Item | Value |
---|---|
geneid | 3912 |
ensemblid | ENSG00000091136.15 |
hgncid | 6486 |
symbol | LAMB1 |
name | laminin subunit beta 1 |
refseq_nuc | NM_002291.3 |
refseq_prot | NP_002282.2 |
ensembl_nuc | ENST00000222399.11 |
ensembl_prot | ENSP00000222399.6 |
mane_status | MANE Select |
chr | chr7 |
start | 107923799 |
end | 108003161 |
strand | - |
ver | v1.2 |
region | chr7:107923799-108003161 |
region5000 | chr7:107918799-108008161 |
regionname0 | LAMB1_chr7_107923799_108003161 |
regionname5000 | LAMB1_chr7_107918799_108008161 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 1786 | 212 | 49 | 36 | 99 | 6 | 21 | 70 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0002 | 1/0 | 1786 | 72 | 17 | 16 | 21 | 7 | 10 | 19 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0003 | 0/0 | 1786 | 30 | 1 | 6 | 23 | 0 | 0 | 19 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0004 | 0/0 | 1786 | 10 | 9 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0005 | 0/0 | 1786 | 5 | 3 | 1 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0006 | 0/0 | 1786 | 4 | 1 | 1 | 0 | 0 | 2 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0007 | 0/0 | 1786 | 3 | 1 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0008 | 0/0 | 1786 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0009 | 0/0 | 1786 | 2 | 0 | 1 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0010 | 0/0 | 1786 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0011 | 0/0 | 1786 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0012 | 0/0 | 1786 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0013 | 0/0 | 1786 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0014 | 0/0 | 1786 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0015 | 0/0 | 1786 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0016 | 0/0 | 1786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0017 | 0/0 | 1786 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0018 | 0/0 | 1786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0019 | 0/0 | 1786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0020 | 0/0 | 1786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0021 | 0/0 | 1786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0022 | 0/0 | 1786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0023 | 0/0 | 1786 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0024 | 0/0 | 1786 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0025 | 0/0 | 1786 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0026 | 0/0 | 1786 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0027 | 0/0 | 1786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0028 | 0/0 | 1786 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0029 | 0/0 | 1786 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
a0030 | 0/0 | 1786 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | MGLLQ others(1781): Show |
chr7 | 107918799 | 108008161 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | aseq | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 5358 | 83 | 7 | 18 | 45 | 4 | 9 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0002 | 0/1 | 5358 | 50 | 3 | 12 | 30 | 1 | 3 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0005 | 0/0 | 5358 | 17 | 6 | 1 | 9 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0006 | 0/0 | 5358 | 14 | 6 | 1 | 2 | 0 | 5 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0007 | 0/0 | 5358 | 11 | 11 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0009 | 0/0 | 5358 | 8 | 1 | 3 | 4 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0014 | 0/0 | 5358 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0017 | 0/0 | 5358 | 3 | 0 | 0 | 3 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0018 | 0/0 | 5358 | 3 | 0 | 0 | 2 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0022 | 0/0 | 5358 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0027 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0028 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0029 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0032 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0035 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0042 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0043 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0044 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0045 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0056 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0058 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0059 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0063 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0072 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0073 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0077 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0078 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0001c0083 | 0/0 | 5358 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0002c0003 | 1/0 | 5358 | 44 | 7 | 7 | 18 | 5 | 6 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0002c0008 | 0/0 | 5358 | 9 | 1 | 3 | 2 | 1 | 2 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0002c0010 | 0/0 | 5358 | 6 | 3 | 2 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0002c0013 | 0/0 | 5358 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0002c0019 | 0/0 | 5358 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0002c0021 | 0/0 | 5358 | 2 | 0 | 1 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0002c0026 | 0/0 | 5358 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0002c0039 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0002c0052 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0002c0053 | 0/0 | 5358 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0002c0054 | 0/0 | 5358 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0002c0081 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0003c0004 | 0/0 | 5358 | 24 | 1 | 4 | 19 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0003c0020 | 0/0 | 5358 | 2 | 0 | 0 | 2 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0003c0038 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0003c0049 | 0/0 | 5358 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0003c0050 | 0/0 | 5358 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0003c0079 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0004c0015 | 0/0 | 5358 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0004c0016 | 0/0 | 5358 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0004c0066 | 0/0 | 5358 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0004c0067 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0004c0068 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0004c0069 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0005c0012 | 0/0 | 5358 | 4 | 2 | 1 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0005c0065 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0006c0011 | 0/0 | 5358 | 4 | 1 | 1 | 0 | 0 | 2 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0007c0023 | 0/0 | 5358 | 2 | 0 | 2 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0007c0080 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0008c0024 | 0/0 | 5358 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0008c0031 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0009c0062 | 0/0 | 5358 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0009c0082 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0010c0025 | 0/0 | 5358 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0011c0070 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0011c0071 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0012c0075 | 0/0 | 5358 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0013c0040 | 0/0 | 5358 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0014c0041 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0015c0055 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0016c0060 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0017c0051 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0018c0048 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0019c0036 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0020c0034 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0021c0046 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0022c0033 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0023c0037 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0024c0030 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0025c0061 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0026c0064 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0027c0047 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0028c0074 | 0/0 | 5358 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0029c0076 | 0/0 | 5358 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 | ||
a0030c0057 | 0/0 | 5358 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | ATGGG others(5353): Show |
chr7 | 107918799 | 108008161 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 5650 | 70 | 7 | 9 | 44 | 2 | 8 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0001t0002 | 0/0 | 5650 | 13 | 0 | 9 | 1 | 2 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0002t0001 | 0/1 | 5650 | 50 | 3 | 12 | 30 | 1 | 3 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0005t0001 | 0/0 | 5650 | 17 | 6 | 1 | 9 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0006t0001 | 0/0 | 5650 | 9 | 6 | 0 | 1 | 0 | 2 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0006t0002 | 0/0 | 5650 | 5 | 0 | 1 | 1 | 0 | 3 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0007t0001 | 0/0 | 5650 | 9 | 9 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0007t0003 | 0/0 | 5650 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0009t0001 | 0/0 | 5650 | 8 | 1 | 3 | 4 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0014t0001 | 0/0 | 5650 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0014t0003 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0017t0001 | 0/0 | 5650 | 3 | 0 | 0 | 3 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0018t0001 | 0/0 | 5650 | 2 | 0 | 0 | 2 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0018t0002 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0022t0001 | 0/0 | 5650 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0027t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0028t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0029t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0032t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0035t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0042t0001 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0043t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0044t0002 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0045t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0056t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0058t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0059t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0063t0001 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0072t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0073t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0077t0001 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0078t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0001c0083t0002 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0002c0003t0001 | 0/0 | 5650 | 5 | 2 | 1 | 1 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0002c0003t0002 | 1/0 | 5650 | 39 | 5 | 6 | 17 | 4 | 6 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0002c0008t0002 | 0/0 | 5650 | 9 | 1 | 3 | 2 | 1 | 2 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0002c0010t0001 | 0/0 | 5650 | 6 | 3 | 2 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0002c0013t0001 | 0/0 | 5650 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0002c0019t0002 | 0/0 | 5650 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0002c0021t0002 | 0/0 | 5650 | 2 | 0 | 1 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0002c0026t0002 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0002c0039t0002 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0002c0052t0002 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0002c0053t0002 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0002c0054t0001 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0002c0081t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0003c0004t0001 | 0/0 | 5650 | 23 | 1 | 4 | 18 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0003c0004t0002 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0003c0020t0001 | 0/0 | 5650 | 2 | 0 | 0 | 2 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0003c0038t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0003c0049t0001 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0003c0050t0002 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0003c0079t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0004c0015t0001 | 0/0 | 5650 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0004c0015t0002 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0004c0016t0001 | 0/0 | 5650 | 3 | 3 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0004c0066t0004 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0004c0067t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0004c0068t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0004c0069t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0005c0012t0002 | 0/0 | 5650 | 4 | 2 | 1 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0005c0065t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0006c0011t0002 | 0/0 | 5650 | 4 | 1 | 1 | 0 | 0 | 2 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0007c0023t0001 | 0/0 | 5650 | 2 | 0 | 2 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0007c0080t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0008c0024t0001 | 0/0 | 5650 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0008c0031t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0009c0062t0002 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0009c0082t0002 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0010c0025t0001 | 0/0 | 5650 | 2 | 2 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0011c0070t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0011c0071t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0012c0075t0001 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0013c0040t0001 | 0/0 | 5650 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0014c0041t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0015c0055t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0016c0060t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0017c0051t0001 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0018c0048t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0019c0036t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0020c0034t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0021c0046t0002 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0022c0033t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0023c0037t0002 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0024c0030t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0025c0061t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0026c0064t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0027c0047t0003 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0028c0074t0001 | 0/0 | 5650 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0029c0076t0001 | 0/0 | 5650 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
a0030c0057t0002 | 0/0 | 5650 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | CTTCT others(5645): Show |
chr7 | 107918799 | 108008161 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0015 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0303 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0001g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0002g0002 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0002g0003 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0002g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0001t0002g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0014 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0053 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0103 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0144 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0237 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0297 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0002t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0005t0001g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0005t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0005t0001g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0005t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0005t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0005t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0005t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0005t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0005t0001g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0005t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0005t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0005t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0005t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0005t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0005t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0005t0001g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0005t0001g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0006t0001g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0006t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0006t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0006t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0006t0001g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0006t0001g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0006t0001g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0006t0001g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0006t0001g0358 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0006t0002g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0006t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0006t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0006t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0006t0002g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0007t0001g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0007t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0007t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0007t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0007t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0007t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0007t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0007t0001g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0007t0001g0343 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0007t0003g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0007t0003g0362 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0009t0001g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0009t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0009t0001g0270 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0009t0001g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0009t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0009t0001g0281 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0009t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0009t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0014t0001g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0014t0001g0346 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0014t0003g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0017t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0017t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0017t0001g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0018t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0018t0001g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0018t0002g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0022t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0022t0001g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0027t0001g0349 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0028t0001g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0029t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0032t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0035t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0042t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0043t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0044t0002g0345 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0045t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0056t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0058t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0059t0001g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0063t0001g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0072t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0073t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0077t0001g0275 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0078t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0001c0083t0002g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0001g0284 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0023 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0242 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0285 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0288 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0003t0002g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0008t0002g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0008t0002g0098 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0008t0002g0156 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0008t0002g0268 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0008t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0008t0002g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0008t0002g0274 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0008t0002g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0008t0002g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0010t0001g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0010t0001g0155 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0010t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0010t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0010t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0010t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0013t0001g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0013t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0013t0001g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0019t0002g0304 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0019t0002g0308 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0021t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0021t0002g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0026t0002g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0039t0002g0203 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0052t0002g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0053t0002g0145 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0054t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0002c0081t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0004t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0020t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0020t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0038t0001g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0049t0001g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0050t0002g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0003c0079t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0004c0015t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0004c0015t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0004c0015t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0004c0016t0001g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0004c0016t0001g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0004c0016t0001g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0004c0066t0004g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0004c0067t0001g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0004c0068t0001g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0004c0069t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0005c0012t0002g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0005c0012t0002g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0005c0012t0002g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0005c0012t0002g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0005c0065t0001g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0006c0011t0002g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0006c0011t0002g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0006c0011t0002g0259 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0006c0011t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0007c0023t0001g0051 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0007c0023t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0007c0080t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0008c0024t0001g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0008c0024t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0008c0031t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0009c0062t0002g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0009c0082t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0010c0025t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0010c0025t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0011c0070t0001g0348 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0011c0071t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0012c0075t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0013c0040t0001g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0014c0041t0001g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0015c0055t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0016c0060t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0017c0051t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0018c0048t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0019c0036t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0020c0034t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0021c0046t0002g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0022c0033t0001g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0023c0037t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0024c0030t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0025c0061t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0026c0064t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0027c0047t0003g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0028c0074t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0029c0076t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
a0030c0057t0002g0090 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0002 | c0003 | t0001 | g0284 | EUR | GBR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00099 | hp2 | a0002 | c0003 | t0002 | g0258 | EUR | GBR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00140 | hp1 | a0002 | c0003 | t0002 | g0161 | EUR | GBR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00140 | hp2 | a0001 | c0002 | t0001 | g0049 | EUR | GBR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00323 | hp1 | a0002 | c0010 | t0001 | g0155 | EUR | FIN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0015 | EUR | FIN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00408 | hp1 | a0001 | c0009 | t0001 | g0280 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00408 | hp2 | a0001 | c0005 | t0001 | g0101 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00423 | hp1 | a0001 | c0006 | t0001 | g0251 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00423 | hp2 | a0001 | c0002 | t0001 | g0107 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00438 | hp1 | a0003 | c0004 | t0001 | g0081 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0260 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00558 | hp1 | a0001 | c0002 | t0001 | g0344 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00609 | hp2 | a0001 | c0005 | t0001 | g0129 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00621 | hp2 | a0001 | c0073 | t0001 | g0256 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00639 | hp1 | a0003 | c0004 | t0001 | g0148 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00639 | hp2 | a0002 | c0010 | t0001 | g0227 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00642 | hp2 | a0001 | c0002 | t0001 | g0103 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00673 | hp1 | a0002 | c0003 | t0002 | g0128 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00673 | hp2 | a0001 | c0002 | t0001 | g0216 | EAS | CHS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00733 | hp1 | a0002 | c0003 | t0002 | g0013 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00733 | hp2 | a0001 | c0006 | t0002 | g0124 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00735 | hp1 | a0001 | c0009 | t0001 | g0018 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00735 | hp2 | a0002 | c0008 | t0002 | g0273 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00738 | hp1 | a0002 | c0026 | t0002 | g0352 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0047 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00741 | hp1 | a0003 | c0004 | t0001 | g0171 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG00741 | hp2 | a0006 | c0011 | t0002 | g0060 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01069 | hp1 | a0002 | c0003 | t0002 | g0010 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01069 | hp2 | a0007 | c0023 | t0001 | g0051 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01070 | hp2 | a0002 | c0021 | t0002 | g0066 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01081 | hp1 | a0002 | c0003 | t0001 | g0165 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01081 | hp2 | a0001 | c0002 | t0001 | g0104 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01099 | hp1 | a0001 | c0002 | t0001 | g0105 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01099 | hp2 | a0002 | c0054 | t0001 | g0181 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01106 | hp1 | a0012 | c0075 | t0001 | g0043 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0048 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01109 | hp1 | a0002 | c0003 | t0002 | g0017 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01168 | hp1 | a0002 | c0008 | t0002 | g0272 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01168 | hp2 | a0001 | c0002 | t0001 | g0057 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01175 | hp1 | a0001 | c0083 | t0002 | g0074 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01175 | hp2 | a0001 | c0005 | t0001 | g0059 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01192 | hp1 | a0001 | c0002 | t0001 | g0212 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01192 | hp2 | a0009 | c0062 | t0002 | g0293 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01243 | hp1 | a0005 | c0012 | t0002 | g0353 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01243 | hp2 | a0001 | c0001 | t0002 | g0089 | AMR | PUR | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01255 | hp2 | a0001 | c0002 | t0001 | g0065 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01256 | hp1 | a0003 | c0049 | t0001 | g0056 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01256 | hp2 | a0002 | c0003 | t0002 | g0045 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0294 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0153 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01258 | hp1 | a0002 | c0003 | t0002 | g0046 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01258 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01261 | hp1 | a0001 | c0001 | t0002 | g0061 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01261 | hp2 | a0003 | c0004 | t0001 | g0215 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0320 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01361 | hp1 | a0003 | c0050 | t0002 | g0146 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01361 | hp2 | a0001 | c0002 | t0001 | g0106 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01433 | hp1 | a0004 | c0066 | t0004 | g0021 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01433 | hp2 | a0007 | c0023 | t0001 | g0052 | AMR | CLM | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01515 | hp2 | a0001 | c0042 | t0001 | g0112 | EUR | IBS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01517 | hp1 | a0002 | c0003 | t0002 | g0288 | EUR | IBS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0002 | EUR | IBS | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01884 | hp1 | a0007 | c0080 | t0001 | g0276 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01884 | hp2 | a0002 | c0010 | t0001 | g0044 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01891 | hp1 | a0001 | c0007 | t0001 | g0130 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01891 | hp2 | a0001 | c0014 | t0003 | g0360 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01928 | hp1 | a0001 | c0002 | t0001 | g0265 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01928 | hp2 | a0002 | c0053 | t0002 | g0145 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01943 | hp2 | a0002 | c0010 | t0001 | g0162 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01952 | hp1 | a0013 | c0040 | t0001 | g0241 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01952 | hp2 | a0001 | c0002 | t0001 | g0064 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01975 | hp1 | a0002 | c0008 | t0002 | g0268 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01975 | hp2 | a0001 | c0002 | t0001 | g0014 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01981 | hp2 | a0001 | c0002 | t0001 | g0240 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01993 | hp1 | a0001 | c0009 | t0001 | g0281 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG01993 | hp2 | a0002 | c0003 | t0002 | g0242 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02004 | hp2 | a0001 | c0002 | t0001 | g0144 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02015 | hp1 | a0001 | c0009 | t0001 | g0282 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02015 | hp2 | a0001 | c0002 | t0001 | g0211 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02027 | hp1 | a0001 | c0002 | t0001 | g0209 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0263 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02055 | hp1 | a0001 | c0007 | t0003 | g0361 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02055 | hp2 | a0001 | c0005 | t0001 | g0351 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02056 | hp1 | a0003 | c0004 | t0001 | g0164 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02080 | hp1 | a0005 | c0012 | t0002 | g0323 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02080 | hp2 | a0001 | c0005 | t0001 | g0244 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02083 | hp1 | a0001 | c0002 | t0001 | g0202 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0221 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02129 | hp2 | a0001 | c0006 | t0002 | g0235 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0228 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02132 | hp2 | a0002 | c0003 | t0002 | g0315 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02135 | hp2 | a0001 | c0005 | t0001 | g0326 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02145 | hp1 | a0002 | c0003 | t0002 | g0092 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02145 | hp2 | a0001 | c0005 | t0001 | g0150 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0019 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02148 | hp2 | a0003 | c0004 | t0001 | g0238 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02155 | hp1 | a0014 | c0041 | t0001 | g0322 | EAS | CDX | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | CDX | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | CDX | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02165 | hp2 | a0015 | c0055 | t0001 | g0243 | EAS | CDX | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02257 | hp1 | a0001 | c0002 | t0001 | g0237 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02257 | hp2 | a0005 | c0012 | t0002 | g0135 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0335 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02258 | hp2 | a0001 | c0006 | t0001 | g0341 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02280 | hp1 | a0001 | c0043 | t0001 | g0116 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02280 | hp2 | a0002 | c0013 | t0001 | g0030 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0131 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02293 | hp2 | a0001 | c0009 | t0001 | g0270 | AMR | PEL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02451 | hp1 | a0001 | c0007 | t0001 | g0343 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02451 | hp2 | a0001 | c0009 | t0001 | g0271 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0246 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02523 | hp2 | a0001 | c0009 | t0001 | g0194 | EAS | KHV | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02572 | hp1 | a0001 | c0007 | t0003 | g0362 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02572 | hp2 | a0001 | c0078 | t0001 | g0024 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02615 | hp1 | a0010 | c0025 | t0001 | g0340 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02622 | hp1 | a0001 | c0035 | t0001 | g0037 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02622 | hp2 | a0001 | c0007 | t0001 | g0009 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02630 | hp1 | a0002 | c0003 | t0002 | g0347 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02630 | hp2 | a0001 | c0032 | t0001 | g0028 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02647 | hp1 | a0004 | c0015 | t0001 | g0138 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02647 | hp2 | a0004 | c0067 | t0001 | g0137 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02698 | hp1 | a0009 | c0082 | t0002 | g0204 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0226 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02717 | hp1 | a0001 | c0002 | t0001 | g0337 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02717 | hp2 | a0001 | c0007 | t0001 | g0113 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02723 | hp1 | a0016 | c0060 | t0001 | g0036 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02723 | hp2 | a0008 | c0031 | t0001 | g0072 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02735 | hp2 | a0002 | c0039 | t0002 | g0203 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02738 | hp1 | a0017 | c0051 | t0001 | g0253 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02738 | hp2 | a0002 | c0003 | t0002 | g0054 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02809 | hp1 | a0011 | c0070 | t0001 | g0348 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02809 | hp2 | a0018 | c0048 | t0001 | g0027 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02818 | hp1 | a0002 | c0003 | t0002 | g0075 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02818 | hp2 | a0004 | c0069 | t0001 | g0134 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02886 | hp1 | a0019 | c0036 | t0001 | g0068 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02886 | hp2 | a0008 | c0024 | t0001 | g0184 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02895 | hp1 | a0004 | c0015 | t0002 | g0008 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02895 | hp2 | a0002 | c0003 | t0002 | g0339 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02896 | hp1 | a0001 | c0006 | t0001 | g0356 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02896 | hp2 | a0020 | c0034 | t0001 | g0031 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02897 | hp1 | a0002 | c0003 | t0002 | g0338 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02897 | hp2 | a0001 | c0006 | t0001 | g0358 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02922 | hp1 | a0021 | c0046 | t0002 | g0333 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0342 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02965 | hp1 | a0001 | c0059 | t0001 | g0041 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02965 | hp2 | a0001 | c0007 | t0001 | g0319 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02970 | hp1 | a0001 | c0022 | t0001 | g0029 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0151 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02976 | hp1 | a0002 | c0003 | t0001 | g0071 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02976 | hp2 | a0004 | c0016 | t0001 | g0354 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03017 | hp1 | a0001 | c0006 | t0001 | g0133 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03017 | hp2 | a0002 | c0003 | t0002 | g0233 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03041 | hp1 | a0002 | c0010 | t0001 | g0180 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03041 | hp2 | a0005 | c0012 | t0002 | g0136 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03098 | hp1 | a0002 | c0010 | t0001 | g0334 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0247 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03130 | hp1 | a0008 | c0024 | t0001 | g0032 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03130 | hp2 | a0005 | c0065 | t0001 | g0147 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03139 | hp1 | a0001 | c0014 | t0001 | g0336 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03139 | hp2 | a0002 | c0019 | t0002 | g0308 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03209 | hp1 | a0001 | c0028 | t0001 | g0350 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03209 | hp2 | a0001 | c0007 | t0001 | g0115 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03225 | hp1 | a0011 | c0071 | t0001 | g0067 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03225 | hp2 | a0001 | c0072 | t0001 | g0025 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0267 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03239 | hp2 | a0006 | c0011 | t0002 | g0259 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03486 | hp1 | a0022 | c0033 | t0001 | g0040 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03486 | hp2 | a0004 | c0068 | t0001 | g0139 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03490 | hp2 | a0001 | c0006 | t0002 | g0224 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0100 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03491 | hp2 | a0001 | c0002 | t0001 | g0310 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03492 | hp2 | a0001 | c0002 | t0001 | g0298 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03516 | hp1 | a0001 | c0045 | t0001 | g0038 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03516 | hp2 | a0002 | c0019 | t0002 | g0304 | AFR | ESN | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03540 | hp1 | a0001 | c0007 | t0001 | g0122 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03540 | hp2 | a0001 | c0005 | t0001 | g0035 | AFR | GWD | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03579 | hp1 | a0001 | c0044 | t0002 | g0345 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03579 | hp2 | a0001 | c0022 | t0001 | g0039 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03654 | hp1 | a0001 | c0006 | t0002 | g0327 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03654 | hp2 | a0002 | c0008 | t0002 | g0156 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03669 | hp1 | a0001 | c0006 | t0002 | g0185 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03669 | hp2 | a0002 | c0003 | t0002 | g0176 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03710 | hp1 | a0002 | c0003 | t0002 | g0168 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03710 | hp2 | a0002 | c0003 | t0002 | g0175 | SAS | PJL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03831 | hp1 | a0006 | c0011 | t0002 | g0330 | SAS | BEB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03831 | hp2 | a0002 | c0052 | t0002 | g0160 | SAS | BEB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03834 | hp1 | a0023 | c0037 | t0002 | g0232 | SAS | BEB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03834 | hp2 | a0001 | c0018 | t0002 | g0269 | SAS | BEB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG04115 | hp1 | a0001 | c0077 | t0001 | g0275 | SAS | STU | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG04115 | hp2 | a0001 | c0006 | t0001 | g0193 | SAS | STU | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG04184 | hp1 | a0001 | c0005 | t0001 | g0248 | SAS | BEB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG04184 | hp2 | a0001 | c0063 | t0001 | g0324 | SAS | BEB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG04199 | hp1 | a0002 | c0003 | t0002 | g0285 | SAS | STU | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0287 | SAS | STU | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0170 | SAS | STU | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG04204 | hp2 | a0001 | c0002 | t0001 | g0297 | SAS | STU | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG04228 | hp1 | a0002 | c0008 | t0002 | g0274 | SAS | STU | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | STU | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18522 | hp1 | a0001 | c0006 | t0001 | g0254 | AFR | YRI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18522 | hp2 | a0002 | c0013 | t0001 | g0069 | AFR | YRI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18612 | hp1 | a0003 | c0004 | t0001 | g0080 | EAS | CHB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18612 | hp2 | a0003 | c0004 | t0001 | g0229 | EAS | CHB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18906 | hp1 | a0002 | c0008 | t0002 | g0006 | AFR | YRI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18906 | hp2 | a0001 | c0027 | t0001 | g0349 | AFR | YRI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0188 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18939 | hp2 | a0003 | c0004 | t0001 | g0082 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18942 | hp1 | a0001 | c0002 | t0001 | g0309 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18942 | hp2 | a0002 | c0003 | t0002 | g0163 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18944 | hp2 | a0001 | c0002 | t0001 | g0222 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18945 | hp1 | a0003 | c0020 | t0001 | g0195 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18945 | hp2 | a0002 | c0003 | t0002 | g0120 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18946 | hp1 | a0001 | c0002 | t0001 | g0123 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0217 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18948 | hp1 | a0002 | c0003 | t0002 | g0264 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0234 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18949 | hp1 | a0001 | c0002 | t0001 | g0055 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18949 | hp2 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18952 | hp1 | a0024 | c0030 | t0001 | g0312 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0022 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18953 | hp2 | a0003 | c0004 | t0001 | g0158 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18954 | hp2 | a0001 | c0005 | t0001 | g0096 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18960 | hp1 | a0002 | c0003 | t0002 | g0127 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18960 | hp2 | a0003 | c0004 | t0001 | g0252 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18962 | hp1 | a0002 | c0003 | t0002 | g0076 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18962 | hp2 | a0025 | c0061 | t0001 | g0119 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18966 | hp1 | a0001 | c0017 | t0001 | g0093 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18966 | hp2 | a0001 | c0002 | t0001 | g0223 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18967 | hp1 | a0003 | c0004 | t0001 | g0084 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18969 | hp1 | a0002 | c0003 | t0001 | g0291 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18969 | hp2 | a0001 | c0002 | t0001 | g0328 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18971 | hp1 | a0001 | c0029 | t0001 | g0311 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18971 | hp2 | a0003 | c0004 | t0001 | g0318 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18975 | hp1 | a0001 | c0009 | t0001 | g0283 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18977 | hp2 | a0002 | c0008 | t0002 | g0279 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18981 | hp1 | a0003 | c0004 | t0001 | g0191 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18982 | hp1 | a0001 | c0002 | t0001 | g0295 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18982 | hp2 | a0003 | c0004 | t0001 | g0230 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18984 | hp1 | a0001 | c0002 | t0001 | g0197 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18984 | hp2 | a0003 | c0004 | t0001 | g0317 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18985 | hp1 | a0001 | c0017 | t0001 | g0257 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18985 | hp2 | a0002 | c0003 | t0002 | g0142 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18988 | hp1 | a0002 | c0003 | t0002 | g0198 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18989 | hp1 | a0001 | c0002 | t0001 | g0078 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18990 | hp1 | a0026 | c0064 | t0001 | g0255 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18990 | hp2 | a0001 | c0002 | t0001 | g0306 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0305 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18993 | hp2 | a0002 | c0003 | t0002 | g0208 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18994 | hp2 | a0002 | c0021 | t0002 | g0108 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0218 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18995 | hp2 | a0001 | c0002 | t0001 | g0331 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18998 | hp1 | a0002 | c0003 | t0002 | g0301 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA18998 | hp2 | a0003 | c0004 | t0002 | g0154 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19001 | hp1 | a0003 | c0004 | t0001 | g0250 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19001 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19003 | hp1 | a0001 | c0005 | t0001 | g0121 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19007 | hp1 | a0003 | c0020 | t0001 | g0187 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19007 | hp2 | a0001 | c0058 | t0001 | g0143 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19009 | hp1 | a0003 | c0004 | t0001 | g0087 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19009 | hp2 | a0001 | c0002 | t0001 | g0239 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19010 | hp1 | a0001 | c0002 | t0001 | g0286 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19011 | hp2 | a0001 | c0002 | t0001 | g0210 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19012 | hp1 | a0001 | c0002 | t0001 | g0110 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19012 | hp2 | a0001 | c0005 | t0001 | g0329 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19030 | hp1 | a0027 | c0047 | t0003 | g0359 | AFR | LWK | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0303 | AFR | LWK | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19043 | hp1 | a0001 | c0006 | t0001 | g0042 | AFR | LWK | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19043 | hp2 | a0004 | c0015 | t0001 | g0140 | AFR | LWK | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19055 | hp1 | a0003 | c0004 | t0001 | g0079 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19055 | hp2 | a0001 | c0018 | t0001 | g0178 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19056 | hp1 | a0001 | c0005 | t0001 | g0190 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19056 | hp2 | a0001 | c0002 | t0001 | g0314 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19057 | hp1 | a0001 | c0002 | t0001 | g0118 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19057 | hp2 | a0002 | c0003 | t0002 | g0220 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19058 | hp2 | a0028 | c0074 | t0001 | g0200 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19060 | hp2 | a0001 | c0002 | t0001 | g0266 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19062 | hp1 | a0003 | c0038 | t0001 | g0231 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19062 | hp2 | a0001 | c0002 | t0001 | g0199 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0249 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19065 | hp2 | a0001 | c0018 | t0001 | g0277 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19066 | hp1 | a0003 | c0004 | t0001 | g0157 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19066 | hp2 | a0001 | c0002 | t0001 | g0132 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19068 | hp1 | a0002 | c0003 | t0002 | g0213 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19070 | hp1 | a0001 | c0017 | t0001 | g0095 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19076 | hp2 | a0002 | c0008 | t0002 | g0278 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19080 | hp1 | a0001 | c0002 | t0001 | g0125 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19081 | hp1 | a0001 | c0002 | t0001 | g0077 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19081 | hp2 | a0002 | c0003 | t0002 | g0099 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19082 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19082 | hp2 | a0003 | c0004 | t0001 | g0225 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19084 | hp2 | a0001 | c0002 | t0001 | g0302 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19085 | hp1 | a0003 | c0004 | t0001 | g0236 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19087 | hp1 | a0001 | c0002 | t0001 | g0196 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0174 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19088 | hp1 | a0001 | c0056 | t0001 | g0088 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19088 | hp2 | a0001 | c0005 | t0001 | g0219 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19090 | hp1 | a0002 | c0003 | t0002 | g0182 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19090 | hp2 | a0003 | c0079 | t0001 | g0179 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19091 | hp1 | a0002 | c0003 | t0002 | g0159 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19091 | hp2 | a0002 | c0003 | t0002 | g0169 | EAS | JPT | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19240 | hp1 | a0004 | c0016 | t0001 | g0332 | AFR | YRI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA19240 | hp2 | a0001 | c0005 | t0001 | g0126 | AFR | YRI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA20129 | hp1 | a0029 | c0076 | t0001 | g0005 | AFR | ASW | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA20129 | hp2 | a0002 | c0013 | t0001 | g0034 | AFR | ASW | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0004 | EUR | TSI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA20752 | hp2 | a0002 | c0008 | t0002 | g0098 | EUR | TSI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA20805 | hp1 | a0002 | c0003 | t0002 | g0166 | EUR | TSI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA20805 | hp2 | a0030 | c0057 | t0002 | g0090 | EUR | TSI | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02109 | hp1 | a0010 | c0025 | t0001 | g0141 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02109 | hp2 | a0001 | c0005 | t0001 | g0357 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0033 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02559 | hp1 | a0004 | c0016 | t0001 | g0355 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG02559 | hp2 | a0001 | c0007 | t0001 | g0007 | AFR | ACB | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03471 | hp1 | a0002 | c0081 | t0001 | g0020 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG03471 | hp2 | a0001 | c0007 | t0001 | g0114 | AFR | MSL | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG06807 | hp1 | a0001 | c0014 | t0001 | g0346 | AFR | USA | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
HG06807 | hp2 | a0006 | c0011 | t0002 | g0058 | AFR | USA | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA20300 | hp1 | a0003 | c0004 | t0001 | g0207 | AFR | USA | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA20300 | hp2 | a0002 | c0003 | t0001 | g0070 | AFR | USA | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA21309 | hp1 | a0001 | c0006 | t0001 | g0117 | AFR | LWK | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
NA21309 | hp2 | a0001 | c0005 | t0001 | g0026 | AFR | LWK | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
homoSapiens | chm13v2 | a0001 | c0002 | t0001 | g0053 | REF | REF | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
homoSapiens | grch38p0 | a0002 | c0003 | t0002 | g0023 | REF | REF | LAMB1_chr7_107918799_108008161 | LAMB1 | chr7 | 107918799 | 108008161 |
view | chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:107929427 | T | G | 1 | a0017 | 1 | HG02738.hp1 | missense_variant | MODERATE | c.4730A>C | p.Glu1577Ala | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 30/34 | 4867/5650 | 4730/5361 | 1577/1786 | chr7 | 107929427 | |||
chr7:107929517 | A | G | 2 | a0006 a0030 |
5 | HG00741.hp2 HG03239.hp2 HG03831.hp1 others(2): Show |
missense_variant | MODERATE | c.4640T>C | p.Ile1547Thr | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 30/34 | 4777/5650 | 4640/5361 | 1547/1786 | chr7 | 107929517 | |||
chr7:107937131 | G | T | 1 | a0015 | 1 | HG02165.hp2 | missense_variant | MODERATE | c.3908C>A | p.Ala1303Asp | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/34 | 4045/5650 | 3908/5361 | 1303/1786 | chr7 | 107937131 | |||
chr7:107940100 | C | A | 2 | a0018 a0019 |
2 | HG02809.hp2 HG02886.hp1 |
missense_variant | MODERATE | c.3650G>T | p.Arg1217Leu | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/34 | 3787/5650 | 3650/5361 | 1217/1786 | chr7 | 107940100 | |||
chr7:107940127 | T | C | 1 | a0024 | 1 | NA18952.hp1 | missense_variant | MODERATE | c.3623A>G | p.Lys1208Arg | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/34 | 3760/5650 | 3623/5361 | 1208/1786 | chr7 | 107940127 | |||
chr7:107952179 | C | T | 2 | a0014 a0028 |
2 | HG02155.hp1 NA19058.hp2 |
missense_variant | MODERATE | c.3124G>A | p.Gly1042Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/34 | 3261/5650 | 3124/5361 | 1042/1786 | chr7 | 107952179 | |||
chr7:107953544 | T | C | 25 | a0001 a0003 a0004 others(22): Show |
279 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(276): Show |
missense_variant | MODERATE | c.3065A>G | p.Gln1022Arg | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/34 | 3202/5650 | 3065/5361 | 1022/1786 | chr7 | 107953544 | |||
chr7:107953689 | G | C | 1 | a0008 | 3 | HG02723.hp2 HG02886.hp2 HG03130.hp1 |
missense_variant | MODERATE | c.2920C>G | p.Gln974Glu | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/34 | 3057/5650 | 2920/5361 | 974/1786 | chr7 | 107953689 | |||
chr7:107953740 | C | T | 1 | a0007 | 3 | HG01069.hp2 HG01433.hp2 HG01884.hp1 |
missense_variant | MODERATE | c.2869G>A | p.Asp957Asn | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/34 | 3006/5650 | 2869/5361 | 957/1786 | chr7 | 107953740 | |||
chr7:107955551 | C | T | 1 | a0013 | 1 | HG01952.hp1 | missense_variant | MODERATE | c.2770G>A | p.Asp924Asn | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/34 | 2907/5650 | 2770/5361 | 924/1786 | chr7 | 107955551 | |||
chr7:107959361 | C | T | 2 | a0003 a0017 |
31 | HG00438.hp1 HG00639.hp1 HG00741.hp1 others(28): Show |
missense_variant | MODERATE | c.2578G>A | p.Gly860Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/34 | 2715/5650 | 2578/5361 | 860/1786 | chr7 | 107959361 | |||
chr7:107959382 | G | A | 1 | a0016 | 1 | HG02723.hp1 | missense_variant | MODERATE | c.2557C>T | p.Arg853Trp | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/34 | 2694/5650 | 2557/5361 | 853/1786 | chr7 | 107959382 | |||
chr7:107959394 | G | A | 1 | a0025 | 1 | NA18962.hp2 | missense_variant | MODERATE | c.2545C>T | p.Arg849Trp | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/34 | 2682/5650 | 2545/5361 | 849/1786 | chr7 | 107959394 | |||
chr7:107959397 | C | G | 1 | a0020 | 1 | HG02896.hp2 | missense_variant | MODERATE | c.2542G>C | p.Ala848Pro | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/34 | 2679/5650 | 2542/5361 | 848/1786 | chr7 | 107959397 | |||
chr7:107959738 | T | C | 1 | a0021 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.2411A>G | p.Asn804Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 19/34 | 2548/5650 | 2411/5361 | 804/1786 | chr7 | 107959738 | |||
chr7:107959766 | G | C | 1 | a0009 | 2 | HG01192.hp2 HG02698.hp1 |
missense_variant | MODERATE | c.2383C>G | p.Arg795Gly | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 19/34 | 2520/5650 | 2383/5361 | 795/1786 | chr7 | 107959766 | |||
chr7:107960646 | C | G | 1 | a0022 | 1 | HG03486.hp1 | missense_variant | MODERATE | c.2113G>C | p.Val705Leu | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 18/34 | 2250/5650 | 2113/5361 | 705/1786 | chr7 | 107960646 | |||
chr7:107961219 | G | A | 1 | a0027 | 1 | NA19030.hp1 | missense_variant | MODERATE | c.2096C>T | p.Thr699Met | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 17/34 | 2233/5650 | 2096/5361 | 699/1786 | chr7 | 107961219 | |||
chr7:107961306 | A | G | 4 | a0010 a0018 a0019 others(1): Show |
5 | HG02109.hp1 HG02615.hp1 HG02809.hp2 others(2): Show |
missense_variant | MODERATE | c.2009T>C | p.Val670Ala | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 17/34 | 2146/5650 | 2009/5361 | 670/1786 | chr7 | 107961306 | |||
chr7:107962996 | A | G | 1 | a0023 | 1 | HG03834.hp1 | missense_variant | MODERATE | c.1766T>C | p.Val589Ala | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/34 | 1903/5650 | 1766/5361 | 589/1786 | chr7 | 107962996 | |||
chr7:107973066 | C | G | 1 | a0019 | 1 | HG02886.hp1 | missense_variant | MODERATE | c.1488G>C | p.Glu496Asp | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/34 | 1625/5650 | 1488/5361 | 496/1786 | chr7 | 107973066 | |||
chr7:107975021 | G | A | 1 | a0026 | 1 | NA18990.hp1 | missense_variant | MODERATE | c.1447C>T | p.Arg483Cys | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/34 | 1584/5650 | 1447/5361 | 483/1786 | chr7 | 107975021 | |||
chr7:107975743 | G | A | 3 | a0004 a0005 a0010 |
17 | HG01243.hp1 HG01433.hp1 HG02080.hp1 others(14): Show |
missense_variant | MODERATE | c.1135C>T | p.Pro379Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 10/34 | 1272/5650 | 1135/5361 | 379/1786 | chr7 | 107975743 | |||
chr7:107978116 | G | A | 1 | a0011 | 2 | HG02809.hp1 HG03225.hp1 |
missense_variant | MODERATE | c.931C>T | p.Leu311Phe | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/34 | 1068/5650 | 931/5361 | 311/1786 | chr7 | 107978116 | |||
chr7:107986288 | C | A | 1 | a0028 | 1 | NA19058.hp2 | missense_variant | MODERATE | c.499G>T | p.Ala167Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 6/34 | 636/5650 | 499/5361 | 167/1786 | chr7 | 107986288 | |||
chr7:107986311 | G | C | 1 | a0012 | 1 | HG01106.hp1 | missense_variant | MODERATE | c.476C>G | p.Thr159Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 6/34 | 613/5650 | 476/5361 | 159/1786 | chr7 | 107986311 |
view | chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:107924065 | G | A | 1 | a0001c0058 | 1 | NA19007.hp2 | synonymous_variant | LOW | c.5247C>T | p.Asp1749Asp | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 34/34 | 5384/5650 | 5247/5361 | 1749/1786 | chr7 | 107924065 | |||
chr7:107926300 | G | A | 1 | a0002c0054 | 1 | HG01099.hp2 | synonymous_variant | LOW | c.4947C>T | p.Ser1649Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/34 | 5084/5650 | 4947/5361 | 1649/1786 | chr7 | 107926300 | |||
chr7:107926318 | G | A | 3 | a0001c0022 a0001c0078 a0004c0067 |
4 | HG02572.hp2 HG02647.hp2 HG02970.hp1 others(1): Show |
synonymous_variant | LOW | c.4929C>T | p.Asn1643Asn | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/34 | 5066/5650 | 4929/5361 | 1643/1786 | chr7 | 107926318 | |||
chr7:107926357 | A | G | 1 | a0004c0069 | 1 | HG02818.hp2 | splice_region_variant&synonymous_variant | LOW | c.4890T>C | p.Ile1630Ile | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/34 | 5027/5650 | 4890/5361 | 1630/1786 | chr7 | 107926357 | |||
chr7:107929072 | A | G | 44 | a0001c0002 a0001c0005 a0001c0007 others(41): Show |
159 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(156): Show |
synonymous_variant | LOW | c.4879T>C | p.Leu1627Leu | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/34 | 5016/5650 | 4879/5361 | 1627/1786 | chr7 | 107929072 | |||
chr7:107929572 | A | G | 1 | a0001c0056 | 1 | NA19088.hp1 | synonymous_variant | LOW | c.4585T>C | p.Leu1529Leu | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 30/34 | 4722/5650 | 4585/5361 | 1529/1786 | chr7 | 107929572 | |||
chr7:107932285 | C | A | 1 | a0001c0045 | 1 | HG03516.hp1 | synonymous_variant | LOW | c.4281G>T | p.Gly1427Gly | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 28/34 | 4418/5650 | 4281/5361 | 1427/1786 | chr7 | 107932285 | |||
chr7:107932330 | G | A | 3 | a0010c0025 a0011c0070 a0029c0076 |
4 | HG02109.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
synonymous_variant | LOW | c.4236C>T | p.Gly1412Gly | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 28/34 | 4373/5650 | 4236/5361 | 1412/1786 | chr7 | 107932330 | |||
chr7:107932345 | G | A | 1 | a0008c0024 | 2 | HG02886.hp2 HG03130.hp1 |
synonymous_variant | LOW | c.4221C>T | p.Ser1407Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 28/34 | 4358/5650 | 4221/5361 | 1407/1786 | chr7 | 107932345 | |||
chr7:107935421 | G | A | 1 | a0001c0042 | 1 | HG01515.hp2 | synonymous_variant | LOW | c.4182C>T | p.Ala1394Ala | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/34 | 4319/5650 | 4182/5361 | 1394/1786 | chr7 | 107935421 | |||
chr7:107940045 | C | T | 1 | a0002c0053 | 1 | HG01928.hp2 | synonymous_variant | LOW | c.3705G>A | p.Ala1235Ala | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/34 | 3842/5650 | 3705/5361 | 1235/1786 | chr7 | 107940045 | |||
chr7:107940120 | A | G | 1 | a0003c0049 | 1 | HG01256.hp1 | synonymous_variant | LOW | c.3630T>C | p.Ser1210Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/34 | 3767/5650 | 3630/5361 | 1210/1786 | chr7 | 107940120 | |||
chr7:107940282 | A | C | 1 | a0002c0052 | 1 | HG03831.hp2 | synonymous_variant | LOW | c.3468T>G | p.Gly1156Gly | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/34 | 3605/5650 | 3468/5361 | 1156/1786 | chr7 | 107940282 | |||
chr7:107940303 | G | A | 1 | a0004c0066 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.3447C>T | p.Gly1149Gly | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/34 | 3584/5650 | 3447/5361 | 1149/1786 | chr7 | 107940303 | |||
chr7:107951275 | G | A | 12 | a0001c0014 a0001c0027 a0001c0035 others(9): Show |
16 | HG01891.hp2 HG02280.hp1 HG02559.hp1 others(13): Show |
synonymous_variant | LOW | c.3342C>T | p.Cys1114Cys | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/34 | 3479/5650 | 3342/5361 | 1114/1786 | chr7 | 107951275 | |||
chr7:107952162 | G | A | 3 | a0001c0007 a0001c0028 a0001c0032 |
13 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(10): Show |
synonymous_variant | LOW | c.3141C>T | p.Cys1047Cys | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/34 | 3278/5650 | 3141/5361 | 1047/1786 | chr7 | 107952162 | |||
chr7:107953597 | C | T | 1 | a0004c0069 | 1 | HG02818.hp2 | synonymous_variant | LOW | c.3012G>A | p.Thr1004Thr | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/34 | 3149/5650 | 3012/5361 | 1004/1786 | chr7 | 107953597 | |||
chr7:107960509 | C | T | 1 | a0011c0070 | 1 | HG02809.hp1 | synonymous_variant | LOW | c.2250G>A | p.Pro750Pro | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 18/34 | 2387/5650 | 2250/5361 | 750/1786 | chr7 | 107960509 | |||
chr7:107961275 | C | T | 1 | a0001c0032 | 1 | HG02630.hp2 | synonymous_variant | LOW | c.2040G>A | p.Val680Val | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 17/34 | 2177/5650 | 2040/5361 | 680/1786 | chr7 | 107961275 | |||
chr7:107962917 | G | A | 1 | a0001c0063 | 1 | HG04184.hp2 | synonymous_variant | LOW | c.1845C>T | p.Arg615Arg | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/34 | 1982/5650 | 1845/5361 | 615/1786 | chr7 | 107962917 | |||
chr7:107962986 | A | C | 33 | a0001c0002 a0001c0006 a0001c0007 others(30): Show |
117 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(114): Show |
synonymous_variant | LOW | c.1776T>G | p.Pro592Pro | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/34 | 1913/5650 | 1776/5361 | 592/1786 | chr7 | 107962986 | |||
chr7:107964657 | G | A | 2 | a0004c0069 a0011c0071 |
2 | HG02818.hp2 HG03225.hp1 |
synonymous_variant | LOW | c.1593C>T | p.Cys531Cys | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/34 | 1730/5650 | 1593/5361 | 531/1786 | chr7 | 107964657 | |||
chr7:107964678 | C | T | 3 | a0002c0039 a0003c0038 a0023c0037 |
3 | HG02735.hp2 HG03834.hp1 NA19062.hp1 |
synonymous_variant | LOW | c.1572G>A | p.Ala524Ala | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/34 | 1709/5650 | 1572/5361 | 524/1786 | chr7 | 107964678 | |||
chr7:107975061 | C | T | 18 | a0001c0009 a0001c0018 a0001c0029 others(15): Show |
35 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
synonymous_variant | LOW | c.1407G>A | p.Gly469Gly | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/34 | 1544/5650 | 1407/5361 | 469/1786 | chr7 | 107975061 | |||
chr7:107975741 | C | T | 3 | a0001c0027 a0001c0028 a0002c0019 |
4 | HG03139.hp2 HG03209.hp1 HG03516.hp2 others(1): Show |
synonymous_variant | LOW | c.1137G>A | p.Pro379Pro | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 10/34 | 1274/5650 | 1137/5361 | 379/1786 | chr7 | 107975741 | |||
chr7:107978156 | G | A | 1 | a0001c0072 | 1 | HG03225.hp2 | synonymous_variant | LOW | c.891C>T | p.His297His | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/34 | 1028/5650 | 891/5361 | 297/1786 | chr7 | 107978156 | |||
chr7:107980633 | T | C | 2 | a0001c0017 a0001c0073 |
4 | HG00621.hp2 NA18966.hp1 NA18985.hp1 others(1): Show |
synonymous_variant | LOW | c.855A>G | p.Gly285Gly | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/34 | 992/5650 | 855/5361 | 285/1786 | chr7 | 107980633 | |||
chr7:107986319 | A | G | 1 | a0002c0026 | 1 | HG00738.hp1 | synonymous_variant | LOW | c.468T>C | p.Phe156Phe | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 6/34 | 605/5650 | 468/5361 | 156/1786 | chr7 | 107986319 | |||
chr7:107986325 | G | A | 11 | a0001c0009 a0001c0018 a0001c0077 others(8): Show |
28 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(25): Show |
synonymous_variant | LOW | c.462C>T | p.Ser154Ser | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 6/34 | 599/5650 | 462/5361 | 154/1786 | chr7 | 107986325 |
view | chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:107923866 | T | C | 1 | a0004c0066t0004 | 1 | HG01433.hp1 | 3_prime_UTR_variant | MODIFIER | c.*85A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 34/34 | 85 | chr7 | 107923866 | ||||||
chr7:107923921 | T | G | 68 | a0001c0001t0001 a0001c0002t0001 a0001c0005t0001 others(65): Show |
270 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*30A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 34/34 | 30 | chr7 | 107923921 | ||||||
chr7:108002907 | G | A | 3 | a0001c0007t0003 a0001c0014t0003 a0027c0047t0003 |
4 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-22C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/34 | 22 | chr7 | 108002907 |
view | chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:107924094 | G | A | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(266): Show |
270 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(267): Show |
splice_region_variant&intron_variant | LOW | c.5225-7C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 33/33 | chr7 | 107924094 | |||||||
chr7:107924097 | G | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(266): Show |
270 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.5225-10C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 33/33 | chr7 | 107924097 | |||||||
chr7:107924525 | T | G | 1 | a0001c0001t0001g0174 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.5065-136A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107924525 | |||||||
chr7:107924538 | A | G | 13 | a0001c0005t0001g0357 a0001c0007t0001g0007 a0001c0007t0001g0009 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.5065-149T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107924538 | |||||||
chr7:107924562 | A | C | 221 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(218): Show |
222 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(219): Show |
intron_variant | MODIFIER | c.5065-173T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107924562 | |||||||
chr7:107924580 | T | G | 7 | a0001c0001t0001g0012 a0001c0001t0001g0151 a0001c0001t0001g0335 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.5065-191A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107924580 | |||||||
chr7:107924649 | T | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0260 |
2 | HG00438.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.5065-260A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107924649 | |||||||
chr7:107924667 | A | C | 1 | a0001c0002t0001g0286 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.5065-278T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107924667 | |||||||
chr7:107924693 | C | T | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(266): Show |
