C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 13/33 | chr7 | 108092050 | ||||||
| chr7:108092106
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1550+231G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 13/33 | chr7 | 108092106 | ||||||
| chr7:108092223
|
A | T | 1 | a0010c0013t0002g0173 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1550+114T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 13/33 | chr7 | 108092223 | ||||||
| chr7:108092242
|
A | G | 1 | a0008c0039t0002g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1550+95T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 13/33 | chr7 | 108092242 | ||||||
| chr7:108092480
|
C | T | 1 | a0001c0063t0001g0270 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1471-64G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108092480 | ||||||
| chr7:108092844
|
G | C | 159 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(156): Show | 159 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(156): Show |
intron_variant | MODIFIER | c.1471-428C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108092844 | ||||||
| chr7:108092858
|
C | T | 2 | a0020c0021t0002g0098a0020c0021t0002g0099 | 2 | HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1471-442G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108092858 | ||||||
| chr7:108092954
|
T | C | 1 | a0001c0002t0001g0021 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1471-538A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108092954 | ||||||
| chr7:108093034
|
C | T | 1 | a0024c0047t0001g0165 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1471-618G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108093034 | ||||||
| chr7:108093129
|
G | A | 1 | a0029c0067t0002g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1471-713C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108093129 | ||||||
| chr7:108093191
|
C | T | 1 | a0001c0070t0001g0246 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.1471-775G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108093191 | ||||||
| chr7:108093211
|
C | T | 1 | a0001c0002t0003g0022 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1471-795G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108093211 | ||||||
| chr7:108093349
|
G | A | 1 | a0036c0045t0003g0251 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1471-933C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108093349 | ||||||
| chr7:108093411
|
C | T | 161 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(158): Show | 161 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1471-995G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108093411 | ||||||
| chr7:108093548
|
A | G | 161 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(158): Show | 161 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(158): Show |
intron_variant | MODIFIER | c.1471-1132T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108093548 | ||||||
| chr7:108093646
|
G | A | 13 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(10): Show | 13 | HG02258.hp2 HG02615.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1471-1230C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108093646 | ||||||
| chr7:108093729
|
C | T | 1 | a0001c0002t0001g0066 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.1471-1313G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108093729 | ||||||
| chr7:108094077
|
A | G | 1 | a0021c0028t0002g0092 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1470+1151T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108094077 | ||||||
| chr7:108094214
|
G | C | 54 | a0001c0006t0001g0142a0001c0006t0001g0144a0001c0006t0001g0145others(51): Show | 54 | HG00323.hp1 HG00621.hp1 HG01074.hp2 others(51): Show |
intron_variant | MODIFIER | c.1470+1014C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108094214 | ||||||
| chr7:108094312
|
C | T | 13 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(10): Show | 13 | HG02258.hp2 HG02615.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1470+916G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108094312 | ||||||
| chr7:108094392
|
C | T | 1 | a0003c0004t0002g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1470+836G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108094392 | ||||||
| chr7:108094577
|
GT | G | 147 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(144): Show | 147 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(144): Show |
intron_variant | MODIFIER | c.1470+650delA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108094577 | ||||||
| chr7:108094579
|
T | G | 2 | a0007c0019t0002g0005a0040c0031t0002g0006 | 2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1470+649A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108094579 | ||||||
| chr7:108094788
|
A | G | 9 | a0001c0054t0001g0146a0006c0010t0001g0288a0006c0010t0001g0289others(6): Show | 9 | HG01074.hp2 HG02486.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1470+440T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108094788 | ||||||
| chr7:108094789
|
C | A | 9 | a0001c0054t0001g0146a0006c0010t0001g0288a0006c0010t0001g0289others(6): Show | 9 | HG01074.hp2 HG02486.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1470+439G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108094789 | ||||||
| chr7:108094796
|
C | G | 1 | a0001c0001t0003g0186 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1470+432G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 12/33 | chr7 | 108094796 | ||||||
| chr7:108095707
|
G | A | 1 | a0002c0003t0001g0082 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.1361-370C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108095707 | ||||||
| chr7:108095884
|
C | T | 13 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(10): Show | 13 | HG02258.hp2 HG02615.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1361-547G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108095884 | ||||||
| chr7:108095912
|
T | C | 1 | a0017c0030t0002g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1361-575A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108095912 | ||||||
| chr7:108096158
|
C | G | 1 | a0001c0060t0004g0216 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1361-821G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096158 | ||||||
| chr7:108096349
|
AG | A | 7 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(4): Show | 7 | HG01074.hp2 HG02486.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1361-1013delC | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096349 | ||||||
| chr7:108096575
|
A | G | 6 | a0001c0006t0001g0144a0001c0006t0001g0145a0003c0004t0002g0268others(3): Show | 6 | HG02258.hp2 HG02965.hp2 HG03579.hp1 others(3): Show |
intron_variant | MODIFIER | c.1361-1238T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096575 | ||||||
| chr7:108096698
|
G | A | 1 | a0006c0027t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1361-1361C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096698 | ||||||
| chr7:108096764
|
T | C | 1 | a0008c0015t0002g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1361-1427A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096764 | ||||||
| chr7:108096767
|
C | CA | 13 | a0001c0001t0001g0030a0001c0001t0001g0230a0001c0001t0001g0240others(10): Show | 13 | HG00544.hp1 HG01099.hp1 HG01433.hp2 others(10): Show |
intron_variant | MODIFIER | c.1361-1431dupT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096767 | ||||||
| chr7:108096767
|
CA | C | 52 | a0001c0001t0001g0150a0001c0001t0001g0264a0001c0002t0001g0047others(49): Show | 52 | HG00323.hp1 HG00323.hp2 HG00621.hp1 others(49): Show |
intron_variant | MODIFIER | c.1361-1431delT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096767 | ||||||
| chr7:108096795
|
G | T | 1 | a0009c0009t0001g0228 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.1361-1458C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096795 | ||||||
| chr7:108096833
|
T | C | 68 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(65): Show | 68 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.1361-1496A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096833 | ||||||
| chr7:108096887
|
G | A | 1 | a0021c0028t0002g0092 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1360+1516C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096887 | ||||||
| chr7:108096926
|
ACT | A | 68 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(65): Show | 68 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(65): Show |
intron_variant | MODIFIER | c.1360+1475_1360+147 others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096926 | ||||||
| chr7:108096939
|
C | CA | 9 | a0001c0001t0001g0202a0001c0001t0001g0203a0001c0001t0001g0253others(6): Show | 9 | HG01433.hp1 HG01943.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+1463dupT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096939 | ||||||
| chr7:108096939
|
CA | C | 82 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0042others(79): Show | 82 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.1360+1463delT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096939 | ||||||
| chr7:108096939
|
CAA | C | 22 | a0001c0001t0001g0166a0001c0001t0001g0177a0001c0001t0001g0188others(19): Show | 22 | HG00621.hp2 HG01069.hp1 HG01975.hp2 others(19): Show |
intron_variant | MODIFIER | c.1360+1462_1360+146 others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096939 | ||||||
| chr7:108096939
|
CAAA | C | 38 | a0001c0006t0001g0144a0001c0006t0001g0145a0001c0006t0003g0121others(35): Show | 38 | HG00323.hp1 HG00621.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.1360+1461_1360+146 others(7): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096939 | ||||||
| chr7:108096939
|
CAAAA | C | 16 | a0001c0006t0001g0142a0006c0010t0001g0288a0006c0010t0001g0289others(13): Show | 16 | HG01074.hp2 HG02055.hp2 HG02451.hp2 others(13): Show |
intron_variant | MODIFIER | c.1360+1460_1360+146 others(8): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096939 | ||||||
| chr7:108096939
|
CAAAAAAA | C | 7 | a0001c0002t0001g0017a0001c0002t0001g0019a0001c0002t0001g0025others(4): Show | 7 | HG01361.hp2 HG02080.hp1 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.1360+1457_1360+146 others(11): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096939 | ||||||
| chr7:108096939
|
CAAAAAAA others(1): Show |
C | 53 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(50): Show | 53 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.1360+1456_1360+146 others(12): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096939 | ||||||
| chr7:108096939
|
CAAAAAAA others(2): Show |
C | 8 | a0001c0002t0001g0029a0001c0002t0001g0047a0001c0002t0001g0049others(5): Show | 8 | HG01167.hp2 HG01169.hp1 HG01515.hp1 others(5): Show |
intron_variant | MODIFIER | c.1360+1455_1360+146 others(13): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096939 | ||||||
| chr7:108096939
|
CAAAAAAA others(4): Show |
C | 2 | a0002c0003t0001g0137a0006c0016t0002g0086 | 2 | HG02165.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1360+1453_1360+146 others(15): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096939 | ||||||
| chr7:108096939
|
CAAAAAAA others(5): Show |
C | 3 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281 | 3 | HG02258.hp2 HG03579.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1360+1452_1360+146 others(16): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096939 | ||||||
| chr7:108096939
|
CAAAAAAA others(6): Show |
C | 11 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0104others(8): Show | 11 | HG01981.hp2 HG02040.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.1360+1451_1360+146 others(17): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096939 | ||||||
| chr7:108096939
|
CAAAAAAA others(7): Show |
C | 1 | a0029c0067t0002g0257 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1360+1450_1360+146 others(18): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096939 | ||||||
| chr7:108096956
|
A | T | 1 | a0006c0027t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1360+1447T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096956 | ||||||
| chr7:108096959
|
AAAAAAAA others(7): Show |
A | 1 | a0018c0024t0001g0109 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.1360+1430_1360+144 others(18): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096959 | ||||||
| chr7:108096964
|
A | T | 1 | a0006c0027t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1360+1439T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096964 | ||||||
| chr7:108096994
|
C | T | 1 | a0001c0002t0001g0025 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.1360+1409G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108096994 | ||||||
| chr7:108097086
|
G | T | 1 | a0010c0013t0002g0221 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1360+1317C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108097086 | ||||||
| chr7:108097189
|
A | G | 8 | a0001c0002t0001g0018a0001c0002t0001g0028a0001c0002t0001g0029others(5): Show | 8 | HG00558.hp2 NA18612.hp1 NA18962.hp1 others(5): Show |
intron_variant | MODIFIER | c.1360+1214T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108097189 | ||||||
| chr7:108097301
|
C | G | 1 | a0001c0001t0001g0220 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1360+1102G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108097301 | ||||||
| chr7:108097339
