geneid | 3993 |
---|---|
ensemblid | ENSG00000073350.14 |
hgncid | 6629 |
symbol | LLGL2 |
name | LLGL scribble cell polarity complex component 2 |
refseq_nuc | NM_001031803.2 |
refseq_prot | NP_001026973.1 |
ensembl_nuc | ENST00000392550.8 |
ensembl_prot | ENSP00000376333.4 |
mane_status | MANE Select |
chr | chr17 |
start | 75525697 |
end | 75575209 |
strand | + |
ver | v1.2 |
region | chr17:75525697-75575209 |
region5000 | chr17:75520697-75580209 |
regionname0 | LLGL2_chr17_75525697_75575209 |
regionname5000 | LLGL2_chr17_75520697_75580209 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/0 | 1020 | 123 | 6 | 22 | 67 | 7 | 21 | 52 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002 | 0/1 | 1020 | 97 | 38 | 23 | 19 | 6 | 10 | 13 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0003 | 1/0 | 1020 | 74 | 4 | 18 | 44 | 2 | 5 | 33 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0004 | 0/0 | 1020 | 36 | 16 | 4 | 13 | 0 | 3 | 4 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0005 | 0/0 | 1020 | 6 | 0 | 6 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0006 | 0/0 | 1020 | 6 | 2 | 1 | 3 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0007 | 0/0 | 1020 | 4 | 0 | 0 | 4 | 0 | 0 | 4 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0008 | 0/0 | 1020 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0009 | 0/0 | 1020 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0010 | 0/0 | 1020 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0011 | 0/0 | 1020 | 2 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0012 | 0/0 | 1020 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0013 | 0/0 | 1020 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0014 | 0/0 | 1020 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0015 | 0/0 | 1020 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0016 | 0/0 | 1020 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0017 | 0/0 | 1020 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0018 | 0/0 | 1020 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0019 | 0/0 | 1020 | 1 | 0 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0020 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0021 | 0/0 | 1020 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0022 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0023 | 0/0 | 538 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0024 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0025 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0026 | 0/0 | 1020 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0027 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0028 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0029 | 0/0 | 1020 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0030 | 0/0 | 1020 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0031 | 0/0 | 1020 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0032 | 0/0 | 1020 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0033 | 0/0 | 1020 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/0 | 3063 | 119 | 6 | 22 | 65 | 6 | 20 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0002 | 1/0 | 3063 | 69 | 2 | 17 | 42 | 2 | 5 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0003 | 0/1 | 3063 | 40 | 3 | 11 | 19 | 3 | 3 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0004 | 0/0 | 3063 | 33 | 18 | 11 | 0 | 2 | 2 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0005 | 0/0 | 3063 | 25 | 7 | 3 | 13 | 0 | 2 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0006 | 0/0 | 3063 | 14 | 14 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0007 | 0/0 | 3063 | 8 | 6 | 1 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0008 | 0/0 | 3063 | 5 | 0 | 5 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0009 | 0/0 | 3063 | 4 | 0 | 1 | 3 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0010 | 0/0 | 3063 | 4 | 0 | 0 | 4 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0011 | 0/0 | 3063 | 3 | 3 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0012 | 0/0 | 3063 | 3 | 0 | 0 | 0 | 0 | 3 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0013 | 0/0 | 3063 | 3 | 1 | 0 | 0 | 1 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0014 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0015 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0016 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0017 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0018 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0019 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0020 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0021 | 0/0 | 3063 | 2 | 0 | 1 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0022 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0023 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0024 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0025 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0026 | 0/0 | 3080 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0027 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0028 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0029 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0030 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0031 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0032 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0033 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0034 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0035 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0036 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0037 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0038 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0039 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0040 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0041 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0042 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0043 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0044 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0045 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0046 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0047 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0048 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0049 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0050 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0051 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0052 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0053 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0054 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0055 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
c0056 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 501 | 112 | 6 | 25 | 56 | 4 | 21 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
t0002 | 1/0 | 491 | 105 | 6 | 22 | 62 | 6 | 8 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
t0003 | 0/0 | 491 | 101 | 56 | 19 | 15 | 3 | 8 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
t0004 | 0/0 | 491 | 27 | 9 | 4 | 12 | 0 | 2 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
t0005 | 0/1 | 501 | 27 | 7 | 9 | 4 | 3 | 3 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
t0006 | 0/0 | 491 | 4 | 4 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
t0007 | 0/0 | 501 | 4 | 0 | 0 | 4 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
t0008 | 0/0 | 501 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
t0009 | 0/0 | 501 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0131 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0251 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/0 | 3063 | 119 | 6 | 22 | 65 | 6 | 20 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0001c0023 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0001c0024 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0001c0029 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0001c0037 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0003 | 0/1 | 3063 | 40 | 3 | 11 | 19 | 3 | 3 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0004 | 0/0 | 3063 | 33 | 18 | 11 | 0 | 2 | 2 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0006 | 0/0 | 3063 | 14 | 14 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0012 | 0/0 | 3063 | 3 | 0 | 0 | 0 | 0 | 3 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0013 | 0/0 | 3063 | 3 | 1 | 0 | 0 | 1 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0045 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0046 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0048 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0055 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0003c0002 | 1/0 | 3063 | 69 | 2 | 17 | 42 | 2 | 5 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0003c0019 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0003c0021 | 0/0 | 3063 | 2 | 0 | 1 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0003c0054 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0004c0005 | 0/0 | 3063 | 25 | 7 | 3 | 13 | 0 | 2 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0004c0007 | 0/0 | 3063 | 8 | 6 | 1 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0004c0018 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0004c0050 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0005c0008 | 0/0 | 3063 | 5 | 0 | 5 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0005c0036 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0006c0009 | 0/0 | 3063 | 4 | 0 | 1 | 3 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0006c0015 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0007c0010 | 0/0 | 3063 | 4 | 0 | 0 | 4 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0008c0041 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0008c0043 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0008c0044 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0009c0011 | 0/0 | 3063 | 3 | 3 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0010c0014 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0011c0027 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0011c0028 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0012c0022 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0013c0016 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0014c0020 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0015c0017 | 0/0 | 3063 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0016c0056 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0017c0034 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0018c0031 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0019c0030 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0020c0032 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0021c0033 | 0/0 | 3063 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0022c0035 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0023c0026 | 0/0 | 3080 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0024c0025 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0025c0039 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0026c0042 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0027c0040 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0028c0052 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0029c0051 | 0/0 | 3063 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0030c0053 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0031c0049 | 0/0 | 3063 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0032c0047 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0033c0038 | 0/0 | 3063 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 3563 | 91 | 5 | 16 | 52 | 2 | 16 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0001c0001t0002 | 0/0 | 3553 | 26 | 1 | 5 | 12 | 4 | 4 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0001c0001t0008 | 0/0 | 3563 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0001c0001t0009 | 0/0 | 3563 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0001c0023t0002 | 0/0 | 3553 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0001c0024t0002 | 0/0 | 3553 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0001c0029t0001 | 0/0 | 3563 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0001c0037t0001 | 0/0 | 3563 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0003t0003 | 0/0 | 3553 | 20 | 1 | 4 | 15 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0003t0005 | 0/1 | 3563 | 20 | 2 | 7 | 4 | 3 | 3 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0004t0003 | 0/0 | 3553 | 33 | 18 | 11 | 0 | 2 | 2 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0006t0003 | 0/0 | 3553 | 13 | 13 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0006t0005 | 0/0 | 3563 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0012t0003 | 0/0 | 3553 | 3 | 0 | 0 | 0 | 0 | 3 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0013t0003 | 0/0 | 3553 | 3 | 1 | 0 | 0 | 1 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0045t0003 | 0/0 | 3553 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0046t0005 | 0/0 | 3563 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0048t0004 | 0/0 | 3553 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0002c0055t0003 | 0/0 | 3553 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0003c0002t0001 | 0/0 | 3563 | 5 | 0 | 2 | 1 | 0 | 2 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0003c0002t0002 | 1/0 | 3553 | 64 | 2 | 15 | 41 | 2 | 3 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0003c0019t0002 | 0/0 | 3553 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0003c0021t0002 | 0/0 | 3553 | 2 | 0 | 1 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0003c0054t0001 | 0/0 | 3563 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0004c0005t0004 | 0/0 | 3553 | 23 | 7 | 3 | 11 | 0 | 2 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0004c0005t0007 | 0/0 | 3563 | 2 | 0 | 0 | 2 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0004c0007t0003 | 0/0 | 3553 | 8 | 6 | 1 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0004c0018t0005 | 0/0 | 3563 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0004c0050t0006 | 0/0 | 3553 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0005c0008t0001 | 0/0 | 3563 | 5 | 0 | 5 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0005c0036t0001 | 0/0 | 3563 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0006c0009t0002 | 0/0 | 3553 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0006c0009t0004 | 0/0 | 3553 | 2 | 0 | 1 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0006c0009t0007 | 0/0 | 3563 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0006c0015t0005 | 0/0 | 3563 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0007c0010t0002 | 0/0 | 3553 | 4 | 0 | 0 | 4 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0008c0041t0003 | 0/0 | 3553 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0008c0043t0003 | 0/0 | 3553 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0008c0044t0003 | 0/0 | 3553 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0009c0011t0006 | 0/0 | 3553 | 3 | 3 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0010c0014t0003 | 0/0 | 3553 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0011c0027t0005 | 0/0 | 3563 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0011c0028t0003 | 0/0 | 3553 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0012c0022t0003 | 0/0 | 3553 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0013c0016t0003 | 0/0 | 3553 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0014c0020t0003 | 0/0 | 3553 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0015c0017t0003 | 0/0 | 3553 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0016c0056t0001 | 0/0 | 3563 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0017c0034t0001 | 0/0 | 3563 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0018c0031t0001 | 0/0 | 3563 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0019c0030t0001 | 0/0 | 3563 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0020c0032t0002 | 0/0 | 3553 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0021c0033t0001 | 0/0 | 3563 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0022c0035t0001 | 0/0 | 3563 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0023c0026t0001 | 0/0 | 3580 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0024c0025t0007 | 0/0 | 3563 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0025c0039t0004 | 0/0 | 3553 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0026c0042t0003 | 0/0 | 3553 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0027c0040t0003 | 0/0 | 3553 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0028c0052t0002 | 0/0 | 3553 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0029c0051t0002 | 0/0 | 3553 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0030c0053t0002 | 0/0 | 3553 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0031c0049t0003 | 0/0 | 3553 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0032c0047t0003 | 0/0 | 3553 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
a0033c0038t0003 | 0/0 | 3553 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | copy fasta | chr17 | 75520697 | 75580209 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0224 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0300 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0315 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0316 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0325 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0326 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0354 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0002g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0008g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0001t0009g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0023t0002g0229 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0024t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0029t0001g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0001c0037t0001g0149 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0276 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0320 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0003g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0005 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0113 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0130 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0131 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0003t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0014 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0017 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0195 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0339 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0340 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0344 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0345 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0347 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0349 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0350 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0363 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0364 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0004t0003g0365 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0006t0003g0004 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0006t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0006t0003g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0006t0003g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0006t0003g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0006t0003g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0006t0003g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0006t0003g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0006t0003g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0006t0003g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0006t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0006t0003g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0006t0005g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0012t0003g0311 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0012t0003g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0012t0003g0324 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0013t0003g0192 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0013t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0013t0003g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0045t0003g0310 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0046t0005g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0048t0004g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0002c0055t0003g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0001g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0001g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0001g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0010 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0251 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0261 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0263 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0264 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0272 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0274 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0279 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0288 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0289 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0291 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0314 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0002t0002g0343 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0019t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0019t0002g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0021t0002g0277 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0021t0002g0331 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0003c0054t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0356 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0359 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0004g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0007g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0005t0007g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0007t0003g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0007t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0007t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0007t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0007t0003g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0007t0003g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0007t0003g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0007t0003g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0018t0005g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0018t0005g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0004c0050t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0005c0008t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0005c0008t0001g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0005c0008t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0005c0008t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0005c0008t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0005c0036t0001g0002 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0006c0009t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0006c0009t0004g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0006c0009t0004g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0006c0009t0007g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0006c0015t0005g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0006c0015t0005g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0007c0010t0002g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0007c0010t0002g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0007c0010t0002g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0008c0041t0003g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0008c0043t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0008c0044t0003g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0009c0011t0006g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0009c0011t0006g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0009c0011t0006g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0010c0014t0003g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0010c0014t0003g0338 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0011c0027t0005g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0011c0028t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0012c0022t0003g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0012c0022t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0013c0016t0003g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0013c0016t0003g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0014c0020t0003g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0014c0020t0003g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0015c0017t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0015c0017t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0016c0056t0001g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0017c0034t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0018c0031t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0019c0030t0001g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0020c0032t0002g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0021c0033t0001g0185 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0022c0035t0001g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0023c0026t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0024c0025t0007g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0025c0039t0004g0367 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0026c0042t0003g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0027c0040t0003g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0028c0052t0002g0001 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0029c0051t0002g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0030c0053t0002g0290 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0031c0049t0003g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0032c0047t0003g0366 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
a0033c0038t0003g0278 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0033 | EUR | GBR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00099 | hp2 | a0002 | c0003 | t0005 | g0130 | EUR | GBR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00140 | hp1 | a0002 | c0013 | t0003 | g0196 | EUR | GBR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00140 | hp2 | a0003 | c0002 | t0002 | g0234 | EUR | GBR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00323 | hp1 | a0001 | c0037 | t0001 | g0149 | EUR | FIN | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00323 | hp2 | a0001 | c0001 | t0002 | g0224 | EUR | FIN | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0071 | EAS | CHS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00408 | hp2 | a0002 | c0003 | t0005 | g0105 | EAS | CHS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00423 | hp1 | a0003 | c0002 | t0002 | g0218 | EAS | CHS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00423 | hp2 | a0029 | c0051 | t0002 | g0009 | EAS | CHS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00438 | hp1 | a0004 | c0005 | t0004 | g0307 | EAS | CHS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00438 | hp2 | a0001 | c0029 | t0001 | g0048 | EAS | CHS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0243 | EAS | CHS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0357 | EAS | CHS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | CHS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00597 | hp1 | a0003 | c0002 | t0002 | g0275 | EAS | CHS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00597 | hp2 | a0004 | c0005 | t0004 | g0361 | EAS | CHS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00609 | hp1 | a0006 | c0009 | t0007 | g0036 | EAS | CHS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00609 | hp2 | a0003 | c0002 | t0002 | g0297 | EAS | CHS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00621 | hp1 | a0003 | c0002 | t0002 | g0011 | EAS | CHS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | CHS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00639 | hp1 | a0002 | c0004 | t0003 | g0066 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00639 | hp2 | a0030 | c0053 | t0002 | g0290 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0123 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00642 | hp2 | a0002 | c0003 | t0005 | g0114 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00733 | hp1 | a0005 | c0036 | t0001 | g0002 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00733 | hp2 | a0003 | c0002 | t0002 | g0343 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00735 | hp1 | a0002 | c0004 | t0003 | g0350 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00735 | hp2 | a0026 | c0042 | t0003 | g0214 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0253 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00738 | hp2 | a0002 | c0004 | t0003 | g0013 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00741 | hp1 | a0005 | c0008 | t0001 | g0043 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG00741 | hp2 | a0006 | c0009 | t0004 | g0322 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01069 | hp1 | a0002 | c0004 | t0003 | g0017 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01069 | hp2 | a0002 | c0003 | t0003 | g0320 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01070 | hp2 | a0005 | c0008 | t0001 | g0046 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01071 | hp1 | a0002 | c0003 | t0003 | g0321 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01071 | hp2 | a0005 | c0008 | t0001 | g0002 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01074 | hp1 | a0003 | c0002 | t0002 | g0314 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01081 | hp1 | a0002 | c0003 | t0003 | g0248 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01099 | hp1 | a0003 | c0002 | t0002 | g0291 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01099 | hp2 | a0004 | c0005 | t0004 | g0207 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01106 | hp1 | a0004 | c0007 | t0003 | g0329 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0301 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01109 | hp1 | a0032 | c0047 | t0003 | g0366 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01109 | hp2 | a0003 | c0021 | t0002 | g0331 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01167 | hp1 | a0002 | c0004 | t0003 | g0346 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0300 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01168 | hp2 | a0001 | c0001 | t0009 | g0142 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0006 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01169 | hp2 | a0001 | c0001 | t0002 | g0299 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0099 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01243 | hp1 | a0002 | c0004 | t0003 | g0340 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01255 | hp1 | a0002 | c0003 | t0005 | g0125 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01255 | hp2 | a0003 | c0002 | t0002 | g0332 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01256 | hp1 | a0003 | c0002 | t0002 | g0252 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01256 | hp2 | a0002 | c0003 | t0005 | g0124 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01257 | hp1 | a0003 | c0002 | t0001 | g0171 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01257 | hp2 | a0004 | c0005 | t0004 | g0356 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01258 | hp1 | a0002 | c0003 | t0005 | g0129 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01258 | hp2 | a0004 | c0005 | t0004 | g0355 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0076 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0174 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01346 | hp2 | a0003 | c0002 | t0001 | g0170 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01358 | hp1 | a0002 | c0003 | t0005 | g0128 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01358 | hp2 | a0005 | c0008 | t0001 | g0030 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01361 | hp1 | a0002 | c0004 | t0003 | g0282 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01361 | hp2 | a0002 | c0004 | t0003 | g0195 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01433 | hp1 | a0003 | c0002 | t0002 | g0279 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01433 | hp2 | a0002 | c0004 | t0003 | g0348 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01496 | hp1 | a0003 | c0002 | t0002 | g0289 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0317 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01515 | hp1 | a0002 | c0003 | t0005 | g0005 | EUR | IBS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0318 | EUR | IBS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0326 | EUR | IBS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01516 | hp2 | a0003 | c0002 | t0002 | g0330 | EUR | IBS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01517 | hp1 | a0002 | c0003 | t0005 | g0005 | EUR | IBS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01517 | hp2 | a0001 | c0001 | t0002 | g0325 | EUR | IBS | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01884 | hp1 | a0002 | c0004 | t0003 | g0342 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01884 | hp2 | a0002 | c0006 | t0003 | g0313 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01891 | hp1 | a0025 | c0039 | t0004 | g0367 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01891 | hp2 | a0020 | c0032 | t0002 | g0055 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01928 | hp1 | a0033 | c0038 | t0003 | g0278 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01928 | hp2 | a0001 | c0001 | t0002 | g0327 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01934 | hp1 | a0002 | c0004 | t0003 | g0344 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01934 | hp2 | a0002 | c0046 | t0005 | g0119 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01943 | hp1 | a0003 | c0002 | t0002 | g0238 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01943 | hp2 | a0005 | c0008 | t0001 | g0032 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01952 | hp1 | a0003 | c0002 | t0002 | g0261 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0039 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01975 | hp1 | a0003 | c0002 | t0002 | g0010 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01975 | hp2 | a0002 | c0003 | t0003 | g0259 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01981 | hp1 | a0003 | c0002 | t0002 | g0272 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01981 | hp2 | a0003 | c0002 | t0002 | g0288 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01993 | hp1 | a0018 | c0031 | t0001 | g0177 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01993 | hp2 | a0003 | c0002 | t0002 | g0010 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02015 | hp1 | a0002 | c0003 | t0003 | g0250 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02027 | hp1 | a0003 | c0002 | t0002 | g0052 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0286 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02040 | hp1 | a0002 | c0003 | t0003 | g0226 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02040 | hp2 | a0006 | c0009 | t0004 | g0203 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02055 | hp1 | a0004 | c0007 | t0003 | g0021 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02055 | hp2 | a0022 | c0035 | t0001 | g0038 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02056 | hp1 | a0004 | c0005 | t0007 | g0069 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02056 | hp2 | a0003 | c0002 | t0002 | g0050 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02071 | hp1 | a0003 | c0002 | t0002 | g0237 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02071 | hp2 | a0004 | c0005 | t0004 | g0305 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02074 | hp1 | a0006 | c0009 | t0002 | g0204 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02074 | hp2 | a0003 | c0021 | t0002 | g0277 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02080 | hp1 | a0024 | c0025 | t0007 | g0037 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02080 | hp2 | a0004 | c0005 | t0004 | g0304 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02083 | hp1 | a0004 | c0005 | t0004 | g0302 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0180 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02129 | hp2 | a0003 | c0002 | t0002 | g0001 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02132 | hp1 | a0004 | c0005 | t0004 | g0303 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02132 | hp2 | a0003 | c0002 | t0002 | g0239 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02135 | hp1 | a0002 | c0003 | t0003 | g0241 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02145 | hp1 | a0010 | c0014 | t0003 | g0338 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02145 | hp2 | a0014 | c0020 | t0003 | g0094 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02148 | hp1 | a0011 | c0027 | t0005 | g0175 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02148 | hp2 | a0003 | c0002 | t0002 | g0264 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02155 | hp1 | a0004 | c0005 | t0004 | g0308 | EAS | CDX | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0155 | EAS | CDX | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | CDX | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02165 | hp2 | a0002 | c0003 | t0003 | g0246 | EAS | CDX | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02257 | hp1 | a0002 | c0004 | t0003 | g0283 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0200 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02258 | hp1 | a0013 | c0016 | t0003 | g0056 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02258 | hp2 | a0002 | c0006 | t0003 | g0004 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02280 | hp1 | a0006 | c0015 | t0005 | g0173 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02280 | hp2 | a0002 | c0003 | t0005 | g0126 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02293 | hp1 | a0003 | c0002 | t0002 | g0263 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0040 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02300 | hp2 | a0002 | c0003 | t0005 | g0054 | AMR | PEL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02451 | hp1 | a0004 | c0007 | t0003 | g0027 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02523 | hp1 | a0004 | c0005 | t0004 | g0306 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | KHV | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02572 | hp1 | a0002 | c0006 | t0003 | g0210 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02572 | hp2 | a0008 | c0044 | t0003 | g0097 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0315 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02615 | hp1 | a0015 | c0017 | t0003 | g0016 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02615 | hp2 | a0002 | c0006 | t0003 | g0086 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02622 | hp1 | a0002 | c0004 | t0003 | g0333 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02622 | hp2 | a0009 | c0011 | t0006 | g0018 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02630 | hp1 | a0009 | c0011 | t0006 | g0020 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02630 | hp2 | a0004 | c0007 | t0003 | g0312 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02647 | hp1 | a0009 | c0011 | t0006 | g0019 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02647 | hp2 | a0003 | c0019 | t0002 | g0212 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02683 | hp1 | a0002 | c0045 | t0003 | g0310 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0070 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02717 | hp1 | a0002 | c0048 | t0004 | g0087 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02717 | hp2 | a0002 | c0004 | t0003 | g0063 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0176 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02738 | hp1 | a0002 | c0003 | t0005 | g0108 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0316 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02809 | hp1 | a0012 | c0022 | t0003 | g0024 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02809 | hp2 | a0002 | c0004 | t0003 | g0351 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0201 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02818 | hp2 | a0014 | c0020 | t0003 | g0064 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02886 | hp2 | a0012 | c0022 | t0003 | g0022 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02895 | hp1 | a0004 | c0018 | t0005 | g0190 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02895 | hp2 | a0015 | c0017 | t0003 | g0026 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02896 | hp1 | a0004 | c0005 | t0004 | g0057 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02896 | hp2 | a0004 | c0007 | t0003 | g0199 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02897 | hp1 | a0004 | c0005 | t0004 | g0058 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02897 | hp2 | a0004 | c0018 | t0005 | g0109 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02922 | hp1 | a0031 | c0049 | t0003 | g0065 | AFR | ESN | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02922 | hp2 | a0004 | c0005 | t0004 | g0211 | AFR | ESN | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02965 | hp1 | a0002 | c0004 | t0003 | g0363 | AFR | ESN | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02965 | hp2 | a0004 | c0005 | t0004 | g0208 | AFR | ESN | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02970 | hp1 | a0004 | c0005 | t0004 | g0003 | AFR | ESN | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02970 | hp2 | a0002 | c0004 | t0003 | g0067 | AFR | ESN | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02976 | hp1 | a0008 | c0043 | t0003 | g0023 | AFR | ESN | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02976 | hp2 | a0002 | c0013 | t0003 | g0334 | AFR | ESN | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03017 | hp1 | a0002 | c0012 | t0003 | g0323 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0147 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03041 | hp1 | a0004 | c0007 | t0003 | g0309 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03041 | hp2 | a0002 | c0004 | t0003 | g0089 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03139 | hp1 | a0002 | c0004 | t0003 | g0365 | AFR | ESN | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03139 | hp2 | a0002 | c0004 | t0003 | g0339 | AFR | ESN | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03195 | hp1 | a0002 | c0004 | t0003 | g0336 | AFR | ESN | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03195 | hp2 | a0013 | c0016 | t0003 | g0061 | AFR | ESN | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03209 | hp1 | a0003 | c0019 | t0002 | g0095 | AFR | MSL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03209 | hp2 | a0002 | c0006 | t0003 | g0025 | AFR | MSL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03225 | hp1 | a0011 | c0028 | t0003 | g0187 | AFR | MSL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03225 | hp2 | a0004 | c0050 | t0006 | g0062 | AFR | MSL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03239 | hp1 | a0001 | c0001 | t0002 | g0230 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0145 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03486 | hp1 | a0002 | c0006 | t0005 | g0112 | AFR | MSL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03486 | hp2 | a0027 | c0040 | t0003 | g0188 | AFR | MSL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03490 | hp2 | a0002 | c0003 | t0005 | g0113 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0169 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03491 | hp2 | a0003 | c0002 | t0002 | g0206 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03492 | hp1 | a0003 | c0002 | t0002 | g0209 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03492 | hp2 | a0002 | c0003 | t0005 | g0127 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03516 | hp1 | a0002 | c0004 | t0003 | g0364 | AFR | ESN | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03516 | hp2 | a0002 | c0006 | t0003 | g0093 | AFR | ESN | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03540 | hp1 | a0010 | c0014 | t0003 | g0015 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03540 | hp2 | a0004 | c0005 | t0004 | g0060 | AFR | GWD | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03654 | hp1 | a0002 | c0004 | t0003 | g0345 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0144 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03688 | hp1 | a0001 | c0023 | t0002 | g0229 | SAS | STU | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0068 | SAS | STU | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03704 | hp1 | a0003 | c0002 | t0002 | g0266 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03704 | hp2 | a0016 | c0056 | t0001 | g0136 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03710 | hp1 | a0004 | c0005 | t0004 | g0194 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03831 | hp2 | a0002 | c0004 | t0003 | g0349 | SAS | BEB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0163 | SAS | BEB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03834 | hp2 | a0003 | c0002 | t0001 | g0102 | SAS | BEB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03927 | hp1 | a0004 | c0005 | t0004 | g0359 | SAS | BEB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03927 | hp2 | a0003 | c0002 | t0001 | g0083 | SAS | BEB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03942 | hp2 | a0002 | c0012 | t0003 | g0324 | SAS | BEB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG04115 | hp1 | a0002 | c0012 | t0003 | g0311 | SAS | STU | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | STU | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0228 | SAS | STU | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | STU | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG04204 | hp1 | a0017 | c0034 | t0001 | g0141 | SAS | STU | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG04204 | hp2 | a0002 | c0013 | t0003 | g0192 | SAS | STU | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18522 | hp1 | a0008 | c0041 | t0003 | g0092 | AFR | YRI | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18522 | hp2 | a0002 | c0055 | t0003 | g0215 | AFR | YRI | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18747 | hp1 | a0002 | c0003 | t0003 | g0242 | EAS | CHB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18747 | hp2 | a0003 | c0002 | t0002 | g0265 | EAS | CHB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18906 | hp1 | a0002 | c0006 | t0003 | g0096 | AFR | YRI | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18906 | hp2 | a0002 | c0004 | t0003 | g0352 | AFR | YRI | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18940 | hp1 | a0003 | c0002 | t0002 | g0274 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18941 | hp1 | a0001 | c0001 | t0002 | g0293 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18941 | hp2 | a0003 | c0002 | t0002 | g0223 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18943 | hp1 | a0001 | c0024 | t0002 | g0217 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18943 | hp2 | a0001 | c0001 | t0002 | g0284 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18944 | hp1 | a0003 | c0002 | t0002 | g0011 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18947 | hp2 | a0003 | c0002 | t0002 | g0294 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18948 | hp1 | a0028 | c0052 | t0002 | g0001 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18950 | hp1 | a0003 | c0002 | t0002 | g0232 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18953 | hp2 | a0003 | c0002 | t0002 | g0292 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18954 | hp1 | a0003 | c0002 | t0002 | g0227 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0049 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18957 | hp1 | a0003 | c0002 | t0002 | g0257 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0081 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18961 | hp2 | a0003 | c0002 | t0002 | g0009 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18962 | hp1 | a0003 | c0002 | t0002 | g0262 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18962 | hp2 | a0004 | c0005 | t0007 | g0106 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0074 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0073 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18969 | hp1 | a0007 | c0010 | t0002 | g0287 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18969 | hp2 | a0004 | c0005 | t0004 | g0298 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18970 | hp2 | a0002 | c0003 | t0003 | g0244 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18971 | hp1 | a0002 | c0003 | t0003 | g0247 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18971 | hp2 | a0003 | c0002 | t0002 | g0051 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18972 | hp2 | a0003 | c0002 | t0002 | g0225 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18977 | hp1 | a0004 | c0005 | t0004 | g0273 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18977 | hp2 | a0002 | c0003 | t0003 | g0271 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18979 | hp2 | a0003 | c0054 | t0001 | g0107 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18980 | hp1 | a0003 | c0002 | t0002 | g0295 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18980 | hp2 | a0001 | c0001 | t0002 | g0216 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18981 | hp2 | a0003 | c0002 | t0002 | g0213 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18982 | hp2 | a0004 | c0005 | t0004 | g0360 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0116 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18983 | hp2 | a0003 | c0002 | t0002 | g0008 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18987 | hp1 | a0002 | c0003 | t0003 | g0256 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18987 | hp2 | a0001 | c0001 | t0001 | g0077 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18989 | hp2 | a0002 | c0003 | t0003 | g0240 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18990 | hp1 | a0003 | c0002 | t0002 | g0008 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0035 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18995 | hp1 | a0002 | c0003 | t0003 | g0270 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18995 | hp2 | a0003 | c0002 | t0002 | g0280 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18999 | hp1 | a0007 | c0010 | t0002 | g0012 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18999 | hp2 | a0023 | c0026 | t0001 | g0151 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19005 | hp1 | a0003 | c0002 | t0002 | g0222 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19005 | hp2 | a0003 | c0002 | t0001 | g0053 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19007 | hp1 | a0007 | c0010 | t0002 | g0296 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19010 | hp1 | a0003 | c0002 | t0002 | g0255 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19011 | hp2 | a0002 | c0003 | t0005 | g0104 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19012 | hp1 | a0002 | c0003 | t0003 | g0276 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19030 | hp1 | a0002 | c0003 | t0003 | g0328 | AFR | LWK | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19030 | hp2 | a0003 | c0002 | t0002 | g0202 | AFR | LWK | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19043 | hp1 | a0002 | c0004 | t0003 | g0335 | AFR | LWK | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19043 | hp2 | a0002 | c0006 | t0003 | g0088 | AFR | LWK | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19054 | hp2 | a0003 | c0002 | t0002 | g0235 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19055 | hp1 | a0002 | c0003 | t0005 | g0103 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19056 | hp2 | a0003 | c0002 | t0002 | g0258 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19057 | hp1 | a0003 | c0002 | t0002 | g0236 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19058 | hp1 | a0003 | c0002 | t0002 | g0260 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19058 | hp2 | a0002 | c0003 | t0003 | g0220 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0285 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19074 | hp1 | a0002 | c0003 | t0003 | g0249 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19077 | hp1 | a0003 | c0002 | t0002 | g0268 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0028 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0358 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19079 | hp2 | a0007 | c0010 | t0002 | g0012 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19080 | hp1 | a0002 | c0003 | t0005 | g0118 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19080 | hp2 | a0001 | c0001 | t0002 | g0362 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19081 | hp1 | a0001 | c0001 | t0008 | g0041 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19081 | hp2 | a0003 | c0002 | t0002 | g0231 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19084 | hp1 | a0002 | c0003 | t0003 | g0245 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19084 | hp2 | a0003 | c0002 | t0002 | g0254 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19085 | hp1 | a0003 | c0002 | t0002 | g0233 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0084 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0354 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19088 | hp2 | a0003 | c0002 | t0002 | g0269 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19090 | hp1 | a0003 | c0002 | t0002 | g0281 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19091 | hp1 | a0003 | c0002 | t0002 | g0001 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19240 | hp1 | a0002 | c0004 | t0003 | g0341 | AFR | YRI | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA19240 | hp2 | a0002 | c0006 | t0003 | g0098 | AFR | YRI | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA20129 | hp1 | a0002 | c0003 | t0005 | g0133 | AFR | ASW | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA20129 | hp2 | a0004 | c0007 | t0003 | g0091 | AFR | ASW | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA20752 | hp1 | a0002 | c0004 | t0003 | g0014 | EUR | TSI | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | TSI | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA20805 | hp1 | a0002 | c0004 | t0003 | g0014 | EUR | TSI | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA20805 | hp2 | a0019 | c0030 | t0001 | g0138 | EUR | TSI | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA20905 | hp1 | a0021 | c0033 | t0001 | g0185 | SAS | GIH | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA20905 | hp2 | a0004 | c0007 | t0003 | g0205 | SAS | GIH | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01123 | hp1 | a0002 | c0003 | t0005 | g0132 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG01123 | hp2 | a0002 | c0004 | t0003 | g0353 | AMR | CLM | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02109 | hp1 | a0002 | c0004 | t0003 | g0337 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02109 | hp2 | a0002 | c0006 | t0003 | g0059 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02486 | hp1 | a0002 | c0006 | t0003 | g0004 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0319 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02559 | hp1 | a0002 | c0004 | t0003 | g0347 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG02559 | hp2 | a0006 | c0015 | t0005 | g0172 | AFR | ACB | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03471 | hp1 | a0002 | c0004 | t0003 | g0013 | AFR | MSL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG03471 | hp2 | a0004 | c0005 | t0004 | g0003 | AFR | MSL | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0168 | AFR | USA | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
HG06807 | hp2 | a0002 | c0006 | t0003 | g0090 | AFR | USA | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18955 | hp1 | a0003 | c0002 | t0002 | g0267 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA20300 | hp1 | a0003 | c0002 | t0002 | g0189 | AFR | USA | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
NA20300 | hp2 | a0002 | c0006 | t0003 | g0085 | AFR | USA | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
homoSapiens_chm13v2 | hp1 | a0002 | c0003 | t0005 | g0131 | REF | REF | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
homoSapiens_grch38 | hp1 | a0003 | c0002 | t0002 | g0251 | REF | REF | LLGL2_chr17_75520697_75580209 | LLGL2 | chr17 | 75520697 | 75580209 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:75543479
|
G | A | 1 | a0010 | 2 | HG02145.hp1 HG03540.hp1 |
missense_variant | MODERATE | c.53G>A | p.Arg18Gln | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/26 | 212/3553 | 53/3063 | 18/1020 | chr17 | 75543479 | ||
chr17:75556047
|
C | T | 1 | a0016 | 1 | HG03704.hp2 | missense_variant&splice_region_variant | MODERATE | c.77C>T | p.Thr26Met | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/26 | 236/3553 | 77/3063 | 26/1020 | chr17 | 75556047 | ||
chr17:75556104
|
G | A | 13 | a0001a0005a0006others(10): Show | 146 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(143): Show |
missense_variant | MODERATE | c.134G>A | p.Arg45His | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/26 | 293/3553 | 134/3063 | 45/1020 | chr17 | 75556104 | ||
chr17:75558211
|
C | T | 1 | a0012 | 2 | HG02809.hp1 HG02886.hp2 |
missense_variant | MODERATE | c.230C>T | p.Thr77Met | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 4/26 | 389/3553 | 230/3063 | 77/1020 | chr17 | 75558211 | ||
chr17:75558231
|
G | A | 1 | a0033 | 1 | HG01928.hp1 | missense_variant | MODERATE | c.250G>A | p.Gly84Ser | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 4/26 | 409/3553 | 250/3063 | 84/1020 | chr17 | 75558231 | ||
chr17:75559365
|
G | A | 1 | a0025 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.485G>A | p.Arg162His | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/26 | 644/3553 | 485/3063 | 162/1020 | chr17 | 75559365 | ||
chr17:75559397
|
G | A | 1 | a0009 | 3 | HG02622.hp2 HG02630.hp1 HG02647.hp1 |
missense_variant | MODERATE | c.517G>A | p.Ala173Thr | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/26 | 676/3553 | 517/3063 | 173/1020 | chr17 | 75559397 | ||
chr17:75563412
|
G | A | 4 | a0008a0012a0026others(1): Show | 7 | HG00735.hp2 HG02572.hp2 HG02809.hp1 others(4): Show |
missense_variant | MODERATE | c.775G>A | p.Val259Met | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 8/26 | 934/3553 | 775/3063 | 259/1020 | chr17 | 75563412 | ||
chr17:75563412
|
G | T | 1 | a0005 | 6 | HG00733.hp1 HG00741.hp1 HG01070.hp2 others(3): Show |
missense_variant | MODERATE | c.775G>T | p.Val259Leu | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 8/26 | 934/3553 | 775/3063 | 259/1020 | chr17 | 75563412 | ||
chr17:75568676
|
G | A | 1 | a0024 | 1 | HG02080.hp1 | missense_variant | MODERATE | c.1237G>A | p.Ala413Thr | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 11/26 | 1396/3553 | 1237/3063 | 413/1020 | chr17 | 75568676 | ||
chr17:75568800
|
T | TGACCCCA others(10): Show |
1 | a0023 | 1 | NA18999.hp2 | frameshift_variant | HIGH | c.1284_1300dupGACCCC others(11): Show |
p.Gln434fs | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 12/26 | 1460/3553 | 1301/3063 | 434/1020 | INFO_REALIGN_3_PRIME | chr17 | 75568800 | |
chr17:75569090
|
T | C | 18 | a0002a0004a0006others(15): Show | 164 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(161): Show |
missense_variant | MODERATE | c.1435T>C | p.Phe479Leu | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 13/26 | 1594/3553 | 1435/3063 | 479/1020 | chr17 | 75569090 | ||
chr17:75569286
|
G | T | 1 | a0030 | 1 | HG00639.hp2 | missense_variant | MODERATE | c.1542G>T | p.Lys514Asn | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 14/26 | 1701/3553 | 1542/3063 | 514/1020 | chr17 | 75569286 | ||
chr17:75570013
|
G | C | 2 | a0013a0014 | 4 | HG02145.hp2 HG02258.hp1 HG02818.hp2 others(1): Show |
missense_variant | MODERATE | c.1632G>C | p.Gln544His | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 15/26 | 1791/3553 | 1632/3063 | 544/1020 | chr17 | 75570013 | ||
chr17:75570020
|
G | A | 1 | a0007 | 4 | NA18969.hp1 NA18999.hp1 NA19007.hp1 others(1): Show |
missense_variant | MODERATE | c.1639G>A | p.Ala547Thr | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 15/26 | 1798/3553 | 1639/3063 | 547/1020 | chr17 | 75570020 | ||
chr17:75570036
|
A | G | 1 | a0022 | 1 | HG02055.hp2 | missense_variant | MODERATE | c.1655A>G | p.Asp552Gly | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 15/26 | 1814/3553 | 1655/3063 | 552/1020 | chr17 | 75570036 | ||
chr17:75570080
|
C | T | 1 | a0017 | 1 | HG04204.hp1 | missense_variant | MODERATE | c.1699C>T | p.Arg567Cys | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 15/26 | 1858/3553 | 1699/3063 | 567/1020 | chr17 | 75570080 | ||
chr17:75570090
|
C | G | 1 | a0021 | 1 | NA20905.hp1 | missense_variant | MODERATE | c.1709C>G | p.Pro570Arg | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 15/26 | 1868/3553 | 1709/3063 | 570/1020 | chr17 | 75570090 | ||
chr17:75570388
|
C | T | 1 | a0014 | 2 | HG02145.hp2 HG02818.hp2 |
missense_variant | MODERATE | c.1915C>T | p.Pro639Ser | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 16/26 | 2074/3553 | 1915/3063 | 639/1020 | chr17 | 75570388 | ||
chr17:75570959
|
G | A | 1 | a0032 | 1 | HG01109.hp1 | missense_variant | MODERATE | c.2035G>A | p.Gly679Arg | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 17/26 | 2194/3553 | 2035/3063 | 679/1020 | chr17 | 75570959 | ||
chr17:75571016
|
C | T | 1 | a0028 | 1 | NA18948.hp1 | missense_variant | MODERATE | c.2092C>T | p.Arg698Cys | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 17/26 | 2251/3553 | 2092/3063 | 698/1020 | chr17 | 75571016 | ||
chr17:75571079
|
G | A | 1 | a0027 | 1 | HG03486.hp2 | missense_variant | MODERATE | c.2155G>A | p.Ala719Thr | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 17/26 | 2314/3553 | 2155/3063 | 719/1020 | chr17 | 75571079 | ||
chr17:75571733
|
G | A | 1 | a0015 | 2 | HG02615.hp1 HG02895.hp2 |
missense_variant | MODERATE | c.2243G>A | p.Arg748His | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 18/26 | 2402/3553 | 2243/3063 | 748/1020 | chr17 | 75571733 | ||
chr17:75571765
|
C | T | 8 | a0002a0009a0010others(5): Show | 110 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(107): Show |
missense_variant | MODERATE | c.2275C>T | p.Pro759Ser | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 18/26 | 2434/3553 | 2275/3063 | 759/1020 | chr17 | 75571765 | ||
chr17:75573227
|
C | T | 1 | a0020 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.2674C>T | p.Arg892Trp | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 20/26 | 2833/3553 | 2674/3063 | 892/1020 | chr17 | 75573227 | ||
chr17:75573257
|
G | A | 1 | a0020 | 1 | HG01891.hp2 | missense_variant | MODERATE | c.2704G>A | p.Val902Ile | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 20/26 | 2863/3553 | 2704/3063 | 902/1020 | chr17 | 75573257 | ||
chr17:75573585
|
C | T | 1 | a0018 | 1 | HG01993.hp1 | missense_variant | MODERATE | c.2830C>T | p.Arg944Cys | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 21/26 | 2989/3553 | 2830/3063 | 944/1020 | chr17 | 75573585 | ||
chr17:75573625
|
G | A | 1 | a0026 | 1 | HG00735.hp2 | missense_variant | MODERATE | c.2870G>A | p.Arg957Gln | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 21/26 | 3029/3553 | 2870/3063 | 957/1020 | chr17 | 75573625 | ||
chr17:75574251
|
A | T | 1 | a0029 | 1 | HG00423.hp2 | missense_variant | MODERATE | c.2944A>T | p.Ser982Cys | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 23/26 | 3103/3553 | 2944/3063 | 982/1020 | chr17 | 75574251 | ||
chr17:75574614
|
G | A | 1 | a0019 | 1 | NA20805.hp2 | missense_variant | MODERATE | c.3001G>A | p.Gly1001Ser | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 25/26 | 3160/3553 | 3001/3063 | 1001/1020 | chr17 | 75574614 | ||
chr17:75574623
|
C | T | 1 | a0031 | 1 | HG02922.hp1 | missense_variant | MODERATE | c.3010C>T | p.Arg1004Cys | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 25/26 | 3169/3553 | 3010/3063 | 1004/1020 | chr17 | 75574623 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:75558203
|
C | T | 1 | a0001c0037 | 1 | HG00323.hp1 | synonymous_variant | LOW | c.222C>T | p.Asn74Asn | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 4/26 | 381/3553 | 222/3063 | 74/1020 | chr17 | 75558203 | ||
chr17:75558212
|
G | A | 1 | a0001c0023 | 1 | HG03688.hp1 | synonymous_variant | LOW | c.231G>A | p.Thr77Thr | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 4/26 | 390/3553 | 231/3063 | 77/1020 | chr17 | 75558212 | ||
chr17:75558230
|
C | T | 1 | a0003c0021 | 2 | HG01109.hp2 HG02074.hp2 |
synonymous_variant | LOW | c.249C>T | p.Pro83Pro | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 4/26 | 408/3553 | 249/3063 | 83/1020 | chr17 | 75558230 | ||
chr17:75559396
|
C | T | 1 | a0002c0055 | 1 | NA18522.hp2 | synonymous_variant | LOW | c.516C>T | p.Asp172Asp | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/26 | 675/3553 | 516/3063 | 172/1020 | chr17 | 75559396 | ||
chr17:75563360
|
C | T | 1 | a0002c0013 | 3 | HG00140.hp1 HG02976.hp2 HG04204.hp2 |
synonymous_variant | LOW | c.723C>T | p.Asp241Asp | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 8/26 | 882/3553 | 723/3063 | 241/1020 | chr17 | 75563360 | ||
chr17:75563372
|
C | T | 1 | a0014c0020 | 2 | HG02145.hp2 HG02818.hp2 |
synonymous_variant | LOW | c.735C>T | p.Leu245Leu | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 8/26 | 894/3553 | 735/3063 | 245/1020 | chr17 | 75563372 | ||
chr17:75564401
|
G | A | 1 | a0002c0012 | 3 | HG03017.hp1 HG03942.hp2 HG04115.hp1 |
synonymous_variant | LOW | c.930G>A | p.Gly310Gly | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/26 | 1089/3553 | 930/3063 | 310/1020 | chr17 | 75564401 | ||
chr17:75568558
|
G | A | 1 | a0001c0024 | 1 | NA18943.hp1 | synonymous_variant | LOW | c.1119G>A | p.Pro373Pro | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 11/26 | 1278/3553 | 1119/3063 | 373/1020 | chr17 | 75568558 | ||
chr17:75568657
|
C | T | 1 | a0003c0054 | 1 | NA18979.hp2 | synonymous_variant | LOW | c.1218C>T | p.Ala406Ala | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 11/26 | 1377/3553 | 1218/3063 | 406/1020 | chr17 | 75568657 | ||
chr17:75568795
|
C | A | 1 | a0023c0026 | 1 | NA18999.hp2 | synonymous_variant | LOW | c.1278C>A | p.Thr426Thr | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 12/26 | 1437/3553 | 1278/3063 | 426/1020 | chr17 | 75568795 | ||
chr17:75568831
|
G | A | 1 | a0002c0045 | 1 | HG02683.hp1 | synonymous_variant | LOW | c.1314G>A | p.Leu438Leu | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 12/26 | 1473/3553 | 1314/3063 | 438/1020 | chr17 | 75568831 | ||
chr17:75569083
|
C | T | 5 | a0003c0019a0008c0043a0008c0044others(2): Show | 7 | HG00735.hp2 HG02572.hp2 HG02647.hp2 others(4): Show |
synonymous_variant | LOW | c.1428C>T | p.Asn476Asn | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 13/26 | 1587/3553 | 1428/3063 | 476/1020 | chr17 | 75569083 | ||
chr17:75569119
|
C | T | 5 | a0004c0018a0004c0050a0008c0041others(2): Show | 7 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(4): Show |
synonymous_variant | LOW | c.1464C>T | p.Pro488Pro | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 13/26 | 1623/3553 | 1464/3063 | 488/1020 | chr17 | 75569119 | ||
chr17:75570480
|
G | A | 6 | a0002c0003a0002c0012a0002c0045others(3): Show | 47 | HG00099.hp2 HG00408.hp2 HG00642.hp2 others(44): Show |
synonymous_variant | LOW | c.2007G>A | p.Pro669Pro | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 16/26 | 2166/3553 | 2007/3063 | 669/1020 | chr17 | 75570480 | ||
chr17:75571764
|
G | A | 1 | a0001c0029 | 1 | HG00438.hp2 | synonymous_variant | LOW | c.2274G>A | p.Glu758Glu | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 18/26 | 2433/3553 | 2274/3063 | 758/1020 | chr17 | 75571764 | ||
chr17:75571950
|
C | T | 2 | a0004c0007a0006c0015 | 10 | HG01106.hp1 HG02055.hp1 HG02280.hp1 others(7): Show |
synonymous_variant | LOW | c.2346C>T | p.Leu782Leu | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/26 | 2505/3553 | 2346/3063 | 782/1020 | chr17 | 75571950 | ||
chr17:75571974
|
C | T | 9 | a0002c0003a0002c0004a0002c0012others(6): Show | 83 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(80): Show |