270 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(267): Show |
intron_variant | MODIFIER | c.5065-304G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107924693 | |||||||
chr7:107924998 | T | C | 2 | a0001c0005t0001g0126 a0002c0081t0001g0020 |
2 | HG03471.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.5065-609A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107924998 | |||||||
chr7:107925138 | A | T | 4 | a0001c0022t0001g0029 a0001c0022t0001g0039 a0001c0078t0001g0024 others(1): Show |
4 | HG02572.hp2 HG02647.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.5065-749T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107925138 | |||||||
chr7:107925270 | G | A | 2 | a0001c0006t0001g0042 a0001c0006t0001g0117 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.5065-881C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107925270 | |||||||
chr7:107925380 | T | C | 13 | a0001c0005t0001g0357 a0001c0007t0001g0007 a0001c0007t0001g0009 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.5064+803A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107925380 | |||||||
chr7:107925436 | A | C | 31 | a0001c0001t0001g0012 a0001c0001t0001g0151 a0001c0001t0001g0335 others(28): Show |
31 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.5064+747T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107925436 | |||||||
chr7:107925542 | A | G | 10 | a0001c0002t0001g0306 a0001c0005t0001g0129 a0003c0004t0001g0084 others(7): Show |
10 | HG00609.hp2 NA18612.hp2 NA18967.hp1 others(7): Show |
intron_variant | MODIFIER | c.5064+641T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107925542 | |||||||
chr7:107925558 | C | T | 1 | a0001c0028t0001g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.5064+625G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107925558 | |||||||
chr7:107925898 | T | TA | 12 | a0001c0001t0001g0299 a0001c0005t0001g0026 a0001c0005t0001g0351 others(9): Show |
12 | HG02055.hp2 HG02109.hp1 HG02451.hp2 others(9): Show |
intron_variant | MODIFIER | c.5064+284dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107925898 | |||||||
chr7:107925898 | T | TAA | 262 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(259): Show |
264 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(261): Show |
intron_variant | MODIFIER | c.5064+283_5064+284d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107925898 | |||||||
chr7:107925985 | A | G | 275 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(272): Show |
276 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.5064+198T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107925985 | |||||||
chr7:107926043 | G | T | 275 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(272): Show |
276 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.5064+140C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107926043 | |||||||
chr7:107926044 | G | A | 1 | a0001c0001t0001g0170 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.5064+139C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 32/33 | chr7 | 107926044 | |||||||
chr7:107926367 | C | T | 3 | a0001c0005t0001g0026 a0001c0005t0001g0351 a0004c0069t0001g0134 |
3 | HG02055.hp2 HG02818.hp2 NA21309.hp2 |
splice_region_variant&intron_variant | LOW | c.4888-8G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107926367 | |||||||
chr7:107926641 | T | C | 30 | a0001c0001t0001g0012 a0001c0001t0001g0151 a0001c0001t0001g0335 others(27): Show |
30 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.4888-282A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107926641 | |||||||
chr7:107926761 | T | C | 26 | a0001c0001t0001g0012 a0001c0001t0001g0151 a0001c0001t0001g0335 others(23): Show |
26 | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(23): Show |
intron_variant | MODIFIER | c.4888-402A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107926761 | |||||||
chr7:107926844 | G | A | 1 | a0001c0001t0001g0300 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.4888-485C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107926844 | |||||||
chr7:107926994 | T | C | 1 | a0001c0006t0002g0327 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.4888-635A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107926994 | |||||||
chr7:107927028 | A | G | 31 | a0001c0001t0001g0012 a0001c0001t0001g0151 a0001c0001t0001g0335 others(28): Show |
31 | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(28): Show |
intron_variant | MODIFIER | c.4888-669T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107927028 | |||||||
chr7:107927349 | T | C | 30 | a0001c0001t0001g0012 a0001c0001t0001g0151 a0001c0001t0001g0335 others(27): Show |
30 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.4888-990A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107927349 | |||||||
chr7:107927414 | TTCAG | T | 82 | a0001c0002t0001g0014 a0001c0002t0001g0049 a0001c0002t0001g0055 others(79): Show |
82 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.4888-1059_4888-105 others(8): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107927414 | |||||||
chr7:107927571 | A | T | 1 | a0003c0004t0001g0080 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.4888-1212T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107927571 | |||||||
chr7:107927599 | C | G | 7 | a0001c0001t0001g0012 a0001c0001t0001g0151 a0001c0001t0001g0335 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4888-1240G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107927599 | |||||||
chr7:107927703 | C | G | 1 | a0001c0001t0001g0325 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.4888-1344G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107927703 | |||||||
chr7:107927742 | A | AT | 29 | a0001c0001t0001g0012 a0001c0001t0001g0151 a0001c0001t0001g0335 others(26): Show |
29 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.4887+1321dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107927742 | |||||||
chr7:107927967 | G | A | 2 | a0008c0024t0001g0032 a0008c0024t0001g0184 |
2 | HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4887+1097C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107927967 | |||||||
chr7:107928064 | G | A | 29 | a0001c0001t0001g0012 a0001c0001t0001g0151 a0001c0001t0001g0335 others(26): Show |
29 | HG02055.hp2 HG02109.hp1 HG02258.hp1 others(26): Show |
intron_variant | MODIFIER | c.4887+1000C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928064 | |||||||
chr7:107928094 | A | T | 1 | a0003c0004t0001g0250 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.4887+970T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928094 | |||||||
chr7:107928154 | G | A | 307 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(304): Show |
308 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(305): Show |
intron_variant | MODIFIER | c.4887+910C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928154 | |||||||
chr7:107928218 | T | C | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(271): Show |
275 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(272): Show |
intron_variant | MODIFIER | c.4887+846A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928218 | |||||||
chr7:107928365 | T | A | 9 | a0001c0005t0001g0026 a0001c0005t0001g0351 a0001c0007t0001g0319 others(6): Show |
9 | HG02055.hp2 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.4887+699A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928365 | |||||||
chr7:107928488 | A | G | 9 | a0001c0001t0001g0086 a0001c0001t0001g0188 a0001c0001t0001g0189 others(6): Show |
9 | HG02132.hp1 HG02523.hp1 NA18939.hp1 others(6): Show |
intron_variant | MODIFIER | c.4887+576T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928488 | |||||||
chr7:107928501 | CT | C | 19 | a0001c0002t0001g0247 a0001c0005t0001g0026 a0001c0005t0001g0351 others(16): Show |
19 | HG01433.hp1 HG02055.hp2 HG02280.hp1 others(16): Show |
intron_variant | MODIFIER | c.4887+562delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928501 | |||||||
chr7:107928683 | G | T | 4 | a0001c0005t0001g0101 a0001c0005t0001g0190 a0001c0005t0001g0219 others(1): Show |
4 | HG00408.hp2 HG02080.hp2 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.4887+381C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928683 | |||||||
chr7:107928744 | C | T | 1 | a0002c0003t0002g0168 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.4887+320G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928744 | |||||||
chr7:107928789 | G | A | 18 | a0001c0002t0001g0247 a0001c0005t0001g0026 a0001c0005t0001g0351 others(15): Show |
18 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.4887+275C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928789 | |||||||
chr7:107928826 | T | G | 1 | a0001c0002t0001g0197 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.4887+238A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928826 | |||||||
chr7:107928865 | TGAA | T | 18 | a0001c0002t0001g0247 a0001c0005t0001g0026 a0001c0005t0001g0351 others(15): Show |
18 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.4887+196_4887+198d others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928865 | |||||||
chr7:107928969 | T | A | 19 | a0001c0005t0001g0126 a0001c0005t0001g0357 a0001c0007t0001g0007 others(16): Show |
19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.4887+95A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 31/33 | chr7 | 107928969 | |||||||
chr7:107929253 | A | T | 13 | a0001c0005t0001g0357 a0001c0007t0001g0007 a0001c0007t0001g0009 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.4746-48T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 30/33 | chr7 | 107929253 | |||||||
chr7:107929748 | T | A | 20 | a0001c0005t0001g0357 a0001c0007t0001g0007 a0001c0007t0001g0009 others(17): Show |
20 | HG01433.hp1 HG01891.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.4538-129A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107929748 | |||||||
chr7:107929974 | A | G | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.4538-355T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107929974 | |||||||
chr7:107930074 | C | T | 3 | a0010c0025t0001g0141 a0010c0025t0001g0340 a0029c0076t0001g0005 |
3 | HG02109.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.4538-455G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107930074 | |||||||
chr7:107930232 | G | A | 8 | a0001c0002t0001g0337 a0001c0005t0001g0026 a0001c0005t0001g0351 others(5): Show |
8 | HG02055.hp2 HG02572.hp2 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.4538-613C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107930232 | |||||||
chr7:107930482 | T | C | 282 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(279): Show |
284 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(281): Show |
intron_variant | MODIFIER | c.4538-863A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107930482 | |||||||
chr7:107930620 | A | G | 2 | a0001c0007t0001g0009 a0001c0007t0001g0122 |
2 | HG02622.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4537+736T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107930620 | |||||||
chr7:107930805 | A | G | 19 | a0001c0005t0001g0126 a0001c0005t0001g0357 a0001c0007t0001g0007 others(16): Show |
19 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(16): Show |
intron_variant | MODIFIER | c.4537+551T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107930805 | |||||||
chr7:107930813 | C | G | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4537+543G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107930813 | |||||||
chr7:107930943 | A | G | 9 | a0003c0004t0001g0079 a0003c0004t0001g0080 a0003c0004t0001g0081 others(6): Show |
9 | HG00438.hp1 NA18612.hp1 NA18953.hp2 others(6): Show |
intron_variant | MODIFIER | c.4537+413T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107930943 | |||||||
chr7:107931000 | A | G | 1 | a0002c0008t0002g0268 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.4537+356T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107931000 | |||||||
chr7:107931094 | C | T | 1 | a0001c0001t0001g0221 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.4537+262G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107931094 | |||||||
chr7:107931096 | C | T | 2 | a0002c0003t0002g0013 a0002c0008t0002g0098 |
2 | HG00733.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.4537+260G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107931096 | |||||||
chr7:107931170 | G | A | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.4537+186C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 29/33 | chr7 | 107931170 | |||||||
chr7:107931517 | A | G | 1 | a0002c0003t0002g0076 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.4393-17T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 28/33 | chr7 | 107931517 | |||||||
chr7:107931703 | A | G | 7 | a0001c0001t0001g0012 a0001c0001t0001g0151 a0001c0001t0001g0335 others(4): Show |
7 | HG02258.hp1 HG02486.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.4393-203T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 28/33 | chr7 | 107931703 | |||||||
chr7:107932140 | A | G | 2 | a0008c0024t0001g0032 a0008c0024t0001g0184 |
2 | HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.4392+34T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 28/33 | chr7 | 107932140 | |||||||
chr7:107932547 | G | A | 6 | a0001c0001t0001g0109 a0001c0001t0001g0217 a0001c0001t0001g0218 others(3): Show |
6 | HG02135.hp1 NA18946.hp2 NA18989.hp2 others(3): Show |
intron_variant | MODIFIER | c.4189-170C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107932547 | |||||||
chr7:107932728 | G | A | 1 | a0001c0001t0001g0262 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.4189-351C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107932728 | |||||||
chr7:107932731 | T | TA | 28 | a0001c0002t0001g0247 a0001c0005t0001g0026 a0001c0005t0001g0126 others(25): Show |
28 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.4189-355dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107932731 | |||||||
chr7:107932742 | C | G | 28 | a0001c0002t0001g0247 a0001c0005t0001g0026 a0001c0005t0001g0126 others(25): Show |
28 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(25): Show |
intron_variant | MODIFIER | c.4189-365G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107932742 | |||||||
chr7:107932765 | C | A | 27 | a0001c0002t0001g0247 a0001c0005t0001g0026 a0001c0005t0001g0126 others(24): Show |
27 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.4189-388G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107932765 | |||||||
chr7:107932799 | T | C | 2 | a0003c0004t0001g0082 a0003c0004t0001g0317 |
2 | NA18939.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.4189-422A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107932799 | |||||||
chr7:107932809 | T | G | 274 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(271): Show |
276 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(273): Show |
intron_variant | MODIFIER | c.4189-432A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107932809 | |||||||
chr7:107932823 | C | A | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(249): Show |
254 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(251): Show |
intron_variant | MODIFIER | c.4189-446G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107932823 | |||||||
chr7:107932902 | C | G | 2 | a0002c0003t0002g0159 a0002c0003t0002g0213 |
2 | NA19068.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.4189-525G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107932902 | |||||||
chr7:107933009 | C | G | 1 | a0001c0001t0001g0226 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.4189-632G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933009 | |||||||
chr7:107933062 | C | G | 4 | a0010c0025t0001g0141 a0010c0025t0001g0340 a0011c0070t0001g0348 others(1): Show |
4 | HG02109.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.4189-685G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933062 | |||||||
chr7:107933297 | T | G | 1 | a0001c0002t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4189-920A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933297 | |||||||
chr7:107933303 | A | G | 2 | a0018c0048t0001g0027 a0019c0036t0001g0068 |
2 | HG02809.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.4189-926T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933303 | |||||||
chr7:107933516 | T | G | 27 | a0001c0002t0001g0247 a0001c0005t0001g0026 a0001c0005t0001g0126 others(24): Show |
27 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(24): Show |
intron_variant | MODIFIER | c.4189-1139A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933516 | |||||||
chr7:107933593 | G | C | 17 | a0001c0002t0001g0247 a0001c0005t0001g0126 a0001c0022t0001g0029 others(14): Show |
17 | HG01243.hp1 HG02280.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.4189-1216C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933593 | |||||||
chr7:107933603 | G | GA | 13 | a0001c0002t0001g0337 a0001c0005t0001g0026 a0001c0005t0001g0351 others(10): Show |
13 | HG02055.hp2 HG02109.hp1 HG02615.hp1 others(10): Show |
intron_variant | MODIFIER | c.4189-1227dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933603 | |||||||
chr7:107933603 | G | GAA | 16 | a0001c0002t0001g0247 a0001c0005t0001g0126 a0001c0022t0001g0029 others(13): Show |
16 | HG01243.hp1 HG02280.hp1 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.4189-1228_4189-122 others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933603 | |||||||
chr7:107933615 | C | A | 26 | a0001c0002t0001g0247 a0001c0005t0001g0026 a0001c0005t0001g0126 others(23): Show |
26 | HG01243.hp1 HG02055.hp2 HG02109.hp1 others(23): Show |
intron_variant | MODIFIER | c.4189-1238G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933615 | |||||||
chr7:107933683 | A | G | 143 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(140): Show |
144 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.4189-1306T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933683 | |||||||
chr7:107933692 | C | T | 9 | a0001c0001t0002g0192 a0002c0003t0002g0099 a0002c0003t0002g0120 others(6): Show |
9 | HG01993.hp2 NA18945.hp2 NA18948.hp1 others(6): Show |
intron_variant | MODIFIER | c.4189-1315G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933692 | |||||||
chr7:107933830 | A | G | 1 | a0002c0081t0001g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4189-1453T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933830 | |||||||
chr7:107933843 | G | C | 2 | a0001c0005t0001g0026 a0001c0005t0001g0351 |
2 | HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.4189-1466C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933843 | |||||||
chr7:107933859 | C | T | 1 | a0002c0081t0001g0020 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.4189-1482G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933859 | |||||||
chr7:107933861 | C | T | 1 | a0001c0001t0002g0061 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.4189-1484G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933861 | |||||||
chr7:107933901 | G | A | 3 | a0001c0002t0001g0247 a0001c0027t0001g0349 a0001c0043t0001g0116 |
3 | HG02280.hp1 HG03098.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.4188+1514C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933901 | |||||||
chr7:107933913 | G | A | 2 | a0001c0078t0001g0024 a0004c0067t0001g0137 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.4188+1502C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933913 | |||||||
chr7:107933937 | A | G | 1 | a0001c0002t0001g0331 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.4188+1478T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933937 | |||||||
chr7:107933954 | G | A | 1 | a0004c0066t0004g0021 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4188+1461C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933954 | |||||||
chr7:107933982 | A | G | 141 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(138): Show |
142 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.4188+1433T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933982 | |||||||
chr7:107933986 | AT | A | 8 | a0001c0006t0001g0133 a0002c0003t0002g0347 a0002c0013t0001g0030 others(5): Show |
8 | HG01243.hp1 HG02280.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.4188+1428delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107933986 | |||||||
chr7:107934050 | T | C | 1 | a0002c0010t0001g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.4188+1365A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934050 | |||||||
chr7:107934339 | G | A | 101 | a0001c0002t0001g0014 a0001c0002t0001g0049 a0001c0002t0001g0055 others(98): Show |
101 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(98): Show |
intron_variant | MODIFIER | c.4188+1076C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934339 | |||||||
chr7:107934390 | C | T | 2 | a0001c0001t0001g0085 a0001c0001t0001g0316 |
2 | NA18977.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.4188+1025G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934390 | |||||||
chr7:107934433 | A | G | 1 | a0004c0015t0002g0008 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4188+982T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934433 | |||||||
chr7:107934659 | C | T | 1 | a0002c0010t0001g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.4188+756G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934659 | |||||||
chr7:107934717 | C | T | 145 | a0001c0002t0001g0014 a0001c0002t0001g0049 a0001c0002t0001g0055 others(142): Show |
145 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.4188+698G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934717 | |||||||
chr7:107934835 | G | A | 3 | a0001c0005t0001g0035 a0001c0005t0001g0150 a0004c0068t0001g0139 |
3 | HG02145.hp2 HG03486.hp2 HG03540.hp2 |
intron_variant | MODIFIER | c.4188+580C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934835 | |||||||
chr7:107934902 | T | TA | 6 | a0001c0001t0002g0002 a0001c0001t0002g0061 a0002c0003t0002g0159 others(3): Show |
7 | HG01261.hp1 HG01515.hp1 HG01517.hp2 others(4): Show |
intron_variant | MODIFIER | c.4188+512dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934902 | |||||||
chr7:107934902 | TA | T | 28 | a0001c0002t0001g0247 a0001c0005t0001g0026 a0001c0005t0001g0126 others(25): Show |
28 | HG01891.hp1 HG01993.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.4188+512delT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934902 | |||||||
chr7:107934902 | TAA | T | 14 | a0001c0001t0001g0033 a0001c0001t0001g0342 a0001c0002t0001g0337 others(11): Show |
14 | HG01433.hp1 HG02109.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.4188+511_4188+512d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934902 | |||||||
chr7:107934902 | TAAA | T | 222 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(219): Show |
223 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(220): Show |
intron_variant | MODIFIER | c.4188+510_4188+512d others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934902 | |||||||
chr7:107934903 | A | T | 4 | a0001c0022t0001g0029 a0001c0022t0001g0039 a0001c0078t0001g0024 others(1): Show |
4 | HG02572.hp2 HG02647.hp2 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.4188+512T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107934903 | |||||||
chr7:107935067 | T | A | 1 | a0001c0002t0001g0125 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.4188+348A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935067 | |||||||
chr7:107935112 | G | A | 103 | a0001c0002t0001g0014 a0001c0002t0001g0049 a0001c0002t0001g0055 others(100): Show |
103 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(100): Show |
intron_variant | MODIFIER | c.4188+303C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935112 | |||||||
chr7:107935113 | G | A | 20 | a0001c0002t0001g0247 a0001c0005t0001g0026 a0001c0005t0001g0126 others(17): Show |
20 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.4188+302C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935113 | |||||||
chr7:107935148 | G | A | 20 | a0001c0002t0001g0247 a0001c0005t0001g0026 a0001c0005t0001g0126 others(17): Show |
20 | HG02055.hp2 HG02280.hp1 HG02280.hp2 others(17): Show |
intron_variant | MODIFIER | c.4188+267C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935148 | |||||||
chr7:107935282 | T | C | 2 | a0001c0001t0001g0022 a0001c0001t0001g0245 |
2 | NA18944.hp1 NA18952.hp2 |
intron_variant | MODIFIER | c.4188+133A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935282 | |||||||
chr7:107935342 | TCTTTG | T | 4 | a0002c0010t0001g0334 a0008c0024t0001g0032 a0008c0024t0001g0184 others(1): Show |
4 | HG02723.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.4188+68_4188+72del others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935342 | |||||||
chr7:107935343 | CTTTGTTT others(7): Show |
C | 13 | a0001c0005t0001g0357 a0001c0007t0001g0007 a0001c0007t0001g0009 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.4188+58_4188+71del others(14): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935343 | |||||||
chr7:107935347 | G | GT | 41 | a0001c0001t0001g0012 a0001c0001t0001g0073 a0001c0001t0001g0151 others(38): Show |
41 | HG00423.hp2 HG00438.hp2 HG00609.hp2 others(38): Show |
intron_variant | MODIFIER | c.4188+67dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935347 | |||||||
chr7:107935347 | G | GTT | 6 | a0001c0002t0001g0337 a0001c0035t0001g0037 a0002c0003t0001g0070 others(3): Show |
6 | HG01361.hp1 HG02622.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.4188+66_4188+67dup others(2): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935347 | |||||||
chr7:107935347 | G | GTTTTTTT others(3): Show |
1 | a0001c0005t0001g0351 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.4188+58_4188+67dup others(10): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935347 | |||||||
chr7:107935347 | G | GTTTTTTT others(7): Show |
2 | a0001c0007t0001g0319 a0011c0071t0001g0067 |
2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.4188+54_4188+67dup others(14): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935347 | |||||||
chr7:107935347 | G | GTTTTTTT others(11): Show |
1 | a0001c0032t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.4188+50_4188+67dup others(18): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935347 | |||||||
chr7:107935347 | GTTTT | G | 11 | a0001c0002t0001g0247 a0001c0022t0001g0029 a0001c0027t0001g0349 others(8): Show |
11 | HG02280.hp1 HG02280.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.4188+64_4188+67del others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935347 | |||||||
chr7:107935347 | GTTTTTTT others(6): Show |
G | 102 | a0001c0001t0001g0263 a0001c0002t0001g0014 a0001c0002t0001g0049 others(99): Show |
102 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.4188+55_4188+67del others(13): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935347 | |||||||
chr7:107935348 | T | G | 4 | a0002c0010t0001g0334 a0008c0024t0001g0032 a0008c0024t0001g0184 others(1): Show |
4 | HG02723.hp2 HG02886.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.4188+67A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935348 | |||||||
chr7:107935350 | T | G | 1 | a0004c0066t0004g0021 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4188+65A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935350 | |||||||
chr7:107935352 | T | TC | 4 | a0001c0001t0001g0100 a0001c0001t0001g0111 a0001c0001t0001g0226 others(1): Show |
4 | HG02698.hp2 HG02735.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.4188+62_4188+63ins others(1): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935352 | |||||||
chr7:107935353 | T | G | 1 | a0001c0005t0001g0126 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4188+62A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935353 | |||||||
chr7:107935354 | T | G | 12 | a0001c0002t0001g0247 a0001c0027t0001g0349 a0001c0043t0001g0116 others(9): Show |
12 | HG02280.hp1 HG02280.hp2 HG02723.hp1 others(9): Show |
intron_variant | MODIFIER | c.4188+61A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935354 | |||||||
chr7:107935356 | T | G | 4 | a0001c0001t0001g0100 a0001c0001t0001g0111 a0001c0001t0001g0226 others(1): Show |
4 | HG02698.hp2 HG02735.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.4188+59A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935356 | |||||||
chr7:107935357 | T | G | 9 | a0001c0002t0001g0247 a0001c0027t0001g0349 a0001c0043t0001g0116 others(6): Show |
9 | HG01433.hp1 HG02280.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.4188+58A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935357 | |||||||
chr7:107935358 | T | G | 3 | a0001c0006t0001g0133 a0001c0006t0001g0193 a0001c0077t0001g0275 |
3 | HG03017.hp1 HG04115.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.4188+57A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 27/33 | chr7 | 107935358 | |||||||
chr7:107935704 | C | T | 4 | a0001c0044t0002g0345 a0002c0019t0002g0308 a0002c0026t0002g0352 others(1): Show |
4 | HG00738.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3947-48G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107935704 | |||||||
chr7:107935848 | G | A | 2 | a0001c0007t0001g0319 a0011c0071t0001g0067 |
2 | HG02965.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.3947-192C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107935848 | |||||||
chr7:107935908 | T | C | 2 | a0001c0001t0001g0172 a0001c0001t0001g0260 |
2 | HG00438.hp2 HG02155.hp2 |
intron_variant | MODIFIER | c.3947-252A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107935908 | |||||||
chr7:107935910 | T | C | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3947-254A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107935910 | |||||||
chr7:107936001 | G | C | 1 | a0011c0070t0001g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.3947-345C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936001 | |||||||
chr7:107936045 | G | A | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3947-389C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936045 | |||||||
chr7:107936375 | T | A | 2 | a0001c0001t0001g0083 a0001c0001t0001g0300 |
2 | NA19010.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.3946+718A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936375 | |||||||
chr7:107936419 | A | G | 5 | a0006c0011t0002g0058 a0006c0011t0002g0060 a0006c0011t0002g0259 others(2): Show |
5 | HG00741.hp2 HG03239.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.3946+674T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936419 | |||||||
chr7:107936460 | A | G | 1 | a0001c0001t0001g0214 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3946+633T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936460 | |||||||
chr7:107936637 | T | G | 1 | a0001c0001t0002g0003 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3946+456A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936637 | |||||||
chr7:107936661 | A | T | 1 | a0001c0001t0002g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3946+432T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936661 | |||||||
chr7:107936817 | G | A | 1 | a0001c0059t0001g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3946+276C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936817 | |||||||
chr7:107936822 | GA | G | 241 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(238): Show |
242 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(239): Show |
intron_variant | MODIFIER | c.3946+270delT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936822 | |||||||
chr7:107936836 | C | T | 5 | a0002c0013t0001g0030 a0002c0013t0001g0034 a0002c0013t0001g0069 others(2): Show |
5 | HG02280.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3946+257G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936836 | |||||||
chr7:107936905 | G | A | 1 | a0003c0004t0001g0229 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.3946+188C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936905 | |||||||
chr7:107936921 | T | C | 1 | a0017c0051t0001g0253 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3946+172A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936921 | |||||||
chr7:107936945 | T | G | 123 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(120): Show |
124 | HG00099.hp1 HG00323.hp2 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.3946+148A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107936945 | |||||||
chr7:107937003 | CT | C | 108 | a0001c0001t0001g0249 a0001c0002t0001g0014 a0001c0002t0001g0049 others(105): Show |
108 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.3946+89delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107937003 | |||||||
chr7:107937011 | T | C | 102 | a0001c0001t0001g0249 a0001c0002t0001g0014 a0001c0002t0001g0049 others(99): Show |
102 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(99): Show |
intron_variant | MODIFIER | c.3946+82A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107937011 | |||||||
chr7:107937049 | G | A | 5 | a0001c0002t0001g0077 a0001c0002t0001g0078 a0001c0002t0001g0118 others(2): Show |
5 | NA18966.hp2 NA18989.hp1 NA19057.hp1 others(2): Show |
intron_variant | MODIFIER | c.3946+44C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 26/33 | chr7 | 107937049 | |||||||
chr7:107937560 | G | A | 18 | a0001c0002t0001g0337 a0001c0005t0001g0357 a0001c0007t0001g0007 others(15): Show |
18 | HG01433.hp1 HG01891.hp1 HG02055.hp1 others(15): Show |
intron_variant | MODIFIER | c.3762-283C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107937560 | |||||||
chr7:107937649 | A | G | 2 | a0001c0002t0001g0196 a0001c0002t0001g0210 |
2 | NA19011.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.3762-372T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107937649 | |||||||
chr7:107937791 | A | G | 1 | a0001c0001t0001g0249 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3762-514T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107937791 | |||||||
chr7:107937806 | G | A | 4 | a0001c0001t0001g0151 a0002c0003t0001g0070 a0002c0003t0001g0071 others(1): Show |
4 | HG02970.hp2 HG02976.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.3762-529C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107937806 | |||||||
chr7:107937877 | TAAG | T | 18 | a0001c0002t0001g0239 a0003c0004t0001g0082 a0003c0004t0001g0084 others(15): Show |
18 | HG00741.hp1 HG01256.hp1 HG01261.hp2 others(15): Show |
intron_variant | MODIFIER | c.3762-603_3762-601d others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107937877 | |||||||
chr7:107937954 | C | T | 4 | a0001c0001t0001g0100 a0001c0001t0001g0111 a0001c0001t0001g0226 others(1): Show |
4 | HG02698.hp2 HG02735.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.3762-677G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107937954 | |||||||
chr7:107937970 | A | G | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3762-693T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107937970 | |||||||
chr7:107938088 | G | C | 1 | a0001c0002t0001g0240 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3762-811C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107938088 | |||||||
chr7:107938096 | C | T | 4 | a0001c0044t0002g0345 a0002c0019t0002g0308 a0002c0026t0002g0352 others(1): Show |
4 | HG00738.hp1 HG03041.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.3762-819G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107938096 | |||||||
chr7:107938416 | AT | A | 104 | a0001c0002t0001g0014 a0001c0002t0001g0049 a0001c0002t0001g0055 others(101): Show |
104 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(101): Show |
intron_variant | MODIFIER | c.3762-1140delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107938416 | |||||||
chr7:107938460 | G | A | 2 | a0008c0024t0001g0032 a0008c0024t0001g0184 |
2 | HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3762-1183C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107938460 | |||||||
chr7:107938499 | T | C | 6 | a0001c0002t0001g0337 a0010c0025t0001g0141 a0010c0025t0001g0340 others(3): Show |
6 | HG02109.hp1 HG02615.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.3762-1222A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107938499 | |||||||
chr7:107938508 | A | G | 1 | a0001c0017t0001g0257 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.3762-1231T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107938508 | |||||||
chr7:107938587 | G | A | 1 | a0001c0001t0001g0214 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3762-1310C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107938587 | |||||||
chr7:107938747 | C | T | 1 | a0001c0005t0001g0121 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.3761+1242G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107938747 | |||||||
chr7:107938939 | T | G | 1 | a0008c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3761+1050A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107938939 | |||||||
chr7:107939158 | A | G | 252 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(249): Show |
253 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(250): Show |
