geneid | 51056 |
---|---|
ensemblid | ENSG00000002549.13 |
hgncid | 18449 |
symbol | LAP3 |
name | leucine aminopeptidase 3 |
refseq_nuc | NM_015907.3 |
refseq_prot | NP_056991.2 |
ensembl_nuc | ENST00000226299.9 |
ensembl_prot | ENSP00000226299.4 |
mane_status | MANE Select |
chr | chr4 |
start | 17577198 |
end | 17607970 |
strand | + |
ver | v1.2 |
region | chr4:17577198-17607970 |
region5000 | chr4:17572198-17612970 |
regionname0 | LAP3_chr4_17577198_17607970 |
regionname5000 | LAP3_chr4_17572198_17612970 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 519 | 300 | 100 | 56 | 92 | 14 | 36 | 60 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1560 | 187 | 37 | 39 | 78 | 8 | 24 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
c0002 | 1/0 | 1560 | 59 | 17 | 11 | 13 | 6 | 11 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
c0003 | 0/0 | 1560 | 18 | 18 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
c0004 | 0/0 | 1560 | 15 | 13 | 1 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
c0005 | 0/0 | 1560 | 15 | 14 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
c0006 | 0/0 | 1560 | 4 | 0 | 4 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
c0007 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
c0008 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 650 | 189 | 50 | 41 | 66 | 8 | 23 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
t0002 | 1/0 | 650 | 54 | 13 | 11 | 12 | 6 | 11 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
t0003 | 0/0 | 640 | 28 | 27 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
t0004 | 0/0 | 637 | 18 | 0 | 3 | 14 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
t0005 | 0/0 | 650 | 4 | 4 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
t0006 | 0/0 | 640 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
t0007 | 0/0 | 666 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
t0008 | 0/0 | 650 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
t0009 | 0/0 | 650 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
t0010 | 0/0 | 640 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
t0011 | 0/0 | 621 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 9 | 3 | 0 | 6 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0002 | 0/0 | 8 | 1 | 4 | 2 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0005 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0006 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0007 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0013 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0249 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1560 | 187 | 37 | 39 | 78 | 8 | 24 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0002 | 1/0 | 1560 | 59 | 17 | 11 | 13 | 6 | 11 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0003 | 0/0 | 1560 | 18 | 18 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0004 | 0/0 | 1560 | 15 | 13 | 1 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0005 | 0/0 | 1560 | 15 | 14 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0006 | 0/0 | 1560 | 4 | 0 | 4 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0007 | 0/0 | 1560 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0008 | 0/0 | 1560 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2209 | 167 | 36 | 36 | 64 | 8 | 22 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0001t0004 | 0/0 | 2196 | 18 | 0 | 3 | 14 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0001t0008 | 0/0 | 2209 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0001t0011 | 0/0 | 2180 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0002t0001 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0002t0002 | 1/0 | 2209 | 53 | 12 | 11 | 12 | 6 | 11 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0002t0005 | 0/0 | 2209 | 4 | 4 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0002t0010 | 0/0 | 2199 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0003t0001 | 0/0 | 2209 | 3 | 3 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0003t0003 | 0/0 | 2199 | 15 | 15 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0004t0001 | 0/0 | 2209 | 13 | 11 | 1 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0004t0007 | 0/0 | 2225 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0004t0009 | 0/0 | 2209 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0005t0003 | 0/0 | 2199 | 13 | 12 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0005t0006 | 0/0 | 2199 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0006t0001 | 0/0 | 2209 | 4 | 0 | 4 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0007t0001 | 0/0 | 2209 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
a0001c0008t0002 | 0/0 | 2209 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | copy fasta | chr4 | 17572198 | 17612970 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0006 | 0/0 | 3 | 1 | 1 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 2 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0011 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0049 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0052 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0172 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0228 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0004g0003 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0004g0016 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0004g0017 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0004g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0004g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0004g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0004g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0004g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0004g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0008g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0001t0011g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0001g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0001 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0002 | 0/0 | 8 | 1 | 4 | 2 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0005 | 0/0 | 4 | 0 | 2 | 0 | 2 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0013 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0018 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0019 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0236 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0239 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0249 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0253 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0255 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0002g0258 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0005g0001 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0005g0244 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0002t0010g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0003t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0003t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0003t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0003t0003g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0003t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0003t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0003t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0003t0003g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0003t0003g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0003t0003g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0003t0003g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0003t0003g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0003t0003g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0003t0003g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0003t0003g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0003t0003g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0003t0003g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0004t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0004t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0004t0001g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0004t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0004t0001g0161 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0004t0001g0162 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0004t0001g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0004t0001g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0004t0001g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0004t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0004t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0004t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0004t0001g0188 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0004t0007g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0004t0009g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0005t0003g0015 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0005t0003g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0005t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0005t0003g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0005t0003g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0005t0003g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0005t0003g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0005t0003g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0005t0003g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0005t0003g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0005t0003g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0005t0003g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0005t0006g0215 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0005t0006g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0006t0001g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0006t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0006t0001g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0006t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0007t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
a0001c0008t0002g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0002 | t0002 | g0013 | EUR | GBR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0104 | EUR | GBR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00140 | hp1 | a0001 | c0002 | t0002 | g0258 | EUR | GBR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0006 | EUR | GBR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0119 | EUR | FIN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00280 | hp2 | a0001 | c0002 | t0002 | g0005 | EUR | FIN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00323 | hp1 | a0001 | c0002 | t0002 | g0239 | EUR | FIN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00323 | hp2 | a0001 | c0001 | t0001 | g0080 | EUR | FIN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00423 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0050 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00438 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00544 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00597 | hp1 | a0001 | c0002 | t0002 | g0242 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00609 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00673 | hp1 | a0001 | c0002 | t0002 | g0002 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0036 | EAS | CHS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00733 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00733 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00735 | hp1 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00735 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00738 | hp1 | a0001 | c0002 | t0002 | g0248 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00738 | hp2 | a0001 | c0002 | t0002 | g0005 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0182 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0100 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01099 | hp1 | a0001 | c0002 | t0002 | g0002 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0045 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01109 | hp1 | a0001 | c0005 | t0003 | g0015 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0120 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01169 | hp2 | a0001 | c0002 | t0002 | g0253 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01175 | hp1 | a0001 | c0002 | t0002 | g0252 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0098 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0111 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01192 | hp2 | a0001 | c0001 | t0004 | g0017 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01243 | hp1 | a0001 | c0004 | t0001 | g0168 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01255 | hp1 | a0001 | c0002 | t0002 | g0247 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0151 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0033 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0006 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0152 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0237 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0052 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0046 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01361 | hp1 | a0001 | c0001 | t0001 | g0039 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01361 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0042 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0035 | EUR | IBS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0054 | EUR | IBS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01516 | hp1 | a0001 | c0002 | t0002 | g0005 | EUR | IBS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0007 | EUR | IBS | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01884 | hp1 | a0001 | c0005 | t0003 | g0015 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01884 | hp2 | a0001 | c0002 | t0002 | g0234 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01891 | hp1 | a0001 | c0004 | t0001 | g0167 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01891 | hp2 | a0001 | c0004 | t0001 | g0164 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01928 | hp2 | a0001 | c0006 | t0001 | g0096 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0091 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01943 | hp2 | a0001 | c0006 | t0001 | g0047 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0227 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0142 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0064 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01978 | hp2 | a0001 | c0006 | t0001 | g0124 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0034 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02027 | hp1 | a0001 | c0002 | t0002 | g0238 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0071 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02055 | hp1 | a0001 | c0005 | t0003 | g0207 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02055 | hp2 | a0001 | c0002 | t0002 | g0002 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0123 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02071 | hp2 | a0001 | c0002 | t0001 | g0070 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0072 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02132 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02135 | hp2 | a0001 | c0002 | t0002 | g0245 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02145 | hp1 | a0001 | c0003 | t0003 | g0194 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0171 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02257 | hp2 | a0001 | c0004 | t0007 | g0183 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02258 | hp1 | a0001 | c0005 | t0006 | g0216 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02258 | hp2 | a0001 | c0002 | t0002 | g0251 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0094 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0063 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02280 | hp1 | a0001 | c0005 | t0003 | g0186 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0179 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02293 | hp1 | a0001 | c0006 | t0001 | g0084 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02293 | hp2 | a0001 | c0002 | t0002 | g0002 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0129 | AMR | PEL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0011 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02451 | hp2 | a0001 | c0004 | t0001 | g0157 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0177 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02572 | hp2 | a0001 | c0002 | t0002 | g0018 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0230 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02615 | hp2 | a0001 | c0004 | t0001 | g0165 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02622 | hp1 | a0001 | c0003 | t0003 | g0014 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02622 | hp2 | a0001 | c0002 | t0002 | g0255 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02630 | hp1 | a0001 | c0004 | t0001 | g0163 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02630 | hp2 | a0001 | c0005 | t0003 | g0192 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02647 | hp1 | a0001 | c0002 | t0002 | g0254 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02647 | hp2 | a0001 | c0002 | t0002 | g0189 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02683 | hp1 | a0001 | c0002 | t0002 | g0002 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0076 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02698 | hp2 | a0001 | c0002 | t0002 | g0257 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02717 | hp2 | a0001 | c0005 | t0003 | g0210 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02723 | hp1 | a0001 | c0005 | t0003 | g0212 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02723 | hp2 | a0001 | c0002 | t0005 | g0001 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0141 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0114 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0148 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0069 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02809 | hp1 | a0001 | c0003 | t0003 | g0196 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02809 | hp2 | a0001 | c0002 | t0002 | g0013 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0118 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02818 | hp2 | a0001 | c0003 | t0003 | g0197 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02886 | hp1 | a0001 | c0002 | t0002 | g0190 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0122 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02895 | hp1 | a0001 | c0004 | t0001 | g0166 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02895 | hp2 | a0001 | c0003 | t0003 | g0201 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02896 | hp1 | a0001 | c0003 | t0003 | g0014 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0180 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02897 | hp1 | a0001 | c0003 | t0003 | g0200 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0178 