geneid | 122060 |
---|---|
ensemblid | ENSG00000139737.23 |
hgncid | 26387 |
symbol | SLAIN1 |
name | SLAIN motif family member 1 |
refseq_nuc | NM_001242868.2 |
refseq_prot | NP_001229797.1 |
ensembl_nuc | ENST00000418532.6 |
ensembl_prot | ENSP00000400921.2 |
mane_status | MANE Select |
chr | chr13 |
start | 77697687 |
end | 77764229 |
strand | + |
ver | v1.2 |
region | chr13:77697687-77764229 |
region5000 | chr13:77692687-77769229 |
regionname0 | SLAIN1_chr13_77697687_77764229 |
regionname5000 | SLAIN1_chr13_77692687_77769229 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 0/1 | 591 | 290 | 73 | 58 | 108 | 14 | 36 | 78 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0002 | 0/0 | 592 | 8 | 7 | 0 | 1 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0003 | 0/0 | 591 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0004 | 1/0 | 590 | 1 | 0 | 0 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1776 | 285 | 70 | 56 | 108 | 14 | 36 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
c0002 | 0/0 | 1779 | 8 | 7 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
c0003 | 0/0 | 1776 | 3 | 3 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
c0004 | 0/0 | 1776 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
c0005 | 1/0 | 1773 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
c0006 | 0/0 | 1776 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 1237 | 222 | 48 | 46 | 93 | 7 | 26 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
t0002 | 0/0 | 1237 | 63 | 20 | 9 | 17 | 7 | 10 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
t0003 | 0/0 | 1236 | 10 | 9 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
t0004 | 0/0 | 1237 | 2 | 1 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
t0005 | 0/0 | 1237 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
t0006 | 0/0 | 1237 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
t0007 | 0/0 | 1236 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0274 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1776 | 285 | 70 | 56 | 108 | 14 | 36 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0001c0003 | 0/0 | 1776 | 3 | 3 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0001c0004 | 0/0 | 1776 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0002c0002 | 0/0 | 1779 | 8 | 7 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0003c0006 | 0/0 | 1776 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0004c0005 | 1/0 | 1773 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 3012 | 208 | 39 | 44 | 91 | 7 | 26 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0001c0001t0002 | 0/0 | 3012 | 62 | 19 | 9 | 17 | 7 | 10 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0001c0001t0003 | 0/0 | 3011 | 10 | 9 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0001c0001t0004 | 0/0 | 3012 | 2 | 1 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0001c0001t0005 | 0/0 | 3012 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0001c0001t0006 | 0/0 | 3012 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0001c0001t0007 | 0/0 | 3011 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0001c0003t0001 | 0/0 | 3012 | 3 | 3 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0001c0004t0001 | 0/0 | 3012 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0002c0002t0001 | 0/0 | 3015 | 7 | 6 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0002c0002t0002 | 0/0 | 3015 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0003c0006t0001 | 0/0 | 3012 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
a0004c0005t0001 | 1/0 | 3009 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | copy fasta | chr13 | 77692687 | 77769229 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 2 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0002 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0014 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0034 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0048 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0084 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0246 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0250 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0251 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0253 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0259 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0119 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0131 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0233 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0234 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0235 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0263 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0277 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0002g0282 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0003g0010 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0003g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0003g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0003g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0003g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0003g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0003g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0004g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0005g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0006g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0001t0007g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0003t0001g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0003t0001g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0003t0001g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0001c0004t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0002c0002t0001g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0002c0002t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0002c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0002c0002t0001g0168 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0002c0002t0001g0169 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0002c0002t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0002c0002t0002g0158 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0003c0006t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
a0004c0005t0001g0274 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0230 | EUR | GBR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0240 | EUR | GBR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0236 | EUR | FIN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0119 | EUR | FIN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0273 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0053 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0035 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00544 | hp2 | a0001 | c0001 | t0002 | g0141 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0249 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0268 | EAS | CHS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0244 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0094 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00735 | hp1 | a0001 | c0001 | t0003 | g0149 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0120 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0259 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0233 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0139 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01070 | hp1 | a0001 | c0001 | t0002 | g0282 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0135 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01071 | hp1 | a0001 | c0001 | t0002 | g0133 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0015 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0130 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0129 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0095 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0262 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0063 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0060 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0283 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01109 | hp2 | a0001 | c0001 | t0004 | g0114 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0231 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01167 | hp2 | a0001 | c0001 | t0001 | g0106 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01168 | hp2 | a0001 | c0004 | t0001 | g0016 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0107 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01169 | hp2 | a0001 | c0004 | t0001 | g0016 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0189 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PUR | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0235 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0171 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0239 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0217 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0238 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0013 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0172 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0257 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | IBS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0132 | EUR | IBS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0134 | EUR | IBS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0162 | EUR | IBS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01517 | hp1 | a0001 | c0001 | t0002 | g0131 | EUR | IBS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0161 | EUR | IBS | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0193 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0223 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0224 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01934 | hp2 | a0001 | c0001 | t0006 | g0082 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0226 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0258 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0160 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02015 | hp1 | a0001 | c0001 | t0002 | g0007 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0178 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0124 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0144 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0203 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0272 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0269 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0046 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0037 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0255 | EAS | KHV | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0062 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0251 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | CDX | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0143 | EAS | CDX | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0069 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PEL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0202 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02572 | hp1 | a0001 | c0001 | t0002 | g0064 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02572 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0254 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0029 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0027 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0225 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02630 | hp1 | a0001 | c0003 | t0001 | g0068 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0081 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02647 | hp2 | a0001 | c0001 | t0003 | g0147 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0263 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0248 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0218 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0059 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02717 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0113 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0205 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0034 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0165 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0243 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0091 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0072 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02818 | hp1 | a0002 | c0002 | t0001 | g0168 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02886 | hp1 | a0001 | c0001 | t0003 | g0145 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02886 | hp2 | a0002 | c0002 | t0001 | g0167 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02896 | hp1 | a0001 | c0001 | t0002 | g0079 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02896 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0049 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02897 | hp2 | a0001 | c0001 | t0002 | g0006 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02970 | hp1 | a0001 | c0001 | t0005 | g0222 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0077 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0229 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02976 | hp2 | a0001 | c0001 | t0004 | g0112 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0271 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0146 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03041 | hp2 | a0001 | c0001 | t0002 | g0076 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0176 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03139 | hp1 | a0001 | c0001 | t0002 | g0065 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03139 | hp2 | a0001 | c0001 | t0001 | g0221 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0156 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0118 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03209 | hp1 | a0001 | c0001 | t0002 | g0067 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03209 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03225 | hp1 | a0001 | c0003 | t0001 | g0071 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0028 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0242 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03453 | hp2 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03486 | hp1 | a0001 | c0001 | t0007 | g0155 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03486 | hp2 | a0001 | c0001 | t0003 | g0187 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0036 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0164 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0009 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03516 | hp1 | a0001 | c0001 | t0002 | g0066 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03516 | hp2 | a0002 | c0002 | t0001 | g0166 | AFR | ESN | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03540 | hp1 | a0001 | c0001 | t0003 | g0151 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03540 | hp2 | a0001 | c0001 | t0003 | g0010 | AFR | GWD | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0128 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0247 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03710 | hp1 | a0001 | c0001 | t0001 | g0200 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0253 | SAS | BEB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0138 | SAS | BEB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0088 | SAS | STU | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0250 | SAS | STU | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0277 | SAS | BEB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0270 | SAS | STU | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0054 | SAS | STU | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0048 | SAS | STU | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0022 | SAS | STU | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG04228 | hp1 | a0001 | c0001 | t0002 | g0261 | SAS | STU | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0256 | SAS | STU | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18522 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | YRI | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0206 | AFR | YRI | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0127 | EAS | CHB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | CHB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0220 | EAS | CHB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0185 | EAS | CHB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18940 | hp1 | a0001 | c0001 | t0002 | g0252 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18943 | hp2 | a0001 | c0001 | t0001 | g0043 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18944 | hp1 | a0003 | c0006 | t0001 | g0052 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0033 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0056 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18947 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0050 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18953 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18956 | hp1 | a0001 | c0001 | t0002 | g0125 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0044 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0030 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0175 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0020 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18974 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0142 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18975 | hp2 | a0002 | c0002 | t0001 | g0228 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0038 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18979 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18981 | hp1 | a0001 | c0001 | t0002 | g0123 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0023 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0279 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0019 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0021 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0121 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0057 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19002 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0011 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0275 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0190 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0089 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19030 | hp1 | a0002 | c0002 | t0002 | g0158 | AFR | LWK | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | LWK | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0241 | AFR | LWK | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0245 | AFR | LWK | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19054 | hp1 | a0001 | c0001 | t0001 | g0090 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19054 | hp2 | a0001 | c0001 | t0001 | g0041 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0032 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0017 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19064 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0047 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0194 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0026 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0186 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0045 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19091 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19240 | hp1 | a0002 | c0002 | t0001 | g0169 | AFR | YRI | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0078 | AFR | YRI | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA20129 | hp1 | a0001 | c0001 | t0003 | g0148 | AFR | ASW | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | ASW | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0234 | EUR | TSI | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0136 | EUR | TSI | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0177 | EUR | TSI | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA20805 | hp2 | a0001 | c0001 | t0001 | g0276 | EUR | TSI | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0159 | SAS | GIH | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | GIH | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01123 | hp1 | a0001 | c0001 | t0001 | g0181 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0100 | AMR | CLM | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0083 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0246 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0073 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02559 | hp1 | a0001 | c0003 | t0001 | g0070 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG02559 | hp2 | a0002 | c0002 | t0001 | g0157 | AFR | ACB | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0232 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
HG03471 | hp2 | a0001 | c0001 | t0003 | g0150 | AFR | MSL | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0108 | AFR | USA | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0227 | AFR | USA | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA21309 | hp1 | a0001 | c0001 | t0002 | g0126 | AFR | LWK | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
NA21309 | hp2 | a0002 | c0002 | t0001 | g0170 | AFR | LWK | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0084 | REF | REF | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
homoSapiens_grch38 | hp1 | a0004 | c0005 | t0001 | g0274 | REF | REF | SLAIN1_chr13_77692687_77769229 | SLAIN1 | chr13 | 77692687 | 77769229 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:77698098
|
T | TGCC | 1 | a0002 | 8 | HG02559.hp2 HG02818.hp1 HG02886.hp2 others(5): Show |
disruptive_inframe_insertion | MODERATE | c.198_200dupGCC | p.Pro67dup | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/7 | 428/3009 | 201/1773 | 67/590 | INFO_REALIGN_3_PRIME | chr13 | 77698098 | |
chr13:77698132
|
T | TGG | 3 | a0001a0002a0003 | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
frameshift_variant | HIGH | c.220_221dupGG | p.Leu75fs | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/7 | 449/3009 | 222/1773 | 74/590 | INFO_REALIGN_3_PRIME | chr13 | 77698132 | |
chr13:77698141
|
G | GC | 3 | a0001a0002a0003 | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
frameshift_variant | HIGH | c.230dupC | p.Leu78fs | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/7 | 458/3009 | 231/1773 | 77/590 | INFO_REALIGN_3_PRIME | chr13 | 77698141 | |
chr13:77746676
|
G | A | 1 | a0003 | 1 | NA18944.hp1 | missense_variant | MODERATE | c.1079G>A | p.Arg360His | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/7 | 1306/3009 | 1079/1773 | 360/590 | chr13 | 77746676 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:77753279
|
G | A | 1 | a0001c0003 | 3 | HG02559.hp1 HG02630.hp1 HG03225.hp1 |
synonymous_variant | LOW | c.1335G>A | p.Pro445Pro | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/7 | 1562/3009 | 1335/1773 | 445/590 | chr13 | 77753279 | ||
chr13:77761012
|
A | G | 1 | a0001c0004 | 2 | HG01168.hp2 HG01169.hp2 |
synonymous_variant | LOW | c.1599A>G | p.Ala533Ala | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/7 | 1826/3009 | 1599/1773 | 533/590 | chr13 | 77761012 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:77697898
|
GC | G | 2 | a0001c0001t0003a0001c0001t0007 | 11 | HG00735.hp1 HG02647.hp2 HG02717.hp2 others(8): Show |
5_prime_UTR_variant | MODIFIER | c.-13delC | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/7 | 13 | INFO_REALIGN_3_PRIME | chr13 | 77697898 | ||||
chr13:77763356
|
A | G | 1 | a0001c0001t0006 | 1 | HG01934.hp2 | 3_prime_UTR_variant | MODIFIER | c.*136A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 7/7 | 136 | chr13 | 77763356 | |||||
chr13:77763784
|
C | T | 1 | a0001c0001t0005 | 1 | HG02970.hp1 | 3_prime_UTR_variant | MODIFIER | c.*564C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 7/7 | 564 | chr13 | 77763784 | |||||
chr13:77763826
|
C | G | 1 | a0001c0001t0004 | 2 | HG01109.hp2 HG02976.hp2 |
3_prime_UTR_variant | MODIFIER | c.*606C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 7/7 | 606 | chr13 | 77763826 | |||||
chr13:77763881
|
A | G | 4 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(1): Show | 66 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(63): Show |
3_prime_UTR_variant | MODIFIER | c.*661A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 7/7 | 661 | chr13 | 77763881 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:77698541
|
T | G | 1 | a0001c0001t0001g0017 | 1 | NA19064.hp1 | splice_donor_variant&intron_variant | HIGH | c.626+2T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77698541 | ||||||
chr13:77698619
|
C | G | 1 | a0001c0001t0001g0283 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.626+80C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77698619 | ||||||
chr13:77698771