intron_variant | MODIFIER | c.3761+831T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939158 | |||||||
chr7:107939158 | A | T | 1 | a0001c0018t0001g0178 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.3761+831T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939158 | |||||||
chr7:107939186 | T | C | 1 | a0001c0009t0001g0283 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.3761+803A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939186 | |||||||
chr7:107939200 | G | A | 3 | a0001c0002t0001g0197 a0001c0002t0001g0216 a0001c0009t0001g0283 |
3 | HG00673.hp2 NA18975.hp1 NA18984.hp1 |
intron_variant | MODIFIER | c.3761+789C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939200 | |||||||
chr7:107939206 | C | G | 9 | a0001c0005t0001g0026 a0001c0005t0001g0351 a0001c0022t0001g0029 others(6): Show |
9 | HG02055.hp2 HG02572.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3761+783G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939206 | |||||||
chr7:107939226 | G | A | 1 | a0004c0066t0004g0021 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3761+763C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939226 | |||||||
chr7:107939229 | A | T | 251 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(248): Show |
252 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.3761+760T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939229 | |||||||
chr7:107939311 | C | CA | 44 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(41): Show |
44 | HG00423.hp2 HG00558.hp2 HG00621.hp1 others(41): Show |
intron_variant | MODIFIER | c.3761+677dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939311 | |||||||
chr7:107939428 | G | A | 3 | a0001c0001t0002g0192 a0002c0003t0002g0182 a0002c0008t0002g0278 |
3 | NA18994.hp1 NA19076.hp2 NA19090.hp1 |
intron_variant | MODIFIER | c.3761+561C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939428 | |||||||
chr7:107939438 | A | G | 13 | a0001c0005t0001g0357 a0001c0007t0001g0007 a0001c0007t0001g0009 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.3761+551T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939438 | |||||||
chr7:107939503 | A | T | 1 | a0001c0002t0001g0064 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3761+486T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939503 | |||||||
chr7:107939532 | T | C | 1 | a0021c0046t0002g0333 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3761+457A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939532 | |||||||
chr7:107939614 | G | A | 1 | a0001c0059t0001g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3761+375C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939614 | |||||||
chr7:107939658 | C | T | 5 | a0002c0013t0001g0030 a0002c0013t0001g0034 a0002c0013t0001g0069 others(2): Show |
5 | HG02280.hp2 HG02723.hp1 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.3761+331G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 25/33 | chr7 | 107939658 | |||||||
chr7:107940394 | A | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(263): Show |
268 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.3392-36T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107940394 | |||||||
chr7:107940589 | T | C | 1 | a0001c0002t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3392-231A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107940589 | |||||||
chr7:107940590 | A | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(263): Show |
268 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.3392-232T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107940590 | |||||||
chr7:107940650 | A | G | 1 | a0021c0046t0002g0333 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3392-292T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107940650 | |||||||
chr7:107940660 | T | A | 1 | a0004c0066t0004g0021 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3392-302A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107940660 | |||||||
chr7:107940670 | C | G | 269 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(266): Show |
271 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(268): Show |
intron_variant | MODIFIER | c.3392-312G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107940670 | |||||||
chr7:107940836 | A | G | 1 | a0016c0060t0001g0036 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.3392-478T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107940836 | |||||||
chr7:107940840 | A | G | 1 | a0001c0007t0001g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3392-482T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107940840 | |||||||
chr7:107940901 | T | C | 266 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(263): Show |
268 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.3392-543A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107940901 | |||||||
chr7:107941024 | A | G | 1 | a0007c0023t0001g0052 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.3392-666T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941024 | |||||||
chr7:107941049 | G | A | 4 | a0010c0025t0001g0141 a0010c0025t0001g0340 a0011c0070t0001g0348 others(1): Show |
4 | HG02109.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3392-691C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941049 | |||||||
chr7:107941134 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(258): Show |
263 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(260): Show |
intron_variant | MODIFIER | c.3392-776G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941134 | |||||||
chr7:107941246 | G | A | 1 | a0001c0005t0001g0248 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.3392-888C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941246 | |||||||
chr7:107941491 | A | G | 267 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(264): Show |
268 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(265): Show |
intron_variant | MODIFIER | c.3392-1133T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941491 | |||||||
chr7:107941539 | T | A | 1 | a0004c0068t0001g0139 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.3392-1181A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941539 | |||||||
chr7:107941653 | G | A | 1 | a0001c0006t0002g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3392-1295C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941653 | |||||||
chr7:107941655 | AT | A | 247 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(244): Show |
248 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(245): Show |
intron_variant | MODIFIER | c.3392-1298delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941655 | |||||||
chr7:107941816 | A | G | 1 | a0003c0004t0001g0250 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.3392-1458T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941816 | |||||||
chr7:107941819 | C | T | 1 | a0001c0028t0001g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.3392-1461G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941819 | |||||||
chr7:107941822 | C | CT | 12 | a0001c0001t0002g0019 a0001c0001t0002g0089 a0001c0001t0002g0177 others(9): Show |
12 | HG01243.hp2 HG01346.hp2 HG01928.hp2 others(9): Show |
intron_variant | MODIFIER | c.3392-1465dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941822 | |||||||
chr7:107941822 | CT | C | 30 | a0001c0001t0002g0003 a0001c0001t0002g0047 a0001c0001t0002g0267 others(27): Show |
30 | HG00099.hp2 HG00140.hp1 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.3392-1465delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941822 | |||||||
chr7:107941822 | CTT | C | 8 | a0001c0005t0001g0026 a0001c0045t0001g0038 a0002c0003t0002g0010 others(5): Show |
8 | HG01069.hp1 HG02818.hp2 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.3392-1466_3392-146 others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941822 | |||||||
chr7:107941822 | CTTTTTT | C | 7 | a0001c0001t0001g0292 a0001c0007t0001g0009 a0001c0007t0001g0130 others(4): Show |
7 | HG01891.hp1 HG01891.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.3392-1470_3392-146 others(10): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941822 | |||||||
chr7:107941822 | CTTTTTTT | C | 30 | a0001c0001t0001g0004 a0001c0001t0001g0012 a0001c0001t0001g0170 others(27): Show |
30 | HG02027.hp2 HG02055.hp1 HG02109.hp2 others(27): Show |
intron_variant | MODIFIER | c.3392-1471_3392-146 others(11): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941822 | |||||||
chr7:107941822 | CTTTTTTT others(1): Show |
C | 94 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0015 others(91): Show |
95 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.3392-1472_3392-146 others(12): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941822 | |||||||
chr7:107941822 | CTTTTTTT others(2): Show |
C | 25 | a0001c0001t0001g0063 a0001c0001t0001g0086 a0001c0001t0001g0111 others(22): Show |
25 | HG00558.hp2 HG00621.hp2 HG01070.hp1 others(22): Show |
intron_variant | MODIFIER | c.3392-1473_3392-146 others(13): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941822 | |||||||
chr7:107941822 | CTTTTTTT others(3): Show |
C | 93 | a0001c0002t0001g0014 a0001c0002t0001g0049 a0001c0002t0001g0055 others(90): Show |
93 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(90): Show |
intron_variant | MODIFIER | c.3392-1474_3392-146 others(14): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941822 | |||||||
chr7:107941822 | CTTTTTTT others(4): Show |
C | 3 | a0001c0005t0001g0150 a0001c0042t0001g0112 a0011c0070t0001g0348 |
3 | HG01515.hp2 HG02145.hp2 HG02809.hp1 |
intron_variant | MODIFIER | c.3392-1475_3392-146 others(15): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941822 | |||||||
chr7:107941878 | T | C | 126 | a0001c0001t0001g0249 a0001c0002t0001g0014 a0001c0002t0001g0049 others(123): Show |
126 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(123): Show |
intron_variant | MODIFIER | c.3392-1520A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107941878 | |||||||
chr7:107942001 | C | T | 1 | a0002c0008t0002g0278 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3392-1643G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942001 | |||||||
chr7:107942001 | CTT | C | 251 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(248): Show |
252 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(249): Show |
intron_variant | MODIFIER | c.3392-1645_3392-164 others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942001 | |||||||
chr7:107942106 | C | T | 1 | a0001c0002t0001g0297 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.3392-1748G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942106 | |||||||
chr7:107942176 | G | A | 1 | a0001c0002t0001g0106 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.3392-1818C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942176 | |||||||
chr7:107942182 | G | T | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.3392-1824C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942182 | |||||||
chr7:107942233 | G | A | 17 | a0001c0005t0001g0357 a0001c0007t0001g0007 a0001c0007t0001g0009 others(14): Show |
17 | HG01433.hp1 HG01891.hp1 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.3392-1875C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942233 | |||||||
chr7:107942277 | A | G | 4 | a0010c0025t0001g0141 a0010c0025t0001g0340 a0011c0070t0001g0348 others(1): Show |
4 | HG02109.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3392-1919T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942277 | |||||||
chr7:107942280 | G | T | 2 | a0002c0003t0002g0347 a0005c0012t0002g0353 |
2 | HG01243.hp1 HG02630.hp1 |
intron_variant | MODIFIER | c.3392-1922C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942280 | |||||||
chr7:107942282 | G | A | 1 | a0001c0001t0001g0063 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.3392-1924C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942282 | |||||||
chr7:107942335 | T | C | 1 | a0001c0072t0001g0025 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3392-1977A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942335 | |||||||
chr7:107942355 | G | T | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3392-1997C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942355 | |||||||
chr7:107942497 | G | C | 16 | a0001c0005t0001g0357 a0001c0007t0001g0007 a0001c0007t0001g0009 others(13): Show |
16 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(13): Show |
intron_variant | MODIFIER | c.3392-2139C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942497 | |||||||
chr7:107942726 | T | C | 1 | a0001c0002t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3392-2368A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942726 | |||||||
chr7:107942740 | A | G | 121 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(118): Show |
122 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(119): Show |
intron_variant | MODIFIER | c.3392-2382T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942740 | |||||||
chr7:107942796 | G | A | 108 | a0001c0002t0001g0014 a0001c0002t0001g0049 a0001c0002t0001g0055 others(105): Show |
108 | HG00140.hp2 HG00323.hp1 HG00408.hp1 others(105): Show |
intron_variant | MODIFIER | c.3392-2438C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107942796 | |||||||
chr7:107943063 | G | T | 1 | a0024c0030t0001g0312 | 1 | NA18952.hp1 | intron_variant | MODIFIER | c.3392-2705C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943063 | |||||||
chr7:107943073 | G | A | 1 | a0001c0002t0001g0202 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.3392-2715C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943073 | |||||||
chr7:107943132 | C | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(115): Show |
119 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.3392-2774G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943132 | |||||||
chr7:107943181 | G | A | 248 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(245): Show |
249 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(246): Show |
intron_variant | MODIFIER | c.3392-2823C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943181 | |||||||
chr7:107943246 | G | A | 1 | a0001c0005t0001g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.3392-2888C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943246 | |||||||
chr7:107943310 | G | T | 1 | a0001c0001t0002g0061 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3392-2952C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943310 | |||||||
chr7:107943456 | A | T | 118 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(115): Show |
119 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.3392-3098T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943456 | |||||||
chr7:107943634 | C | T | 2 | a0001c0001t0001g0083 a0001c0001t0001g0300 |
2 | NA19010.hp2 NA19070.hp2 |
intron_variant | MODIFIER | c.3392-3276G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943634 | |||||||
chr7:107943716 | G | A | 2 | a0008c0024t0001g0032 a0008c0024t0001g0184 |
2 | HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3392-3358C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943716 | |||||||
chr7:107943829 | C | G | 2 | a0001c0078t0001g0024 a0004c0067t0001g0137 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.3392-3471G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943829 | |||||||
chr7:107943876 | G | A | 1 | a0008c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3392-3518C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943876 | |||||||
chr7:107943944 | CG | C | 3 | a0008c0024t0001g0032 a0008c0024t0001g0184 a0008c0031t0001g0072 |
3 | HG02723.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.3392-3587delC | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107943944 | |||||||
chr7:107944087 | A | G | 1 | a0001c0002t0001g0209 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3392-3729T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107944087 | |||||||
chr7:107944144 | A | C | 1 | a0001c0001t0001g0170 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3392-3786T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107944144 | |||||||
chr7:107944335 | G | T | 245 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(242): Show |
246 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(243): Show |
intron_variant | MODIFIER | c.3392-3977C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107944335 | |||||||
chr7:107944401 | C | T | 2 | a0001c0005t0001g0026 a0001c0005t0001g0351 |
2 | HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.3392-4043G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107944401 | |||||||
chr7:107944452 | T | C | 1 | a0001c0002t0001g0065 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3392-4094A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107944452 | |||||||
chr7:107944480 | A | C | 1 | a0002c0010t0001g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.3392-4122T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107944480 | |||||||
chr7:107944705 | AC | A | 61 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0015 others(58): Show |
62 | HG00099.hp1 HG00323.hp2 HG00423.hp1 others(59): Show |
intron_variant | MODIFIER | c.3392-4348delG | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107944705 | |||||||
chr7:107944925 | G | A | 20 | a0001c0005t0001g0121 a0001c0005t0001g0129 a0001c0005t0001g0326 others(17): Show |
20 | HG00609.hp2 HG00741.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.3392-4567C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107944925 | |||||||
chr7:107945028 | C | T | 236 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(233): Show |
237 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(234): Show |
intron_variant | MODIFIER | c.3392-4670G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945028 | |||||||
chr7:107945041 | G | T | 20 | a0001c0005t0001g0121 a0001c0005t0001g0129 a0001c0005t0001g0326 others(17): Show |
20 | HG00609.hp2 HG00741.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.3392-4683C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945041 | |||||||
chr7:107945076 | T | A | 1 | a0021c0046t0002g0333 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3392-4718A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945076 | |||||||
chr7:107945083 | T | C | 1 | a0001c0001t0002g0267 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3392-4725A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945083 | |||||||
chr7:107945098 | G | A | 1 | a0003c0004t0001g0084 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.3392-4740C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945098 | |||||||
chr7:107945181 | A | G | 2 | a0001c0027t0001g0349 a0001c0043t0001g0116 |
2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.3392-4823T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945181 | |||||||
chr7:107945399 | C | T | 111 | a0001c0001t0002g0061 a0001c0002t0001g0014 a0001c0002t0001g0049 others(108): Show |
111 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.3392-5041G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945399 | |||||||
chr7:107945475 | C | A | 1 | a0001c0002t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3392-5117G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945475 | |||||||
chr7:107945809 | C | T | 107 | a0001c0001t0002g0061 a0001c0002t0001g0014 a0001c0002t0001g0049 others(104): Show |
107 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.3391+5417G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945809 | |||||||
chr7:107945910 | T | G | 1 | a0001c0002t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3391+5316A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107945910 | |||||||
chr7:107946026 | T | C | 26 | a0001c0001t0001g0012 a0001c0001t0001g0335 a0001c0002t0001g0247 others(23): Show |
26 | HG01891.hp2 HG02055.hp2 HG02258.hp1 others(23): Show |
intron_variant | MODIFIER | c.3391+5200A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946026 | |||||||
chr7:107946073 | A | C | 258 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(255): Show |
260 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(257): Show |
intron_variant | MODIFIER | c.3391+5153T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946073 | |||||||
chr7:107946139 | C | T | 2 | a0001c0006t0001g0042 a0001c0006t0001g0117 |
2 | NA19043.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3391+5087G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946139 | |||||||
chr7:107946309 | T | C | 7 | a0001c0001t0001g0102 a0001c0001t0001g0186 a0001c0001t0001g0234 others(4): Show |
7 | HG02056.hp2 HG02165.hp1 HG02165.hp2 others(4): Show |
intron_variant | MODIFIER | c.3391+4917A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946309 | |||||||
chr7:107946526 | A | C | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3391+4700T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946526 | |||||||
chr7:107946530 | A | G | 1 | a0001c0005t0001g0059 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.3391+4696T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946530 | |||||||
chr7:107946563 | C | T | 2 | a0002c0003t0001g0291 a0008c0031t0001g0072 |
2 | HG02723.hp2 NA18969.hp1 |
intron_variant | MODIFIER | c.3391+4663G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946563 | |||||||
chr7:107946583 | C | T | 14 | a0001c0005t0001g0357 a0001c0007t0001g0007 a0001c0007t0001g0009 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02109.hp2 others(11): Show |
intron_variant | MODIFIER | c.3391+4643G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946583 | |||||||
chr7:107946589 | C | T | 1 | a0001c0002t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3391+4637G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946589 | |||||||
chr7:107946640 | T | C | 1 | a0001c0044t0002g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.3391+4586A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946640 | |||||||
chr7:107946660 | A | G | 17 | a0001c0001t0001g0012 a0001c0001t0001g0335 a0001c0014t0001g0336 others(14): Show |
17 | HG01891.hp2 HG02258.hp1 HG02280.hp1 others(14): Show |
intron_variant | MODIFIER | c.3391+4566T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946660 | |||||||
chr7:107946930 | G | C | 1 | a0004c0066t0004g0021 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3391+4296C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107946930 | |||||||
chr7:107947072 | G | A | 1 | a0001c0002t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3391+4154C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947072 | |||||||
chr7:107947124 | C | T | 3 | a0001c0001t0002g0047 a0001c0001t0002g0152 a0001c0001t0002g0153 |
3 | HG00738.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.3391+4102G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947124 | |||||||
chr7:107947422 | T | C | 1 | a0001c0002t0001g0247 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.3391+3804A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947422 | |||||||
chr7:107947434 | A | G | 8 | a0001c0002t0001g0247 a0001c0005t0001g0026 a0001c0005t0001g0351 others(5): Show |
8 | HG02055.hp2 HG02723.hp2 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.3391+3792T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947434 | |||||||
chr7:107947941 | C | T | 1 | a0001c0002t0001g0065 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.3391+3285G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947941 | |||||||
chr7:107947972 | ATCT | A | 3 | a0002c0003t0002g0176 a0002c0003t0002g0258 a0002c0003t0002g0288 |
3 | HG00099.hp2 HG01517.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.3391+3251_3391+325 others(7): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947972 | |||||||
chr7:107947983 | C | CT | 14 | a0001c0001t0001g0063 a0001c0001t0001g0086 a0001c0001t0001g0100 others(11): Show |
15 | HG01070.hp1 HG01168.hp2 HG01515.hp1 others(12): Show |
intron_variant | MODIFIER | c.3391+3242dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947983 | |||||||
chr7:107947983 | C | CTT | 221 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(218): Show |
222 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(219): Show |
intron_variant | MODIFIER | c.3391+3241_3391+324 others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947983 | |||||||
chr7:107947983 | C | CTTT | 11 | a0001c0001t0001g0303 a0001c0001t0001g0321 a0001c0002t0001g0125 others(8): Show |
11 | HG01433.hp1 HG02109.hp2 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.3391+3240_3391+324 others(7): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947983 | |||||||
chr7:107947983 | C | CTTTT | 9 | a0001c0002t0001g0247 a0001c0005t0001g0026 a0001c0005t0001g0351 others(6): Show |
9 | HG02055.hp2 HG02622.hp2 HG02630.hp2 others(6): Show |
intron_variant | MODIFIER | c.3391+3239_3391+324 others(8): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947983 | |||||||
chr7:107947983 | C | CTTTTT | 8 | a0001c0007t0001g0007 a0001c0007t0001g0113 a0001c0007t0001g0114 others(5): Show |
8 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.3391+3238_3391+324 others(9): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947983 | |||||||
chr7:107947983 | C | T | 4 | a0001c0002t0001g0297 a0008c0024t0001g0032 a0008c0024t0001g0184 others(1): Show |
4 | HG02723.hp2 HG02886.hp2 HG03130.hp1 others(1): Show |
intron_variant | MODIFIER | c.3391+3243G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947983 | |||||||
chr7:107947983 | CT | C | 14 | a0001c0014t0001g0336 a0001c0014t0001g0346 a0001c0027t0001g0349 others(11): Show |
14 | HG02280.hp1 HG02559.hp1 HG02572.hp2 others(11): Show |
intron_variant | MODIFIER | c.3391+3242delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107947983 | |||||||
chr7:107948135 | C | T | 1 | a0001c0006t0001g0193 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.3391+3091G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948135 | |||||||
chr7:107948150 | T | C | 1 | a0001c0001t0001g0249 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.3391+3076A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948150 | |||||||
chr7:107948159 | G | A | 168 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(165): Show |
169 | HG00099.hp1 HG00408.hp2 HG00423.hp2 others(166): Show |
intron_variant | MODIFIER | c.3391+3067C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948159 | |||||||
chr7:107948282 | C | T | 1 | a0001c0001t0001g0073 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.3391+2944G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948282 | |||||||
chr7:107948388 | A | G | 1 | a0001c0001t0001g0261 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.3391+2838T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948388 | |||||||
chr7:107948488 | G | A | 4 | a0001c0027t0001g0349 a0001c0043t0001g0116 a0001c0078t0001g0024 others(1): Show |
4 | HG02280.hp1 HG02572.hp2 HG02647.hp2 others(1): Show |
intron_variant | MODIFIER | c.3391+2738C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948488 | |||||||
chr7:107948690 | G | A | 1 | a0001c0059t0001g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3391+2536C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948690 | |||||||
chr7:107948732 | A | T | 14 | a0001c0014t0001g0336 a0001c0014t0001g0346 a0001c0014t0003g0360 others(11): Show |
14 | HG01891.hp2 HG02280.hp1 HG02559.hp1 others(11): Show |
intron_variant | MODIFIER | c.3391+2494T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948732 | |||||||
chr7:107948781 | C | G | 1 | a0008c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3391+2445G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948781 | |||||||
chr7:107948821 | G | A | 1 | a0001c0002t0001g0049 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.3391+2405C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107948821 | |||||||
chr7:107949054 | C | T | 12 | a0001c0007t0001g0007 a0001c0007t0001g0009 a0001c0007t0001g0113 others(9): Show |
12 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3391+2172G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107949054 | |||||||
chr7:107949061 | A | G | 1 | a0001c0006t0002g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.3391+2165T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107949061 | |||||||
chr7:107949116 | T | C | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3391+2110A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107949116 | |||||||
chr7:107949205 | G | A | 1 | a0004c0067t0001g0137 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.3391+2021C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107949205 | |||||||
chr7:107949471 | T | TTTAACAG others(30): Show |
1 | a0002c0008t0002g0278 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3391+1718_3391+175 others(41): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107949471 | |||||||
chr7:107949799 | A | C | 1 | a0001c0002t0001g0337 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.3391+1427T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107949799 | |||||||
chr7:107949889 | A | G | 13 | a0001c0007t0001g0007 a0001c0007t0001g0009 a0001c0007t0001g0113 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.3391+1337T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107949889 | |||||||
chr7:107949952 | C | T | 97 | a0001c0001t0002g0061 a0001c0002t0001g0014 a0001c0002t0001g0049 others(94): Show |
97 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.3391+1274G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107949952 | |||||||
chr7:107950003 | G | A | 4 | a0010c0025t0001g0141 a0010c0025t0001g0340 a0011c0070t0001g0348 others(1): Show |
4 | HG02109.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.3391+1223C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950003 | |||||||
chr7:107950018 | T | A | 97 | a0001c0001t0002g0061 a0001c0002t0001g0014 a0001c0002t0001g0049 others(94): Show |
97 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.3391+1208A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950018 | |||||||
chr7:107950067 | T | C | 2 | a0001c0001t0001g0001 a0001c0001t0001g0004 |
3 | HG03490.hp1 HG03492.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.3391+1159A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950067 | |||||||
chr7:107950111 | C | T | 32 | a0001c0002t0001g0337 a0001c0005t0001g0357 a0001c0007t0001g0007 others(29): Show |
32 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(29): Show |
intron_variant | MODIFIER | c.3391+1115G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950111 | |||||||
chr7:107950229 | C | CA | 9 | a0001c0001t0001g0086 a0001c0001t0001g0217 a0001c0001t0001g0218 others(6): Show |
9 | HG02723.hp2 HG02886.hp2 HG02970.hp1 others(6): Show |
intron_variant | MODIFIER | c.3391+996dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950229 | |||||||
chr7:107950293 | G | C | 271 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(268): Show |
273 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(270): Show |
intron_variant | MODIFIER | c.3391+933C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950293 | |||||||
chr7:107950386 | A | G | 13 | a0001c0007t0001g0007 a0001c0007t0001g0009 a0001c0007t0001g0113 others(10): Show |
13 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.3391+840T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950386 | |||||||
chr7:107950494 | G | T | 25 | a0001c0014t0001g0336 a0001c0014t0001g0346 a0001c0014t0003g0360 others(22): Show |
25 | HG01433.hp1 HG01891.hp2 HG02109.hp1 others(22): Show |
intron_variant | MODIFIER | c.3391+732C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950494 | |||||||
chr7:107950523 | G | T | 1 | a0002c0008t0002g0278 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3391+703C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950523 | |||||||
chr7:107950524 | T | G | 1 | a0002c0008t0002g0278 | 1 | NA19076.hp2 | intron_variant | MODIFIER | c.3391+702A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950524 | |||||||
chr7:107950776 | T | A | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3391+450A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950776 | |||||||
chr7:107950923 | G | GGT | 21 | a0001c0002t0001g0110 a0001c0002t0001g0202 a0001c0002t0001g0212 others(18): Show |
21 | HG00323.hp1 HG01192.hp1 HG01256.hp2 others(18): Show |
intron_variant | MODIFIER | c.3391+301_3391+302d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | |||||||
chr7:107950923 | G | GGTGT | 62 | a0001c0001t0002g0002 a0001c0001t0002g0047 a0001c0002t0001g0049 others(59): Show |
63 | HG00140.hp2 HG00423.hp1 HG00558.hp1 others(60): Show |
intron_variant | MODIFIER | c.3391+299_3391+302d others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | |||||||
chr7:107950923 | G | GGTGTGT | 9 | a0001c0002t0001g0196 a0001c0005t0001g0248 a0001c0009t0001g0283 others(6): Show |
9 | HG01361.hp1 HG02572.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.3391+297_3391+302d others(8): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | |||||||
chr7:107950923 | G | GGTGTGTG others(1): Show |
7 | a0001c0001t0002g0152 a0001c0001t0002g0153 a0001c0042t0001g0112 others(4): Show |
7 | HG00741.hp1 HG01257.hp2 HG01258.hp2 others(4): Show |
intron_variant | MODIFIER | c.3391+295_3391+302d others(10): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | |||||||
chr7:107950923 | GGT | G | 84 | a0001c0001t0002g0050 a0001c0001t0002g0267 a0001c0005t0001g0357 others(81): Show |
84 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(81): Show |
intron_variant | MODIFIER | c.3391+301_3391+302d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | |||||||
chr7:107950923 | GGTGT | G | 5 | a0002c0013t0001g0030 a0002c0013t0001g0069 a0005c0012t0002g0353 others(2): Show |
5 | HG01243.hp1 HG02280.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.3391+299_3391+302d others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | |||||||
chr7:107950923 | GGTGTGT | G | 10 | a0001c0002t0001g0337 a0001c0005t0001g0026 a0001c0005t0001g0351 others(7): Show |
10 | HG02055.hp2 HG02165.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.3391+297_3391+302d others(8): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | |||||||
chr7:107950923 | GGTGTGTG others(1): Show |
G | 7 | a0001c0001t0001g0015 a0001c0001t0001g0316 a0001c0001t0002g0192 others(4): Show |
7 | HG00323.hp2 HG00408.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.3391+295_3391+302d others(10): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | |||||||
chr7:107950923 | GGTGTGTG others(3): Show |
G | 120 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(117): Show |
121 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(118): Show |
intron_variant | MODIFIER | c.3391+293_3391+302d others(12): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | |||||||
chr7:107950923 | GGTGTGTG others(11): Show |
G | 1 | a0001c0002t0001g0331 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.3391+285_3391+302d others(20): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950923 | |||||||
chr7:107950971 | C | A | 4 | a0002c0003t0002g0166 a0002c0008t0002g0272 a0002c0010t0001g0155 others(1): Show |
4 | HG00323.hp1 HG01070.hp2 HG01168.hp1 others(1): Show |
intron_variant | MODIFIER | c.3391+255G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107950971 | |||||||
chr7:107951126 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3391+100C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107951126 | |||||||
chr7:107951205 | G | A | 1 | a0001c0014t0001g0346 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.3391+21C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107951205 | |||||||
chr7:107951207 | G | A | 3 | a0001c0002t0001g0247 a0001c0022t0001g0029 a0001c0022t0001g0039 |
3 | HG02970.hp1 HG03098.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.3391+19C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 24/33 | chr7 | 107951207 | |||||||
chr7:107951381 | CT | C | 4 | a0001c0001t0002g0047 a0001c0001t0002g0152 a0001c0001t0002g0153 others(1): Show |
4 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.3295-60delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951381 | |||||||
chr7:107951469 | A | G | 105 | a0001c0001t0002g0002 a0001c0001t0002g0047 a0001c0001t0002g0050 others(102): Show |
106 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.3295-147T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951469 | |||||||
chr7:107951471 | C | T | 6 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0010t0001g0334 others(3): Show |
6 | HG00738.hp1 HG02976.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.3295-149G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951471 | |||||||
chr7:107951622 | C | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0342 |
2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.3295-300G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951622 | |||||||
chr7:107951662 | C | CA | 124 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(121): Show |
125 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(122): Show |
intron_variant | MODIFIER | c.3295-341dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951662 | |||||||
chr7:107951680 | T | C | 2 | a0001c0005t0001g0126 a0011c0071t0001g0067 |