synonymous_variant | LOW | c.2370C>T | p.Pro790Pro | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/26 | 2529/3553 | 2370/3063 | 790/1020 | chr17 | 75571974 | ||
chr17:75573034
|
G | A | 1 | a0005c0036 | 1 | HG00733.hp1 | synonymous_variant | LOW | c.2481G>A | p.Val827Val | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 20/26 | 2640/3553 | 2481/3063 | 827/1020 | chr17 | 75573034 | ||
chr17:75573077
|
A | C | 1 | a0032c0047 | 1 | HG01109.hp1 | synonymous_variant | LOW | c.2524A>C | p.Arg842Arg | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 20/26 | 2683/3553 | 2524/3063 | 842/1020 | chr17 | 75573077 | ||
chr17:75573500
|
C | T | 1 | a0015c0017 | 2 | HG02615.hp1 HG02895.hp2 |
synonymous_variant | LOW | c.2745C>T | p.Pro915Pro | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 21/26 | 2904/3553 | 2745/3063 | 915/1020 | chr17 | 75573500 | ||
chr17:75573620
|
G | A | 2 | a0002c0046a0032c0047 | 2 | HG01109.hp1 HG01934.hp2 |
synonymous_variant | LOW | c.2865G>A | p.Pro955Pro | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 21/26 | 3024/3553 | 2865/3063 | 955/1020 | chr17 | 75573620 | ||
chr17:75574637
|
C | G | 19 | a0002c0003a0002c0004a0002c0006others(16): Show | 112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
synonymous_variant | LOW | c.3024C>G | p.Ala1008Ala | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 25/26 | 3183/3553 | 3024/3063 | 1008/1020 | chr17 | 75574637 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:75525777
|
G | GCGCCGAG others(3): Show |
25 | a0001c0001t0001a0001c0001t0008a0001c0001t0009others(22): Show | 145 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(142): Show |
5_prime_UTR_variant | MODIFIER | c.-70_-61dupGACGCCGA others(2): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/26 | 17631 | INFO_REALIGN_3_PRIME | chr17 | 75525777 | ||||
chr17:75574949
|
A | G | 37 | a0002c0003t0003a0002c0003t0005a0002c0004t0003others(34): Show | 163 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(160): Show |
3_prime_UTR_variant | MODIFIER | c.*71A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 26/26 | 71 | chr17 | 75574949 | |||||
chr17:75574977
|
C | A | 2 | a0004c0050t0006a0009c0011t0006 | 4 | HG02622.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*99C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 26/26 | 99 | chr17 | 75574977 | |||||
chr17:75575007
|
A | G | 1 | a0001c0001t0009 | 1 | HG01168.hp2 | 3_prime_UTR_variant | MODIFIER | c.*129A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 26/26 | 129 | chr17 | 75575007 | |||||
chr17:75575074
|
T | C | 7 | a0002c0048t0004a0004c0005t0004a0004c0005t0007others(4): Show | 31 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
3_prime_UTR_variant | MODIFIER | c.*196T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 26/26 | 196 | chr17 | 75575074 | |||||
chr17:75575153
|
T | C | 1 | a0001c0001t0008 | 1 | NA19081.hp1 | 3_prime_UTR_variant | MODIFIER | c.*275T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 26/26 | 275 | chr17 | 75575153 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:75525980
|
G | C | 1 | a0010c0014t0003g0015 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.-31+155G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75525980 | ||||||
chr17:75526022
|
A | G | 62 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(59): Show | 64 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.-31+197A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75526022 | ||||||
chr17:75526164
|
C | G | 1 | a0025c0039t0004g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-31+339C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75526164 | ||||||
chr17:75526364
|
C | A | 11 | a0002c0004t0003g0017a0002c0006t0003g0025a0004c0007t0003g0021others(8): Show | 11 | HG01069.hp1 HG02055.hp1 HG02615.hp1 others(8): Show |
intron_variant | MODIFIER | c.-31+539C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75526364 | ||||||
chr17:75526489
|
A | T | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-31+664A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75526489 | ||||||
chr17:75526552
|
G | T | 1 | a0015c0017t0003g0026 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.-31+727G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75526552 | ||||||
chr17:75526632
|
C | T | 7 | a0004c0005t0004g0302a0004c0005t0004g0303a0004c0005t0004g0304others(4): Show | 7 | HG00438.hp1 HG02071.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+807C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75526632 | ||||||
chr17:75526702
|
G | T | 1 | a0001c0001t0001g0301 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.-31+877G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75526702 | ||||||
chr17:75526740
|
G | C | 21 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(18): Show | 21 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(18): Show |
intron_variant | MODIFIER | c.-31+915G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75526740 | ||||||
chr17:75526768
|
G | A | 6 | a0002c0004t0003g0017a0009c0011t0006g0018a0009c0011t0006g0019others(3): Show | 6 | HG01069.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-31+943G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75526768 | ||||||
chr17:75526923
|
T | C | 28 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0031others(25): Show | 28 | HG00099.hp1 HG00438.hp2 HG00609.hp1 others(25): Show |
intron_variant | MODIFIER | c.-31+1098T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75526923 | ||||||
chr17:75526931
|
G | A | 2 | a0025c0039t0004g0367a0032c0047t0003g0366 | 2 | HG01109.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.-31+1106G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75526931 | ||||||
chr17:75526960
|
G | A | 1 | a0002c0003t0005g0054 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-31+1135G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75526960 | ||||||
chr17:75527050
|
TC | T | 14 | a0002c0004t0003g0063a0002c0004t0003g0066a0002c0004t0003g0067others(11): Show | 15 | HG00639.hp1 HG01891.hp2 HG02109.hp2 others(12): Show |
intron_variant | MODIFIER | c.-31+1228delC | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75527050 | |||||
chr17:75527142
|
C | T | 3 | a0002c0004t0003g0363a0002c0004t0003g0364a0002c0004t0003g0365 | 3 | HG02965.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.-31+1317C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75527142 | ||||||
chr17:75527167
|
C | CA | 58 | a0001c0001t0001g0191a0001c0001t0001g0193a0001c0001t0001g0197others(55): Show | 59 | HG00140.hp1 HG00438.hp1 HG00639.hp1 others(56): Show |
intron_variant | MODIFIER | c.-31+1359dupA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75527167 | |||||
chr17:75527167
|
C | CAA | 141 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0029others(138): Show | 145 | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(142): Show |
intron_variant | MODIFIER | c.-31+1358_-31+1359d others(4): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75527167 | |||||
chr17:75527167
|
C | CAAA | 13 | a0001c0001t0001g0028a0001c0001t0001g0068a0001c0001t0001g0070others(10): Show | 13 | HG00408.hp1 HG01261.hp2 HG02056.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+1357_-31+1359d others(5): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75527167 | |||||
chr17:75527167
|
CA | C | 53 | a0001c0001t0002g0299a0001c0001t0002g0300a0001c0001t0002g0315others(50): Show | 55 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.-31+1359delA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75527167 | |||||
chr17:75527167
|
CAAAA | C | 9 | a0001c0001t0002g0354a0001c0001t0002g0357a0001c0001t0002g0358others(6): Show | 9 | HG00544.hp2 HG00597.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31+1356_-31+1359d others(6): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75527167 | |||||
chr17:75527331
|
A | G | 1 | a0001c0001t0001g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-31+1506A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75527331 | ||||||
chr17:75527369
|
C | T | 1 | a0021c0033t0001g0185 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.-31+1544C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75527369 | ||||||
chr17:75527405
|
T | C | 1 | a0025c0039t0004g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-31+1580T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75527405 | ||||||
chr17:75527490
|
G | T | 9 | a0001c0001t0002g0354a0001c0001t0002g0357a0001c0001t0002g0358others(6): Show | 9 | HG00544.hp2 HG00597.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31+1665G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75527490 | ||||||
chr17:75527529
|
C | T | 8 | a0001c0001t0001g0007a0001c0001t0001g0079a0001c0001t0001g0179others(5): Show | 9 | HG00621.hp2 HG02083.hp2 HG02135.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31+1704C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75527529 | ||||||
chr17:75527562
|
A | G | 2 | a0001c0001t0001g0178a0018c0031t0001g0177 | 2 | HG01070.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.-31+1737A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75527562 | ||||||
chr17:75527732
|
G | A | 1 | a0003c0002t0002g0213 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.-31+1907G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75527732 | ||||||
chr17:75527775
|
CT | C | 64 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(61): Show | 66 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(63): Show |
intron_variant | MODIFIER | c.-31+1961delT | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75527775 | |||||
chr17:75527918
|
G | T | 30 | a0002c0004t0003g0013a0002c0004t0003g0014a0002c0004t0003g0333others(27): Show | 32 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.-31+2093G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75527918 | ||||||
chr17:75527919
|
C | A | 30 | a0002c0004t0003g0013a0002c0004t0003g0014a0002c0004t0003g0333others(27): Show | 32 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.-31+2094C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75527919 | ||||||
chr17:75527961
|
AT | A | 62 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(59): Show | 64 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(61): Show |
intron_variant | MODIFIER | c.-31+2146delT | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75527961 | |||||
chr17:75528060
|
G | T | 30 | a0002c0004t0003g0013a0002c0004t0003g0014a0002c0004t0003g0333others(27): Show | 32 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(29): Show |
intron_variant | MODIFIER | c.-31+2235G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75528060 | ||||||
chr17:75528091
|
T | C | 3 | a0001c0001t0001g0080a0001c0001t0001g0081a0001c0001t0001g0082 | 3 | NA18957.hp2 NA19010.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.-31+2266T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75528091 | ||||||
chr17:75528146
|
C | T | 2 | a0003c0019t0002g0212a0004c0005t0004g0211 | 2 | HG02647.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.-31+2321C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75528146 | ||||||
chr17:75528178
|
A | C | 63 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(60): Show | 65 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.-31+2353A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75528178 | ||||||
chr17:75528185
|
G | T | 15 | a0002c0006t0003g0210a0003c0002t0002g0206a0003c0002t0002g0209others(12): Show | 15 | HG00438.hp1 HG01099.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.-31+2360G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75528185 | ||||||
chr17:75528298
|
G | A | 1 | a0026c0042t0003g0214 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.-31+2473G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75528298 | ||||||
chr17:75528336
|
C | T | 1 | a0002c0003t0005g0054 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.-31+2511C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75528336 | ||||||
chr17:75528394
|
C | T | 1 | a0002c0004t0003g0067 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-31+2569C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75528394 | ||||||
chr17:75528395
|
G | C | 3 | a0002c0004t0003g0017a0015c0017t0003g0016a0015c0017t0003g0026 | 3 | HG01069.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-31+2570G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75528395 | ||||||
chr17:75528406
|
C | T | 1 | a0003c0002t0002g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-31+2581C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75528406 | ||||||
chr17:75528569
|
T | C | 3 | a0003c0002t0002g0330a0003c0002t0002g0332a0003c0021t0002g0331 | 3 | HG01109.hp2 HG01255.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-31+2744T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75528569 | ||||||
chr17:75528739
|
A | AAAACAAA others(1): Show |
63 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(60): Show | 65 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(62): Show |
intron_variant | MODIFIER | c.-31+2926_-31+2933d others(10): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75528739 | |||||
chr17:75528844
|
G | T | 1 | a0003c0002t0002g0332 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.-31+3019G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75528844 | ||||||
chr17:75529072
|
C | T | 1 | a0001c0001t0001g0176 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-31+3247C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75529072 | ||||||
chr17:75529147
|
C | CTT | 275 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(272): Show | 282 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(279): Show |
intron_variant | MODIFIER | c.-31+3323_-31+3324i others(4): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75529147 | |||||
chr17:75529198
|
T | C | 1 | a0001c0001t0001g0029 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.-31+3373T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75529198 | ||||||
chr17:75529236
|
G | A | 24 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(21): Show | 24 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-31+3411G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75529236 | ||||||
chr17:75529290
|
A | C | 2 | a0001c0001t0001g0174a0011c0027t0005g0175 | 2 | HG01346.hp1 HG02148.hp1 |
intron_variant | MODIFIER | c.-31+3465A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75529290 | ||||||
chr17:75529346
|
A | G | 66 | a0001c0001t0001g0201a0001c0001t0002g0315a0001c0001t0002g0316others(63): Show | 68 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(65): Show |
intron_variant | MODIFIER | c.-31+3521A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75529346 | ||||||
chr17:75529476
|
A | G | 1 | a0003c0002t0002g0297 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.-31+3651A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75529476 | ||||||
chr17:75529589
|
T | G | 217 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(214): Show | 222 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(219): Show |
intron_variant | MODIFIER | c.-31+3764T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75529589 | ||||||
chr17:75529603
|
C | G | 204 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(201): Show | 209 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(206): Show |
intron_variant | MODIFIER | c.-31+3778C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75529603 | ||||||
chr17:75529721
|
C | T | 1 | a0004c0007t0003g0199 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.-31+3896C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75529721 | ||||||
chr17:75529728
|
G | A | 1 | a0001c0001t0002g0216 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.-31+3903G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75529728 | ||||||
chr17:75529751
|
C | T | 2 | a0002c0055t0003g0215a0026c0042t0003g0214 | 2 | HG00735.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.-31+3926C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75529751 | ||||||
chr17:75529776
|
G | A | 1 | a0002c0004t0003g0353 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.-31+3951G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75529776 | ||||||
chr17:75529810
|
G | A | 1 | a0003c0002t0001g0083 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.-31+3985G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75529810 | ||||||
chr17:75529898
|
A | G | 15 | a0002c0006t0003g0210a0003c0002t0002g0206a0003c0002t0002g0209others(12): Show | 15 | HG00438.hp1 HG01099.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.-31+4073A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75529898 | ||||||
chr17:75529899
|
G | A | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-31+4074G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75529899 | ||||||
chr17:75529944
|
A | G | 12 | a0001c0001t0002g0293a0003c0002t0002g0189a0003c0002t0002g0288others(9): Show | 13 | HG00639.hp2 HG01099.hp1 HG01496.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+4119A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75529944 | ||||||
chr17:75530078
|
C | A | 3 | a0003c0002t0002g0330a0003c0002t0002g0332a0003c0021t0002g0331 | 3 | HG01109.hp2 HG01255.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.-31+4253C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530078 | ||||||
chr17:75530113
|
C | A | 1 | a0001c0001t0001g0084 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-31+4288C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530113 | ||||||
chr17:75530287
|
G | T | 24 | a0001c0001t0002g0315a0001c0001t0002g0316a0001c0001t0002g0317others(21): Show | 24 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-31+4462G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530287 | ||||||
chr17:75530296
|
A | G | 1 | a0001c0001t0001g0184 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.-31+4471A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530296 | ||||||
chr17:75530298
|
T | C | 1 | a0005c0008t0001g0030 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.-31+4473T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530298 | ||||||
chr17:75530330
|
G | A | 1 | a0007c0010t0002g0287 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.-31+4505G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530330 | ||||||
chr17:75530349
|
T | A | 1 | a0004c0007t0003g0309 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.-31+4524T>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530349 | ||||||
chr17:75530378
|
C | T | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-31+4553C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530378 | ||||||
chr17:75530389
|
G | A | 2 | a0002c0006t0003g0085a0002c0006t0003g0086 | 2 | HG02615.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.-31+4564G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530389 | ||||||
chr17:75530393
|
G | C | 9 | a0001c0001t0002g0354a0001c0001t0002g0357a0001c0001t0002g0358others(6): Show | 9 | HG00544.hp2 HG00597.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31+4568G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530393 | ||||||
chr17:75530398
|
T | C | 274 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(271): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.-31+4573T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530398 | ||||||
chr17:75530410
|
G | A | 7 | a0004c0005t0004g0302a0004c0005t0004g0303a0004c0005t0004g0304others(4): Show | 7 | HG00438.hp1 HG02071.hp2 HG02080.hp2 others(4): Show |
intron_variant | MODIFIER | c.-31+4585G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530410 | ||||||
chr17:75530416
|
C | T | 1 | a0004c0005t0004g0308 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.-31+4591C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530416 | ||||||
chr17:75530619
|
C | T | 2 | a0003c0002t0001g0083a0003c0002t0001g0171 | 2 | HG01257.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.-31+4794C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530619 | ||||||
chr17:75530645
|
AT | A | 3 | a0001c0001t0001g0031a0002c0055t0003g0215a0015c0017t0003g0016 | 3 | HG02615.hp1 NA18522.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.-31+4823delT | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75530645 | |||||
chr17:75530647
|
TTC | T | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(186): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.-31+4823_-31+4824d others(4): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530647 | ||||||
chr17:75530648
|
T | C | 15 | a0002c0004t0003g0089a0002c0006t0003g0004a0002c0006t0003g0085others(12): Show | 16 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-31+4823T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530648 | ||||||
chr17:75530649
|
C | A | 15 | a0002c0004t0003g0089a0002c0006t0003g0004a0002c0006t0003g0085others(12): Show | 16 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-31+4824C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530649 | ||||||
chr17:75530649
|
C | CA | 9 | a0001c0001t0002g0354a0001c0001t0002g0357a0001c0001t0002g0358others(6): Show | 9 | HG00544.hp2 HG00597.hp2 HG01106.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31+4841dupA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75530649 | |||||
chr17:75530650
|
A | C | 189 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(186): Show | 193 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(190): Show |
intron_variant | MODIFIER | c.-31+4825A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530650 | ||||||
chr17:75530680
|
G | A | 15 | a0002c0006t0003g0210a0003c0002t0002g0206a0003c0002t0002g0209others(12): Show | 15 | HG00438.hp1 HG01099.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.-31+4855G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530680 | ||||||
chr17:75530800
|
G | C | 9 | a0001c0001t0002g0354a0001c0001t0002g0357a0001c0001t0002g0358others(6): Show | 9 | HG00544.hp2 HG00597.hp2 HG01257.hp2 others(6): Show |
intron_variant | MODIFIER | c.-31+4975G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530800 | ||||||
chr17:75530894
|
G | A | 2 | a0001c0001t0002g0216a0004c0005t0004g0298 | 2 | NA18969.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.-31+5069G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75530894 | ||||||
chr17:75531007
|
C | T | 1 | a0002c0004t0003g0014 | 2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-31+5182C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75531007 | ||||||
chr17:75531082
|
C | G | 1 | a0001c0001t0001g0084 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.-31+5257C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75531082 | ||||||
chr17:75531219
|
G | A | 1 | a0001c0001t0001g0068 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.-31+5394G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75531219 | ||||||
chr17:75531274
|
C | T | 1 | a0003c0002t0001g0170 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-31+5449C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75531274 | ||||||
chr17:75531479
|
A | G | 144 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(141): Show | 147 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(144): Show |
intron_variant | MODIFIER | c.-31+5654A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75531479 | ||||||
chr17:75531507
|
A | G | 52 | a0001c0001t0001g0201a0001c0001t0002g0354a0001c0001t0002g0357others(49): Show | 54 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.-31+5682A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75531507 | ||||||
chr17:75531514
|
A | G | 52 | a0001c0001t0001g0201a0001c0001t0002g0354a0001c0001t0002g0357others(49): Show | 54 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.-31+5689A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75531514 | ||||||
chr17:75531581
|
G | A | 1 | a0002c0003t0005g0108 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-31+5756G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75531581 | ||||||
chr17:75531631
|
A | C | 52 | a0001c0001t0001g0201a0001c0001t0002g0354a0001c0001t0002g0357others(49): Show | 54 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.-31+5806A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75531631 | ||||||
chr17:75531664
|
T | A | 1 | a0002c0045t0003g0310 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-31+5839T>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75531664 | ||||||
chr17:75531707
|
G | T | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-31+5882G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75531707 | ||||||
chr17:75531848
|
A | T | 15 | a0002c0004t0003g0089a0002c0006t0003g0004a0002c0006t0003g0085others(12): Show | 16 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.-31+6023A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75531848 | ||||||
chr17:75532048
|
G | C | 2 | a0004c0018t0005g0109a0004c0018t0005g0190 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-31+6223G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532048 | ||||||
chr17:75532051
|
T | TACACACA others(5): Show |
8 | a0002c0004t0003g0063a0002c0006t0003g0059a0004c0005t0004g0003others(5): Show | 9 | HG02109.hp2 HG02717.hp2 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.-31+6227_-31+6228i others(14): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532051 | |||||
chr17:75532051
|
T | TACACACA others(7): Show |
1 | a0013c0016t0003g0056 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.-31+6227_-31+6228i others(16): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532051 | |||||
chr17:75532053
|
T | C | 9 | a0002c0004t0003g0063a0002c0006t0003g0059a0004c0005t0004g0003others(6): Show | 10 | HG02109.hp2 HG02258.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.-31+6228T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532053 | ||||||
chr17:75532053
|
T | TAC | 16 | a0002c0004t0003g0014a0002c0004t0003g0282a0002c0004t0003g0283others(13): Show | 17 | HG00735.hp1 HG01109.hp2 HG01123.hp2 others(14): Show |
intron_variant | MODIFIER | c.-31+6229_-31+6230i others(4): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532053 | |||||
chr17:75532053
|
T | TACAC | 4 | a0001c0001t0001g0201a0002c0004t0003g0342a0003c0002t0002g0343others(1): Show | 4 | HG00733.hp2 HG01106.hp1 HG01884.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+6229_-31+6230i others(6): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532053 | |||||
chr17:75532053
|
T | TACACAC | 12 | a0002c0004t0003g0013a0002c0004t0003g0333a0002c0004t0003g0335others(9): Show | 13 | HG00738.hp2 HG01243.hp1 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+6229_-31+6230i others(8): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532053 | |||||
chr17:75532053
|
T | TACACACA others(1): Show |
3 | a0002c0003t0003g0328a0003c0002t0002g0202a0032c0047t0003g0366 | 3 | HG01109.hp1 NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-31+6229_-31+6230i others(10): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532053 | |||||
chr17:75532053
|
T | TACACACA others(3): Show |
5 | a0001c0001t0001g0110a0004c0007t0003g0021a0008c0043t0003g0023others(2): Show | 5 | HG02055.hp1 HG02809.hp1 HG02886.hp2 others(2): Show |
intron_variant | MODIFIER | c.-31+6229_-31+6230i others(12): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532053 | |||||
chr17:75532053
|
T | TACACACA others(5): Show |
2 | a0004c0018t0005g0190a0014c0020t0003g0064 | 2 | HG02818.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.-31+6229_-31+6230i others(14): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532053 | |||||
chr17:75532053
|
T | TACACACA others(7): Show |
17 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(14): Show | 17 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.-31+6229_-31+6230i others(16): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532053 | |||||
chr17:75532053
|
T | TACACACA others(9): Show |
15 | a0002c0006t0003g0313a0003c0002t0002g0206a0003c0002t0002g0209others(12): Show | 15 | HG00438.hp1 HG01099.hp2 HG01884.hp2 others(12): Show |
intron_variant | MODIFIER | c.-31+6229_-31+6230i others(18): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532053 | |||||
chr17:75532053
|
T | TACACACA others(11): Show |
3 | a0002c0012t0003g0311a0006c0009t0002g0204a0006c0009t0004g0203 | 3 | HG02040.hp2 HG02074.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.-31+6229_-31+6230i others(20): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532053 | |||||
chr17:75532055
|
T | C | 103 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(100): Show | 106 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(103): Show |
intron_variant | MODIFIER | c.-31+6230T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532055 | ||||||
chr17:75532055
|
T | TAC | 3 | a0001c0001t0002g0219a0002c0055t0003g0215a0003c0002t0002g0218 | 3 | HG00423.hp1 NA18522.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.-31+6251_-31+6252d others(4): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532055 | |||||
chr17:75532055
|
T | TACACACA others(1): Show |
5 | a0001c0001t0001g0068a0001c0001t0001g0162a0001c0001t0001g0163others(2): Show | 5 | HG02735.hp1 HG03688.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.-31+6245_-31+6252d others(10): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532055 | |||||
chr17:75532055
|
T | TACACACA others(3): Show |
30 | a0001c0001t0001g0007a0001c0001t0001g0075a0001c0001t0001g0076others(27): Show | 31 | HG00558.hp1 HG00558.hp2 HG00621.hp2 others(28): Show |
intron_variant | MODIFIER | c.-31+6243_-31+6252d others(12): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532055 | |||||
chr17:75532055
|
T | TACACACA others(5): Show |
8 | a0001c0001t0001g0074a0001c0001t0001g0179a0002c0003t0005g0124others(5): Show | 8 | HG00639.hp1 HG01256.hp2 HG02135.hp2 others(5): Show |
intron_variant | MODIFIER | c.-31+6241_-31+6252d others(14): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532055 | |||||
chr17:75532055
|
T | TACACACA others(7): Show |
41 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0039others(38): Show | 41 | HG00408.hp1 HG00438.hp2 HG00733.hp1 others(38): Show |
intron_variant | MODIFIER | c.-31+6239_-31+6252d others(16): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532055 | |||||
chr17:75532055
|
T | TACACACA others(9): Show |
18 | a0001c0001t0001g0035a0001c0001t0001g0080a0001c0001t0001g0081others(15): Show | 18 | HG00609.hp1 HG01074.hp2 HG01261.hp1 others(15): Show |
intron_variant | MODIFIER | c.-31+6237_-31+6252d others(18): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532055 | |||||
chr17:75532055
|
T | TACACACA others(11): Show |
6 | a0001c0001t0001g0111a0001c0001t0001g0191a0002c0006t0003g0025others(3): Show | 6 | HG03209.hp2 HG03225.hp1 HG03486.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+6235_-31+6252d others(20): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532055 | |||||
chr17:75532055
|
T | TATACACA others(7): Show |
4 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0174others(1): Show | 4 | HG01346.hp1 HG02148.hp1 HG03491.hp1 others(1): Show |
intron_variant | MODIFIER | c.-31+6231_-31+6232i others(16): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532055 | |||||
chr17:75532055
|
T | TATACACA others(9): Show |
1 | a0001c0001t0001g0006 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.-31+6231_-31+6232i others(18): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532055 | |||||
chr17:75532057
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-31+6232C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532057 | ||||||
chr17:75532077
|
C | CACACACA others(4): Show |
2 | a0004c0007t0003g0199a0004c0018t0005g0109 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.-31+6252_-31+6253i others(13): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532077 | ||||||
chr17:75532077
|
C | CACACACA others(6): Show |
16 | a0001c0001t0001g0033a0001c0001t0001g0167a0002c0003t0005g0125others(13): Show | 16 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(13): Show |
intron_variant | MODIFIER | c.-31+6252_-31+6253i others(15): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532077 | ||||||
chr17:75532077
|
C | CACACACA others(8): Show |
7 | a0001c0001t0001g0034a0001c0001t0001g0123a0002c0003t0005g0113others(4): Show | 7 | HG00642.hp1 HG00642.hp2 HG02083.hp1 others(4): Show |
intron_variant | MODIFIER | c.-31+6252_-31+6253i others(17): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532077 | ||||||
chr17:75532077
|
C | CACACACA others(14): Show |
2 | a0001c0001t0002g0354a0001c0001t0002g0362 | 2 | NA19080.hp2 NA19088.hp1 |
intron_variant | MODIFIER | c.-31+6252_-31+6253i others(23): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532077 | ||||||
chr17:75532077
|
C | CACACACA others(12): Show |
3 | a0004c0005t0004g0355a0004c0005t0004g0356a0004c0005t0007g0106 | 3 | HG01257.hp2 HG01258.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.-31+6252_-31+6253i others(21): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532077 | ||||||
chr17:75532077
|
C | CACACACA others(10): Show |
12 | a0001c0001t0001g0031a0001c0001t0001g0121a0001c0001t0001g0122others(9): Show | 13 | HG00544.hp2 HG00597.hp2 HG01106.hp2 others(10): Show |
intron_variant | MODIFIER | c.-31+6252_-31+6253i others(19): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532077 | ||||||
chr17:75532077
|
C | CACACACA others(11): Show |
1 | a0004c0005t0007g0069 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-31+6252_-31+6253i others(20): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532077 | ||||||
chr17:75532077
|
C | CACACACA others(8): Show |
6 | a0001c0001t0001g0049a0001c0001t0001g0150a0001c0037t0001g0149others(3): Show | 6 | HG00323.hp1 HG02622.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+6252_-31+6253i others(17): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532077 | ||||||
chr17:75532077
|
C | CACACACA others(6): Show |
1 | a0020c0032t0002g0055 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.-31+6252_-31+6253i others(15): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532077 | ||||||
chr17:75532077
|
C | CACACACA others(4): Show |
3 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG03942.hp1 NA18940.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.-31+6252_-31+6253i others(13): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532077 | ||||||
chr17:75532077
|
C | CT | 34 | a0002c0003t0003g0259a0002c0003t0003g0270a0002c0003t0003g0271others(31): Show | 38 | HG00597.hp1 HG00621.hp1 HG01433.hp1 others(35): Show |
intron_variant | MODIFIER | c.-31+6273dupT | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75532077 | |||||
chr17:75532078
|