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.626+232G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77698771 | ||||||
chr13:77698909
|
G | C | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021 | 3 | NA18974.hp1 NA18990.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.626+370G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77698909 | ||||||
chr13:77698910
|
A | T | 3 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021 | 3 | NA18974.hp1 NA18990.hp1 NA18990.hp2 |
intron_variant | MODIFIER | c.626+371A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77698910 | ||||||
chr13:77698918
|
C | T | 1 | a0001c0001t0002g0282 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.626+379C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77698918 | ||||||
chr13:77698921
|
G | A | 1 | a0001c0001t0001g0022 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.626+382G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77698921 | ||||||
chr13:77699039
|
G | A | 3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025 | 3 | NA18951.hp2 NA18979.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.626+500G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77699039 | ||||||
chr13:77699152
|
A | C | 1 | a0001c0001t0001g0017 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.626+613A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77699152 | ||||||
chr13:77699253
|
A | T | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.626+714A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77699253 | ||||||
chr13:77699260
|
T | C | 1 | a0001c0001t0001g0026 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.626+721T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77699260 | ||||||
chr13:77699536
|
T | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(88): Show | 96 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.626+997T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77699536 | ||||||
chr13:77699555
|
A | G | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(88): Show | 96 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.626+1016A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77699555 | ||||||
chr13:77699796
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.626+1257A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77699796 | ||||||
chr13:77699815
|
G | T | 1 | a0001c0001t0001g0279 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.626+1276G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77699815 | ||||||
chr13:77699859
|
A | AGCCCAGG others(7): Show |
145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 154 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.626+1321_626+1322i others(16): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77699859 | |||||
chr13:77700179
|
AG | A | 8 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(5): Show | 8 | HG01109.hp2 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.626+1641delG | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77700179 | ||||||
chr13:77700409
|
C | A | 1 | a0001c0001t0001g0159 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.626+1870C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77700409 | ||||||
chr13:77700591
|
G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG02615.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.626+2052G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77700591 | ||||||
chr13:77700799
|
A | G | 2 | a0002c0002t0001g0157a0002c0002t0002g0158 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.626+2260A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77700799 | ||||||
chr13:77700852
|
A | G | 1 | a0001c0001t0001g0278 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.626+2313A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77700852 | ||||||
chr13:77700897
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.626+2358C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77700897 | ||||||
chr13:77701240
|
TA | T | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 154 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.626+2706delA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77701240 | |||||
chr13:77701481
|
A | G | 2 | a0002c0002t0001g0157a0002c0002t0002g0158 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.626+2942A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77701481 | ||||||
chr13:77701589
|
A | G | 1 | a0001c0001t0002g0277 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.626+3050A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77701589 | ||||||
chr13:77701597
|
A | T | 1 | a0001c0001t0001g0279 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.626+3058A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77701597 | ||||||
chr13:77701670
|
A | G | 2 | a0002c0002t0001g0157a0002c0002t0002g0158 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.626+3131A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77701670 | ||||||
chr13:77701714
|
G | A | 2 | a0002c0002t0001g0157a0002c0002t0002g0158 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.626+3175G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77701714 | ||||||
chr13:77701731
|
ATTCT | A | 32 | a0001c0001t0001g0017a0001c0001t0001g0122a0001c0001t0001g0127others(29): Show | 35 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(32): Show |
intron_variant | MODIFIER | c.626+3215_626+3218d others(6): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77701731 | |||||
chr13:77701948
|
T | C | 2 | a0002c0002t0001g0157a0002c0002t0002g0158 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.626+3409T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77701948 | ||||||
chr13:77702161
|
C | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(85): Show | 93 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(90): Show |
intron_variant | MODIFIER | c.626+3622C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77702161 | ||||||
chr13:77702168
|
T | C | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG02615.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.626+3629T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77702168 | ||||||
chr13:77702169
|
G | A | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG02615.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.626+3630G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77702169 | ||||||
chr13:77702239
|
A | G | 2 | a0002c0002t0001g0157a0002c0002t0002g0158 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.626+3700A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77702239 | ||||||
chr13:77702550
|
A | C | 2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.626+4011A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77702550 | ||||||
chr13:77702629
|
G | A | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG01175.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.626+4090G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77702629 | ||||||
chr13:77702716
|
A | AT | 116 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(113): Show | 122 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(119): Show |
intron_variant | MODIFIER | c.626+4186dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77702716 | |||||
chr13:77703258
|
T | A | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG02735.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.626+4719T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703258 | ||||||
chr13:77703279
|
C | T | 28 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(25): Show | 28 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(25): Show |
intron_variant | MODIFIER | c.626+4740C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703279 | ||||||
chr13:77703286
|
A | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG02735.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.626+4747A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703286 | ||||||
chr13:77703333
|
T | C | 52 | a0001c0001t0001g0018a0001c0001t0001g0111a0001c0001t0001g0113others(49): Show | 56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.626+4794T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703333 | ||||||
chr13:77703400
|
T | A | 1 | a0001c0001t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.626+4861T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703400 | ||||||
chr13:77703420
|
A | G | 1 | a0002c0002t0002g0158 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.626+4881A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703420 | ||||||
chr13:77703462
|
T | C | 2 | a0002c0002t0001g0157a0002c0002t0002g0158 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.626+4923T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703462 | ||||||
chr13:77703489
|
C | T | 1 | a0001c0001t0001g0276 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.626+4950C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703489 | ||||||
chr13:77703889
|
T | TTA | 4 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163others(1): Show | 4 | HG01175.hp2 HG01516.hp2 HG01517.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+5365_626+5366d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703889 | |||||
chr13:77703904
|
TAC | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(88): Show | 96 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.626+5375_626+5376d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703904 | |||||
chr13:77703948
|
T | TAAAATAT others(528): Show |
1 | a0002c0002t0001g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(537): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(566): Show |
2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG01256.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.626+5434_626+5435i others(575): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(528): Show |
1 | a0001c0001t0001g0173 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(537): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(612): Show |
2 | a0001c0001t0001g0175a0001c0001t0001g0176 | 2 | HG03098.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.626+5434_626+5435i others(621): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(572): Show |
1 | a0001c0001t0002g0177 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(581): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(612): Show |
1 | a0001c0001t0001g0160 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(621): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(572): Show |
48 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(45): Show | 52 | HG00423.hp2 HG00735.hp2 HG00741.hp2 others(49): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(581): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(860): Show |
1 | a0001c0001t0001g0226 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(869): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(533): Show |
1 | a0001c0001t0001g0280 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(542): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(532): Show |
13 | a0001c0001t0001g0164a0001c0001t0001g0232a0001c0001t0001g0251others(10): Show | 13 | HG00741.hp1 HG01070.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(541): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(534): Show |
1 | a0001c0001t0002g0263 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(543): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(616): Show |
7 | a0001c0001t0001g0021a0001c0001t0001g0264a0001c0001t0001g0265others(4): Show | 7 | HG00558.hp2 HG02080.hp2 HG03704.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(625): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(656): Show |
1 | a0001c0001t0001g0269 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(665): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(744): Show |
1 | a0001c0001t0001g0270 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(753): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(574): Show |
3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025 | 3 | NA18951.hp2 NA18979.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.626+5434_626+5435i others(583): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(570): Show |
1 | a0001c0001t0001g0273 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(579): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(758): Show |
1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(767): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(802): Show |
1 | a0001c0001t0001g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(811): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(831): Show |
1 | a0001c0001t0003g0145 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(840): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(661): Show |
2 | a0002c0002t0001g0157a0002c0002t0002g0158 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.626+5434_626+5435i others(670): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(697): Show |
1 | a0001c0001t0001g0111 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(706): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(699): Show |
1 | a0001c0001t0001g0115 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(708): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(785): Show |
3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG02615.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.626+5434_626+5435i others(794): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(791): Show |
1 | a0001c0001t0003g0146 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(800): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(753): Show |
1 | a0001c0001t0003g0149 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(762): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(795): Show |
3 | a0001c0001t0003g0010a0001c0001t0003g0147a0001c0001t0003g0148 | 4 | HG02647.hp2 HG02717.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(804): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(791): Show |
1 | a0001c0001t0003g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(800): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(833): Show |
1 | a0001c0001t0003g0150 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(842): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(540): Show |
3 | a0001c0001t0002g0119a0001c0001t0002g0137a0001c0001t0002g0138 | 3 | HG00280.hp2 HG03831.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.626+5434_626+5435i others(549): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(582): Show |
20 | a0001c0001t0001g0122a0001c0001t0001g0127a0001c0001t0001g0130others(17): Show | 23 | HG00438.hp2 HG00738.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(591): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(797): Show |
1 | a0001c0001t0001g0152 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(806): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(584): Show |
1 | a0001c0001t0002g0140 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(593): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(628): Show |
1 | a0001c0001t0002g0141 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(637): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(879): Show |
1 | a0001c0001t0007g0155 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(888): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(797): Show |
1 | a0001c0001t0001g0156 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(806): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(494): Show |
1 | a0001c0001t0002g0143 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.626+5437_626+5438i others(503): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TAAAATAT others(616): Show |
1 | a0001c0001t0001g0275 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.626+5422_626+5423i others(625): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703948 | |||||
chr13:77703948
|
T | TTAAAATA others(583): Show |
1 | a0001c0001t0002g0142 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.626+5409_626+5410i others(592): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703948 | ||||||
chr13:77703949
|
A | AAAATATA others(530): Show |
1 | a0001c0001t0001g0178 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(539): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703949 | |||||
chr13:77703950
|
A | AAATATAT others(697): Show |
1 | a0001c0001t0004g0112 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(706): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703950 | |||||
chr13:77703950
|
A | AAATATAT others(657): Show |
1 | a0001c0001t0004g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(666): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703950 | |||||
chr13:77703950
|
A | AAATATAT others(579): Show |
1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(588): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703950 | |||||
chr13:77703950
|
A | AAATATAT others(498): Show |
1 | a0001c0001t0002g0139 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(507): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703950 | |||||
chr13:77703950
|
A | AAATATAT others(789): Show |
1 | a0001c0001t0001g0153 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(798): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703950 | |||||
chr13:77703950
|
A | AAATATAT others(709): Show |
1 | a0001c0001t0001g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(718): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703950 | |||||
chr13:77703963
|
T | TATGTTTT others(812): Show |
1 | a0002c0002t0001g0166 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(821): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | |||||
chr13:77703963
|
T | TATGTTTT others(814): Show |
3 | a0002c0002t0001g0168a0002c0002t0001g0169a0002c0002t0001g0170 | 3 | HG02818.hp1 NA19240.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.626+5434_626+5435i others(823): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | |||||
chr13:77703963
|
T | TATGTTTT others(812): Show |
1 | a0001c0001t0001g0174 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(821): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | |||||
chr13:77703963
|
T | TATGTTTT others(612): Show |
4 | a0001c0001t0001g0223a0001c0001t0001g0224a0001c0001t0001g0225others(1): Show | 4 | HG01928.hp2 HG01934.hp1 HG02622.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(621): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | |||||
chr13:77703963
|
T | TATGTTTT others(856): Show |
1 | a0001c0001t0001g0179 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(865): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | |||||
chr13:77703963
|
T | TATGTTTT others(858): Show |
4 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0184others(1): Show | 4 | HG02572.hp2 HG02717.hp1 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(867): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | |||||
chr13:77703963
|
T | TATGTTTT others(858): Show |
1 | a0002c0002t0001g0228 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(867): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | |||||
chr13:77703963
|
T | TATGTTTT others(818): Show |
1 | a0001c0001t0001g0231 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(827): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | |||||
chr13:77703963
|
T | TATGTTTT others(898): Show |
1 | a0001c0001t0001g0230 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(907): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | |||||
chr13:77703963
|
T | TATGTTTT others(818): Show |
20 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0159others(17): Show | 23 | HG00140.hp2 HG00280.hp1 HG00639.hp1 others(20): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(827): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | |||||
chr13:77703963
|
T | TATGTTTT others(858): Show |
3 | a0001c0001t0001g0253a0001c0001t0002g0249a0001c0001t0002g0277 | 3 | HG00558.hp1 HG03831.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.626+5434_626+5435i others(867): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | |||||
chr13:77703963
|
T | TATGTTTT others(898): Show |
2 | a0001c0001t0002g0254a0001c0001t0002g0255 | 2 | HG02135.hp2 HG02602.hp1 |
intron_variant | MODIFIER | c.626+5434_626+5435i others(907): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | |||||
chr13:77703963
|
T | TATGTTTT others(816): Show |
1 | a0001c0001t0001g0259 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(825): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | |||||
chr13:77703963
|
T | TATGTTTT others(818): Show |
1 | a0001c0001t0001g0165 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(827): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | |||||
chr13:77703963
|
T | TATGTTTT others(816): Show |
1 | a0001c0001t0002g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(825): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | |||||
chr13:77703963
|
T | TATGTTTT others(816): Show |
1 | a0001c0001t0001g0262 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.626+5434_626+5435i others(825): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | |||||
chr13:77703963
|
T | TATGTTTT others(948): Show |
1 | a0001c0001t0001g0271 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(957): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | |||||
chr13:77703963
|
T | TATGTTTT others(858): Show |
1 | a0001c0001t0002g0272 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.626+5434_626+5435i others(867): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703963 | |||||
chr13:77703963
|
T | TGTTTTAT others(812): Show |
1 | a0001c0004t0001g0016 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.626+5424_626+5425i others(821): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703963 | ||||||
chr13:77703973
|
A | AAG | 51 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(48): Show | 51 | HG00642.hp2 HG01081.hp1 HG01099.hp1 others(48): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703973 | ||||||
chr13:77703973
|
A | AAGTGTAT others(127): Show |
38 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(35): Show | 42 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(39): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(136): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703973 | ||||||
chr13:77703973
|
A | AAGTGTAT others(215): Show |
5 | a0001c0001t0002g0006a0001c0001t0002g0067a0001c0001t0002g0069others(2): Show | 5 | HG02257.hp1 HG02559.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.626+5434_626+5435i others(224): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703973 | ||||||
chr13:77703977
|
A | ATATATAC others(776): Show |
1 | a0001c0001t0001g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.626+5444_626+5445i others(785): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703977 | |||||
chr13:77703977
|
A | ATATATAC others(653): Show |
1 | a0001c0001t0001g0113 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.626+5444_626+5445i others(662): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77703977 | |||||
chr13:77703983
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.626+5444A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703983 | ||||||
chr13:77703984
|
T | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(88): Show | 96 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.626+5445T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703984 | ||||||
chr13:77703990
|
G | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(88): Show | 96 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(93): Show |
intron_variant | MODIFIER | c.626+5451G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77703990 | ||||||
chr13:77704003
|
C | CAT | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(127): Show | 138 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(135): Show |
intron_variant | MODIFIER | c.626+5465_626+5466d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704003 | |||||
chr13:77704003
|
C | CATATGTT others(88): Show |
2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.626+5466_626+5467i others(97): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704003 | |||||
chr13:77704003
|
C | CATATGTT others(90): Show |
1 | a0001c0001t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.626+5466_626+5467i others(99): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704003 | |||||
chr13:77704003
|
C | CATATGTT others(308): Show |
1 | a0001c0001t0002g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.626+5466_626+5467i others(317): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704003 | |||||
chr13:77704003
|
C | CATATGTT others(255): Show |
7 | a0001c0001t0002g0006a0001c0001t0002g0063a0001c0001t0002g0064others(4): Show | 7 | HG01099.hp1 HG02572.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+5466_626+5467i others(264): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704003 | |||||
chr13:77704003
|
C | CATATGTT others(310): Show |
6 | a0001c0001t0002g0074a0001c0001t0002g0075a0001c0001t0002g0076others(3): Show | 6 | HG02630.hp2 HG02896.hp1 HG02970.hp2 others(3): Show |
intron_variant | MODIFIER | c.626+5466_626+5467i others(319): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704003 | |||||