2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3294+329A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951680 | |||||||
chr7:107951753 | A | G | 23 | a0001c0002t0001g0306 a0001c0005t0001g0121 a0001c0005t0001g0129 others(20): Show |
23 | HG00609.hp2 HG00741.hp1 HG01256.hp1 others(20): Show |
intron_variant | MODIFIER | c.3294+256T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951753 | |||||||
chr7:107951900 | C | T | 1 | a0001c0001t0001g0214 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3294+109G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951900 | |||||||
chr7:107951946 | C | A | 1 | a0008c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.3294+63G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951946 | |||||||
chr7:107951958 | G | A | 160 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(157): Show |
161 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(158): Show |
intron_variant | MODIFIER | c.3294+51C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 23/33 | chr7 | 107951958 | |||||||
chr7:107952337 | G | A | 7 | a0002c0003t0002g0076 a0002c0003t0002g0169 a0002c0003t0002g0198 others(4): Show |
7 | NA18962.hp1 NA18988.hp1 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.3080-114C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107952337 | |||||||
chr7:107952400 | C | T | 2 | a0001c0005t0001g0126 a0011c0071t0001g0067 |
2 | HG03225.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.3080-177G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107952400 | |||||||
chr7:107952437 | A | G | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3080-214T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107952437 | |||||||
chr7:107952512 | A | C | 35 | a0001c0001t0001g0183 a0001c0002t0001g0247 a0001c0007t0001g0007 others(32): Show |
35 | HG01891.hp1 HG01891.hp2 HG02055.hp1 others(32): Show |
intron_variant | MODIFIER | c.3080-289T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107952512 | |||||||
chr7:107952526 | T | A | 1 | a0001c0059t0001g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3080-303A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107952526 | |||||||
chr7:107952835 | G | A | 16 | a0001c0014t0001g0336 a0001c0014t0001g0346 a0001c0014t0003g0360 others(13): Show |
16 | HG01891.hp2 HG02280.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.3080-612C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107952835 | |||||||
chr7:107952906 | A | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0321 |
2 | NA19076.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.3079+624T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107952906 | |||||||
chr7:107952997 | A | C | 1 | a0002c0003t0002g0264 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.3079+533T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107952997 | |||||||
chr7:107953128 | G | A | 1 | a0001c0059t0001g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.3079+402C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953128 | |||||||
chr7:107953152 | T | A | 1 | a0001c0018t0001g0277 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3079+378A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953152 | |||||||
chr7:107953162 | A | T | 1 | a0001c0018t0001g0277 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3079+368T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953162 | |||||||
chr7:107953167 | A | G | 1 | a0001c0018t0001g0277 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3079+363T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953167 | |||||||
chr7:107953169 | C | T | 1 | a0001c0018t0001g0277 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3079+361G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953169 | |||||||
chr7:107953174 | T | A | 1 | a0001c0018t0001g0277 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3079+356A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953174 | |||||||
chr7:107953193 | T | C | 1 | a0001c0018t0001g0277 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3079+337A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953193 | |||||||
chr7:107953200 | T | C | 1 | a0004c0066t0004g0021 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.3079+330A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953200 | |||||||
chr7:107953202 | C | CAAAAAAT others(238): Show |
1 | a0001c0018t0001g0277 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.3079+327_3079+328i others(247): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953202 | |||||||
chr7:107953295 | T | C | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.3079+235A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953295 | |||||||
chr7:107953359 | TA | T | 263 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(260): Show |
264 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(261): Show |
intron_variant | MODIFIER | c.3079+170delT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953359 | |||||||
chr7:107953425 | A | C | 1 | a0001c0001t0001g0205 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.3079+105T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 22/33 | chr7 | 107953425 | |||||||
chr7:107953816 | A | C | 1 | a0011c0071t0001g0067 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.2855-62T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107953816 | |||||||
chr7:107954060 | C | T | 1 | a0001c0005t0001g0035 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.2855-306G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954060 | |||||||
chr7:107954104 | G | A | 95 | a0001c0001t0002g0050 a0001c0001t0002g0061 a0001c0002t0001g0014 others(92): Show |
95 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(92): Show |
intron_variant | MODIFIER | c.2855-350C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954104 | |||||||
chr7:107954166 | T | G | 6 | a0002c0003t0002g0347 a0002c0013t0001g0030 a0002c0013t0001g0034 others(3): Show |
6 | HG01243.hp1 HG02280.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.2855-412A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954166 | |||||||
chr7:107954272 | A | G | 20 | a0001c0002t0001g0306 a0001c0005t0001g0129 a0003c0004t0001g0082 others(17): Show |
20 | HG00609.hp2 HG00741.hp1 HG01256.hp1 others(17): Show |
intron_variant | MODIFIER | c.2855-518T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954272 | |||||||
chr7:107954331 | AT | A | 101 | a0001c0001t0001g0214 a0001c0001t0002g0050 a0001c0002t0001g0014 others(98): Show |
101 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.2855-578delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954331 | |||||||
chr7:107954332 | T | A | 3 | a0001c0001t0002g0061 a0001c0005t0001g0059 a0001c0059t0001g0041 |
3 | HG01175.hp2 HG01261.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.2855-578A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954332 | |||||||
chr7:107954556 | C | T | 1 | a0001c0006t0002g0235 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.2855-802G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954556 | |||||||
chr7:107954638 | C | T | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2854+829G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954638 | |||||||
chr7:107954683 | C | A | 1 | a0003c0004t0001g0087 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2854+784G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954683 | |||||||
chr7:107954707 | C | T | 3 | a0008c0024t0001g0032 a0008c0024t0001g0184 a0008c0031t0001g0072 |
3 | HG02723.hp2 HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.2854+760G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954707 | |||||||
chr7:107954881 | A | T | 16 | a0001c0001t0001g0183 a0001c0014t0001g0336 a0001c0014t0001g0346 others(13): Show |
16 | HG01891.hp2 HG02280.hp1 HG02559.hp1 others(13): Show |
intron_variant | MODIFIER | c.2854+586T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954881 | |||||||
chr7:107954939 | C | A | 1 | a0008c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2854+528G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954939 | |||||||
chr7:107954939 | C | T | 3 | a0002c0003t0002g0175 a0002c0039t0002g0203 a0023c0037t0002g0232 |
3 | HG02735.hp2 HG03710.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2854+528G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954939 | |||||||
chr7:107954945 | C | T | 261 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(258): Show |
262 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(259): Show |
intron_variant | MODIFIER | c.2854+522G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954945 | |||||||
chr7:107954952 | TG | T | 35 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(32): Show |
35 | HG00558.hp2 HG00621.hp1 HG02083.hp2 others(32): Show |
intron_variant | MODIFIER | c.2854+514delC | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107954952 | |||||||
chr7:107955144 | T | G | 14 | a0001c0006t0001g0042 a0001c0006t0001g0117 a0001c0007t0001g0007 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2854+323A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107955144 | |||||||
chr7:107955167 | G | C | 2 | a0001c0002t0001g0123 a0001c0002t0001g0125 |
2 | NA18946.hp1 NA19080.hp1 |
intron_variant | MODIFIER | c.2854+300C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107955167 | |||||||
chr7:107955287 | A | G | 4 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0294 others(1): Show |
4 | HG01109.hp2 HG01255.hp1 HG01257.hp1 others(1): Show |
intron_variant | MODIFIER | c.2854+180T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107955287 | |||||||
chr7:107955371 | A | T | 1 | a0002c0003t0002g0159 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.2854+96T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107955371 | |||||||
chr7:107955447 | A | C | 4 | a0010c0025t0001g0141 a0010c0025t0001g0340 a0011c0070t0001g0348 others(1): Show |
4 | HG02109.hp1 HG02615.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2854+20T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 21/33 | chr7 | 107955447 | |||||||
chr7:107955648 | G | A | 1 | a0001c0002t0001g0331 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2691-18C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107955648 | |||||||
chr7:107955898 | G | GT | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(137): Show |
141 | HG00323.hp2 HG00408.hp2 HG00423.hp2 others(138): Show |
intron_variant | MODIFIER | c.2691-269dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107955898 | |||||||
chr7:107955902 | T | G | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2691-272A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107955902 | |||||||
chr7:107955927 | G | A | 2 | a0009c0062t0002g0293 a0009c0082t0002g0204 |
2 | HG01192.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2691-297C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107955927 | |||||||
chr7:107955928 | C | T | 1 | a0001c0002t0001g0199 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.2691-298G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107955928 | |||||||
chr7:107955975 | G | A | 15 | a0001c0014t0001g0336 a0001c0014t0001g0346 a0001c0014t0003g0360 others(12): Show |
15 | HG01891.hp2 HG02280.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.2691-345C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107955975 | |||||||
chr7:107956056 | C | G | 14 | a0001c0006t0001g0042 a0001c0006t0001g0117 a0001c0007t0001g0007 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2691-426G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107956056 | |||||||
chr7:107956281 | C | T | 2 | a0001c0027t0001g0349 a0001c0043t0001g0116 |
2 | HG02280.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.2691-651G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107956281 | |||||||
chr7:107956459 | G | A | 1 | a0003c0004t0001g0250 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.2691-829C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107956459 | |||||||
chr7:107956664 | T | C | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2691-1034A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107956664 | |||||||
chr7:107956811 | G | A | 2 | a0001c0005t0001g0026 a0001c0005t0001g0351 |
2 | HG02055.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.2691-1181C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107956811 | |||||||
chr7:107956829 | T | C | 2 | a0004c0015t0002g0008 a0004c0069t0001g0134 |
2 | HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.2691-1199A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107956829 | |||||||
chr7:107956930 | G | A | 14 | a0001c0006t0001g0042 a0001c0006t0001g0117 a0001c0007t0001g0007 others(11): Show |
14 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.2691-1300C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107956930 | |||||||
chr7:107956931 | C | T | 6 | a0001c0006t0001g0254 a0001c0006t0001g0341 a0001c0006t0001g0356 others(3): Show |
6 | HG01433.hp1 HG02258.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.2691-1301G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107956931 | |||||||
chr7:107957045 | A | G | 7 | a0001c0001t0002g0050 a0001c0006t0001g0133 a0001c0006t0002g0224 others(4): Show |
7 | HG00408.hp1 HG00642.hp1 HG00735.hp1 others(4): Show |
intron_variant | MODIFIER | c.2691-1415T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957045 | |||||||
chr7:107957058 | G | A | 15 | a0001c0014t0001g0346 a0001c0027t0001g0349 a0001c0035t0001g0037 others(12): Show |
15 | HG02280.hp1 HG02559.hp1 HG02572.hp2 others(12): Show |
intron_variant | MODIFIER | c.2691-1428C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957058 | |||||||
chr7:107957116 | G | A | 3 | a0001c0001t0002g0047 a0001c0001t0002g0152 a0001c0001t0002g0153 |
3 | HG00738.hp2 HG01257.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.2691-1486C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957116 | |||||||
chr7:107957118 | G | A | 1 | a0004c0015t0002g0008 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.2691-1488C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957118 | |||||||
chr7:107957345 | C | T | 1 | a0002c0053t0002g0145 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.2691-1715G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957345 | |||||||
chr7:107957506 | C | G | 82 | a0001c0001t0002g0002 a0001c0001t0002g0047 a0001c0001t0002g0050 others(79): Show |
83 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(80): Show |
intron_variant | MODIFIER | c.2690+1743G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957506 | |||||||
chr7:107957529 | C | T | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2690+1720G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957529 | |||||||
chr7:107957544 | G | A | 2 | a0001c0001t0001g0033 a0001c0001t0001g0342 |
2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2690+1705C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957544 | |||||||
chr7:107957555 | A | G | 4 | a0001c0022t0001g0039 a0010c0025t0001g0141 a0010c0025t0001g0340 others(1): Show |
4 | HG02109.hp1 HG02615.hp1 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.2690+1694T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957555 | |||||||
chr7:107957833 | A | G | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2690+1416T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957833 | |||||||
chr7:107957858 | A | C | 1 | a0001c0005t0001g0126 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2690+1391T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107957858 | |||||||
chr7:107958336 | G | C | 1 | a0002c0003t0002g0168 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.2690+913C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107958336 | |||||||
chr7:107958348 | A | G | 1 | a0001c0007t0001g0343 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.2690+901T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107958348 | |||||||
chr7:107958644 | G | A | 20 | a0001c0002t0001g0337 a0001c0014t0001g0336 a0001c0014t0001g0346 others(17): Show |
20 | HG01243.hp1 HG01891.hp2 HG02559.hp1 others(17): Show |
intron_variant | MODIFIER | c.2690+605C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107958644 | |||||||
chr7:107958691 | T | G | 1 | a0001c0002t0001g0302 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.2690+558A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107958691 | |||||||
chr7:107958837 | A | C | 1 | a0001c0001t0002g0003 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.2690+412T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107958837 | |||||||
chr7:107958948 | G | C | 1 | a0003c0049t0001g0056 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.2690+301C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107958948 | |||||||
chr7:107959001 | G | A | 1 | a0002c0010t0001g0227 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.2690+248C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107959001 | |||||||
chr7:107959038 | G | C | 1 | a0001c0005t0001g0248 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.2690+211C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 20/33 | chr7 | 107959038 | |||||||
chr7:107959502 | G | A | 1 | a0001c0072t0001g0025 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2459-22C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 19/33 | chr7 | 107959502 | |||||||
chr7:107960113 | C | T | 116 | a0001c0001t0002g0050 a0001c0002t0001g0014 a0001c0002t0001g0049 others(113): Show |
116 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(113): Show |
intron_variant | MODIFIER | c.2315-279G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 18/33 | chr7 | 107960113 | |||||||
chr7:107960142 | G | A | 2 | a0009c0062t0002g0293 a0009c0082t0002g0204 |
2 | HG01192.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.2314+303C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 18/33 | chr7 | 107960142 | |||||||
chr7:107960688 | G | T | 1 | a0011c0070t0001g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2110-39C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 17/33 | chr7 | 107960688 | |||||||
chr7:107961078 | T | C | 87 | a0001c0001t0002g0002 a0001c0001t0002g0047 a0001c0001t0002g0050 others(84): Show |
88 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(85): Show |
intron_variant | MODIFIER | c.2109+128A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 17/33 | chr7 | 107961078 | |||||||
chr7:107961091 | G | T | 4 | a0001c0001t0002g0002 a0001c0001t0002g0047 a0001c0001t0002g0152 others(1): Show |
5 | HG00738.hp2 HG01257.hp2 HG01258.hp2 others(2): Show |
intron_variant | MODIFIER | c.2109+115C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 17/33 | chr7 | 107961091 | |||||||
chr7:107961138 | C | G | 1 | a0011c0070t0001g0348 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2109+68G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 17/33 | chr7 | 107961138 | |||||||
chr7:107961402 | C | G | 1 | a0002c0008t0002g0273 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1986-73G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 16/33 | chr7 | 107961402 | |||||||
chr7:107961537 | C | T | 3 | a0010c0025t0001g0141 a0010c0025t0001g0340 a0029c0076t0001g0005 |
3 | HG02109.hp1 HG02615.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1985+12G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 16/33 | chr7 | 107961537 | |||||||
chr7:107961781 | C | G | 2 | a0001c0001t0001g0033 a0001c0001t0001g0342 |
2 | HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.1858-105G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107961781 | |||||||
chr7:107961853 | C | T | 1 | a0001c0002t0001g0222 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1858-177G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107961853 | |||||||
chr7:107961869 | C | G | 22 | a0001c0006t0001g0042 a0001c0006t0001g0117 a0001c0006t0001g0254 others(19): Show |
22 | HG01433.hp1 HG01891.hp1 HG02055.hp1 others(19): Show |
intron_variant | MODIFIER | c.1858-193G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107961869 | |||||||
chr7:107962061 | T | G | 1 | a0015c0055t0001g0243 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.1858-385A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962061 | |||||||
chr7:107962083 | C | T | 1 | a0028c0074t0001g0200 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1858-407G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962083 | |||||||
chr7:107962179 | C | T | 43 | a0001c0005t0001g0026 a0001c0005t0001g0351 a0001c0014t0001g0336 others(40): Show |
43 | HG00099.hp1 HG00099.hp2 HG00738.hp1 others(40): Show |
intron_variant | MODIFIER | c.1858-503G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962179 | |||||||
chr7:107962216 | C | T | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.1858-540G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962216 | |||||||
chr7:107962359 | C | T | 7 | a0001c0035t0001g0037 a0002c0003t0001g0070 a0002c0003t0001g0071 others(4): Show |
7 | HG00738.hp1 HG02622.hp1 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1857+546G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962359 | |||||||
chr7:107962387 | G | C | 2 | a0008c0024t0001g0032 a0008c0024t0001g0184 |
2 | HG02886.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.1857+518C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962387 | |||||||
chr7:107962416 | GA | G | 11 | a0001c0002t0001g0337 a0001c0014t0003g0360 a0001c0027t0001g0349 others(8): Show |
11 | HG01891.hp2 HG02572.hp2 HG02647.hp2 others(8): Show |
intron_variant | MODIFIER | c.1857+488delT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962416 | |||||||
chr7:107962512 | A | G | 23 | a0001c0006t0001g0042 a0001c0006t0001g0117 a0001c0006t0001g0254 others(20): Show |
23 | HG01433.hp1 HG01891.hp1 HG02055.hp1 others(20): Show |
intron_variant | MODIFIER | c.1857+393T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962512 | |||||||
chr7:107962582 | C | T | 3 | a0001c0027t0001g0349 a0001c0078t0001g0024 a0004c0067t0001g0137 |
3 | HG02572.hp2 HG02647.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.1857+323G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962582 | |||||||
chr7:107962664 | A | G | 1 | a0004c0016t0001g0354 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.1857+241T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962664 | |||||||
chr7:107962697 | G | C | 1 | a0001c0006t0001g0341 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1857+208C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962697 | |||||||
chr7:107962700 | C | G | 6 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(3): Show |
6 | HG00642.hp2 HG00733.hp2 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.1857+205G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962700 | |||||||
chr7:107962707 | CA | C | 79 | a0001c0001t0001g0111 a0001c0001t0001g0228 a0001c0002t0001g0014 others(76): Show |
79 | HG00140.hp2 HG00408.hp1 HG00423.hp1 others(76): Show |
intron_variant | MODIFIER | c.1857+197delT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962707 | |||||||
chr7:107962707 | CAA | C | 65 | a0001c0001t0001g0048 a0001c0002t0001g0123 a0001c0002t0001g0247 others(62): Show |
65 | HG00639.hp1 HG01070.hp2 HG01106.hp2 others(62): Show |
intron_variant | MODIFIER | c.1857+196_1857+197d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962707 | |||||||
chr7:107962722 | A | G | 3 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0002c0003t0002g0092 |
4 | HG02145.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.1857+183T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962722 | |||||||
chr7:107962810 | A | G | 2 | a0001c0001t0001g0173 a0001c0001t0001g0321 |
2 | NA19076.hp1 NA19084.hp1 |
intron_variant | MODIFIER | c.1857+95T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962810 | |||||||
chr7:107962837 | T | G | 20 | a0001c0001t0001g0048 a0001c0005t0001g0126 a0001c0005t0001g0129 others(17): Show |
20 | HG00609.hp2 HG00639.hp1 HG01106.hp2 others(17): Show |
intron_variant | MODIFIER | c.1857+68A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962837 | |||||||
chr7:107962848 | A | G | 5 | a0001c0002t0001g0247 a0001c0005t0001g0357 a0001c0022t0001g0029 others(2): Show |
5 | HG02109.hp2 HG02630.hp2 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1857+57T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 15/33 | chr7 | 107962848 | |||||||
chr7:107963222 | T | C | 1 | a0001c0001t0001g0245 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.1699-159A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107963222 | |||||||
chr7:107963303 | G | C | 1 | a0003c0004t0001g0236 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.1699-240C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107963303 | |||||||
chr7:107963639 | C | T | 5 | a0001c0006t0001g0254 a0001c0006t0001g0341 a0001c0006t0001g0356 others(2): Show |
5 | HG02258.hp2 HG02896.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1699-576G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107963639 | |||||||
chr7:107963721 | A | C | 1 | a0002c0008t0002g0273 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1699-658T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107963721 | |||||||
chr7:107963817 | C | T | 6 | a0001c0002t0001g0222 a0001c0002t0001g0266 a0001c0002t0001g0295 others(3): Show |
6 | HG02622.hp2 NA18944.hp2 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.1698+735G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107963817 | |||||||
chr7:107963818 | G | A | 2 | a0001c0078t0001g0024 a0004c0067t0001g0137 |
2 | HG02572.hp2 HG02647.hp2 |
intron_variant | MODIFIER | c.1698+734C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107963818 | |||||||
chr7:107963869 | C | T | 7 | a0001c0001t0001g0011 a0001c0001t0001g0016 a0001c0001t0001g0033 others(4): Show |
7 | HG00642.hp1 HG01109.hp2 HG01255.hp1 others(4): Show |
intron_variant | MODIFIER | c.1698+683G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107963869 | |||||||
chr7:107963870 | G | A | 1 | a0002c0008t0002g0273 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1698+682C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107963870 | |||||||
chr7:107964028 | C | T | 3 | a0001c0006t0002g0224 a0008c0024t0001g0184 a0020c0034t0001g0031 |
3 | HG02886.hp2 HG02896.hp2 HG03490.hp2 |
intron_variant | MODIFIER | c.1698+524G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107964028 | |||||||
chr7:107964050 | T | C | 21 | a0001c0014t0001g0336 a0001c0044t0002g0345 a0002c0003t0001g0284 others(18): Show |
21 | HG00099.hp1 HG00099.hp2 HG01192.hp2 others(18): Show |
intron_variant | MODIFIER | c.1698+502A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107964050 | |||||||
chr7:107964097 | C | T | 1 | a0001c0006t0002g0327 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1698+455G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107964097 | |||||||
chr7:107964098 | G | A | 1 | a0001c0002t0001g0223 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1698+454C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107964098 | |||||||
chr7:107964373 | T | G | 243 | a0001c0001t0001g0011 a0001c0001t0001g0012 a0001c0001t0001g0015 others(240): Show |
243 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(240): Show |
intron_variant | MODIFIER | c.1698+179A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107964373 | |||||||
chr7:107964476 | G | A | 1 | a0001c0017t0001g0257 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1698+76C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 14/33 | chr7 | 107964476 | |||||||
chr7:107964741 | C | T | 1 | a0001c0001t0001g0111 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1563-54G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107964741 | |||||||
chr7:107964836 | AG | A | 8 | a0001c0001t0001g0083 a0001c0002t0001g0077 a0001c0002t0001g0110 others(5): Show |
8 | NA18967.hp1 NA18982.hp1 NA18985.hp1 others(5): Show |
intron_variant | MODIFIER | c.1563-150delC | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107964836 | |||||||
chr7:107964837 | G | A | 60 | a0001c0001t0001g0085 a0001c0001t0001g0188 a0001c0001t0001g0189 others(57): Show |
60 | HG00140.hp2 HG00408.hp2 HG00621.hp1 others(57): Show |
intron_variant | MODIFIER | c.1563-150C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107964837 | |||||||
chr7:107964859 | A | T | 14 | a0001c0001t0001g0033 a0001c0001t0001g0303 a0001c0001t0001g0342 others(11): Show |
14 | HG01433.hp1 HG02109.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1563-172T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107964859 | |||||||
chr7:107964867 | G | A | 16 | a0001c0001t0001g0033 a0001c0001t0001g0342 a0001c0006t0001g0117 others(13): Show |
16 | HG00738.hp1 HG01433.hp1 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.1563-180C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107964867 | |||||||
chr7:107964964 | A | G | 6 | a0001c0007t0001g0122 a0001c0022t0001g0029 a0001c0022t0001g0039 others(3): Show |
6 | HG02572.hp2 HG02809.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1563-277T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107964964 | |||||||
chr7:107964967 | C | T | 299 | a0001c0001t0001g0004 a0001c0001t0001g0011 a0001c0001t0001g0015 others(296): Show |
300 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(297): Show |
intron_variant | MODIFIER | c.1563-280G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107964967 | |||||||
chr7:107965080 | G | A | 1 | a0001c0005t0001g0059 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1563-393C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965080 | |||||||
chr7:107965088 | G | A | 5 | a0001c0006t0001g0341 a0001c0027t0001g0349 a0001c0078t0001g0024 others(2): Show |
5 | HG02258.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1563-401C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965088 | |||||||
chr7:107965108 | C | T | 1 | a0001c0032t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1563-421G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965108 | |||||||
chr7:107965111 | A | G | 1 | a0002c0010t0001g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1563-424T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965111 | |||||||
chr7:107965161 | A | G | 1 | a0001c0072t0001g0025 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1563-474T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965161 | |||||||
chr7:107965232 | A | G | 13 | a0001c0001t0001g0335 a0001c0001t0001g0342 a0001c0006t0001g0341 others(10): Show |
13 | HG01243.hp1 HG01433.hp1 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.1563-545T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965232 | |||||||
chr7:107965233 | C | A | 1 | a0001c0035t0001g0037 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1563-546G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965233 | |||||||
chr7:107965264 | C | T | 7 | a0001c0001t0001g0015 a0001c0001t0001g0172 a0001c0001t0001g0260 others(4): Show |
7 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(4): Show |
intron_variant | MODIFIER | c.1563-577G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965264 | |||||||
chr7:107965299 | G | T | 3 | a0004c0016t0001g0354 a0004c0016t0001g0355 a0005c0012t0002g0353 |
3 | HG01243.hp1 HG02559.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.1563-612C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965299 | |||||||
chr7:107965367 | G | A | 1 | a0002c0008t0002g0274 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1563-680C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965367 | |||||||
chr7:107965486 | C | G | 157 | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0001g0033 others(154): Show |
157 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.1563-799G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965486 | |||||||
chr7:107965503 | C | T | 1 | a0001c0001t0002g0019 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1563-816G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965503 | |||||||
chr7:107965516 | T | C | 14 | a0001c0001t0001g0033 a0001c0007t0003g0361 a0002c0013t0001g0034 others(11): Show |
14 | HG02055.hp1 HG02109.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1563-829A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965516 | |||||||
chr7:107965520 | G | T | 3 | a0001c0002t0001g0286 a0001c0002t0001g0298 a0001c0002t0001g0310 |
3 | HG03491.hp2 HG03492.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1563-833C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965520 | |||||||
chr7:107965521 | G | A | 3 | a0001c0002t0001g0286 a0001c0002t0001g0298 a0001c0002t0001g0310 |
3 | HG03491.hp2 HG03492.hp2 NA19010.hp1 |
intron_variant | MODIFIER | c.1563-834C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965521 | |||||||
chr7:107965562 | A | G | 1 | a0002c0008t0002g0156 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1563-875T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965562 | |||||||
chr7:107965602 | G | A | 1 | a0002c0010t0001g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1563-915C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965602 | |||||||
chr7:107965603 | T | C | 2 | a0001c0001t0001g0262 a0001c0001t0001g0263 |
2 | HG02027.hp2 HG02056.hp2 |
intron_variant | MODIFIER | c.1563-916A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965603 | |||||||
chr7:107965714 | G | T | 2 | a0001c0005t0001g0035 a0016c0060t0001g0036 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1563-1027C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965714 | |||||||
chr7:107965759 | A | C | 2 | a0001c0006t0002g0235 a0003c0004t0001g0230 |
2 | HG02129.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.1563-1072T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965759 | |||||||
chr7:107965782 | C | T | 2 | a0001c0005t0001g0035 a0016c0060t0001g0036 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1563-1095G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965782 | |||||||
chr7:107965828 | G | A | 2 | a0004c0015t0002g0008 a0010c0025t0001g0141 |
2 | HG02109.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.1563-1141C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965828 | |||||||
chr7:107965831 | G | C | 7 | a0001c0001t0001g0201 a0001c0001t0001g0205 a0001c0001t0001g0217 others(4): Show |
7 | HG00673.hp2 HG02129.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1563-1144C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107965831 | |||||||
chr7:107966102 | T | C | 1 | a0001c0006t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1563-1415A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966102 | |||||||
chr7:107966139 | C | T | 3 | a0001c0032t0001g0028 a0001c0072t0001g0025 a0001c0078t0001g0024 |
3 | HG02572.hp2 HG02630.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1563-1452G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966139 | |||||||
chr7:107966189 | G | C | 28 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(25): Show |
28 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1563-1502C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966189 | |||||||
chr7:107966235 | G | T | 1 | a0001c0007t0003g0362 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1563-1548C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966235 | |||||||
chr7:107966250 | G | A | 3 | a0001c0035t0001g0037 a0020c0034t0001g0031 a0022c0033t0001g0040 |
3 | HG02622.hp1 HG02896.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.1563-1563C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966250 | |||||||
chr7:107966286 | C | T | 1 | a0002c0010t0001g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1563-1599G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966286 | |||||||
chr7:107966296 | C | T | 1 | a0001c0005t0001g0150 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1563-1609G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966296 | |||||||
chr7:107966373 | G | A | 14 | a0001c0001t0001g0033 a0002c0013t0001g0034 a0002c0019t0002g0308 others(11): Show |
14 | HG02109.hp1 HG02257.hp2 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.1563-1686C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966373 | |||||||
chr7:107966402 | G | T | 2 | a0001c0005t0001g0035 a0016c0060t0001g0036 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1563-1715C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966402 | |||||||
chr7:107966501 | G | A | 3 | a0002c0003t0002g0045 a0002c0003t0002g0046 a0006c0011t0002g0259 |
3 | HG01256.hp2 HG01258.hp1 HG03239.hp2 |
intron_variant | MODIFIER | c.1563-1814C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966501 | |||||||
chr7:107966772 | G | A | 1 | a0001c0032t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1563-2085C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107966772 | |||||||
chr7:107967078 | T | C | 1 | a0001c0002t0001g0240 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1563-2391A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967078 | |||||||
chr7:107967108 | A | G | 1 | a0001c0005t0001g0219 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1563-2421T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967108 | |||||||