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02922 | hp1 | a0001 | c0005 | t0003 | g0208 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02922 | hp2 | a0001 | c0001 | t0008 | g0021 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02965 | hp1 | a0001 | c0002 | t0010 | g0185 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0259 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02970 | hp2 | a0001 | c0004 | t0009 | g0020 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0024 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02976 | hp2 | a0001 | c0002 | t0005 | g0244 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03017 | hp1 | a0001 | c0004 | t0001 | g0188 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03098 | hp1 | a0001 | c0003 | t0001 | g0059 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03098 | hp2 | a0001 | c0003 | t0003 | g0204 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03130 | hp1 | a0001 | c0002 | t0005 | g0001 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0025 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03139 | hp1 | a0001 | c0003 | t0003 | g0199 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03139 | hp2 | a0001 | c0003 | t0003 | g0198 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03195 | hp1 | a0001 | c0005 | t0003 | g0206 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03195 | hp2 | a0001 | c0003 | t0001 | g0061 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03209 | hp1 | a0001 | c0003 | t0003 | g0202 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0011 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03225 | hp1 | a0001 | c0003 | t0003 | g0195 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03225 | hp2 | a0001 | c0004 | t0001 | g0159 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0062 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0085 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03453 | hp2 | a0001 | c0005 | t0003 | g0213 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03486 | hp2 | a0001 | c0004 | t0001 | g0156 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03490 | hp1 | a0001 | c0002 | t0002 | g0256 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03490 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0027 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03491 | hp2 | a0001 | c0002 | t0002 | g0243 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0026 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03516 | hp1 | a0001 | c0003 | t0003 | g0205 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03516 | hp2 | a0001 | c0005 | t0003 | g0209 | AFR | ESN | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03540 | hp1 | a0001 | c0003 | t0003 | g0193 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03540 | hp2 | a0001 | c0003 | t0001 | g0058 | AFR | GWD | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0160 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03579 | hp2 | a0001 | c0008 | t0002 | g0217 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03654 | hp1 | a0001 | c0002 | t0002 | g0233 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0131 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03704 | hp2 | a0001 | c0002 | t0002 | g0235 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03710 | hp1 | a0001 | c0002 | t0002 | g0232 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | BEB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03831 | hp2 | a0001 | c0001 | t0011 | g0218 | SAS | BEB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03942 | hp1 | a0001 | c0002 | t0002 | g0240 | SAS | BEB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0037 | SAS | BEB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG04184 | hp1 | a0001 | c0002 | t0002 | g0246 | SAS | BEB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | BEB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG04199 | hp1 | a0001 | c0001 | t0004 | g0224 | SAS | STU | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG04199 | hp2 | a0001 | c0002 | t0002 | g0019 | SAS | STU | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG04228 | hp1 | a0001 | c0002 | t0002 | g0250 | SAS | STU | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0048 | SAS | STU | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18522 | hp1 | a0001 | c0004 | t0001 | g0158 | AFR | YRI | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18522 | hp2 | a0001 | c0003 | t0003 | g0203 | AFR | YRI | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18612 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | CHB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0154 | EAS | CHB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0137 | EAS | CHB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0065 | EAS | CHB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18906 | hp2 | a0001 | c0002 | t0005 | g0001 | AFR | YRI | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18939 | hp1 | a0001 | c0007 | t0001 | g0187 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0055 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18946 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18950 | hp1 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18956 | hp1 | a0001 | c0001 | t0004 | g0222 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18978 | hp1 | a0001 | c0001 | t0001 | g0031 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18978 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18995 | hp1 | a0001 | c0001 | t0004 | g0220 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0075 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18998 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19000 | hp2 | a0001 | c0001 | t0004 | g0221 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19001 | hp1 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19001 | hp2 | a0001 | c0002 | t0002 | g0241 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19012 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19030 | hp1 | a0001 | c0005 | t0003 | g0214 | AFR | LWK | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19030 | hp2 | a0001 | c0004 | t0001 | g0161 | AFR | LWK | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | LWK | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0173 | AFR | LWK | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19056 | hp1 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19058 | hp1 | a0001 | c0001 | t0001 | g0139 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19058 | hp2 | a0001 | c0001 | t0004 | g0226 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19064 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0184 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19068 | hp2 | a0001 | c0001 | t0004 | g0225 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19081 | hp1 | a0001 | c0001 | t0001 | g0110 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19081 | hp2 | a0001 | c0002 | t0002 | g0001 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19085 | hp2 | a0001 | c0001 | t0004 | g0003 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19240 | hp1 | a0001 | c0002 | t0002 | g0018 | AFR | YRI | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | YRI | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0169 | AFR | ASW | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA20129 | hp2 | a0001 | c0002 | t0002 | g0236 | AFR | ASW | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA20752 | hp1 | a0001 | c0002 | t0002 | g0019 | EUR | TSI | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0101 | EUR | TSI | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | GIH | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | GIH | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0223 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0174 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02486 | hp1 | a0001 | c0005 | t0003 | g0211 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0175 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG02559 | hp2 | a0001 | c0005 | t0006 | g0215 | AFR | ACB | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03471 | hp1 | a0001 | c0004 | t0001 | g0162 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG03471 | hp2 | a0001 | c0002 | t0002 | g0191 | AFR | MSL | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | USA | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0172 | AFR | USA | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA18955 | hp2 | a0001 | c0001 | t0004 | g0219 | EAS | JPT | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | USA | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0228 | AFR | USA | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
NA21309 | hp2 | a0001 | c0001 | t0001 | g0043 | AFR | LWK | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0049 | REF | REF | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
homoSapiens_grch38 | hp1 | a0001 | c0002 | t0002 | g0249 | REF | REF | LAP3_chr4_17572198_17612970 | LAP3 | chr4 | 17572198 | 17612970 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:17579826
|
C | T | 1 | a0001c0006 | 4 | HG01928.hp2 HG01943.hp2 HG01978.hp2 others(1): Show |
splice_region_variant&synonymous_variant | LOW | c.105C>T | p.Gly35Gly | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/13 | 373/2209 | 105/1560 | 35/519 | chr4 | 17579826 | ||
chr4:17585080
|
T | C | 6 | a0001c0001a0001c0003a0001c0004others(3): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
synonymous_variant | LOW | c.648T>C | p.Ala216Ala | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/13 | 916/2209 | 648/1560 | 216/519 | chr4 | 17585080 | ||
chr4:17588882
|
C | T | 1 | a0001c0005 | 15 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(12): Show |
synonymous_variant | LOW | c.768C>T | p.Asp256Asp | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/13 | 1036/2209 | 768/1560 | 256/519 | chr4 | 17588882 | ||
chr4:17598509
|
C | T | 2 | a0001c0003a0001c0005 | 33 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(30): Show |
synonymous_variant | LOW | c.1131C>T | p.Tyr377Tyr | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/13 | 1399/2209 | 1131/1560 | 377/519 | chr4 | 17598509 | ||
chr4:17607502
|
A | G | 3 | a0001c0004a0001c0007a0001c0008 | 17 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(14): Show |
synonymous_variant | LOW | c.1473A>G | p.Glu491Glu | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 13/13 | 1741/2209 | 1473/1560 | 491/519 | chr4 | 17607502 | ||
chr4:17607547
|
T | G | 1 | a0001c0007 | 1 | NA18939.hp1 | synonymous_variant | LOW | c.1518T>G | p.Thr506Thr | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 13/13 | 1786/2209 | 1518/1560 | 506/519 | chr4 | 17607547 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:17577206
|
A | C | 2 | a0001c0001t0008a0001c0004t0009 | 2 | HG02922.hp2 HG02970.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-260A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/13 | chr4 | 17577206 | ||||||
chr4:17577209
|
C | CGGGCGCA others(9): Show |
1 | a0001c0004t0007 | 1 | HG02257.hp2 | 5_prime_UTR_variant | MODIFIER | c.-242_-241insGGGGCG others(10): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/13 | 241 | INFO_REALIGN_3_PRIME | chr4 | 17577209 | ||||
chr4:17577222
|
A | C | 2 | a0001c0001t0008a0001c0004t0009 | 2 | HG02922.hp2 HG02970.hp2 |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-244A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/13 | chr4 | 17577222 | ||||||
chr4:17577238
|
A | C | 1 | a0001c0004t0009 | 1 | HG02970.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-228A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/13 | chr4 | 17577238 | ||||||
chr4:17577268
|
A | G | 14 | a0001c0001t0001a0001c0001t0004a0001c0001t0008others(11): Show | 241 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(238): Show |
5_prime_UTR_variant | MODIFIER | c.-198A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/13 | 198 | chr4 | 17577268 | |||||
chr4:17577295
|
C | G | 1 | a0001c0002t0005 | 4 | HG02723.hp2 HG02976.hp2 HG03130.hp1 others(1): Show |
5_prime_UTR_variant | MODIFIER | c.-171C>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/13 | 171 | chr4 | 17577295 | |||||
chr4:17577352
|
C | G | 1 | a0001c0002t0010 | 1 | HG02965.hp1 | 5_prime_UTR_variant | MODIFIER | c.-114C>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/13 | 114 | chr4 | 17577352 | |||||
chr4:17607678
|
C | T | 1 | a0001c0005t0006 | 2 | HG02258.hp1 HG02559.hp2 |
3_prime_UTR_variant | MODIFIER | c.*89C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 13/13 | 89 | chr4 | 17607678 | |||||
chr4:17607795
|
ATTT | A | 2 | a0001c0001t0004a0001c0001t0011 | 19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*209_*211delTTT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 13/13 | 209 | INFO_REALIGN_3_PRIME | chr4 | 17607795 | ||||
chr4:17607912
|
G | T | 2 | a0001c0001t0004a0001c0001t0011 | 19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*323G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 13/13 | 323 | chr4 | 17607912 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr4:17577627
|
G | T | 1 | a0001c0001t0001g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.102+60G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17577627 | ||||||
chr4:17577792
|
T | C | 227 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(224): Show | 248 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(245): Show |
intron_variant | MODIFIER | c.102+225T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17577792 | ||||||
chr4:17577850
|
C | T | 4 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(1): Show | 4 | HG01243.hp2 HG02615.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.102+283C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17577850 | ||||||
chr4:17577908
|
G | A | 2 | a0001c0002t0002g0232a0001c0002t0002g0233 | 2 | HG03654.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.102+341G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17577908 | ||||||
chr4:17578055
|
G | C | 174 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(171): Show | 186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.102+488G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578055 | ||||||
chr4:17578162
|
G | T | 1 | a0001c0001t0001g0184 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.102+595G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578162 | ||||||
chr4:17578163
|
G | T | 1 | a0001c0001t0001g0184 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.102+596G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578163 | ||||||
chr4:17578246
|
G | T | 1 | a0001c0004t0007g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.102+679G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578246 | ||||||
chr4:17578324
|
T | C | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.102+757T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578324 | ||||||
chr4:17578371
|
C | T | 2 | a0001c0001t0001g0181a0001c0001t0001g0182 | 2 | HG00741.hp2 HG01433.hp2 |
intron_variant | MODIFIER | c.102+804C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578371 | ||||||
chr4:17578515
|
G | A | 1 | a0001c0002t0002g0234 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.102+948G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578515 | ||||||
chr4:17578542
|
TACCAC | T | 174 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(171): Show | 186 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(183): Show |
intron_variant | MODIFIER | c.102+983_102+987del others(5): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | INFO_REALIGN_3_PRIME | chr4 | 17578542 | |||||
chr4:17578554
|
C | T | 13 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0017others(10): Show | 19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.102+987C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578554 | ||||||
chr4:17578597
|
C | G | 1 | a0001c0008t0002g0217 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.102+1030C>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578597 | ||||||
chr4:17578802
|
T | C | 2 | a0001c0001t0008g0021a0001c0004t0009g0020 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.103-1022T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578802 | ||||||
chr4:17578872
|
C | T | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0169others(16): Show | 21 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.103-952C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17578872 | ||||||
chr4:17579013
|
G | A | 2 | a0001c0001t0008g0021a0001c0004t0009g0020 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.103-811G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579013 | ||||||
chr4:17579120
|
G | A | 13 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0017others(10): Show | 19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.103-704G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579120 | ||||||
chr4:17579137
|
A | G | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180 | 3 | HG02280.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.103-687A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579137 | ||||||
chr4:17579313
|
C | T | 1 | a0001c0002t0002g0005 | 4 | HG00280.hp2 HG00735.hp1 HG00738.hp2 others(1): Show |
intron_variant | MODIFIER | c.103-511C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579313 | ||||||
chr4:17579323
|
T | C | 1 | a0001c0005t0003g0186 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.103-501T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579323 | ||||||
chr4:17579332
|
G | A | 173 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(170): Show | 185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.103-492G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579332 | ||||||
chr4:17579447
|
G | A | 5 | a0001c0004t0001g0164a0001c0004t0001g0165a0001c0004t0001g0166others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.103-377G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579447 | ||||||
chr4:17579597
|
T | C | 1 | a0001c0008t0002g0217 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.103-227T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579597 | ||||||
chr4:17579600
|
A | G | 11 | a0001c0005t0003g0206a0001c0005t0003g0207a0001c0005t0003g0208others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.103-224A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579600 | ||||||
chr4:17579675
|
C | T | 32 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(29): Show | 34 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.103-149C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579675 | ||||||
chr4:17579715
|
A | G | 8 | a0001c0001t0001g0160a0001c0004t0001g0156a0001c0004t0001g0157others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.103-109A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579715 | ||||||
chr4:17579719
|
G | A | 1 | a0001c0004t0007g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.103-105G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579719 | ||||||
chr4:17579763
|
T | C | 1 | a0001c0001t0001g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.103-61T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 1/12 | chr4 | 17579763 | ||||||