chr13:77704003
|
C | CATGTTTT others(308): Show |
1 | a0001c0001t0002g0081 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.626+5474_626+5475i others(317): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704003 | |||||
chr13:77704013
|
A | AAG | 31 | a0001c0001t0001g0058a0001c0001t0001g0083a0001c0001t0001g0084others(28): Show | 31 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(28): Show |
intron_variant | MODIFIER | c.626+5474_626+5475i others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704013 | ||||||
chr13:77704013
|
A | ATG | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG02615.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.626+5476_626+5477d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704013 | |||||
chr13:77704015
|
GTA | G | 57 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(54): Show | 62 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.626+5485_626+5486d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704015 | |||||
chr13:77704017
|
A | ATATATAC others(161): Show |
1 | a0001c0001t0001g0058 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.626+5484_626+5485i others(170): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704017 | |||||
chr13:77704024
|
T | C | 33 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(30): Show | 33 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.626+5485T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704024 | ||||||
chr13:77704030
|
G | T | 33 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(30): Show | 33 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(30): Show |
intron_variant | MODIFIER | c.626+5491G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704030 | ||||||
chr13:77704040
|
A | G | 57 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(54): Show | 62 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(59): Show |
intron_variant | MODIFIER | c.626+5501A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704040 | ||||||
chr13:77704043
|
C | CAT | 149 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 158 | HG00140.hp1 HG00280.hp2 HG00408.hp1 others(155): Show |
intron_variant | MODIFIER | c.626+5505_626+5506d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704043 | |||||
chr13:77704051
|
A | C | 46 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(43): Show | 50 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(47): Show |
intron_variant | MODIFIER | c.626+5512A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704051 | ||||||
chr13:77704053
|
A | ATG | 29 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(26): Show | 29 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.626+5516_626+5517d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704053 | |||||
chr13:77704055
|
G | GTGTATAT others(167): Show |
1 | a0001c0001t0006g0082 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.626+5517_626+5518i others(176): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704055 | |||||
chr13:77704055
|
GTA | G | 61 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(58): Show | 66 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.626+5525_626+5526d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704055 | |||||
chr13:77704057
|
A | G | 1 | a0001c0001t0006g0082 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.626+5518A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704057 | ||||||
chr13:77704064
|
T | C | 29 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(26): Show | 29 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.626+5525T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704064 | ||||||
chr13:77704070
|
G | T | 29 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(26): Show | 29 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.626+5531G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704070 | ||||||
chr13:77704080
|
A | ATACATAT others(251): Show |
23 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(20): Show | 23 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(20): Show |
intron_variant | MODIFIER | c.626+5559_626+5560i others(260): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704080 | |||||
chr13:77704080
|
A | ATACATAT others(249): Show |
2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | HG01167.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.626+5559_626+5560i others(258): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704080 | |||||
chr13:77704080
|
A | ATACATAT others(295): Show |
2 | a0001c0001t0001g0108a0001c0001t0001g0109 | 2 | NA20129.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.626+5559_626+5560i others(304): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704080 | |||||
chr13:77704080
|
A | ATACATAT others(220): Show |
1 | a0001c0001t0002g0080 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.626+5559_626+5560i others(229): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704080 | |||||
chr13:77704080
|
A | G | 24 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(21): Show | 25 | HG01099.hp1 HG01934.hp2 HG02257.hp1 others(22): Show |
intron_variant | MODIFIER | c.626+5541A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704080 | ||||||
chr13:77704084
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.626+5545A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704084 | ||||||
chr13:77704093
|
A | C | 14 | a0001c0001t0001g0005a0001c0001t0001g0059a0001c0001t0001g0060others(11): Show | 15 | HG00639.hp2 HG01099.hp2 HG01168.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5554A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704093 | ||||||
chr13:77704097
|
GTA | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(87): Show | 95 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.626+5567_626+5568d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704097 | |||||
chr13:77704099
|
A | G | 1 | a0001c0001t0002g0073 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626+5560A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704099 | ||||||
chr13:77704108
|
C | CACATATA others(52): Show |
1 | a0001c0001t0002g0073 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626+5570_626+5571i others(61): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704108 | |||||
chr13:77704112
|
G | T | 1 | a0001c0001t0002g0073 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626+5573G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704112 | ||||||
chr13:77704117
|
T | C | 1 | a0001c0001t0001g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.626+5578T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704117 | ||||||
chr13:77704122
|
A | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(74): Show | 81 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(78): Show |
intron_variant | MODIFIER | c.626+5583A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704122 | ||||||
chr13:77704125
|
CAT | C | 15 | a0001c0001t0002g0006a0001c0001t0002g0031a0001c0001t0002g0063others(12): Show | 15 | HG01099.hp1 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5589_626+5590d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704125 | |||||
chr13:77704126
|
A | G | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01981.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.626+5587A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704126 | ||||||
chr13:77704127
|
T | TACGTTTT others(193): Show |
1 | a0002c0002t0001g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.626+5589_626+5590i others(202): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704127 | |||||
chr13:77704127
|
T | TACGTTTT others(195): Show |
1 | a0001c0001t0001g0164 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.626+5589_626+5590i others(204): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704127 | |||||
chr13:77704129
|
T | C | 13 | a0001c0001t0001g0232a0001c0001t0001g0251a0001c0001t0001g0256others(10): Show | 13 | HG00741.hp1 HG01070.hp1 HG01255.hp2 others(10): Show |
intron_variant | MODIFIER | c.626+5590T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704129 | ||||||
chr13:77704135
|
A | C | 30 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(27): Show | 30 | HG00642.hp2 HG01069.hp1 HG01081.hp1 others(27): Show |
intron_variant | MODIFIER | c.626+5596A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704135 | ||||||
chr13:77704139
|
GTA | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(87): Show | 95 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.626+5609_626+5610d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704139 | |||||
chr13:77704148
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626+5609T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704148 | ||||||
chr13:77704154
|
G | T | 1 | a0001c0001t0002g0073 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626+5615G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704154 | ||||||
chr13:77704164
|
A | G | 78 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(75): Show | 82 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(79): Show |
intron_variant | MODIFIER | c.626+5625A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704164 | ||||||
chr13:77704167
|
CAT | C | 5 | a0001c0001t0002g0006a0001c0001t0002g0067a0001c0001t0002g0069others(2): Show | 5 | HG02257.hp1 HG02559.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.626+5631_626+5632d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704167 | |||||
chr13:77704168
|
A | G | 1 | a0001c0001t0001g0153 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.626+5629A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704168 | ||||||
chr13:77704171
|
T | C | 1 | a0001c0001t0001g0232 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.626+5632T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704171 | ||||||
chr13:77704177
|
A | C | 29 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(26): Show | 29 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(26): Show |
intron_variant | MODIFIER | c.626+5638A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704177 | ||||||
chr13:77704181
|
GTA | G | 76 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(73): Show | 80 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.626+5651_626+5652d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704181 | |||||
chr13:77704183
|
A | ATATATAT others(117): Show |
1 | a0001c0001t0001g0179 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.626+5666_626+5667i others(126): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704183 | |||||
chr13:77704188
|
TATAC | T | 15 | a0001c0001t0002g0006a0001c0001t0002g0031a0001c0001t0002g0063others(12): Show | 15 | HG01099.hp1 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5653_626+5656d others(6): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704188 | |||||
chr13:77704190
|
T | C | 1 | a0001c0001t0002g0073 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626+5651T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704190 | ||||||
chr13:77704196
|
G | T | 1 | a0001c0001t0002g0073 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626+5657G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704196 | ||||||
chr13:77704199
|
AAT | A | 15 | a0001c0001t0002g0006a0001c0001t0002g0031a0001c0001t0002g0063others(12): Show | 15 | HG01099.hp1 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5668_626+5669d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704199 | |||||
chr13:77704206
|
A | ATACATAT others(405): Show |
1 | a0001c0001t0001g0185 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.626+5706_626+5707i others(414): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704206 | |||||
chr13:77704206
|
A | ATACATAT others(523): Show |
1 | a0001c0001t0001g0215 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.626+5706_626+5707i others(532): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704206 | |||||
chr13:77704206
|
A | ATACATAT others(363): Show |
1 | a0001c0001t0002g0252 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.626+5706_626+5707i others(372): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704206 | |||||
chr13:77704206
|
A | G | 80 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0116others(77): Show | 88 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(85): Show |
intron_variant | MODIFIER | c.626+5667A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704206 | ||||||
chr13:77704209
|
C | CGTATGTT others(153): Show |
1 | a0001c0001t0001g0153 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.626+5670_626+5671i others(162): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704209 | ||||||
chr13:77704209
|
CAT | C | 71 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(68): Show | 75 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(72): Show |
intron_variant | MODIFIER | c.626+5673_626+5674d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704209 | |||||
chr13:77704211
|
T | C | 1 | a0001c0001t0001g0153 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.626+5672T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704211 | ||||||
chr13:77704211
|
T | TATGTTTT others(111): Show |
1 | a0001c0001t0001g0152 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.626+5706_626+5707i others(120): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(521): Show |
2 | a0001c0001t0002g0233a0001c0001t0002g0282 | 2 | HG00741.hp1 HG01070.hp1 |
intron_variant | MODIFIER | c.626+5706_626+5707i others(530): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(483): Show |
1 | a0001c0001t0002g0234 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.626+5706_626+5707i others(492): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(441): Show |
3 | a0001c0001t0002g0177a0001c0001t0002g0235a0001c0001t0002g0263 | 3 | HG01255.hp2 HG02683.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.626+5706_626+5707i others(450): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(521): Show |
2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG01256.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.626+5706_626+5707i others(530): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(481): Show |
1 | a0001c0001t0001g0175 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.626+5706_626+5707i others(490): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(523): Show |
1 | a0001c0001t0001g0186 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.626+5706_626+5707i others(532): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(477): Show |
1 | a0001c0001t0001g0011 | 2 | NA18998.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.626+5706_626+5707i others(486): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(481): Show |
28 | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(25): Show | 28 | HG00408.hp2 HG00741.hp2 HG01884.hp1 others(25): Show |
intron_variant | MODIFIER | c.626+5706_626+5707i others(490): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(519): Show |
1 | a0001c0001t0001g0189 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.626+5706_626+5707i others(528): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(557): Show |
2 | a0001c0001t0001g0188a0001c0001t0003g0187 | 2 | HG00735.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.626+5706_626+5707i others(566): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(481): Show |
10 | a0001c0001t0001g0012a0001c0001t0001g0208a0001c0001t0001g0209others(7): Show | 11 | HG00438.hp1 HG02074.hp2 HG02132.hp1 others(8): Show |
intron_variant | MODIFIER | c.626+5706_626+5707i others(490): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(519): Show |
1 | a0001c0001t0001g0206 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.626+5706_626+5707i others(528): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(481): Show |
1 | a0001c0001t0001g0269 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.626+5706_626+5707i others(490): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(481): Show |
1 | a0001c0001t0001g0216 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.626+5706_626+5707i others(490): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(355): Show |
1 | a0001c0001t0001g0178 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.626+5706_626+5707i others(364): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(481): Show |
2 | a0001c0001t0001g0013a0001c0001t0001g0217 | 3 | HG01258.hp1 HG01261.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.626+5706_626+5707i others(490): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(479): Show |
1 | a0001c0001t0001g0218 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.626+5706_626+5707i others(488): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(193): Show |
1 | a0002c0002t0001g0168 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.626+5734_626+5735i others(202): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(523): Show |
3 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258 | 3 | HG01433.hp2 HG01952.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.626+5692_626+5693i others(532): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(523): Show |
4 | a0001c0001t0001g0014a0001c0001t0001g0219a0001c0001t0001g0267others(1): Show | 5 | HG02257.hp2 HG02809.hp2 HG03704.hp1 others(2): Show |
intron_variant | MODIFIER | c.626+5692_626+5693i others(532): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(523): Show |
1 | a0001c0001t0001g0221 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.626+5692_626+5693i others(532): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(523): Show |
1 | a0001c0001t0001g0021 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.626+5692_626+5693i others(532): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(481): Show |
1 | a0001c0001t0001g0268 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.626+5692_626+5693i others(490): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(195): Show |
1 | a0001c0001t0002g0139 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.626+5692_626+5693i others(204): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(485): Show |
1 | a0001c0001t0001g0227 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.626+5692_626+5693i others(494): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(195): Show |
24 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0159others(21): Show | 28 | HG00280.hp1 HG00639.hp1 HG00642.hp1 others(25): Show |
intron_variant | MODIFIER | c.626+5692_626+5693i others(204): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(235): Show |
1 | a0001c0001t0001g0248 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.626+5692_626+5693i others(244): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(237): Show |
1 | a0002c0002t0001g0170 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.626+5692_626+5693i others(246): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(279): Show |
1 | a0001c0001t0001g0226 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.626+5692_626+5693i others(288): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(237): Show |
3 | a0001c0001t0001g0182a0001c0001t0001g0183a0001c0001t0001g0278 | 3 | HG02572.hp2 NA18946.hp2 NA19062.hp1 |
intron_variant | MODIFIER | c.626+5692_626+5693i others(246): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(239): Show |
1 | a0001c0001t0001g0184 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.626+5692_626+5693i others(248): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(195): Show |
2 | a0001c0001t0001g0250a0002c0002t0001g0228 | 2 | HG04115.hp2 NA18975.hp2 |
intron_variant | MODIFIER | c.626+5692_626+5693i others(204): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(195): Show |
1 | a0001c0001t0001g0259 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.626+5692_626+5693i others(204): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704211
|
T | TATGTTTT others(155): Show |
2 | a0001c0001t0001g0111a0001c0001t0001g0115 | 2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.626+5692_626+5693i others(164): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704211 | |||||
chr13:77704219
|
A | C | 1 | a0001c0001t0002g0073 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626+5680A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704219 | ||||||
chr13:77704223
|
G | GTA | 23 | a0001c0001t0001g0018a0001c0001t0001g0113a0001c0001t0001g0154others(20): Show | 23 | HG00140.hp2 HG00558.hp1 HG00735.hp1 others(20): Show |
intron_variant | MODIFIER | c.626+5691_626+5692d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704223 | |||||
chr13:77704223
|
G | GTATATAT others(113): Show |
3 | a0001c0001t0001g0176a0001c0001t0001g0207a0001c0001t0001g0251 | 3 | HG02148.hp2 HG03098.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.626+5706_626+5707i others(122): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704223 | |||||
chr13:77704223
|
G | GTATATAT others(155): Show |
3 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025 | 3 | NA18951.hp2 NA18979.hp2 NA18985.hp1 |
intron_variant | MODIFIER | c.626+5706_626+5707i others(164): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704223 | |||||
chr13:77704223
|
G | GTATATAT others(239): Show |
1 | a0001c0001t0001g0270 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.626+5706_626+5707i others(248): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704223 | |||||
chr13:77704223
|
G | GTATATAT others(153): Show |
1 | a0001c0001t0001g0225 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.626+5706_626+5707i others(162): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704223 | |||||
chr13:77704230
|
TAC | T | 5 | a0001c0001t0002g0006a0001c0001t0002g0067a0001c0001t0002g0069others(2): Show | 5 | HG02257.hp1 HG02559.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.626+5693_626+5694d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704230 | |||||
chr13:77704240
|
A | C | 15 | a0001c0001t0002g0006a0001c0001t0002g0031a0001c0001t0002g0063others(12): Show | 15 | HG01099.hp1 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5701A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704240 | ||||||
chr13:77704242
|
A | G | 15 | a0001c0001t0002g0006a0001c0001t0002g0031a0001c0001t0002g0063others(12): Show | 15 | HG01099.hp1 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5703A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704242 | ||||||
chr13:77704244
|
ATG | A | 5 | a0001c0001t0002g0006a0001c0001t0002g0067a0001c0001t0002g0069others(2): Show | 5 | HG02257.hp1 HG02559.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.626+5707_626+5708d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704244 | |||||
chr13:77704246
|
G | A | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(106): Show | 113 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(110): Show |
intron_variant | MODIFIER | c.626+5707G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704246 | ||||||
chr13:77704249
|
CAT | C | 3 | a0001c0001t0001g0160a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG01123.hp1 HG01255.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.626+5713_626+5714d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704249 | |||||
chr13:77704251
|
T | TGTTTTAT others(31): Show |
1 | a0001c0001t0002g0247 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+5712_626+5713i others(40): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704251 | ||||||
chr13:77704253
|
T | G | 15 | a0001c0001t0002g0006a0001c0001t0002g0031a0001c0001t0002g0063others(12): Show | 15 | HG01099.hp1 HG02572.hp1 HG02630.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5714T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704253 | ||||||
chr13:77704258
|
T | C | 3 | a0001c0001t0001g0111a0001c0001t0001g0115a0001c0001t0002g0139 | 3 | HG01069.hp1 HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.626+5719T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704258 | ||||||
chr13:77704258
|
T | TATATGTA others(111): Show |
11 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118others(8): Show | 11 | HG00738.hp1 HG01070.hp2 HG01071.hp1 others(8): Show |
intron_variant | MODIFIER | c.626+5732_626+5733i others(120): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704258 | |||||
chr13:77704258
|
T | TATATGTA others(149): Show |
1 | a0001c0001t0002g0129 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.626+5732_626+5733i others(158): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704258 | |||||
chr13:77704270
|
T | TAC | 62 | a0001c0001t0001g0018a0001c0001t0001g0113a0001c0001t0001g0122others(59): Show | 67 | HG00140.hp1 HG00280.hp2 HG00423.hp2 others(64): Show |
intron_variant | MODIFIER | c.626+5732_626+5733i others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704270 | |||||
chr13:77704270
|
T | TACATAGA others(157): Show |
2 | a0001c0001t0001g0220a0001c0001t0001g0232 | 2 | HG03471.hp1 NA18747.hp1 |
intron_variant | MODIFIER | c.626+5732_626+5733i others(166): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704270 | |||||
chr13:77704270
|
T | TATAC | 24 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(21): Show | 24 | HG00140.hp2 HG00558.hp1 HG01109.hp2 others(21): Show |