|
G | A | 9 | a0001c0054t0001g0146a0006c0010t0001g0288a0006c0010t0001g0289others(6): Show | 9 | HG01074.hp2 HG02486.hp2 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.1360+1064C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108097339 | ||||||
| chr7:108097481
|
A | G | 36 | a0001c0006t0001g0142a0001c0006t0001g0144a0001c0006t0001g0145others(33): Show | 36 | HG00323.hp1 HG00621.hp1 HG01256.hp2 others(33): Show |
intron_variant | MODIFIER | c.1360+922T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108097481 | ||||||
| chr7:108097517
|
G | A | 2 | a0003c0004t0002g0175a0003c0004t0002g0231 | 2 | HG03139.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.1360+886C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108097517 | ||||||
| chr7:108097521
|
C | T | 1 | a0001c0001t0001g0219 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1360+882G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108097521 | ||||||
| chr7:108097707
|
C | A | 4 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(1): Show | 4 | HG02258.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1360+696G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108097707 | ||||||
| chr7:108097715
|
CAAAT | C | 19 | a0001c0054t0001g0146a0006c0010t0001g0288a0006c0010t0001g0289others(16): Show | 19 | HG00741.hp1 HG01074.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.1360+684_1360+687d others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108097715 | ||||||
| chr7:108097765
|
G | C | 1 | a0001c0001t0001g0263 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1360+638C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108097765 | ||||||
| chr7:108097893
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1360+510A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108097893 | ||||||
| chr7:108098010
|
C | T | 1 | a0008c0015t0002g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1360+393G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108098010 | ||||||
| chr7:108098086
|
A | G | 90 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1360+317T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108098086 | ||||||
| chr7:108098107
|
C | T | 90 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1360+296G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108098107 | ||||||
| chr7:108098188
|
C | A | 1 | a0006c0027t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.1360+215G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108098188 | ||||||
| chr7:108098317
|
A | C | 2 | a0009c0009t0001g0266a0009c0009t0001g0267 | 2 | HG02970.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.1360+86T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108098317 | ||||||
| chr7:108098356
|
A | ACATAGGG others(52): Show |
89 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(86): Show | 89 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(86): Show |
intron_variant | MODIFIER | c.1360+46_1360+47ins others(59): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108098356 | ||||||
| chr7:108098356
|
A | ACATAGGG others(52): Show |
1 | a0015c0017t0001g0070 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1360+46_1360+47ins others(59): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108098356 | ||||||
| chr7:108098377
|
C | T | 3 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0066t0001g0012 | 3 | HG01981.hp2 HG02293.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.1360+26G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108098377 | ||||||
| chr7:108098391
|
T | C | 90 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1360+12A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 11/33 | chr7 | 108098391 | ||||||
| chr7:108098736
|
A | G | 90 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1181-154T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108098736 | ||||||
| chr7:108098904
|
C | T | 2 | a0007c0019t0002g0005a0040c0031t0002g0006 | 2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1181-322G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108098904 | ||||||
| chr7:108099040
|
A | G | 90 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1181-458T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108099040 | ||||||
| chr7:108099073
|
G | A | 1 | a0002c0003t0001g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1181-491C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108099073 | ||||||
| chr7:108099093
|
A | C | 90 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1181-511T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108099093 | ||||||
| chr7:108099180
|
G | C | 1 | a0001c0001t0001g0042 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1181-598C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108099180 | ||||||
| chr7:108099213
|
A | C | 73 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(70): Show | 73 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(70): Show |
intron_variant | MODIFIER | c.1181-631T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108099213 | ||||||
| chr7:108099282
|
A | G | 90 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1181-700T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108099282 | ||||||
| chr7:108099333
|
A | G | 1 | a0001c0001t0001g0258 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.1181-751T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108099333 | ||||||
| chr7:108099336
|
A | G | 13 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(10): Show | 13 | HG02258.hp2 HG02615.hp1 HG02717.hp1 others(10): Show |
intron_variant | MODIFIER | c.1181-754T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108099336 | ||||||
| chr7:108099461
|
A | T | 142 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(139): Show | 142 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(139): Show |
intron_variant | MODIFIER | c.1181-879T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108099461 | ||||||
| chr7:108099767
|
C | A | 1 | a0041c0033t0001g0090 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.1181-1185G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108099767 | ||||||
| chr7:108099790
|
G | A | 14 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(11): Show | 14 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1181-1208C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108099790 | ||||||
| chr7:108099930
|
A | G | 1 | a0022c0029t0002g0284 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1181-1348T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108099930 | ||||||
| chr7:108099952
|
C | G | 4 | a0008c0015t0002g0001a0008c0015t0002g0002a0017c0041t0001g0003others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.1181-1370G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108099952 | ||||||
| chr7:108100216
|
A | G | 1 | a0001c0002t0001g0170 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1181-1634T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108100216 | ||||||
| chr7:108100299
|
T | C | 14 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(11): Show | 14 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1181-1717A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108100299 | ||||||
| chr7:108100356
|
G | A | 1 | a0007c0011t0001g0100 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1181-1774C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108100356 | ||||||
| chr7:108100609
|
C | G | 6 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(3): Show | 6 | HG01074.hp2 HG03098.hp2 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.1181-2027G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108100609 | ||||||
| chr7:108100610
|
A | G | 90 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1181-2028T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108100610 | ||||||
| chr7:108100647
|
C | G | 90 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1181-2065G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108100647 | ||||||
| chr7:108100892
|
T | A | 90 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1180+2152A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108100892 | ||||||
| chr7:108100901
|
G | A | 14 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(11): Show | 14 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1180+2143C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108100901 | ||||||
| chr7:108101198
|
A | G | 1 | a0008c0015t0002g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1180+1846T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108101198 | ||||||
| chr7:108101206
|
C | T | 10 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(7): Show | 10 | HG02258.hp2 HG02615.hp1 HG02717.hp1 others(7): Show |
intron_variant | MODIFIER | c.1180+1838G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108101206 | ||||||
| chr7:108101322
|
A | T | 3 | a0001c0002t0003g0022a0001c0002t0003g0046a0001c0002t0003g0078 | 3 | HG01243.hp1 HG02683.hp1 HG03017.hp2 |
intron_variant | MODIFIER | c.1180+1722T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108101322 | ||||||
| chr7:108101792
|
G | A | 1 | a0001c0002t0001g0036 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1180+1252C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108101792 | ||||||
| chr7:108101964
|
G | A | 1 | a0001c0063t0001g0270 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1180+1080C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108101964 | ||||||
| chr7:108101981
|
C | T | 7 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(4): Show | 7 | HG01074.hp2 HG02486.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.1180+1063G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108101981 | ||||||
| chr7:108102164
|
T | C | 90 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1180+880A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108102164 | ||||||
| chr7:108102697
|
T | C | 14 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(11): Show | 14 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1180+347A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108102697 | ||||||
| chr7:108102757
|
C | A | 1 | a0001c0001t0001g0264 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.1180+287G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108102757 | ||||||
| chr7:108102770
|
C | T | 1 | a0040c0031t0002g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1180+274G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108102770 | ||||||
| chr7:108102775
|
A | C | 2 | a0001c0002t0002g0149a0023c0018t0002g0095 | 2 | HG02818.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1180+269T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108102775 | ||||||
| chr7:108102798
|
G | T | 90 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.1180+246C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108102798 | ||||||
| chr7:108102799
|
C | T | 145 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(142): Show | 145 | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.1180+245G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108102799 | ||||||
| chr7:108102964
|
A | G | 104 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(101): Show | 104 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(101): Show |
intron_variant | MODIFIER | c.1180+80T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108102964 | ||||||
| chr7:108102970
|
C | T | 14 | a0003c0004t0002g0268a0003c0004t0002g0269a0003c0004t0002g0281others(11): Show | 14 | HG02055.hp2 HG02258.hp2 HG02615.hp1 others(11): Show |
intron_variant | MODIFIER | c.1180+74G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 10/33 | chr7 | 108102970 | ||||||
| chr7:108103305
|
C | G | 1 | a0001c0002t0001g0017 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.992-73G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 9/33 | chr7 | 108103305 | ||||||
| chr7:108103635
|
C | T | 4 | a0001c0002t0001g0059a0001c0002t0001g0060a0001c0002t0001g0061others(1): Show | 4 | HG01069.hp2 HG01496.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.992-403G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 9/33 | chr7 | 108103635 | ||||||
| chr7:108103772
|
A | G | 131 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(128): Show | 131 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.992-540T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 9/33 | chr7 | 108103772 | ||||||
| chr7:108103775
|
A | C | 1 | a0002c0012t0001g0159 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.992-543T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 9/33 | chr7 | 108103775 | ||||||
| chr7:108103842
|
C | T | 1 | a0001c0002t0001g0170 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.992-610G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 9/33 | chr7 | 108103842 | ||||||
| chr7:108103998
|
T | C | 1 | a0001c0002t0001g0037 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.991+501A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 9/33 | chr7 | 108103998 | ||||||
| chr7:108104098
|
A | G | 71 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(68): Show | 71 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.991+401T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 9/33 | chr7 | 108104098 | ||||||
| chr7:108104123
|
G | A | 1 | a0001c0001t0001g0282 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.991+376C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 9/33 | chr7 | 108104123 | ||||||
| chr7:108104286
|