chr4:17579967
|
T | A | 13 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0017others(10): Show | 19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.218+28T>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17579967 | ||||||
chr4:17579994
|
T | A | 173 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(170): Show | 185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.218+55T>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17579994 | ||||||
chr4:17580004
|
C | A | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.218+65C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580004 | ||||||
chr4:17580020
|
CAG | C | 144 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(141): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.218+84_218+85delAG | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580020 | |||||
chr4:17580159
|
G | A | 11 | a0001c0005t0003g0206a0001c0005t0003g0207a0001c0005t0003g0208others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.218+220G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580159 | ||||||
chr4:17580165
|
C | CATATATA others(5): Show |
1 | a0001c0004t0001g0188 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.218+231_218+242dup others(12): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(461): Show |
1 | a0001c0004t0001g0156 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.218+239_218+240ins others(468): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(469): Show |
1 | a0001c0004t0001g0157 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.218+239_218+240ins others(476): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(117): Show |
1 | a0001c0001t0001g0169 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.218+239_218+240ins others(124): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(99): Show |
1 | a0001c0001t0001g0023 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.218+241_218+242ins others(106): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(467): Show |
1 | a0001c0004t0001g0158 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.218+241_218+242ins others(474): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(451): Show |
1 | a0001c0004t0001g0159 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.218+241_218+242ins others(458): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(136): Show |
1 | a0001c0001t0001g0033 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.218+242_218+243ins others(143): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(141): Show |
1 | a0001c0001t0001g0127 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.218+242_218+243ins others(148): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(139): Show |
1 | a0001c0001t0001g0128 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.218+242_218+243ins others(146): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(125): Show |
1 | a0001c0001t0001g0130 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(132): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(115): Show |
1 | a0001c0001t0001g0131 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.218+240_218+241ins others(122): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(134): Show |
1 | a0001c0001t0001g0132 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.218+240_218+241ins others(141): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(117): Show |
3 | a0001c0001t0001g0133a0001c0001t0001g0134a0001c0001t0001g0135 | 3 | HG02129.hp1 NA18978.hp2 NA19079.hp2 |
intron_variant | MODIFIER | c.218+240_218+241ins others(124): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(130): Show |
1 | a0001c0001t0001g0140 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(137): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(132): Show |
1 | a0001c0001t0001g0139 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(139): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(134): Show |
2 | a0001c0001t0001g0137a0001c0001t0001g0138 | 2 | HG02257.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.218+240_218+241ins others(141): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(138): Show |
1 | a0001c0001t0001g0136 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(145): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(137): Show |
1 | a0001c0001t0001g0141 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(144): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(117): Show |
5 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0143others(2): Show | 9 | HG00597.hp2 HG02015.hp1 HG02132.hp1 others(6): Show |
intron_variant | MODIFIER | c.218+240_218+241ins others(124): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(133): Show |
1 | a0001c0001t0001g0142 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.218+240_218+241ins others(140): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(143): Show |
1 | a0001c0001t0001g0146 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.218+240_218+241ins others(150): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(136): Show |
1 | a0001c0001t0001g0147 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(143): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(137): Show |
1 | a0001c0001t0001g0149 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(144): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(143): Show |
1 | a0001c0001t0001g0148 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(150): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(119): Show |
2 | a0001c0001t0001g0150a0001c0001t0001g0151 | 2 | HG01255.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.218+240_218+241ins others(126): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(139): Show |
1 | a0001c0001t0001g0153 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.218+240_218+241ins others(146): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(141): Show |
1 | a0001c0001t0001g0152 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(148): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(147): Show |
1 | a0001c0001t0001g0154 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.218+240_218+241ins others(154): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(143): Show |
1 | a0001c0001t0001g0155 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.218+240_218+241ins others(150): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(115): Show |
1 | a0001c0001t0001g0177 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.218+238_218+239ins others(122): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580165
|
C | CATATATA others(29): Show |
2 | a0001c0005t0006g0215a0001c0005t0006g0216 | 2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.218+234_218+235ins others(36): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580165 | |||||
chr4:17580178
|
A | G | 1 | a0001c0005t0003g0214 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.218+239A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580178 | ||||||
chr4:17580182
|
G | A | 179 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(176): Show | 195 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(192): Show |
intron_variant | MODIFIER | c.218+243G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580182 | ||||||
chr4:17580184
|
A | AT | 36 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0127others(33): Show | 40 | HG00438.hp1 HG00438.hp2 HG00597.hp2 others(37): Show |
intron_variant | MODIFIER | c.218+259dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATACAC others(121): Show |
1 | a0001c0004t0001g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(128): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATACAC others(115): Show |
1 | a0001c0004t0001g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(122): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATACAC others(117): Show |
1 | a0001c0004t0001g0166 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(124): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATACAC others(116): Show |
2 | a0001c0004t0001g0167a0001c0004t0001g0168 | 2 | HG01243.hp1 HG01891.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(123): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATACAT others(194): Show |
1 | a0001c0004t0009g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(201): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAC others(121): Show |
1 | a0001c0001t0001g0011 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(128): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAC others(148): Show |
1 | a0001c0001t0008g0021 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(155): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAT others(118): Show |
3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180 | 3 | HG02280.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(125): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAT others(116): Show |
1 | a0001c0001t0001g0170 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(123): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAT others(121): Show |
1 | a0001c0001t0001g0171 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(128): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAT others(127): Show |
1 | a0001c0001t0001g0172 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(134): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAT others(123): Show |
3 | a0001c0001t0001g0012a0001c0001t0001g0173a0001c0001t0001g0174 | 4 | HG02109.hp2 NA18906.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+246_218+247ins others(130): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAT others(121): Show |
1 | a0001c0001t0001g0175 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(128): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAT others(454): Show |
1 | a0001c0001t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(461): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAT others(151): Show |
1 | a0001c0001t0001g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(158): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAT others(458): Show |
1 | a0001c0004t0001g0161 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(465): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAT others(460): Show |
1 | a0001c0004t0001g0162 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(467): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAT others(452): Show |
1 | a0001c0004t0001g0163 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(459): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAT others(29): Show |
1 | a0001c0005t0003g0206 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(36): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAT others(27): Show |
1 | a0001c0005t0003g0207 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(34): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAT others(25): Show |
1 | a0001c0005t0003g0208 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(32): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAT others(23): Show |
3 | a0001c0005t0003g0209a0001c0005t0003g0210a0001c0005t0003g0211 | 3 | HG02486.hp1 HG02717.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(30): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAT others(21): Show |
1 | a0001c0005t0003g0212 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(28): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAT others(19): Show |
1 | a0001c0005t0003g0213 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(26): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATATAT others(12): Show |
1 | a0001c0007t0001g0187 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(19): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATGTGT others(132): Show |
1 | a0001c0001t0001g0024 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(139): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATGTGT others(134): Show |
1 | a0001c0001t0001g0025 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(141): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATGTGT others(137): Show |
2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(144): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATGTGT others(143): Show |
1 | a0001c0001t0001g0129 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(150): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATGTGT others(138): Show |
1 | a0001c0001t0001g0259 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(145): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATGTGT others(136): Show |
1 | a0001c0001t0001g0028 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(143): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATGTGT others(142): Show |
1 | a0001c0001t0001g0029 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(149): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATGTGT others(137): Show |
1 | a0001c0001t0001g0030 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(144): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATATGTGT others(144): Show |
1 | a0001c0001t0001g0031 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(151): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(126): Show |
1 | a0001c0001t0001g0032 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(133): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(132): Show |
2 | a0001c0001t0001g0034a0001c0001t0001g0181 | 2 | HG01433.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(139): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(131): Show |
1 | a0001c0001t0001g0006 | 3 | HG00140.hp2 HG01256.hp2 HG02486.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(138): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(129): Show |
1 | a0001c0001t0001g0035 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(136): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(127): Show |
1 | a0001c0001t0001g0036 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(134): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(139): Show |
1 | a0001c0001t0001g0037 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(146): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(137): Show |
1 | a0001c0001t0001g0038 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(144): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(133): Show |
1 | a0001c0001t0001g0039 | 1 | HG01361.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(140): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(134): Show |
2 | a0001c0001t0001g0040a0001c0001t0001g0041 | 2 | HG01123.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(141): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(132): Show |
1 | a0001c0001t0001g0042 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(139): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(138): Show |
1 | a0001c0001t0001g0043 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(145): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(132): Show |
1 | a0001c0001t0001g0044 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(139): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(137): Show |
1 | a0001c0001t0001g0045 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(144): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(141): Show |
1 | a0001c0001t0001g0046 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(148): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(143): Show |
1 | a0001c0006t0001g0047 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(150): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(141): Show |
1 | a0001c0001t0001g0048 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(148): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(137): Show |
2 | a0001c0001t0001g0049a0001c0001t0001g0050 | 2 | HG00423.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(144): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(135): Show |
2 | a0001c0001t0001g0051a0001c0001t0001g0052 | 2 | HG01261.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(142): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(133): Show |
2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG01515.hp2 HG02300.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(140): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(129): Show |
1 | a0001c0001t0001g0055 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(136): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(142): Show |
2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | NA18942.hp1 NA18947.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(149): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(158): Show |
1 | a0001c0003t0001g0058 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(165): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(160): Show |
1 | a0001c0003t0001g0059 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(167): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(140): Show |
3 | a0001c0001t0001g0060a0001c0001t0001g0062a0001c0003t0001g0061 | 3 | HG03195.hp2 HG03239.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(147): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(138): Show |
4 | a0001c0001t0001g0063a0001c0001t0001g0064a0001c0001t0001g0065others(1): Show | 4 | HG01978.hp1 HG01981.hp2 HG02273.hp2 others(1): Show |
intron_variant | MODIFIER | c.218+246_218+247ins others(145): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(136): Show |
5 | a0001c0001t0001g0007a0001c0001t0001g0067a0001c0001t0001g0068others(2): Show | 7 | HG01516.hp2 HG02071.hp2 HG02738.hp2 others(4): Show |
intron_variant | MODIFIER | c.218+246_218+247ins others(143): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(134): Show |
1 | a0001c0001t0001g0184 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(141): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(122): Show |
1 | a0001c0001t0001g0071 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(129): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(118): Show |
3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG02074.hp2 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(125): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(145): Show |
1 | a0001c0001t0001g0075 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(152): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(136): Show |
1 | a0001c0001t0001g0076 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(143): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(134): Show |
1 | a0001c0001t0001g0077 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(141): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(136): Show |
2 | a0001c0001t0001g0078a0001c0001t0001g0079 | 2 | HG02148.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(143): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(138): Show |
1 | a0001c0001t0001g0080 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(145): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(131): Show |
1 | a0001c0001t0001g0081 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(138): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(133): Show |
1 | a0001c0001t0001g0082 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(140): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(136): Show |