T | A | 27 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(24): Show | 27 | HG00741.hp2 HG01069.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.-31+6253T>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532078 | ||||||
chr17:75532078
|
T | C | 27 | a0001c0001t0001g0033a0001c0001t0001g0034a0001c0001t0001g0164others(24): Show | 27 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(24): Show |
intron_variant | MODIFIER | c.-31+6253T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532078 | ||||||
chr17:75532079
|
T | A | 2 | a0001c0001t0001g0033a0003c0002t0002g0314 | 2 | HG00099.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-31+6254T>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532079 | ||||||
chr17:75532079
|
T | C | 27 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(24): Show | 27 | HG00741.hp2 HG01069.hp1 HG01069.hp2 others(24): Show |
intron_variant | MODIFIER | c.-31+6254T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532079 | ||||||
chr17:75532080
|
T | A | 3 | a0002c0004t0003g0017a0015c0017t0003g0016a0015c0017t0003g0026 | 3 | HG01069.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-31+6255T>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532080 | ||||||
chr17:75532080
|
T | C | 2 | a0001c0001t0001g0033a0003c0002t0002g0314 | 2 | HG00099.hp1 HG01074.hp1 |
intron_variant | MODIFIER | c.-31+6255T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532080 | ||||||
chr17:75532081
|
T | C | 3 | a0002c0004t0003g0017a0015c0017t0003g0016a0015c0017t0003g0026 | 3 | HG01069.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.-31+6256T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532081 | ||||||
chr17:75532127
|
T | C | 278 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(275): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.-31+6302T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532127 | ||||||
chr17:75532162
|
T | C | 52 | a0001c0001t0001g0201a0001c0001t0002g0354a0001c0001t0002g0357others(49): Show | 54 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(51): Show |
intron_variant | MODIFIER | c.-31+6337T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532162 | ||||||
chr17:75532267
|
T | C | 24 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(21): Show | 24 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-31+6442T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532267 | ||||||
chr17:75532396
|
G | A | 1 | a0004c0007t0003g0329 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.-31+6571G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532396 | ||||||
chr17:75532399
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-31+6574C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532399 | ||||||
chr17:75532454
|
C | T | 2 | a0004c0007t0003g0199a0026c0042t0003g0214 | 2 | HG00735.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.-31+6629C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532454 | ||||||
chr17:75532517
|
G | A | 24 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(21): Show | 24 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(21): Show |
intron_variant | MODIFIER | c.-31+6692G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532517 | ||||||
chr17:75532528
|
A | G | 27 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(24): Show | 27 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(24): Show |
intron_variant | MODIFIER | c.-31+6703A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532528 | ||||||
chr17:75532866
|
A | G | 3 | a0001c0001t0002g0325a0001c0001t0002g0326a0001c0001t0002g0327 | 3 | HG01516.hp1 HG01517.hp2 HG01928.hp2 |
intron_variant | MODIFIER | c.-31+7041A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532866 | ||||||
chr17:75532911
|
C | T | 17 | a0001c0001t0002g0354a0001c0001t0002g0357a0001c0001t0002g0358others(14): Show | 17 | HG00544.hp2 HG00597.hp2 HG01074.hp1 others(14): Show |
intron_variant | MODIFIER | c.-31+7086C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75532911 | ||||||
chr17:75533062
|
C | T | 1 | a0025c0039t0004g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-31+7237C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75533062 | ||||||
chr17:75533069
|
G | A | 1 | a0002c0004t0003g0067 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.-31+7244G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75533069 | ||||||
chr17:75533160
|
C | T | 13 | a0001c0001t0002g0354a0001c0001t0002g0357a0001c0001t0002g0358others(10): Show | 13 | HG00544.hp2 HG00597.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+7335C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75533160 | ||||||
chr17:75533235
|
G | A | 1 | a0002c0045t0003g0310 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.-31+7410G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75533235 | ||||||
chr17:75533289
|
G | A | 1 | a0004c0007t0003g0027 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-31+7464G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75533289 | ||||||
chr17:75533299
|
C | CT | 76 | a0001c0001t0001g0079a0001c0001t0001g0122a0001c0001t0001g0123others(73): Show | 77 | HG00140.hp1 HG00544.hp2 HG00597.hp2 others(74): Show |
intron_variant | MODIFIER | c.-31+7497dupT | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75533299 | |||||
chr17:75533299
|
C | CTT | 14 | a0001c0001t0001g0186a0002c0003t0003g0328a0002c0004t0003g0350others(11): Show | 14 | HG00438.hp1 HG00735.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.-31+7496_-31+7497d others(4): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75533299 | |||||
chr17:75533299
|
C | CTTT | 16 | a0001c0001t0001g0100a0001c0001t0001g0101a0001c0001t0002g0317others(13): Show | 16 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(13): Show |
intron_variant | MODIFIER | c.-31+7495_-31+7497d others(5): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75533299 | |||||
chr17:75533299
|
CTTTTTTT others(7): Show |
C | 12 | a0002c0004t0003g0013a0002c0004t0003g0333a0002c0004t0003g0335others(9): Show | 13 | HG00738.hp2 HG01243.hp1 HG02109.hp1 others(10): Show |
intron_variant | MODIFIER | c.-31+7484_-31+7497d others(16): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75533299 | |||||
chr17:75533368
|
G | A | 1 | a0001c0001t0001g0193 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.-31+7543G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75533368 | ||||||
chr17:75533406
|
A | G | 53 | a0001c0001t0001g0201a0001c0001t0002g0354a0001c0001t0002g0357others(50): Show | 55 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-31+7581A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75533406 | ||||||
chr17:75533467
|
G | A | 2 | a0002c0004t0003g0017a0015c0017t0003g0016 | 2 | HG01069.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-31+7642G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75533467 | ||||||
chr17:75533516
|
G | A | 1 | a0001c0001t0002g0357 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.-31+7691G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75533516 | ||||||
chr17:75533526
|
G | A | 1 | a0018c0031t0001g0177 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-31+7701G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75533526 | ||||||
chr17:75533550
|
C | T | 14 | a0003c0002t0002g0206a0003c0002t0002g0209a0004c0005t0004g0207others(11): Show | 14 | HG00438.hp1 HG01099.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.-31+7725C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75533550 | ||||||
chr17:75533578
|
G | A | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.-31+7753G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75533578 | ||||||
chr17:75533584
|
A | C | 1 | a0002c0013t0003g0192 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.-31+7759A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75533584 | ||||||
chr17:75533595
|
C | T | 2 | a0002c0004t0003g0282a0002c0004t0003g0283 | 2 | HG01361.hp1 HG02257.hp1 |
intron_variant | MODIFIER | c.-31+7770C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75533595 | ||||||
chr17:75533669
|
A | C | 1 | a0002c0004t0003g0341 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.-31+7844A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75533669 | ||||||
chr17:75534028
|
G | GT | 53 | a0001c0001t0001g0201a0001c0001t0002g0354a0001c0001t0002g0357others(50): Show | 55 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-31+8203_-31+8204i others(3): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75534028 | ||||||
chr17:75534072
|
C | T | 2 | a0001c0001t0001g0073a0001c0029t0001g0048 | 2 | HG00438.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.-31+8247C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75534072 | ||||||
chr17:75534339
|
G | A | 6 | a0002c0004t0003g0066a0002c0004t0003g0067a0002c0004t0003g0363others(3): Show | 6 | HG00639.hp1 HG01891.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.-31+8514G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75534339 | ||||||
chr17:75534349
|
G | C | 1 | a0001c0001t0001g0110 | 1 | NA18964.hp1 | intron_variant | MODIFIER | c.-31+8524G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75534349 | ||||||
chr17:75534390
|
T | C | 1 | a0003c0002t0002g0218 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.-31+8565T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75534390 | ||||||
chr17:75534552
|
C | T | 1 | a0001c0001t0001g0167 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.-31+8727C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75534552 | ||||||
chr17:75534678
|
C | T | 4 | a0004c0007t0003g0021a0008c0043t0003g0023a0012c0022t0003g0022others(1): Show | 4 | HG02055.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-8719C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75534678 | ||||||
chr17:75534681
|
A | G | 1 | a0003c0019t0002g0095 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.-30-8716A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75534681 | ||||||
chr17:75534701
|
G | A | 14 | a0003c0002t0002g0206a0003c0002t0002g0209a0004c0005t0004g0207others(11): Show | 14 | HG00438.hp1 HG01099.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.-30-8696G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75534701 | ||||||
chr17:75534742
|
A | G | 36 | a0001c0001t0001g0201a0002c0004t0003g0013a0002c0004t0003g0014others(33): Show | 38 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.-30-8655A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75534742 | ||||||
chr17:75534936
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.-30-8461C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75534936 | ||||||
chr17:75535024
|
G | A | 16 | a0002c0004t0003g0089a0002c0006t0003g0004a0002c0006t0003g0085others(13): Show | 17 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.-30-8373G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75535024 | ||||||
chr17:75535242
|
C | T | 1 | a0002c0003t0003g0256 | 1 | NA18987.hp1 | intron_variant | MODIFIER | c.-30-8155C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75535242 | ||||||
chr17:75535420
|
G | A | 1 | a0002c0003t0003g0220 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-30-7977G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75535420 | ||||||
chr17:75535468
|
G | A | 53 | a0001c0001t0001g0201a0001c0001t0002g0354a0001c0001t0002g0357others(50): Show | 55 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30-7929G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75535468 | ||||||
chr17:75535605
|
G | A | 1 | a0025c0039t0004g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-30-7792G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75535605 | ||||||
chr17:75535728
|
C | T | 1 | a0003c0002t0002g0343 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.-30-7669C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75535728 | ||||||
chr17:75535768
|
G | A | 1 | a0003c0019t0002g0212 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-30-7629G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75535768 | ||||||
chr17:75535838
|
A | C | 8 | a0002c0004t0003g0017a0004c0007t0003g0199a0009c0011t0006g0018others(5): Show | 8 | HG00735.hp2 HG01069.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30-7559A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75535838 | ||||||
chr17:75535935
|
C | T | 2 | a0002c0004t0003g0017a0015c0017t0003g0016 | 2 | HG01069.hp1 HG02615.hp1 |
intron_variant | MODIFIER | c.-30-7462C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75535935 | ||||||
chr17:75535996
|
G | A | 6 | a0002c0004t0003g0017a0009c0011t0006g0018a0009c0011t0006g0019others(3): Show | 6 | HG01069.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.-30-7401G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75535996 | ||||||
chr17:75536011
|
C | T | 2 | a0002c0012t0003g0323a0002c0012t0003g0324 | 2 | HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.-30-7386C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75536011 | ||||||
chr17:75536132
|
G | A | 2 | a0001c0001t0001g0178a0018c0031t0001g0177 | 2 | HG01070.hp1 HG01993.hp1 |
intron_variant | MODIFIER | c.-30-7265G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75536132 | ||||||
chr17:75536207
|
G | A | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-30-7190G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75536207 | ||||||
chr17:75536286
|
C | T | 1 | a0004c0005t0007g0069 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.-30-7111C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75536286 | ||||||
chr17:75536368
|
T | C | 8 | a0002c0004t0003g0017a0004c0007t0003g0199a0009c0011t0006g0018others(5): Show | 8 | HG00735.hp2 HG01069.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30-7029T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75536368 | ||||||
chr17:75536471
|
G | A | 50 | a0001c0001t0002g0354a0001c0001t0002g0357a0001c0001t0002g0358others(47): Show | 52 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(49): Show |
intron_variant | MODIFIER | c.-30-6926G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75536471 | ||||||
chr17:75536492
|
C | G | 269 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(266): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-30-6905C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75536492 | ||||||
chr17:75536493
|
C | G | 269 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(266): Show | 276 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(273): Show |
intron_variant | MODIFIER | c.-30-6904C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75536493 | ||||||
chr17:75536494
|
G | C | 1 | a0025c0039t0004g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.-30-6903G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75536494 | ||||||
chr17:75536578
|
A | T | 13 | a0001c0001t0002g0354a0001c0001t0002g0357a0001c0001t0002g0358others(10): Show | 13 | HG00544.hp2 HG00597.hp2 HG01074.hp1 others(10): Show |
intron_variant | MODIFIER | c.-30-6819A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75536578 | ||||||
chr17:75537021
|
G | C | 66 | a0001c0001t0002g0354a0001c0001t0002g0357a0001c0001t0002g0358others(63): Show | 69 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(66): Show |
intron_variant | MODIFIER | c.-30-6376G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75537021 | ||||||
chr17:75537041
|
G | A | 5 | a0001c0001t0002g0221a0003c0002t0002g0213a0003c0002t0002g0218others(2): Show | 5 | HG00423.hp1 NA18941.hp2 NA18981.hp2 others(2): Show |
intron_variant | MODIFIER | c.-30-6356G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75537041 | ||||||
chr17:75537371
|
G | T | 2 | a0011c0028t0003g0187a0027c0040t0003g0188 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-30-6026G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75537371 | ||||||
chr17:75537399
|
T | C | 1 | a0002c0004t0003g0333 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-30-5998T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75537399 | ||||||
chr17:75537522
|
A | C | 105 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(102): Show | 108 | HG00438.hp1 HG00544.hp2 HG00597.hp2 others(105): Show |
intron_variant | MODIFIER | c.-30-5875A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75537522 | ||||||
chr17:75537653
|
C | T | 1 | a0003c0002t0002g0255 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.-30-5744C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75537653 | ||||||
chr17:75537803
|
G | T | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-30-5594G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75537803 | ||||||
chr17:75537809
|
C | CT | 17 | a0001c0001t0001g0078a0001c0001t0002g0219a0001c0001t0002g0316others(14): Show | 17 | HG00741.hp2 HG01109.hp1 HG01433.hp1 others(14): Show |
intron_variant | MODIFIER | c.-30-5569dupT | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75537809 | |||||
chr17:75537809
|
C | CTT | 11 | a0001c0001t0002g0354a0001c0001t0002g0357a0001c0001t0002g0358others(8): Show | 11 | HG00544.hp2 HG01074.hp1 HG01257.hp2 others(8): Show |
intron_variant | MODIFIER | c.-30-5570_-30-5569d others(4): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75537809 | |||||
chr17:75537809
|
C | CTTT | 33 | a0001c0001t0001g0201a0002c0004t0003g0013a0002c0004t0003g0014others(30): Show | 35 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.-30-5571_-30-5569d others(5): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75537809 | |||||
chr17:75537809
|
C | T | 2 | a0004c0005t0004g0360a0004c0005t0004g0361 | 2 | HG00597.hp2 NA18982.hp2 |
intron_variant | MODIFIER | c.-30-5588C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75537809 | ||||||
chr17:75537852
|
C | T | 1 | a0001c0001t0001g0147 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.-30-5545C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75537852 | ||||||
chr17:75537969
|
C | G | 14 | a0003c0002t0002g0206a0003c0002t0002g0209a0004c0005t0004g0207others(11): Show | 14 | HG00438.hp1 HG01099.hp2 HG02040.hp2 others(11): Show |
intron_variant | MODIFIER | c.-30-5428C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75537969 | ||||||
chr17:75538057
|
C | T | 2 | a0011c0028t0003g0187a0027c0040t0003g0188 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-30-5340C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75538057 | ||||||
chr17:75538058
|
G | A | 4 | a0004c0007t0003g0021a0008c0043t0003g0023a0012c0022t0003g0022others(1): Show | 4 | HG02055.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-5339G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75538058 | ||||||
chr17:75538090
|
C | T | 53 | a0001c0001t0001g0201a0001c0001t0002g0354a0001c0001t0002g0357others(50): Show | 55 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30-5307C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75538090 | ||||||
chr17:75538103
|
G | A | 3 | a0003c0002t0002g0202a0025c0039t0004g0367a0032c0047t0003g0366 | 3 | HG01109.hp1 HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-30-5294G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75538103 | ||||||
chr17:75538123
|
C | T | 53 | a0001c0001t0001g0201a0001c0001t0002g0354a0001c0001t0002g0357others(50): Show | 55 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30-5274C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75538123 | ||||||
chr17:75538263
|
G | T | 1 | a0001c0001t0001g0160 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.-30-5134G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75538263 | ||||||
chr17:75538300
|
G | A | 1 | a0002c0003t0005g0108 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.-30-5097G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75538300 | ||||||
chr17:75538375
|
A | T | 1 | a0003c0002t0002g0314 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.-30-5022A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75538375 | ||||||
chr17:75538404
|
T | C | 79 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(76): Show | 81 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(78): Show |
intron_variant | MODIFIER | c.-30-4993T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75538404 | ||||||
chr17:75538535
|
C | T | 1 | a0018c0031t0001g0177 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.-30-4862C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75538535 | ||||||
chr17:75538665
|
T | G | 69 | a0001c0001t0001g0201a0001c0001t0002g0354a0001c0001t0002g0357others(66): Show | 72 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(69): Show |
intron_variant | MODIFIER | c.-30-4732T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75538665 | ||||||
chr17:75538762
|
G | A | 1 | a0002c0006t0003g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-30-4635G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75538762 | ||||||
chr17:75538809
|
G | A | 1 | a0003c0002t0001g0102 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.-30-4588G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75538809 | ||||||
chr17:75538914
|
CAA | C | 53 | a0001c0001t0001g0201a0001c0001t0002g0354a0001c0001t0002g0357others(50): Show | 55 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30-4482_-30-4481d others(4): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75538914 | ||||||
chr17:75539005
|
G | A | 37 | a0001c0001t0001g0201a0002c0004t0003g0013a0002c0004t0003g0014others(34): Show | 39 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(36): Show |
intron_variant | MODIFIER | c.-30-4392G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75539005 | ||||||
chr17:75539119
|
T | C | 53 | a0001c0001t0001g0201a0001c0001t0002g0354a0001c0001t0002g0357others(50): Show | 55 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30-4278T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75539119 | ||||||
chr17:75539167
|
T | G | 26 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(23): Show | 26 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(23): Show |
intron_variant | MODIFIER | c.-30-4230T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75539167 | ||||||
chr17:75539275
|
G | T | 23 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(20): Show | 23 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-30-4122G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75539275 | ||||||
chr17:75539405
|
G | C | 53 | a0001c0001t0001g0201a0001c0001t0002g0354a0001c0001t0002g0357others(50): Show | 55 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30-3992G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75539405 | ||||||
chr17:75539413
|
C | CT | 7 | a0002c0004t0003g0066a0002c0004t0003g0067a0002c0004t0003g0363others(4): Show | 7 | HG00639.hp1 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-3974dupT | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75539413 | |||||
chr17:75539455
|
GGTC | G | 53 | a0001c0001t0001g0201a0001c0001t0002g0354a0001c0001t0002g0357others(50): Show | 55 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30-3938_-30-3936d others(5): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75539455 | |||||
chr17:75539493
|
C | T | 12 | a0002c0004t0003g0063a0002c0006t0003g0059a0004c0005t0004g0003others(9): Show | 13 | HG02109.hp2 HG02258.hp1 HG02717.hp2 others(10): Show |
intron_variant | MODIFIER | c.-30-3904C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75539493 | ||||||
chr17:75539566
|
A | G | 23 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(20): Show | 23 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-30-3831A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75539566 | ||||||
chr17:75539608
|
CT | C | 59 | a0001c0001t0001g0029a0001c0001t0001g0123a0001c0001t0001g0134others(56): Show | 61 | HG00544.hp2 HG00597.hp2 HG00639.hp1 others(58): Show |
intron_variant | MODIFIER | c.-30-3771delT | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75539608 | |||||
chr17:75539625
|
T | A | 21 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(18): Show | 21 | HG00741.hp2 HG01081.hp2 HG01192.hp1 others(18): Show |
intron_variant | MODIFIER | c.-30-3772T>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75539625 | ||||||
chr17:75539626
|
T | A | 19 | a0001c0001t0002g0354a0001c0001t0002g0357a0001c0001t0002g0358others(16): Show | 19 | HG00408.hp2 HG00544.hp2 HG00597.hp2 others(16): Show |
intron_variant | MODIFIER | c.-30-3771T>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75539626 | ||||||
chr17:75539861
|
G | A | 1 | a0016c0056t0001g0136 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.-30-3536G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75539861 | ||||||
chr17:75539929
|
A | T | 1 | a0003c0019t0002g0212 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-30-3468A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75539929 | ||||||
chr17:75540050
|
T | TC | 53 | a0001c0001t0001g0201a0001c0001t0002g0354a0001c0001t0002g0357others(50): Show | 55 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30-3342dupC | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75540050 | |||||
chr17:75540065
|
G | A | 8 | a0002c0004t0003g0017a0004c0007t0003g0199a0009c0011t0006g0018others(5): Show | 8 | HG00735.hp2 HG01069.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30-3332G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75540065 | ||||||
chr17:75540066
|
A | C | 1 | a0002c0004t0003g0014 | 2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.-30-3331A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75540066 | ||||||
chr17:75540086
|
T | C | 53 | a0001c0001t0001g0201a0001c0001t0002g0354a0001c0001t0002g0357others(50): Show | 55 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(52): Show |
intron_variant | MODIFIER | c.-30-3311T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75540086 | ||||||
chr17:75540145
|
C | T | 1 | a0001c0001t0001g0146 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.-30-3252C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75540145 | ||||||
chr17:75540218
|
C | T | 1 | a0004c0005t0004g0359 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.-30-3179C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75540218 | ||||||
chr17:75540265
|
G | T | 1 | a0002c0003t0003g0220 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.-30-3132G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75540265 | ||||||
chr17:75540531
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-30-2866C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75540531 | ||||||
chr17:75540634
|
T | C | 1 | a0002c0048t0004g0087 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-30-2763T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75540634 | ||||||
chr17:75540724
|
C | T | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.-30-2673C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75540724 | ||||||
chr17:75540858
|
A | G | 33 | a0001c0001t0001g0201a0002c0004t0003g0013a0002c0004t0003g0014others(30): Show | 35 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(32): Show |
intron_variant | MODIFIER | c.-30-2539A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75540858 | ||||||
chr17:75541181
|
A | T | 1 | a0001c0001t0001g0200 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.-30-2216A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75541181 | ||||||
chr17:75541182
|
G | T | 1 | a0001c0001t0001g0176 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-30-2215G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75541182 | ||||||
chr17:75541456
|
G | A | 54 | a0001c0001t0001g0201a0001c0001t0002g0354a0001c0001t0002g0357others(51): Show | 56 | HG00544.hp2 HG00597.hp2 HG00733.hp2 others(53): Show |
intron_variant | MODIFIER | c.-30-1941G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75541456 | ||||||
chr17:75541512
|
C | T | 23 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(20): Show | 23 | HG00741.hp2 HG01069.hp2 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.-30-1885C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75541512 | ||||||
chr17:75541547
|
C | T | 3 | a0003c0002t0002g0202a0025c0039t0004g0367a0032c0047t0003g0366 | 3 | HG01109.hp1 HG01891.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.-30-1850C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75541547 | ||||||
chr17:75541660
|
G | A | 11 | a0002c0006t0003g0059a0004c0005t0004g0003a0004c0005t0004g0057others(8): Show | 12 | HG02109.hp2 HG02258.hp1 HG02818.hp2 others(9): Show |
intron_variant | MODIFIER | c.-30-1737G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75541660 | ||||||
chr17:75541678
|
C | T | 1 | a0003c0021t0002g0277 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.-30-1719C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75541678 | ||||||
chr17:75541715
|
CT | C | 147 | a0001c0001t0001g0007a0001c0001t0001g0028a0001c0001t0001g0029others(144): Show | 154 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(151): Show |
intron_variant | MODIFIER | c.-30-1651delT | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75541715 | |||||
chr17:75541715
|
CTT | C | 67 | a0001c0001t0001g0006a0001c0001t0001g0068a0001c0001t0001g0073others(64): Show | 69 | HG00323.hp2 HG00558.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.-30-1652_-30-1651d others(4): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75541715 | |||||
chr17:75541715
|
CTTT | C | 8 | a0001c0001t0001g0160a0001c0001t0001g0197a0001c0001t0002g0315others(5): Show | 8 | HG02074.hp1 HG02486.hp2 HG02602.hp2 others(5): Show |
intron_variant | MODIFIER | c.-30-1653_-30-1651d others(5): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75541715 | |||||
chr17:75541715
|
CTTTT | C | 31 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(28): Show | 31 | HG00438.hp1 HG00741.hp2 HG01071.hp1 others(28): Show |
intron_variant | MODIFIER | c.-30-1654_-30-1651d others(6): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75541715 | |||||
chr17:75541715
|
CTTTTT | C | 51 | a0001c0001t0001g0201a0001c0001t0002g0325a0002c0003t0003g0320others(48): Show | 54 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.-30-1655_-30-1651d others(7): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75541715 | |||||
chr17:75541715
|
CTTTTTT | C | 10 | a0002c0004t0003g0335a0002c0004t0003g0336a0002c0013t0003g0334others(7): Show | 10 | HG02055.hp1 HG02280.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.-30-1656_-30-1651d others(8): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr17 | 75541715 | |||||
chr17:75541753
|
C | T | 2 | a0011c0028t0003g0187a0027c0040t0003g0188 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.-30-1644C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75541753 | ||||||
chr17:75541777
|
C | T | 369 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(366): Show | 381 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(378): Show |
intron_variant | MODIFIER | c.-30-1620C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75541777 | ||||||
chr17:75541804
|
A | G | 1 | a0003c0002t0002g0272 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.-30-1593A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75541804 | ||||||
chr17:75541860
|
G | T | 5 | a0003c0002t0002g0202a0011c0028t0003g0187a0025c0039t0004g0367others(2): Show | 5 | HG01109.hp1 HG01891.hp1 HG03225.hp1 others(2): Show |
intron_variant | MODIFIER | c.-30-1537G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75541860 | ||||||
chr17:75541874
|
C | T | 1 | a0002c0013t0003g0196 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.-30-1523C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75541874 | ||||||
chr17:75541891
|
G | A | 3 | a0001c0001t0001g0197a0011c0028t0003g0187a0027c0040t0003g0188 | 3 | HG03225.hp1 HG03486.hp2 NA18981.hp1 |
intron_variant | MODIFIER | c.-30-1506G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75541891 | ||||||
chr17:75542062
|
A | G | 127 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(124): Show | 130 | HG00408.hp2 HG00438.hp1 HG00544.hp1 others(127): Show |
intron_variant | MODIFIER | c.-30-1335A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542062 | ||||||
chr17:75542086
|
G | A | 37 | a0001c0001t0001g0201a0002c0004t0003g0013a0002c0004t0003g0014others(34): Show | 39 | HG00140.hp1 HG00733.hp2 HG00735.hp1 others(36): Show |
intron_variant | MODIFIER | c.-30-1311G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542086 | ||||||
chr17:75542112
|
C | T | 2 | a0004c0018t0005g0109a0004c0018t0005g0190 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.-30-1285C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542112 | ||||||
chr17:75542142
|
T | G | 221 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(218): Show | 227 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(224): Show |
intron_variant | MODIFIER | c.-30-1255T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542142 | ||||||
chr17:75542143
|
T | C | 296 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(293): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.-30-1254T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542143 | ||||||
chr17:75542192
|
G | A | 1 | a0003c0002t0002g0227 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.-30-1205G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542192 | ||||||
chr17:75542209
|
C | T | 7 | a0003c0002t0002g0202a0004c0007t0003g0021a0008c0043t0003g0023others(4): Show | 7 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-1188C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542209 | ||||||
chr17:75542236
|
ACCT | A | 21 | a0001c0001t0002g0354a0001c0001t0002g0357a0001c0001t0002g0358others(18): Show | 21 | HG00544.hp2 HG00597.hp2 HG00735.hp2 others(18): Show |
intron_variant | MODIFIER | c.-30-1160_-30-1158d others(5): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542236 | ||||||
chr17:75542237
|
C | T | 90 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(87): Show | 92 | HG00140.hp1 HG00408.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.-30-1160C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542237 | ||||||
chr17:75542357
|
G | A | 7 | a0003c0002t0002g0202a0004c0007t0003g0021a0008c0043t0003g0023others(4): Show | 7 | HG01109.hp1 HG01891.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-1040G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542357 | ||||||
chr17:75542408
|
G | A | 17 | a0002c0006t0003g0059a0003c0002t0002g0206a0003c0002t0002g0209others(14): Show | 18 | HG00438.hp1 HG01099.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.-30-989G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542408 | ||||||
chr17:75542538
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.-30-859A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542538 | ||||||
chr17:75542586
|
G | A | 1 | a0002c0006t0003g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.-30-811G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542586 | ||||||