T | TA | 90 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.991+212dupT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 9/33 | chr7 | 108104286 | ||||||
| chr7:108104290
|
G | A | 90 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(87): Show | 90 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(87): Show |
intron_variant | MODIFIER | c.991+209C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 9/33 | chr7 | 108104290 | ||||||
| chr7:108104314
|
A | G | 131 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(128): Show | 131 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.991+185T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 9/33 | chr7 | 108104314 | ||||||
| chr7:108104431
|
C | T | 8 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(5): Show | 8 | HG01433.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.991+68G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 9/33 | chr7 | 108104431 | ||||||
| chr7:108104643
|
G | A | 1 | a0006c0027t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.871-24C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104643 | ||||||
| chr7:108104742
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-123T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104742 | ||||||
| chr7:108104743
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-124T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104743 | ||||||
| chr7:108104748
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-129T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104748 | ||||||
| chr7:108104749
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-130T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104749 | ||||||
| chr7:108104751
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-132T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104751 | ||||||
| chr7:108104752
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-133G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104752 | ||||||
| chr7:108104753
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-134G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104753 | ||||||
| chr7:108104754
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-135T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104754 | ||||||
| chr7:108104755
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-136T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104755 | ||||||
| chr7:108104756
|
C | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-137G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104756 | ||||||
| chr7:108104757
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-138G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104757 | ||||||
| chr7:108104761
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-142T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104761 | ||||||
| chr7:108104764
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-145T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104764 | ||||||
| chr7:108104766
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-147G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104766 | ||||||
| chr7:108104769
|
C | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-150G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104769 | ||||||
| chr7:108104771
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-152T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104771 | ||||||
| chr7:108104774
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-155T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104774 | ||||||
| chr7:108104775
|
T | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-156A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104775 | ||||||
| chr7:108104779
|
C | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-160G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104779 | ||||||
| chr7:108104784
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-165G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104784 | ||||||
| chr7:108104786
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-167T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104786 | ||||||
| chr7:108104788
|
C | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-169G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104788 | ||||||
| chr7:108104790
|
T | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-171A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104790 | ||||||
| chr7:108104792
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-173T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104792 | ||||||
| chr7:108104793
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-174T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104793 | ||||||
| chr7:108104794
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-175T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104794 | ||||||
| chr7:108104795
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-176G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104795 | ||||||
| chr7:108104798
|
T | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-179A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104798 | ||||||
| chr7:108104799
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-180T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104799 | ||||||
| chr7:108104801
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-182T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104801 | ||||||
| chr7:108104802
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-183T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104802 | ||||||
| chr7:108104803
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-184T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104803 | ||||||
| chr7:108104804
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-185T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104804 | ||||||
| chr7:108104805
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-186T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104805 | ||||||
| chr7:108104810
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-191T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104810 | ||||||
| chr7:108104811
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-192T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104811 | ||||||
| chr7:108104812
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-193T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104812 | ||||||
| chr7:108104813
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-194T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104813 | ||||||
| chr7:108104815
|
T | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-196A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104815 | ||||||
| chr7:108104817
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-198G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104817 | ||||||
| chr7:108104818
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-199T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104818 | ||||||
| chr7:108104822
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-203T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104822 | ||||||
| chr7:108104823
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-204T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104823 | ||||||
| chr7:108104824
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-205G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104824 | ||||||
| chr7:108104827
|
C | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-208G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104827 | ||||||
| chr7:108104829
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-210T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104829 | ||||||
| chr7:108104830
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-211T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104830 | ||||||
| chr7:108104831
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-212T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104831 | ||||||
| chr7:108104832
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-213T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104832 | ||||||
| chr7:108104834
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-215T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104834 | ||||||
| chr7:108104835
|
C | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-216G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104835 | ||||||
| chr7:108104836
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-217T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104836 | ||||||
| chr7:108104837
|
A | T | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-218T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104837 | ||||||
| chr7:108104839
|
A | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-220T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104839 | ||||||
| chr7:108104840
|
C | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-221G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104840 | ||||||
| chr7:108104841
|
T | G | 1 | a0001c0001t0001g0030 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.871-222A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104841 | ||||||
| chr7:108104938
|
G | A | 1 | a0002c0003t0001g0137 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.871-319C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104938 | ||||||
| chr7:108104939
|
G | C | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.871-320C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104939 | ||||||
| chr7:108104954
|
A | G | 125 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(122): Show | 125 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.871-335T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104954 | ||||||
| chr7:108104998
|
G | A | 124 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(121): Show | 124 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.871-379C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108104998 | ||||||
| chr7:108105109
|
T | C | 124 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(121): Show | 124 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(121): Show |
intron_variant | MODIFIER | c.871-490A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108105109 | ||||||
| chr7:108105244
|
C | T | 1 | a0022c0029t0002g0284 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.870+573G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108105244 | ||||||
| chr7:108105387
|
G | T | 1 | a0036c0045t0003g0251 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.870+430C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108105387 | ||||||
| chr7:108105680
|
T | C | 2 | a0012c0022t0002g0279a0025c0057t0002g0280 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.870+137A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108105680 | ||||||
| chr7:108105769
|
T | G | 125 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(122): Show | 125 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.870+48A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108105769 | ||||||
| chr7:108105770
|
G | C | 88 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(85): Show | 88 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(85): Show |
intron_variant | MODIFIER | c.870+47C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108105770 | ||||||
| chr7:108105793
|
T | C | 1 | a0005c0008t0002g0110 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.870+24A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108105793 | ||||||
| chr7:108105801
|
T | C | 131 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(128): Show | 131 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(128): Show |
intron_variant | MODIFIER | c.870+16A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108105801 | ||||||
| chr7:108105808
|
A | G | 125 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(122): Show | 125 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.870+9T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 8/33 | chr7 | 108105808 | ||||||
| chr7:108106141
|
G | A | 37 | a0001c0006t0001g0142a0001c0006t0001g0144a0001c0006t0001g0145others(34): Show | 37 | HG00621.hp1 HG01243.hp2 HG01256.hp2 others(34): Show |
intron_variant | MODIFIER | c.656-110C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 7/33 | chr7 | 108106141 | ||||||
| chr7:108106413
|
G | A | 3 | a0007c0019t0002g0005a0016c0055t0002g0213a0040c0031t0002g0006 | 3 | HG02922.hp1 HG03486.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.655+96C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 7/33 | chr7 | 108106413 | ||||||
| chr7:108106420
|
GA | G | 130 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(127): Show | 130 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.655+88delT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 7/33 | chr7 | 108106420 | ||||||
| chr7:108106428
|
A | T | 1 | a0006c0016t0002g0101 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.655+81T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 7/33 | chr7 | 108106428 | ||||||
| chr7:108106618
|
G | A | 1 | a0001c0006t0003g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.592-46C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 6/33 | chr7 | 108106618 | ||||||
| chr7:108106636
|
C | CT | 71 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(68): Show | 71 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(68): Show |