1 | a0001c0001t0001g0083 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(143): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(145): Show |
1 | a0001c0006t0001g0084 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(152): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(135): Show |
1 | a0001c0001t0001g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(142): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(144): Show |
1 | a0001c0001t0001g0086 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(151): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(140): Show |
2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | NA18946.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(147): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(138): Show |
3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG01943.hp1 NA18984.hp1 NA19085.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(145): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(136): Show |
1 | a0001c0001t0001g0092 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(143): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(138): Show |
3 | a0001c0001t0001g0093a0001c0001t0001g0094a0001c0001t0001g0095 | 3 | HG01928.hp1 HG02273.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(145): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(143): Show |
1 | a0001c0006t0001g0096 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(150): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(137): Show |
2 | a0001c0001t0001g0097a0001c0001t0001g0098 | 2 | HG01169.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(144): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(135): Show |
1 | a0001c0001t0001g0008 | 2 | HG00609.hp2 NA19065.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(142): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(144): Show |
1 | a0001c0001t0001g0099 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(151): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(142): Show |
1 | a0001c0001t0001g0100 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(149): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(140): Show |
2 | a0001c0001t0001g0009a0001c0001t0001g0182 | 3 | HG00741.hp1 HG00741.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(147): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(140): Show |
1 | a0001c0001t0001g0101 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(147): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(141): Show |
1 | a0001c0001t0001g0102 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(148): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(142): Show |
1 | a0001c0001t0001g0103 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(149): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(139): Show |
1 | a0001c0001t0001g0104 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(146): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(146): Show |
2 | a0001c0001t0001g0105a0001c0001t0001g0106 | 2 | NA18956.hp2 NA19004.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(153): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(144): Show |
2 | a0001c0001t0001g0107a0001c0001t0001g0108 | 2 | HG00544.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(151): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(142): Show |
1 | a0001c0001t0001g0109 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(149): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(145): Show |
1 | a0001c0001t0001g0110 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(152): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(144): Show |
1 | a0001c0001t0001g0111 | 1 | HG01192.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(151): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(141): Show |
1 | a0001c0001t0001g0112 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(148): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(184): Show |
1 | a0001c0001t0001g0113 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(191): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(180): Show |
1 | a0001c0001t0001g0114 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(187): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(211): Show |
1 | a0001c0001t0001g0115 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(218): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(208): Show |
1 | a0001c0001t0001g0116 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(215): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(190): Show |
1 | a0001c0001t0001g0117 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(197): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTAT others(190): Show |
1 | a0001c0001t0001g0118 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(197): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTGT others(134): Show |
1 | a0001c0001t0001g0022 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(141): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTGT others(141): Show |
1 | a0001c0001t0001g0119 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(148): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTGT others(137): Show |
1 | a0001c0001t0001g0120 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(144): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTGT others(132): Show |
1 | a0001c0001t0001g0121 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(139): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTGT others(136): Show |
1 | a0001c0001t0001g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(143): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTGT others(139): Show |
1 | a0001c0001t0001g0123 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(146): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTGT others(145): Show |
1 | a0001c0006t0001g0124 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(152): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTGT others(135): Show |
1 | a0001c0001t0001g0125 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(142): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | ATGTGTGT others(148): Show |
1 | a0001c0001t0001g0126 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(155): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17580184 | |||||
chr4:17580184
|
A | G | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.218+245A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580184 | ||||||
chr4:17580184
|
A | T | 1 | a0001c0001t0001g0033 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.218+245A>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580184 | ||||||
chr4:17580185
|
T | TATATATA others(44): Show |
2 | a0001c0001t0001g0228a0001c0005t0003g0186 | 2 | HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.218+246_218+247ins others(51): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | ||||||
chr4:17580185
|
T | TATATATA others(40): Show |
1 | a0001c0005t0003g0192 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(47): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | ||||||
chr4:17580185
|
T | TATATATA others(42): Show |
1 | a0001c0003t0003g0193 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(49): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | ||||||
chr4:17580185
|
T | TATATATA others(40): Show |
1 | a0001c0003t0003g0194 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(47): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | ||||||
chr4:17580185
|
T | TATATATA others(38): Show |
1 | a0001c0003t0003g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(45): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | ||||||
chr4:17580185
|
T | TATATATA others(36): Show |
1 | a0001c0003t0003g0196 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(43): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | ||||||
chr4:17580185
|
T | TATATATA others(34): Show |
1 | a0001c0003t0003g0197 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(41): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | ||||||
chr4:17580185
|
T | TATATATA others(32): Show |
1 | a0001c0003t0003g0198 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(39): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | ||||||
chr4:17580185
|
T | TATATATA others(26): Show |
1 | a0001c0004t0007g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(33): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | ||||||
chr4:17580185
|
T | TATATATA others(30): Show |
4 | a0001c0003t0003g0014a0001c0003t0003g0199a0001c0003t0003g0200others(1): Show | 5 | HG02622.hp1 HG02895.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.218+246_218+247ins others(37): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | ||||||
chr4:17580185
|
T | TATATATA others(28): Show |
1 | a0001c0003t0003g0202 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.218+246_218+247ins others(35): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | ||||||
chr4:17580185
|
T | TATATATA others(22): Show |
3 | a0001c0001t0001g0229a0001c0001t0001g0230a0001c0001t0001g0231 | 3 | HG01243.hp2 HG02615.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(29): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | ||||||
chr4:17580185
|
T | TATATATA others(26): Show |
1 | a0001c0003t0003g0203 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.218+246_218+247ins others(33): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | ||||||
chr4:17580185
|
T | TATATATA others(24): Show |
2 | a0001c0003t0003g0204a0001c0003t0003g0205 | 2 | HG03098.hp2 HG03516.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(31): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | ||||||
chr4:17580185
|
T | TATATATA others(8): Show |
1 | a0001c0005t0003g0015 | 2 | HG01109.hp1 HG01884.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(15): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | ||||||
chr4:17580185
|
T | TATATATA others(6): Show |
2 | a0001c0001t0004g0016a0001c0001t0011g0218 | 3 | HG03831.hp2 NA18998.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.218+246_218+247ins others(13): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | ||||||
chr4:17580185
|
T | TATATATA others(4): Show |
5 | a0001c0001t0004g0003a0001c0001t0004g0219a0001c0001t0004g0220others(2): Show | 9 | NA18945.hp1 NA18955.hp2 NA18956.hp1 others(6): Show |
intron_variant | MODIFIER | c.218+246_218+247ins others(11): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | ||||||
chr4:17580185
|
T | TATATATG others(2): Show |
6 | a0001c0001t0004g0017a0001c0001t0004g0223a0001c0001t0004g0224others(3): Show | 7 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.218+246_218+247ins others(9): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580185 | ||||||
chr4:17580186
|
T | A | 8 | a0001c0005t0003g0206a0001c0005t0003g0207a0001c0005t0003g0208others(5): Show | 8 | HG02055.hp1 HG02486.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.218+247T>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580186 | ||||||
chr4:17580331
|
T | C | 1 | a0001c0002t0002g0189 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.218+392T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580331 | ||||||
chr4:17580334
|
A | G | 1 | a0001c0004t0007g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.218+395A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580334 | ||||||
chr4:17580428
|
G | A | 144 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(141): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.218+489G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580428 | ||||||
chr4:17580729
|
A | G | 19 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0169others(16): Show | 21 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.218+790A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580729 | ||||||
chr4:17580819
|
T | C | 226 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(223): Show | 247 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(244): Show |
intron_variant | MODIFIER | c.218+880T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580819 | ||||||
chr4:17580897
|
G | A | 1 | a0001c0001t0001g0112 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.219-863G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580897 | ||||||
chr4:17580917
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.219-843A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580917 | ||||||
chr4:17580996
|
G | A | 11 | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0133others(8): Show | 15 | HG00438.hp1 HG00597.hp2 HG01255.hp2 others(12): Show |
intron_variant | MODIFIER | c.219-764G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17580996 | ||||||
chr4:17581011
|
T | C | 1 | a0001c0001t0004g0223 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.219-749T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581011 | ||||||
chr4:17581108
|
G | A | 13 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0017others(10): Show | 19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.219-652G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581108 | ||||||
chr4:17581167
|
G | A | 13 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0017others(10): Show | 19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.219-593G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581167 | ||||||
chr4:17581181
|
G | A | 1 | a0001c0004t0001g0188 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.219-579G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581181 | ||||||
chr4:17581241
|
A | G | 6 | a0001c0003t0003g0014a0001c0003t0003g0193a0001c0003t0003g0198others(3): Show | 7 | HG02622.hp1 HG02895.hp2 HG02896.hp1 others(4): Show |
intron_variant | MODIFIER | c.219-519A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581241 | ||||||
chr4:17581292
|
G | A | 1 | a0001c0002t0002g0235 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.219-468G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581292 | ||||||
chr4:17581307
|
C | T | 1 | a0001c0002t0002g0258 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.219-453C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581307 | ||||||
chr4:17581360
|
T | C | 1 | a0001c0004t0001g0188 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.219-400T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581360 | ||||||
chr4:17581377
|
A | G | 8 | a0001c0001t0001g0160a0001c0004t0001g0156a0001c0004t0001g0157others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(5): Show |
intron_variant | MODIFIER | c.219-383A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581377 | ||||||
chr4:17581458
|
G | A | 1 | a0001c0003t0003g0199 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.219-302G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581458 | ||||||
chr4:17581497
|
G | A | 1 | a0001c0001t0001g0160 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.219-263G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581497 | ||||||
chr4:17581514
|
G | A | 1 | a0001c0004t0001g0188 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.219-246G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581514 | ||||||
chr4:17581523
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.219-237G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581523 | ||||||
chr4:17581577
|
TA | T | 18 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0017others(15): Show | 24 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(21): Show |
intron_variant | MODIFIER | c.219-169delA | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17581577 | |||||
chr4:17581577
|
TAA | T | 173 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(170): Show | 185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.219-170_219-169del others(2): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr4 | 17581577 | |||||
chr4:17581725
|
A | G | 3 | a0001c0005t0003g0015a0001c0005t0003g0186a0001c0005t0003g0192 | 4 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.219-35A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581725 | ||||||
chr4:17581738
|
C | T | 2 | a0001c0001t0001g0231a0001c0004t0007g0183 | 2 | HG01243.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.219-22C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581738 | ||||||
chr4:17581743
|
A | G | 13 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0017others(10): Show | 19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.219-17A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 2/12 | chr4 | 17581743 | ||||||
chr4:17582183
|
A | C | 173 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(170): Show | 185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.274-105A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 3/12 | chr4 | 17582183 | ||||||
chr4:17582412
|
T | A | 11 | a0001c0005t0003g0206a0001c0005t0003g0207a0001c0005t0003g0208others(8): Show | 11 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.379+19T>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 4/12 | chr4 | 17582412 | ||||||
chr4:17582550
|
G | A | 1 | a0001c0002t0002g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.379+157G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 4/12 | chr4 | 17582550 | ||||||
chr4:17582813
|
G | GT | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0062 | 3 | HG01123.hp2 HG02698.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.379+421dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 4/12 | INFO_REALIGN_3_PRIME | chr4 | 17582813 | |||||
chr4:17582910
|
C | A | 1 | a0001c0001t0001g0072 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.379+517C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 4/12 | chr4 | 17582910 | ||||||
chr4:17582939
|
A | G | 1 | a0001c0003t0003g0203 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.380-544A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 4/12 | chr4 | 17582939 | ||||||
chr4:17583391
|
G | C | 173 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(170): Show | 185 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(182): Show |
intron_variant | MODIFIER | c.380-92G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 4/12 | chr4 | 17583391 | ||||||
chr4:17583468
|
C | T | 14 | a0001c0005t0003g0015a0001c0005t0003g0186a0001c0005t0003g0192others(11): Show | 15 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.380-15C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 4/12 | chr4 | 17583468 | ||||||
chr4:17583658
|
TAGG | T | 32 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(29): Show | 34 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.539+23_539+25delAG others(1): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | INFO_REALIGN_3_PRIME | chr4 | 17583658 | |||||
chr4:17583744
|
G | A | 1 | a0001c0001t0004g0016 | 2 | NA18998.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.539+102G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17583744 | ||||||
chr4:17583860
|
C | A | 29 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0160others(26): Show | 31 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(28): Show |
intron_variant | MODIFIER | c.539+218C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17583860 | ||||||
chr4:17583876
|