chr17:75542595
|
A | G | 156 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(153): Show | 160 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.-30-802A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542595 | ||||||
chr17:75542625
|
G | A | 1 | a0001c0001t0001g0186 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.-30-772G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542625 | ||||||
chr17:75542683
|
A | C | 148 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(145): Show | 151 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.-30-714A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542683 | ||||||
chr17:75542695
|
C | A | 273 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(270): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-30-702C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542695 | ||||||
chr17:75542720
|
A | T | 273 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(270): Show | 279 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(276): Show |
intron_variant | MODIFIER | c.-30-677A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542720 | ||||||
chr17:75542879
|
C | G | 1 | a0004c0005t0004g0298 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.-30-518C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75542879 | ||||||
chr17:75543104
|
C | T | 8 | a0002c0004t0003g0017a0004c0007t0003g0199a0009c0011t0006g0018others(5): Show | 8 | HG00735.hp2 HG01069.hp1 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.-30-293C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75543104 | ||||||
chr17:75543216
|
G | A | 4 | a0004c0007t0003g0021a0008c0043t0003g0023a0012c0022t0003g0022others(1): Show | 4 | HG02055.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-181G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75543216 | ||||||
chr17:75543282
|
C | G | 7 | a0002c0004t0003g0066a0002c0004t0003g0067a0002c0004t0003g0363others(4): Show | 7 | HG00639.hp1 HG01891.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.-30-115C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75543282 | ||||||
chr17:75543283
|
G | A | 1 | a0004c0007t0003g0027 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.-30-114G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75543283 | ||||||
chr17:75543304
|
T | C | 124 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(121): Show | 127 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(124): Show |
intron_variant | MODIFIER | c.-30-93T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75543304 | ||||||
chr17:75543321
|
C | T | 4 | a0004c0007t0003g0021a0008c0043t0003g0023a0012c0022t0003g0022others(1): Show | 4 | HG02055.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.-30-76C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 1/25 | chr17 | 75543321 | ||||||
chr17:75543550
|
A | G | 289 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(286): Show | 295 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(292): Show |
intron_variant | MODIFIER | c.75+49A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75543550 | ||||||
chr17:75543714
|
G | C | 304 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(301): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.75+213G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75543714 | ||||||
chr17:75543799
|
C | T | 1 | a0002c0003t0005g0114 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.75+298C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75543799 | ||||||
chr17:75543829
|
T | G | 1 | a0001c0001t0001g0144 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.75+328T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75543829 | ||||||
chr17:75543834
|
A | T | 1 | a0001c0001t0001g0006 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.75+333A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75543834 | ||||||
chr17:75543867
|
A | T | 4 | a0004c0007t0003g0021a0008c0043t0003g0023a0012c0022t0003g0022others(1): Show | 4 | HG02055.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+366A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75543867 | ||||||
chr17:75543898
|
C | T | 1 | a0003c0019t0002g0095 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.75+397C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75543898 | ||||||
chr17:75543950
|
C | T | 1 | a0024c0025t0007g0037 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.75+449C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75543950 | ||||||
chr17:75544006
|
G | A | 1 | a0003c0002t0001g0083 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.75+505G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75544006 | ||||||
chr17:75544010
|
G | A | 1 | a0003c0002t0002g0218 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.75+509G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75544010 | ||||||
chr17:75544011
|
G | C | 1 | a0002c0006t0003g0210 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.75+510G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75544011 | ||||||
chr17:75544056
|
T | G | 2 | a0004c0007t0003g0199a0026c0042t0003g0214 | 2 | HG00735.hp2 HG02896.hp2 |
intron_variant | MODIFIER | c.75+555T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75544056 | ||||||
chr17:75544156
|
C | T | 16 | a0002c0004t0003g0063a0002c0004t0003g0089a0002c0006t0003g0004others(13): Show | 17 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.75+655C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75544156 | ||||||
chr17:75544238
|
C | G | 48 | a0001c0001t0002g0354a0001c0001t0002g0357a0001c0001t0002g0358others(45): Show | 49 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.75+737C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75544238 | ||||||
chr17:75544288
|
G | A | 2 | a0004c0018t0005g0109a0004c0018t0005g0190 | 2 | HG02895.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.75+787G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75544288 | ||||||
chr17:75544432
|
T | G | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75+931T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75544432 | ||||||
chr17:75544488
|
C | G | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75+987C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75544488 | ||||||
chr17:75544532
|
T | C | 264 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.75+1031T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75544532 | ||||||
chr17:75544588
|
C | T | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75+1087C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75544588 | ||||||
chr17:75544635
|
T | C | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75+1134T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75544635 | ||||||
chr17:75544636
|
G | A | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75+1135G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75544636 | ||||||
chr17:75544684
|
G | C | 1 | a0003c0002t0002g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.75+1183G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75544684 | ||||||
chr17:75544752
|
T | C | 279 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(276): Show | 285 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(282): Show |
intron_variant | MODIFIER | c.75+1251T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75544752 | ||||||
chr17:75544774
|
T | G | 263 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.75+1273T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75544774 | ||||||
chr17:75544840
|
G | A | 1 | a0026c0042t0003g0214 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.75+1339G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75544840 | ||||||
chr17:75545001
|
G | A | 265 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(262): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.75+1500G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545001 | ||||||
chr17:75545055
|
T | G | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75+1554T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545055 | ||||||
chr17:75545112
|
C | T | 1 | a0001c0001t0001g0042 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.75+1611C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545112 | ||||||
chr17:75545124
|
C | T | 1 | a0003c0019t0002g0095 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.75+1623C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545124 | ||||||
chr17:75545131
|
A | C | 265 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(262): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.75+1630A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545131 | ||||||
chr17:75545145
|
G | A | 1 | a0002c0003t0003g0242 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.75+1644G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545145 | ||||||
chr17:75545363
|
C | G | 1 | a0001c0001t0001g0145 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.75+1862C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545363 | ||||||
chr17:75545385
|
C | T | 1 | a0002c0003t0003g0241 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.75+1884C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545385 | ||||||
chr17:75545490
|
C | T | 1 | a0004c0007t0003g0199 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.75+1989C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545490 | ||||||
chr17:75545502
|
A | C | 2 | a0003c0002t0002g0202a0032c0047t0003g0366 | 2 | HG01109.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.75+2001A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545502 | ||||||
chr17:75545549
|
T | C | 1 | a0003c0002t0002g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.75+2048T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545549 | ||||||
chr17:75545580
|
G | A | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0002g0299others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+2079G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545580 | ||||||
chr17:75545690
|
T | C | 2 | a0002c0003t0003g0320a0002c0003t0003g0321 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.75+2189T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545690 | ||||||
chr17:75545694
|
A | G | 265 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(262): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.75+2193A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545694 | ||||||
chr17:75545720
|
G | A | 1 | a0001c0001t0001g0162 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.75+2219G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545720 | ||||||
chr17:75545770
|
A | C | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75+2269A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545770 | ||||||
chr17:75545781
|
C | T | 31 | a0001c0001t0001g0201a0002c0004t0003g0013a0002c0004t0003g0014others(28): Show | 33 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(30): Show |
intron_variant | MODIFIER | c.75+2280C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545781 | ||||||
chr17:75545924
|
T | C | 275 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(272): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.75+2423T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545924 | ||||||
chr17:75545929
|
G | A | 125 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(122): Show | 128 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.75+2428G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545929 | ||||||
chr17:75545936
|
A | G | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75+2435A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545936 | ||||||
chr17:75545983
|
A | C | 15 | a0001c0001t0002g0354a0001c0001t0002g0357a0001c0001t0002g0358others(12): Show | 15 | HG00544.hp2 HG00597.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.75+2482A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75545983 | ||||||
chr17:75546045
|
G | A | 1 | a0001c0001t0002g0228 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.75+2544G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546045 | ||||||
chr17:75546061
|
C | T | 4 | a0004c0007t0003g0021a0008c0043t0003g0023a0012c0022t0003g0022others(1): Show | 4 | HG02055.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+2560C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546061 | ||||||
chr17:75546115
|
G | A | 125 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(122): Show | 128 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.75+2614G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546115 | ||||||
chr17:75546198
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.75+2697G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546198 | ||||||
chr17:75546198
|
G | T | 1 | a0002c0004t0003g0014 | 2 | NA20752.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.75+2697G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546198 | ||||||
chr17:75546222
|
G | A | 5 | a0004c0018t0005g0109a0004c0018t0005g0190a0004c0050t0006g0062others(2): Show | 5 | HG02258.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+2721G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546222 | ||||||
chr17:75546395
|
T | C | 3 | a0009c0011t0006g0018a0009c0011t0006g0019a0009c0011t0006g0020 | 3 | HG02622.hp2 HG02630.hp1 HG02647.hp1 |
intron_variant | MODIFIER | c.75+2894T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546395 | ||||||
chr17:75546416
|
T | C | 2 | a0002c0004t0003g0335a0002c0004t0003g0337 | 2 | HG02109.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.75+2915T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546416 | ||||||
chr17:75546435
|
A | G | 6 | a0004c0018t0005g0109a0004c0018t0005g0190a0004c0050t0006g0062others(3): Show | 6 | HG02258.hp1 HG02818.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+2934A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546435 | ||||||
chr17:75546468
|
T | C | 6 | a0004c0018t0005g0109a0004c0018t0005g0190a0004c0050t0006g0062others(3): Show | 6 | HG02258.hp1 HG02818.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+2967T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546468 | ||||||
chr17:75546472
|
T | C | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75+2971T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546472 | ||||||
chr17:75546533
|
T | G | 1 | a0002c0003t0003g0244 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.75+3032T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546533 | ||||||
chr17:75546554
|
CCCAGCAG others(17): Show |
C | 2 | a0001c0023t0002g0229a0002c0006t0003g0088 | 2 | HG03688.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.75+3185_75+3208del others(24): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75546554 | |||||
chr17:75546554
|
CCCAGCAG others(233): Show |
C | 2 | a0001c0001t0002g0315a0002c0004t0003g0351 | 2 | HG02602.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.75+3131_75+3370del | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75546554 | |||||
chr17:75546566
|
GCGGAGGG others(209): Show |
G | 272 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(269): Show | 278 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(275): Show |
intron_variant | MODIFIER | c.75+3155_75+3370del | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75546566 | |||||
chr17:75546590
|
G | A | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75+3089G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546590 | ||||||
chr17:75546614
|
GCGGAGGG others(161): Show |
G | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.75+3203_75+3370del | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75546614 | |||||
chr17:75546686
|
G | GCGGAGGG others(17): Show |
12 | a0001c0001t0002g0354a0001c0001t0002g0362a0003c0002t0002g0227others(9): Show | 12 | HG00597.hp2 HG01074.hp1 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.75+3200_75+3201ins others(24): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75546686 | |||||
chr17:75546686
|
G | GCGGAGGG others(17): Show |
1 | a0003c0002t0002g0268 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.75+3209_75+3232dup others(24): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75546686 | |||||
chr17:75546686
|
GCGGAGGG others(17): Show |
G | 1 | a0003c0002t0002g0275 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.75+3209_75+3232del others(24): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75546686 | |||||
chr17:75546702
|
G | A | 2 | a0001c0001t0002g0357a0001c0001t0002g0358 | 2 | HG00544.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.75+3201G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546702 | ||||||
chr17:75546710
|
A | G | 1 | a0003c0002t0002g0255 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.75+3209A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546710 | ||||||
chr17:75546734
|
G | A | 2 | a0001c0001t0002g0357a0001c0001t0002g0358 | 2 | HG00544.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.75+3233G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546734 | ||||||
chr17:75546734
|
GCGGAGGG others(41): Show |
G | 2 | a0002c0006t0003g0090a0002c0006t0003g0098 | 2 | HG06807.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.75+3281_75+3328del others(48): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75546734 | |||||
chr17:75546758
|
GCGGAGGG others(17): Show |
G | 2 | a0001c0001t0002g0357a0001c0001t0002g0358 | 2 | HG00544.hp2 NA19079.hp1 |
intron_variant | MODIFIER | c.75+3281_75+3304del others(24): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75546758 | |||||
chr17:75546782
|
A | G | 3 | a0003c0002t0002g0254a0004c0005t0004g0360a0004c0005t0004g0361 | 3 | HG00597.hp2 NA18982.hp2 NA19084.hp2 |
intron_variant | MODIFIER | c.75+3281A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546782 | ||||||
chr17:75546782
|
ACGGAGGG others(17): Show |
A | 15 | a0002c0004t0003g0063a0002c0004t0003g0089a0002c0006t0003g0004others(12): Show | 16 | HG02145.hp2 HG02258.hp2 HG02486.hp1 others(13): Show |
intron_variant | MODIFIER | c.75+3347_75+3370del others(24): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75546782 | |||||
chr17:75546806
|
G | A | 264 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(261): Show | 270 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(267): Show |
intron_variant | MODIFIER | c.75+3305G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546806 | ||||||
chr17:75546830
|
G | A | 4 | a0001c0001t0002g0315a0001c0001t0002g0357a0001c0001t0002g0358others(1): Show | 4 | HG00544.hp2 HG02602.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+3329G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546830 | ||||||
chr17:75546857
|
G | A | 1 | a0004c0005t0004g0194 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.75+3356G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546857 | ||||||
chr17:75546858
|
AG | A | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0002g0299others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+3360delG | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75546858 | |||||
chr17:75546861
|
G | C | 4 | a0001c0001t0001g0075a0001c0001t0001g0076a0001c0001t0002g0299others(1): Show | 4 | HG01168.hp1 HG01169.hp2 HG01261.hp2 others(1): Show |
intron_variant | MODIFIER | c.75+3360G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546861 | ||||||
chr17:75546917
|
T | C | 144 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(141): Show | 147 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(144): Show |
intron_variant | MODIFIER | c.75+3416T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546917 | ||||||
chr17:75546918
|
G | C | 128 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(125): Show | 131 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(128): Show |
intron_variant | MODIFIER | c.75+3417G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75546918 | ||||||
chr17:75547055
|
G | A | 6 | a0002c0004t0003g0017a0009c0011t0006g0018a0009c0011t0006g0019others(3): Show | 6 | HG01069.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+3554G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75547055 | ||||||
chr17:75547097
|
T | C | 140 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(137): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.75+3596T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75547097 | ||||||
chr17:75547108
|
T | G | 140 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(137): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.75+3607T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75547108 | ||||||
chr17:75547110
|
T | C | 275 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(272): Show | 281 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(278): Show |
intron_variant | MODIFIER | c.75+3609T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75547110 | ||||||
chr17:75547143
|
G | A | 1 | a0004c0007t0003g0199 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.75+3642G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75547143 | ||||||
chr17:75547173
|
C | G | 140 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(137): Show | 143 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(140): Show |
intron_variant | MODIFIER | c.75+3672C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75547173 | ||||||
chr17:75547250
|
G | C | 17 | a0002c0006t0003g0059a0003c0002t0002g0206a0003c0002t0002g0209others(14): Show | 18 | HG00438.hp1 HG01099.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.75+3749G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75547250 | ||||||
chr17:75547300
|
G | T | 17 | a0002c0006t0003g0059a0003c0002t0002g0206a0003c0002t0002g0209others(14): Show | 18 | HG00438.hp1 HG01099.hp2 HG02071.hp2 others(15): Show |
intron_variant | MODIFIER | c.75+3799G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75547300 | ||||||
chr17:75547439
|
C | T | 1 | a0002c0003t0003g0220 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.75+3938C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75547439 | ||||||
chr17:75547538
|
C | T | 5 | a0004c0018t0005g0109a0004c0018t0005g0190a0004c0050t0006g0062others(2): Show | 5 | HG02258.hp1 HG02895.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.75+4037C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75547538 | ||||||
chr17:75547541
|
G | C | 10 | a0004c0007t0003g0021a0004c0018t0005g0109a0004c0018t0005g0190others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+4040G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75547541 | ||||||
chr17:75547592
|
A | G | 130 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(127): Show | 133 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.75+4091A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75547592 | ||||||
chr17:75547602
|
A | G | 6 | a0002c0004t0003g0017a0009c0011t0006g0018a0009c0011t0006g0019others(3): Show | 6 | HG01069.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+4101A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75547602 | ||||||
chr17:75547641
|
A | G | 6 | a0002c0004t0003g0017a0009c0011t0006g0018a0009c0011t0006g0019others(3): Show | 6 | HG01069.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+4140A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75547641 | ||||||
chr17:75547692
|
G | A | 135 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(132): Show | 138 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(135): Show |
intron_variant | MODIFIER | c.75+4191G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75547692 | ||||||
chr17:75547824
|
CA | C | 147 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(144): Show | 150 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.75+4337delA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75547824 | |||||
chr17:75547908
|
G | C | 6 | a0004c0018t0005g0109a0004c0018t0005g0190a0004c0050t0006g0062others(3): Show | 6 | HG02258.hp1 HG02818.hp2 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.75+4407G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75547908 | ||||||
chr17:75548079
|
C | T | 125 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(122): Show | 128 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(125): Show |
intron_variant | MODIFIER | c.75+4578C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548079 | ||||||
chr17:75548096
|
G | T | 145 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(142): Show | 148 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.75+4595G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548096 | ||||||
chr17:75548118
|
C | T | 145 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(142): Show | 148 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.75+4617C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548118 | ||||||
chr17:75548130
|
T | C | 145 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(142): Show | 148 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.75+4629T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548130 | ||||||
chr17:75548143
|
A | C | 1 | a0003c0002t0002g0275 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.75+4642A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548143 | ||||||
chr17:75548178
|
T | TC | 15 | a0001c0001t0002g0354a0001c0001t0002g0357a0001c0001t0002g0358others(12): Show | 15 | HG00544.hp2 HG00597.hp2 HG01074.hp1 others(12): Show |
intron_variant | MODIFIER | c.75+4678dupC | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75548178 | |||||
chr17:75548267
|
A | G | 290 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(287): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.75+4766A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548267 | ||||||
chr17:75548268
|
T | C | 290 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(287): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.75+4767T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548268 | ||||||
chr17:75548273
|
T | C | 290 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(287): Show | 296 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(293): Show |
intron_variant | MODIFIER | c.75+4772T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548273 | ||||||
chr17:75548279
|
CTTT | C | 60 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(57): Show | 61 | HG00408.hp2 HG00438.hp1 HG00741.hp2 others(58): Show |
intron_variant | MODIFIER | c.75+4792_75+4794del others(3): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75548279 | |||||
chr17:75548279
|
CTTTT | C | 75 | a0001c0001t0001g0201a0002c0003t0005g0054a0002c0003t0005g0108others(72): Show | 77 | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(74): Show |
intron_variant | MODIFIER | c.75+4791_75+4794del others(4): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75548279 | |||||
chr17:75548296
|
G | A | 145 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(142): Show | 148 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.75+4795G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548296 | ||||||
chr17:75548307
|
A | C | 145 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(142): Show | 148 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.75+4806A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548307 | ||||||
chr17:75548320
|
C | T | 10 | a0004c0007t0003g0021a0004c0018t0005g0109a0004c0018t0005g0190others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+4819C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548320 | ||||||
chr17:75548371
|
G | A | 11 | a0002c0055t0003g0215a0004c0007t0003g0021a0004c0018t0005g0109others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02809.hp1 others(8): Show |
intron_variant | MODIFIER | c.75+4870G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548371 | ||||||
chr17:75548402
|
C | T | 2 | a0003c0002t0002g0222a0003c0002t0002g0223 | 2 | NA18941.hp2 NA19005.hp1 |
intron_variant | MODIFIER | c.75+4901C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548402 | ||||||
chr17:75548403
|
A | G | 145 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(142): Show | 148 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.75+4902A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548403 | ||||||
chr17:75548742
|
T | C | 145 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(142): Show | 148 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.75+5241T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548742 | ||||||
chr17:75548755
|
CAAA | C | 145 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(142): Show | 148 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.75+5267_75+5269del others(3): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75548755 | |||||
chr17:75548786
|
T | G | 2 | a0001c0001t0001g0033a0001c0001t0001g0034 | 2 | HG00099.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.75+5285T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548786 | ||||||
chr17:75548818
|
G | A | 145 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(142): Show | 148 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.75+5317G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548818 | ||||||
chr17:75548820
|
A | G | 145 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(142): Show | 148 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(145): Show |
intron_variant | MODIFIER | c.75+5319A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548820 | ||||||
chr17:75548858
|
A | G | 104 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(101): Show | 106 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.75+5357A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548858 | ||||||
chr17:75548966
|
T | A | 1 | a0019c0030t0001g0138 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.75+5465T>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548966 | ||||||
chr17:75548984
|
G | A | 10 | a0004c0007t0003g0021a0004c0018t0005g0109a0004c0018t0005g0190others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.75+5483G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75548984 | ||||||
chr17:75549192
|
GGACA | G | 15 | a0001c0001t0001g0031a0001c0001t0001g0039a0001c0001t0001g0040others(12): Show | 15 | HG00438.hp2 HG00733.hp1 HG00741.hp1 others(12): Show |
intron_variant | MODIFIER | c.75+5700_75+5703del others(4): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75549192 | |||||
chr17:75549343
|
C | T | 6 | a0002c0003t0005g0124a0002c0003t0005g0125a0002c0003t0005g0128others(3): Show | 6 | HG01123.hp1 HG01255.hp1 HG01256.hp2 others(3): Show |
intron_variant | MODIFIER | c.75+5842C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75549343 | ||||||
chr17:75549415
|
C | T | 2 | a0002c0012t0003g0323a0002c0012t0003g0324 | 2 | HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.75+5914C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75549415 | ||||||
chr17:75549449
|
G | A | 8 | a0003c0002t0002g0189a0003c0002t0002g0288a0003c0002t0002g0289others(5): Show | 8 | HG00639.hp2 HG01099.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.75+5948G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75549449 | ||||||
chr17:75549460
|
T | C | 263 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(260): Show | 269 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(266): Show |
intron_variant | MODIFIER | c.75+5959T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75549460 | ||||||
chr17:75549602
|
G | T | 130 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(127): Show | 133 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.75+6101G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75549602 | ||||||
chr17:75549603
|
C | T | 2 | a0011c0028t0003g0187a0027c0040t0003g0188 | 2 | HG03225.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.75+6102C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75549603 | ||||||
chr17:75549644
|
G | A | 1 | a0002c0012t0003g0311 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.75+6143G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75549644 | ||||||
chr17:75549644
|
G | T | 1 | a0001c0001t0001g0167 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.75+6143G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75549644 | ||||||
chr17:75549684
|
T | C | 265 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(262): Show | 271 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(268): Show |
intron_variant | MODIFIER | c.75+6183T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75549684 | ||||||
chr17:75549762
|
A | G | 131 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(128): Show | 134 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(131): Show |
intron_variant | MODIFIER | c.75+6261A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75549762 | ||||||
chr17:75549847
|
G | C | 130 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(127): Show | 133 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.76-6199G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75549847 | ||||||
chr17:75549864
|
T | C | 1 | a0001c0001t0001g0028 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.76-6182T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75549864 | ||||||
chr17:75549877
|
C | T | 2 | a0003c0002t0002g0206a0003c0002t0002g0209 | 2 | HG03491.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.76-6169C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75549877 | ||||||
chr17:75549906
|
C | T | 130 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(127): Show | 133 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.76-6140C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75549906 | ||||||
chr17:75549920
|
C | T | 130 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(127): Show | 133 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(130): Show |
intron_variant | MODIFIER | c.76-6126C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75549920 | ||||||
chr17:75549941
|
G | A | 128 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(125): Show | 130 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(127): Show |
intron_variant | MODIFIER | c.76-6105G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75549941 | ||||||
chr17:75549965
|
A | G | 1 | a0002c0004t0003g0347 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.76-6081A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75549965 | ||||||
chr17:75550062
|
G | A | 6 | a0001c0001t0002g0316a0001c0001t0002g0317a0001c0001t0002g0318others(3): Show | 6 | HG01496.hp2 HG01515.hp2 HG01516.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-5984G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75550062 | ||||||
chr17:75550226
|