intron_variant | MODIFIER | c.592-65dupA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 6/33 | chr7 | 108106636 | ||||||
| chr7:108106715
|
C | T | 1 | a0002c0003t0001g0111 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.592-143G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 6/33 | chr7 | 108106715 | ||||||
| chr7:108106867
|
G | A | 3 | a0015c0017t0001g0011a0015c0017t0001g0070a0015c0017t0001g0071 | 3 | HG01261.hp1 HG01346.hp2 HG01978.hp1 |
intron_variant | MODIFIER | c.592-295C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 6/33 | chr7 | 108106867 | ||||||
| chr7:108106888
|
G | T | 1 | a0002c0003t0001g0120 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.592-316C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 6/33 | chr7 | 108106888 | ||||||
| chr7:108107020
|
C | T | 125 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(122): Show | 125 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.592-448G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 6/33 | chr7 | 108107020 | ||||||
| chr7:108107114
|
A | G | 1 | a0017c0030t0002g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.591+517T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 6/33 | chr7 | 108107114 | ||||||
| chr7:108107293
|
G | T | 1 | a0022c0029t0002g0284 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.591+338C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 6/33 | chr7 | 108107293 | ||||||
| chr7:108107303
|
T | C | 1 | a0002c0003t0001g0114 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.591+328A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 6/33 | chr7 | 108107303 | ||||||
| chr7:108107483
|
A | C | 125 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(122): Show | 125 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.591+148T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 6/33 | chr7 | 108107483 | ||||||
| chr7:108107492
|
G | A | 125 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(122): Show | 125 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.591+139C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 6/33 | chr7 | 108107492 | ||||||
| chr7:108107553
|
G | A | 6 | a0008c0015t0002g0001a0008c0015t0002g0002a0017c0041t0001g0003others(3): Show | 6 | HG02615.hp1 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.591+78C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 6/33 | chr7 | 108107553 | ||||||
| chr7:108107870
|
A | G | 8 | a0001c0060t0004g0216a0003c0004t0002g0007a0003c0004t0002g0217others(5): Show | 8 | HG00738.hp1 HG01943.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.403-51T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 5/33 | chr7 | 108107870 | ||||||
| chr7:108107892
|
G | A | 125 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(122): Show | 125 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.403-73C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 5/33 | chr7 | 108107892 | ||||||
| chr7:108107908
|
T | C | 7 | a0007c0019t0002g0005a0007c0019t0002g0096a0016c0055t0002g0213others(4): Show | 7 | HG00741.hp1 HG02615.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.403-89A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 5/33 | chr7 | 108107908 | ||||||
| chr7:108108015
|
A | T | 1 | a0037c0042t0001g0151 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.403-196T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 5/33 | chr7 | 108108015 | ||||||
| chr7:108108104
|
A | G | 125 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(122): Show | 125 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.403-285T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 5/33 | chr7 | 108108104 | ||||||
| chr7:108108255
|
C | T | 2 | a0019c0020t0001g0088a0019c0020t0001g0097 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.403-436G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 5/33 | chr7 | 108108255 | ||||||
| chr7:108108256
|
A | G | 125 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(122): Show | 125 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.403-437T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 5/33 | chr7 | 108108256 | ||||||
| chr7:108108334
|
T | A | 1 | a0004c0005t0003g0180 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.403-515A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 5/33 | chr7 | 108108334 | ||||||
| chr7:108108489
|
A | G | 125 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(122): Show | 125 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.403-670T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 5/33 | chr7 | 108108489 | ||||||
| chr7:108108573
|
C | G | 1 | a0007c0019t0002g0005 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.402+598G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 5/33 | chr7 | 108108573 | ||||||
| chr7:108108656
|
T | G | 1 | a0002c0003t0001g0138 | 1 | HG01258.hp1 | intron_variant | MODIFIER | c.402+515A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 5/33 | chr7 | 108108656 | ||||||
| chr7:108108812
|
A | T | 125 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(122): Show | 125 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.402+359T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 5/33 | chr7 | 108108812 | ||||||
| chr7:108108830
|
A | C | 1 | a0008c0015t0002g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.402+341T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 5/33 | chr7 | 108108830 | ||||||
| chr7:108108923
|
C | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208 | 3 | HG02895.hp2 HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.402+248G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 5/33 | chr7 | 108108923 | ||||||
| chr7:108108966
|
A | T | 36 | a0001c0002t0001g0008a0001c0002t0001g0016a0001c0002t0001g0019others(33): Show | 36 | HG00140.hp1 HG00280.hp2 HG00544.hp2 others(33): Show |
intron_variant | MODIFIER | c.402+205T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 5/33 | chr7 | 108108966 | ||||||
| chr7:108109361
|
G | A | 1 | a0001c0002t0001g0043 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.329-117C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108109361 | ||||||
| chr7:108109435
|
T | G | 129 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(126): Show | 129 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.329-191A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108109435 | ||||||
| chr7:108109712
|
G | A | 129 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(126): Show | 129 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.329-468C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108109712 | ||||||
| chr7:108109820
|
A | G | 8 | a0001c0060t0004g0216a0003c0004t0002g0007a0003c0004t0002g0217others(5): Show | 8 | HG00738.hp1 HG01943.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.329-576T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108109820 | ||||||
| chr7:108109848
|
C | T | 1 | a0008c0015t0002g0087 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.329-604G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108109848 | ||||||
| chr7:108109868
|
C | G | 1 | a0001c0002t0001g0079 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.329-624G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108109868 | ||||||
| chr7:108109912
|
G | A | 129 | a0001c0002t0001g0008a0001c0002t0001g0009a0001c0002t0001g0016others(126): Show | 129 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(126): Show |
intron_variant | MODIFIER | c.329-668C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108109912 | ||||||
| chr7:108110001
|
T | A | 130 | a0001c0001t0001g0240a0001c0002t0001g0008a0001c0002t0001g0009others(127): Show | 130 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.329-757A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108110001 | ||||||
| chr7:108110061
|
G | T | 1 | a0006c0027t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.329-817C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108110061 | ||||||
| chr7:108110171
|
T | C | 130 | a0001c0001t0001g0240a0001c0002t0001g0008a0001c0002t0001g0009others(127): Show | 130 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.329-927A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108110171 | ||||||
| chr7:108110257
|
G | C | 2 | a0008c0044t0002g0091a0012c0069t0001g0158 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.329-1013C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108110257 | ||||||
| chr7:108110286
|
C | T | 1 | a0001c0001t0001g0164 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.329-1042G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108110286 | ||||||
| chr7:108110377
|
T | C | 8 | a0007c0019t0002g0005a0007c0019t0002g0096a0016c0055t0002g0213others(5): Show | 8 | HG00741.hp1 HG02615.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.329-1133A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108110377 | ||||||
| chr7:108110467
|
C | T | 1 | a0021c0028t0002g0092 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.329-1223G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108110467 | ||||||
| chr7:108110588
|
C | T | 3 | a0004c0005t0003g0235a0004c0005t0003g0236a0004c0072t0003g0245 | 3 | NA18747.hp1 NA18945.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.328+1223G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108110588 | ||||||
| chr7:108110595
|
A | G | 1 | a0001c0002t0001g0045 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.328+1216T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108110595 | ||||||
| chr7:108110787
|
T | C | 130 | a0001c0001t0001g0240a0001c0002t0001g0008a0001c0002t0001g0009others(127): Show | 130 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(127): Show |
intron_variant | MODIFIER | c.328+1024A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108110787 | ||||||
| chr7:108110924
|
T | C | 38 | a0001c0001t0001g0119a0001c0006t0001g0142a0001c0006t0001g0144others(35): Show | 38 | HG00621.hp1 HG01243.hp2 HG01256.hp2 others(35): Show |
intron_variant | MODIFIER | c.328+887A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108110924 | ||||||
| chr7:108110956
|
T | C | 1 | a0003c0004t0002g0175 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.328+855A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108110956 | ||||||
| chr7:108110971
|
T | TC | 291 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0030others(288): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.328+839dupG | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108110971 | ||||||
| chr7:108111104
|
A | G | 2 | a0008c0044t0002g0091a0012c0069t0001g0158 | 2 | HG02451.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.328+707T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108111104 | ||||||
| chr7:108111251
|
A | G | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.328+560T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108111251 | ||||||
| chr7:108111518
|
A | C | 151 | a0001c0001t0001g0119a0001c0001t0001g0240a0001c0001t0003g0186others(148): Show | 151 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(148): Show |
intron_variant | MODIFIER | c.328+293T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108111518 | ||||||
| chr7:108111521
|
A | C | 135 | a0001c0001t0001g0119a0001c0001t0001g0240a0001c0002t0001g0008others(132): Show | 135 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.328+290T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108111521 | ||||||
| chr7:108111633
|
A | G | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.328+178T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108111633 | ||||||
| chr7:108111640
|
T | C | 6 | a0001c0070t0001g0246a0006c0027t0001g0085a0008c0044t0002g0091others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.328+171A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108111640 | ||||||
| chr7:108111757
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.328+54A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108111757 | ||||||
| chr7:108111798
|
A | G | 1 | a0001c0002t0001g0075 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.328+13T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 4/33 | chr7 | 108111798 | ||||||
| chr7:108112025
|
A | T | 141 | a0001c0001t0001g0119a0001c0001t0001g0240a0001c0002t0001g0008others(138): Show | 141 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.193-79T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108112025 | ||||||
| chr7:108112032
|
A | G | 135 | a0001c0001t0001g0119a0001c0001t0001g0240a0001c0002t0001g0008others(132): Show | 135 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.193-86T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108112032 | ||||||
| chr7:108112129
|
A | C | 1 | a0001c0001t0003g0185 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.193-183T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108112129 | ||||||
| chr7:108112316
|
ATT | A | 132 | a0001c0001t0001g0119a0001c0001t0001g0240a0001c0002t0001g0009others(129): Show | 132 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(129): Show |
intron_variant | MODIFIER | c.193-372_193-371del others(2): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108112316 | ||||||
| chr7:108112319
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.193-373A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108112319 | ||||||
| chr7:108112416
|