intron_variant | MODIFIER | c.626+5734_626+5735i others(6): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704270 | |||||
chr13:77704274
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.626+5735G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704274 | ||||||
chr13:77704277
|
A | AAT | 38 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(35): Show | 41 | HG00438.hp2 HG00544.hp2 HG01070.hp2 others(38): Show |
intron_variant | MODIFIER | c.626+5744_626+5745d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704277 | |||||
chr13:77704277
|
A | ACT | 20 | a0001c0001t0001g0215a0001c0001t0002g0006a0001c0001t0002g0031others(17): Show | 21 | HG00423.hp2 HG01099.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.626+5738_626+5739i others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704277 | ||||||
chr13:77704277
|
A | C | 1 | a0001c0001t0001g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.626+5738A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704277 | ||||||
chr13:77704278
|
A | ATATATAC others(33): Show |
7 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0103others(4): Show | 7 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+5749_626+5750i others(42): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704278 | |||||
chr13:77704278
|
A | ATATATAT others(189): Show |
1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.626+5745_626+5746i others(198): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704278 | |||||
chr13:77704278
|
A | ATATATAT others(149): Show |
2 | a0001c0001t0001g0144a0001c0001t0002g0009 | 3 | HG02055.hp1 HG03490.hp2 HG03492.hp2 |
intron_variant | MODIFIER | c.626+5745_626+5746i others(158): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704278 | |||||
chr13:77704278
|
A | ATATATAT others(189): Show |
1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.626+5745_626+5746i others(198): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704278 | |||||
chr13:77704278
|
A | ATATATGT others(267): Show |
1 | a0002c0002t0002g0158 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.626+5744_626+5745i others(276): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704278 | |||||
chr13:77704278
|
A | ATATATGT others(545): Show |
1 | a0002c0002t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.626+5744_626+5745i others(554): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704278 | |||||
chr13:77704278
|
A | ATATATGT others(227): Show |
1 | a0001c0001t0002g0073 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.626+5744_626+5745i others(236): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704278 | |||||
chr13:77704278
|
A | G | 20 | a0001c0001t0001g0215a0001c0001t0002g0006a0001c0001t0002g0031others(17): Show | 21 | HG00423.hp2 HG01099.hp1 HG02257.hp1 others(18): Show |
intron_variant | MODIFIER | c.626+5739A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704278 | ||||||
chr13:77704282
|
A | ATG | 24 | a0001c0001t0001g0113a0001c0001t0001g0154a0001c0001t0001g0156others(21): Show | 24 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(21): Show |
intron_variant | MODIFIER | c.626+5744_626+5745i others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704282 | |||||
chr13:77704282
|
A | G | 1 | a0001c0001t0001g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.626+5743A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704282 | ||||||
chr13:77704284
|
A | G | 1 | a0001c0001t0002g0234 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.626+5745A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704284 | ||||||
chr13:77704285
|
C | T | 6 | a0001c0001t0001g0160a0001c0001t0001g0179a0001c0001t0001g0180others(3): Show | 6 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.626+5746C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704285 | ||||||
chr13:77704287
|
T | C | 6 | a0001c0001t0001g0160a0001c0001t0001g0179a0001c0001t0001g0180others(3): Show | 6 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(3): Show |
intron_variant | MODIFIER | c.626+5748T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704287 | ||||||
chr13:77704287
|
T | G | 2 | a0002c0002t0001g0157a0002c0002t0002g0158 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.626+5748T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704287 | ||||||
chr13:77704287
|
T | TAGGTTTT others(33): Show |
64 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0013others(61): Show | 69 | HG00423.hp2 HG00438.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.626+6491_626+6530d others(42): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704287 | |||||
chr13:77704287
|
T | TAGGTTTT others(73): Show |
15 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0173others(12): Show | 16 | HG00735.hp2 HG01243.hp1 HG02015.hp2 others(13): Show |
intron_variant | MODIFIER | c.626+6451_626+6530d others(82): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704287 | |||||
chr13:77704287
|
T | TAGGTTTT others(113): Show |
4 | a0001c0001t0001g0020a0001c0001t0001g0183a0001c0001t0001g0205others(1): Show | 4 | HG00408.hp2 HG02723.hp2 NA18946.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+6411_626+6530d others(122): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704287 | |||||
chr13:77704289
|
G | T | 143 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 150 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(147): Show |
intron_variant | MODIFIER | c.626+5750G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704289 | ||||||
chr13:77704294
|
T | C | 7 | a0001c0001t0001g0130a0001c0001t0002g0131a0001c0001t0002g0132others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+5755T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704294 | ||||||
chr13:77704295
|
A | C | 1 | a0001c0001t0001g0271 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.626+5756A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704295 | ||||||
chr13:77704299
|
G | GTA | 19 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(16): Show | 19 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(16): Show |
intron_variant | MODIFIER | c.626+5767_626+5768d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704299 | |||||
chr13:77704306
|
TAC | T | 7 | a0001c0001t0001g0130a0001c0001t0002g0131a0001c0001t0002g0132others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+5769_626+5770d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704306 | |||||
chr13:77704315
|
ACT | A | 7 | a0001c0001t0001g0130a0001c0001t0002g0131a0001c0001t0002g0132others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01074.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+5777_626+5778d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704315 | ||||||
chr13:77704316
|
C | A | 62 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(59): Show | 65 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(62): Show |
intron_variant | MODIFIER | c.626+5777C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704316 | ||||||
chr13:77704317
|
T | TATATATA others(107): Show |
2 | a0001c0001t0002g0119a0001c0001t0002g0138 | 2 | HG00280.hp2 HG03831.hp2 |
intron_variant | MODIFIER | c.626+5778_626+5779i others(116): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704317 | ||||||
chr13:77704317
|
T | TATATATA others(67): Show |
15 | a0001c0001t0001g0122a0001c0001t0001g0127a0001c0001t0002g0007others(12): Show | 17 | HG00438.hp2 HG00544.hp2 HG02015.hp1 others(14): Show |
intron_variant | MODIFIER | c.626+5778_626+5779i others(76): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704317 | ||||||
chr13:77704317
|
T | TATATATA others(513): Show |
1 | a0001c0001t0005g0222 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.626+5778_626+5779i others(522): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704317 | ||||||
chr13:77704318
|
G | A | 69 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(66): Show | 72 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(69): Show |
intron_variant | MODIFIER | c.626+5779G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704318 | ||||||
chr13:77704322
|
A | G | 24 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(21): Show | 24 | HG00140.hp2 HG00558.hp1 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.626+5783A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704322 | ||||||
chr13:77704325
|
CAG | C | 11 | a0001c0001t0001g0156a0001c0001t0001g0185a0001c0001t0001g0230others(8): Show | 12 | HG00140.hp1 HG02647.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.626+5789_626+5790d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704325 | |||||
chr13:77704327
|
G | T | 161 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(158): Show | 169 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(166): Show |
intron_variant | MODIFIER | c.626+5788G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704327 | ||||||
chr13:77704329
|
G | T | 70 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(67): Show | 73 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(70): Show |
intron_variant | MODIFIER | c.626+5790G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704329 | ||||||
chr13:77704335
|
A | C | 2 | a0001c0001t0001g0270a0001c0001t0001g0271 | 2 | HG03017.hp1 HG04199.hp1 |
intron_variant | MODIFIER | c.626+5796A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704335 | ||||||
chr13:77704339
|
G | GTA | 15 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(12): Show | 15 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5807_626+5808d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704339 | |||||
chr13:77704356
|
C | A | 43 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(40): Show | 44 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.626+5817C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704356 | ||||||
chr13:77704357
|
T | TATATATA others(67): Show |
2 | a0001c0001t0001g0154a0001c0001t0003g0149 | 2 | HG00735.hp1 HG01884.hp2 |
intron_variant | MODIFIER | c.626+5818_626+5819i others(76): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704357 | ||||||
chr13:77704357
|
T | TATATGTA others(107): Show |
1 | a0001c0001t0001g0241 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.626+5818_626+5819i others(116): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704357 | ||||||
chr13:77704358
|
G | A | 44 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(41): Show | 45 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(42): Show |
intron_variant | MODIFIER | c.626+5819G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704358 | ||||||
chr13:77704358
|
G | GTATATAC others(31): Show |
1 | a0001c0001t0002g0075 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.626+5821_626+5858d others(40): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704358 | |||||
chr13:77704362
|
A | G | 24 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(21): Show | 24 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(21): Show |
intron_variant | MODIFIER | c.626+5823A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704362 | ||||||
chr13:77704367
|
G | T | 152 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(149): Show | 159 | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(156): Show |
intron_variant | MODIFIER | c.626+5828G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704367 | ||||||
chr13:77704369
|
G | T | 42 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(39): Show | 43 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(40): Show |
intron_variant | MODIFIER | c.626+5830G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704369 | ||||||
chr13:77704379
|
G | GTA | 13 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(10): Show | 13 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.626+5847_626+5848d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704379 | |||||
chr13:77704386
|
TAC | T | 11 | a0001c0001t0001g0156a0001c0001t0001g0185a0001c0001t0001g0230others(8): Show | 12 | HG00140.hp1 HG02647.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.626+5849_626+5850d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704386 | |||||
chr13:77704395
|
ACT | A | 11 | a0001c0001t0001g0156a0001c0001t0001g0185a0001c0001t0001g0230others(8): Show | 12 | HG00140.hp1 HG02647.hp2 HG02717.hp2 others(9): Show |
intron_variant | MODIFIER | c.626+5857_626+5858d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704395 | ||||||
chr13:77704396
|
C | A | 29 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(26): Show | 29 | HG00140.hp2 HG00558.hp1 HG01109.hp2 others(26): Show |
intron_variant | MODIFIER | c.626+5857C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704396 | ||||||
chr13:77704396
|
CTG | C | 15 | a0001c0001t0002g0006a0001c0001t0002g0031a0001c0001t0002g0063others(12): Show | 15 | HG01099.hp1 HG02486.hp2 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5859_626+5860d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704396 | |||||
chr13:77704397
|
T | TATATATA others(67): Show |
1 | a0001c0001t0001g0240 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.626+5858_626+5859i others(76): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704397 | ||||||
chr13:77704398
|
G | A | 40 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(37): Show | 41 | HG00140.hp1 HG00140.hp2 HG00558.hp1 others(38): Show |
intron_variant | MODIFIER | c.626+5859G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704398 | ||||||
chr13:77704398
|
G | GTATATAC others(31): Show |
2 | a0001c0001t0002g0006a0001c0001t0002g0067 | 2 | HG02897.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.626+5861_626+5898d others(40): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704398 | |||||
chr13:77704398
|
G | GTATATAC others(31): Show |
1 | a0001c0001t0002g0080 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.626+5867_626+5868i others(40): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704398 | |||||
chr13:77704402
|
A | G | 18 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(15): Show | 18 | HG00558.hp1 HG02135.hp2 HG02148.hp2 others(15): Show |
intron_variant | MODIFIER | c.626+5863A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704402 | ||||||
chr13:77704405
|
CAG | C | 5 | a0001c0001t0002g0254a0001c0001t0002g0272a0001c0001t0002g0277others(2): Show | 5 | HG01109.hp2 HG02080.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.626+5869_626+5870d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704405 | |||||
chr13:77704407
|
G | T | 124 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(121): Show | 132 | HG00140.hp2 HG00280.hp2 HG00408.hp1 others(129): Show |
intron_variant | MODIFIER | c.626+5868G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704407 | ||||||
chr13:77704409
|
G | T | 39 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(36): Show | 40 | HG00558.hp1 HG00735.hp1 HG01109.hp2 others(37): Show |
intron_variant | MODIFIER | c.626+5870G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704409 | ||||||
chr13:77704414
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.626+5875T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704414 | ||||||
chr13:77704415
|
A | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02622.hp2 HG02976.hp1 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.626+5876A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704415 | ||||||
chr13:77704419
|
G | GTA | 8 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0180others(5): Show | 8 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.626+5887_626+5888d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704419 | |||||
chr13:77704427
|
A | T | 2 | a0001c0001t0002g0249a0001c0001t0002g0255 | 2 | HG00558.hp1 HG02135.hp2 |
intron_variant | MODIFIER | c.626+5888A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704427 | ||||||
chr13:77704436
|
C | A | 26 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(23): Show | 26 | HG00558.hp1 HG01109.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.626+5897C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704436 | ||||||
chr13:77704436
|
CTG | C | 10 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0103others(7): Show | 10 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(7): Show |
intron_variant | MODIFIER | c.626+5899_626+5900d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704436 | |||||
chr13:77704438
|
G | A | 28 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(25): Show | 28 | HG00558.hp1 HG01109.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.626+5899G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704438 | ||||||
chr13:77704438
|
G | GTATATAC others(31): Show |
39 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(36): Show | 43 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(40): Show |
intron_variant | MODIFIER | c.626+5901_626+5938d others(40): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704438 | |||||
chr13:77704438
|
G | GTATATAC others(33): Show |
1 | a0001c0001t0001g0190 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.626+5938_626+5939i others(42): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704438 | |||||
chr13:77704442
|
A | G | 18 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(15): Show | 18 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(15): Show |
intron_variant | MODIFIER | c.626+5903A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704442 | ||||||
chr13:77704445
|
CAG | C | 6 | a0001c0001t0001g0229a0001c0001t0001g0270a0001c0001t0001g0271others(3): Show | 6 | HG00558.hp1 HG02135.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.626+5909_626+5910d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704445 | |||||
chr13:77704447
|
G | T | 35 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(32): Show | 36 | HG00735.hp1 HG01109.hp2 HG01123.hp1 others(33): Show |
intron_variant | MODIFIER | c.626+5908G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704447 | ||||||
chr13:77704449
|
G | T | 36 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(33): Show | 37 | HG00558.hp1 HG01109.hp2 HG01123.hp1 others(34): Show |
intron_variant | MODIFIER | c.626+5910G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704449 | ||||||
chr13:77704454
|
T | C | 2 | a0001c0001t0004g0112a0001c0001t0004g0114 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.626+5915T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704454 | ||||||
chr13:77704455
|
A | C | 3 | a0001c0001t0001g0176a0001c0001t0001g0207a0001c0001t0001g0220 | 3 | HG03098.hp1 HG03704.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.626+5916A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704455 | ||||||
chr13:77704459
|
G | GTA | 4 | a0001c0001t0001g0160a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+5927_626+5928d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704459 | |||||
chr13:77704466
|
TAC | T | 3 | a0001c0001t0002g0254a0001c0001t0002g0272a0001c0001t0002g0277 | 3 | HG02080.hp1 HG02602.hp1 HG04184.hp1 |
intron_variant | MODIFIER | c.626+5929_626+5930d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704466 | |||||
chr13:77704468
|
C | T | 2 | a0001c0001t0004g0112a0001c0001t0004g0114 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.626+5929C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704468 | ||||||
chr13:77704473
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG02615.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.626+5934A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704473 | ||||||
chr13:77704475
|
ACT | A | 5 | a0001c0001t0002g0254a0001c0001t0002g0272a0001c0001t0002g0277others(2): Show | 5 | HG01109.hp2 HG02080.hp1 HG02602.hp1 others(2): Show |
intron_variant | MODIFIER | c.626+5937_626+5938d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704475 | ||||||
chr13:77704476
|
C | A | 21 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(18): Show | 21 | HG00558.hp1 HG01123.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.626+5937C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704476 | ||||||
chr13:77704476
|
CTG | C | 25 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(22): Show | 25 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(22): Show |
intron_variant | MODIFIER | c.626+5939_626+5940d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704476 | |||||
chr13:77704477
|
T | TATATGTA others(29): Show |
1 | a0001c0001t0002g0261 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.626+5938_626+5939i others(38): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704477 | ||||||
chr13:77704478
|
G | A | 26 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(23): Show | 26 | HG00558.hp1 HG01109.hp2 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.626+5939G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704478 | ||||||
chr13:77704478
|
G | GTATATAC others(71): Show |
1 | a0001c0001t0003g0187 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.626+5941_626+6018d others(80): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704478 | |||||
chr13:77704482
|
A | G | 18 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(15): Show | 18 | HG00558.hp1 HG01123.hp1 HG01255.hp1 others(15): Show |
intron_variant | MODIFIER | c.626+5943A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704482 | ||||||
chr13:77704487
|
G | T | 35 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(32): Show | 36 | HG00558.hp1 HG00735.hp1 HG01109.hp2 others(33): Show |
intron_variant | MODIFIER | c.626+5948G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704487 | ||||||
chr13:77704489
|
G | T | 22 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(19): Show | 22 | HG00558.hp1 HG01109.hp2 HG01123.hp1 others(19): Show |
intron_variant | MODIFIER | c.626+5950G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704489 | ||||||
chr13:77704495
|
A | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0220 | 2 | HG03704.hp2 NA18747.hp1 |
intron_variant | MODIFIER | c.626+5956A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704495 | ||||||
chr13:77704499
|
G | GTA | 4 | a0001c0001t0001g0160a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+5967_626+5968d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704499 | |||||
chr13:77704506
|
TAC | T | 5 | a0001c0001t0001g0229a0001c0001t0001g0270a0001c0001t0001g0271others(2): Show | 5 | HG00558.hp1 HG02135.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.626+5969_626+5970d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704506 | |||||
chr13:77704515
|
ACT | A | 5 | a0001c0001t0001g0229a0001c0001t0001g0270a0001c0001t0001g0271others(2): Show | 5 | HG00558.hp1 HG02135.hp2 HG02976.hp1 others(2): Show |
intron_variant | MODIFIER | c.626+5977_626+5978d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704515 | ||||||
chr13:77704516
|
C | A | 15 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(12): Show | 15 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5977C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704516 | ||||||
chr13:77704518
|
G | A | 20 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(17): Show | 20 | HG00558.hp1 HG01123.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.626+5979G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704518 | ||||||
chr13:77704522
|
A | G | 10 | a0001c0001t0001g0160a0001c0001t0001g0164a0001c0001t0001g0176others(7): Show | 10 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.626+5983A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704522 | ||||||
chr13:77704525
|
CAG | C | 5 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(2): Show | 5 | HG02148.hp2 HG02622.hp2 NA18951.hp2 others(2): Show |
intron_variant | MODIFIER | c.626+5989_626+5990d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704525 | |||||
chr13:77704527
|
G | T | 27 | a0001c0001t0001g0156a0001c0001t0001g0160a0001c0001t0001g0164others(24): Show | 28 | HG00558.hp1 HG01109.hp2 HG01123.hp1 others(25): Show |
intron_variant | MODIFIER | c.626+5988G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704527 | ||||||
chr13:77704529
|
G | T | 15 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(12): Show | 15 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+5990G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704529 | ||||||
chr13:77704535
|
A | C | 3 | a0001c0001t0001g0160a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG01123.hp1 HG01255.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.626+5996A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704535 | ||||||
chr13:77704556
|
C | A | 13 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(10): Show | 13 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.626+6017C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704556 | ||||||
chr13:77704558
|
G | A | 15 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(12): Show | 15 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+6019G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704558 | ||||||
chr13:77704562
|
A | G | 8 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(5): Show | 8 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.626+6023A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704562 | ||||||