T | C | 2 | a0001c0001t0008g0021a0001c0004t0009g0020 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.539+234T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17583876 | ||||||
chr4:17583883
|
A | G | 13 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0017others(10): Show | 19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.539+241A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17583883 | ||||||
chr4:17584002
|
T | C | 219 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(216): Show | 239 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(236): Show |
intron_variant | MODIFIER | c.539+360T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17584002 | ||||||
chr4:17584361
|
T | C | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.540-611T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17584361 | ||||||
chr4:17584418
|
A | T | 4 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(1): Show | 4 | HG01243.hp2 HG02615.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.540-554A>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17584418 | ||||||
chr4:17584451
|
C | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0028others(1): Show | 4 | HG02970.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.540-521C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17584451 | ||||||
chr4:17584787
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.540-185C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17584787 | ||||||
chr4:17584850
|
A | G | 1 | a0001c0008t0002g0217 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.540-122A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17584850 | ||||||
chr4:17584893
|
G | C | 1 | a0001c0001t0001g0087 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.540-79G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17584893 | ||||||
chr4:17584937
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.540-35G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 5/12 | chr4 | 17584937 | ||||||
chr4:17585150
|
G | A | 7 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+14G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585150 | ||||||
chr4:17585218
|
T | G | 14 | a0001c0003t0003g0014a0001c0003t0003g0193a0001c0003t0003g0194others(11): Show | 15 | HG02145.hp1 HG02622.hp1 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.704+82T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585218 | ||||||
chr4:17585264
|
G | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01257.hp1 HG01975.hp2 |
intron_variant | MODIFIER | c.704+128G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585264 | ||||||
chr4:17585334
|
A | G | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.704+198A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585334 | ||||||
chr4:17585395
|
A | G | 2 | a0001c0002t0002g0019a0001c0002t0002g0235 | 3 | HG03704.hp2 HG04199.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.704+259A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585395 | ||||||
chr4:17585435
|
A | AT | 164 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(161): Show | 181 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(178): Show |
intron_variant | MODIFIER | c.704+318dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17585435 | |||||
chr4:17585435
|
A | ATT | 14 | a0001c0001t0001g0032a0001c0001t0001g0068a0001c0001t0001g0069others(11): Show | 14 | HG00323.hp2 HG01952.hp1 HG01975.hp1 others(11): Show |
intron_variant | MODIFIER | c.704+317_704+318dup others(2): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17585435 | |||||
chr4:17585514
|
T | A | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.704+378T>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585514 | ||||||
chr4:17585610
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.704+474A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585610 | ||||||
chr4:17585639
|
G | A | 1 | a0001c0001t0001g0172 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.704+503G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585639 | ||||||
chr4:17585715
|
C | T | 3 | a0001c0002t0002g0013a0001c0002t0002g0189a0001c0002t0002g0190 | 4 | HG00099.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.704+579C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585715 | ||||||
chr4:17585738
|
C | T | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.704+602C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585738 | ||||||
chr4:17585942
|
C | T | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.704+806C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17585942 | ||||||
chr4:17586148
|
C | T | 7 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+1012C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17586148 | ||||||
chr4:17586162
|
G | A | 1 | a0001c0004t0001g0188 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.704+1026G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17586162 | ||||||
chr4:17586292
|
CT | C | 6 | a0001c0001t0001g0011a0001c0004t0001g0164a0001c0004t0001g0165others(3): Show | 7 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.704+1158delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17586292 | |||||
chr4:17586380
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.704+1244A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17586380 | ||||||
chr4:17586697
|
A | G | 188 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(185): Show | 206 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(203): Show |
intron_variant | MODIFIER | c.704+1561A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17586697 | ||||||
chr4:17586722
|
G | A | 32 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(29): Show | 34 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.704+1586G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17586722 | ||||||
chr4:17586814
|
A | G | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.704+1678A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17586814 | ||||||
chr4:17586965
|
G | C | 1 | a0001c0003t0003g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.704+1829G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17586965 | ||||||
chr4:17587092
|
A | G | 1 | a0001c0001t0001g0125 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.705-1727A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587092 | ||||||
chr4:17587130
|
A | G | 5 | a0001c0001t0001g0036a0001c0001t0001g0102a0001c0001t0001g0103others(2): Show | 5 | HG00438.hp2 HG00673.hp2 NA18960.hp1 others(2): Show |
intron_variant | MODIFIER | c.705-1689A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587130 | ||||||
chr4:17587143
|
G | A | 1 | a0001c0004t0009g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.705-1676G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587143 | ||||||
chr4:17587148
|
G | T | 4 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(1): Show | 4 | HG01243.hp2 HG02615.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.705-1671G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587148 | ||||||
chr4:17587155
|
C | T | 32 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(29): Show | 34 | HG01109.hp1 HG01243.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.705-1664C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587155 | ||||||
chr4:17587207
|
T | C | 1 | a0001c0002t0002g0237 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.705-1612T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587207 | ||||||
chr4:17587289
|
C | T | 3 | a0001c0002t0002g0013a0001c0002t0002g0189a0001c0002t0002g0190 | 4 | HG00099.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.705-1530C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587289 | ||||||
chr4:17587327
|
G | A | 220 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(217): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.705-1492G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587327 | ||||||
chr4:17587413
|
C | T | 1 | a0001c0004t0001g0165 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.705-1406C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587413 | ||||||
chr4:17587429
|
G | GT | 16 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0017others(13): Show | 22 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.705-1374dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17587429 | |||||
chr4:17587429
|
G | GTT | 19 | a0001c0003t0003g0014a0001c0003t0003g0193a0001c0003t0003g0194others(16): Show | 21 | HG01109.hp1 HG01884.hp1 HG02145.hp1 others(18): Show |
intron_variant | MODIFIER | c.705-1375_705-1374d others(4): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17587429 | |||||
chr4:17587429
|
G | GTTT | 13 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(10): Show | 13 | HG01243.hp2 HG02258.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.705-1376_705-1374d others(5): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17587429 | |||||
chr4:17587429
|
GTTTT | G | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.705-1377_705-1374d others(6): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17587429 | |||||
chr4:17587436
|
T | G | 2 | a0001c0001t0001g0143a0001c0001t0001g0150 | 2 | NA18950.hp2 NA19065.hp1 |
intron_variant | MODIFIER | c.705-1383T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587436 | ||||||
chr4:17587437
|
T | A | 1 | a0001c0001t0001g0114 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.705-1382T>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587437 | ||||||
chr4:17587667
|
T | C | 14 | a0001c0003t0003g0014a0001c0003t0003g0193a0001c0003t0003g0194others(11): Show | 15 | HG02145.hp1 HG02622.hp1 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.705-1152T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587667 | ||||||
chr4:17587706
|
G | T | 1 | a0001c0002t0002g0234 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.705-1113G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587706 | ||||||
chr4:17587752
|
G | A | 1 | a0001c0004t0001g0188 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.705-1067G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587752 | ||||||
chr4:17587758
|
A | G | 2 | a0001c0003t0003g0197a0001c0003t0003g0199 | 2 | HG02818.hp2 HG03139.hp1 |
intron_variant | MODIFIER | c.705-1061A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587758 | ||||||
chr4:17587934
|
C | T | 225 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(222): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.705-885C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587934 | ||||||
chr4:17587936
|
G | C | 1 | a0001c0004t0007g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.705-883G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17587936 | ||||||
chr4:17587944
|
A | AT | 18 | a0001c0001t0001g0151a0001c0001t0004g0222a0001c0003t0003g0014others(15): Show | 19 | HG01255.hp2 HG02145.hp1 HG02622.hp1 others(16): Show |
intron_variant | MODIFIER | c.705-861dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17587944 | |||||
chr4:17587944
|
AT | A | 9 | a0001c0001t0008g0021a0001c0004t0001g0156a0001c0004t0001g0157others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.705-861delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17587944 | |||||
chr4:17588201
|
CT | C | 164 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(161): Show | 176 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(173): Show |
intron_variant | MODIFIER | c.705-606delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | INFO_REALIGN_3_PRIME | chr4 | 17588201 | |||||
chr4:17588579
|
A | C | 5 | a0001c0004t0001g0164a0001c0004t0001g0165a0001c0004t0001g0166others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.705-240A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17588579 | ||||||
chr4:17588596
|
A | G | 220 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(217): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.705-223A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17588596 | ||||||
chr4:17588657
|
T | G | 1 | a0001c0003t0003g0204 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.705-162T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17588657 | ||||||
chr4:17588684
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.705-135A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17588684 | ||||||
chr4:17588769
|
T | C | 1 | a0001c0001t0001g0135 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.705-50T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17588769 | ||||||
chr4:17588816
|
T | C | 20 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0160others(17): Show | 22 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(19): Show |
splice_region_variant&intron_variant | LOW | c.705-3T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 6/12 | chr4 | 17588816 | ||||||
chr4:17589018
|
A | G | 1 | a0001c0001t0001g0147 | 1 | HG00733.hp1 | intron_variant | MODIFIER | c.863+41A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589018 | ||||||
chr4:17589048
|
G | A | 106 | a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008others(103): Show | 112 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.863+71G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589048 | ||||||
chr4:17589053
|
TTTTGG | T | 3 | a0001c0002t0002g0013a0001c0002t0002g0189a0001c0002t0002g0190 | 4 | HG00099.hp1 HG02647.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.863+81_863+85delGT others(3): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17589053 | |||||
chr4:17589063
|
AT | A | 200 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(197): Show | 214 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(211): Show |
intron_variant | MODIFIER | c.863+101delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17589063 | |||||
chr4:17589111
|
A | T | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.863+134A>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589111 | ||||||
chr4:17589161
|
A | C | 7 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.863+184A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589161 | ||||||
chr4:17589272
|
G | A | 1 | a0001c0001t0004g0016 | 2 | NA18998.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.863+295G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589272 | ||||||
chr4:17589332
|
A | C | 1 | a0001c0007t0001g0187 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.863+355A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589332 | ||||||
chr4:17589389
|
G | T | 9 | a0001c0001t0008g0021a0001c0004t0001g0156a0001c0004t0001g0157others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.863+412G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589389 | ||||||
chr4:17589565
|
T | C | 1 | a0001c0001t0001g0086 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.863+588T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589565 | ||||||
chr4:17589794
|
C | T | 1 | a0001c0001t0001g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.863+817C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589794 | ||||||
chr4:17589821
|
T | C | 1 | a0001c0008t0002g0217 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.863+844T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589821 | ||||||
chr4:17589845
|
C | T | 13 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0160others(10): Show | 15 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.863+868C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17589845 | ||||||
chr4:17590004
|
T | G | 14 | a0001c0003t0003g0014a0001c0003t0003g0193a0001c0003t0003g0194others(11): Show | 15 | HG02145.hp1 HG02622.hp1 HG02809.hp1 others(12): Show |
intron_variant | MODIFIER | c.863+1027T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590004 | ||||||
chr4:17590025
|
A | G | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.863+1048A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590025 | ||||||
chr4:17590121
|
C | A | 1 | a0001c0004t0007g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.863+1144C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590121 | ||||||
chr4:17590123
|
A | G | 1 | a0001c0004t0007g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.863+1146A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590123 | ||||||
chr4:17590217
|
G | A | 7 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.863+1240G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590217 | ||||||
chr4:17590276
|
C | T | 7 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.863+1299C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590276 | ||||||
chr4:17590587
|
T | G | 3 | a0001c0004t0001g0166a0001c0004t0001g0167a0001c0004t0001g0168 | 3 | HG01243.hp1 HG01891.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.863+1610T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590587 | ||||||
chr4:17590657
|
C | T | 1 | a0001c0001t0001g0052 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.863+1680C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590657 | ||||||
chr4:17590664
|
C | T | 1 | a0001c0001t0004g0221 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.863+1687C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590664 | ||||||
chr4:17590665
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.863+1688G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590665 | ||||||
chr4:17590688
|
C | T | 1 | a0001c0004t0001g0163 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.863+1711C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590688 | ||||||
chr4:17590765
|
G | A | 1 | a0001c0005t0003g0214 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.863+1788G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590765 | ||||||
chr4:17590776
|
T | A | 1 | a0001c0007t0001g0187 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.863+1799T>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590776 | ||||||
chr4:17590840
|
G | C | 2 | a0001c0001t0008g0021a0001c0004t0009g0020 | 2 | HG02922.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.863+1863G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590840 | ||||||
chr4:17590845
|
C | T | 4 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(1): Show | 4 | HG01243.hp2 HG02615.hp1 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.863+1868C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590845 | ||||||
chr4:17590898
|
A | G | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.863+1921A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590898 | ||||||
chr4:17590923
|
CT | C | 164 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(161): Show | 176 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(173): Show |
intron_variant | MODIFIER | c.863+1971delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17590923 | |||||
chr4:17590923
|
CTT | C | 49 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0030others(46): Show | 57 | HG01109.hp1 HG01123.hp1 HG01192.hp2 others(54): Show |
intron_variant | MODIFIER | c.863+1970_863+1971d others(4): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17590923 | |||||
chr4:17590925
|
T | A | 1 | a0001c0002t0002g0238 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.863+1948T>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590925 | ||||||
chr4:17590951
|