T | C | 135 | a0001c0001t0001g0119a0001c0001t0001g0240a0001c0002t0001g0008others(132): Show | 135 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.193-470A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108112416 | ||||||
| chr7:108112425
|
G | C | 6 | a0001c0070t0001g0246a0006c0027t0001g0085a0008c0044t0002g0091others(3): Show | 6 | HG02451.hp2 HG02572.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.193-479C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108112425 | ||||||
| chr7:108112499
|
G | GC | 135 | a0001c0001t0001g0119a0001c0001t0001g0240a0001c0002t0001g0008others(132): Show | 135 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.193-554dupG | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108112499 | ||||||
| chr7:108112513
|
G | A | 135 | a0001c0001t0001g0119a0001c0001t0001g0240a0001c0002t0001g0008others(132): Show | 135 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(132): Show |
intron_variant | MODIFIER | c.193-567C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108112513 | ||||||
| chr7:108112551
|
C | T | 3 | a0001c0001t0001g0044a0001c0001t0001g0150a0001c0001t0001g0163 | 3 | HG00323.hp2 HG02257.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.193-605G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108112551 | ||||||
| chr7:108112552
|
G | A | 1 | a0005c0008t0002g0271 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.193-606C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108112552 | ||||||
| chr7:108112794
|
C | T | 4 | a0008c0015t0002g0001a0008c0015t0002g0002a0017c0041t0001g0003others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-848G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108112794 | ||||||
| chr7:108113233
|
T | G | 1 | a0001c0052t0003g0072 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.193-1287A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108113233 | ||||||
| chr7:108113289
|
C | T | 1 | a0038c0036t0002g0089 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.193-1343G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108113289 | ||||||
| chr7:108113304
|
A | G | 30 | a0001c0054t0001g0146a0006c0010t0001g0288a0006c0010t0001g0289others(27): Show | 30 | HG00741.hp1 HG01074.hp2 HG02055.hp2 others(27): Show |
intron_variant | MODIFIER | c.193-1358T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108113304 | ||||||
| chr7:108113352
|
G | T | 1 | a0001c0002t0001g0028 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.193-1406C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108113352 | ||||||
| chr7:108113494
|
G | A | 1 | a0001c0054t0001g0146 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.193-1548C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108113494 | ||||||
| chr7:108113604
|
G | T | 1 | a0001c0001t0001g0272 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.193-1658C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108113604 | ||||||
| chr7:108113917
|
CTT | C | 4 | a0008c0015t0002g0001a0008c0015t0002g0002a0017c0041t0001g0003others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.193-1973_193-1972d others(4): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108113917 | ||||||
| chr7:108113952
|
G | T | 7 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(4): Show | 7 | HG01074.hp2 HG02486.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.193-2006C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108113952 | ||||||
| chr7:108114084
|
G | A | 37 | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0006t0001g0142others(34): Show | 37 | HG00621.hp1 HG01256.hp2 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.192+1920C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108114084 | ||||||
| chr7:108114145
|
A | G | 15 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(12): Show | 15 | HG01074.hp2 HG02258.hp1 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.192+1859T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108114145 | ||||||
| chr7:108114440
|
A | AAAAT | 36 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(33): Show | 36 | HG00741.hp1 HG01074.hp2 HG02055.hp2 others(33): Show |
intron_variant | MODIFIER | c.192+1560_192+1563d others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108114440 | ||||||
| chr7:108114443
|
A | ATAAG | 4 | a0008c0015t0002g0001a0008c0015t0002g0002a0017c0041t0001g0003others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+1560_192+1561i others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108114443 | ||||||
| chr7:108114444
|
T | G | 8 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(5): Show | 8 | HG01433.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.192+1560A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108114444 | ||||||
| chr7:108114530
|
T | A | 1 | a0017c0030t0002g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.192+1474A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108114530 | ||||||
| chr7:108114679
|
A | T | 8 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(5): Show | 8 | HG01433.hp2 HG02055.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.192+1325T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108114679 | ||||||
| chr7:108114766
|
C | T | 1 | a0005c0023t0002g0215 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.192+1238G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108114766 | ||||||
| chr7:108114782
|
G | A | 2 | a0007c0019t0002g0005a0040c0031t0002g0006 | 2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.192+1222C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108114782 | ||||||
| chr7:108114885
|
T | C | 1 | a0003c0004t0002g0244 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.192+1119A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108114885 | ||||||
| chr7:108114887
|
C | T | 25 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(22): Show | 25 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.192+1117G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108114887 | ||||||
| chr7:108114917
|
G | C | 21 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(18): Show | 21 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.192+1087C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108114917 | ||||||
| chr7:108114980
|
T | C | 2 | a0001c0001t0001g0234a0014c0025t0002g0233 | 2 | HG02165.hp1 NA18993.hp2 |
intron_variant | MODIFIER | c.192+1024A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108114980 | ||||||
| chr7:108115013
|
A | C | 14 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(11): Show | 14 | HG01243.hp2 HG01433.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.192+991T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108115013 | ||||||
| chr7:108115070
|
G | A | 1 | a0001c0001t0001g0115 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.192+934C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108115070 | ||||||
| chr7:108115202
|
C | T | 3 | a0008c0015t0002g0087a0020c0021t0002g0098a0020c0021t0002g0099 | 3 | HG02055.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.192+802G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108115202 | ||||||
| chr7:108115653
|
AAG | A | 11 | a0007c0019t0002g0096a0007c0037t0002g0093a0008c0044t0002g0091others(8): Show | 11 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(8): Show |
intron_variant | MODIFIER | c.192+349_192+350del others(2): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108115653 | ||||||
| chr7:108115785
|
A | G | 4 | a0008c0015t0002g0001a0008c0015t0002g0002a0017c0041t0001g0003others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.192+219T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108115785 | ||||||
| chr7:108115819
|
C | T | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.192+185G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108115819 | ||||||
| chr7:108115897
|
A | G | 40 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(37): Show | 40 | HG00741.hp1 HG01074.hp2 HG02055.hp2 others(37): Show |
intron_variant | MODIFIER | c.192+107T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 3/33 | chr7 | 108115897 | ||||||
| chr7:108116162
|
C | G | 1 | a0039c0032t0002g0287 | 1 | NA21309.hp2 | splice_acceptor_variant&intron_variant | HIGH | c.35-1G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108116162 | ||||||
| chr7:108116188
|
C | T | 22 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(19): Show | 22 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.35-27G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108116188 | ||||||
| chr7:108116189
|
G | A | 2 | a0001c0001t0001g0209a0001c0001t0001g0210 | 2 | HG02895.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.35-28C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108116189 | ||||||
| chr7:108116330
|
T | G | 1 | a0004c0071t0001g0239 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.35-169A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108116330 | ||||||
| chr7:108116402
|
A | G | 56 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(53): Show | 56 | HG00741.hp1 HG01074.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.35-241T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108116402 | ||||||
| chr7:108116413
|
C | T | 2 | a0007c0019t0002g0005a0040c0031t0002g0006 | 2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.35-252G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108116413 | ||||||
| chr7:108116823
|
A | G | 56 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(53): Show | 56 | HG00741.hp1 HG01074.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.35-662T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108116823 | ||||||
| chr7:108117028
|
C | A | 13 | a0001c0001t0001g0237a0001c0001t0001g0241a0001c0001t0003g0181others(10): Show | 13 | HG02080.hp2 HG03239.hp2 HG03688.hp1 others(10): Show |
intron_variant | MODIFIER | c.35-867G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117028 | ||||||
| chr7:108117133
|
G | A | 3 | a0001c0002t0001g0009a0001c0002t0001g0076a0001c0002t0001g0077 | 3 | HG03688.hp2 HG03834.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.35-972C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117133 | ||||||
| chr7:108117186
|
T | G | 4 | a0008c0015t0002g0001a0008c0015t0002g0002a0017c0041t0001g0003others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.35-1025A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117186 | ||||||
| chr7:108117358
|
G | T | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-1197C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117358 | ||||||
| chr7:108117398
|
T | C | 162 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(159): Show | 162 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(159): Show |
intron_variant | MODIFIER | c.35-1237A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117398 | ||||||
| chr7:108117466
|
T | C | 1 | a0001c0001t0001g0042 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.35-1305A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117466 | ||||||
| chr7:108117510
|
A | T | 1 | a0004c0005t0003g0184 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.35-1349T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117510 | ||||||
| chr7:108117573
|
C | T | 2 | a0001c0001t0001g0030a0001c0001t0003g0255 | 2 | NA19087.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.35-1412G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117573 | ||||||
| chr7:108117582
|
C | A | 2 | a0008c0038t0002g0152a0037c0042t0001g0151 | 2 | HG02280.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.35-1421G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117582 | ||||||
| chr7:108117603
|
C | T | 1 | a0008c0039t0002g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.35-1442G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117603 | ||||||
| chr7:108117628
|
G | A | 1 | a0012c0069t0001g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.35-1467C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117628 | ||||||
| chr7:108117722
|
G | A | 1 | a0003c0004t0002g0007 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.35-1561C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117722 | ||||||
| chr7:108117736
|
C | T | 1 | a0001c0002t0001g0043 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.35-1575G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117736 | ||||||
| chr7:108117748
|
G | T | 7 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(4): Show | 7 | HG01074.hp2 HG02486.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.35-1587C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117748 | ||||||
| chr7:108117783
|
C | A | 16 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(13): Show | 16 | HG01243.hp2 HG01433.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.35-1622G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117783 | ||||||
| chr7:108117879
|
A | G | 1 | a0021c0028t0002g0092 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.35-1718T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117879 | ||||||
| chr7:108117891
|
C | T | 21 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(18): Show | 21 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.35-1730G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117891 | ||||||
| chr7:108117951
|
G | T | 1 | a0001c0002t0001g0020 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.35-1790C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117951 | ||||||
| chr7:108117996
|