chr13:77704565
|
CAG | C | 5 | a0001c0001t0001g0176a0001c0001t0001g0207a0001c0001t0001g0220others(2): Show | 5 | HG02622.hp2 HG03098.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.626+6029_626+6030d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704565 | |||||
chr13:77704567
|
G | T | 10 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(7): Show | 10 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.626+6028G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704567 | ||||||
chr13:77704569
|
G | T | 13 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(10): Show | 13 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.626+6030G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704569 | ||||||
chr13:77704586
|
TAC | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | HG02148.hp2 NA18951.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+6049_626+6050d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704586 | |||||
chr13:77704589
|
A | T | 1 | a0001c0001t0003g0149 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.626+6050A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704589 | ||||||
chr13:77704595
|
ACT | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(1): Show | 4 | HG02148.hp2 NA18951.hp2 NA18979.hp2 others(1): Show |
intron_variant | MODIFIER | c.626+6057_626+6058d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704595 | ||||||
chr13:77704596
|
C | A | 9 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0180others(6): Show | 9 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.626+6057C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704596 | ||||||
chr13:77704598
|
G | A | 13 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(10): Show | 13 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(10): Show |
intron_variant | MODIFIER | c.626+6059G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704598 | ||||||
chr13:77704602
|
A | G | 9 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0180others(6): Show | 9 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.626+6063A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704602 | ||||||
chr13:77704607
|
G | GAGGTTTT others(33): Show |
1 | a0002c0002t0002g0158 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.626+6107_626+6108i others(42): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704607 | |||||
chr13:77704607
|
G | T | 15 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(12): Show | 15 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+6068G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704607 | ||||||
chr13:77704609
|
G | T | 9 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0180others(6): Show | 9 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.626+6070G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704609 | ||||||
chr13:77704626
|
TAC | T | 5 | a0001c0001t0001g0176a0001c0001t0001g0207a0001c0001t0001g0220others(2): Show | 5 | HG02622.hp2 HG03098.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.626+6089_626+6090d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704626 | |||||
chr13:77704629
|
A | T | 8 | a0001c0001t0003g0010a0001c0001t0003g0145a0001c0001t0003g0146others(5): Show | 9 | HG02647.hp2 HG02717.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.626+6090A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704629 | ||||||
chr13:77704635
|
ACT | A | 5 | a0001c0001t0001g0176a0001c0001t0001g0207a0001c0001t0001g0220others(2): Show | 5 | HG02622.hp2 HG03098.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.626+6097_626+6098d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704635 | ||||||
chr13:77704636
|
C | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+6097C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704636 | ||||||
chr13:77704638
|
G | A | 9 | a0001c0001t0001g0160a0001c0001t0001g0176a0001c0001t0001g0180others(6): Show | 9 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(6): Show |
intron_variant | MODIFIER | c.626+6099G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704638 | ||||||
chr13:77704642
|
A | G | 1 | a0001c0001t0002g0247 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+6103A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704642 | ||||||
chr13:77704645
|
CAG | C | 3 | a0001c0001t0001g0160a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG01123.hp1 HG01255.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.626+6109_626+6110d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704645 | |||||
chr13:77704647
|
G | T | 7 | a0001c0001t0001g0105a0001c0001t0001g0176a0001c0001t0001g0220others(4): Show | 7 | HG02622.hp2 HG02809.hp1 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.626+6108G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704647 | ||||||
chr13:77704649
|
G | T | 4 | a0001c0001t0001g0160a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+6110G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704649 | ||||||
chr13:77704676
|
C | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+6137C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704676 | ||||||
chr13:77704677
|
T | TATATGTA others(29): Show |
3 | a0001c0001t0001g0160a0001c0001t0001g0180a0001c0001t0001g0181 | 3 | HG01123.hp1 HG01255.hp1 HG01981.hp1 |
intron_variant | MODIFIER | c.626+6138_626+6139i others(38): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704677 | ||||||
chr13:77704678
|
G | A | 4 | a0001c0001t0001g0160a0001c0001t0001g0180a0001c0001t0001g0181others(1): Show | 4 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+6139G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704678 | ||||||
chr13:77704678
|
G | GTATATAC others(31): Show |
5 | a0001c0001t0001g0015a0001c0001t0001g0236a0001c0001t0001g0237others(2): Show | 6 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.626+6141_626+6178d others(40): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704678 | |||||
chr13:77704687
|
G | T | 4 | a0001c0001t0001g0029a0001c0001t0001g0160a0001c0001t0001g0180others(1): Show | 4 | HG01123.hp1 HG01255.hp1 HG01981.hp1 others(1): Show |
intron_variant | MODIFIER | c.626+6148G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704687 | ||||||
chr13:77704689
|
G | T | 1 | a0001c0001t0002g0247 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+6150G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704689 | ||||||
chr13:77704716
|
C | A | 1 | a0001c0001t0002g0247 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+6177C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704716 | ||||||
chr13:77704718
|
G | A | 1 | a0001c0001t0002g0247 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+6179G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704718 | ||||||
chr13:77704722
|
A | G | 1 | a0001c0001t0002g0247 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+6183A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704722 | ||||||
chr13:77704727
|
G | T | 1 | a0001c0001t0002g0247 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+6188G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704727 | ||||||
chr13:77704729
|
G | T | 1 | a0001c0001t0002g0247 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+6190G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704729 | ||||||
chr13:77704758
|
G | A | 1 | a0001c0001t0002g0247 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+6219G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704758 | ||||||
chr13:77704767
|
G | T | 1 | a0001c0001t0002g0247 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.626+6228G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704767 | ||||||
chr13:77704819
|
G | GTATATAT others(35): Show |
1 | a0001c0001t0001g0021 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.626+6287_626+6328d others(44): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77704819 | |||||
chr13:77704967
|
G | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(61): Show | 68 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.626+6428G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77704967 | ||||||
chr13:77705007
|
G | T | 80 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(77): Show | 84 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(81): Show |
intron_variant | MODIFIER | c.626+6468G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77705007 | ||||||
chr13:77705047
|
G | GAGGTTTT others(153): Show |
1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.626+6530_626+6531i others(162): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77705047 | |||||
chr13:77705047
|
G | GAGGTTTT others(113): Show |
11 | a0001c0001t0002g0006a0001c0001t0002g0063a0001c0001t0002g0064others(8): Show | 12 | HG01099.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.626+6530_626+6531i others(122): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77705047 | |||||
chr13:77705047
|
G | T | 118 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(115): Show | 126 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(123): Show |
intron_variant | MODIFIER | c.626+6508G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77705047 | ||||||
chr13:77705097
|
C | T | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 154 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.626+6558C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77705097 | ||||||
chr13:77705202
|
A | G | 1 | a0001c0001t0001g0057 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.626+6663A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77705202 | ||||||
chr13:77705243
|
A | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0250 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.626+6704A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77705243 | ||||||
chr13:77705393
|
A | G | 1 | a0001c0001t0001g0019 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.626+6854A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77705393 | ||||||
chr13:77705615
|
A | T | 1 | a0002c0002t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.626+7076A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77705615 | ||||||
chr13:77705644
|
A | AT | 72 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(69): Show | 76 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(73): Show |
intron_variant | MODIFIER | c.626+7120dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77705644 | |||||
chr13:77705644
|
A | ATT | 14 | a0001c0001t0001g0056a0001c0001t0002g0006a0001c0001t0002g0063others(11): Show | 15 | HG01099.hp1 HG02257.hp1 HG02559.hp1 others(12): Show |
intron_variant | MODIFIER | c.626+7119_626+7120d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77705644 | |||||
chr13:77705660
|
A | T | 1 | a0001c0001t0001g0102 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.626+7121A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77705660 | ||||||
chr13:77706124
|
T | C | 1 | a0002c0002t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.626+7585T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77706124 | ||||||
chr13:77706671
|
AT | A | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 147 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.626+8140delT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77706671 | |||||
chr13:77707490
|
T | G | 14 | a0001c0001t0001g0018a0001c0001t0001g0152a0001c0001t0001g0153others(11): Show | 15 | HG00735.hp1 HG01884.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.626+8951T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77707490 | ||||||
chr13:77707584
|
A | G | 8 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(5): Show | 8 | HG01109.hp2 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.626+9045A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77707584 | ||||||
chr13:77707753
|
A | G | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 89 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.626+9214A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77707753 | ||||||
chr13:77707794
|
G | A | 1 | a0001c0001t0001g0086 | 1 | NA18969.hp1 | intron_variant | MODIFIER | c.626+9255G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77707794 | ||||||
chr13:77707878
|
C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0250 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.626+9339C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77707878 | ||||||
chr13:77707917
|
G | T | 1 | a0001c0001t0001g0101 | 1 | NA18943.hp1 | intron_variant | MODIFIER | c.626+9378G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77707917 | ||||||
chr13:77707957
|
G | C | 3 | a0001c0001t0001g0161a0001c0001t0001g0162a0001c0001t0001g0163 | 3 | HG01175.hp2 HG01516.hp2 HG01517.hp2 |
intron_variant | MODIFIER | c.626+9418G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77707957 | ||||||
chr13:77707957
|
G | T | 1 | a0001c0001t0001g0054 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.626+9418G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77707957 | ||||||
chr13:77708020
|
T | C | 1 | a0001c0001t0001g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.626+9481T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708020 | ||||||
chr13:77708054
|
C | G | 2 | a0001c0001t0001g0241a0001c0001t0001g0242 | 2 | HG03453.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.626+9515C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708054 | ||||||
chr13:77708058
|
A | G | 52 | a0001c0001t0001g0018a0001c0001t0001g0111a0001c0001t0001g0113others(49): Show | 56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.626+9519A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708058 | ||||||
chr13:77708107
|
A | T | 1 | a0001c0001t0001g0260 | 1 | NA19077.hp1 | intron_variant | MODIFIER | c.626+9568A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708107 | ||||||
chr13:77708486
|
T | C | 2 | a0001c0001t0001g0209a0001c0001t0001g0220 | 2 | NA18747.hp1 NA18995.hp1 |
intron_variant | MODIFIER | c.626+9947T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708486 | ||||||
chr13:77708794
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.626+10255C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708794 | ||||||
chr13:77708871
|
A | G | 1 | a0001c0001t0002g0072 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.626+10332A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708871 | ||||||
chr13:77708944
|
G | A | 14 | a0001c0001t0001g0018a0001c0001t0001g0152a0001c0001t0001g0153others(11): Show | 15 | HG00735.hp1 HG01884.hp2 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.626+10405G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708944 | ||||||
chr13:77708967
|
G | A | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 89 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.626+10428G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708967 | ||||||
chr13:77708980
|
A | G | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG02615.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.626+10441A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77708980 | ||||||
chr13:77709046
|
C | T | 8 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(5): Show | 8 | HG01109.hp2 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.627-10486C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709046 | ||||||
chr13:77709048
|
A | G | 38 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(35): Show | 41 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.627-10484A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709048 | ||||||
chr13:77709061
|
A | G | 5 | a0001c0001t0001g0111a0001c0001t0001g0115a0001c0001t0001g0116others(2): Show | 5 | HG02615.hp1 HG02818.hp2 HG03130.hp2 others(2): Show |
intron_variant | MODIFIER | c.627-10471A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709061 | ||||||
chr13:77709163
|
C | A | 2 | a0001c0001t0004g0112a0001c0001t0004g0114 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.627-10369C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709163 | ||||||
chr13:77709197
|
T | C | 52 | a0001c0001t0001g0018a0001c0001t0001g0111a0001c0001t0001g0113others(49): Show | 56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-10335T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709197 | ||||||
chr13:77709367
|
C | T | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 36 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.627-10165C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709367 | ||||||
chr13:77709383
|
A | G | 11 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0003g0010others(8): Show | 12 | HG00735.hp1 HG01884.hp2 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.627-10149A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709383 | ||||||
chr13:77709833
|
C | T | 2 | a0002c0002t0001g0157a0002c0002t0002g0158 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.627-9699C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709833 | ||||||
chr13:77709856
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.627-9676C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709856 | ||||||
chr13:77709960
|
C | T | 9 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(6): Show | 9 | HG01109.hp2 HG02602.hp1 HG02615.hp1 others(6): Show |
intron_variant | MODIFIER | c.627-9572C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77709960 | ||||||
chr13:77710008
|
A | G | 3 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029 | 3 | HG02615.hp2 HG02622.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.627-9524A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710008 | ||||||
chr13:77710062
|
G | A | 1 | a0001c0001t0001g0229 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.627-9470G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710062 | ||||||
chr13:77710073
|
T | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01981.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.627-9459T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710073 | ||||||
chr13:77710102
|
C | T | 1 | a0001c0001t0004g0112 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.627-9430C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710102 | ||||||
chr13:77710116
|
G | A | 1 | a0001c0001t0002g0063 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.627-9416G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710116 | ||||||
chr13:77710410
|
A | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0256a0002c0002t0001g0157others(1): Show | 4 | HG02559.hp2 HG03831.hp1 HG04228.hp2 others(1): Show |
intron_variant | MODIFIER | c.627-9122A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710410 | ||||||
chr13:77710564
|
C | G | 28 | a0001c0001t0001g0122a0001c0001t0001g0127a0001c0001t0001g0130others(25): Show | 31 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.627-8968C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710564 | ||||||
chr13:77710723
|
G | C | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 154 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.627-8809G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710723 | ||||||
chr13:77710775
|
C | T | 1 | a0001c0001t0001g0163 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.627-8757C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710775 | ||||||
chr13:77710796
|
C | T | 6 | a0001c0001t0001g0021a0001c0001t0001g0264a0001c0001t0001g0265others(3): Show | 6 | HG00558.hp2 HG02080.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.627-8736C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710796 | ||||||
chr13:77710839
|
T | A | 1 | a0001c0001t0001g0061 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.627-8693T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77710839 | ||||||
chr13:77711447
|
C | T | 1 | a0001c0001t0002g0080 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.627-8085C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711447 | ||||||
chr13:77711461
|
AC | A | 52 | a0001c0001t0001g0018a0001c0001t0001g0111a0001c0001t0001g0113others(49): Show | 56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-8070delC | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711461 | ||||||
chr13:77711586
|
A | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 154 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.627-7946A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711586 | ||||||
chr13:77711604
|
G | C | 1 | a0001c0001t0001g0185 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.627-7928G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711604 | ||||||
chr13:77711660
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.627-7872G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711660 | ||||||
chr13:77711669
|
C | T | 1 | a0002c0002t0002g0158 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.627-7863C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711669 | ||||||
chr13:77711738
|
A | T | 2 | a0001c0001t0004g0112a0001c0001t0004g0114 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.627-7794A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711738 | ||||||
chr13:77711888
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.627-7644G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711888 | ||||||
chr13:77711945
|
T | A | 2 | a0001c0001t0001g0013a0001c0001t0001g0217 | 3 | HG01258.hp1 HG01261.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.627-7587T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711945 | ||||||
chr13:77711999
|
C | T | 5 | a0001c0001t0003g0010a0001c0001t0003g0146a0001c0001t0003g0147others(2): Show | 6 | HG00735.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.627-7533C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77711999 | ||||||
chr13:77712003
|
G | A | 11 | a0001c0001t0002g0006a0001c0001t0002g0063a0001c0001t0002g0064others(8): Show | 12 | HG01099.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.627-7529G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712003 | ||||||
chr13:77712121
|
T | C | 1 | a0001c0001t0001g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.627-7411T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712121 | ||||||
chr13:77712156
|
C | T | 1 | a0001c0001t0002g0263 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.627-7376C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712156 | ||||||
chr13:77712316
|
A | G | 1 | a0001c0001t0002g0282 | 1 | HG01070.hp1 | intron_variant | MODIFIER | c.627-7216A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712316 | ||||||
chr13:77712693
|
T | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 154 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.627-6839T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712693 | ||||||
chr13:77712730
|
A | C | 1 | a0001c0001t0001g0159 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.627-6802A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712730 | ||||||
chr13:77712980
|
A | G | 1 | a0001c0001t0001g0159 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.627-6552A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712980 | ||||||
chr13:77712988
|
G | A | 1 | a0001c0001t0001g0230 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.627-6544G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712988 | ||||||
chr13:77712989
|
G | T | 1 | a0001c0001t0001g0230 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.627-6543G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712989 | ||||||
chr13:77712990
|
G | T | 1 | a0001c0001t0001g0230 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.627-6542G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712990 | ||||||
chr13:77712991
|
A | T | 1 | a0001c0001t0001g0230 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.627-6541A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712991 | ||||||
chr13:77712993
|
A | ATAAATGG others(10): Show |
1 | a0001c0001t0001g0230 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.627-6539_627-6538i others(19): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712993 | ||||||
chr13:77712995
|
C | A | 1 | a0001c0001t0001g0230 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.627-6537C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77712995 | ||||||
chr13:77713082
|
C | T | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01981.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.627-6450C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77713082 | ||||||
chr13:77713108
|
T | A | 38 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(35): Show | 38 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.627-6424T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77713108 | ||||||
chr13:77713287
|
C | G | 145 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(142): Show | 154 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(151): Show |
intron_variant | MODIFIER | c.627-6245C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77713287 | ||||||
chr13:77713811
|
C | T | 13 | a0001c0001t0001g0011a0001c0001t0001g0021a0001c0001t0001g0179others(10): Show | 14 | HG00558.hp2 HG02080.hp2 HG02132.hp2 others(11): Show |
intron_variant | MODIFIER | c.627-5721C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77713811 | ||||||
chr13:77713835