C | A | 32 | a0001c0001t0001g0201a0002c0004t0003g0013a0002c0004t0003g0014others(29): Show | 34 | HG00733.hp2 HG00735.hp1 HG00738.hp2 others(31): Show |
intron_variant | MODIFIER | c.76-5820C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75550226 | ||||||
chr17:75550243
|
G | C | 133 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(130): Show | 136 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.76-5803G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75550243 | ||||||
chr17:75550376
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.76-5670G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75550376 | ||||||
chr17:75550460
|
G | A | 6 | a0002c0004t0003g0017a0009c0011t0006g0018a0009c0011t0006g0019others(3): Show | 6 | HG01069.hp1 HG02615.hp1 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.76-5586G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75550460 | ||||||
chr17:75550507
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0139 | 2 | HG04115.hp2 HG04199.hp2 |
intron_variant | MODIFIER | c.76-5539G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75550507 | ||||||
chr17:75550690
|
T | C | 4 | a0004c0007t0003g0021a0008c0043t0003g0023a0012c0022t0003g0022others(1): Show | 4 | HG02055.hp1 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.76-5356T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75550690 | ||||||
chr17:75550715
|
A | T | 11 | a0004c0007t0003g0021a0004c0018t0005g0109a0004c0018t0005g0190others(8): Show | 11 | HG02055.hp1 HG02145.hp2 HG02258.hp1 others(8): Show |
intron_variant | MODIFIER | c.76-5331A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75550715 | ||||||
chr17:75550754
|
C | A | 127 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(124): Show | 130 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.76-5292C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75550754 | ||||||
chr17:75550780
|
C | CA | 73 | a0001c0001t0002g0224a0001c0001t0002g0228a0001c0001t0002g0230others(70): Show | 80 | HG00140.hp2 HG00323.hp2 HG00423.hp1 others(77): Show |
intron_variant | MODIFIER | c.76-5242dupA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75550780 | |||||
chr17:75550780
|
C | CAA | 9 | a0003c0002t0002g0213a0003c0002t0002g0222a0003c0002t0002g0252others(6): Show | 9 | HG01099.hp2 HG01256.hp1 HG01952.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-5243_76-5242dup others(2): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75550780 | |||||
chr17:75550780
|
CA | C | 24 | a0001c0001t0001g0201a0001c0001t0002g0316a0002c0003t0003g0240others(21): Show | 24 | HG00438.hp1 HG01255.hp2 HG01358.hp1 others(21): Show |
intron_variant | MODIFIER | c.76-5242delA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75550780 | |||||
chr17:75550780
|
CAA | C | 89 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(86): Show | 91 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(88): Show |
intron_variant | MODIFIER | c.76-5243_76-5242del others(2): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75550780 | |||||
chr17:75550780
|
CAAA | C | 10 | a0001c0001t0002g0318a0001c0001t0002g0326a0002c0003t0005g0054others(7): Show | 10 | HG00140.hp1 HG01074.hp1 HG01515.hp2 others(7): Show |
intron_variant | MODIFIER | c.76-5244_76-5242del others(3): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75550780 | |||||
chr17:75550780
|
CAAAAA | C | 8 | a0001c0001t0001g0111a0001c0001t0001g0134a0001c0001t0001g0139others(5): Show | 8 | HG00741.hp1 HG03831.hp1 HG04199.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-5246_76-5242del others(5): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75550780 | |||||
chr17:75550780
|
CAAAAAA | C | 119 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(116): Show | 122 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(119): Show |
intron_variant | MODIFIER | c.76-5247_76-5242del others(6): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75550780 | |||||
chr17:75550799
|
AAAAAAC | A | 10 | a0004c0018t0005g0109a0004c0018t0005g0190a0004c0050t0006g0062others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02809.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-5245_76-5240del others(6): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75550799 | |||||
chr17:75550803
|
A | AC | 13 | a0001c0001t0002g0354a0001c0001t0002g0357a0001c0001t0002g0358others(10): Show | 13 | HG00544.hp2 HG00597.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.76-5243_76-5242ins others(1): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75550803 | ||||||
chr17:75550803
|
A | C | 127 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(124): Show | 130 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.76-5243A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75550803 | ||||||
chr17:75550826
|
G | A | 113 | a0001c0001t0001g0099a0001c0001t0001g0100a0001c0001t0001g0101others(110): Show | 115 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.76-5220G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75550826 | ||||||
chr17:75550829
|
AC | A | 10 | a0003c0002t0002g0206a0003c0002t0002g0209a0004c0005t0004g0302others(7): Show | 10 | HG00438.hp1 HG02071.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.76-5216delC | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75550829 | ||||||
chr17:75550941
|
C | T | 13 | a0001c0001t0002g0354a0001c0001t0002g0357a0001c0001t0002g0358others(10): Show | 13 | HG00544.hp2 HG00597.hp2 HG01257.hp2 others(10): Show |
intron_variant | MODIFIER | c.76-5105C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75550941 | ||||||
chr17:75550971
|
C | T | 11 | a0002c0003t0003g0250a0003c0002t0002g0206a0003c0002t0002g0209others(8): Show | 11 | HG00438.hp1 HG02015.hp1 HG02071.hp2 others(8): Show |
intron_variant | MODIFIER | c.76-5075C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75550971 | ||||||
chr17:75551088
|
G | C | 139 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(136): Show | 142 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(139): Show |
intron_variant | MODIFIER | c.76-4958G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75551088 | ||||||
chr17:75551099
|
C | T | 1 | a0002c0004t0003g0342 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-4947C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75551099 | ||||||
chr17:75551286
|
A | G | 143 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(140): Show | 146 | HG00099.hp1 HG00323.hp1 HG00408.hp1 others(143): Show |
intron_variant | MODIFIER | c.76-4760A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75551286 | ||||||
chr17:75551300
|
A | G | 4 | a0002c0006t0003g0085a0002c0006t0003g0086a0002c0006t0003g0093others(1): Show | 4 | HG02615.hp2 HG03516.hp2 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-4746A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75551300 | ||||||
chr17:75551536
|
G | A | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.76-4510G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75551536 | ||||||
chr17:75551561
|
G | T | 1 | a0001c0001t0001g0028 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.76-4485G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75551561 | ||||||
chr17:75551603
|
T | G | 1 | a0001c0001t0001g0080 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.76-4443T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75551603 | ||||||
chr17:75551661
|
T | C | 303 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(300): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.76-4385T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75551661 | ||||||
chr17:75551694
|
C | T | 30 | a0003c0002t0002g0206a0003c0002t0002g0209a0003c0002t0002g0227others(27): Show | 30 | HG00438.hp1 HG00597.hp2 HG01257.hp2 others(27): Show |
intron_variant | MODIFIER | c.76-4352C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75551694 | ||||||
chr17:75551754
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0301 | 2 | HG01106.hp2 HG01243.hp2 |
intron_variant | MODIFIER | c.76-4292T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75551754 | ||||||
chr17:75551799
|
A | G | 1 | a0003c0002t0001g0053 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.76-4247A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75551799 | ||||||
chr17:75551854
|
T | C | 1 | a0001c0001t0002g0317 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.76-4192T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75551854 | ||||||
chr17:75551910
|
C | T | 1 | a0012c0022t0003g0024 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.76-4136C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75551910 | ||||||
chr17:75551947
|
G | A | 1 | a0003c0002t0002g0231 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.76-4099G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75551947 | ||||||
chr17:75552062
|
G | A | 147 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(144): Show | 149 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.76-3984G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75552062 | ||||||
chr17:75552068
|
G | T | 2 | a0002c0004t0003g0342a0004c0007t0003g0329 | 2 | HG01106.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.76-3978G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75552068 | ||||||
chr17:75552128
|
T | TA | 155 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(152): Show | 157 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(154): Show |
intron_variant | MODIFIER | c.76-3909dupA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75552128 | |||||
chr17:75552136
|
A | C | 1 | a0004c0007t0003g0199 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.76-3910A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75552136 | ||||||
chr17:75552228
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.76-3818C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75552228 | ||||||
chr17:75552229
|
C | T | 8 | a0004c0005t0004g0302a0004c0005t0004g0303a0004c0005t0004g0304others(5): Show | 8 | HG00438.hp1 HG02071.hp2 HG02080.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-3817C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75552229 | ||||||
chr17:75552333
|
A | G | 1 | a0001c0001t0008g0041 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.76-3713A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75552333 | ||||||
chr17:75552528
|
A | C | 1 | a0001c0001t0001g0101 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.76-3518A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75552528 | ||||||
chr17:75552642
|
A | G | 1 | a0003c0021t0002g0277 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.76-3404A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75552642 | ||||||
chr17:75552643
|
A | T | 1 | a0003c0021t0002g0277 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.76-3403A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75552643 | ||||||
chr17:75552644
|
T | A | 1 | a0003c0021t0002g0277 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.76-3402T>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75552644 | ||||||
chr17:75552753
|
G | C | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.76-3293G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75552753 | ||||||
chr17:75552782
|
C | A | 146 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(143): Show | 148 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(145): Show |
intron_variant | MODIFIER | c.76-3264C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75552782 | ||||||
chr17:75552832
|
T | G | 2 | a0001c0001t0001g0168a0001c0001t0001g0200 | 2 | HG02257.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.76-3214T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75552832 | ||||||
chr17:75552982
|
A | G | 52 | a0001c0001t0001g0201a0002c0004t0003g0013a0002c0004t0003g0014others(49): Show | 54 | HG00733.hp2 HG00735.hp1 HG00735.hp2 others(51): Show |
intron_variant | MODIFIER | c.76-3064A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75552982 | ||||||
chr17:75552989
|
T | C | 2 | a0004c0007t0003g0027a0004c0007t0003g0312 | 2 | HG02451.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.76-3057T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75552989 | ||||||
chr17:75552994
|
T | A | 1 | a0001c0001t0001g0161 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.76-3052T>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75552994 | ||||||
chr17:75553107
|
A | C | 1 | a0011c0028t0003g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.76-2939A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75553107 | ||||||
chr17:75553224
|
C | T | 10 | a0003c0002t0002g0206a0003c0002t0002g0209a0004c0005t0004g0302others(7): Show | 10 | HG00438.hp1 HG02071.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.76-2822C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75553224 | ||||||
chr17:75553265
|
G | T | 6 | a0002c0004t0003g0066a0002c0004t0003g0067a0002c0004t0003g0363others(3): Show | 6 | HG00639.hp1 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-2781G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75553265 | ||||||
chr17:75553314
|
A | G | 10 | a0003c0002t0002g0206a0003c0002t0002g0209a0004c0005t0004g0302others(7): Show | 10 | HG00438.hp1 HG02071.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.76-2732A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75553314 | ||||||
chr17:75553427
|
T | C | 6 | a0002c0004t0003g0066a0002c0004t0003g0067a0002c0004t0003g0363others(3): Show | 6 | HG00639.hp1 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-2619T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75553427 | ||||||
chr17:75553449
|
G | A | 3 | a0003c0002t0002g0288a0003c0002t0002g0289a0030c0053t0002g0290 | 3 | HG00639.hp2 HG01496.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.76-2597G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75553449 | ||||||
chr17:75553701
|
C | T | 8 | a0004c0007t0003g0021a0008c0043t0003g0023a0008c0044t0003g0097others(5): Show | 8 | HG02055.hp1 HG02572.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.76-2345C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75553701 | ||||||
chr17:75553726
|
G | T | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.76-2320G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75553726 | ||||||
chr17:75553750
|
C | G | 1 | a0001c0001t0001g0143 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.76-2296C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75553750 | ||||||
chr17:75553966
|
A | G | 286 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(283): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.76-2080A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75553966 | ||||||
chr17:75553978
|
A | C | 164 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(161): Show | 166 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.76-2068A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75553978 | ||||||
chr17:75554023
|
C | G | 9 | a0003c0002t0002g0227a0003c0054t0001g0107a0004c0005t0004g0355others(6): Show | 9 | HG00597.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-2023C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554023 | ||||||
chr17:75554025
|
G | A | 1 | a0003c0002t0002g0232 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.76-2021G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554025 | ||||||
chr17:75554044
|
G | A | 1 | a0016c0056t0001g0136 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.76-2002G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554044 | ||||||
chr17:75554115
|
A | T | 14 | a0002c0004t0003g0089a0002c0006t0003g0004a0002c0006t0003g0085others(11): Show | 15 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(12): Show |
intron_variant | MODIFIER | c.76-1931A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554115 | ||||||
chr17:75554201
|
C | T | 3 | a0002c0004t0003g0017a0015c0017t0003g0016a0015c0017t0003g0026 | 3 | HG01069.hp1 HG02615.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.76-1845C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554201 | ||||||
chr17:75554270
|
C | T | 11 | a0002c0004t0003g0017a0004c0007t0003g0021a0008c0043t0003g0023others(8): Show | 11 | HG01069.hp1 HG02055.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.76-1776C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554270 | ||||||
chr17:75554299
|
T | C | 10 | a0003c0002t0002g0206a0003c0002t0002g0209a0004c0005t0004g0302others(7): Show | 10 | HG00438.hp1 HG02071.hp2 HG02080.hp2 others(7): Show |
intron_variant | MODIFIER | c.76-1747T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554299 | ||||||
chr17:75554302
|
C | CA | 131 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(128): Show | 135 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(132): Show |
intron_variant | MODIFIER | c.76-1726dupA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75554302 | |||||
chr17:75554302
|
C | CAA | 9 | a0002c0003t0003g0245a0002c0004t0003g0363a0002c0006t0003g0090others(6): Show | 9 | HG00733.hp2 HG02896.hp2 HG02965.hp1 others(6): Show |
intron_variant | MODIFIER | c.76-1727_76-1726dup others(2): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75554302 | |||||
chr17:75554302
|
CAAAAAAA others(1): Show |
C | 158 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(155): Show | 160 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(157): Show |
intron_variant | MODIFIER | c.76-1733_76-1726del others(8): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75554302 | |||||
chr17:75554364
|
C | T | 147 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(144): Show | 149 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.76-1682C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554364 | ||||||
chr17:75554377
|
C | T | 147 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(144): Show | 149 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(146): Show |
intron_variant | MODIFIER | c.76-1669C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554377 | ||||||
chr17:75554392
|
G | A | 1 | a0001c0001t0001g0146 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.76-1654G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554392 | ||||||
chr17:75554404
|
A | G | 286 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(283): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.76-1642A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554404 | ||||||
chr17:75554409
|
T | C | 164 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(161): Show | 166 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.76-1637T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554409 | ||||||
chr17:75554471
|
T | C | 286 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(283): Show | 291 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(288): Show |
intron_variant | MODIFIER | c.76-1575T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554471 | ||||||
chr17:75554497
|
G | C | 1 | a0003c0002t0002g0232 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.76-1549G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554497 | ||||||
chr17:75554579
|
C | T | 2 | a0004c0005t0004g0057a0004c0005t0004g0058 | 2 | HG02896.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.76-1467C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554579 | ||||||
chr17:75554580
|
G | A | 164 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(161): Show | 166 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.76-1466G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554580 | ||||||
chr17:75554755
|
G | A | 3 | a0001c0001t0001g0201a0006c0015t0005g0172a0006c0015t0005g0173 | 3 | HG02280.hp1 HG02559.hp2 HG02818.hp1 |
intron_variant | MODIFIER | c.76-1291G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554755 | ||||||
chr17:75554821
|
G | A | 2 | a0003c0002t0002g0225a0003c0002t0002g0233 | 2 | NA18972.hp2 NA19085.hp1 |
intron_variant | MODIFIER | c.76-1225G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554821 | ||||||
chr17:75554863
|
TG | T | 6 | a0002c0004t0003g0066a0002c0004t0003g0067a0002c0004t0003g0363others(3): Show | 6 | HG00639.hp1 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-1180delG | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75554863 | |||||
chr17:75554888
|
C | CA | 142 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(139): Show | 144 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(141): Show |
intron_variant | MODIFIER | c.76-1143dupA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75554888 | |||||
chr17:75554903
|
A | T | 2 | a0002c0055t0003g0215a0003c0054t0001g0107 | 2 | NA18522.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.76-1143A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554903 | ||||||
chr17:75554946
|
C | T | 1 | a0002c0004t0003g0342 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.76-1100C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75554946 | ||||||
chr17:75555070
|
G | A | 5 | a0001c0001t0001g0152a0001c0001t0001g0164a0007c0010t0002g0012others(2): Show | 6 | NA18969.hp1 NA18979.hp1 NA18982.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-976G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75555070 | ||||||
chr17:75555101
|
C | T | 1 | a0003c0002t0001g0053 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.76-945C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75555101 | ||||||
chr17:75555119
|
G | A | 143 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(140): Show | 145 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.76-927G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75555119 | ||||||
chr17:75555221
|
A | G | 11 | a0002c0004t0003g0017a0004c0007t0003g0021a0008c0043t0003g0023others(8): Show | 11 | HG01069.hp1 HG02055.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.76-825A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75555221 | ||||||
chr17:75555240
|
A | C | 1 | a0001c0001t0008g0041 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.76-806A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75555240 | ||||||
chr17:75555290
|
CT | C | 117 | a0002c0003t0003g0220a0002c0003t0003g0240a0002c0003t0003g0241others(114): Show | 119 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(116): Show |
intron_variant | MODIFIER | c.76-739delT | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75555290 | |||||
chr17:75555290
|
CTTT | C | 160 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(157): Show | 162 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(159): Show |
intron_variant | MODIFIER | c.76-741_76-739delTT others(1): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr17 | 75555290 | |||||
chr17:75555310
|
G | A | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.76-736G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75555310 | ||||||
chr17:75555352
|
G | T | 1 | a0002c0003t0003g0240 | 1 | NA18989.hp2 | intron_variant | MODIFIER | c.76-694G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75555352 | ||||||
chr17:75555405
|
A | G | 4 | a0002c0006t0003g0025a0002c0006t0005g0112a0003c0002t0002g0202others(1): Show | 4 | HG01109.hp1 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-641A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75555405 | ||||||
chr17:75555501
|
A | G | 6 | a0002c0004t0003g0066a0002c0004t0003g0067a0002c0004t0003g0363others(3): Show | 6 | HG00639.hp1 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.76-545A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75555501 | ||||||
chr17:75555718
|
C | T | 4 | a0002c0006t0003g0025a0002c0006t0005g0112a0003c0002t0002g0202others(1): Show | 4 | HG01109.hp1 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.76-328C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75555718 | ||||||
chr17:75555870
|
CA | C | 11 | a0002c0004t0003g0017a0004c0007t0003g0021a0008c0043t0003g0023others(8): Show | 11 | HG01069.hp1 HG02055.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.76-175delA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75555870 | ||||||
chr17:75555870
|
CAG | C | 9 | a0003c0002t0002g0227a0003c0054t0001g0107a0004c0005t0004g0355others(6): Show | 9 | HG00597.hp2 HG01257.hp2 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.76-175_76-174delAG | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75555870 | ||||||
chr17:75555955
|
C | T | 10 | a0002c0004t0003g0066a0002c0004t0003g0067a0002c0004t0003g0363others(7): Show | 10 | HG00639.hp1 HG01109.hp1 HG02922.hp1 others(7): Show |
intron_variant | MODIFIER | c.76-91C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75555955 | ||||||
chr17:75555965
|
G | A | 11 | a0002c0004t0003g0017a0004c0007t0003g0021a0008c0043t0003g0023others(8): Show | 11 | HG01069.hp1 HG02055.hp1 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.76-81G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75555965 | ||||||
chr17:75555981
|
G | C | 165 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(162): Show | 167 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(164): Show |
intron_variant | MODIFIER | c.76-65G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 2/25 | chr17 | 75555981 | ||||||
chr17:75556267
|
C | T | 1 | a0019c0030t0001g0138 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.173+124C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75556267 | ||||||
chr17:75556341
|
C | A | 2 | a0002c0006t0003g0025a0002c0006t0005g0112 | 2 | HG03209.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.173+198C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75556341 | ||||||
chr17:75556408
|
T | C | 3 | a0002c0004t0003g0363a0002c0004t0003g0364a0002c0004t0003g0365 | 3 | HG02965.hp1 HG03139.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.173+265T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75556408 | ||||||
chr17:75556445
|
C | G | 164 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(161): Show | 166 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.173+302C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75556445 | ||||||
chr17:75556776
|
G | A | 4 | a0002c0006t0003g0025a0002c0006t0005g0112a0003c0002t0002g0202others(1): Show | 4 | HG01109.hp1 HG03209.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.173+633G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75556776 | ||||||
chr17:75556779
|
A | C | 21 | a0002c0004t0003g0017a0002c0004t0003g0066a0002c0004t0003g0067others(18): Show | 21 | HG00639.hp1 HG01069.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.173+636A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75556779 | ||||||
chr17:75556786
|
G | A | 21 | a0002c0004t0003g0017a0002c0004t0003g0066a0002c0004t0003g0067others(18): Show | 21 | HG00639.hp1 HG01069.hp1 HG01109.hp1 others(18): Show |
intron_variant | MODIFIER | c.173+643G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75556786 | ||||||
chr17:75556827
|
G | A | 164 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(161): Show | 166 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.173+684G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75556827 | ||||||
chr17:75556943
|
C | T | 1 | a0001c0001t0002g0357 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.173+800C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75556943 | ||||||
chr17:75556944
|
G | A | 6 | a0002c0004t0003g0066a0002c0004t0003g0067a0002c0004t0003g0363others(3): Show | 6 | HG00639.hp1 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.173+801G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75556944 | ||||||
chr17:75556985
|
T | C | 164 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(161): Show | 166 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(163): Show |
intron_variant | MODIFIER | c.173+842T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75556985 | ||||||
chr17:75557007
|
C | A | 3 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0153 | 3 | NA18964.hp2 NA18966.hp1 NA18987.hp2 |
intron_variant | MODIFIER | c.173+864C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75557007 | ||||||
chr17:75557034
|
C | CT | 113 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(110): Show | 116 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(113): Show |
intron_variant | MODIFIER | c.173+916dupT | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr17 | 75557034 | |||||
chr17:75557034
|
C | CTT | 17 | a0002c0003t0005g0127a0002c0004t0003g0195a0002c0004t0003g0282others(14): Show | 17 | HG00735.hp1 HG01109.hp2 HG01361.hp1 others(14): Show |
intron_variant | MODIFIER | c.173+915_173+916dup others(2): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr17 | 75557034 | |||||
chr17:75557034
|
C | CTTTTTTT others(8): Show |
3 | a0002c0004t0003g0363a0002c0004t0003g0365a0031c0049t0003g0065 | 3 | HG02922.hp1 HG02965.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.173+902_173+916dup others(15): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr17 | 75557034 | |||||
chr17:75557034
|
C | CTTTTTTT others(9): Show |
3 | a0002c0004t0003g0066a0002c0004t0003g0067a0002c0004t0003g0364 | 3 | HG00639.hp1 HG02970.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.173+901_173+916dup others(16): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr17 | 75557034 | |||||
chr17:75557034
|
CTTTTTTT others(5): Show |
C | 143 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(140): Show | 145 | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(142): Show |
intron_variant | MODIFIER | c.173+905_173+916del others(12): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr17 | 75557034 | |||||
chr17:75557130
|
T | C | 24 | a0001c0001t0001g0074a0001c0001t0001g0077a0001c0001t0001g0080others(21): Show | 24 | HG00558.hp1 HG00558.hp2 HG02027.hp2 others(21): Show |
intron_variant | MODIFIER | c.173+987T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75557130 | ||||||
chr17:75557373
|
C | T | 2 | a0001c0001t0001g0120a0001c0001t0001g0122 | 2 | NA18953.hp1 NA18955.hp2 |
intron_variant | MODIFIER | c.174-782C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75557373 | ||||||
chr17:75557437
|
TG | T | 6 | a0002c0004t0003g0066a0002c0004t0003g0067a0002c0004t0003g0363others(3): Show | 6 | HG00639.hp1 HG02922.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.174-713delG | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr17 | 75557437 | |||||
chr17:75557482
|
G | A | 1 | a0001c0001t0001g0168 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.174-673G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75557482 | ||||||
chr17:75557540
|
A | G | 11 | a0003c0002t0002g0227a0003c0002t0002g0268a0003c0002t0002g0274others(8): Show | 11 | HG00597.hp2 HG01257.hp2 HG01258.hp2 others(8): Show |
intron_variant | MODIFIER | c.174-615A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75557540 | ||||||
chr17:75557594
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.174-561C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75557594 | ||||||
chr17:75557815
|
A | T | 8 | a0004c0007t0003g0199a0004c0018t0005g0109a0004c0018t0005g0190others(5): Show | 8 | HG02145.hp2 HG02258.hp1 HG02818.hp2 others(5): Show |
intron_variant | MODIFIER | c.174-340A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75557815 | ||||||
chr17:75557847
|
T | C | 111 | a0001c0001t0001g0044a0002c0003t0003g0220a0002c0003t0003g0226others(108): Show | 114 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.174-308T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75557847 | ||||||
chr17:75557919
|
CCACCGGC others(31): Show |
C | 1 | a0001c0001t0001g0167 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.174-232_174-195del others(38): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr17 | 75557919 | |||||
chr17:75557984
|
G | A | 1 | a0002c0004t0003g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.174-171G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75557984 | ||||||
chr17:75558052
|
T | C | 4 | a0002c0006t0003g0059a0004c0005t0004g0003a0004c0005t0004g0057others(1): Show | 5 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(2): Show |
intron_variant | MODIFIER | c.174-103T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75558052 | ||||||
chr17:75558083
|
C | T | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.174-72C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75558083 | ||||||
chr17:75558105
|
G | C | 20 | a0001c0001t0001g0176a0003c0002t0002g0227a0003c0002t0002g0268others(17): Show | 20 | HG00438.hp1 HG00597.hp2 HG01257.hp2 others(17): Show |
intron_variant | MODIFIER | c.174-50G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 3/25 | chr17 | 75558105 | ||||||
chr17:75558282
|
T | C | 7 | a0002c0004t0003g0066a0002c0004t0003g0067a0002c0004t0003g0342others(4): Show | 7 | HG00639.hp1 HG01884.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.255+46T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 4/25 | chr17 | 75558282 | ||||||
chr17:75558369
|
C | T | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.255+133C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 4/25 | chr17 | 75558369 | ||||||
chr17:75558442
|
C | G | 183 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0029others(180): Show | 191 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(188): Show |
intron_variant | MODIFIER | c.256-70C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 4/25 | chr17 | 75558442 | ||||||
chr17:75558675
|
C | T | 15 | a0002c0003t0005g0005a0002c0003t0005g0054a0002c0003t0005g0108others(12): Show | 16 | HG00642.hp2 HG01123.hp1 HG01255.hp1 others(13): Show |
intron_variant | MODIFIER | c.371+48C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558675 | ||||||
chr17:75558730
|
C | T | 1 | a0008c0044t0003g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.371+103C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558730 | ||||||
chr17:75558803
|
C | A | 1 | a0002c0004t0003g0335 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.371+176C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558803 | ||||||
chr17:75558805
|
T | TGCCTCCT others(33): Show |
2 | a0003c0002t0002g0330a0003c0021t0002g0331 | 2 | HG01109.hp2 HG01516.hp2 |
intron_variant | MODIFIER | c.371+211_371+212ins others(40): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr17 | 75558805 | |||||
chr17:75558806
|
GCCTCCTC others(73): Show |
G | 231 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(228): Show | 238 | HG00099.hp1 HG00140.hp2 HG00323.hp2 others(235): Show |
intron_variant | MODIFIER | c.371+259_372-287del others(80): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr17 | 75558806 | |||||
chr17:75558824
|
A | ACGCCTCC others(213): Show |
1 | a0002c0006t0003g0313 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.371+211_371+212ins others(220): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr17 | 75558824 | |||||
chr17:75558824
|
A | ACGCCTCC others(193): Show |