chr7:107967127 | G | C | 1 | a0001c0002t0001g0297 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.1563-2440C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967127 | |||||||
chr7:107967281 | T | G | 1 | a0001c0001t0002g0002 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.1563-2594A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967281 | |||||||
chr7:107967311 | C | T | 1 | a0001c0001t0001g0342 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.1563-2624G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967311 | |||||||
chr7:107967312 | G | A | 1 | a0008c0024t0001g0184 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1563-2625C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967312 | |||||||
chr7:107967367 | A | T | 1 | a0002c0003t0002g0013 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1563-2680T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967367 | |||||||
chr7:107967429 | T | G | 1 | a0006c0011t0002g0330 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1563-2742A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967429 | |||||||
chr7:107967444 | TTTCA | T | 5 | a0001c0001t0001g0226 a0001c0001t0001g0287 a0001c0006t0001g0133 others(2): Show |
5 | HG01361.hp1 HG02698.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.1563-2761_1563-275 others(8): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967444 | |||||||
chr7:107967457 | C | T | 74 | a0001c0001t0001g0011 a0001c0001t0001g0022 a0001c0001t0001g0062 others(71): Show |
75 | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(72): Show |
intron_variant | MODIFIER | c.1563-2770G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967457 | |||||||
chr7:107967476 | C | T | 1 | a0001c0032t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1563-2789G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967476 | |||||||
chr7:107967503 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1563-2816C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967503 | |||||||
chr7:107967525 | T | C | 32 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(29): Show |
32 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1563-2838A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967525 | |||||||
chr7:107967649 | C | T | 6 | a0001c0001t0001g0012 a0001c0002t0001g0247 a0001c0006t0001g0254 others(3): Show |
6 | HG02080.hp1 HG02258.hp2 HG02486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1563-2962G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967649 | |||||||
chr7:107967740 | T | C | 1 | a0021c0046t0002g0333 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1563-3053A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967740 | |||||||
chr7:107967890 | T | A | 1 | a0001c0006t0002g0327 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1563-3203A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967890 | |||||||
chr7:107967919 | T | C | 125 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(122): Show |
127 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(124): Show |
intron_variant | MODIFIER | c.1563-3232A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107967919 | |||||||
chr7:107968093 | G | C | 1 | a0001c0006t0002g0235 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1563-3406C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107968093 | |||||||
chr7:107968386 | G | A | 2 | a0001c0005t0001g0035 a0016c0060t0001g0036 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1563-3699C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107968386 | |||||||
chr7:107968437 | G | A | 33 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(30): Show |
33 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1563-3750C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107968437 | |||||||
chr7:107968494 | T | C | 1 | a0001c0014t0001g0346 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1563-3807A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107968494 | |||||||
chr7:107968594 | G | C | 32 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(29): Show |
32 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(29): Show |
intron_variant | MODIFIER | c.1563-3907C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107968594 | |||||||
chr7:107968613 | T | C | 1 | a0001c0001t0002g0019 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.1563-3926A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107968613 | |||||||
chr7:107968681 | G | A | 2 | a0001c0005t0001g0035 a0016c0060t0001g0036 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1563-3994C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107968681 | |||||||
chr7:107968846 | G | C | 2 | a0001c0072t0001g0025 a0001c0078t0001g0024 |
2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1562+4146C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107968846 | |||||||
chr7:107969026 | C | T | 1 | a0001c0032t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1562+3966G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969026 | |||||||
chr7:107969061 | A | G | 33 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(30): Show |
33 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1562+3931T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969061 | |||||||
chr7:107969287 | C | CA | 57 | a0001c0001t0001g0011 a0001c0001t0001g0048 a0001c0001t0001g0091 others(54): Show |
57 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(54): Show |
intron_variant | MODIFIER | c.1562+3704dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969287 | |||||||
chr7:107969287 | CA | C | 38 | a0001c0002t0001g0077 a0001c0002t0001g0078 a0001c0002t0001g0132 others(35): Show |
38 | HG00438.hp1 HG01243.hp1 HG01256.hp2 others(35): Show |
intron_variant | MODIFIER | c.1562+3704delT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969287 | |||||||
chr7:107969428 | T | TA | 33 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(30): Show |
33 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1562+3563dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969428 | |||||||
chr7:107969465 | C | T | 1 | a0008c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1562+3527G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969465 | |||||||
chr7:107969466 | G | A | 2 | a0001c0005t0001g0035 a0016c0060t0001g0036 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1562+3526C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969466 | |||||||
chr7:107969596 | A | G | 2 | a0001c0072t0001g0025 a0001c0078t0001g0024 |
2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1562+3396T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969596 | |||||||
chr7:107969708 | G | C | 3 | a0001c0014t0001g0346 a0001c0022t0001g0029 a0002c0013t0001g0030 |
3 | HG02280.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1562+3284C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969708 | |||||||
chr7:107969716 | C | T | 109 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(106): Show |
111 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(108): Show |
intron_variant | MODIFIER | c.1562+3276G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107969716 | |||||||
chr7:107970094 | A | G | 5 | a0001c0001t0001g0012 a0001c0001t0001g0342 a0001c0002t0001g0247 others(2): Show |
5 | HG02258.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1562+2898T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970094 | |||||||
chr7:107970106 | C | T | 2 | a0001c0072t0001g0025 a0001c0078t0001g0024 |
2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1562+2886G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970106 | |||||||
chr7:107970170 | G | A | 1 | a0001c0002t0001g0202 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1562+2822C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970170 | |||||||
chr7:107970230 | T | C | 2 | a0001c0072t0001g0025 a0001c0078t0001g0024 |
2 | HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1562+2762A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970230 | |||||||
chr7:107970433 | A | G | 4 | a0001c0001t0002g0177 a0002c0003t0002g0045 a0002c0003t0002g0046 others(1): Show |
4 | HG01256.hp2 HG01258.hp1 HG01346.hp2 others(1): Show |
intron_variant | MODIFIER | c.1562+2559T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970433 | |||||||
chr7:107970450 | C | G | 2 | a0001c0005t0001g0035 a0016c0060t0001g0036 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1562+2542G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970450 | |||||||
chr7:107970488 | C | CA | 18 | a0001c0002t0001g0196 a0001c0002t0001g0328 a0001c0005t0001g0035 others(15): Show |
18 | HG00738.hp1 HG01891.hp2 HG02055.hp2 others(15): Show |
intron_variant | MODIFIER | c.1562+2503dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970488 | |||||||
chr7:107970504 | A | AG | 6 | a0001c0022t0001g0039 a0001c0056t0001g0088 a0002c0003t0002g0220 others(3): Show |
6 | HG02895.hp2 HG02897.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.1562+2487_1562+248 others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970504 | |||||||
chr7:107970505 | A | AAG | 50 | a0001c0001t0001g0303 a0001c0001t0001g0321 a0001c0009t0001g0018 others(47): Show |
50 | HG00735.hp1 HG00735.hp2 HG01168.hp1 others(47): Show |
intron_variant | MODIFIER | c.1562+2486_1562+248 others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970505 | |||||||
chr7:107970505 | A | AG | 158 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0073 others(155): Show |
158 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1562+2486dupC | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970505 | |||||||
chr7:107970505 | A | G | 8 | a0001c0022t0001g0039 a0001c0028t0001g0350 a0001c0056t0001g0088 others(5): Show |
8 | HG02895.hp2 HG02897.hp1 HG03139.hp2 others(5): Show |
intron_variant | MODIFIER | c.1562+2487T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970505 | |||||||
chr7:107970506 | G | T | 1 | a0001c0007t0001g0007 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1562+2486C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970506 | |||||||
chr7:107970733 | AT | A | 35 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(32): Show |
35 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1562+2258delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970733 | |||||||
chr7:107970736 | T | A | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1562+2256A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970736 | |||||||
chr7:107970815 | T | A | 1 | a0001c0006t0002g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1562+2177A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970815 | |||||||
chr7:107970869 | A | G | 2 | a0002c0003t0002g0301 a0003c0004t0002g0154 |
2 | NA18998.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1562+2123T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970869 | |||||||
chr7:107970980 | C | T | 2 | a0001c0005t0001g0035 a0016c0060t0001g0036 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1562+2012G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970980 | |||||||
chr7:107970983 | C | T | 6 | a0001c0002t0001g0057 a0001c0005t0001g0059 a0002c0021t0002g0066 others(3): Show |
6 | HG00741.hp2 HG01070.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.1562+2009G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107970983 | |||||||
chr7:107971024 | G | A | 3 | a0001c0014t0003g0360 a0001c0044t0002g0345 a0027c0047t0003g0359 |
3 | HG01891.hp2 HG03579.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.1562+1968C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971024 | |||||||
chr7:107971049 | A | G | 9 | a0001c0001t0001g0083 a0001c0001t0001g0085 a0001c0001t0001g0086 others(6): Show |
9 | NA18954.hp1 NA18967.hp1 NA18971.hp2 others(6): Show |
intron_variant | MODIFIER | c.1562+1943T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971049 | |||||||
chr7:107971095 | T | G | 1 | a0001c0058t0001g0143 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.1562+1897A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971095 | |||||||
chr7:107971205 | G | T | 33 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(30): Show |
33 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1562+1787C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971205 | |||||||
chr7:107971260 | T | C | 1 | a0001c0006t0001g0254 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1562+1732A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971260 | |||||||
chr7:107971418 | G | T | 1 | a0012c0075t0001g0043 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1562+1574C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971418 | |||||||
chr7:107971602 | T | C | 1 | a0001c0005t0001g0326 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1562+1390A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971602 | |||||||
chr7:107971673 | T | G | 1 | a0002c0010t0001g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1562+1319A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971673 | |||||||
chr7:107971688 | C | T | 1 | a0001c0032t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1562+1304G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971688 | |||||||
chr7:107971704 | T | C | 1 | a0001c0006t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1562+1288A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971704 | |||||||
chr7:107971757 | G | A | 2 | a0001c0005t0001g0219 a0001c0005t0001g0244 |
2 | HG02080.hp2 NA19088.hp2 |
intron_variant | MODIFIER | c.1562+1235C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971757 | |||||||
chr7:107971877 | G | T | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1562+1115C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971877 | |||||||
chr7:107971900 | C | A | 33 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(30): Show |
33 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.1562+1092G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107971900 | |||||||
chr7:107972128 | G | A | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1562+864C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972128 | |||||||
chr7:107972171 | A | G | 17 | a0004c0015t0001g0138 a0004c0015t0001g0140 a0004c0015t0002g0008 others(14): Show |
17 | HG01243.hp1 HG01433.hp1 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.1562+821T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972171 | |||||||
chr7:107972184 | A | G | 164 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0073 others(161): Show |
164 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.1562+808T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972184 | |||||||
chr7:107972258 | G | C | 2 | a0001c0001t0001g0173 a0001c0001t0001g0174 |
2 | NA19084.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.1562+734C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972258 | |||||||
chr7:107972339 | C | T | 28 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(25): Show |
28 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1562+653G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972339 | |||||||
chr7:107972372 | A | G | 1 | a0001c0005t0001g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1562+620T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972372 | |||||||
chr7:107972391 | A | G | 5 | a0001c0014t0003g0360 a0001c0044t0002g0345 a0002c0003t0002g0347 others(2): Show |
5 | HG00738.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1562+601T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972391 | |||||||
chr7:107972402 | G | T | 1 | a0007c0023t0001g0051 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.1562+590C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972402 | |||||||
chr7:107972539 | T | C | 1 | a0021c0046t0002g0333 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1562+453A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972539 | |||||||
chr7:107972587 | C | CA | 20 | a0001c0001t0001g0289 a0001c0007t0001g0319 a0001c0032t0001g0028 others(17): Show |
20 | HG01243.hp1 HG01433.hp1 HG02080.hp1 others(17): Show |
intron_variant | MODIFIER | c.1562+404dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972587 | |||||||
chr7:107972587 | CA | C | 164 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0073 others(161): Show |
164 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.1562+404delT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972587 | |||||||
chr7:107972719 | A | G | 12 | a0001c0006t0001g0042 a0001c0007t0001g0009 a0001c0014t0001g0346 others(9): Show |
12 | HG00738.hp1 HG01891.hp2 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.1562+273T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972719 | |||||||
chr7:107972762 | T | C | 172 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0073 others(169): Show |
172 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(169): Show |
intron_variant | MODIFIER | c.1562+230A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972762 | |||||||
chr7:107972934 | G | A | 240 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0048 others(237): Show |
240 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(237): Show |
intron_variant | MODIFIER | c.1562+58C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972934 | |||||||
chr7:107972941 | A | C | 1 | a0001c0028t0001g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1562+51T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 13/33 | chr7 | 107972941 | |||||||
chr7:107973273 | A | G | 1 | a0001c0002t0001g0328 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1483-202T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973273 | |||||||
chr7:107973360 | T | C | 1 | a0001c0007t0003g0362 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1483-289A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973360 | |||||||
chr7:107973452 | A | C | 1 | a0001c0005t0001g0248 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1483-381T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973452 | |||||||
chr7:107973462 | T | C | 2 | a0001c0001t0002g0192 a0002c0003t0002g0159 |
2 | NA18994.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1483-391A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973462 | |||||||
chr7:107973505 | G | A | 2 | a0001c0001t0001g0188 a0001c0001t0001g0189 |
2 | NA18939.hp1 NA18949.hp2 |
intron_variant | MODIFIER | c.1483-434C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973505 | |||||||
chr7:107973509 | C | T | 1 | a0001c0002t0001g0222 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.1483-438G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973509 | |||||||
chr7:107973558 | A | G | 28 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(25): Show |
28 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1483-487T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973558 | |||||||
chr7:107973851 | G | A | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1483-780C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973851 | |||||||
chr7:107973925 | T | G | 200 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0073 others(197): Show |
200 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.1483-854A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973925 | |||||||
chr7:107973961 | T | C | 17 | a0004c0015t0001g0138 a0004c0015t0001g0140 a0004c0015t0002g0008 others(14): Show |
17 | HG01243.hp1 HG01433.hp1 HG02080.hp1 others(14): Show |
intron_variant | MODIFIER | c.1483-890A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107973961 | |||||||
chr7:107974042 | A | C | 1 | a0001c0009t0001g0194 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1482+944T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974042 | |||||||
chr7:107974118 | A | G | 266 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(263): Show |
267 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.1482+868T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974118 | |||||||
chr7:107974224 | T | A | 35 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(32): Show |
35 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1482+762A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974224 | |||||||
chr7:107974357 | G | GT | 30 | a0001c0005t0001g0035 a0001c0006t0001g0042 a0001c0007t0001g0009 others(27): Show |
30 | HG00323.hp1 HG01243.hp1 HG01433.hp1 others(27): Show |
intron_variant | MODIFIER | c.1482+628dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974357 | |||||||
chr7:107974357 | GT | G | 6 | a0001c0032t0001g0028 a0002c0003t0002g0045 a0002c0003t0002g0046 others(3): Show |
6 | HG01256.hp2 HG01258.hp1 HG02630.hp2 others(3): Show |
intron_variant | MODIFIER | c.1482+628delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974357 | |||||||
chr7:107974485 | T | C | 193 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0073 others(190): Show |
193 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.1482+501A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974485 | |||||||
chr7:107974576 | A | G | 2 | a0001c0007t0001g0319 a0001c0022t0001g0039 |
2 | HG02965.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1482+410T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974576 | |||||||
chr7:107974579 | G | A | 249 | a0001c0001t0001g0012 a0001c0001t0001g0033 a0001c0001t0001g0048 others(246): Show |
249 | HG00140.hp1 HG00323.hp1 HG00408.hp1 others(246): Show |
intron_variant | MODIFIER | c.1482+407C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974579 | |||||||
chr7:107974760 | T | A | 3 | a0001c0014t0001g0346 a0001c0022t0001g0029 a0002c0013t0001g0030 |
3 | HG02280.hp2 HG02970.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.1482+226A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974760 | |||||||
chr7:107974817 | A | G | 5 | a0001c0001t0001g0131 a0001c0001t0001g0201 a0001c0002t0001g0286 others(2): Show |
5 | HG02129.hp1 HG02293.hp1 HG03491.hp2 others(2): Show |
intron_variant | MODIFIER | c.1482+169T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974817 | |||||||
chr7:107974829 | C | T | 35 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(32): Show |
35 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1482+157G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974829 | |||||||
chr7:107974889 | G | T | 15 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0173 others(12): Show |
15 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(12): Show |
intron_variant | MODIFIER | c.1482+97C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 12/33 | chr7 | 107974889 | |||||||
chr7:107975116 | G | A | 1 | a0002c0010t0001g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1370-18C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 11/33 | chr7 | 107975116 | |||||||
chr7:107975550 | C | T | 1 | a0003c0079t0001g0179 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1190-137G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 10/33 | chr7 | 107975550 | |||||||
chr7:107975566 | C | G | 35 | a0001c0006t0001g0042 a0001c0009t0001g0018 a0001c0009t0001g0194 others(32): Show |
35 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1189+123G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 10/33 | chr7 | 107975566 | |||||||
chr7:107975604 | C | A | 28 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(25): Show |
28 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(25): Show |
intron_variant | MODIFIER | c.1189+85G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 10/33 | chr7 | 107975604 | |||||||
chr7:107975623 | T | C | 35 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(32): Show |
35 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1189+66A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 10/33 | chr7 | 107975623 | |||||||
chr7:107975633 | G | A | 35 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(32): Show |
35 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(32): Show |
intron_variant | MODIFIER | c.1189+56C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 10/33 | chr7 | 107975633 | |||||||
chr7:107975920 | T | C | 2 | a0001c0035t0001g0037 a0020c0034t0001g0031 |
2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1001-43A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107975920 | |||||||
chr7:107975958 | A | G | 1 | a0001c0002t0001g0118 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.1001-81T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107975958 | |||||||
chr7:107976130 | A | T | 1 | a0001c0017t0001g0093 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1001-253T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976130 | |||||||
chr7:107976177 | C | G | 1 | a0001c0001t0002g0050 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.1001-300G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976177 | |||||||
chr7:107976245 | A | G | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1001-368T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976245 | |||||||
chr7:107976317 | G | A | 18 | a0001c0007t0001g0319 a0004c0015t0001g0138 a0004c0015t0001g0140 others(15): Show |
18 | HG01243.hp1 HG01433.hp1 HG02080.hp1 others(15): Show |
intron_variant | MODIFIER | c.1001-440C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976317 | |||||||
chr7:107976329 | G | C | 1 | a0012c0075t0001g0043 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1001-452C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976329 | |||||||
chr7:107976347 | G | A | 21 | a0001c0001t0001g0048 a0001c0001t0002g0047 a0001c0007t0001g0009 others(18): Show |
21 | HG00738.hp2 HG01106.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1001-470C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976347 | |||||||
chr7:107976372 | C | T | 1 | a0001c0005t0001g0026 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1001-495G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976372 | |||||||
chr7:107976440 | C | T | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1001-563G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976440 | |||||||
chr7:107976500 | G | A | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1001-623C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976500 | |||||||
chr7:107976544 | C | T | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1001-667G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976544 | |||||||
chr7:107976645 | T | C | 1 | a0010c0025t0001g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1001-768A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976645 | |||||||
chr7:107976655 | T | A | 5 | a0001c0002t0001g0196 a0001c0002t0001g0199 a0002c0003t0002g0076 others(2): Show |
5 | NA18962.hp1 NA18988.hp1 NA19058.hp2 others(2): Show |
intron_variant | MODIFIER | c.1001-778A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976655 | |||||||
chr7:107976703 | A | G | 2 | a0001c0001t0001g0245 a0001c0001t0001g0246 |
2 | HG02523.hp1 NA18944.hp1 |
intron_variant | MODIFIER | c.1001-826T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976703 | |||||||
chr7:107976759 | C | A | 27 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(24): Show |
27 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1001-882G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976759 | |||||||
chr7:107976778 | G | A | 1 | a0001c0032t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1001-901C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976778 | |||||||
chr7:107976838 | T | C | 1 | a0001c0007t0001g0009 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1001-961A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976838 | |||||||
chr7:107976854 | CCTCTCCT others(63): Show |
C | 26 | a0001c0001t0001g0048 a0001c0001t0002g0047 a0001c0007t0001g0009 others(23): Show |
26 | HG00738.hp1 HG00738.hp2 HG01106.hp2 others(23): Show |
intron_variant | MODIFIER | c.1001-1047_1001-978 others(73): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976854 | |||||||
chr7:107976856 | TCTCCTTC others(19): Show |
T | 2 | a0001c0035t0001g0037 a0020c0034t0001g0031 |
2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1001-1005_1001-980 others(29): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976856 | |||||||
chr7:107976856 | TCTCCTTC others(85): Show |
T | 30 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(27): Show |
30 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1001-1071_1001-980 others(95): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976856 | |||||||
chr7:107976861 | T | C | 1 | a0002c0003t0002g0013 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.1001-984A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976861 | |||||||
chr7:107976861 | T | TTCCTTCC others(11): Show |
123 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(120): Show |
124 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(121): Show |
intron_variant | MODIFIER | c.1001-985_1001-984i others(20): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976861 | |||||||
chr7:107976861 | T | TTCCTTCC others(33): Show |
3 | a0001c0002t0001g0118 a0001c0007t0001g0007 a0025c0061t0001g0119 |
3 | HG02559.hp2 NA18962.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1001-985_1001-984i others(42): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976861 | |||||||
chr7:107976881 | T | C | 134 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(131): Show |
135 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(132): Show |
intron_variant | MODIFIER | c.1001-1004A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976881 | |||||||
chr7:107976882 | G | C | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(134): Show |
138 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.1001-1005C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976882 | |||||||
chr7:107976887 | T | G | 9 | a0001c0006t0001g0042 a0001c0014t0001g0346 a0001c0022t0001g0029 others(6): Show |
9 | HG02280.hp2 HG02970.hp1 HG02976.hp1 others(6): Show |
intron_variant | MODIFIER | c.1001-1010A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976887 | |||||||
chr7:107976903 | T | C | 10 | a0001c0002t0001g0118 a0001c0006t0001g0042 a0001c0014t0001g0346 others(7): Show |
10 | HG02280.hp2 HG02622.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1001-1026A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976903 | |||||||
chr7:107976904 | G | C | 130 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(127): Show |
131 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(128): Show |
intron_variant | MODIFIER | c.1001-1027C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976904 | |||||||
chr7:107976904 | G | GCTCCTTC others(59): Show |
1 | a0001c0002t0001g0209 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1001-1028_1001-102 others(70): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976904 | |||||||
chr7:107976924 | T | TCTCTCCT others(77): Show |
5 | a0001c0001t0001g0012 a0001c0001t0001g0342 a0001c0006t0001g0341 others(2): Show |
5 | HG02258.hp2 HG02486.hp2 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1001-1048_1001-104 others(88): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976924 | |||||||
chr7:107976926 | T | C | 6 | a0001c0002t0001g0118 a0001c0002t0001g0209 a0001c0007t0001g0007 others(3): Show |
6 | HG02027.hp1 HG02559.hp2 HG02622.hp1 others(3): Show |
intron_variant | MODIFIER | c.1001-1049A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976926 | |||||||
chr7:107976926 | T | TCTCCTTC others(15): Show |
4 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0003t0002g0288 others(1): Show |
4 | HG01517.hp1 HG02976.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.1001-1071_1001-105 others(26): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976926 | |||||||
chr7:107976926 | T | TCTCCTTC others(37): Show |
161 | a0001c0001t0001g0033 a0001c0001t0001g0073 a0001c0001t0001g0083 others(158): Show |
162 | HG00099.hp2 HG00140.hp1 HG00323.hp1 others(159): Show |
intron_variant | MODIFIER | c.1000+1077_1001-105 others(48): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976926 | |||||||
chr7:107976926 | T | TCTCCTTC others(59): Show |
2 | a0001c0001t0001g0151 a0021c0046t0002g0333 |
2 | HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1001-1050_1001-104 others(70): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976926 | |||||||
chr7:107976926 | T | TCTCCTTC others(279): Show |
1 | a0001c0001t0001g0313 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1001-1050_1001-104 others(290): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976926 | |||||||
chr7:107976947 | C | T | 5 | a0001c0014t0003g0360 a0001c0044t0002g0345 a0002c0003t0002g0347 others(2): Show |
5 | HG00738.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1001-1070G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976947 | |||||||
chr7:107976948 | C | CCTCCTTC others(11): Show |
3 | a0001c0002t0001g0118 a0002c0003t0002g0013 a0025c0061t0001g0119 |
3 | HG00733.hp1 NA18962.hp2 NA19057.hp1 |
intron_variant | MODIFIER | c.1000+1081_1001-107 others(22): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976948 | |||||||
chr7:107976948 | C | CCTCCTTC others(33): Show |
5 | a0003c0004t0001g0079 a0003c0004t0001g0080 a0003c0004t0001g0157 others(2): Show |
5 | NA18612.hp1 NA18953.hp2 NA18981.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+1059_1001-107 others(44): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976948 | |||||||
chr7:107976948 | C | CCTCCTTC others(55): Show |
71 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0015 others(68): Show |
72 | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(69): Show |
intron_variant | MODIFIER | c.1001-1072_1001-107 others(66): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976948 | |||||||
chr7:107976948 | C | CCTCCTTC others(77): Show |
1 | a0003c0004t0001g0082 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.1001-1072_1001-107 others(88): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976948 | |||||||
chr7:107976948 | C | CCTCCTTC others(121): Show |
1 | a0001c0001t0001g0294 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.1001-1072_1001-107 others(132): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976948 | |||||||
chr7:107976948 | C | T | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1001-1071G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976948 | |||||||
chr7:107976969 | C | T | 1 | a0002c0010t0001g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1000+1078G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976969 | |||||||
chr7:107976970 | C | CCTCCTTC others(681): Show |
5 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0002g0061 others(2): Show |
5 | HG01070.hp1 HG01255.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+1076_1000+107 others(692): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976970 | |||||||
chr7:107976970 | C | T | 5 | a0001c0006t0001g0042 a0001c0014t0001g0346 a0001c0022t0001g0029 others(2): Show |
5 | HG02280.hp2 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+1077G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976970 | |||||||
chr7:107976990 | T | TCTCTCCT others(554): Show |
1 | a0002c0010t0001g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1000+1056_1000+105 others(565): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976990 | |||||||
chr7:107976990 | TTC | T | 5 | a0001c0006t0001g0042 a0001c0014t0001g0346 a0001c0022t0001g0029 others(2): Show |
5 | HG02280.hp2 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+1055_1000+105 others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976990 | |||||||
chr7:107976991 | T | C | 167 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(164): Show |
168 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(165): Show |
intron_variant | MODIFIER | c.1000+1056A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976991 | |||||||
chr7:107976992 | C | T | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1000+1055G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976992 | |||||||
chr7:107976995 | C | T | 5 | a0001c0006t0001g0042 a0001c0014t0001g0346 a0001c0022t0001g0029 others(2): Show |
5 | HG02280.hp2 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+1052G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976995 | |||||||
chr7:107976996 | C | T | 5 | a0001c0006t0001g0042 a0001c0014t0001g0346 a0001c0022t0001g0029 others(2): Show |
5 | HG02280.hp2 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+1051G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976996 | |||||||
chr7:107976998 | T | C | 5 | a0001c0006t0001g0042 a0001c0014t0001g0346 a0001c0022t0001g0029 others(2): Show |
5 | HG02280.hp2 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+1049A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107976998 | |||||||
chr7:107977000 | C | T | 5 | a0001c0006t0001g0042 a0001c0014t0001g0346 a0001c0022t0001g0029 others(2): Show |
5 | HG02280.hp2 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+1047G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977000 | |||||||
chr7:107977003 | C | CCTTTCCT others(13): Show |
1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1000+1043_1000+104 others(24): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977003 | |||||||
chr7:107977003 | C | T | 5 | a0001c0006t0001g0042 a0001c0014t0001g0346 a0001c0022t0001g0029 others(2): Show |