|
T | G | 87 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(84): Show | 91 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.627-5697T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77713835 | ||||||
chr13:77713966
|
G | A | 1 | a0001c0001t0001g0251 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.627-5566G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77713966 | ||||||
chr13:77714028
|
G | T | 1 | a0001c0001t0001g0113 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.627-5504G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714028 | ||||||
chr13:77714087
|
G | T | 52 | a0001c0001t0001g0018a0001c0001t0001g0111a0001c0001t0001g0113others(49): Show | 56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-5445G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714087 | ||||||
chr13:77714174
|
TA | T | 85 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(82): Show | 89 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(86): Show |
intron_variant | MODIFIER | c.627-5351delA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77714174 | |||||
chr13:77714183
|
A | G | 8 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(5): Show | 8 | HG01109.hp2 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.627-5349A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714183 | ||||||
chr13:77714230
|
G | T | 3 | a0001c0003t0001g0068a0001c0003t0001g0070a0001c0003t0001g0071 | 3 | HG02559.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.627-5302G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714230 | ||||||
chr13:77714285
|
C | T | 7 | a0001c0001t0002g0129a0001c0001t0002g0131a0001c0001t0002g0132others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.627-5247C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714285 | ||||||
chr13:77714376
|
C | T | 1 | a0001c0001t0001g0203 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.627-5156C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714376 | ||||||
chr13:77714792
|
T | C | 2 | a0001c0001t0001g0201a0001c0001t0001g0203 | 2 | HG02074.hp1 NA18962.hp1 |
intron_variant | MODIFIER | c.627-4740T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714792 | ||||||
chr13:77714804
|
A | T | 2 | a0001c0001t0001g0238a0001c0001t0001g0239 | 2 | HG01256.hp2 HG01258.hp2 |
intron_variant | MODIFIER | c.627-4728A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714804 | ||||||
chr13:77714811
|
C | T | 8 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(5): Show | 8 | HG01109.hp2 HG02615.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.627-4721C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714811 | ||||||
chr13:77714860
|
C | A | 28 | a0001c0001t0001g0122a0001c0001t0001g0127a0001c0001t0001g0130others(25): Show | 31 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(28): Show |
intron_variant | MODIFIER | c.627-4672C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77714860 | ||||||
chr13:77715020
|
A | T | 1 | a0001c0001t0002g0263 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.627-4512A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77715020 | ||||||
chr13:77715057
|
A | G | 1 | a0001c0001t0001g0184 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.627-4475A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77715057 | ||||||
chr13:77715440
|
T | C | 52 | a0001c0001t0001g0018a0001c0001t0001g0111a0001c0001t0001g0113others(49): Show | 56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-4092T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77715440 | ||||||
chr13:77715551
|
TA | T | 52 | a0001c0001t0001g0018a0001c0001t0001g0111a0001c0001t0001g0113others(49): Show | 56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-3979delA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77715551 | |||||
chr13:77715633
|
A | G | 2 | a0002c0002t0001g0157a0002c0002t0002g0158 | 2 | HG02559.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.627-3899A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77715633 | ||||||
chr13:77715896
|
A | G | 33 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(30): Show | 36 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(33): Show |
intron_variant | MODIFIER | c.627-3636A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77715896 | ||||||
chr13:77716244
|
A | AT | 11 | a0001c0001t0002g0006a0001c0001t0002g0063a0001c0001t0002g0064others(8): Show | 12 | HG01099.hp1 HG02257.hp1 HG02559.hp1 others(9): Show |
intron_variant | MODIFIER | c.627-3281dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77716244 | |||||
chr13:77716331
|
A | AT | 259 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(256): Show | 275 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(272): Show |
intron_variant | MODIFIER | c.627-3189dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77716331 | |||||
chr13:77716331
|
A | ATT | 19 | a0001c0001t0001g0034a0001c0001t0001g0188a0001c0001t0001g0189others(16): Show | 20 | HG00735.hp2 HG01099.hp1 HG01243.hp1 others(17): Show |
intron_variant | MODIFIER | c.627-3190_627-3189d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77716331 | |||||
chr13:77716359
|
A | G | 1 | a0001c0001t0001g0113 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.627-3173A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77716359 | ||||||
chr13:77716664
|
A | G | 1 | a0002c0002t0002g0158 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.627-2868A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77716664 | ||||||
chr13:77716672
|
G | A | 2 | a0001c0001t0001g0210a0001c0001t0001g0219 | 2 | NA18952.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.627-2860G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77716672 | ||||||
chr13:77716679
|
G | A | 1 | a0001c0001t0001g0035 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.627-2853G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77716679 | ||||||
chr13:77716915
|
C | T | 4 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0245others(1): Show | 4 | HG02486.hp1 HG03453.hp1 NA19043.hp1 others(1): Show |
intron_variant | MODIFIER | c.627-2617C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77716915 | ||||||
chr13:77716916
|
G | A | 52 | a0001c0001t0001g0018a0001c0001t0001g0111a0001c0001t0001g0113others(49): Show | 56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-2616G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77716916 | ||||||
chr13:77716953
|
G | A | 6 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0036others(3): Show | 7 | HG01168.hp1 HG01243.hp2 HG01433.hp1 others(4): Show |
intron_variant | MODIFIER | c.627-2579G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77716953 | ||||||
chr13:77717134
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.627-2398T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77717134 | ||||||
chr13:77717360
|
T | C | 52 | a0001c0001t0001g0018a0001c0001t0001g0111a0001c0001t0001g0113others(49): Show | 56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-2172T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77717360 | ||||||
chr13:77717457
|
G | A | 6 | a0001c0001t0001g0021a0001c0001t0001g0264a0001c0001t0001g0265others(3): Show | 6 | HG00558.hp2 HG02080.hp2 NA18988.hp2 others(3): Show |
intron_variant | MODIFIER | c.627-2075G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77717457 | ||||||
chr13:77717519
|
T | A | 52 | a0001c0001t0001g0018a0001c0001t0001g0111a0001c0001t0001g0113others(49): Show | 56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-2013T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77717519 | ||||||
chr13:77717551
|
A | G | 1 | a0001c0001t0002g0128 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.627-1981A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77717551 | ||||||
chr13:77717752
|
C | T | 3 | a0001c0001t0001g0014a0001c0001t0001g0191a0001c0001t0001g0192 | 4 | HG00741.hp2 HG02257.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.627-1780C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77717752 | ||||||
chr13:77718098
|
GA | G | 6 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0053others(3): Show | 6 | HG00423.hp1 HG01261.hp2 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.627-1423delA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77718098 | |||||
chr13:77718107
|
A | T | 52 | a0001c0001t0001g0018a0001c0001t0001g0111a0001c0001t0001g0113others(49): Show | 56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-1425A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77718107 | ||||||
chr13:77718205
|
C | T | 139 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(136): Show | 147 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(144): Show |
intron_variant | MODIFIER | c.627-1327C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77718205 | ||||||
chr13:77718353
|
A | G | 1 | a0001c0001t0001g0199 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.627-1179A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77718353 | ||||||
chr13:77718545
|
C | T | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.627-987C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77718545 | ||||||
chr13:77718987
|
A | G | 52 | a0001c0001t0001g0018a0001c0001t0001g0111a0001c0001t0001g0113others(49): Show | 56 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(53): Show |
intron_variant | MODIFIER | c.627-545A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77718987 | ||||||
chr13:77719258
|
T | TA | 120 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(117): Show | 127 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(124): Show |
intron_variant | MODIFIER | c.627-259dupA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr13 | 77719258 | |||||
chr13:77719311
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.627-221G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 1/6 | chr13 | 77719311 | ||||||
chr13:77720032
|
A | G | 51 | a0001c0001t0001g0018a0001c0001t0001g0111a0001c0001t0001g0113others(48): Show | 55 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.766+361A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720032 | ||||||
chr13:77720316
|
G | C | 51 | a0001c0001t0001g0018a0001c0001t0001g0111a0001c0001t0001g0113others(48): Show | 55 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(52): Show |
intron_variant | MODIFIER | c.766+645G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720316 | ||||||
chr13:77720362
|
A | C | 92 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(89): Show | 97 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(94): Show |
intron_variant | MODIFIER | c.766+691A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720362 | ||||||
chr13:77720392
|
C | T | 3 | a0001c0001t0001g0164a0001c0001t0001g0165a0001c0001t0001g0265 | 3 | HG02735.hp2 HG03492.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.766+721C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720392 | ||||||
chr13:77720414
|
G | C | 146 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(143): Show | 155 | HG00280.hp2 HG00408.hp1 HG00423.hp1 others(152): Show |
intron_variant | MODIFIER | c.766+743G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720414 | ||||||
chr13:77720471
|
T | C | 50 | a0001c0001t0001g0018a0001c0001t0001g0111a0001c0001t0001g0113others(47): Show | 54 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(51): Show |
intron_variant | MODIFIER | c.766+800T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720471 | ||||||
chr13:77720517
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.766+846A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720517 | ||||||
chr13:77720565
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.766+894T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720565 | ||||||
chr13:77720667
|
C | T | 1 | a0001c0001t0001g0047 | 1 | NA19066.hp1 | intron_variant | MODIFIER | c.766+996C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720667 | ||||||
chr13:77720830
|
C | T | 37 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(34): Show | 37 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(34): Show |
intron_variant | MODIFIER | c.766+1159C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720830 | ||||||
chr13:77720831
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.766+1160G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720831 | ||||||
chr13:77720931
|
T | C | 1 | a0002c0002t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.766+1260T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720931 | ||||||
chr13:77720952
|
G | T | 1 | a0001c0001t0006g0082 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.766+1281G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720952 | ||||||
chr13:77720957
|
A | G | 7 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0197others(4): Show | 7 | HG01928.hp2 HG01934.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.766+1286A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77720957 | ||||||
chr13:77721132
|
G | A | 1 | a0001c0001t0002g0139 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.766+1461G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721132 | ||||||
chr13:77721154
|
C | T | 1 | a0001c0001t0001g0226 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.766+1483C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721154 | ||||||
chr13:77721203
|
T | C | 56 | a0001c0001t0001g0028a0001c0001t0001g0039a0001c0001t0001g0086others(53): Show | 60 | HG00280.hp2 HG00408.hp1 HG00438.hp2 others(57): Show |
intron_variant | MODIFIER | c.766+1532T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721203 | ||||||
chr13:77721240
|
TGCCACCA others(6): Show |
T | 1 | a0001c0001t0001g0087 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.766+1571_766+1583d others(15): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77721240 | |||||
chr13:77721369
|
C | G | 1 | a0001c0001t0001g0057 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.766+1698C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721369 | ||||||
chr13:77721388
|
A | G | 1 | a0001c0001t0001g0216 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.766+1717A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721388 | ||||||
chr13:77721515
|
A | C | 2 | a0001c0001t0001g0144a0001c0001t0001g0281 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.766+1844A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721515 | ||||||
chr13:77721779
|
G | A | 35 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(32): Show | 37 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(34): Show |
intron_variant | MODIFIER | c.766+2108G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721779 | ||||||
chr13:77721812
|
TA | T | 34 | a0001c0001t0001g0130a0001c0001t0002g0006a0001c0001t0002g0007others(31): Show | 38 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.766+2148delA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77721812 | |||||
chr13:77721817
|
A | C | 36 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(33): Show | 38 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(35): Show |
intron_variant | MODIFIER | c.766+2146A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721817 | ||||||
chr13:77721907
|
G | A | 17 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0036others(14): Show | 18 | HG01109.hp2 HG01168.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.766+2236G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721907 | ||||||
chr13:77721916
|
T | C | 38 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(35): Show | 38 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.766+2245T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721916 | ||||||
chr13:77721955
|
T | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(35): Show | 40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+2284T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77721955 | ||||||
chr13:77721996
|
G | GT | 38 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(35): Show | 40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+2334dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77721996 | |||||
chr13:77721996
|
GTTTTT | G | 27 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(24): Show | 27 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.766+2330_766+2334d others(7): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77721996 | |||||
chr13:77722049
|
T | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.766+2378T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77722049 | ||||||
chr13:77722071
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.766+2400C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77722071 | ||||||
chr13:77722106
|
A | T | 1 | a0001c0001t0005g0222 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.766+2435A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77722106 | ||||||
chr13:77722147
|
T | C | 2 | a0001c0001t0001g0207a0001c0001t0001g0250 | 2 | HG03704.hp2 HG04115.hp2 |
intron_variant | MODIFIER | c.766+2476T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77722147 | ||||||
chr13:77722420
|
C | T | 1 | a0001c0001t0002g0272 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.766+2749C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77722420 | ||||||
chr13:77722420
|
CA | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(35): Show | 40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+2752delA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77722420 | |||||
chr13:77722502
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(35): Show | 40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+2831A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77722502 | ||||||
chr13:77723645
|
A | G | 1 | a0001c0001t0001g0028 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.766+3974A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77723645 | ||||||
chr13:77723652
|
T | C | 15 | a0001c0001t0001g0229a0001c0001t0002g0177a0001c0001t0002g0233others(12): Show | 15 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.766+3981T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77723652 | ||||||
chr13:77723851
|
A | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(35): Show | 40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+4180A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77723851 | ||||||
chr13:77723932
|
TA | T | 159 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 170 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(167): Show |
intron_variant | MODIFIER | c.766+4276delA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77723932 | |||||
chr13:77723932
|
TAA | T | 40 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0027others(37): Show | 42 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.766+4275_766+4276d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77723932 | |||||
chr13:77723977
|
T | G | 38 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(35): Show | 40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+4306T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77723977 | ||||||
chr13:77724040
|
G | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(35): Show | 40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+4369G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77724040 | ||||||
chr13:77724171
|
T | C | 1 | a0001c0001t0002g0272 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.766+4500T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77724171 | ||||||
chr13:77724320
|
G | A | 38 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(35): Show | 40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+4649G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77724320 | ||||||
chr13:77724327
|
C | T | 1 | a0001c0001t0002g0277 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.766+4656C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77724327 | ||||||
chr13:77724445
|
G | A | 1 | a0001c0001t0003g0187 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.766+4774G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77724445 | ||||||
chr13:77724744
|
CT | C | 38 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(35): Show | 40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+5081delT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77724744 | |||||
chr13:77724855
|
A | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(35): Show | 40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+5184A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77724855 | ||||||
chr13:77725263
|
C | G | 90 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(87): Show | 92 | HG00558.hp1 HG00642.hp2 HG00735.hp1 others(89): Show |
intron_variant | MODIFIER | c.766+5592C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77725263 | ||||||
chr13:77725311
|
C | T | 2 | a0001c0001t0001g0017a0001c0001t0001g0185 | 2 | NA18747.hp2 NA19064.hp1 |
intron_variant | MODIFIER | c.766+5640C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77725311 | ||||||
chr13:77725576
|
C | T | 1 | a0001c0001t0001g0275 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.766+5905C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77725576 | ||||||
chr13:77725602
|
G | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(35): Show | 40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+5931G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77725602 | ||||||
chr13:77725962
|
G | T | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | HG02486.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.766+6291G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77725962 | ||||||
chr13:77725963
|
C | T | 3 | a0001c0001t0001g0241a0001c0001t0001g0245a0001c0001t0001g0246 | 3 | HG02486.hp1 NA19043.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.766+6292C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77725963 | ||||||
chr13:77725991
|
A | G | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.766+6320A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77725991 | ||||||
chr13:77726232
|
C | T | 38 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(35): Show | 40 | HG00735.hp1 HG01109.hp2 HG01168.hp1 others(37): Show |
intron_variant | MODIFIER | c.766+6561C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77726232 | ||||||
chr13:77726344
|
G | C | 1 | a0001c0001t0001g0221 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.766+6673G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77726344 | ||||||
chr13:77726374
|
A | G | 36 | a0001c0001t0001g0130a0001c0001t0002g0006a0001c0001t0002g0007others(33): Show | 40 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(37): Show |
intron_variant | MODIFIER | c.766+6703A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77726374 | ||||||
chr13:77726378
|
G | C | 3 | a0001c0003t0001g0068a0001c0003t0001g0070a0001c0003t0001g0071 | 3 | HG02559.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.766+6707G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77726378 | ||||||
chr13:77726488
|
G | A | 27 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(24): Show | 27 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(24): Show |
intron_variant | MODIFIER | c.766+6817G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77726488 | ||||||
chr13:77726625
|
G | T | 1 | a0001c0001t0002g0277 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.766+6954G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77726625 | ||||||
chr13:77727157
|
T | G | 1 | a0001c0001t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.766+7486T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727157 | ||||||
chr13:77727168
|
C | G | 3 | a0001c0001t0001g0015a0001c0001t0001g0236a0001c0001t0001g0237 | 4 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(1): Show |
intron_variant | MODIFIER | c.766+7497C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727168 | ||||||
chr13:77727431
|
G | A | 4 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0106others(1): Show | 4 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(1): Show |
intron_variant | MODIFIER | c.766+7760G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727431 | ||||||
chr13:77727437
|
C | CA | 38 | a0001c0001t0001g0002a0001c0001t0001g0014a0001c0001t0001g0018others(35): Show | 41 | HG00735.hp1 HG00741.hp2 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.766+7777dupA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77727437 | |||||
chr13:77727448
|
AC | A | 33 | a0001c0001t0001g0084a0001c0001t0001g0085a0001c0001t0001g0086others(30): Show | 33 | HG00642.hp2 HG01081.hp1 HG01167.hp2 others(30): Show |
intron_variant | MODIFIER | c.766+7778delC | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727448 | ||||||
chr13:77727449
|
C | A | 5 | a0001c0001t0001g0083a0001c0001t0001g0091a0001c0001t0001g0092others(2): Show | 5 | HG01123.hp2 HG02109.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.766+7778C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727449 | ||||||
chr13:77727504
|
C | CAA | 38 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(35): Show | 38 | HG00642.hp2 HG01081.hp1 HG01123.hp2 others(35): Show |