1 | a0002c0006t0003g0086 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.371+211_371+212ins others(200): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr17 | 75558824 | |||||
chr17:75558824
|
A | ACGCCTCC others(213): Show |
9 | a0002c0004t0003g0089a0002c0006t0003g0004a0002c0006t0003g0085others(6): Show | 10 | HG02258.hp2 HG02486.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.371+211_371+212ins others(220): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr17 | 75558824 | |||||
chr17:75558825
|
C | T | 1 | a0002c0003t0005g0105 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.371+198C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558825 | ||||||
chr17:75558826
|
GCCTCCTC others(53): Show |
G | 2 | a0001c0037t0001g0149a0027c0040t0003g0188 | 2 | HG00323.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.371+212_371+271del others(60): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr17 | 75558826 | |||||
chr17:75558837
|
CCGCACCC others(75): Show |
C | 19 | a0002c0004t0003g0342a0003c0019t0002g0095a0003c0019t0002g0212others(16): Show | 19 | HG00735.hp2 HG01106.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.371+212_371+293del others(82): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr17 | 75558837 | |||||
chr17:75558839
|
G | A | 60 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0002g0243others(57): Show | 62 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(59): Show |
intron_variant | MODIFIER | c.371+212G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558839 | ||||||
chr17:75558843
|
C | CACGCCTC others(11): Show |
3 | a0001c0001t0001g0162a0001c0001t0001g0163a0002c0004t0003g0063 | 3 | HG02717.hp2 HG03834.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.371+216_371+217ins others(18): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558843 | ||||||
chr17:75558843
|
C | CACGCCTC others(31): Show |
1 | a0002c0004t0003g0349 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.371+216_371+217ins others(38): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558843 | ||||||
chr17:75558843
|
C | CACGCCTC others(51): Show |
2 | a0002c0004t0003g0351a0003c0002t0002g0332 | 2 | HG01255.hp2 HG02809.hp2 |
intron_variant | MODIFIER | c.371+216_371+217ins others(58): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558843 | ||||||
chr17:75558843
|
C | CACGCCTC others(131): Show |
1 | a0002c0004t0003g0195 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.371+216_371+217ins others(138): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558843 | ||||||
chr17:75558843
|
C | CATGCCTC others(11): Show |
2 | a0002c0003t0003g0245a0002c0003t0003g0271 | 2 | NA18977.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.371+216_371+217ins others(18): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558843 | ||||||
chr17:75558844
|
C | A | 53 | a0001c0001t0002g0243a0002c0003t0003g0220a0002c0003t0003g0226others(50): Show | 55 | HG00544.hp1 HG00735.hp1 HG00738.hp2 others(52): Show |
intron_variant | MODIFIER | c.371+217C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558844 | ||||||
chr17:75558844
|
CCACCTCC others(53): Show |
C | 4 | a0002c0013t0003g0192a0002c0013t0003g0196a0002c0013t0003g0334others(1): Show | 4 | HG00140.hp1 HG02976.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.371+219_371+278del others(60): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr17 | 75558844 | |||||
chr17:75558845
|
C | T | 36 | a0001c0001t0002g0243a0002c0003t0003g0220a0002c0003t0003g0226others(33): Show | 37 | HG00544.hp1 HG00738.hp2 HG01069.hp2 others(34): Show |
intron_variant | MODIFIER | c.371+218C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558845 | ||||||
chr17:75558846
|
A | ACCTCCTC others(13): Show |
2 | a0002c0004t0003g0017a0015c0017t0003g0026 | 2 | HG01069.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.371+239_371+258dup others(20): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr17 | 75558846 | |||||
chr17:75558846
|
A | ACG | 6 | a0001c0001t0001g0162a0001c0001t0001g0163a0002c0004t0003g0195others(3): Show | 6 | HG01255.hp2 HG01361.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.371+220_371+221ins others(2): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr17 | 75558846 | |||||
chr17:75558846
|
A | ATG | 3 | a0002c0003t0003g0245a0002c0003t0003g0271a0002c0004t0003g0063 | 3 | HG02717.hp2 NA18977.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.371+219_371+220ins others(2): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558846 | ||||||
chr17:75558846
|
A | G | 65 | a0001c0001t0002g0243a0002c0003t0003g0220a0002c0003t0003g0226others(62): Show | 68 | HG00408.hp2 HG00544.hp1 HG00735.hp1 others(65): Show |
intron_variant | MODIFIER | c.371+219A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558846 | ||||||
chr17:75558859
|
G | A | 37 | a0001c0001t0002g0243a0002c0003t0003g0220a0002c0003t0003g0226others(34): Show | 38 | HG00544.hp1 HG00735.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.371+232G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558859 | ||||||
chr17:75558864
|
C | A | 42 | a0001c0001t0002g0243a0002c0003t0003g0220a0002c0003t0003g0226others(39): Show | 43 | HG00544.hp1 HG00735.hp1 HG01069.hp2 others(40): Show |
intron_variant | MODIFIER | c.371+237C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558864 | ||||||
chr17:75558864
|
CCGCCTCC others(33): Show |
C | 16 | a0002c0003t0005g0105a0002c0004t0003g0066a0002c0004t0003g0363others(13): Show | 17 | HG00408.hp2 HG00639.hp1 HG01099.hp2 others(14): Show |
intron_variant | MODIFIER | c.371+272_371+311del others(40): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr17 | 75558864 | |||||
chr17:75558865
|
C | T | 37 | a0001c0001t0002g0243a0002c0003t0003g0220a0002c0003t0003g0226others(34): Show | 38 | HG00544.hp1 HG00735.hp1 HG01069.hp2 others(35): Show |
intron_variant | MODIFIER | c.371+238C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558865 | ||||||
chr17:75558866
|
GCCTCCTC others(53): Show |
G | 1 | a0001c0024t0002g0217 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.371+259_372-307del others(60): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr17 | 75558866 | |||||
chr17:75558884
|
CCACCTCC others(13): Show |
C | 31 | a0001c0001t0002g0243a0002c0003t0003g0249a0002c0003t0005g0005others(28): Show | 33 | HG00099.hp2 HG00544.hp1 HG00642.hp2 others(30): Show |
intron_variant | MODIFIER | c.371+259_371+278del others(20): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr17 | 75558884 | |||||
chr17:75558886
|
A | G | 63 | a0001c0001t0001g0162a0001c0001t0001g0163a0002c0003t0003g0220others(60): Show | 65 | HG00735.hp1 HG01069.hp2 HG01071.hp1 others(62): Show |
intron_variant | MODIFIER | c.371+259A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558886 | ||||||
chr17:75558899
|
A | G | 74 | a0001c0001t0001g0162a0001c0001t0001g0163a0002c0003t0003g0220others(71): Show | 76 | HG00735.hp1 HG01069.hp1 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.371+272A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558899 | ||||||
chr17:75558904
|
A | C | 74 | a0001c0001t0001g0162a0001c0001t0001g0163a0002c0003t0003g0220others(71): Show | 76 | HG00735.hp1 HG01069.hp1 HG01069.hp2 others(73): Show |
intron_variant | MODIFIER | c.371+277A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558904 | ||||||
chr17:75558905
|
C | T | 2 | a0001c0037t0001g0149a0002c0006t0003g0096 | 2 | HG00323.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.371+278C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558905 | ||||||
chr17:75558919
|
G | A | 11 | a0002c0004t0003g0089a0002c0006t0003g0004a0002c0006t0003g0085others(8): Show | 12 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.371+292G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558919 | ||||||
chr17:75558923
|
C | A | 19 | a0002c0004t0003g0342a0003c0019t0002g0095a0003c0019t0002g0212others(16): Show | 19 | HG00735.hp2 HG01106.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.371+296C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558923 | ||||||
chr17:75558924
|
C | A | 11 | a0002c0004t0003g0089a0002c0006t0003g0004a0002c0006t0003g0085others(8): Show | 12 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.371+297C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558924 | ||||||
chr17:75558925
|
C | CGCCTCCT others(193): Show |
1 | a0002c0006t0003g0096 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.371+298_371+299ins others(200): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558925 | ||||||
chr17:75558925
|
C | T | 11 | a0002c0004t0003g0089a0002c0006t0003g0004a0002c0006t0003g0085others(8): Show | 12 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(9): Show |
intron_variant | MODIFIER | c.371+298C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558925 | ||||||
chr17:75558926
|
A | ATG | 19 | a0002c0004t0003g0342a0003c0019t0002g0095a0003c0019t0002g0212others(16): Show | 19 | HG00735.hp2 HG01106.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.371+299_371+300ins others(2): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558926 | ||||||
chr17:75558926
|
A | G | 126 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0002g0243others(123): Show | 131 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.371+299A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558926 | ||||||
chr17:75558946
|
G | A | 19 | a0002c0004t0003g0342a0003c0019t0002g0095a0003c0019t0002g0212others(16): Show | 19 | HG00735.hp2 HG01106.hp1 HG01884.hp1 others(16): Show |
intron_variant | MODIFIER | c.372-306G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558946 | ||||||
chr17:75558963
|
C | T | 33 | a0001c0001t0001g0162a0001c0001t0001g0163a0002c0003t0003g0271others(30): Show | 34 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(31): Show |
intron_variant | MODIFIER | c.372-289C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558963 | ||||||
chr17:75558966
|
G | A | 10 | a0002c0006t0003g0025a0002c0006t0005g0112a0004c0018t0005g0109others(7): Show | 10 | HG02145.hp2 HG02258.hp1 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.372-286G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558966 | ||||||
chr17:75558978
|
C | CGCACCCC others(13): Show |
12 | a0002c0003t0003g0244a0002c0003t0003g0276a0002c0004t0003g0195others(9): Show | 12 | HG01109.hp2 HG01123.hp2 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.372-255_372-254ins others(20): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr17 | 75558978 | |||||
chr17:75558978
|
C | CGCACTCC others(13): Show |
60 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(57): Show | 63 | HG00099.hp2 HG00408.hp2 HG00642.hp2 others(60): Show |
intron_variant | MODIFIER | c.372-270_372-269ins others(20): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | INFO_REALIGN_3_PRIME | chr17 | 75558978 | |||||
chr17:75558978
|
C | G | 39 | a0001c0001t0001g0162a0001c0001t0001g0163a0002c0003t0003g0245others(36): Show | 40 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.372-274C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558978 | ||||||
chr17:75558983
|
C | T | 1 | a0002c0046t0005g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.372-269C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558983 | ||||||
chr17:75558998
|
T | C | 12 | a0002c0004t0003g0089a0002c0006t0003g0004a0002c0006t0003g0085others(9): Show | 13 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.372-254T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558998 | ||||||
chr17:75558998
|
T | G | 1 | a0002c0046t0005g0119 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.372-254T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75558998 | ||||||
chr17:75559005
|
C | T | 5 | a0002c0004t0003g0066a0002c0004t0003g0363a0002c0004t0003g0364others(2): Show | 5 | HG00639.hp1 HG02922.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.372-247C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75559005 | ||||||
chr17:75559012
|
T | C | 1 | a0003c0002t0002g0263 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.372-240T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75559012 | ||||||
chr17:75559028
|
G | T | 1 | a0023c0026t0001g0151 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.372-224G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75559028 | ||||||
chr17:75559210
|
G | A | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.372-42G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 5/25 | chr17 | 75559210 | ||||||
chr17:75559504
|
T | A | 29 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(26): Show | 29 | HG00408.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.530+94T>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75559504 | ||||||
chr17:75559579
|
T | C | 1 | a0004c0007t0003g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.530+169T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75559579 | ||||||
chr17:75559606
|
A | T | 5 | a0002c0006t0003g0025a0002c0006t0005g0112a0002c0013t0003g0192others(2): Show | 5 | HG00140.hp1 HG02976.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.530+196A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75559606 | ||||||
chr17:75559730
|
G | A | 1 | a0001c0001t0001g0075 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.530+320G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75559730 | ||||||
chr17:75559738
|
C | T | 1 | a0011c0028t0003g0187 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.530+328C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75559738 | ||||||
chr17:75559739
|
G | A | 2 | a0004c0007t0003g0091a0004c0007t0003g0199 | 2 | HG02896.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.530+329G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75559739 | ||||||
chr17:75559821
|
G | A | 3 | a0001c0001t0001g0029a0001c0001t0001g0049a0001c0001t0002g0243 | 3 | HG00544.hp1 NA18954.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.530+411G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75559821 | ||||||
chr17:75559824
|
A | G | 161 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(158): Show | 166 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530+414A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75559824 | ||||||
chr17:75559954
|
A | T | 1 | a0008c0044t0003g0097 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.530+544A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75559954 | ||||||
chr17:75560002
|
G | C | 2 | a0004c0005t0004g0207a0004c0005t0004g0208 | 2 | HG01099.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.530+592G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560002 | ||||||
chr17:75560066
|
G | A | 1 | a0003c0002t0002g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.530+656G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560066 | ||||||
chr17:75560142
|
G | C | 1 | a0002c0004t0003g0335 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.530+732G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560142 | ||||||
chr17:75560178
|
G | A | 17 | a0002c0003t0005g0005a0002c0003t0005g0054a0002c0003t0005g0108others(14): Show | 18 | HG00099.hp2 HG00642.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.530+768G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560178 | ||||||
chr17:75560183
|
T | C | 1 | a0014c0020t0003g0064 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.530+773T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560183 | ||||||
chr17:75560411
|
C | T | 4 | a0013c0016t0003g0056a0013c0016t0003g0061a0014c0020t0003g0064others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.530+1001C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560411 | ||||||
chr17:75560426
|
C | CG | 98 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(95): Show | 101 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.530+1023dupG | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr17 | 75560426 | |||||
chr17:75560486
|
A | T | 1 | a0019c0030t0001g0138 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.530+1076A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560486 | ||||||
chr17:75560526
|
C | G | 161 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(158): Show | 166 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.530+1116C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560526 | ||||||
chr17:75560696
|
A | G | 98 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(95): Show | 101 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.530+1286A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560696 | ||||||
chr17:75560709
|
C | T | 1 | a0025c0039t0004g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.530+1299C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560709 | ||||||
chr17:75560802
|
T | TA | 94 | a0001c0001t0001g0007a0001c0001t0001g0029a0001c0001t0001g0033others(91): Show | 96 | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(93): Show |
intron_variant | MODIFIER | c.530+1422dupA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr17 | 75560802 | |||||
chr17:75560802
|
T | TAA | 6 | a0001c0001t0001g0123a0001c0001t0001g0148a0001c0001t0001g0301others(3): Show | 6 | HG00642.hp1 HG01106.hp2 HG01192.hp2 others(3): Show |
intron_variant | MODIFIER | c.530+1421_530+1422d others(4): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr17 | 75560802 | |||||
chr17:75560802
|
TA | T | 8 | a0001c0001t0001g0074a0001c0001t0001g0078a0001c0001t0001g0080others(5): Show | 8 | HG00735.hp2 HG01256.hp1 HG02027.hp2 others(5): Show |
intron_variant | MODIFIER | c.530+1422delA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr17 | 75560802 | |||||
chr17:75560802
|
TAAA | T | 31 | a0001c0001t0001g0143a0002c0004t0003g0089a0002c0004t0003g0342others(28): Show | 32 | HG00438.hp1 HG00597.hp2 HG00741.hp2 others(29): Show |
intron_variant | MODIFIER | c.530+1420_530+1422d others(5): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr17 | 75560802 | |||||
chr17:75560802
|
TAAAAAAA others(3): Show |
T | 2 | a0003c0002t0002g0314a0004c0018t0005g0109 | 2 | HG01074.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.530+1413_530+1422d others(12): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr17 | 75560802 | |||||
chr17:75560802
|
TAAAAAAA others(7): Show |
T | 4 | a0002c0006t0003g0059a0004c0005t0004g0003a0004c0005t0004g0057others(1): Show | 5 | HG02109.hp2 HG02896.hp1 HG02970.hp1 others(2): Show |
intron_variant | MODIFIER | c.530+1409_530+1422d others(16): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr17 | 75560802 | |||||
chr17:75560802
|
TAAAAAAA others(8): Show |
T | 1 | a0004c0005t0004g0058 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.530+1408_530+1422d others(17): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr17 | 75560802 | |||||
chr17:75560803
|
A | T | 83 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(80): Show | 85 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(82): Show |
intron_variant | MODIFIER | c.530+1393A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560803 | ||||||
chr17:75560813
|
A | T | 1 | a0004c0018t0005g0109 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.530+1403A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560813 | ||||||
chr17:75560815
|
A | C | 5 | a0002c0006t0003g0025a0002c0006t0005g0112a0002c0013t0003g0192others(2): Show | 5 | HG00140.hp1 HG02976.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.530+1405A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560815 | ||||||
chr17:75560818
|
A | C | 1 | a0025c0039t0004g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.530+1408A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560818 | ||||||
chr17:75560819
|
A | C | 5 | a0004c0005t0004g0207a0004c0005t0004g0208a0004c0005t0004g0211others(2): Show | 5 | HG01099.hp2 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.530+1409A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560819 | ||||||
chr17:75560821
|
A | C | 4 | a0002c0003t0003g0245a0002c0003t0005g0126a0002c0003t0005g0130others(1): Show | 4 | HG00099.hp2 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.530+1411A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560821 | ||||||
chr17:75560822
|
A | C | 83 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(80): Show | 86 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.530+1412A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560822 | ||||||
chr17:75560822
|
A | G | 1 | a0025c0039t0004g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.530+1412A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560822 | ||||||
chr17:75560823
|
A | C | 9 | a0002c0004t0003g0017a0002c0004t0003g0195a0002c0004t0003g0282others(6): Show | 9 | HG01069.hp1 HG01123.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.530+1413A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560823 | ||||||
chr17:75560823
|
A | G | 5 | a0004c0005t0004g0207a0004c0005t0004g0208a0004c0005t0004g0211others(2): Show | 5 | HG01099.hp2 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.530+1413A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560823 | ||||||
chr17:75560823
|
AAAAAAAA others(7): Show |
A | 1 | a0025c0039t0004g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.530+1420_530+1433d others(16): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr17 | 75560823 | |||||
chr17:75560824
|
A | C | 1 | a0002c0004t0003g0345 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.530+1414A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560824 | ||||||
chr17:75560824
|
AAAAAAAA others(6): Show |
A | 5 | a0004c0005t0004g0207a0004c0005t0004g0208a0004c0005t0004g0211others(2): Show | 5 | HG01099.hp2 HG02922.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.530+1421_530+1433d others(15): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr17 | 75560824 | |||||
chr17:75560825
|
A | G | 4 | a0002c0003t0003g0245a0002c0003t0005g0126a0002c0003t0005g0130others(1): Show | 4 | HG00099.hp2 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.530+1415A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560825 | ||||||
chr17:75560826
|
A | C | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.530+1416A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560826 | ||||||
chr17:75560826
|
A | G | 82 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(79): Show | 85 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.530+1416A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560826 | ||||||
chr17:75560826
|
AAAAAAAC others(4): Show |
A | 4 | a0002c0003t0003g0245a0002c0003t0005g0126a0002c0003t0005g0130others(1): Show | 4 | HG00099.hp2 HG02280.hp2 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.530+1425_530+1435d others(13): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr17 | 75560826 | |||||
chr17:75560827
|
A | G | 9 | a0002c0004t0003g0017a0002c0004t0003g0195a0002c0004t0003g0282others(6): Show | 9 | HG01069.hp1 HG01123.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.530+1417A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560827 | ||||||
chr17:75560827
|
AAAAAACA others(3): Show |
A | 82 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(79): Show | 85 | HG00140.hp1 HG00408.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.530+1423_530+1432d others(12): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr17 | 75560827 | |||||
chr17:75560828
|
A | C | 12 | a0002c0004t0003g0089a0002c0006t0003g0004a0002c0006t0003g0085others(9): Show | 13 | HG01884.hp2 HG02258.hp2 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.530+1418A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560828 | ||||||
chr17:75560828
|
A | G | 1 | a0002c0004t0003g0345 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.530+1418A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560828 | ||||||
chr17:75560828
|
AAAAACAA others(2): Show |
A | 9 | a0002c0004t0003g0017a0002c0004t0003g0195a0002c0004t0003g0282others(6): Show | 9 | HG01069.hp1 HG01123.hp2 HG01361.hp1 others(6): Show |
intron_variant | MODIFIER | c.530+1423_530+1431d others(11): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr17 | 75560828 | |||||
chr17:75560829
|
A | C | 3 | a0004c0005t0004g0306a0004c0005t0004g0356a0004c0005t0007g0106 | 3 | HG01257.hp2 HG02523.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.530+1419A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560829 | ||||||
chr17:75560830
|
A | G | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.530+1420A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560830 | ||||||
chr17:75560833
|
C | A | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.530+1423C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560833 | ||||||
chr17:75560833
|
C | G | 3 | a0004c0005t0004g0306a0004c0005t0004g0356a0004c0005t0007g0106 | 3 | HG01257.hp2 HG02523.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.530+1423C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560833 | ||||||
chr17:75560837
|
G | C | 1 | a0001c0001t0001g0135 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.530+1427G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560837 | ||||||
chr17:75560837
|
G | GA | 39 | a0002c0004t0003g0089a0002c0004t0003g0342a0002c0006t0003g0004others(36): Show | 40 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(37): Show |
intron_variant | MODIFIER | c.530+1433dupA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr17 | 75560837 | |||||
chr17:75560844
|
C | A | 6 | a0002c0006t0003g0059a0004c0005t0004g0003a0004c0005t0004g0057others(3): Show | 7 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.530+1434C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560844 | ||||||
chr17:75560845
|
A | C | 6 | a0002c0006t0003g0059a0004c0005t0004g0003a0004c0005t0004g0057others(3): Show | 7 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.530+1435A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560845 | ||||||
chr17:75560846
|
T | A | 6 | a0002c0006t0003g0059a0004c0005t0004g0003a0004c0005t0004g0057others(3): Show | 7 | HG02109.hp2 HG02896.hp1 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.530+1436T>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560846 | ||||||
chr17:75560849
|
T | G | 10 | a0004c0007t0003g0021a0004c0007t0003g0027a0004c0007t0003g0091others(7): Show | 10 | HG01106.hp1 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.530+1439T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560849 | ||||||
chr17:75560956
|
C | T | 97 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(94): Show | 100 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.530+1546C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560956 | ||||||
chr17:75560992
|
C | T | 1 | a0002c0004t0003g0333 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.530+1582C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75560992 | ||||||
chr17:75561019
|
A | T | 1 | a0004c0007t0003g0329 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.530+1609A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75561019 | ||||||
chr17:75561099
|
T | C | 1 | a0001c0001t0001g0179 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.530+1689T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75561099 | ||||||
chr17:75561153
|
C | T | 2 | a0004c0005t0007g0069a0004c0005t0007g0106 | 2 | HG02056.hp1 NA18962.hp2 |
intron_variant | MODIFIER | c.530+1743C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75561153 | ||||||
chr17:75561171
|
T | TA | 5 | a0008c0043t0003g0023a0008c0044t0003g0097a0012c0022t0003g0022others(2): Show | 5 | HG00735.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.530+1762dupA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr17 | 75561171 | |||||
chr17:75561210
|
A | ACT | 129 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(126): Show | 133 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(130): Show |
intron_variant | MODIFIER | c.530+1801_530+1802d others(4): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr17 | 75561210 | |||||
chr17:75561462
|
T | C | 161 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(158): Show | 166 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(163): Show |
intron_variant | MODIFIER | c.531-1554T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75561462 | ||||||
chr17:75561465
|
C | T | 2 | a0001c0001t0001g0167a0025c0039t0004g0367 | 2 | HG01891.hp1 HG02886.hp1 |
intron_variant | MODIFIER | c.531-1551C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75561465 | ||||||
chr17:75561493
|
G | A | 10 | a0004c0007t0003g0021a0004c0007t0003g0027a0004c0007t0003g0091others(7): Show | 10 | HG01106.hp1 HG02055.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.531-1523G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75561493 | ||||||
chr17:75561597
|
G | C | 1 | a0025c0039t0004g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.531-1419G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75561597 | ||||||
chr17:75561647
|
G | A | 97 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(94): Show | 100 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.531-1369G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75561647 | ||||||
chr17:75561656
|
C | T | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.531-1360C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75561656 | ||||||
chr17:75561861
|
G | C | 1 | a0001c0001t0001g0101 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.531-1155G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75561861 | ||||||
chr17:75561922
|
CA | C | 11 | a0001c0001t0001g0155a0002c0003t0005g0113a0002c0006t0003g0059others(8): Show | 12 | HG01099.hp2 HG02109.hp2 HG02155.hp2 others(9): Show |
intron_variant | MODIFIER | c.531-1082delA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr17 | 75561922 | |||||
chr17:75562100
|
T | C | 1 | a0027c0040t0003g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.531-916T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75562100 | ||||||
chr17:75562116
|
T | C | 2 | a0001c0001t0001g0159a0001c0001t0002g0216 | 2 | HG02165.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.531-900T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75562116 | ||||||
chr17:75562132
|
G | GT | 98 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(95): Show | 101 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.531-877dupT | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | INFO_REALIGN_3_PRIME | chr17 | 75562132 | |||||
chr17:75562169
|
C | T | 2 | a0002c0003t0005g0113a0002c0003t0005g0127 | 2 | HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.531-847C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75562169 | ||||||
chr17:75562212
|
G | A | 3 | a0004c0018t0005g0109a0004c0018t0005g0190a0004c0050t0006g0062 | 3 | HG02895.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.531-804G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75562212 | ||||||
chr17:75562236
|
T | C | 97 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(94): Show | 100 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.531-780T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75562236 | ||||||
chr17:75562384
|
G | T | 29 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(26): Show | 29 | HG00408.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.531-632G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75562384 | ||||||
chr17:75562428
|
C | A | 4 | a0009c0011t0006g0018a0009c0011t0006g0019a0009c0011t0006g0020others(1): Show | 4 | HG02622.hp2 HG02630.hp1 HG02647.hp1 others(1): Show |
intron_variant | MODIFIER | c.531-588C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75562428 | ||||||
chr17:75562462
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.531-554T>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75562462 | ||||||
chr17:75562479
|
G | A | 1 | a0001c0001t0002g0228 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.531-537G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75562479 | ||||||
chr17:75562638
|
G | A | 5 | a0008c0043t0003g0023a0008c0044t0003g0097a0012c0022t0003g0022others(2): Show | 5 | HG00735.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.531-378G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75562638 | ||||||
chr17:75562680
|
C | T | 77 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(74): Show | 80 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(77): Show |
intron_variant | MODIFIER | c.531-336C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75562680 | ||||||
chr17:75562719
|
C | T | 1 | a0002c0004t0003g0282 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.531-297C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75562719 | ||||||
chr17:75562761
|
G | A | 22 | a0004c0005t0004g0194a0004c0005t0004g0273a0004c0005t0004g0298others(19): Show | 22 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(19): Show |
intron_variant | MODIFIER | c.531-255G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75562761 | ||||||
chr17:75562912
|
A | G | 1 | a0003c0002t0002g0267 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.531-104A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75562912 | ||||||
chr17:75562982
|
G | A | 9 | a0002c0006t0003g0059a0004c0005t0004g0003a0004c0005t0004g0057others(6): Show | 10 | HG01099.hp2 HG01891.hp1 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.531-34G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 6/25 | chr17 | 75562982 | ||||||
chr17:75563211
|
G | C | 29 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(26): Show | 29 | HG00408.hp2 HG01069.hp2 HG01071.hp1 others(26): Show |
intron_variant | MODIFIER | c.693+33G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 7/25 | chr17 | 75563211 | ||||||
chr17:75563261
|
G | A | 97 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(94): Show | 100 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.694-70G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 7/25 | chr17 | 75563261 | ||||||
chr17:75563282
|
C | T | 13 | a0002c0006t0003g0025a0002c0006t0005g0112a0002c0013t0003g0192others(10): Show | 13 | HG00140.hp1 HG02145.hp2 HG02258.hp1 others(10): Show |
intron_variant | MODIFIER | c.694-49C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 7/25 | chr17 | 75563282 | ||||||
chr17:75563284
|
C | T | 4 | a0013c0016t0003g0056a0013c0016t0003g0061a0014c0020t0003g0064others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.694-47C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 7/25 | chr17 | 75563284 | ||||||
chr17:75563296
|
G | A | 1 | a0002c0004t0003g0340 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.694-35G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 7/25 | chr17 | 75563296 | ||||||
chr17:75563482
|