C | G | 1 | a0011c0014t0001g0214 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.35-1835G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108117996 | ||||||
| chr7:108118112
|
T | C | 1 | a0012c0069t0001g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.35-1951A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108118112 | ||||||
| chr7:108118120
|
G | GT | 5 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(2): Show | 5 | HG01261.hp2 HG01943.hp1 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.35-1960dupA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108118120 | ||||||
| chr7:108118139
|
A | G | 37 | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0006t0001g0142others(34): Show | 37 | HG00621.hp1 HG01256.hp2 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.35-1978T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108118139 | ||||||
| chr7:108118245
|
C | G | 1 | a0003c0004t0002g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.35-2084G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108118245 | ||||||
| chr7:108118307
|
G | A | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.35-2146C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108118307 | ||||||
| chr7:108118377
|
G | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0003g0015others(4): Show | 7 | HG01943.hp2 HG01978.hp1 HG01981.hp2 others(4): Show |
intron_variant | MODIFIER | c.35-2216C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108118377 | ||||||
| chr7:108118570
|
T | C | 56 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(53): Show | 56 | HG00741.hp1 HG01074.hp2 HG01243.hp2 others(53): Show |
intron_variant | MODIFIER | c.35-2409A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108118570 | ||||||
| chr7:108118915
|
C | A | 1 | a0001c0001t0001g0240 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.35-2754G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108118915 | ||||||
| chr7:108119198
|
A | G | 1 | a0012c0069t0001g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.35-3037T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108119198 | ||||||
| chr7:108119255
|
A | C | 1 | a0001c0002t0001g0028 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.35-3094T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108119255 | ||||||
| chr7:108119461
|
T | C | 1 | a0001c0002t0001g0029 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.35-3300A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108119461 | ||||||
| chr7:108119470
|
G | T | 40 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(37): Show | 40 | HG00741.hp1 HG01074.hp2 HG02055.hp2 others(37): Show |
intron_variant | MODIFIER | c.35-3309C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108119470 | ||||||
| chr7:108119503
|
C | T | 2 | a0001c0002t0001g0020a0001c0002t0001g0021 | 2 | HG00140.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.35-3342G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108119503 | ||||||
| chr7:108119504
|
G | A | 3 | a0001c0002t0003g0073a0002c0003t0001g0138a0002c0003t0001g0141 | 3 | HG01256.hp2 HG01258.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.35-3343C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108119504 | ||||||
| chr7:108119528
|
C | T | 8 | a0001c0002t0001g0019a0001c0002t0001g0032a0001c0002t0001g0033others(5): Show | 8 | HG00544.hp2 HG02129.hp2 HG02155.hp1 others(5): Show |
intron_variant | MODIFIER | c.35-3367G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108119528 | ||||||
| chr7:108119568
|
T | C | 1 | a0001c0001t0001g0206 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.35-3407A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108119568 | ||||||
| chr7:108119683
|
G | A | 1 | a0007c0019t0002g0096 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.34+3448C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108119683 | ||||||
| chr7:108119711
|
A | G | 18 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(15): Show | 18 | HG01074.hp2 HG02280.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.34+3420T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108119711 | ||||||
| chr7:108119735
|
T | C | 18 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(15): Show | 18 | HG01074.hp2 HG02280.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.34+3396A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108119735 | ||||||
| chr7:108119775
|
G | A | 1 | a0001c0006t0001g0142 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.34+3356C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108119775 | ||||||
| chr7:108119833
|
G | A | 39 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(36): Show | 39 | HG00741.hp1 HG01074.hp2 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.34+3298C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108119833 | ||||||
| chr7:108119931
|
A | G | 1 | a0010c0013t0002g0171 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.34+3200T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108119931 | ||||||
| chr7:108120076
|
A | G | 2 | a0012c0022t0002g0279a0025c0057t0002g0280 | 2 | HG01243.hp2 HG02109.hp1 |
intron_variant | MODIFIER | c.34+3055T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108120076 | ||||||
| chr7:108120288
|
A | C | 39 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(36): Show | 39 | HG00741.hp1 HG01074.hp2 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.34+2843T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108120288 | ||||||
| chr7:108120289
|
C | T | 6 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(3): Show | 6 | HG02055.hp1 HG02280.hp1 HG03195.hp2 others(3): Show |
intron_variant | MODIFIER | c.34+2842G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108120289 | ||||||
| chr7:108120382
|
C | A | 1 | a0001c0001t0001g0241 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.34+2749G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108120382 | ||||||
| chr7:108120518
|
T | G | 1 | a0002c0012t0001g0207 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.34+2613A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108120518 | ||||||
| chr7:108120550
|
A | G | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0003g0015others(5): Show | 8 | HG00738.hp1 HG01943.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.34+2581T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108120550 | ||||||
| chr7:108120584
|
C | T | 39 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(36): Show | 39 | HG00741.hp1 HG01074.hp2 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.34+2547G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108120584 | ||||||
| chr7:108120841
|
C | G | 1 | a0034c0073t0003g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.34+2290G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108120841 | ||||||
| chr7:108120854
|
C | T | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+2277G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108120854 | ||||||
| chr7:108120900
|
A | C | 1 | a0034c0073t0003g0212 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.34+2231T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108120900 | ||||||
| chr7:108120929
|
T | C | 1 | a0008c0039t0002g0147 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.34+2202A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108120929 | ||||||
| chr7:108120979
|
A | G | 24 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(21): Show | 24 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.34+2152T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108120979 | ||||||
| chr7:108121038
|
A | G | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.34+2093T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108121038 | ||||||
| chr7:108121118
|
A | G | 2 | a0019c0020t0001g0088a0019c0020t0001g0097 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.34+2013T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108121118 | ||||||
| chr7:108121124
|
A | C | 1 | a0010c0013t0002g0161 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.34+2007T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108121124 | ||||||
| chr7:108121155
|
G | A | 39 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(36): Show | 39 | HG00741.hp1 HG01074.hp2 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.34+1976C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108121155 | ||||||
| chr7:108121224
|
A | G | 2 | a0001c0002t0001g0183a0001c0002t0003g0162 | 2 | NA18950.hp2 NA18990.hp2 |
intron_variant | MODIFIER | c.34+1907T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108121224 | ||||||
| chr7:108121465
|
T | C | 1 | a0011c0014t0001g0242 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.34+1666A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108121465 | ||||||
| chr7:108121643
|
G | A | 2 | a0002c0003t0001g0138a0002c0003t0001g0141 | 2 | HG01256.hp2 HG01258.hp1 |
intron_variant | MODIFIER | c.34+1488C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108121643 | ||||||
| chr7:108121728
|
C | T | 18 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(15): Show | 18 | HG01074.hp2 HG02280.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.34+1403G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108121728 | ||||||
| chr7:108121750
|
T | TA | 49 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(46): Show | 49 | HG00741.hp1 HG01074.hp2 HG02055.hp1 others(46): Show |
intron_variant | MODIFIER | c.34+1380dupT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108121750 | ||||||
| chr7:108121750
|
T | TAA | 38 | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0006t0001g0142others(35): Show | 38 | HG00621.hp1 HG01256.hp2 HG01258.hp1 others(35): Show |
intron_variant | MODIFIER | c.34+1379_34+1380dup others(2): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108121750 | ||||||
| chr7:108121796
|
A | C | 49 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(46): Show | 49 | HG00741.hp1 HG01074.hp2 HG01433.hp2 others(46): Show |
intron_variant | MODIFIER | c.34+1335T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108121796 | ||||||
| chr7:108121981
|
C | A | 21 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(18): Show | 21 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.34+1150G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108121981 | ||||||
| chr7:108122039
|
G | A | 2 | a0007c0011t0002g0156a0007c0011t0002g0157 | 2 | HG03041.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.34+1092C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108122039 | ||||||
| chr7:108122088
|
A | G | 20 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(17): Show | 20 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.34+1043T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108122088 | ||||||
| chr7:108122189
|
C | T | 39 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(36): Show | 39 | HG00741.hp1 HG01074.hp2 HG02055.hp2 others(36): Show |
intron_variant | MODIFIER | c.34+942G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108122189 | ||||||
| chr7:108122195
|
C | T | 16 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(13): Show | 16 | HG01243.hp2 HG01433.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.34+936G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108122195 | ||||||
| chr7:108122268
|
G | A | 3 | a0001c0002t0001g0018a0001c0002t0001g0028a0001c0002t0001g0029 | 3 | NA18962.hp1 NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.34+863C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108122268 | ||||||
| chr7:108122274
|
C | A | 2 | a0019c0020t0001g0088a0019c0020t0001g0097 | 2 | HG02615.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.34+857G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108122274 | ||||||
| chr7:108122295
|
G | A | 55 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(52): Show | 55 | HG00741.hp1 HG01074.hp2 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.34+836C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108122295 | ||||||
| chr7:108122299
|
T | G | 18 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(15): Show | 18 | HG01074.hp2 HG02280.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.34+832A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108122299 | ||||||
| chr7:108122308
|
A | G | 16 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(13): Show | 16 | HG01243.hp2 HG01433.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.34+823T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108122308 | ||||||
| chr7:108122334
|
A | G | 4 | a0008c0015t0002g0001a0008c0015t0002g0002a0017c0041t0001g0003others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.34+797T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108122334 | ||||||
| chr7:108122361
|
T | C | 1 | a0031c0053t0001g0074 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.34+770A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108122361 | ||||||
| chr7:108122552
|
A | G | 18 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(15): Show | 18 | HG01074.hp2 HG02280.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.34+579T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108122552 | ||||||
| chr7:108122567
|
A | G | 3 | a0003c0004t0002g0268a0003c0004t0002g0269a0035c0046t0002g0211 | 3 | HG02258.hp2 HG02886.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.34+564T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108122567 | ||||||
| chr7:108122735
|