intron_variant | MODIFIER | c.766+7844_766+7845d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77727504 | |||||
chr13:77727522
|
A | G | 1 | a0001c0001t0001g0194 | 1 | NA19066.hp2 | intron_variant | MODIFIER | c.766+7851A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727522 | ||||||
chr13:77727728
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.766+8057G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727728 | ||||||
chr13:77727812
|
T | C | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG01256.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.766+8141T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727812 | ||||||
chr13:77727824
|
T | C | 3 | a0001c0001t0001g0040a0001c0001t0002g0121a0001c0001t0002g0125 | 3 | NA18956.hp1 NA18998.hp1 NA19088.hp2 |
intron_variant | MODIFIER | c.766+8153T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727824 | ||||||
chr13:77727923
|
A | T | 25 | a0001c0001t0001g0040a0001c0001t0002g0007a0001c0001t0002g0008others(22): Show | 28 | HG00280.hp2 HG00438.hp2 HG00738.hp1 others(25): Show |
intron_variant | MODIFIER | c.766+8252A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77727923 | ||||||
chr13:77728011
|
C | T | 1 | a0001c0001t0003g0148 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.766+8340C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77728011 | ||||||
chr13:77728052
|
T | A | 1 | a0001c0001t0001g0035 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.766+8381T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77728052 | ||||||
chr13:77728055
|
A | G | 1 | a0001c0001t0001g0176 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.766+8384A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77728055 | ||||||
chr13:77728130
|
G | A | 282 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(279): Show | 299 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.766+8459G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77728130 | ||||||
chr13:77728166
|
C | G | 1 | a0002c0002t0001g0167 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.766+8495C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77728166 | ||||||
chr13:77728712
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.766+9041G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77728712 | ||||||
chr13:77729001
|
A | G | 8 | a0001c0001t0001g0027a0001c0001t0002g0073a0001c0001t0002g0074others(5): Show | 8 | HG02486.hp2 HG02622.hp1 HG02630.hp2 others(5): Show |
intron_variant | MODIFIER | c.766+9330A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77729001 | ||||||
chr13:77729054
|
A | C | 1 | a0001c0001t0001g0198 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.766+9383A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77729054 | ||||||
chr13:77729135
|
G | GT | 14 | a0001c0001t0002g0177a0001c0001t0002g0233a0001c0001t0002g0234others(11): Show | 14 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.766+9465dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77729135 | |||||
chr13:77729468
|
C | T | 1 | a0001c0001t0001g0098 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.766+9797C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77729468 | ||||||
chr13:77729503
|
CT | C | 47 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(44): Show | 51 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.766+9845delT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77729503 | |||||
chr13:77729505
|
T | A | 1 | a0001c0001t0001g0091 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.766+9834T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77729505 | ||||||
chr13:77729901
|
C | CTG | 40 | a0001c0001t0001g0099a0001c0001t0001g0250a0001c0001t0001g0280others(37): Show | 44 | HG00280.hp2 HG00438.hp1 HG00438.hp2 others(41): Show |
intron_variant | MODIFIER | c.766+10248_766+1024 others(6): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77729901 | |||||
chr13:77730093
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.766+10422T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77730093 | ||||||
chr13:77730295
|
A | G | 3 | a0001c0001t0001g0103a0001c0001t0001g0104a0001c0001t0001g0105 | 3 | NA18962.hp2 NA18966.hp2 NA18985.hp2 |
intron_variant | MODIFIER | c.766+10624A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77730295 | ||||||
chr13:77730300
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.766+10629C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77730300 | ||||||
chr13:77730516
|
C | T | 1 | a0001c0003t0001g0071 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.766+10845C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77730516 | ||||||
chr13:77730671
|
A | G | 1 | a0001c0001t0002g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.766+11000A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77730671 | ||||||
chr13:77730821
|
C | T | 84 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(81): Show | 88 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(85): Show |
intron_variant | MODIFIER | c.766+11150C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77730821 | ||||||
chr13:77731162
|
A | G | 1 | a0001c0001t0001g0062 | 1 | HG02148.hp1 | intron_variant | MODIFIER | c.766+11491A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77731162 | ||||||
chr13:77731510
|
T | C | 1 | a0001c0001t0002g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.766+11839T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77731510 | ||||||
chr13:77731667
|
G | A | 25 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(22): Show | 28 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.766+11996G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77731667 | ||||||
chr13:77731746
|
A | T | 17 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0036others(14): Show | 18 | HG01109.hp2 HG01168.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.766+12075A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77731746 | ||||||
chr13:77731934
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.766+12263G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77731934 | ||||||
chr13:77732205
|
C | T | 2 | a0001c0001t0002g0077a0001c0001t0002g0078 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.767-12078C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77732205 | ||||||
chr13:77732499
|
G | GT | 34 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(31): Show | 38 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.767-11781dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77732499 | |||||
chr13:77732763
|
A | G | 1 | a0001c0001t0001g0156 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.767-11520A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77732763 | ||||||
chr13:77732801
|
T | C | 3 | a0001c0001t0001g0116a0001c0001t0001g0117a0001c0001t0001g0118 | 3 | HG02615.hp1 HG03130.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.767-11482T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77732801 | ||||||
chr13:77732918
|
G | A | 2 | a0001c0001t0004g0112a0001c0001t0004g0114 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.767-11365G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77732918 | ||||||
chr13:77733390
|
T | C | 1 | a0001c0001t0001g0269 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.767-10893T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733390 | ||||||
chr13:77733395
|
T | A | 1 | a0001c0001t0001g0180 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.767-10888T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733395 | ||||||
chr13:77733396
|
T | G | 3 | a0001c0003t0001g0068a0001c0003t0001g0070a0001c0003t0001g0071 | 3 | HG02559.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.767-10887T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733396 | ||||||
chr13:77733408
|
T | C | 1 | a0001c0001t0001g0019 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.767-10875T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733408 | ||||||
chr13:77733428
|
A | G | 1 | a0001c0001t0001g0085 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.767-10855A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733428 | ||||||
chr13:77733584
|
A | G | 1 | a0001c0001t0001g0109 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.767-10699A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733584 | ||||||
chr13:77733595
|
T | C | 4 | a0001c0001t0001g0026a0001c0001t0001g0175a0001c0001t0001g0201others(1): Show | 4 | HG02074.hp1 NA18961.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.767-10688T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733595 | ||||||
chr13:77733768
|
A | G | 1 | a0001c0001t0001g0011 | 2 | NA18998.hp2 NA19007.hp1 |
intron_variant | MODIFIER | c.767-10515A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733768 | ||||||
chr13:77733808
|
G | A | 3 | a0001c0001t0003g0010a0001c0001t0003g0148a0001c0001t0003g0149 | 4 | HG00735.hp1 HG02717.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.767-10475G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733808 | ||||||
chr13:77733850
|
A | G | 1 | a0001c0001t0002g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.767-10433A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77733850 | ||||||
chr13:77734105
|
G | T | 1 | a0001c0001t0002g0137 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.767-10178G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77734105 | ||||||
chr13:77734156
|
G | A | 1 | a0001c0001t0001g0163 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.767-10127G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77734156 | ||||||
chr13:77734612
|
G | A | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.767-9671G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77734612 | ||||||
chr13:77734659
|
A | G | 27 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0030others(24): Show | 29 | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.767-9624A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77734659 | ||||||
chr13:77734682
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.767-9601A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77734682 | ||||||
chr13:77735001
|
C | T | 1 | a0001c0001t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.767-9282C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735001 | ||||||
chr13:77735078
|
A | G | 2 | a0001c0001t0004g0112a0001c0001t0004g0114 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.767-9205A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735078 | ||||||
chr13:77735185
|
A | G | 1 | a0001c0001t0001g0246 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.767-9098A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735185 | ||||||
chr13:77735366
|
G | A | 1 | a0001c0001t0001g0201 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.767-8917G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735366 | ||||||
chr13:77735471
|
C | T | 34 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(31): Show | 38 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.767-8812C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735471 | ||||||
chr13:77735472
|
G | A | 2 | a0001c0001t0001g0111a0001c0001t0001g0115 | 2 | HG02818.hp2 HG03453.hp2 |
intron_variant | MODIFIER | c.767-8811G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735472 | ||||||
chr13:77735647
|
C | T | 1 | a0002c0002t0001g0168 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.767-8636C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735647 | ||||||
chr13:77735739
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0100 | 2 | HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.767-8544T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735739 | ||||||
chr13:77735815
|
G | A | 14 | a0001c0001t0002g0177a0001c0001t0002g0233a0001c0001t0002g0234others(11): Show | 14 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.767-8468G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735815 | ||||||
chr13:77735991
|
C | T | 2 | a0001c0001t0002g0077a0001c0001t0002g0078 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.767-8292C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77735991 | ||||||
chr13:77736025
|
A | G | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.767-8258A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736025 | ||||||
chr13:77736090
|
G | C | 34 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(31): Show | 38 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.767-8193G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736090 | ||||||
chr13:77736134
|
A | G | 1 | a0001c0001t0001g0179 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.767-8149A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736134 | ||||||
chr13:77736216
|
C | T | 1 | a0001c0001t0002g0140 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.767-8067C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736216 | ||||||
chr13:77736414
|
C | G | 62 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(59): Show | 65 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(62): Show |
intron_variant | MODIFIER | c.767-7869C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736414 | ||||||
chr13:77736758
|
A | G | 14 | a0001c0001t0002g0177a0001c0001t0002g0233a0001c0001t0002g0234others(11): Show | 14 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.767-7525A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736758 | ||||||
chr13:77736792
|
C | CT | 37 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(34): Show | 37 | HG00642.hp2 HG01167.hp2 HG01169.hp1 others(34): Show |
intron_variant | MODIFIER | c.767-7478dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77736792 | |||||
chr13:77736806
|
G | T | 1 | a0001c0001t0001g0193 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.767-7477G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736806 | ||||||
chr13:77736819
|
T | C | 122 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(119): Show | 128 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(125): Show |
intron_variant | MODIFIER | c.767-7464T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736819 | ||||||
chr13:77736949
|
G | A | 68 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(65): Show | 72 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(69): Show |
intron_variant | MODIFIER | c.767-7334G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736949 | ||||||
chr13:77736981
|
T | A | 16 | a0001c0001t0002g0177a0001c0001t0002g0233a0001c0001t0002g0234others(13): Show | 16 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(13): Show |
intron_variant | MODIFIER | c.767-7302T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77736981 | ||||||
chr13:77737092
|
A | AT | 62 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(59): Show | 69 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(66): Show |
intron_variant | MODIFIER | c.767-7181dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77737092 | |||||
chr13:77737099
|
T | G | 5 | a0001c0001t0001g0207a0001c0001t0001g0250a0001c0001t0001g0253others(2): Show | 5 | HG01433.hp2 HG03704.hp2 HG03831.hp1 others(2): Show |
intron_variant | MODIFIER | c.767-7184T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77737099 | ||||||
chr13:77737485
|
G | A | 1 | a0001c0001t0001g0040 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.767-6798G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77737485 | ||||||
chr13:77737671
|
C | T | 1 | a0001c0001t0002g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.767-6612C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77737671 | ||||||
chr13:77737681
|
C | G | 1 | a0001c0001t0002g0128 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.767-6602C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77737681 | ||||||
chr13:77737800
|
G | T | 6 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(3): Show | 6 | HG02615.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.767-6483G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77737800 | ||||||
chr13:77737813
|
AC | A | 36 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(33): Show | 36 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.767-6468delC | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77737813 | |||||
chr13:77738057
|
G | C | 14 | a0001c0001t0002g0177a0001c0001t0002g0233a0001c0001t0002g0234others(11): Show | 14 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.767-6226G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738057 | ||||||
chr13:77738157
|
G | A | 2 | a0001c0001t0001g0152a0001c0001t0001g0153 | 2 | HG01981.hp2 HG02451.hp2 |
intron_variant | MODIFIER | c.767-6126G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738157 | ||||||
chr13:77738200
|
A | C | 1 | a0001c0001t0001g0056 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.767-6083A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738200 | ||||||
chr13:77738202
|
A | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.767-6081A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738202 | ||||||
chr13:77738221
|
T | TACATATA others(3): Show |
189 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(186): Show | 202 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(199): Show |
intron_variant | MODIFIER | c.767-6060_767-6051d others(12): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77738221 | |||||
chr13:77738221
|
T | TACATATA others(3): Show |
2 | a0001c0001t0004g0112a0001c0001t0004g0114 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.767-6054_767-6053i others(12): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77738221 | |||||
chr13:77738274
|
A | T | 4 | a0001c0001t0001g0014a0001c0001t0001g0191a0001c0001t0001g0192others(1): Show | 5 | HG00741.hp2 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.767-6009A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738274 | ||||||
chr13:77738943
|
A | G | 2 | a0001c0001t0001g0171a0001c0001t0001g0172 | 2 | HG01256.hp1 HG01261.hp2 |
intron_variant | MODIFIER | c.767-5340A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738943 | ||||||
chr13:77738955
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.767-5328C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738955 | ||||||
chr13:77738956
|
G | A | 14 | a0001c0001t0002g0177a0001c0001t0002g0233a0001c0001t0002g0234others(11): Show | 14 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.767-5327G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738956 | ||||||
chr13:77738962
|
T | C | 49 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(46): Show | 53 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(50): Show |
intron_variant | MODIFIER | c.767-5321T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738962 | ||||||
chr13:77738994
|
C | T | 1 | a0001c0001t0001g0017 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.767-5289C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77738994 | ||||||
chr13:77739284
|
A | G | 1 | a0001c0001t0001g0004 | 2 | NA18953.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.767-4999A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77739284 | ||||||
chr13:77739415
|
C | T | 58 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(55): Show | 62 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.767-4868C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77739415 | ||||||
chr13:77739765
|
G | A | 2 | a0001c0001t0002g0077a0001c0001t0002g0078 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.767-4518G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77739765 | ||||||
chr13:77739928
|
C | T | 1 | a0001c0001t0002g0272 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.767-4355C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77739928 | ||||||
chr13:77739936
|
A | T | 1 | a0001c0001t0001g0037 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.767-4347A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77739936 | ||||||
chr13:77739973
|
A | G | 26 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(23): Show | 26 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.767-4310A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77739973 | ||||||
chr13:77740054
|
A | C | 1 | a0001c0001t0001g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.767-4229A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77740054 | ||||||
chr13:77740250
|
G | A | 1 | a0001c0001t0001g0053 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.767-4033G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77740250 | ||||||
chr13:77740284
|
A | G | 106 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0028others(103): Show | 111 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(108): Show |
intron_variant | MODIFIER | c.767-3999A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77740284 | ||||||
chr13:77740418
|
C | T | 26 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(23): Show | 26 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.767-3865C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77740418 | ||||||
chr13:77740515
|
A | G | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.767-3768A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77740515 | ||||||
chr13:77740528
|
G | GC | 32 | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0026others(29): Show | 33 | HG00438.hp1 HG00558.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.767-3744dupC | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77740528 | |||||
chr13:77740528
|
GC | G | 84 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(81): Show | 90 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.767-3744delC | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77740528 | |||||
chr13:77740528
|
GCC | G | 76 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0083others(73): Show | 80 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.767-3745_767-3744d others(4): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77740528 | |||||
chr13:77740538
|
C | A | 1 | a0001c0001t0001g0240 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.767-3745C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77740538 | ||||||
chr13:77740861
|
C | G | 57 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(54): Show | 61 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(58): Show |
intron_variant | MODIFIER | c.767-3422C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77740861 | ||||||
chr13:77740928
|
A | G | 5 | a0001c0001t0002g0006a0001c0001t0002g0063a0001c0001t0002g0064others(2): Show | 6 | HG01099.hp1 HG02572.hp1 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.767-3355A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77740928 | ||||||
chr13:77741000
|
G | A | 7 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0036others(4): Show | 8 | HG01168.hp1 HG01243.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.767-3283G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77741000 | ||||||
chr13:77741119
|
G | A | 1 | a0001c0001t0002g0142 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.767-3164G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77741119 | ||||||
chr13:77741151
|
G | A | 1 | a0001c0001t0002g0123 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.767-3132G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77741151 | ||||||
chr13:77741252
|
A | G | 1 | a0001c0001t0001g0237 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.767-3031A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77741252 | ||||||
chr13:77741372
|
A | G | 1 | a0001c0001t0001g0033 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.767-2911A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77741372 | ||||||
chr13:77741450
|
G | A | 1 | a0001c0001t0001g0185 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.767-2833G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77741450 | ||||||
chr13:77741532
|
G | A | 3 | a0001c0001t0001g0253a0001c0001t0001g0256a0001c0001t0001g0257 | 3 | HG01433.hp2 HG03831.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.767-2751G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77741532 | ||||||
chr13:77741570
|
C | A | 1 | a0001c0001t0001g0154 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.767-2713C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77741570 | ||||||
chr13:77741572
|
C | T | 2 | a0001c0001t0001g0231a0001c0001t0001g0276 | 2 | HG01167.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.767-2711C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77741572 | ||||||
chr13:77741646
|
AT | A | 110 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0022others(107): Show | 116 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.767-2618delT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77741646 | |||||
chr13:77741745
|
G | GT | 279 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(276): Show | 296 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(293): Show |
intron_variant | MODIFIER | c.767-2526dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77741745 | |||||
chr13:77742028
|
A | G | 1 | a0001c0001t0002g0075 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.767-2255A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742028 | ||||||
chr13:77742060
|