G | A | 97 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(94): Show | 100 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.826+19G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 8/25 | chr17 | 75563482 | ||||||
chr17:75563547
|
C | T | 2 | a0013c0016t0003g0056a0013c0016t0003g0061 | 2 | HG02258.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.826+84C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 8/25 | chr17 | 75563547 | ||||||
chr17:75563548
|
A | G | 98 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(95): Show | 101 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(98): Show |
intron_variant | MODIFIER | c.826+85A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 8/25 | chr17 | 75563548 | ||||||
chr17:75563565
|
A | C | 1 | a0027c0040t0003g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.826+102A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 8/25 | chr17 | 75563565 | ||||||
chr17:75563624
|
C | T | 1 | a0025c0039t0004g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.827-128C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 8/25 | chr17 | 75563624 | ||||||
chr17:75563658
|
G | A | 1 | a0026c0042t0003g0214 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.827-94G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 8/25 | chr17 | 75563658 | ||||||
chr17:75563958
|
C | T | 2 | a0002c0004t0003g0063a0002c0055t0003g0215 | 2 | HG02717.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.881+152C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 9/25 | chr17 | 75563958 | ||||||
chr17:75564053
|
T | C | 171 | a0001c0001t0001g0039a0002c0003t0003g0220a0002c0003t0003g0226others(168): Show | 177 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.881+247T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 9/25 | chr17 | 75564053 | ||||||
chr17:75564112
|
A | G | 1 | a0004c0007t0003g0309 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.882-241A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 9/25 | chr17 | 75564112 | ||||||
chr17:75564122
|
G | A | 97 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(94): Show | 100 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(97): Show |
intron_variant | MODIFIER | c.882-231G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 9/25 | chr17 | 75564122 | ||||||
chr17:75564137
|
A | G | 110 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(107): Show | 114 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(111): Show |
intron_variant | MODIFIER | c.882-216A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 9/25 | chr17 | 75564137 | ||||||
chr17:75564520
|
C | T | 2 | a0008c0041t0003g0092a0027c0040t0003g0188 | 2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1036+13C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75564520 | ||||||
chr17:75564652
|
C | T | 34 | a0001c0001t0001g0031a0001c0001t0001g0044a0001c0001t0001g0045others(31): Show | 34 | HG00558.hp1 HG00621.hp2 HG00733.hp1 others(31): Show |
intron_variant | MODIFIER | c.1036+145C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75564652 | ||||||
chr17:75564794
|
G | T | 1 | a0001c0001t0001g0068 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.1036+287G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75564794 | ||||||
chr17:75564862
|
C | CA | 80 | a0001c0001t0001g0168a0001c0001t0002g0219a0002c0003t0003g0220others(77): Show | 83 | HG00408.hp2 HG00735.hp1 HG00735.hp2 others(80): Show |
intron_variant | MODIFIER | c.1036+372dupA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr17 | 75564862 | |||||
chr17:75564862
|
C | CAA | 27 | a0001c0001t0002g0316a0002c0003t0003g0271a0002c0004t0003g0017others(24): Show | 28 | HG00140.hp1 HG00639.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.1036+371_1036+372d others(4): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr17 | 75564862 | |||||
chr17:75564879
|
A | AAG | 20 | a0004c0005t0004g0194a0004c0005t0004g0298a0004c0005t0004g0302others(17): Show | 20 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(17): Show |
intron_variant | MODIFIER | c.1036+372_1036+373i others(4): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75564879 | ||||||
chr17:75565049
|
G | A | 4 | a0013c0016t0003g0056a0013c0016t0003g0061a0014c0020t0003g0064others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1036+542G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75565049 | ||||||
chr17:75565238
|
C | G | 111 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(108): Show | 115 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1036+731C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75565238 | ||||||
chr17:75565279
|
G | A | 1 | a0027c0040t0003g0188 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1036+772G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75565279 | ||||||
chr17:75565337
|
T | C | 112 | a0001c0001t0001g0033a0002c0003t0003g0220a0002c0003t0003g0226others(109): Show | 116 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(113): Show |
intron_variant | MODIFIER | c.1036+830T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75565337 | ||||||
chr17:75565409
|
A | G | 3 | a0001c0001t0009g0142a0001c0037t0001g0149a0003c0002t0002g0343 | 3 | HG00323.hp1 HG00733.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1036+902A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75565409 | ||||||
chr17:75565615
|
C | T | 1 | a0004c0005t0004g0302 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1036+1108C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75565615 | ||||||
chr17:75565636
|
G | A | 76 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(73): Show | 79 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(76): Show |
intron_variant | MODIFIER | c.1036+1129G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75565636 | ||||||
chr17:75565728
|
C | T | 32 | a0002c0003t0003g0320a0002c0003t0003g0321a0004c0005t0004g0003others(29): Show | 33 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.1036+1221C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75565728 | ||||||
chr17:75566135
|
G | A | 105 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(102): Show | 109 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1036+1628G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75566135 | ||||||
chr17:75566164
|
C | T | 1 | a0004c0005t0004g0302 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1036+1657C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75566164 | ||||||
chr17:75566170
|
G | C | 2 | a0002c0003t0005g0130a0002c0003t0005g0131 | 2 | HG00099.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1036+1663G>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75566170 | ||||||
chr17:75566210
|
C | T | 102 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(99): Show | 106 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(103): Show |
intron_variant | MODIFIER | c.1036+1703C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75566210 | ||||||
chr17:75566215
|
G | T | 1 | a0033c0038t0003g0278 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1036+1708G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75566215 | ||||||
chr17:75566340
|
C | T | 107 | a0001c0001t0001g0073a0002c0003t0003g0220a0002c0003t0003g0226others(104): Show | 111 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(108): Show |
intron_variant | MODIFIER | c.1036+1833C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75566340 | ||||||
chr17:75566344
|
G | A | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1036+1837G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75566344 | ||||||
chr17:75566357
|
G | A | 80 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(77): Show | 83 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1036+1850G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75566357 | ||||||
chr17:75566510
|
A | G | 30 | a0004c0005t0004g0003a0004c0005t0004g0057a0004c0005t0004g0058others(27): Show | 31 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.1037-1966A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75566510 | ||||||
chr17:75566546
|
C | T | 1 | a0002c0003t0005g0054 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1037-1930C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75566546 | ||||||
chr17:75566592
|
G | A | 3 | a0004c0018t0005g0109a0004c0018t0005g0190a0004c0050t0006g0062 | 3 | HG02895.hp1 HG02897.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1037-1884G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75566592 | ||||||
chr17:75566597
|
C | T | 6 | a0008c0043t0003g0023a0008c0044t0003g0097a0012c0022t0003g0022others(3): Show | 6 | HG00735.hp2 HG01109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-1879C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75566597 | ||||||
chr17:75566626
|
A | G | 1 | a0003c0002t0002g0261 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1037-1850A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75566626 | ||||||
chr17:75566796
|
G | T | 80 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(77): Show | 83 | HG00099.hp2 HG00408.hp2 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.1037-1680G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75566796 | ||||||
chr17:75566799
|
G | A | 6 | a0008c0043t0003g0023a0008c0044t0003g0097a0012c0022t0003g0022others(3): Show | 6 | HG00735.hp2 HG01109.hp1 HG02572.hp2 others(3): Show |
intron_variant | MODIFIER | c.1037-1677G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75566799 | ||||||
chr17:75566824
|
C | A | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1037-1652C>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75566824 | ||||||
chr17:75567060
|
G | A | 4 | a0004c0007t0003g0027a0004c0007t0003g0091a0004c0007t0003g0199others(1): Show | 4 | HG02451.hp1 HG02630.hp2 HG02896.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037-1416G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75567060 | ||||||
chr17:75567129
|
C | T | 31 | a0004c0005t0004g0003a0004c0005t0004g0057a0004c0005t0004g0058others(28): Show | 32 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.1037-1347C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75567129 | ||||||
chr17:75567235
|
T | G | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1037-1241T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75567235 | ||||||
chr17:75567280
|
A | G | 31 | a0004c0005t0004g0003a0004c0005t0004g0057a0004c0005t0004g0058others(28): Show | 32 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.1037-1196A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75567280 | ||||||
chr17:75567332
|
T | C | 159 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(156): Show | 164 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.1037-1144T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75567332 | ||||||
chr17:75567356
|
C | T | 1 | a0001c0001t0001g0073 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.1037-1120C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75567356 | ||||||
chr17:75567459
|
C | T | 1 | a0004c0007t0003g0021 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1037-1017C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75567459 | ||||||
chr17:75567478
|
G | T | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1037-998G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75567478 | ||||||
chr17:75567490
|
T | C | 1 | a0003c0002t0002g0332 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1037-986T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75567490 | ||||||
chr17:75567661
|
A | G | 106 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(103): Show | 110 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1037-815A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75567661 | ||||||
chr17:75567723
|
C | G | 4 | a0013c0016t0003g0056a0013c0016t0003g0061a0014c0020t0003g0064others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.1037-753C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75567723 | ||||||
chr17:75567856
|
C | T | 2 | a0002c0004t0003g0066a0031c0049t0003g0065 | 2 | HG00639.hp1 HG02922.hp1 |
intron_variant | MODIFIER | c.1037-620C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75567856 | ||||||
chr17:75567928
|
G | T | 30 | a0004c0005t0004g0003a0004c0005t0004g0057a0004c0005t0004g0058others(27): Show | 31 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.1037-548G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75567928 | ||||||
chr17:75567943
|
G | A | 149 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(146): Show | 154 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.1037-533G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75567943 | ||||||
chr17:75567950
|
G | GA | 23 | a0001c0001t0001g0039a0003c0002t0002g0001a0003c0002t0002g0010others(20): Show | 26 | HG00621.hp1 HG00735.hp2 HG01433.hp1 others(23): Show |
intron_variant | MODIFIER | c.1037-511dupA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr17 | 75567950 | |||||
chr17:75567950
|
GA | G | 8 | a0001c0001t0002g0285a0004c0018t0005g0109a0004c0018t0005g0190others(5): Show | 8 | HG02615.hp1 HG02895.hp1 HG02895.hp2 others(5): Show |
intron_variant | MODIFIER | c.1037-511delA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr17 | 75567950 | |||||
chr17:75567950
|
GAA | G | 23 | a0004c0005t0004g0194a0004c0005t0004g0273a0004c0005t0004g0298others(20): Show | 23 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1037-512_1037-511d others(4): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr17 | 75567950 | |||||
chr17:75567950
|
GAAAA | G | 7 | a0004c0005t0004g0003a0004c0005t0004g0057a0004c0005t0004g0058others(4): Show | 8 | HG01099.hp2 HG02896.hp1 HG02897.hp1 others(5): Show |
intron_variant | MODIFIER | c.1037-514_1037-511d others(6): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr17 | 75567950 | |||||
chr17:75567955
|
A | G | 106 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(103): Show | 110 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1037-521A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75567955 | ||||||
chr17:75568094
|
G | A | 8 | a0004c0005t0004g0003a0004c0005t0004g0057a0004c0005t0004g0058others(5): Show | 9 | HG01099.hp2 HG01891.hp1 HG02896.hp1 others(6): Show |
intron_variant | MODIFIER | c.1037-382G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75568094 | ||||||
chr17:75568447
|
C | T | 1 | a0004c0005t0004g0359 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.1037-29C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 10/25 | chr17 | 75568447 | ||||||
chr17:75568881
|
A | G | 75 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(72): Show | 78 | HG00099.hp2 HG00408.hp2 HG00642.hp2 others(75): Show |
intron_variant | MODIFIER | c.1322+42A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 12/25 | chr17 | 75568881 | ||||||
chr17:75568887
|
G | A | 31 | a0004c0005t0004g0003a0004c0005t0004g0057a0004c0005t0004g0058others(28): Show | 32 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.1322+48G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 12/25 | chr17 | 75568887 | ||||||
chr17:75569142
|
G | A | 5 | a0008c0043t0003g0023a0008c0044t0003g0097a0012c0022t0003g0022others(2): Show | 5 | HG00735.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1476+11G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 13/25 | chr17 | 75569142 | ||||||
chr17:75569181
|
T | A | 296 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0028others(293): Show | 303 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(300): Show |
intron_variant | MODIFIER | c.1477-40T>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 13/25 | chr17 | 75569181 | ||||||
chr17:75569207
|
C | G | 1 | a0003c0002t0002g0314 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1477-14C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 13/25 | chr17 | 75569207 | ||||||
chr17:75569368
|
C | T | 30 | a0004c0005t0004g0003a0004c0005t0004g0057a0004c0005t0004g0058others(27): Show | 31 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.1581+43C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 14/25 | chr17 | 75569368 | ||||||
chr17:75569429
|
T | G | 150 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(147): Show | 155 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.1581+104T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 14/25 | chr17 | 75569429 | ||||||
chr17:75569507
|
G | A | 31 | a0004c0005t0004g0003a0004c0005t0004g0057a0004c0005t0004g0058others(28): Show | 32 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.1581+182G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 14/25 | chr17 | 75569507 | ||||||
chr17:75569545
|
G | A | 5 | a0008c0043t0003g0023a0008c0044t0003g0097a0012c0022t0003g0022others(2): Show | 5 | HG00735.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.1581+220G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 14/25 | chr17 | 75569545 | ||||||
chr17:75569622
|
G | A | 2 | a0001c0001t0001g0080a0001c0001t0002g0286 | 2 | HG02027.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.1581+297G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 14/25 | chr17 | 75569622 | ||||||
chr17:75569674
|
C | T | 2 | a0008c0041t0003g0092a0027c0040t0003g0188 | 2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1582-289C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 14/25 | chr17 | 75569674 | ||||||
chr17:75569801
|
CA | C | 22 | a0001c0023t0002g0229a0002c0004t0003g0336a0002c0004t0003g0339others(19): Show | 22 | HG00140.hp1 HG00735.hp2 HG01106.hp1 others(19): Show |
intron_variant | MODIFIER | c.1582-144delA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr17 | 75569801 | |||||
chr17:75569801
|
CAA | C | 132 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(129): Show | 137 | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(134): Show |
intron_variant | MODIFIER | c.1582-145_1582-144d others(4): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr17 | 75569801 | |||||
chr17:75569819
|
A | T | 1 | a0001c0001t0001g0147 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1582-144A>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 14/25 | chr17 | 75569819 | ||||||
chr17:75569822
|
C | T | 4 | a0008c0043t0003g0023a0008c0044t0003g0097a0012c0022t0003g0022others(1): Show | 4 | HG02572.hp2 HG02809.hp1 HG02886.hp2 others(1): Show |
intron_variant | MODIFIER | c.1582-141C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 14/25 | chr17 | 75569822 | ||||||
chr17:75570312
|
G | A | 1 | a0006c0009t0004g0322 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.1875-36G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 15/25 | chr17 | 75570312 | ||||||
chr17:75570325
|
T | A | 3 | a0003c0002t0002g0227a0003c0002t0002g0258a0003c0002t0002g0268 | 3 | NA18954.hp1 NA19056.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.1875-23T>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 15/25 | chr17 | 75570325 | ||||||
chr17:75570343
|
C | G | 4 | a0013c0016t0003g0056a0013c0016t0003g0061a0014c0020t0003g0064others(1): Show | 4 | HG02145.hp2 HG02258.hp1 HG02818.hp2 others(1): Show |
splice_region_variant&intron_variant | LOW | c.1875-5C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 15/25 | chr17 | 75570343 | ||||||
chr17:75570343
|
C | T | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | splice_region_variant&intron_variant | LOW | c.1875-5C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 15/25 | chr17 | 75570343 | ||||||
chr17:75570530
|
C | T | 1 | a0002c0006t0003g0059 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2025+32C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 16/25 | chr17 | 75570530 | ||||||
chr17:75570704
|
T | G | 17 | a0002c0003t0005g0005a0002c0003t0005g0054a0002c0003t0005g0108others(14): Show | 18 | HG00099.hp2 HG00642.hp2 HG01123.hp1 others(15): Show |
intron_variant | MODIFIER | c.2025+206T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 16/25 | chr17 | 75570704 | ||||||
chr17:75570800
|
T | G | 2 | a0008c0041t0003g0092a0027c0040t0003g0188 | 2 | HG03486.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2026-150T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 16/25 | chr17 | 75570800 | ||||||
chr17:75570827
|
G | A | 1 | a0003c0002t0002g0202 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2026-123G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 16/25 | chr17 | 75570827 | ||||||
chr17:75570879
|
G | A | 1 | a0001c0001t0001g0164 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.2026-71G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 16/25 | chr17 | 75570879 | ||||||
chr17:75571122
|
G | A | 1 | a0001c0001t0001g0145 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.2176+22G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 17/25 | chr17 | 75571122 | ||||||
chr17:75571127
|
G | T | 3 | a0001c0001t0001g0147a0001c0001t0001g0168a0001c0001t0001g0174 | 3 | HG01346.hp1 HG03017.hp2 HG06807.hp1 |
intron_variant | MODIFIER | c.2176+27G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 17/25 | chr17 | 75571127 | ||||||
chr17:75571134
|
G | T | 1 | a0008c0041t0003g0092 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.2176+34G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 17/25 | chr17 | 75571134 | ||||||
chr17:75571183
|
G | A | 1 | a0003c0002t0002g0294 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.2176+83G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 17/25 | chr17 | 75571183 | ||||||
chr17:75571272
|
A | G | 137 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(134): Show | 142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.2176+172A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 17/25 | chr17 | 75571272 | ||||||
chr17:75571336
|
C | G | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2176+236C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 17/25 | chr17 | 75571336 | ||||||
chr17:75571404
|
C | T | 1 | a0001c0001t0009g0142 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.2177-263C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 17/25 | chr17 | 75571404 | ||||||
chr17:75571454
|
T | G | 137 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(134): Show | 142 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(139): Show |
intron_variant | MODIFIER | c.2177-213T>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 17/25 | chr17 | 75571454 | ||||||
chr17:75571534
|
T | C | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2177-133T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 17/25 | chr17 | 75571534 | ||||||
chr17:75571565
|
C | T | 30 | a0004c0005t0004g0003a0004c0005t0004g0057a0004c0005t0004g0058others(27): Show | 31 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.2177-102C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 17/25 | chr17 | 75571565 | ||||||
chr17:75571859
|
A | AC | 5 | a0001c0001t0001g0160a0002c0003t0003g0240a0003c0002t0002g0050others(2): Show | 5 | HG02056.hp2 HG02148.hp2 NA18940.hp1 others(2): Show |
intron_variant | MODIFIER | c.2294-34dupC | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr17 | 75571859 | |||||
chr17:75572076
|
G | A | 1 | a0004c0005t0004g0359 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.2460+12G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | chr17 | 75572076 | ||||||
chr17:75572084
|
G | A | 2 | a0002c0004t0003g0342a0002c0004t0003g0347 | 2 | HG01884.hp1 HG02559.hp1 |
intron_variant | MODIFIER | c.2460+20G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | chr17 | 75572084 | ||||||
chr17:75572103
|
C | T | 15 | a0002c0006t0003g0004a0002c0006t0003g0059a0002c0006t0003g0085others(12): Show | 16 | HG01884.hp2 HG02109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2460+39C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | chr17 | 75572103 | ||||||
chr17:75572121
|
C | T | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2460+57C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | chr17 | 75572121 | ||||||
chr17:75572253
|
C | T | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2460+189C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | chr17 | 75572253 | ||||||
chr17:75572255
|
C | T | 5 | a0008c0043t0003g0023a0008c0044t0003g0097a0012c0022t0003g0022others(2): Show | 5 | HG00735.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2460+191C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | chr17 | 75572255 | ||||||
chr17:75572360
|
C | CA | 138 | a0001c0001t0001g0167a0002c0003t0003g0220a0002c0003t0003g0226others(135): Show | 143 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(140): Show |
intron_variant | MODIFIER | c.2460+305dupA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr17 | 75572360 | |||||
chr17:75572392
|
G | A | 10 | a0001c0001t0001g0049a0002c0048t0004g0087a0004c0005t0004g0003others(7): Show | 11 | HG01099.hp2 HG01891.hp1 HG02717.hp1 others(8): Show |
intron_variant | MODIFIER | c.2460+328G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | chr17 | 75572392 | ||||||
chr17:75572430
|
G | A | 15 | a0002c0006t0003g0004a0002c0006t0003g0059a0002c0006t0003g0085others(12): Show | 16 | HG01884.hp2 HG02109.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2460+366G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | chr17 | 75572430 | ||||||
chr17:75572596
|
C | T | 5 | a0008c0043t0003g0023a0008c0044t0003g0097a0012c0022t0003g0022others(2): Show | 5 | HG00735.hp2 HG02572.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.2461-418C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | chr17 | 75572596 | ||||||
chr17:75572613
|
C | T | 1 | a0002c0003t0003g0250 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2461-401C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | chr17 | 75572613 | ||||||
chr17:75572625
|
A | G | 1 | a0002c0055t0003g0215 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2461-389A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | chr17 | 75572625 | ||||||
chr17:75572664
|
C | CA | 43 | a0001c0001t0001g0078a0001c0001t0001g0122a0001c0001t0001g0200others(40): Show | 44 | HG00597.hp2 HG00609.hp1 HG00735.hp2 others(41): Show |
intron_variant | MODIFIER | c.2461-333dupA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr17 | 75572664 | |||||
chr17:75572664
|
C | CAA | 15 | a0002c0003t0003g0249a0002c0004t0003g0346a0002c0006t0003g0004others(12): Show | 16 | HG01167.hp1 HG01884.hp2 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2461-334_2461-333d others(4): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr17 | 75572664 | |||||
chr17:75572664
|
C | CAAA | 65 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(62): Show | 67 | HG00639.hp1 HG00735.hp1 HG00738.hp2 others(64): Show |
intron_variant | MODIFIER | c.2461-335_2461-333d others(5): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr17 | 75572664 | |||||
chr17:75572664
|
C | CAAAA | 24 | a0002c0003t0005g0005a0002c0003t0005g0054a0002c0003t0005g0105others(21): Show | 25 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(22): Show |
intron_variant | MODIFIER | c.2461-336_2461-333d others(6): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr17 | 75572664 | |||||
chr17:75572721
|
G | A | 1 | a0002c0004t0003g0063 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.2461-293G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | chr17 | 75572721 | ||||||
chr17:75572768
|
C | T | 10 | a0004c0005t0004g0273a0004c0005t0004g0302a0004c0005t0004g0303others(7): Show | 10 | HG00438.hp1 HG00597.hp2 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.2461-246C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | chr17 | 75572768 | ||||||
chr17:75572769
|
G | A | 1 | a0001c0001t0001g0158 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2461-245G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | chr17 | 75572769 | ||||||
chr17:75572824
|
GA | G | 32 | a0001c0001t0002g0293a0002c0048t0004g0087a0004c0005t0004g0003others(29): Show | 33 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(30): Show |
intron_variant | MODIFIER | c.2461-177delA | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | INFO_REALIGN_3_PRIME | chr17 | 75572824 | |||||
chr17:75572844
|
T | C | 159 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(156): Show | 164 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.2461-170T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | chr17 | 75572844 | ||||||
chr17:75572903
|
G | A | 106 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(103): Show | 110 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.2461-111G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | chr17 | 75572903 | ||||||
chr17:75572929
|
T | C | 149 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(146): Show | 154 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.2461-85T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 19/25 | chr17 | 75572929 | ||||||
chr17:75573305
|
C | T | 12 | a0002c0013t0003g0192a0002c0013t0003g0196a0002c0013t0003g0334others(9): Show | 13 | HG00140.hp1 HG01099.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.2725+27C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 20/25 | chr17 | 75573305 | ||||||
chr17:75573306
|
G | A | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2725+28G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 20/25 | chr17 | 75573306 | ||||||
chr17:75573336
|
G | T | 1 | a0025c0039t0004g0367 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.2725+58G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 20/25 | chr17 | 75573336 | ||||||
chr17:75573372
|
G | A | 1 | a0001c0001t0001g0078 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2725+94G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 20/25 | chr17 | 75573372 | ||||||
chr17:75573430
|
C | T | 1 | a0018c0031t0001g0177 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.2726-51C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 20/25 | chr17 | 75573430 | ||||||
chr17:75573444
|
G | A | 1 | a0012c0022t0003g0022 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2726-37G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 20/25 | chr17 | 75573444 | ||||||
chr17:75573669
|
G | A | 6 | a0002c0006t0003g0025a0002c0006t0005g0112a0002c0013t0003g0192others(3): Show | 6 | HG00140.hp1 HG02572.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2876+38G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 21/25 | chr17 | 75573669 | ||||||
chr17:75573695
|
C | CCT | 139 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(136): Show | 144 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2876+64_2876+65ins others(2): Show |
LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 21/25 | chr17 | 75573695 | ||||||
chr17:75573762
|
G | A | 31 | a0002c0048t0004g0087a0004c0005t0004g0003a0004c0005t0004g0057others(28): Show | 32 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(29): Show |
intron_variant | MODIFIER | c.2876+131G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 21/25 | chr17 | 75573762 | ||||||
chr17:75573846
|
G | T | 139 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(136): Show | 144 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(141): Show |
intron_variant | MODIFIER | c.2877-106G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 21/25 | chr17 | 75573846 | ||||||
chr17:75573922
|
C | T | 1 | a0001c0001t0001g0079 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.2877-30C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 21/25 | chr17 | 75573922 | ||||||
chr17:75574061
|
G | A | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2905+81G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 22/25 | chr17 | 75574061 | ||||||
chr17:75574089
|
A | G | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2905+109A>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 22/25 | chr17 | 75574089 | ||||||
chr17:75574313
|
C | G | 2 | a0004c0005t0004g0298a0006c0009t0004g0203 | 2 | HG02040.hp2 NA18969.hp2 |
intron_variant | MODIFIER | c.2953+53C>G | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 23/25 | chr17 | 75574313 | ||||||
chr17:75574362
|
T | C | 1 | a0032c0047t0003g0366 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.2954-91T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 23/25 | chr17 | 75574362 | ||||||
chr17:75574413
|
C | T | 22 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(19): Show | 22 | HG00408.hp2 HG01081.hp1 HG01928.hp1 others(19): Show |
intron_variant | MODIFIER | c.2954-40C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 23/25 | chr17 | 75574413 | ||||||
chr17:75574505
|
C | T | 1 | a0021c0033t0001g0185 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2996+10C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 24/25 | chr17 | 75574505 | ||||||
chr17:75574531
|
A | C | 3 | a0003c0002t0002g0202a0003c0019t0002g0095a0003c0019t0002g0212 | 3 | HG02647.hp2 HG03209.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.2996+36A>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 24/25 | chr17 | 75574531 | ||||||
chr17:75574675
|
G | T | 108 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(105): Show | 112 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(109): Show |
splice_region_variant&intron_variant | LOW | c.3055+7G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 25/25 | chr17 | 75574675 | ||||||
chr17:75574693
|
G | A | 92 | a0002c0003t0003g0220a0002c0003t0003g0226a0002c0003t0003g0240others(89): Show | 95 | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(92): Show |
intron_variant | MODIFIER | c.3055+25G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 25/25 | chr17 | 75574693 | ||||||
chr17:75574733
|
G | A | 30 | a0002c0048t0004g0087a0004c0005t0004g0003a0004c0005t0004g0057others(27): Show | 31 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.3055+65G>A | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 25/25 | chr17 | 75574733 | ||||||
chr17:75574761
|
T | C | 57 | a0002c0003t0005g0005a0002c0003t0005g0054a0002c0003t0005g0108others(54): Show | 59 | HG00099.hp2 HG00438.hp1 HG00597.hp2 others(56): Show |
intron_variant | MODIFIER | c.3055+93T>C | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 25/25 | chr17 | 75574761 | ||||||
chr17:75574807
|
G | T | 30 | a0002c0048t0004g0087a0004c0005t0004g0003a0004c0005t0004g0057others(27): Show | 31 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(28): Show |
intron_variant | MODIFIER | c.3056-64G>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 25/25 | chr17 | 75574807 | ||||||
chr17:75574834
|
C | T | 21 | a0004c0005t0004g0194a0004c0005t0004g0273a0004c0005t0004g0298others(18): Show | 21 | HG00438.hp1 HG00597.hp2 HG00609.hp1 others(18): Show |
intron_variant | MODIFIER | c.3056-37C>T | LLGL2 | ENSG00000073350.14 | transcript | ENST00000392550.8 | protein_coding | 25/25 | chr17 | 75574834 |