5 | HG02280.hp2 HG02970.hp1 HG03486.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+1044G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977003 | |||||||
chr7:107977006 | T | C | 1 | a0001c0042t0001g0112 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1000+1041A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977006 | |||||||
chr7:107977010 | T | TTCCTTCC others(48): Show |
1 | a0001c0042t0001g0112 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.1000+1036_1000+103 others(59): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977010 | |||||||
chr7:107977012 | T | TCCTTCCT others(51): Show |
30 | a0001c0001t0001g0004 a0001c0001t0002g0050 a0001c0001t0002g0152 others(27): Show |
30 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(27): Show |
intron_variant | MODIFIER | c.1000+1034_1000+103 others(62): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977012 | |||||||
chr7:107977012 | T | TCCTTCCT others(179): Show |
1 | a0002c0054t0001g0181 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.1000+1034_1000+103 others(190): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977012 | |||||||
chr7:107977013 | C | CCCTCCTT others(15): Show |
1 | a0001c0006t0002g0327 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1000+1033_1000+103 others(26): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977013 | |||||||
chr7:107977013 | C | T | 29 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(26): Show |
29 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.1000+1034G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977013 | |||||||
chr7:107977014 | T | C | 135 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(132): Show |
136 | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1000+1033A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977014 | |||||||
chr7:107977014 | T | TCTCCTTC others(37): Show |
6 | a0001c0006t0001g0042 a0001c0014t0001g0346 a0001c0022t0001g0029 others(3): Show |
6 | HG02280.hp2 HG02970.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.1000+1032_1000+103 others(48): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977014 | |||||||
chr7:107977014 | TCTCCTTC others(15): Show |
T | 2 | a0001c0035t0001g0037 a0020c0034t0001g0031 |
2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.1000+1011_1000+103 others(26): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977014 | |||||||
chr7:107977016 | T | TC | 31 | a0001c0001t0001g0004 a0001c0001t0002g0050 a0001c0001t0002g0152 others(28): Show |
31 | HG00140.hp2 HG00642.hp1 HG00741.hp2 others(28): Show |
intron_variant | MODIFIER | c.1000+1030dupG | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977016 | |||||||
chr7:107977016 | T | TCCTTCCT others(144): Show |
1 | a0006c0011t0002g0330 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.1000+1030_1000+103 others(155): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977016 | |||||||
chr7:107977036 | C | T | 30 | a0001c0006t0002g0327 a0001c0009t0001g0018 a0001c0009t0001g0194 others(27): Show |
30 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(27): Show |
intron_variant | MODIFIER | c.1000+1011G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977036 | |||||||
chr7:107977058 | C | T | 5 | a0001c0014t0003g0360 a0001c0044t0002g0345 a0002c0003t0002g0347 others(2): Show |
5 | HG00738.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+989G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977058 | |||||||
chr7:107977125 | T | C | 4 | a0001c0001t0001g0012 a0001c0001t0001g0342 a0001c0006t0001g0341 others(1): Show |
4 | HG02258.hp2 HG02486.hp2 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.1000+922A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977125 | |||||||
chr7:107977192 | T | TC | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(130): Show |
134 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1000+854dupG | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977192 | |||||||
chr7:107977195 | A | T | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(130): Show |
134 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1000+852T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977195 | |||||||
chr7:107977196 | G | A | 133 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(130): Show |
134 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(131): Show |
intron_variant | MODIFIER | c.1000+851C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977196 | |||||||
chr7:107977265 | G | C | 1 | a0003c0004t0001g0238 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1000+782C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977265 | |||||||
chr7:107977323 | G | A | 21 | a0001c0001t0001g0048 a0001c0001t0002g0047 a0001c0007t0001g0009 others(18): Show |
21 | HG00738.hp2 HG01106.hp2 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.1000+724C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977323 | |||||||
chr7:107977483 | G | C | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1000+564C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977483 | |||||||
chr7:107977562 | T | G | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1000+485A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977562 | |||||||
chr7:107977605 | C | T | 321 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(318): Show |
323 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(320): Show |
intron_variant | MODIFIER | c.1000+442G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977605 | |||||||
chr7:107977660 | G | A | 1 | a0001c0005t0001g0129 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.1000+387C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977660 | |||||||
chr7:107977661 | C | T | 5 | a0001c0014t0003g0360 a0001c0044t0002g0345 a0002c0003t0002g0347 others(2): Show |
5 | HG00738.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.1000+386G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977661 | |||||||
chr7:107977667 | T | C | 2 | a0001c0005t0001g0150 a0001c0059t0001g0041 |
2 | HG02145.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1000+380A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977667 | |||||||
chr7:107977745 | A | G | 3 | a0001c0001t0001g0228 a0003c0004t0001g0229 a0003c0020t0001g0187 |
3 | HG02132.hp1 NA18612.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.1000+302T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977745 | |||||||
chr7:107977758 | C | CA | 5 | a0001c0001t0001g0307 a0001c0002t0001g0239 a0001c0007t0001g0130 others(2): Show |
5 | HG01891.hp1 HG02738.hp2 HG03831.hp2 others(2): Show |
intron_variant | MODIFIER | c.1000+288dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977758 | |||||||
chr7:107977950 | A | T | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1000+97T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977950 | |||||||
chr7:107977975 | A | G | 27 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(24): Show |
27 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.1000+72T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 9/33 | chr7 | 107977975 | |||||||
chr7:107978204 | A | T | 1 | a0001c0001t0001g0022 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.880-37T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978204 | |||||||
chr7:107978413 | G | A | 5 | a0001c0014t0003g0360 a0001c0044t0002g0345 a0002c0003t0002g0347 others(2): Show |
5 | HG00738.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.880-246C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978413 | |||||||
chr7:107978455 | T | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.880-288A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978455 | |||||||
chr7:107978455 | T | TA | 7 | a0001c0001t0001g0131 a0001c0001t0001g0201 a0001c0002t0001g0239 others(4): Show |
7 | HG02129.hp1 HG02293.hp1 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.880-289dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978455 | |||||||
chr7:107978455 | TA | T | 37 | a0001c0001t0001g0012 a0001c0001t0001g0048 a0001c0001t0001g0111 others(34): Show |
37 | HG00140.hp1 HG00738.hp2 HG01099.hp1 others(34): Show |
intron_variant | MODIFIER | c.880-289delT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978455 | |||||||
chr7:107978469 | AAAACT | A | 7 | a0001c0018t0002g0269 a0001c0077t0001g0275 a0002c0008t0002g0156 others(4): Show |
7 | HG00735.hp2 HG01168.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.880-307_880-303del others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978469 | |||||||
chr7:107978549 | T | A | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.880-382A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978549 | |||||||
chr7:107978607 | C | A | 1 | a0001c0001t0001g0001 | 2 | HG03490.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.880-440G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978607 | |||||||
chr7:107978647 | G | GT | 119 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(116): Show |
120 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(117): Show |
intron_variant | MODIFIER | c.880-481dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978647 | |||||||
chr7:107978770 | T | A | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.880-603A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107978770 | |||||||
chr7:107979002 | G | A | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.880-835C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979002 | |||||||
chr7:107979010 | C | A | 2 | a0001c0001t0001g0073 a0002c0039t0002g0203 |
2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.880-843G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979010 | |||||||
chr7:107979080 | A | G | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.880-913T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979080 | |||||||
chr7:107979095 | G | A | 31 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(28): Show |
31 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.880-928C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979095 | |||||||
chr7:107979118 | T | A | 31 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(28): Show |
31 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(28): Show |
intron_variant | MODIFIER | c.880-951A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979118 | |||||||
chr7:107979121 | G | C | 6 | a0001c0014t0003g0360 a0001c0044t0002g0345 a0002c0003t0002g0347 others(3): Show |
6 | HG00738.hp1 HG01891.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.880-954C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979121 | |||||||
chr7:107979125 | C | T | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.880-958G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979125 | |||||||
chr7:107979166 | T | C | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.880-999A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979166 | |||||||
chr7:107979196 | T | TTC | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.880-1031_880-1030d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979196 | |||||||
chr7:107979485 | G | C | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.879+1124C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979485 | |||||||
chr7:107979569 | A | G | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.879+1040T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979569 | |||||||
chr7:107979609 | A | ATACTT | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.879+999_879+1000in others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979609 | |||||||
chr7:107979664 | A | G | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.879+945T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979664 | |||||||
chr7:107979789 | G | A | 4 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0002t0001g0064 others(1): Show |
4 | HG01070.hp1 HG01255.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.879+820C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979789 | |||||||
chr7:107979811 | C | T | 3 | a0001c0001t0001g0012 a0001c0001t0001g0342 a0001c0006t0001g0341 |
3 | HG02258.hp2 HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.879+798G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979811 | |||||||
chr7:107979889 | T | C | 1 | a0001c0001t0001g0102 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.879+720A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979889 | |||||||
chr7:107979893 | G | C | 1 | a0002c0003t0002g0166 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.879+716C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107979893 | |||||||
chr7:107980008 | G | T | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.879+601C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107980008 | |||||||
chr7:107980027 | A | G | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.879+582T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107980027 | |||||||
chr7:107980038 | C | T | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.879+571G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107980038 | |||||||
chr7:107980210 | G | GA | 10 | a0001c0001t0001g0073 a0001c0001t0001g0189 a0001c0001t0001g0218 others(7): Show |
10 | HG00741.hp2 HG02055.hp2 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.879+398dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107980210 | |||||||
chr7:107980307 | A | G | 1 | a0020c0034t0001g0031 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.879+302T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107980307 | |||||||
chr7:107980393 | C | G | 1 | a0001c0028t0001g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.879+216G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107980393 | |||||||
chr7:107980410 | G | A | 1 | a0002c0003t0002g0175 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.879+199C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107980410 | |||||||
chr7:107980507 | A | G | 1 | a0001c0002t0001g0328 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.879+102T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 8/33 | chr7 | 107980507 | |||||||
chr7:107980860 | GT | G | 41 | a0001c0001t0001g0048 a0001c0001t0002g0047 a0001c0007t0001g0009 others(38): Show |
41 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(38): Show |
intron_variant | MODIFIER | c.677-50delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107980860 | |||||||
chr7:107980994 | A | C | 1 | a0001c0001t0001g0221 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.677-183T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107980994 | |||||||
chr7:107980996 | G | A | 1 | a0002c0003t0001g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.677-185C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107980996 | |||||||
chr7:107981148 | A | C | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.677-337T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981148 | |||||||
chr7:107981169 | G | A | 26 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(23): Show |
26 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(23): Show |
intron_variant | MODIFIER | c.677-358C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981169 | |||||||
chr7:107981175 | G | A | 17 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0015 others(14): Show |
18 | HG00323.hp2 HG00733.hp1 HG01070.hp1 others(15): Show |
intron_variant | MODIFIER | c.677-364C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981175 | |||||||
chr7:107981409 | T | C | 106 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(103): Show |
107 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(104): Show |
intron_variant | MODIFIER | c.677-598A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981409 | |||||||
chr7:107981445 | TA | T | 137 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(134): Show |
138 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(135): Show |
intron_variant | MODIFIER | c.677-635delT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981445 | |||||||
chr7:107981445 | TAA | T | 8 | a0001c0001t0001g0151 a0001c0002t0001g0077 a0001c0002t0001g0104 others(5): Show |
8 | HG01081.hp2 HG01433.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.677-636_677-635del others(2): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981445 | |||||||
chr7:107981446 | A | T | 2 | a0001c0005t0001g0035 a0016c0060t0001g0036 |
2 | HG02723.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.677-635T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981446 | |||||||
chr7:107981535 | C | T | 1 | a0001c0072t0001g0025 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.677-724G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981535 | |||||||
chr7:107981605 | A | C | 1 | a0001c0002t0001g0049 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.677-794T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981605 | |||||||
chr7:107981705 | A | G | 180 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(177): Show |
181 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.677-894T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981705 | |||||||
chr7:107981843 | G | A | 180 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(177): Show |
181 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(178): Show |
intron_variant | MODIFIER | c.677-1032C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981843 | |||||||
chr7:107981879 | C | T | 1 | a0001c0002t0001g0110 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.677-1068G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981879 | |||||||
chr7:107981970 | C | T | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.677-1159G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981970 | |||||||
chr7:107981979 | G | A | 108 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(105): Show |
109 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(106): Show |
intron_variant | MODIFIER | c.677-1168C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107981979 | |||||||
chr7:107982128 | T | C | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.677-1317A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107982128 | |||||||
chr7:107982191 | G | A | 1 | a0001c0009t0001g0282 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.677-1380C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107982191 | |||||||
chr7:107982420 | T | A | 1 | a0001c0001t0002g0002 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.677-1609A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107982420 | |||||||
chr7:107982553 | TCTCCTGC others(7): Show |
T | 1 | a0001c0006t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.677-1756_677-1743d others(16): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107982553 | |||||||
chr7:107982585 | C | T | 3 | a0001c0001t0001g0048 a0001c0001t0002g0047 a0001c0007t0001g0009 |
3 | HG00738.hp2 HG01106.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.677-1774G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107982585 | |||||||
chr7:107982601 | C | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0342 a0001c0006t0001g0341 |
3 | HG02258.hp2 HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.677-1790G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107982601 | |||||||
chr7:107982666 | T | C | 3 | a0001c0001t0001g0012 a0001c0001t0001g0342 a0001c0006t0001g0341 |
3 | HG02258.hp2 HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.677-1855A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107982666 | |||||||
chr7:107982894 | T | C | 183 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(180): Show |
184 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.677-2083A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107982894 | |||||||
chr7:107983006 | G | C | 2 | a0001c0001t0001g0294 a0019c0036t0001g0068 |
2 | HG01257.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.677-2195C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983006 | |||||||
chr7:107983051 | T | C | 112 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(109): Show |
113 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(110): Show |
intron_variant | MODIFIER | c.677-2240A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983051 | |||||||
chr7:107983097 | A | G | 183 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(180): Show |
184 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.677-2286T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983097 | |||||||
chr7:107983140 | T | G | 1 | a0003c0004t0001g0250 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.677-2329A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983140 | |||||||
chr7:107983145 | G | A | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.677-2334C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983145 | |||||||
chr7:107983422 | A | C | 8 | a0001c0009t0001g0271 a0001c0018t0002g0269 a0001c0077t0001g0275 others(5): Show |
8 | HG00735.hp2 HG01168.hp1 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.676+2600T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983422 | |||||||
chr7:107983427 | A | G | 1 | a0003c0049t0001g0056 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.676+2595T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983427 | |||||||
chr7:107983493 | C | T | 25 | a0001c0001t0001g0094 a0001c0001t0001g0097 a0001c0001t0001g0167 others(22): Show |
26 | HG00408.hp2 HG00423.hp1 HG00621.hp2 others(23): Show |
intron_variant | MODIFIER | c.676+2529G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983493 | |||||||
chr7:107983509 | G | A | 5 | a0001c0014t0003g0360 a0001c0044t0002g0345 a0002c0003t0002g0347 others(2): Show |
5 | HG00738.hp1 HG01891.hp2 HG02630.hp1 others(2): Show |
intron_variant | MODIFIER | c.676+2513C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983509 | |||||||
chr7:107983547 | C | CT | 85 | a0001c0001t0001g0083 a0001c0001t0001g0091 a0001c0001t0001g0097 others(82): Show |
86 | HG00408.hp1 HG00423.hp2 HG00438.hp1 others(83): Show |
intron_variant | MODIFIER | c.676+2474dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983547 | |||||||
chr7:107983547 | C | CTT | 16 | a0001c0002t0001g0055 a0001c0002t0001g0077 a0001c0002t0001g0078 others(13): Show |
16 | HG00738.hp1 HG01175.hp1 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.676+2473_676+2474d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983547 | |||||||
chr7:107983547 | CT | C | 8 | a0001c0001t0001g0062 a0001c0001t0001g0063 a0001c0001t0001g0131 others(5): Show |
8 | HG01070.hp1 HG01255.hp2 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.676+2474delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983547 | |||||||
chr7:107983646 | G | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(178): Show |
182 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.676+2376C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983646 | |||||||
chr7:107983664 | C | T | 27 | a0001c0007t0001g0007 a0001c0009t0001g0018 a0001c0009t0001g0194 others(24): Show |
27 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.676+2358G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983664 | |||||||
chr7:107983674 | T | C | 195 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(192): Show |
196 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(193): Show |
intron_variant | MODIFIER | c.676+2348A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983674 | |||||||
chr7:107983741 | C | T | 1 | a0001c0063t0001g0324 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.676+2281G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983741 | |||||||
chr7:107983895 | G | A | 2 | a0001c0002t0001g0055 a0002c0003t0002g0301 |
2 | NA18949.hp1 NA18998.hp1 |
intron_variant | MODIFIER | c.676+2127C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983895 | |||||||
chr7:107983896 | G | A | 10 | a0001c0001t0001g0048 a0001c0001t0002g0047 a0001c0006t0001g0193 others(7): Show |
10 | HG00738.hp2 HG01106.hp2 HG02080.hp1 others(7): Show |
intron_variant | MODIFIER | c.676+2126C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107983896 | |||||||
chr7:107984271 | CAG | C | 4 | a0001c0001t0001g0091 a0001c0002t0001g0240 a0002c0003t0002g0242 others(1): Show |
4 | HG01952.hp1 HG01981.hp1 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.676+1749_676+1750d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107984271 | |||||||
chr7:107984352 | G | A | 1 | a0002c0003t0002g0092 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.676+1670C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107984352 | |||||||
chr7:107984438 | C | A | 181 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(178): Show |
182 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.676+1584G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107984438 | |||||||
chr7:107984491 | G | A | 110 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(107): Show |
111 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(108): Show |
intron_variant | MODIFIER | c.676+1531C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107984491 | |||||||
chr7:107984553 | C | A | 3 | a0001c0001t0001g0012 a0001c0001t0001g0342 a0001c0006t0001g0341 |
3 | HG02258.hp2 HG02486.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.676+1469G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107984553 | |||||||
chr7:107984977 | C | G | 1 | a0008c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.676+1045G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107984977 | |||||||
chr7:107985058 | C | T | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.676+964G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985058 | |||||||
chr7:107985063 | T | C | 3 | a0001c0022t0001g0029 a0001c0032t0001g0028 a0002c0013t0001g0030 |
3 | HG02280.hp2 HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.676+959A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985063 | |||||||
chr7:107985131 | A | G | 9 | a0001c0001t0001g0102 a0001c0001t0001g0221 a0001c0001t0001g0325 others(6): Show |
9 | HG00609.hp1 HG02083.hp2 HG02132.hp2 others(6): Show |
intron_variant | MODIFIER | c.676+891T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985131 | |||||||
chr7:107985142 | G | A | 7 | a0001c0032t0001g0028 a0001c0035t0001g0037 a0002c0003t0001g0070 others(4): Show |
7 | HG02622.hp1 HG02630.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.676+880C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985142 | |||||||
chr7:107985362 | G | A | 33 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(30): Show |
33 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.676+660C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985362 | |||||||
chr7:107985421 | C | T | 6 | a0001c0002t0001g0103 a0001c0002t0001g0104 a0001c0002t0001g0105 others(3): Show |
6 | HG00642.hp2 HG01069.hp1 HG01081.hp2 others(3): Show |
intron_variant | MODIFIER | c.676+601G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985421 | |||||||
chr7:107985444 | G | C | 1 | a0005c0012t0002g0323 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.676+578C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985444 | |||||||
chr7:107985527 | G | A | 1 | a0002c0003t0002g0099 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.676+495C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985527 | |||||||
chr7:107985614 | A | C | 3 | a0001c0001t0001g0287 a0001c0006t0001g0133 a0003c0050t0002g0146 |
3 | HG01361.hp1 HG03017.hp1 HG04199.hp2 |
intron_variant | MODIFIER | c.676+408T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985614 | |||||||
chr7:107985615 | G | A | 1 | a0003c0004t0002g0154 | 1 | NA18998.hp2 | intron_variant | MODIFIER | c.676+407C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985615 | |||||||
chr7:107985741 | C | T | 183 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(180): Show |
184 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(181): Show |
intron_variant | MODIFIER | c.676+281G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985741 | |||||||
chr7:107985794 | C | T | 77 | a0001c0001t0001g0073 a0001c0001t0001g0091 a0001c0001t0001g0102 others(74): Show |
77 | HG00438.hp1 HG00609.hp1 HG00639.hp2 others(74): Show |
intron_variant | MODIFIER | c.676+228G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 7/33 | chr7 | 107985794 | |||||||
chr7:107986549 | A | G | 186 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(183): Show |
187 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(184): Show |
intron_variant | MODIFIER | c.424-186T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107986549 | |||||||
chr7:107986869 | T | C | 191 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(188): Show |
192 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(189): Show |
intron_variant | MODIFIER | c.424-506A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107986869 | |||||||
chr7:107986873 | A | G | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.424-510T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107986873 | |||||||
chr7:107986957 | C | T | 1 | a0005c0065t0001g0147 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.424-594G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107986957 | |||||||
chr7:107987240 | T | C | 2 | a0001c0006t0001g0356 a0001c0006t0001g0358 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.424-877A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987240 | |||||||
chr7:107987403 | T | A | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(191): Show |
195 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.424-1040A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987403 | |||||||
chr7:107987564 | G | T | 1 | a0003c0020t0001g0195 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.424-1201C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987564 | |||||||
chr7:107987582 | C | T | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.424-1219G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987582 | |||||||
chr7:107987586 | C | T | 2 | a0001c0001t0001g0342 a0001c0006t0001g0341 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.424-1223G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987586 | |||||||
chr7:107987750 | C | T | 2 | a0002c0008t0002g0006 a0029c0076t0001g0005 |
2 | NA18906.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.424-1387G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987750 | |||||||
chr7:107987766 | T | C | 197 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(194): Show |
198 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(195): Show |
intron_variant | MODIFIER | c.424-1403A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987766 | |||||||
chr7:107987794 | G | A | 2 | a0001c0001t0001g0342 a0001c0006t0001g0341 |
2 | HG02258.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.424-1431C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987794 | |||||||
chr7:107987854 | C | T | 1 | a0001c0005t0001g0219 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.424-1491G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987854 | |||||||
chr7:107987969 | G | A | 4 | a0001c0001t0001g0048 a0001c0001t0002g0047 a0001c0007t0001g0009 others(1): Show |
4 | HG00738.hp2 HG01106.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-1606C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107987969 | |||||||
chr7:107988048 | A | C | 1 | a0001c0078t0001g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.424-1685T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107988048 | |||||||
chr7:107988126 | T | A | 1 | a0008c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.424-1763A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107988126 | |||||||
chr7:107988234 | C | A | 336 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(333): Show |
338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.424-1871G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107988234 | |||||||
chr7:107988348 | G | A | 27 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(24): Show |
27 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(24): Show |
intron_variant | MODIFIER | c.424-1985C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107988348 | |||||||
chr7:107988385 | G | A | 4 | a0001c0001t0001g0048 a0001c0001t0002g0047 a0001c0007t0001g0009 others(1): Show |
4 | HG00738.hp2 HG01106.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-2022C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107988385 | |||||||
chr7:107988438 | TCAAA | T | 4 | a0001c0001t0001g0048 a0001c0001t0002g0047 a0001c0007t0001g0009 others(1): Show |
4 | HG00738.hp2 HG01106.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-2079_424-2076d others(6): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107988438 | |||||||
chr7:107988460 | G | T | 4 | a0001c0001t0001g0048 a0001c0001t0002g0047 a0001c0007t0001g0009 others(1): Show |
4 | HG00738.hp2 HG01106.hp2 HG02080.hp1 others(1): Show |
intron_variant | MODIFIER | c.424-2097C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107988460 | |||||||
chr7:107988855 | T | A | 140 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(137): Show |
141 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(138): Show |
intron_variant | MODIFIER | c.424-2492A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107988855 | |||||||
chr7:107988932 | T | C | 1 | a0001c0001t0001g0100 | 1 | HG03491.hp1 | intron_variant | MODIFIER | c.424-2569A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107988932 | |||||||
chr7:107989004 | G | A | 1 | a0001c0007t0001g0007 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.424-2641C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107989004 | |||||||
chr7:107989050 | A | G | 1 | a0001c0059t0001g0041 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.424-2687T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107989050 | |||||||
chr7:107989092 | G | C | 1 | a0001c0032t0001g0028 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.424-2729C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107989092 | |||||||
chr7:107989214 | C | T | 34 | a0001c0009t0001g0018 a0001c0009t0001g0194 a0001c0009t0001g0270 others(31): Show |
34 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.424-2851G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107989214 | |||||||
chr7:107989289 | A | C | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.424-2926T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107989289 | |||||||
chr7:107989364 | C | T | 2 | a0001c0001t0001g0073 a0002c0039t0002g0203 |
2 | HG02735.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.424-3001G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107989364 | |||||||
chr7:107989378 | C | T | 1 | a0002c0026t0002g0352 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.424-3015G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107989378 | |||||||
chr7:107989478 | T | C | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.424-3115A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107989478 | |||||||
chr7:107989799 | G | A | 11 | a0001c0001t0001g0048 a0001c0001t0002g0047 a0001c0007t0001g0009 others(8): Show |
11 | HG00738.hp2 HG01106.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.424-3436C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107989799 | |||||||
chr7:107990026 | T | TG | 138 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(135): Show |
139 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(136): Show |
intron_variant | MODIFIER | c.424-3664dupC | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990026 | |||||||
chr7:107990028 | T | C | 132 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(129): Show |
133 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(130): Show |
intron_variant | MODIFIER | c.424-3665A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990028 | |||||||
chr7:107990028 | T | G | 60 | a0001c0001t0001g0012 a0001c0001t0001g0342 a0001c0006t0001g0042 others(57): Show |
60 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(57): Show |
intron_variant | MODIFIER | c.424-3665A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990028 | |||||||
chr7:107990037 | G | T | 67 | a0001c0001t0001g0012 a0001c0001t0001g0048 a0001c0001t0001g0342 others(64): Show |
67 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(64): Show |
intron_variant | MODIFIER | c.424-3674C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990037 | |||||||
chr7:107990093 | C | G | 1 | a0001c0002t0001g0286 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.424-3730G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990093 | |||||||
chr7:107990151 | A | G | 1 | a0008c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.424-3788T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990151 | |||||||
chr7:107990415 | C | T | 1 | a0001c0005t0001g0101 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.424-4052G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990415 | |||||||
chr7:107990449 | G | A | 1 | a0002c0003t0002g0166 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.424-4086C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990449 | |||||||
chr7:107990535 | C | T | 1 | a0001c0001t0001g0016 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.424-4172G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990535 | |||||||