T | C | 20 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(17): Show | 20 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.34+396A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108122735 | ||||||
| chr7:108122803
|
A | T | 55 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(52): Show | 55 | HG00741.hp1 HG01074.hp2 HG01243.hp2 others(52): Show |
intron_variant | MODIFIER | c.34+328T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108122803 | ||||||
| chr7:108122823
|
C | T | 54 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(51): Show | 54 | HG00741.hp1 HG01074.hp2 HG01243.hp2 others(51): Show |
intron_variant | MODIFIER | c.34+308G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108122823 | ||||||
| chr7:108122924
|
A | T | 3 | a0001c0001t0001g0209a0001c0001t0001g0210a0001c0001t0002g0208 | 3 | HG02895.hp2 HG02897.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.34+207T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108122924 | ||||||
| chr7:108123130
|
C | T | 2 | a0007c0011t0002g0156a0007c0011t0002g0157 | 2 | HG03041.hp1 NA19043.hp2 |
splice_donor_variant&intron_variant | HIGH | c.34+1G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 2/33 | chr7 | 108123130 | ||||||
| chr7:108123256
|
A | G | 7 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(4): Show | 7 | HG01074.hp2 HG02486.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-59T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108123256 | ||||||
| chr7:108123317
|
CCA | C | 20 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(17): Show | 20 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.-33-122_-33-121del others(2): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108123317 | ||||||
| chr7:108123347
|
G | C | 1 | a0003c0004t0002g0243 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.-33-150C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108123347 | ||||||
| chr7:108123348
|
T | A | 14 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(11): Show | 14 | HG01074.hp2 HG02280.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-33-151A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108123348 | ||||||
| chr7:108123433
|
A | G | 2 | a0003c0004t0002g0268a0003c0004t0002g0269 | 2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-33-236T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108123433 | ||||||
| chr7:108123787
|
G | C | 1 | a0001c0002t0001g0075 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-33-590C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108123787 | ||||||
| chr7:108123790
|
C | G | 1 | a0012c0069t0001g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-33-593G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108123790 | ||||||
| chr7:108123828
|
A | G | 1 | a0007c0011t0001g0100 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-33-631T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108123828 | ||||||
| chr7:108123878
|
T | C | 1 | a0009c0009t0001g0267 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.-33-681A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108123878 | ||||||
| chr7:108123899
|
T | C | 7 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(4): Show | 7 | HG01074.hp2 HG02486.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-33-702A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108123899 | ||||||
| chr7:108123914
|
C | T | 58 | a0001c0001t0001g0030a0001c0001t0001g0163a0001c0001t0001g0164others(55): Show | 58 | HG00280.hp1 HG00423.hp1 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.-33-717G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108123914 | ||||||
| chr7:108124010
|
T | C | 5 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(2): Show | 5 | HG02145.hp1 HG02809.hp1 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33-813A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108124010 | ||||||
| chr7:108124013
|
T | G | 3 | a0001c0054t0001g0146a0008c0039t0002g0147a0012c0022t0002g0148 | 3 | HG02258.hp1 HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-33-816A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108124013 | ||||||
| chr7:108124089
|
A | T | 24 | a0001c0054t0001g0146a0003c0004t0002g0281a0006c0010t0001g0288others(21): Show | 24 | HG01074.hp2 HG01243.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-33-892T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108124089 | ||||||
| chr7:108124126
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0003g0015others(4): Show | 7 | HG00738.hp1 HG01943.hp2 HG01978.hp1 others(4): Show |
intron_variant | MODIFIER | c.-33-929G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108124126 | ||||||
| chr7:108124231
|
A | C | 13 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(10): Show | 13 | HG01433.hp2 HG02055.hp1 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.-33-1034T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108124231 | ||||||
| chr7:108124336
|
A | G | 1 | a0002c0003t0001g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-33-1139T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108124336 | ||||||
| chr7:108124490
|
A | T | 3 | a0003c0004t0002g0281a0012c0022t0002g0279a0025c0057t0002g0280 | 3 | HG01243.hp2 HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-33-1293T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108124490 | ||||||
| chr7:108124579
|
C | T | 3 | a0006c0016t0001g0083a0006c0027t0001g0085a0017c0043t0001g0084 | 3 | HG02145.hp1 HG02809.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-33-1382G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108124579 | ||||||
| chr7:108124664
|
C | CA | 70 | a0001c0001t0001g0038a0001c0001t0001g0039a0001c0001t0001g0040others(67): Show | 70 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(67): Show |
intron_variant | MODIFIER | c.-33-1468dupT | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108124664 | ||||||
| chr7:108124682
|
A | C | 37 | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0006t0001g0142others(34): Show | 37 | HG00621.hp1 HG01256.hp2 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.-33-1485T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108124682 | ||||||
| chr7:108124769
|
C | A | 1 | a0001c0006t0003g0139 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.-33-1572G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108124769 | ||||||
| chr7:108124785
|
C | A | 14 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(11): Show | 14 | HG01074.hp2 HG02280.hp2 HG02486.hp2 others(11): Show |
intron_variant | MODIFIER | c.-33-1588G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108124785 | ||||||
| chr7:108124798
|
C | T | 5 | a0001c0001t0003g0181a0002c0003t0001g0182a0004c0005t0001g0178others(2): Show | 5 | HG03239.hp2 HG06807.hp2 NA18985.hp2 others(2): Show |
intron_variant | MODIFIER | c.-33-1601G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108124798 | ||||||
| chr7:108125188
|
T | C | 1 | a0022c0029t0002g0284 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-33-1991A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108125188 | ||||||
| chr7:108125243
|
G | T | 1 | a0017c0030t0002g0286 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.-33-2046C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108125243 | ||||||
| chr7:108125384
|
T | C | 83 | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0006t0001g0142others(80): Show | 83 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(80): Show |
intron_variant | MODIFIER | c.-33-2187A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108125384 | ||||||
| chr7:108125461
|
C | T | 1 | a0016c0062t0001g0160 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.-33-2264G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108125461 | ||||||
| chr7:108125541
|
T | C | 1 | a0040c0031t0002g0006 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.-33-2344A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108125541 | ||||||
| chr7:108126077
|
C | T | 3 | a0001c0002t0001g0018a0001c0002t0001g0028a0001c0002t0001g0029 | 3 | NA18962.hp1 NA19005.hp1 NA19010.hp2 |
intron_variant | MODIFIER | c.-33-2880G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126077 | ||||||
| chr7:108126083
|
G | A | 1 | a0016c0061t0002g0155 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-33-2886C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126083 | ||||||
| chr7:108126086
|
G | A | 1 | a0001c0070t0001g0246 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.-33-2889C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126086 | ||||||
| chr7:108126215
|
A | T | 1 | a0012c0069t0001g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-33-3018T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126215 | ||||||
| chr7:108126263
|
T | A | 18 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(15): Show | 18 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-33-3066A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126263 | ||||||
| chr7:108126295
|
T | A | 3 | a0008c0015t0002g0087a0020c0021t0002g0098a0020c0021t0002g0099 | 3 | HG02055.hp2 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-33-3098A>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126295 | ||||||
| chr7:108126311
|
G | A | 18 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(15): Show | 18 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-33-3114C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126311 | ||||||
| chr7:108126417
|
C | G | 1 | a0001c0001t0001g0177 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.-33-3220G>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126417 | ||||||
| chr7:108126462
|
C | T | 18 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(15): Show | 18 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-33-3265G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126462 | ||||||
| chr7:108126488
|
G | C | 3 | a0001c0002t0001g0009a0001c0002t0001g0076a0001c0002t0001g0077 | 3 | HG03688.hp2 HG03834.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-33-3291C>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126488 | ||||||
| chr7:108126499
|
G | A | 4 | a0008c0015t0002g0001a0008c0015t0002g0002a0017c0041t0001g0003others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-33-3302C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126499 | ||||||
| chr7:108126554
|
C | CCTTTTT | 4 | a0006c0016t0002g0086a0006c0027t0001g0085a0017c0043t0001g0084others(1): Show | 4 | HG02809.hp1 HG02809.hp2 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.-33-3358_-33-3357i others(8): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126554 | ||||||
| chr7:108126554
|
C | CCTTTTTT | 3 | a0006c0016t0001g0083a0020c0021t0002g0098a0020c0021t0002g0099 | 3 | HG02145.hp1 HG03139.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-33-3358_-33-3357i others(9): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126554 | ||||||
| chr7:108126554
|
C | CCTTTTTT others(1): Show |
8 | a0007c0019t0002g0096a0007c0037t0002g0093a0008c0015t0002g0087others(5): Show | 8 | HG00741.hp1 HG02055.hp2 HG02615.hp2 others(5): Show |
intron_variant | MODIFIER | c.-33-3358_-33-3357i others(10): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126554 | ||||||
| chr7:108126554
|
C | CCTTTTTT others(2): Show |
3 | a0008c0044t0002g0091a0038c0036t0002g0089a0041c0033t0001g0090 | 3 | HG02572.hp1 HG02622.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.-33-3358_-33-3357i others(11): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126554 | ||||||
| chr7:108126554
|
C | CTTTTT | 13 | a0001c0001t0001g0150a0001c0001t0001g0249a0001c0001t0003g0247others(10): Show | 13 | HG00323.hp2 HG01169.hp1 HG01256.hp2 others(10): Show |
intron_variant | MODIFIER | c.-33-3362_-33-3358d others(7): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126554 | ||||||
| chr7:108126554
|
C | CTTTTTT | 182 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0030others(179): Show | 182 | HG00140.hp2 HG00280.hp2 HG00323.hp1 others(179): Show |
intron_variant | MODIFIER | c.-33-3363_-33-3358d others(8): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126554 | ||||||
| chr7:108126554
|
C | CTTTTTTT | 53 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(50): Show | 53 | HG00140.hp1 HG00423.hp1 HG00423.hp2 others(50): Show |
intron_variant | MODIFIER | c.-33-3364_-33-3358d others(9): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126554 | ||||||
| chr7:108126554
|
CT | C | 10 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(7): Show | 10 | HG02486.hp2 HG02970.hp2 HG03098.hp2 others(7): Show |
intron_variant | MODIFIER | c.-33-3358delA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126554 | ||||||
| chr7:108126558
|
T | C | 1 | a0001c0001t0001g0254 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-33-3361A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126558 | ||||||
| chr7:108126581
|
G | A | 1 | a0012c0022t0002g0148 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.-33-3384C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126581 | ||||||
| chr7:108126596
|
C | T | 10 | a0007c0019t0002g0096a0007c0037t0002g0093a0008c0044t0002g0091others(7): Show | 10 | HG00741.hp1 HG02572.hp1 HG02615.hp2 others(7): Show |
intron_variant | MODIFIER | c.-33-3399G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126596 | ||||||
| chr7:108126636
|
C | A | 1 | a0002c0003t0001g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-33-3439G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126636 | ||||||