T | G | 1 | a0001c0002t0002g0238 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.863+1974T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17590951 | ||||||
chr4:17591103
|
A | G | 1 | a0001c0008t0002g0217 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.863+2126A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591103 | ||||||
chr4:17591113
|
G | C | 1 | a0001c0001t0001g0031 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.863+2136G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591113 | ||||||
chr4:17591199
|
C | T | 2 | a0001c0001t0001g0026a0001c0001t0001g0027 | 2 | HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.863+2222C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591199 | ||||||
chr4:17591215
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.863+2238T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591215 | ||||||
chr4:17591244
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.863+2267T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591244 | ||||||
chr4:17591298
|
G | A | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.863+2321G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591298 | ||||||
chr4:17591358
|
G | A | 1 | a0001c0004t0007g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.863+2381G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591358 | ||||||
chr4:17591490
|
G | T | 14 | a0001c0005t0003g0015a0001c0005t0003g0186a0001c0005t0003g0192others(11): Show | 15 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(12): Show |
intron_variant | MODIFIER | c.863+2513G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591490 | ||||||
chr4:17591609
|
T | C | 16 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0017others(13): Show | 22 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(19): Show |
intron_variant | MODIFIER | c.863+2632T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591609 | ||||||
chr4:17591673
|
G | C | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0062 | 3 | HG01123.hp2 HG02698.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.863+2696G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591673 | ||||||
chr4:17591739
|
G | T | 9 | a0001c0001t0008g0021a0001c0004t0001g0156a0001c0004t0001g0157others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02922.hp2 others(6): Show |
intron_variant | MODIFIER | c.863+2762G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591739 | ||||||
chr4:17591812
|
T | C | 30 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0017others(27): Show | 36 | HG01123.hp1 HG01192.hp2 HG01243.hp1 others(33): Show |
intron_variant | MODIFIER | c.863+2835T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591812 | ||||||
chr4:17591822
|
C | T | 1 | a0001c0002t0002g0255 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.863+2845C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591822 | ||||||
chr4:17591971
|
CT | C | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.863+2996delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17591971 | |||||
chr4:17591982
|
G | T | 170 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(167): Show | 182 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(179): Show |
intron_variant | MODIFIER | c.863+3005G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17591982 | ||||||
chr4:17592034
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.863+3057T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592034 | ||||||
chr4:17592168
|
C | A | 2 | a0001c0001t0001g0006a0001c0001t0001g0035 | 4 | HG00140.hp2 HG01256.hp2 HG01515.hp1 others(1): Show |
intron_variant | MODIFIER | c.863+3191C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592168 | ||||||
chr4:17592226
|
G | C | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.864-3184G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592226 | ||||||
chr4:17592282
|
A | G | 220 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(217): Show | 240 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(237): Show |
intron_variant | MODIFIER | c.864-3128A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592282 | ||||||
chr4:17592342
|
G | A | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.864-3068G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592342 | ||||||
chr4:17592344
|
C | CTTCT | 225 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(222): Show | 246 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(243): Show |
intron_variant | MODIFIER | c.864-3062_864-3059d others(6): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17592344 | |||||
chr4:17592355
|
G | T | 172 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(169): Show | 184 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(181): Show |
intron_variant | MODIFIER | c.864-3055G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592355 | ||||||
chr4:17592375
|
A | G | 1 | a0001c0001t0001g0120 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.864-3035A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592375 | ||||||
chr4:17592462
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.864-2948A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592462 | ||||||
chr4:17592478
|
T | C | 1 | a0001c0001t0001g0177 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.864-2932T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592478 | ||||||
chr4:17592614
|
A | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0160a0001c0001t0001g0172others(4): Show | 8 | HG02109.hp2 HG02559.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.864-2796A>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592614 | ||||||
chr4:17592840
|
G | A | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.864-2570G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592840 | ||||||
chr4:17592863
|
C | T | 13 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0017others(10): Show | 19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.864-2547C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592863 | ||||||
chr4:17592869
|
G | A | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.864-2541G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592869 | ||||||
chr4:17592876
|
T | C | 1 | a0001c0007t0001g0187 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.864-2534T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17592876 | ||||||
chr4:17593006
|
C | T | 1 | a0001c0002t0002g0253 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.864-2404C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593006 | ||||||
chr4:17593076
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.864-2334G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593076 | ||||||
chr4:17593079
|
T | C | 159 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(156): Show | 169 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(166): Show |
intron_variant | MODIFIER | c.864-2331T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593079 | ||||||
chr4:17593261
|
C | T | 1 | a0001c0004t0009g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.864-2149C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593261 | ||||||
chr4:17593312
|
C | G | 5 | a0001c0004t0001g0164a0001c0004t0001g0165a0001c0004t0001g0166others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.864-2098C>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593312 | ||||||
chr4:17593453
|
C | G | 3 | a0001c0005t0003g0015a0001c0005t0003g0186a0001c0005t0003g0192 | 4 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.864-1957C>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593453 | ||||||
chr4:17593522
|
CAT | C | 143 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(140): Show | 153 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(150): Show |
intron_variant | MODIFIER | c.864-1887_864-1886d others(4): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593522 | ||||||
chr4:17593565
|
G | A | 1 | a0001c0001t0001g0133 | 1 | NA19079.hp2 | intron_variant | MODIFIER | c.864-1845G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593565 | ||||||
chr4:17593589
|
A | G | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.864-1821A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593589 | ||||||
chr4:17593609
|
G | GT | 17 | a0001c0002t0002g0251a0001c0002t0002g0252a0001c0002t0002g0254others(14): Show | 18 | HG00140.hp1 HG01175.hp1 HG02145.hp1 others(15): Show |
intron_variant | MODIFIER | c.864-1781dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17593609 | |||||
chr4:17593609
|
G | GTT | 11 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0017others(8): Show | 17 | HG01192.hp2 HG01952.hp1 HG03098.hp2 others(14): Show |
intron_variant | MODIFIER | c.864-1782_864-1781d others(4): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17593609 | |||||
chr4:17593609
|
G | GTTTTT | 10 | a0001c0005t0003g0015a0001c0005t0003g0186a0001c0005t0003g0192others(7): Show | 11 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.864-1785_864-1781d others(7): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17593609 | |||||
chr4:17593609
|
G | GTTTTTTT | 120 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(117): Show | 132 | HG00099.hp1 HG00140.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.864-1787_864-1781d others(9): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17593609 | |||||
chr4:17593609
|
G | GTTTTTTT others(1): Show |
43 | a0001c0001t0001g0011a0001c0001t0001g0037a0001c0001t0001g0041others(40): Show | 44 | HG00099.hp2 HG00423.hp2 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.864-1788_864-1781d others(10): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17593609 | |||||
chr4:17593609
|
G | GTTTTTTT others(3): Show |
2 | a0001c0001t0001g0231a0001c0007t0001g0187 | 2 | HG01243.hp2 NA18939.hp1 |
intron_variant | MODIFIER | c.864-1790_864-1781d others(12): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17593609 | |||||
chr4:17593609
|
G | GTTTTTTT others(4): Show |
6 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(3): Show | 6 | HG02257.hp2 HG02451.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.864-1791_864-1781d others(13): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17593609 | |||||
chr4:17593609
|
G | GTTTTTTT others(5): Show |
3 | a0001c0004t0001g0159a0001c0004t0001g0161a0001c0004t0009g0020 | 3 | HG02970.hp2 HG03225.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.864-1792_864-1781d others(14): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17593609 | |||||
chr4:17593609
|
GT | G | 6 | a0001c0002t0002g0241a0001c0004t0001g0164a0001c0004t0001g0165others(3): Show | 6 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(3): Show |
intron_variant | MODIFIER | c.864-1781delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17593609 | |||||
chr4:17593631
|
A | G | 1 | a0001c0002t0002g0250 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.864-1779A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593631 | ||||||
chr4:17593637
|
T | C | 1 | a0001c0008t0002g0217 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.864-1773T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593637 | ||||||
chr4:17593697
|
G | A | 1 | a0001c0002t0002g0236 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.864-1713G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593697 | ||||||
chr4:17593738
|
G | C | 8 | a0001c0005t0003g0206a0001c0005t0003g0207a0001c0005t0003g0208others(5): Show | 8 | HG02055.hp1 HG02486.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.864-1672G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593738 | ||||||
chr4:17593742
|
A | T | 158 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(155): Show | 168 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(165): Show |
intron_variant | MODIFIER | c.864-1668A>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593742 | ||||||
chr4:17593845
|
T | C | 7 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.864-1565T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593845 | ||||||
chr4:17593913
|
A | G | 2 | a0001c0001t0001g0081a0001c0001t0001g0111 | 2 | HG01192.hp1 HG03831.hp1 |
intron_variant | MODIFIER | c.864-1497A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593913 | ||||||
chr4:17593971
|
G | C | 1 | a0001c0001t0001g0081 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.864-1439G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593971 | ||||||
chr4:17593975
|
G | A | 19 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(16): Show | 20 | HG01243.hp2 HG02145.hp1 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.864-1435G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17593975 | ||||||
chr4:17594149
|
CA | C | 7 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.864-1258delA | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17594149 | |||||
chr4:17594206
|
T | TA | 7 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.864-1203dupA | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | INFO_REALIGN_3_PRIME | chr4 | 17594206 | |||||
chr4:17594298
|
A | G | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.864-1112A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17594298 | ||||||
chr4:17594384
|
G | A | 1 | a0001c0001t0001g0118 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.864-1026G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17594384 | ||||||
chr4:17594568
|
G | A | 1 | a0001c0004t0007g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.864-842G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17594568 | ||||||
chr4:17594621
|
T | G | 1 | a0001c0004t0009g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.864-789T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17594621 | ||||||
chr4:17594682
|
A | G | 5 | a0001c0004t0001g0164a0001c0004t0001g0165a0001c0004t0001g0166others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.864-728A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17594682 | ||||||
chr4:17594838
|
A | G | 6 | a0001c0001t0001g0009a0001c0001t0001g0034a0001c0001t0001g0065others(3): Show | 7 | HG00741.hp1 HG01071.hp2 HG01943.hp1 others(4): Show |
intron_variant | MODIFIER | c.864-572A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17594838 | ||||||
chr4:17594878
|
T | C | 5 | a0001c0004t0001g0164a0001c0004t0001g0165a0001c0004t0001g0166others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.864-532T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17594878 | ||||||
chr4:17594969
|
C | T | 1 | a0001c0004t0009g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.864-441C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17594969 | ||||||
chr4:17594985
|
A | C | 13 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0017others(10): Show | 19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.864-425A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17594985 | ||||||
chr4:17595073
|
C | T | 13 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0017others(10): Show | 19 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(16): Show |
intron_variant | MODIFIER | c.864-337C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17595073 | ||||||
chr4:17595213
|
G | A | 1 | a0001c0007t0001g0187 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.864-197G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17595213 | ||||||
chr4:17595281
|
G | T | 1 | a0001c0003t0003g0195 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.864-129G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17595281 | ||||||
chr4:17595317
|
C | T | 5 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(2): Show | 5 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.864-93C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17595317 | ||||||
chr4:17595328
|
G | A | 50 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0160others(47): Show | 60 | HG00099.hp1 HG01123.hp1 HG01192.hp2 others(57): Show |
intron_variant | MODIFIER | c.864-82G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17595328 | ||||||
chr4:17595332
|
C | A | 19 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(16): Show | 20 | HG01243.hp2 HG02145.hp1 HG02615.hp1 others(17): Show |
intron_variant | MODIFIER | c.864-78C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17595332 | ||||||
chr4:17595390
|
C | T | 1 | a0001c0001t0001g0010 | 2 | NA18942.hp2 NA18972.hp2 |
intron_variant | MODIFIER | c.864-20C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 7/12 | chr4 | 17595390 | ||||||
chr4:17595639
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.988+105T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17595639 | ||||||
chr4:17595654
|
C | T | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.988+120C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17595654 | ||||||
chr4:17595868
|
C | A | 1 | a0001c0001t0008g0021 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.988+334C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17595868 | ||||||
chr4:17595926
|
A | G | 211 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(208): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.988+392A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17595926 | ||||||
chr4:17596019
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.988+485A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596019 | ||||||
chr4:17596076
|
C | T | 1 | a0001c0004t0001g0188 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.988+542C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596076 | ||||||
chr4:17596084
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.988+550C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596084 | ||||||
chr4:17596339
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.989-707G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596339 | ||||||
chr4:17596355
|
T | G | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.989-691T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596355 | ||||||
chr4:17596402
|
C | T | 5 | a0001c0004t0001g0164a0001c0004t0001g0165a0001c0004t0001g0166others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.989-644C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596402 | ||||||
chr4:17596454
|
C | T | 4 | a0001c0004t0001g0164a0001c0004t0001g0166a0001c0004t0001g0167others(1): Show | 4 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(1): Show |
intron_variant | MODIFIER | c.989-592C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596454 | ||||||
chr4:17596462
|
C | T | 5 | a0001c0004t0001g0164a0001c0004t0001g0165a0001c0004t0001g0166others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.989-584C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596462 | ||||||
chr4:17596519
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.989-527A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596519 | ||||||
chr4:17596581
|
T | C | 24 | a0001c0002t0010g0185a0001c0004t0001g0156a0001c0004t0001g0157others(21): Show | 25 | HG01109.hp1 HG01884.hp1 HG02055.hp1 others(22): Show |
intron_variant | MODIFIER | c.989-465T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596581 | ||||||
chr4:17596690
|
G | A | 3 | a0001c0001t0001g0099a0001c0001t0001g0105a0001c0001t0001g0109 | 3 | NA18956.hp2 NA18971.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.989-356G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596690 | ||||||