chr7:107990546 | A | G | 1 | a0002c0010t0001g0334 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.424-4183T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990546 | |||||||
chr7:107990547 | AT | A | 18 | a0001c0006t0001g0042 a0001c0007t0001g0319 a0004c0015t0001g0138 others(15): Show |
18 | HG01243.hp1 HG01433.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.424-4185delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990547 | |||||||
chr7:107990654 | C | CCA | 21 | a0001c0001t0001g0012 a0001c0001t0001g0342 a0001c0006t0001g0042 others(18): Show |
21 | HG01243.hp1 HG01433.hp1 HG02109.hp1 others(18): Show |
intron_variant | MODIFIER | c.423+4231_423+4232d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990654 | |||||||
chr7:107990709 | G | C | 1 | a0001c0006t0001g0133 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.423+4178C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990709 | |||||||
chr7:107990728 | T | C | 1 | a0003c0004t0001g0318 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.423+4159A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990728 | |||||||
chr7:107990741 | C | T | 2 | a0001c0006t0001g0356 a0001c0006t0001g0358 |
2 | HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.423+4146G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990741 | |||||||
chr7:107990898 | C | T | 1 | a0001c0063t0001g0324 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.423+3989G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990898 | |||||||
chr7:107990960 | C | T | 1 | a0004c0069t0001g0134 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.423+3927G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990960 | |||||||
chr7:107990982 | C | T | 1 | a0001c0002t0001g0202 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.423+3905G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107990982 | |||||||
chr7:107991238 | A | G | 1 | a0002c0010t0001g0180 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.423+3649T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991238 | |||||||
chr7:107991273 | T | C | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.423+3614A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991273 | |||||||
chr7:107991323 | C | T | 129 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(126): Show |
130 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(127): Show |
intron_variant | MODIFIER | c.423+3564G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991323 | |||||||
chr7:107991336 | C | T | 192 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(189): Show |
193 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(190): Show |
intron_variant | MODIFIER | c.423+3551G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991336 | |||||||
chr7:107991444 | G | A | 9 | a0001c0001t0001g0048 a0001c0001t0002g0047 a0001c0007t0001g0009 others(6): Show |
9 | HG00738.hp1 HG00738.hp2 HG01106.hp2 others(6): Show |
intron_variant | MODIFIER | c.423+3443C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991444 | |||||||
chr7:107991449 | T | C | 1 | a0005c0012t0002g0323 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.423+3438A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991449 | |||||||
chr7:107991462 | G | C | 6 | a0001c0002t0001g0057 a0001c0005t0001g0059 a0002c0021t0002g0066 others(3): Show |
6 | HG00741.hp2 HG01070.hp2 HG01168.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+3425C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991462 | |||||||
chr7:107991558 | T | G | 1 | a0003c0050t0002g0146 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.423+3329A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991558 | |||||||
chr7:107991584 | T | G | 1 | a0002c0026t0002g0352 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.423+3303A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991584 | |||||||
chr7:107991588 | C | CA | 16 | a0001c0001t0001g0001 a0001c0001t0001g0016 a0001c0001t0001g0299 others(13): Show |
17 | HG01109.hp1 HG01109.hp2 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.423+3298dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991588 | |||||||
chr7:107991639 | G | A | 1 | a0001c0002t0001g0266 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.423+3248C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991639 | |||||||
chr7:107991698 | C | T | 1 | a0011c0071t0001g0067 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.423+3189G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991698 | |||||||
chr7:107991785 | G | A | 2 | a0011c0071t0001g0067 a0021c0046t0002g0333 |
2 | HG02922.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.423+3102C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991785 | |||||||
chr7:107991786 | T | C | 1 | a0021c0046t0002g0333 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.423+3101A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991786 | |||||||
chr7:107991794 | G | A | 1 | a0001c0072t0001g0025 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.423+3093C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991794 | |||||||
chr7:107991801 | G | A | 1 | a0008c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.423+3086C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991801 | |||||||
chr7:107991905 | C | CA | 193 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(190): Show |
194 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(191): Show |
intron_variant | MODIFIER | c.423+2981dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991905 | |||||||
chr7:107991905 | C | CAA | 10 | a0001c0001t0001g0149 a0001c0001t0001g0300 a0001c0001t0001g0321 others(7): Show |
10 | HG01175.hp1 HG02258.hp2 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.423+2980_423+2981d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991905 | |||||||
chr7:107991905 | C | CAAA | 6 | a0001c0027t0001g0349 a0002c0003t0001g0070 a0002c0003t0001g0071 others(3): Show |
6 | HG02897.hp1 HG02976.hp1 HG03139.hp2 others(3): Show |
intron_variant | MODIFIER | c.423+2979_423+2981d others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991905 | |||||||
chr7:107991970 | T | C | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.423+2917A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107991970 | |||||||
chr7:107992570 | G | A | 1 | a0010c0025t0001g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.423+2317C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107992570 | |||||||
chr7:107992623 | G | A | 2 | a0001c0001t0001g0335 a0002c0003t0002g0075 |
2 | HG02258.hp1 HG02818.hp1 |
intron_variant | MODIFIER | c.423+2264C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107992623 | |||||||
chr7:107992651 | T | C | 45 | a0001c0001t0001g0012 a0001c0001t0001g0342 a0001c0006t0001g0042 others(42): Show |
45 | HG00408.hp1 HG00735.hp1 HG00735.hp2 others(42): Show |
intron_variant | MODIFIER | c.423+2236A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107992651 | |||||||
chr7:107992694 | G | A | 7 | a0001c0027t0001g0349 a0001c0028t0001g0350 a0002c0003t0001g0070 others(4): Show |
7 | HG02976.hp1 HG03139.hp2 HG03209.hp1 others(4): Show |
intron_variant | MODIFIER | c.423+2193C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107992694 | |||||||
chr7:107992726 | C | T | 14 | a0001c0002t0001g0196 a0001c0002t0001g0197 a0001c0002t0001g0199 others(11): Show |
14 | HG00140.hp1 HG00558.hp1 HG01081.hp1 others(11): Show |
intron_variant | MODIFIER | c.423+2161G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107992726 | |||||||
chr7:107992808 | T | C | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.423+2079A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107992808 | |||||||
chr7:107992848 | T | C | 1 | a0001c0072t0001g0025 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.423+2039A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107992848 | |||||||
chr7:107992986 | T | C | 1 | a0021c0046t0002g0333 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.423+1901A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107992986 | |||||||
chr7:107993072 | T | C | 170 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0015 others(167): Show |
171 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(168): Show |
intron_variant | MODIFIER | c.423+1815A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993072 | |||||||
chr7:107993203 | G | A | 3 | a0001c0022t0001g0029 a0001c0032t0001g0028 a0002c0013t0001g0030 |
3 | HG02280.hp2 HG02630.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.423+1684C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993203 | |||||||
chr7:107993212 | C | A | 1 | a0001c0002t0001g0302 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.423+1675G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993212 | |||||||
chr7:107993250 | C | T | 1 | a0001c0001t0001g0004 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.423+1637G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993250 | |||||||
chr7:107993278 | C | T | 1 | a0001c0029t0001g0311 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.423+1609G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993278 | |||||||
chr7:107993287 | C | T | 1 | a0003c0020t0001g0195 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.423+1600G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993287 | |||||||
chr7:107993493 | G | A | 1 | a0003c0004t0001g0158 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.423+1394C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993493 | |||||||
chr7:107993511 | A | G | 9 | a0001c0001t0002g0192 a0001c0006t0001g0193 a0001c0014t0001g0346 others(6): Show |
9 | HG02080.hp1 HG02155.hp1 HG03486.hp1 others(6): Show |
intron_variant | MODIFIER | c.423+1376T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993511 | |||||||
chr7:107993511 | A | T | 2 | a0002c0010t0001g0334 a0008c0031t0001g0072 |
2 | HG02723.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.423+1376T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993511 | |||||||
chr7:107993801 | G | C | 1 | a0001c0001t0001g0303 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.423+1086C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993801 | |||||||
chr7:107993917 | C | T | 1 | a0001c0009t0001g0194 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.423+970G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993917 | |||||||
chr7:107993939 | T | C | 14 | a0001c0001t0001g0151 a0001c0001t0001g0183 a0001c0006t0001g0042 others(11): Show |
14 | HG02615.hp2 HG02630.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.423+948A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107993939 | |||||||
chr7:107994048 | C | G | 13 | a0001c0001t0001g0325 a0001c0001t0002g0192 a0001c0002t0001g0328 others(10): Show |
13 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.423+839G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994048 | |||||||
chr7:107994286 | T | C | 3 | a0002c0081t0001g0020 a0004c0066t0004g0021 a0008c0024t0001g0184 |
3 | HG01433.hp1 HG02886.hp2 HG03471.hp1 |
intron_variant | MODIFIER | c.423+601A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994286 | |||||||
chr7:107994290 | A | G | 3 | a0001c0005t0001g0357 a0001c0006t0001g0356 a0001c0006t0001g0358 |
3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.423+597T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994290 | |||||||
chr7:107994381 | C | T | 1 | a0001c0078t0001g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.423+506G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994381 | |||||||
chr7:107994544 | G | T | 160 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0015 others(157): Show |
161 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(158): Show |
intron_variant | MODIFIER | c.423+343C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994544 | |||||||
chr7:107994660 | G | C | 107 | a0001c0001t0001g0048 a0001c0001t0001g0062 a0001c0001t0001g0063 others(104): Show |
107 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.423+227C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994660 | |||||||
chr7:107994682 | C | A | 2 | a0002c0010t0001g0155 a0003c0004t0001g0148 |
2 | HG00323.hp1 HG00639.hp1 |
intron_variant | MODIFIER | c.423+205G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994682 | |||||||
chr7:107994713 | T | C | 1 | a0001c0009t0001g0018 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.423+174A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994713 | |||||||
chr7:107994738 | G | T | 3 | a0003c0004t0001g0157 a0003c0004t0001g0158 a0003c0004t0001g0191 |
3 | NA18953.hp2 NA18981.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.423+149C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994738 | |||||||
chr7:107994806 | T | C | 1 | a0001c0006t0002g0185 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.423+81A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994806 | |||||||
chr7:107994859 | A | G | 1 | a0001c0005t0001g0351 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.423+28T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 5/33 | chr7 | 107994859 | |||||||
chr7:107995027 | G | C | 12 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0015 others(9): Show |
13 | HG00323.hp2 HG00733.hp1 HG00735.hp1 others(10): Show |
intron_variant | MODIFIER | c.350-67C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107995027 | |||||||
chr7:107995396 | G | A | 3 | a0001c0001t0001g0305 a0001c0001t0001g0307 a0001c0002t0001g0306 |
3 | NA18989.hp2 NA18990.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.350-436C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107995396 | |||||||
chr7:107995457 | C | T | 4 | a0001c0045t0001g0038 a0002c0003t0001g0070 a0002c0003t0001g0071 others(1): Show |
4 | HG02976.hp1 HG03516.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.350-497G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107995457 | |||||||
chr7:107995510 | C | T | 6 | a0001c0014t0001g0346 a0001c0027t0001g0349 a0001c0028t0001g0350 others(3): Show |
6 | HG02630.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-550G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107995510 | |||||||
chr7:107995548 | A | G | 6 | a0001c0014t0001g0346 a0001c0027t0001g0349 a0001c0028t0001g0350 others(3): Show |
6 | HG02630.hp1 HG02809.hp1 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.350-588T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107995548 | |||||||
chr7:107995707 | G | A | 1 | a0019c0036t0001g0068 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.350-747C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107995707 | |||||||
chr7:107995972 | T | C | 1 | a0001c0006t0001g0042 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.350-1012A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107995972 | |||||||
chr7:107996097 | AATGTTAG others(1): Show |
A | 11 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(8): Show |
11 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-1145_350-1138d others(10): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996097 | |||||||
chr7:107996106 | C | T | 11 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(8): Show |
11 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-1146G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996106 | |||||||
chr7:107996237 | A | G | 1 | a0008c0024t0001g0032 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.350-1277T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996237 | |||||||
chr7:107996294 | C | CT | 11 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(8): Show |
11 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-1335dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996294 | |||||||
chr7:107996301 | T | A | 1 | a0008c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.350-1341A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996301 | |||||||
chr7:107996351 | T | C | 11 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(8): Show |
11 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-1391A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996351 | |||||||
chr7:107996382 | G | T | 11 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(8): Show |
11 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-1422C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996382 | |||||||
chr7:107996410 | G | A | 2 | a0001c0001t0001g0151 a0008c0031t0001g0072 |
2 | HG02723.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.350-1450C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996410 | |||||||
chr7:107996457 | C | T | 1 | a0001c0044t0002g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.350-1497G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996457 | |||||||
chr7:107996463 | G | A | 11 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(8): Show |
11 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-1503C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996463 | |||||||
chr7:107996478 | G | A | 8 | a0001c0007t0003g0361 a0001c0007t0003g0362 a0001c0014t0001g0346 others(5): Show |
8 | HG02055.hp1 HG02572.hp1 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.350-1518C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996478 | |||||||
chr7:107996541 | C | G | 1 | a0027c0047t0003g0359 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.350-1581G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996541 | |||||||
chr7:107996718 | G | A | 4 | a0001c0001t0001g0342 a0001c0006t0001g0341 a0001c0007t0001g0343 others(1): Show |
4 | HG02258.hp2 HG02451.hp1 HG02615.hp1 others(1): Show |
intron_variant | MODIFIER | c.349+1639C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996718 | |||||||
chr7:107996832 | A | T | 11 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(8): Show |
11 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.349+1525T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996832 | |||||||
chr7:107996930 | G | A | 11 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(8): Show |
11 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.349+1427C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996930 | |||||||
chr7:107996936 | C | T | 1 | a0002c0003t0002g0075 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.349+1421G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996936 | |||||||
chr7:107996986 | T | C | 1 | a0008c0031t0001g0072 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.349+1371A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996986 | |||||||
chr7:107996995 | G | A | 2 | a0001c0035t0001g0037 a0020c0034t0001g0031 |
2 | HG02622.hp1 HG02896.hp2 |
intron_variant | MODIFIER | c.349+1362C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107996995 | |||||||
chr7:107997157 | T | C | 1 | a0002c0019t0002g0308 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.349+1200A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997157 | |||||||
chr7:107997255 | C | G | 3 | a0001c0005t0001g0357 a0001c0006t0001g0356 a0001c0006t0001g0358 |
3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.349+1102G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997255 | |||||||
chr7:107997347 | C | T | 1 | a0002c0010t0001g0044 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.349+1010G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997347 | |||||||
chr7:107997352 | C | G | 181 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(178): Show |
182 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(179): Show |
intron_variant | MODIFIER | c.349+1005G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997352 | |||||||
chr7:107997428 | TAAAC | T | 12 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(9): Show |
12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.349+925_349+928del others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997428 | |||||||
chr7:107997428 | TAAACAAA others(5): Show |
T | 1 | a0012c0075t0001g0043 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.349+917_349+928del others(12): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997428 | |||||||
chr7:107997477 | C | T | 12 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(9): Show |
12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.349+880G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997477 | |||||||
chr7:107997659 | G | A | 1 | a0001c0002t0001g0309 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.349+698C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997659 | |||||||
chr7:107997769 | A | C | 1 | a0001c0005t0001g0190 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.349+588T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997769 | |||||||
chr7:107997791 | T | C | 141 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0062 others(138): Show |
141 | HG00140.hp2 HG00323.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.349+566A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997791 | |||||||
chr7:107997931 | C | T | 12 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(9): Show |
12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.349+426G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997931 | |||||||
chr7:107997991 | C | T | 3 | a0001c0001t0001g0188 a0001c0001t0001g0189 a0003c0020t0001g0187 |
3 | NA18939.hp1 NA18949.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.349+366G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107997991 | |||||||
chr7:107998016 | T | A | 1 | a0019c0036t0001g0068 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.349+341A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107998016 | |||||||
chr7:107998292 | C | G | 5 | a0001c0002t0001g0337 a0001c0014t0001g0336 a0002c0010t0001g0334 others(2): Show |
5 | HG02717.hp1 HG02922.hp1 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+65G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 4/33 | chr7 | 107998292 | |||||||
chr7:107998628 | T | C | 3 | a0002c0003t0001g0070 a0002c0003t0001g0071 a0002c0013t0001g0069 |
3 | HG02976.hp1 NA18522.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.214-136A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107998628 | |||||||
chr7:107998632 | A | T | 12 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(9): Show |
12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-140T>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107998632 | |||||||
chr7:107998729 | G | C | 7 | a0001c0002t0001g0337 a0001c0014t0001g0336 a0002c0003t0002g0338 others(4): Show |
7 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-237C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107998729 | |||||||
chr7:107998901 | A | G | 12 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(9): Show |
12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-409T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107998901 | |||||||
chr7:107998935 | G | A | 1 | a0001c0005t0001g0150 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.214-443C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107998935 | |||||||
chr7:107999051 | G | A | 2 | a0001c0007t0003g0361 a0001c0007t0003g0362 |
2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.214-559C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999051 | |||||||
chr7:107999116 | C | T | 12 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(9): Show |
12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-624G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999116 | |||||||
chr7:107999146 | C | A | 1 | a0001c0001t0001g0186 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.214-654G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999146 | |||||||
chr7:107999147 | C | T | 2 | a0002c0003t0002g0338 a0002c0003t0002g0339 |
2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.214-655G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999147 | |||||||
chr7:107999182 | G | C | 12 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(9): Show |
12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-690C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999182 | |||||||
chr7:107999196 | A | G | 1 | a0001c0001t0001g0151 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.214-704T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999196 | |||||||
chr7:107999222 | C | A | 12 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(9): Show |
12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-730G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999222 | |||||||
chr7:107999247 | C | T | 2 | a0001c0001t0001g0011 a0002c0003t0002g0010 |
2 | HG01069.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.214-755G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999247 | |||||||
chr7:107999417 | T | G | 3 | a0001c0005t0001g0357 a0001c0006t0001g0356 a0001c0006t0001g0358 |
3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.214-925A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999417 | |||||||
chr7:107999426 | A | C | 2 | a0001c0007t0003g0361 a0001c0007t0003g0362 |
2 | HG02055.hp1 HG02572.hp1 |
intron_variant | MODIFIER | c.214-934T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999426 | |||||||
chr7:107999438 | C | G | 12 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(9): Show |
12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-946G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999438 | |||||||
chr7:107999482 | T | C | 1 | a0001c0001t0002g0019 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.214-990A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999482 | |||||||
chr7:107999519 | T | C | 3 | a0001c0005t0001g0357 a0001c0006t0001g0356 a0001c0006t0001g0358 |
3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.214-1027A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999519 | |||||||
chr7:107999552 | A | G | 12 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(9): Show |
12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-1060T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999552 | |||||||
chr7:107999672 | A | G | 12 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(9): Show |
12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-1180T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999672 | |||||||
chr7:107999695 | C | CCTG | 194 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(191): Show |
195 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.214-1204_214-1203i others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999695 | |||||||
chr7:107999745 | A | G | 1 | a0001c0002t0001g0309 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.214-1253T>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999745 | |||||||
chr7:107999763 | C | CT | 21 | a0001c0001t0001g0033 a0001c0001t0001g0073 a0001c0002t0001g0337 others(18): Show |
21 | HG00738.hp1 HG01175.hp1 HG01243.hp1 others(18): Show |
intron_variant | MODIFIER | c.214-1272dupA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999763 | |||||||
chr7:107999763 | C | CTT | 6 | a0001c0005t0001g0026 a0001c0022t0001g0029 a0001c0032t0001g0028 others(3): Show |
6 | HG02280.hp2 HG02630.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.214-1273_214-1272d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999763 | |||||||
chr7:107999763 | C | CTTT | 13 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(10): Show |
13 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.214-1274_214-1272d others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999763 | |||||||
chr7:107999763 | CT | C | 157 | a0001c0001t0001g0001 a0001c0001t0001g0011 a0001c0001t0001g0012 others(154): Show |
158 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(155): Show |
intron_variant | MODIFIER | c.214-1272delA | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999763 | |||||||
chr7:107999763 | CTT | C | 7 | a0001c0002t0001g0309 a0001c0002t0001g0310 a0001c0002t0001g0314 others(4): Show |
7 | HG02723.hp2 HG02897.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.214-1273_214-1272d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999763 | |||||||
chr7:107999885 | C | T | 12 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(9): Show |
12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.214-1393G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999885 | |||||||
chr7:107999938 | T | C | 4 | a0001c0002t0001g0337 a0001c0014t0001g0336 a0002c0003t0002g0338 others(1): Show |
4 | HG02717.hp1 HG02895.hp2 HG02897.hp1 others(1): Show |
intron_variant | MODIFIER | c.214-1446A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999938 | |||||||
chr7:107999962 | C | T | 2 | a0001c0022t0001g0039 a0008c0031t0001g0072 |
2 | HG02723.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.214-1470G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999962 | |||||||
chr7:107999974 | G | A | 1 | a0019c0036t0001g0068 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.214-1482C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 107999974 | |||||||
chr7:108000008 | G | C | 158 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(155): Show |
159 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(156): Show |
intron_variant | MODIFIER | c.214-1516C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108000008 | |||||||
chr7:108000072 | C | A | 1 | a0001c0028t0001g0350 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.213+1486G>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108000072 | |||||||
chr7:108000198 | C | CA | 176 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(173): Show |
177 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(174): Show |
intron_variant | MODIFIER | c.213+1359dupT | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108000198 | |||||||
chr7:108000198 | C | CAA | 8 | a0001c0001t0001g0321 a0001c0006t0001g0042 a0001c0007t0001g0319 others(5): Show |
8 | HG01433.hp1 HG02895.hp2 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.213+1358_213+1359d others(4): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108000198 | |||||||
chr7:108000198 | C | CAAA | 11 | a0001c0001t0001g0325 a0001c0002t0001g0328 a0001c0002t0001g0331 others(8): Show |
11 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(8): Show |
intron_variant | MODIFIER | c.213+1357_213+1359d others(5): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108000198 | |||||||
chr7:108000212 | G | T | 12 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0002t0001g0328 others(9): Show |
12 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.213+1346C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108000212 | |||||||
chr7:108000556 | T | A | 1 | a0001c0001t0001g0022 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.213+1002A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108000556 | |||||||
chr7:108000700 | C | T | 24 | a0001c0001t0001g0048 a0001c0001t0001g0062 a0001c0001t0001g0063 others(21): Show |
24 | HG00140.hp2 HG00642.hp1 HG00738.hp2 others(21): Show |
intron_variant | MODIFIER | c.213+858G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108000700 | |||||||
chr7:108001115 | G | C | 3 | a0001c0005t0001g0357 a0001c0006t0001g0356 a0001c0006t0001g0358 |
3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.213+443C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108001115 | |||||||
chr7:108001171 | C | T | 190 | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0011 others(187): Show |
191 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(188): Show |
intron_variant | MODIFIER | c.213+387G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108001171 | |||||||
chr7:108001287 | G | A | 20 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0001t0001g0335 others(17): Show |
20 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.213+271C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108001287 | |||||||
chr7:108001288 | C | T | 2 | a0001c0006t0001g0042 a0001c0059t0001g0041 |
2 | HG02965.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.213+270G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108001288 | |||||||
chr7:108001326 | G | A | 1 | a0010c0025t0001g0340 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.213+232C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108001326 | |||||||
chr7:108001430 | G | A | 1 | a0001c0001t0001g0320 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.213+128C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 3/33 | chr7 | 108001430 | |||||||
chr7:108001761 | G | T | 2 | a0001c0014t0003g0360 a0027c0047t0003g0359 |
2 | HG01891.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.38-28C>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108001761 | |||||||
chr7:108001772 | G | A | 20 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0001t0001g0335 others(17): Show |
20 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.38-39C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108001772 | |||||||
chr7:108001814 | G | C | 20 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0001t0001g0335 others(17): Show |
20 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.38-81C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108001814 | |||||||
chr7:108001884 | G | A | 4 | a0002c0026t0002g0352 a0004c0016t0001g0354 a0004c0016t0001g0355 others(1): Show |
4 | HG00738.hp1 HG01243.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.38-151C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108001884 | |||||||
chr7:108001897 | G | A | 1 | a0001c0045t0001g0038 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.38-164C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108001897 | |||||||
chr7:108002117 | G | C | 20 | a0001c0001t0001g0321 a0001c0001t0001g0325 a0001c0001t0001g0335 others(17): Show |
20 | HG00609.hp1 HG02080.hp1 HG02135.hp2 others(17): Show |
intron_variant | MODIFIER | c.38-384C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002117 | |||||||
chr7:108002142 | C | CGCGTGCA others(73): Show |
10 | a0001c0007t0003g0361 a0001c0007t0003g0362 a0001c0014t0001g0346 others(7): Show |
10 | HG01891.hp2 HG02055.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.38-489_38-410dupAC others(78): Show |
LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002142 | |||||||
chr7:108002169 | T | A | 3 | a0001c0001t0001g0342 a0001c0006t0001g0341 a0001c0007t0001g0343 |
3 | HG02258.hp2 HG02451.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.38-436A>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002169 | |||||||
chr7:108002171 | G | A | 18 | a0001c0001t0001g0033 a0001c0005t0001g0026 a0001c0005t0001g0035 others(15): Show |
18 | HG00738.hp1 HG01243.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.38-438C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002171 | |||||||
chr7:108002204 | G | A | 1 | a0001c0002t0001g0344 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.38-471C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002204 | |||||||
chr7:108002585 | A | C | 1 | a0001c0022t0001g0039 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.37+264T>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002585 | |||||||
chr7:108002657 | G | C | 1 | a0001c0044t0002g0345 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.37+192C>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002657 | |||||||
chr7:108002661 | C | T | 18 | a0001c0001t0001g0033 a0001c0005t0001g0026 a0001c0005t0001g0035 others(15): Show |
18 | HG00738.hp1 HG01243.hp1 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.37+188G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002661 | |||||||
chr7:108002678 | C | T | 3 | a0001c0005t0001g0357 a0001c0006t0001g0356 a0001c0006t0001g0358 |
3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.37+171G>A | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002678 | |||||||
chr7:108002704 | G | A | 5 | a0001c0014t0001g0346 a0001c0027t0001g0349 a0001c0028t0001g0350 others(2): Show |
5 | HG02630.hp1 HG02809.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.37+145C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002704 | |||||||
chr7:108002709 | G | A | 1 | a0001c0005t0001g0351 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.37+140C>T | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002709 | |||||||
chr7:108002793 | T | C | 4 | a0002c0026t0002g0352 a0004c0016t0001g0354 a0004c0016t0001g0355 others(1): Show |
4 | HG00738.hp1 HG01243.hp1 HG02559.hp1 others(1): Show |
intron_variant | MODIFIER | c.37+56A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002793 | |||||||
chr7:108002802 | C | G | 1 | a0001c0078t0001g0024 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.37+47G>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002802 | |||||||
chr7:108002805 | T | C | 3 | a0001c0005t0001g0357 a0001c0006t0001g0356 a0001c0006t0001g0358 |
3 | HG02109.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.37+44A>G | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 2/33 | chr7 | 108002805 | |||||||
chr7:108003076 | T | G | 339 | a0001c0001t0001g0033 a0001c0001t0001g0048 a0001c0001t0001g0062 others(336): Show |
340 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(337): Show |
intron_variant | MODIFIER | c.-87+35A>C | LAMB1 | ENSG00000091136.15 | transcript | ENST00000222399.11 | protein_coding | 1/33 | chr7 | 108003076 |