| chr7:108126637
|
T | G | 1 | a0002c0003t0001g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-33-3440A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126637 | ||||||
| chr7:108126648
|
T | G | 1 | a0002c0003t0001g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-33-3451A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126648 | ||||||
| chr7:108126655
|
C | T | 2 | a0007c0019t0002g0005a0040c0031t0002g0006 | 2 | HG02922.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.-33-3458G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126655 | ||||||
| chr7:108126664
|
A | C | 2 | a0001c0006t0001g0144a0001c0006t0001g0145 | 2 | NA18968.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-33-3467T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126664 | ||||||
| chr7:108126720
|
G | A | 13 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0001t0001g0259others(10): Show | 13 | HG00558.hp1 HG02083.hp1 HG02083.hp2 others(10): Show |
intron_variant | MODIFIER | c.-33-3523C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126720 | ||||||
| chr7:108126722
|
G | A | 1 | a0009c0009t0001g0010 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.-33-3525C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126722 | ||||||
| chr7:108126727
|
A | G | 18 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(15): Show | 18 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-33-3530T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126727 | ||||||
| chr7:108126731
|
ATTTT | A | 18 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(15): Show | 18 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-33-3538_-33-3535d others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126731 | ||||||
| chr7:108126847
|
C | A | 2 | a0003c0004t0002g0268a0003c0004t0002g0269 | 2 | HG02258.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.-34+3459G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126847 | ||||||
| chr7:108126864
|
G | A | 1 | a0012c0069t0001g0158 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-34+3442C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126864 | ||||||
| chr7:108126878
|
T | G | 1 | a0002c0003t0001g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-34+3428A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126878 | ||||||
| chr7:108126932
|
G | A | 18 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(15): Show | 18 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-34+3374C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108126932 | ||||||
| chr7:108127057
|
G | A | 1 | a0001c0063t0001g0270 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.-34+3249C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127057 | ||||||
| chr7:108127071
|
C | A | 18 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(15): Show | 18 | HG01074.hp2 HG02280.hp2 HG02486.hp2 others(15): Show |
intron_variant | MODIFIER | c.-34+3235G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127071 | ||||||
| chr7:108127072
|
G | T | 18 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(15): Show | 18 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-34+3234C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127072 | ||||||
| chr7:108127171
|
C | A | 3 | a0003c0004t0002g0281a0012c0022t0002g0279a0025c0057t0002g0280 | 3 | HG01243.hp2 HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-34+3135G>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127171 | ||||||
| chr7:108127174
|
GGTTTTTT others(7): Show |
G | 2 | a0001c0002t0001g0016a0001c0002t0001g0017 | 2 | HG01175.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.-34+3118_-34+3131d others(16): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127174 | ||||||
| chr7:108127175
|
GT | G | 16 | a0006c0016t0001g0083a0006c0016t0002g0086a0007c0019t0002g0096others(13): Show | 16 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.-34+3130delA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127175 | ||||||
| chr7:108127175
|
GTTTTTTT others(8): Show |
G | 66 | a0001c0001t0001g0030a0001c0001t0001g0038a0001c0001t0001g0039others(63): Show | 66 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.-34+3116_-34+3130d others(17): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127175 | ||||||
| chr7:108127180
|
T | G | 1 | a0002c0003t0001g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-34+3126A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127180 | ||||||
| chr7:108127185
|
T | G | 5 | a0005c0008t0002g0271a0007c0019t0002g0005a0016c0061t0002g0155others(2): Show | 5 | HG02056.hp2 HG02922.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.-34+3121A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127185 | ||||||
| chr7:108127186
|
T | G | 1 | a0002c0003t0001g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-34+3120A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127186 | ||||||
| chr7:108127187
|
G | T | 2 | a0003c0004t0002g0007a0009c0009t0001g0010 | 2 | HG00738.hp1 HG01943.hp2 |
intron_variant | MODIFIER | c.-34+3119C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127187 | ||||||
| chr7:108127189
|
G | GT | 27 | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0006t0001g0142others(24): Show | 27 | HG00323.hp1 HG01074.hp2 HG01433.hp2 others(24): Show |
intron_variant | MODIFIER | c.-34+3116dupA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127189 | ||||||
| chr7:108127189
|
G | GTT | 38 | a0001c0001t0001g0104a0001c0001t0001g0115a0001c0001t0001g0119others(35): Show | 38 | HG00621.hp1 HG01256.hp2 HG01258.hp1 others(35): Show |
intron_variant | MODIFIER | c.-34+3115_-34+3116d others(4): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127189 | ||||||
| chr7:108127189
|
G | T | 2 | a0002c0003t0001g0111a0002c0003t0001g0112 | 2 | HG03927.hp1 NA18981.hp2 |
intron_variant | MODIFIER | c.-34+3117C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127189 | ||||||
| chr7:108127189
|
GTTT | G | 16 | a0006c0016t0001g0083a0006c0016t0002g0086a0007c0019t0002g0096others(13): Show | 16 | HG00741.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.-34+3114_-34+3116d others(5): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127189 | ||||||
| chr7:108127191
|
T | G | 1 | a0006c0027t0001g0085 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.-34+3115A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127191 | ||||||
| chr7:108127194
|
T | G | 1 | a0002c0003t0001g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-34+3112A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127194 | ||||||
| chr7:108127203
|
T | G | 1 | a0002c0003t0001g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-34+3103A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127203 | ||||||
| chr7:108127229
|
T | G | 1 | a0002c0003t0001g0143 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-34+3077A>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127229 | ||||||
| chr7:108127299
|
G | T | 88 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(85): Show | 88 | HG00621.hp1 HG00741.hp1 HG01074.hp2 others(85): Show |
intron_variant | MODIFIER | c.-34+3007C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127299 | ||||||
| chr7:108127551
|
G | A | 7 | a0001c0001t0001g0272a0001c0001t0001g0273a0001c0001t0001g0275others(4): Show | 7 | HG02056.hp2 HG02129.hp1 HG02132.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34+2755C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127551 | ||||||
| chr7:108127726
|
C | T | 38 | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0006t0001g0142others(35): Show | 38 | HG00621.hp1 HG01256.hp2 HG01258.hp1 others(35): Show |
intron_variant | MODIFIER | c.-34+2580G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127726 | ||||||
| chr7:108127907
|
C | T | 2 | a0006c0016t0001g0083a0017c0043t0001g0084 | 2 | HG02145.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.-34+2399G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127907 | ||||||
| chr7:108127940
|
A | T | 291 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0030others(288): Show | 291 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(288): Show |
intron_variant | MODIFIER | c.-34+2366T>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108127940 | ||||||
| chr7:108128110
|
G | A | 1 | a0022c0029t0002g0284 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-34+2196C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108128110 | ||||||
| chr7:108128179
|
C | T | 1 | a0001c0001t0001g0150 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.-34+2127G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108128179 | ||||||
| chr7:108128456
|
G | A | 2 | a0001c0006t0001g0144a0001c0006t0001g0145 | 2 | NA18968.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-34+1850C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108128456 | ||||||
| chr7:108128467
|
G | T | 1 | a0001c0002t0002g0149 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.-34+1839C>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108128467 | ||||||
| chr7:108128556
|
C | T | 3 | a0001c0054t0001g0146a0008c0039t0002g0147a0012c0022t0002g0148 | 3 | HG02258.hp1 HG02723.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.-34+1750G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108128556 | ||||||
| chr7:108128631
|
T | C | 3 | a0003c0004t0002g0281a0012c0022t0002g0279a0025c0057t0002g0280 | 3 | HG01243.hp2 HG02109.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.-34+1675A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108128631 | ||||||
| chr7:108128709
|
TGTG | T | 4 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(1): Show | 4 | HG02145.hp1 HG02809.hp1 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.-34+1594_-34+1596d others(5): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108128709 | ||||||
| chr7:108128884
|
TAAAC | T | 18 | a0006c0016t0001g0083a0006c0016t0002g0086a0006c0027t0001g0085others(15): Show | 18 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.-34+1418_-34+1421d others(6): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108128884 | ||||||
| chr7:108128911
|
T | C | 1 | a0003c0004t0002g0281 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.-34+1395A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108128911 | ||||||
| chr7:108129058
|
T | C | 1 | a0001c0001t0001g0282 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.-34+1248A>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108129058 | ||||||
| chr7:108129223
|
G | A | 37 | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0006t0001g0142others(34): Show | 37 | HG00621.hp1 HG01256.hp2 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.-34+1083C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108129223 | ||||||
| chr7:108129224
|
C | T | 37 | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0006t0001g0142others(34): Show | 37 | HG00621.hp1 HG01256.hp2 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.-34+1082G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108129224 | ||||||
| chr7:108129228
|
G | A | 1 | a0028c0064t0002g0283 | 1 | NA18972.hp2 | intron_variant | MODIFIER | c.-34+1078C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108129228 | ||||||
| chr7:108129269
|
GCTC | G | 7 | a0001c0001t0001g0104a0001c0001t0001g0106a0001c0001t0001g0107others(4): Show | 7 | HG01433.hp2 HG02055.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.-34+1034_-34+1036d others(5): Show |
LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108129269 | ||||||
| chr7:108129439
|
A | C | 1 | a0022c0034t0001g0103 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.-34+867T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108129439 | ||||||
| chr7:108129539
|
C | CT | 24 | a0001c0002t0001g0008a0001c0002t0001g0009a0002c0003t0001g0082others(21): Show | 24 | HG00741.hp1 HG02055.hp2 HG02145.hp1 others(21): Show |
intron_variant | MODIFIER | c.-34+766dupA | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108129539 | ||||||
| chr7:108129694
|
C | T | 4 | a0008c0015t0002g0001a0008c0015t0002g0002a0017c0041t0001g0003others(1): Show | 4 | HG02615.hp1 HG02717.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.-34+612G>A | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108129694 | ||||||
| chr7:108129704
|
G | A | 1 | a0022c0029t0002g0284 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-34+602C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108129704 | ||||||
| chr7:108129825
|
G | A | 7 | a0006c0010t0001g0288a0006c0010t0001g0289a0006c0010t0001g0291others(4): Show | 7 | HG01074.hp2 HG02486.hp2 HG03098.hp2 others(4): Show |
intron_variant | MODIFIER | c.-34+481C>T | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108129825 | ||||||
| chr7:108130176
|
A | G | 1 | a0003c0004t0002g0007 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.-34+130T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108130176 | ||||||
| chr7:108130179
|
A | G | 75 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0030others(72): Show | 75 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(72): Show |
intron_variant | MODIFIER | c.-34+127T>C | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108130179 | ||||||
| chr7:108130239
|
A | C | 6 | a0007c0019t0002g0005a0008c0015t0002g0001a0008c0015t0002g0002others(3): Show | 6 | HG02615.hp1 HG02717.hp1 HG02818.hp1 others(3): Show |
intron_variant | MODIFIER | c.-34+67T>G | LAMB4 | ENSG00000091128.13 | transcript | ENST00000388781.8 | protein_coding | 1/33 | chr7 | 108130239 |