chr4:17596732
|
T | G | 9 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.989-314T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596732 | ||||||
chr4:17596736
|
T | C | 1 | a0001c0002t0002g0242 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.989-310T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596736 | ||||||
chr4:17596740
|
C | T | 5 | a0001c0004t0001g0164a0001c0004t0001g0165a0001c0004t0001g0166others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.989-306C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596740 | ||||||
chr4:17596761
|
G | A | 144 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(141): Show | 154 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(151): Show |
intron_variant | MODIFIER | c.989-285G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 8/12 | chr4 | 17596761 | ||||||
chr4:17597217
|
G | A | 2 | a0001c0002t0002g0239a0001c0002t0002g0243 | 2 | HG00323.hp1 HG03491.hp2 |
intron_variant | MODIFIER | c.1077+83G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597217 | ||||||
chr4:17597268
|
T | A | 2 | a0001c0003t0001g0058a0001c0003t0001g0059 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1077+134T>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597268 | ||||||
chr4:17597397
|
G | A | 6 | a0001c0001t0001g0022a0001c0001t0001g0040a0001c0001t0001g0041others(3): Show | 6 | HG01123.hp2 HG02698.hp1 HG02717.hp1 others(3): Show |
intron_variant | MODIFIER | c.1077+263G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597397 | ||||||
chr4:17597410
|
G | A | 10 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(7): Show | 10 | HG01243.hp2 HG02145.hp1 HG02615.hp1 others(7): Show |
intron_variant | MODIFIER | c.1077+276G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597410 | ||||||
chr4:17597463
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1077+329T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597463 | ||||||
chr4:17597714
|
A | T | 2 | a0001c0004t0001g0188a0001c0007t0001g0187 | 2 | HG03017.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1077+580A>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597714 | ||||||
chr4:17597800
|
G | A | 1 | a0001c0002t0002g0251 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1078-656G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597800 | ||||||
chr4:17597833
|
G | C | 259 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(256): Show | 299 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(296): Show |
intron_variant | MODIFIER | c.1078-623G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597833 | ||||||
chr4:17597848
|
G | T | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1078-608G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597848 | ||||||
chr4:17597877
|
G | T | 211 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(208): Show | 231 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(228): Show |
intron_variant | MODIFIER | c.1078-579G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597877 | ||||||
chr4:17597901
|
C | A | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1078-555C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597901 | ||||||
chr4:17597901
|
C | T | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180 | 3 | HG02280.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1078-555C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597901 | ||||||
chr4:17597919
|
A | C | 7 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0171others(4): Show | 7 | HG02145.hp2 HG02280.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1078-537A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17597919 | ||||||
chr4:17598070
|
G | A | 1 | a0001c0001t0001g0011 | 2 | HG02451.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1078-386G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17598070 | ||||||
chr4:17598139
|
C | T | 1 | a0001c0001t0001g0090 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1078-317C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17598139 | ||||||
chr4:17598191
|
G | T | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1078-265G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17598191 | ||||||
chr4:17598206
|
C | T | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1078-250C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17598206 | ||||||
chr4:17598214
|
G | A | 179 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(176): Show | 190 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(187): Show |
intron_variant | MODIFIER | c.1078-242G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17598214 | ||||||
chr4:17598271
|
G | T | 145 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(142): Show | 155 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(152): Show |
intron_variant | MODIFIER | c.1078-185G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17598271 | ||||||
chr4:17598377
|
C | T | 1 | a0001c0001t0001g0110 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1078-79C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17598377 | ||||||
chr4:17598395
|
G | T | 1 | a0001c0002t0002g0248 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1078-61G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 9/12 | chr4 | 17598395 | ||||||
chr4:17598761
|
C | CT | 161 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(158): Show | 174 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(171): Show |
intron_variant | MODIFIER | c.1180+212dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17598761 | |||||
chr4:17598775
|
C | T | 4 | a0001c0001t0001g0036a0001c0001t0001g0102a0001c0001t0001g0103others(1): Show | 4 | HG00673.hp2 NA18960.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180+217C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17598775 | ||||||
chr4:17598787
|
C | CT | 5 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(2): Show | 5 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180+230dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17598787 | |||||
chr4:17598883
|
C | T | 3 | a0001c0001t0001g0010a0001c0001t0001g0143a0001c0001t0001g0150 | 4 | NA18942.hp2 NA18950.hp2 NA18972.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180+325C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17598883 | ||||||
chr4:17598890
|
C | T | 1 | a0001c0005t0003g0214 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1180+332C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17598890 | ||||||
chr4:17598916
|
T | G | 5 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(2): Show | 5 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180+358T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17598916 | ||||||
chr4:17598958
|
G | A | 1 | a0001c0004t0001g0188 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1180+400G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17598958 | ||||||
chr4:17598983
|
C | A | 159 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(156): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1180+425C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17598983 | ||||||
chr4:17598984
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1180+426C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17598984 | ||||||
chr4:17599035
|
G | T | 1 | a0001c0007t0001g0187 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1180+477G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599035 | ||||||
chr4:17599046
|
A | C | 1 | a0001c0001t0001g0036 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.1180+488A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599046 | ||||||
chr4:17599105
|
A | C | 223 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(220): Show | 244 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(241): Show |
intron_variant | MODIFIER | c.1180+547A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599105 | ||||||
chr4:17599260
|
C | T | 3 | a0001c0004t0001g0188a0001c0004t0007g0183a0001c0007t0001g0187 | 3 | HG02257.hp2 HG03017.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1180+702C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599260 | ||||||
chr4:17599261
|
A | G | 181 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1180+703A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599261 | ||||||
chr4:17599291
|
C | A | 2 | a0001c0001t0001g0042a0001c0001t0001g0093 | 2 | HG01433.hp1 NA18960.hp2 |
intron_variant | MODIFIER | c.1180+733C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599291 | ||||||
chr4:17599428
|
C | T | 7 | a0001c0001t0001g0012a0001c0001t0001g0160a0001c0001t0001g0172others(4): Show | 8 | HG02109.hp2 HG02559.hp1 HG03579.hp1 others(5): Show |
intron_variant | MODIFIER | c.1180+870C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599428 | ||||||
chr4:17599434
|
G | T | 1 | a0001c0004t0009g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1180+876G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599434 | ||||||
chr4:17599484
|
C | T | 3 | a0001c0001t0001g0022a0001c0001t0001g0121a0001c0001t0001g0122 | 3 | HG02717.hp1 HG02886.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1180+926C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599484 | ||||||
chr4:17599521
|
C | T | 2 | a0001c0001t0001g0125a0001c0001t0001g0134 | 2 | HG02129.hp1 NA18947.hp1 |
intron_variant | MODIFIER | c.1180+963C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599521 | ||||||
chr4:17599532
|
C | T | 1 | a0001c0008t0002g0217 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1180+974C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599532 | ||||||
chr4:17599533
|
T | C | 1 | a0001c0008t0002g0217 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1180+975T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599533 | ||||||
chr4:17599536
|
A | AAAAAT | 12 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0231others(9): Show | 12 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(9): Show |
intron_variant | MODIFIER | c.1180+997_1180+1001 others(8): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17599536 | |||||
chr4:17599536
|
A | AAAAATAA others(3): Show |
1 | a0001c0001t0001g0230 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1180+992_1180+1001 others(13): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17599536 | |||||
chr4:17599554
|
A | G | 1 | a0001c0004t0009g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1180+996A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599554 | ||||||
chr4:17599704
|
A | AC | 7 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1180+1147dupC | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17599704 | |||||
chr4:17599760
|
A | T | 1 | a0001c0004t0007g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1180+1202A>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599760 | ||||||
chr4:17599820
|
C | T | 4 | a0001c0001t0001g0024a0001c0001t0001g0025a0001c0001t0001g0028others(1): Show | 4 | HG02970.hp1 HG02976.hp1 HG03041.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180+1262C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599820 | ||||||
chr4:17599876
|
C | T | 4 | a0001c0001t0001g0090a0001c0004t0001g0188a0001c0004t0007g0183others(1): Show | 4 | HG02257.hp2 HG03017.hp1 NA18939.hp1 others(1): Show |
intron_variant | MODIFIER | c.1180+1318C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17599876 | ||||||
chr4:17600133
|
A | T | 1 | a0001c0001t0001g0090 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.1180+1575A>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600133 | ||||||
chr4:17600274
|
A | G | 9 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180+1716A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600274 | ||||||
chr4:17600361
|
T | C | 2 | a0001c0003t0001g0058a0001c0003t0001g0059 | 2 | HG03098.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.1180+1803T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600361 | ||||||
chr4:17600382
|
T | G | 8 | a0001c0005t0003g0206a0001c0005t0003g0207a0001c0005t0003g0208others(5): Show | 8 | HG02055.hp1 HG02486.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1180+1824T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600382 | ||||||
chr4:17600410
|
G | C | 164 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(161): Show | 177 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(174): Show |
intron_variant | MODIFIER | c.1180+1852G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600410 | ||||||
chr4:17600450
|
C | T | 9 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180+1892C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600450 | ||||||
chr4:17600518
|
A | C | 9 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180+1960A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600518 | ||||||
chr4:17600560
|
T | C | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1180+2002T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600560 | ||||||
chr4:17600594
|
C | G | 10 | a0001c0005t0003g0206a0001c0005t0003g0207a0001c0005t0003g0208others(7): Show | 10 | HG02055.hp1 HG02258.hp1 HG02486.hp1 others(7): Show |
intron_variant | MODIFIER | c.1180+2036C>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600594 | ||||||
chr4:17600629
|
G | A | 6 | a0001c0001t0001g0012a0001c0001t0001g0160a0001c0001t0001g0172others(3): Show | 7 | HG02109.hp2 HG02559.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.1180+2071G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600629 | ||||||
chr4:17600673
|
G | A | 9 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180+2115G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600673 | ||||||
chr4:17600738
|
A | G | 1 | a0001c0001t0001g0174 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1180+2180A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600738 | ||||||
chr4:17600782
|
C | T | 1 | a0001c0004t0009g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1180+2224C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600782 | ||||||
chr4:17600840
|
G | T | 9 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180+2282G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600840 | ||||||
chr4:17600896
|
C | T | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1180+2338C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600896 | ||||||
chr4:17600898
|
C | T | 1 | a0001c0001t0001g0122 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.1180+2340C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17600898 | ||||||
chr4:17601134
|
C | A | 5 | a0001c0004t0001g0164a0001c0004t0001g0165a0001c0004t0001g0166others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180+2576C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601134 | ||||||
chr4:17601136
|
C | T | 9 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1180+2578C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601136 | ||||||
chr4:17601153
|
T | C | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0001g0180 | 3 | HG02280.hp2 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1180+2595T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601153 | ||||||
chr4:17601188
|
C | T | 1 | a0001c0004t0007g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1180+2630C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601188 | ||||||
chr4:17601346
|
G | C | 1 | a0001c0002t0002g0018 | 2 | HG02572.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1180+2788G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601346 | ||||||
chr4:17601348
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0001g0095 | 2 | HG01928.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1180+2790G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601348 | ||||||
chr4:17601414
|
T | C | 5 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(2): Show | 5 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1180+2856T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601414 | ||||||
chr4:17601461
|
T | G | 7 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1180+2903T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601461 | ||||||
chr4:17601534
|
C | A | 1 | a0001c0001t0001g0131 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1180+2976C>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601534 | ||||||
chr4:17601539
|
A | C | 1 | a0001c0004t0009g0020 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1180+2981A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601539 | ||||||
chr4:17601556
|
T | C | 8 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1180+2998T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601556 | ||||||
chr4:17601565
|
A | G | 3 | a0001c0001t0001g0011a0001c0003t0001g0058a0001c0003t0001g0059 | 4 | HG02451.hp1 HG03098.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1180+3007A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601565 | ||||||
chr4:17601586
|
G | A | 8 | a0001c0004t0001g0164a0001c0004t0001g0165a0001c0004t0001g0166others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1181-3002G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601586 | ||||||
chr4:17601695
|
C | T | 195 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1181-2893C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601695 | ||||||
chr4:17601722
|
A | G | 15 | a0001c0002t0002g0002a0001c0002t0002g0019a0001c0002t0002g0235others(12): Show | 23 | HG00140.hp1 HG00597.hp1 HG00609.hp1 others(20): Show |
intron_variant | MODIFIER | c.1181-2866A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601722 | ||||||
chr4:17601801
|
C | T | 195 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1181-2787C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601801 | ||||||
chr4:17601820
|
T | C | 1 | a0001c0002t0002g0245 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.1181-2768T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601820 | ||||||
chr4:17601835
|
C | T | 1 | a0001c0004t0001g0188 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1181-2753C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601835 | ||||||
chr4:17601863
|
T | C | 1 | a0001c0001t0001g0072 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.1181-2725T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601863 | ||||||
chr4:17601875
|
C | T | 13 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1181-2713C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601875 | ||||||
chr4:17601950
|
A | T | 7 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1181-2638A>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17601950 | ||||||
chr4:17602012
|
T | C | 5 | a0001c0004t0001g0164a0001c0004t0001g0165a0001c0004t0001g0166others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181-2576T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602012 | ||||||
chr4:17602044
|
C | T | 2 | a0001c0003t0003g0198a0001c0003t0003g0202 | 2 | HG03139.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1181-2544C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602044 | ||||||
chr4:17602286
|
C | T | 2 | a0001c0001t0001g0052a0001c0001t0001g0053 | 2 | HG01261.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.1181-2302C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602286 | ||||||
chr4:17602345
|
G | A | 1 | a0001c0001t0001g0114 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1181-2243G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602345 | ||||||
chr4:17602349
|
T | C | 5 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(2): Show | 5 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181-2239T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602349 | ||||||
chr4:17602524
|
A | G | 1 | a0001c0001t0001g0051 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.1181-2064A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602524 | ||||||
chr4:17602629
|
C | T | 2 | a0001c0001t0001g0050a0001c0001t0001g0055 | 2 | HG00423.hp2 NA18945.hp2 |
intron_variant | MODIFIER | c.1181-1959C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602629 | ||||||
chr4:17602672
|
G | C | 159 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(156): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1181-1916G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602672 | ||||||
chr4:17602678
|
A | G | 9 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181-1910A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602678 | ||||||
chr4:17602726
|
G | T | 5 | a0001c0004t0001g0164a0001c0004t0001g0165a0001c0004t0001g0166others(2): Show | 5 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181-1862G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602726 | ||||||
chr4:17602831
|
T | G | 9 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181-1757T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602831 | ||||||
chr4:17602833
|
C | T | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1181-1755C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602833 | ||||||
chr4:17602846
|
G | A | 1 | a0001c0007t0001g0187 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.1181-1742G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602846 | ||||||
chr4:17602871
|
G | A | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1181-1717G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602871 | ||||||
chr4:17602881
|
A | G | 181 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1181-1707A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602881 | ||||||
chr4:17602928
|
C | T | 9 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181-1660C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602928 | ||||||
chr4:17602966
|
G | A | 1 | a0001c0001t0001g0085 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1181-1622G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602966 | ||||||
chr4:17602992
|
A | G | 5 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(2): Show | 5 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1181-1596A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17602992 | ||||||
chr4:17603034
|
G | A | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1181-1554G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603034 | ||||||
chr4:17603036
|
G | A | 8 | a0001c0004t0001g0164a0001c0004t0001g0165a0001c0004t0001g0166others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1181-1552G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603036 | ||||||
chr4:17603082
|
T | C | 181 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1181-1506T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603082 | ||||||
chr4:17603179
|
T | C | 181 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1181-1409T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603179 | ||||||
chr4:17603202
|
A | G | 181 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1181-1386A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603202 | ||||||
chr4:17603505
|
CT | C | 200 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(197): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.1181-1067delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17603505 | |||||
chr4:17603535
|
G | A | 7 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1181-1053G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603535 | ||||||
chr4:17603646
|
G | C | 3 | a0001c0005t0003g0015a0001c0005t0003g0186a0001c0005t0003g0192 | 4 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(1): Show |
intron_variant | MODIFIER | c.1181-942G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603646 | ||||||
chr4:17603669
|
C | G | 9 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181-919C>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603669 | ||||||
chr4:17603671
|
C | T | 1 | a0001c0001t0001g0108 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1181-917C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603671 | ||||||
chr4:17603724
|
G | C | 159 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(156): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1181-864G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603724 | ||||||
chr4:17603779
|
G | A | 9 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181-809G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603779 | ||||||
chr4:17603813
|
C | CT | 12 | a0001c0001t0004g0003a0001c0001t0004g0016a0001c0001t0004g0017others(9): Show | 18 | HG01123.hp1 HG01192.hp2 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.1181-763dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17603813 | |||||
chr4:17603813
|
CT | C | 9 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181-763delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17603813 | |||||
chr4:17603822
|
T | C | 2 | a0001c0002t0010g0185a0001c0008t0002g0217 | 2 | HG02965.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.1181-766T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603822 | ||||||
chr4:17603824
|
TTCTTTCT others(3): Show |
T | 2 | a0001c0001t0001g0063a0001c0001t0001g0142 | 2 | HG01952.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1181-762_1181-753d others(12): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17603824 | |||||
chr4:17603826
|
CTTTCTTT others(2): Show |
C | 157 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(154): Show | 170 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(167): Show |
intron_variant | MODIFIER | c.1181-758_1181-750d others(11): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17603826 | |||||
chr4:17603834
|
C | CT | 8 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1181-744dupT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17603834 | |||||
chr4:17603835
|
T | C | 2 | a0001c0001t0001g0063a0001c0001t0001g0142 | 2 | HG01952.hp2 HG02273.hp2 |
intron_variant | MODIFIER | c.1181-753T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603835 | ||||||
chr4:17603863
|
A | G | 6 | a0001c0001t0001g0012a0001c0001t0001g0160a0001c0001t0001g0172others(3): Show | 7 | HG02109.hp2 HG02559.hp1 HG03579.hp1 others(4): Show |
intron_variant | MODIFIER | c.1181-725A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603863 | ||||||
chr4:17603912
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1181-676C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603912 | ||||||
chr4:17603978
|
G | C | 2 | a0001c0004t0001g0188a0001c0007t0001g0187 | 2 | HG03017.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1181-610G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603978 | ||||||
chr4:17603991
|
T | C | 9 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1181-597T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17603991 | ||||||
chr4:17604009
|
C | T | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0039 | 3 | HG01361.hp1 HG03491.hp1 HG03492.hp1 |
intron_variant | MODIFIER | c.1181-579C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17604009 | ||||||
chr4:17604019
|
A | C | 181 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1181-569A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17604019 | ||||||
chr4:17604177
|
C | T | 7 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(4): Show | 7 | HG02451.hp2 HG02630.hp1 HG03225.hp2 others(4): Show |
intron_variant | MODIFIER | c.1181-411C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17604177 | ||||||
chr4:17604198
|
G | C | 159 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(156): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1181-390G>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17604198 | ||||||
chr4:17604245
|
C | T | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1181-343C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17604245 | ||||||
chr4:17604270
|
C | CA | 19 | a0001c0001t0001g0022a0001c0001t0001g0024a0001c0001t0001g0031others(16): Show | 20 | HG01109.hp2 HG01257.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.1181-296dupA | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17604270 | |||||
chr4:17604270
|
C | CAA | 6 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(3): Show | 6 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(3): Show |
intron_variant | MODIFIER | c.1181-297_1181-296d others(4): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17604270 | |||||
chr4:17604270
|
C | CAAA | 13 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(10): Show | 13 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(10): Show |
intron_variant | MODIFIER | c.1181-298_1181-296d others(5): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17604270 | |||||
chr4:17604270
|
C | CAAAAAAA others(4): Show |
1 | a0001c0004t0001g0188 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.1181-306_1181-296d others(13): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17604270 | |||||
chr4:17604270
|
CA | C | 25 | a0001c0001t0001g0012a0001c0001t0001g0027a0001c0001t0001g0043others(22): Show | 27 | HG00323.hp2 HG01255.hp1 HG02109.hp2 others(24): Show |
intron_variant | MODIFIER | c.1181-296delA | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17604270 | |||||
chr4:17604270
|
CAA | C | 12 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0172others(9): Show | 13 | HG00099.hp1 HG02280.hp2 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.1181-297_1181-296d others(4): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17604270 | |||||
chr4:17604292
|
A | G | 1 | a0001c0001t0001g0176 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1181-296A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17604292 | ||||||
chr4:17604327
|
GT | G | 159 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(156): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1181-259delT | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | INFO_REALIGN_3_PRIME | chr4 | 17604327 | |||||
chr4:17604336
|
T | C | 159 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(156): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1181-252T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 10/12 | chr4 | 17604336 | ||||||
chr4:17604773
|
G | A | 2 | a0001c0005t0006g0215a0001c0005t0006g0216 | 2 | HG02258.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.1260+106G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17604773 | ||||||
chr4:17604778
|
T | C | 1 | a0001c0005t0003g0214 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1260+111T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17604778 | ||||||
chr4:17604883
|
C | T | 5 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(2): Show | 5 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1260+216C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17604883 | ||||||
chr4:17605036
|
G | A | 139 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(136): Show | 149 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1260+369G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605036 | ||||||
chr4:17605118
|
C | CCA | 23 | a0001c0002t0002g0236a0001c0003t0003g0014a0001c0003t0003g0193others(20): Show | 24 | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(21): Show |
intron_variant | MODIFIER | c.1260+481_1260+482d others(4): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 17605118 | |||||
chr4:17605118
|
C | CCACA | 4 | a0001c0001t0004g0224a0001c0005t0003g0015a0001c0005t0003g0186others(1): Show | 5 | HG01109.hp1 HG01884.hp1 HG02280.hp1 others(2): Show |
intron_variant | MODIFIER | c.1260+479_1260+482d others(6): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 17605118 | |||||
chr4:17605118
|
CCA | C | 26 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0027others(23): Show | 28 | HG00099.hp1 HG01243.hp1 HG01361.hp1 others(25): Show |
intron_variant | MODIFIER | c.1260+481_1260+482d others(4): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 17605118 | |||||
chr4:17605118
|
CCACA | C | 154 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(151): Show | 165 | HG00099.hp2 HG00140.hp2 HG00280.hp1 others(162): Show |
intron_variant | MODIFIER | c.1260+479_1260+482d others(6): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 17605118 | |||||
chr4:17605148
|
A | C | 7 | a0001c0004t0001g0164a0001c0004t0001g0165a0001c0004t0001g0166others(4): Show | 7 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(4): Show |
intron_variant | MODIFIER | c.1260+481A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605148 | ||||||
chr4:17605229
|
CTG | C | 8 | a0001c0004t0001g0164a0001c0004t0001g0165a0001c0004t0001g0166others(5): Show | 8 | HG01243.hp1 HG01891.hp1 HG01891.hp2 others(5): Show |
intron_variant | MODIFIER | c.1260+565_1260+566d others(4): Show |
LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 17605229 | |||||
chr4:17605270
|
T | G | 9 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1260+603T>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605270 | ||||||
chr4:17605333
|
C | T | 4 | a0001c0001t0001g0049a0001c0001t0001g0097a0001c0001t0001g0098others(1): Show | 4 | HG00733.hp1 HG01169.hp1 HG01175.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+666C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605333 | ||||||
chr4:17605400
|
G | A | 3 | a0001c0001t0001g0102a0001c0001t0001g0103a0001c0001t0001g0110 | 3 | NA18960.hp1 NA19081.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.1260+733G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605400 | ||||||
chr4:17605444
|
G | T | 8 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(5): Show | 8 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.1260+777G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605444 | ||||||
chr4:17605524
|
T | C | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1260+857T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605524 | ||||||
chr4:17605580
|
TA | T | 159 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(156): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1260+915delA | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 17605580 | |||||
chr4:17605676
|
C | T | 1 | a0001c0002t0010g0185 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.1260+1009C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605676 | ||||||
chr4:17605681
|
A | C | 3 | a0001c0004t0001g0188a0001c0004t0007g0183a0001c0007t0001g0187 | 3 | HG02257.hp2 HG03017.hp1 NA18939.hp1 |
intron_variant | MODIFIER | c.1260+1014A>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605681 | ||||||
chr4:17605700
|
T | C | 181 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(178): Show | 194 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(191): Show |
intron_variant | MODIFIER | c.1260+1033T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605700 | ||||||
chr4:17605718
|
G | A | 3 | a0001c0001t0001g0011a0001c0003t0001g0058a0001c0003t0001g0059 | 4 | HG02451.hp1 HG03098.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.1260+1051G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605718 | ||||||
chr4:17605752
|
C | T | 1 | a0001c0002t0002g0246 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1261-1077C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605752 | ||||||
chr4:17605954
|
T | C | 13 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1261-875T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17605954 | ||||||
chr4:17606097
|
C | G | 9 | a0001c0004t0001g0156a0001c0004t0001g0157a0001c0004t0001g0158others(6): Show | 9 | HG02451.hp2 HG02630.hp1 HG02970.hp2 others(6): Show |
intron_variant | MODIFIER | c.1261-732C>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17606097 | ||||||
chr4:17606150
|
T | C | 13 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(10): Show | 13 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(10): Show |
intron_variant | MODIFIER | c.1261-679T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17606150 | ||||||
chr4:17606208
|
G | T | 1 | a0001c0001t0001g0044 | 1 | HG00733.hp2 | intron_variant | MODIFIER | c.1261-621G>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17606208 | ||||||
chr4:17606374
|
C | T | 5 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(2): Show | 5 | HG01243.hp2 HG02615.hp1 HG02922.hp2 others(2): Show |
intron_variant | MODIFIER | c.1261-455C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17606374 | ||||||
chr4:17606394
|
C | T | 10 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(7): Show | 10 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1261-435C>T | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17606394 | ||||||
chr4:17606395
|
G | A | 1 | a0001c0004t0001g0164 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1261-434G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17606395 | ||||||
chr4:17606484
|
G | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0002t0002g0246 | 3 | HG03491.hp1 HG03492.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.1261-345G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17606484 | ||||||
chr4:17606673
|
TA | T | 10 | a0001c0001t0001g0228a0001c0001t0001g0229a0001c0001t0001g0230others(7): Show | 10 | HG01243.hp1 HG01243.hp2 HG01891.hp1 others(7): Show |
intron_variant | MODIFIER | c.1261-154delA | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | INFO_REALIGN_3_PRIME | chr4 | 17606673 | |||||
chr4:17606676
|
T | C | 159 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(156): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1261-153T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17606676 | ||||||
chr4:17606700
|
A | G | 1 | a0001c0004t0007g0183 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.1261-129A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 11/12 | chr4 | 17606700 | ||||||
chr4:17606997
|
A | G | 159 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(156): Show | 172 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(169): Show |
intron_variant | MODIFIER | c.1370+59A>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 12/12 | chr4 | 17606997 | ||||||
chr4:17607018
|
T | C | 1 | a0001c0001t0001g0171 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1370+80T>C | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 12/12 | chr4 | 17607018 | ||||||
chr4:17607137
|
G | A | 3 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0062 | 3 | HG01123.hp2 HG02698.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.1370+199G>A | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 12/12 | chr4 | 17607137 | ||||||
chr4:17607261
|
C | G | 195 | a0001c0001t0001g0004a0001c0001t0001g0006a0001c0001t0001g0007others(192): Show | 214 | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(211): Show |
intron_variant | MODIFIER | c.1371-139C>G | LAP3 | ENSG00000002549.13 | transcript | ENST00000226299.9 | protein_coding | 12/12 | chr4 | 17607261 |