G | A | 1 | a0001c0001t0003g0151 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.767-2223G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742060 | ||||||
chr13:77742187
|
G | A | 5 | a0001c0001t0002g0007a0001c0001t0002g0121a0001c0001t0002g0124others(2): Show | 6 | HG00438.hp2 HG02015.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.767-2096G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742187 | ||||||
chr13:77742314
|
G | A | 1 | a0001c0001t0001g0270 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.767-1969G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742314 | ||||||
chr13:77742357
|
C | T | 1 | a0001c0001t0002g0124 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.767-1926C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742357 | ||||||
chr13:77742418
|
C | G | 2 | a0001c0001t0001g0164a0001c0001t0001g0165 | 2 | HG02735.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.767-1865C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742418 | ||||||
chr13:77742543
|
C | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | NA18974.hp1 NA18990.hp1 |
intron_variant | MODIFIER | c.767-1740C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742543 | ||||||
chr13:77742806
|
T | TTCAAAAT others(5): Show |
2 | a0001c0001t0004g0112a0001c0001t0004g0114 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.767-1476_767-1475i others(14): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77742806 | |||||
chr13:77742808
|
A | C | 14 | a0001c0001t0002g0177a0001c0001t0002g0233a0001c0001t0002g0234others(11): Show | 14 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.767-1475A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742808 | ||||||
chr13:77742809
|
A | T | 2 | a0001c0001t0004g0112a0001c0001t0004g0114 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.767-1474A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742809 | ||||||
chr13:77742814
|
G | A | 3 | a0001c0003t0001g0068a0001c0003t0001g0070a0001c0003t0001g0071 | 3 | HG02559.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.767-1469G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742814 | ||||||
chr13:77742919
|
CT | C | 24 | a0001c0001t0001g0107a0001c0001t0002g0177a0001c0001t0002g0233others(21): Show | 25 | HG00558.hp1 HG00735.hp1 HG00741.hp1 others(22): Show |
intron_variant | MODIFIER | c.767-1349delT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77742919 | |||||
chr13:77742934
|
T | A | 1 | a0001c0001t0001g0180 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.767-1349T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77742934 | ||||||
chr13:77743327
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.767-956A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77743327 | ||||||
chr13:77743368
|
A | G | 48 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(45): Show | 52 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(49): Show |
intron_variant | MODIFIER | c.767-915A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77743368 | ||||||
chr13:77743495
|
A | AT | 278 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(275): Show | 295 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(292): Show |
intron_variant | MODIFIER | c.767-780dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77743495 | |||||
chr13:77743510
|
T | G | 1 | a0001c0001t0001g0230 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.767-773T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77743510 | ||||||
chr13:77743596
|
C | A | 11 | a0001c0001t0001g0154a0001c0001t0001g0156a0001c0001t0003g0010others(8): Show | 12 | HG00735.hp1 HG01884.hp2 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.767-687C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77743596 | ||||||
chr13:77743667
|
T | TGAAGCCA others(15): Show |
2 | a0001c0001t0001g0036a0001c0001t0001g0037 | 2 | HG02135.hp1 HG03490.hp1 |
intron_variant | MODIFIER | c.767-615_767-594dup others(22): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr13 | 77743667 | |||||
chr13:77743932
|
T | C | 105 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0036others(102): Show | 110 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(107): Show |
intron_variant | MODIFIER | c.767-351T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77743932 | ||||||
chr13:77744254
|
G | A | 14 | a0001c0001t0002g0177a0001c0001t0002g0233a0001c0001t0002g0234others(11): Show | 14 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.767-29G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 2/6 | chr13 | 77744254 | ||||||
chr13:77744464
|
G | T | 10 | a0001c0001t0002g0031a0001c0001t0002g0073a0001c0001t0002g0074others(7): Show | 10 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.916+32G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77744464 | ||||||
chr13:77744665
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.916+233G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77744665 | ||||||
chr13:77744830
|
T | G | 14 | a0001c0001t0002g0177a0001c0001t0002g0233a0001c0001t0002g0234others(11): Show | 14 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.916+398T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77744830 | ||||||
chr13:77745040
|
G | A | 2 | a0001c0001t0004g0112a0001c0001t0004g0114 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.916+608G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77745040 | ||||||
chr13:77745263
|
G | A | 1 | a0001c0001t0001g0195 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.916+831G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77745263 | ||||||
chr13:77745376
|
G | T | 8 | a0001c0001t0001g0012a0001c0001t0001g0204a0001c0001t0001g0208others(5): Show | 9 | HG00423.hp2 HG00438.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.916+944G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77745376 | ||||||
chr13:77745468
|
A | G | 14 | a0001c0001t0002g0177a0001c0001t0002g0233a0001c0001t0002g0234others(11): Show | 14 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(11): Show |
intron_variant | MODIFIER | c.916+1036A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77745468 | ||||||
chr13:77745475
|
A | G | 1 | a0001c0004t0001g0016 | 2 | HG01168.hp2 HG01169.hp2 |
intron_variant | MODIFIER | c.917-1039A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77745475 | ||||||
chr13:77745488
|
G | C | 25 | a0001c0001t0002g0007a0001c0001t0002g0008a0001c0001t0002g0009others(22): Show | 28 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(25): Show |
intron_variant | MODIFIER | c.917-1026G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77745488 | ||||||
chr13:77745526
|
A | G | 8 | a0001c0001t0001g0012a0001c0001t0001g0204a0001c0001t0001g0208others(5): Show | 9 | HG00423.hp2 HG00438.hp1 HG02083.hp1 others(6): Show |
intron_variant | MODIFIER | c.917-988A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77745526 | ||||||
chr13:77745866
|
T | A | 3 | a0001c0001t0001g0171a0001c0001t0001g0172a0001c0001t0007g0155 | 3 | HG01256.hp1 HG01261.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.917-648T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77745866 | ||||||
chr13:77746087
|
T | C | 3 | a0001c0003t0001g0068a0001c0003t0001g0070a0001c0003t0001g0071 | 3 | HG02559.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.917-427T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77746087 | ||||||
chr13:77746251
|
A | G | 2 | a0001c0001t0001g0144a0001c0001t0001g0281 | 2 | HG02055.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.917-263A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 3/6 | chr13 | 77746251 | ||||||
chr13:77746990
|
G | A | 1 | a0001c0001t0001g0039 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1258+135G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77746990 | ||||||
chr13:77747029
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1258+174C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77747029 | ||||||
chr13:77747507
|
A | G | 1 | a0001c0001t0005g0222 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1258+652A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77747507 | ||||||
chr13:77748186
|
TAAG | T | 34 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(31): Show | 38 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.1258+1333_1258+133 others(7): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 77748186 | |||||
chr13:77748277
|
A | C | 1 | a0001c0001t0001g0083 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1258+1422A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77748277 | ||||||
chr13:77748292
|
A | C | 1 | a0001c0001t0001g0280 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1258+1437A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77748292 | ||||||
chr13:77748342
|
G | A | 2 | a0001c0001t0004g0112a0001c0001t0004g0114 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1258+1487G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77748342 | ||||||
chr13:77748398
|
C | CT | 28 | a0001c0001t0001g0020a0001c0001t0001g0025a0001c0001t0001g0034others(25): Show | 29 | HG00544.hp1 HG00735.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.1258+1569dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 77748398 | |||||
chr13:77748398
|
C | CTTTT | 11 | a0001c0001t0002g0073a0001c0001t0002g0074a0001c0001t0002g0075others(8): Show | 11 | HG02486.hp2 HG02559.hp1 HG02630.hp1 others(8): Show |
intron_variant | MODIFIER | c.1258+1566_1258+156 others(8): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 77748398 | |||||
chr13:77748398
|
CT | C | 43 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0036others(40): Show | 44 | HG01167.hp1 HG01167.hp2 HG01168.hp1 others(41): Show |
intron_variant | MODIFIER | c.1258+1569delT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 77748398 | |||||
chr13:77748674
|
C | T | 11 | a0001c0001t0002g0031a0001c0001t0002g0073a0001c0001t0002g0074others(8): Show | 11 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1258+1819C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77748674 | ||||||
chr13:77748855
|
T | C | 1 | a0001c0001t0001g0240 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.1258+2000T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77748855 | ||||||
chr13:77748902
|
C | A | 4 | a0002c0002t0001g0166a0002c0002t0001g0168a0002c0002t0001g0169others(1): Show | 4 | HG02818.hp1 HG03516.hp2 NA19240.hp1 others(1): Show |
intron_variant | MODIFIER | c.1258+2047C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77748902 | ||||||
chr13:77749211
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1258+2356G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77749211 | ||||||
chr13:77749342
|
T | A | 45 | a0001c0001t0001g0011a0001c0001t0001g0012a0001c0001t0001g0013others(42): Show | 48 | HG00408.hp2 HG00423.hp2 HG00438.hp1 others(45): Show |
intron_variant | MODIFIER | c.1258+2487T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77749342 | ||||||
chr13:77749363
|
A | G | 1 | a0001c0001t0001g0118 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1258+2508A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77749363 | ||||||
chr13:77749608
|
C | A | 1 | a0001c0001t0002g0069 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1258+2753C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77749608 | ||||||
chr13:77749660
|
T | C | 3 | a0001c0003t0001g0068a0001c0003t0001g0070a0001c0003t0001g0071 | 3 | HG02559.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1258+2805T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77749660 | ||||||
chr13:77749673
|
C | A | 65 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(62): Show | 69 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1258+2818C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77749673 | ||||||
chr13:77750101
|
T | A | 4 | a0001c0001t0001g0050a0001c0001t0001g0051a0001c0001t0001g0053others(1): Show | 4 | HG00423.hp1 NA18944.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.1259-3102T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77750101 | ||||||
chr13:77750124
|
T | G | 1 | a0001c0001t0001g0093 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1259-3079T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77750124 | ||||||
chr13:77750255
|
C | T | 1 | a0001c0001t0001g0279 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1259-2948C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77750255 | ||||||
chr13:77750396
|
T | C | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1259-2807T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77750396 | ||||||
chr13:77750918
|
A | G | 2 | a0001c0001t0002g0234a0001c0001t0002g0235 | 2 | HG01255.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.1259-2285A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77750918 | ||||||
chr13:77751188
|
C | A | 2 | a0001c0001t0001g0183a0001c0001t0001g0190 | 2 | NA18946.hp2 NA19011.hp1 |
intron_variant | MODIFIER | c.1259-2015C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77751188 | ||||||
chr13:77751189
|
G | A | 3 | a0001c0001t0002g0031a0001c0001t0002g0077a0001c0001t0002g0078 | 3 | HG02970.hp2 NA19030.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1259-2014G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77751189 | ||||||
chr13:77751320
|
G | A | 1 | a0001c0001t0002g0235 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.1259-1883G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77751320 | ||||||
chr13:77751623
|
A | G | 10 | a0001c0001t0002g0031a0001c0001t0002g0073a0001c0001t0002g0074others(7): Show | 10 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1259-1580A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77751623 | ||||||
chr13:77751632
|
A | T | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0018others(126): Show | 136 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(133): Show |
intron_variant | MODIFIER | c.1259-1571A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77751632 | ||||||
chr13:77751901
|
C | T | 6 | a0001c0001t0001g0111a0001c0001t0001g0113a0001c0001t0001g0115others(3): Show | 6 | HG02615.hp1 HG02723.hp1 HG02818.hp2 others(3): Show |
intron_variant | MODIFIER | c.1259-1302C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77751901 | ||||||
chr13:77751992
|
A | G | 1 | a0001c0001t0002g0126 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1259-1211A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77751992 | ||||||
chr13:77752123
|
G | A | 7 | a0001c0001t0002g0129a0001c0001t0002g0131a0001c0001t0002g0132others(4): Show | 7 | HG01070.hp2 HG01071.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1259-1080G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752123 | ||||||
chr13:77752160
|
T | G | 1 | a0001c0001t0004g0114 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1259-1043T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752160 | ||||||
chr13:77752238
|
A | G | 1 | a0001c0001t0001g0045 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.1259-965A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752238 | ||||||
chr13:77752288
|
C | CT | 10 | a0001c0001t0001g0028a0001c0001t0001g0029a0001c0001t0001g0083others(7): Show | 10 | HG00423.hp2 HG02109.hp2 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1259-897dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 77752288 | |||||
chr13:77752288
|
C | CTTTT | 45 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(42): Show | 49 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(46): Show |
intron_variant | MODIFIER | c.1259-900_1259-897d others(6): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 77752288 | |||||
chr13:77752288
|
C | CTTTTT | 13 | a0001c0001t0002g0076a0001c0001t0002g0080a0001c0001t0002g0125others(10): Show | 13 | HG00558.hp1 HG02080.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.1259-901_1259-897d others(7): Show |
SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 77752288 | |||||
chr13:77752288
|
CT | C | 15 | a0001c0001t0001g0038a0001c0001t0001g0054a0001c0001t0001g0090others(12): Show | 15 | HG01081.hp1 HG01081.hp2 HG01167.hp1 others(12): Show |
intron_variant | MODIFIER | c.1259-897delT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr13 | 77752288 | |||||
chr13:77752307
|
A | T | 2 | a0001c0001t0004g0112a0001c0001t0004g0114 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1259-896A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752307 | ||||||
chr13:77752416
|
T | C | 1 | a0001c0001t0002g0139 | 1 | HG01069.hp1 | intron_variant | MODIFIER | c.1259-787T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752416 | ||||||
chr13:77752543
|
G | T | 65 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(62): Show | 69 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(66): Show |
intron_variant | MODIFIER | c.1259-660G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752543 | ||||||
chr13:77752626
|
G | A | 15 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0036others(12): Show | 16 | HG01168.hp1 HG01243.hp2 HG01433.hp1 others(13): Show |
intron_variant | MODIFIER | c.1259-577G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752626 | ||||||
chr13:77752657
|
G | T | 1 | a0001c0001t0001g0280 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1259-546G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752657 | ||||||
chr13:77752687
|
G | A | 10 | a0001c0001t0002g0031a0001c0001t0002g0073a0001c0001t0002g0074others(7): Show | 10 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1259-516G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752687 | ||||||
chr13:77752821
|
C | T | 3 | a0001c0003t0001g0068a0001c0003t0001g0070a0001c0003t0001g0071 | 3 | HG02559.hp1 HG02630.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1259-382C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752821 | ||||||
chr13:77752854
|
G | C | 1 | a0001c0001t0001g0144 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1259-349G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752854 | ||||||
chr13:77752868
|
A | G | 9 | a0001c0001t0002g0006a0001c0001t0002g0063a0001c0001t0002g0064others(6): Show | 10 | HG01099.hp1 HG02257.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1259-335A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752868 | ||||||
chr13:77752919
|
C | T | 1 | a0001c0001t0001g0039 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1259-284C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77752919 | ||||||
chr13:77753171
|
G | A | 10 | a0001c0001t0002g0031a0001c0001t0002g0073a0001c0001t0002g0074others(7): Show | 10 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1259-32G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77753171 | ||||||
chr13:77753194
|
C | A | 1 | a0001c0001t0002g0079 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1259-9C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 4/6 | chr13 | 77753194 | ||||||
chr13:77753598
|
A | G | 1 | a0001c0001t0001g0089 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.1414+240A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77753598 | ||||||
chr13:77753608
|
G | A | 35 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(32): Show | 39 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.1414+250G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77753608 | ||||||
chr13:77753615
|
T | C | 1 | a0001c0001t0001g0038 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1414+257T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77753615 | ||||||
chr13:77753709
|
T | C | 10 | a0001c0001t0002g0031a0001c0001t0002g0073a0001c0001t0002g0074others(7): Show | 10 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(7): Show |
intron_variant | MODIFIER | c.1414+351T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77753709 | ||||||
chr13:77753799
|
G | A | 2 | a0001c0001t0001g0243a0001c0001t0001g0259 | 2 | HG00738.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.1414+441G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77753799 | ||||||
chr13:77754179
|
C | T | 1 | a0001c0001t0001g0207 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1414+821C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77754179 | ||||||
chr13:77754321
|
T | G | 3 | a0001c0001t0001g0090a0001c0001t0001g0093a0001c0001t0001g0096 | 3 | NA18940.hp2 NA18961.hp2 NA19054.hp1 |
intron_variant | MODIFIER | c.1414+963T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77754321 | ||||||
chr13:77754695
|
C | T | 1 | a0001c0001t0002g0120 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1414+1337C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77754695 | ||||||
chr13:77754747
|
A | G | 12 | a0001c0001t0001g0195a0001c0001t0001g0196a0001c0001t0001g0198others(9): Show | 12 | HG01928.hp2 HG01934.hp1 HG02074.hp2 others(9): Show |
intron_variant | MODIFIER | c.1414+1389A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77754747 | ||||||
chr13:77754794
|
T | A | 1 | a0001c0001t0001g0236 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1414+1436T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77754794 | ||||||
chr13:77754820
|
A | G | 1 | a0001c0001t0002g0272 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.1414+1462A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77754820 | ||||||
chr13:77754833
|
T | G | 1 | a0001c0001t0001g0191 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1414+1475T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77754833 | ||||||
chr13:77754860
|
A | G | 1 | a0001c0001t0001g0248 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1414+1502A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77754860 | ||||||
chr13:77754944
|
A | G | 2 | a0001c0001t0004g0112a0001c0001t0004g0114 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1414+1586A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77754944 | ||||||
chr13:77755058
|
T | C | 1 | a0002c0002t0001g0157 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.1414+1700T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77755058 | ||||||
chr13:77755204
|
A | T | 1 | a0002c0002t0002g0158 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1414+1846A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77755204 | ||||||
chr13:77755330
|
GA | G | 26 | a0001c0001t0001g0083a0001c0001t0001g0084a0001c0001t0001g0085others(23): Show | 26 | HG01167.hp2 HG01169.hp1 HG01175.hp1 others(23): Show |
intron_variant | MODIFIER | c.1414+1983delA | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr13 | 77755330 | |||||
chr13:77755337
|
A | C | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1414+1979A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77755337 | ||||||
chr13:77755362
|
G | A | 2 | a0001c0001t0001g0028a0001c0001t0001g0029 | 2 | HG02615.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1414+2004G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77755362 | ||||||
chr13:77755567
|
T | G | 1 | a0001c0001t0001g0202 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1414+2209T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77755567 | ||||||
chr13:77755731
|
G | A | 13 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0036others(10): Show | 14 | HG01168.hp1 HG01243.hp2 HG01433.hp1 others(11): Show |
intron_variant | MODIFIER | c.1414+2373G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77755731 | ||||||
chr13:77755759
|
A | G | 1 | a0001c0001t0001g0267 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.1414+2401A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77755759 | ||||||
chr13:77756073
|
T | C | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1414+2715T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77756073 | ||||||
chr13:77756180
|
C | G | 4 | a0001c0001t0001g0035a0001c0001t0001g0040a0001c0001t0001g0044others(1): Show | 4 | HG00544.hp1 NA18956.hp2 NA18966.hp1 others(1): Show |
intron_variant | MODIFIER | c.1414+2822C>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77756180 | ||||||
chr13:77756721
|
T | C | 1 | a0001c0001t0001g0200 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1414+3363T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77756721 | ||||||
chr13:77756995
|
A | C | 1 | a0001c0001t0001g0251 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.1414+3637A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77756995 | ||||||
chr13:77757050
|
A | G | 2 | a0001c0001t0002g0077a0001c0001t0002g0078 | 2 | HG02970.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.1414+3692A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77757050 | ||||||
chr13:77757201
|
G | C | 1 | a0001c0001t0001g0088 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1415-3627G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77757201 | ||||||
chr13:77757584
|
C | A | 34 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(31): Show | 38 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(35): Show |
intron_variant | MODIFIER | c.1415-3244C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77757584 | ||||||
chr13:77757656
|
C | T | 1 | a0001c0001t0001g0248 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1415-3172C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77757656 | ||||||
chr13:77757760
|
A | T | 3 | a0002c0002t0001g0166a0002c0002t0001g0168a0002c0002t0001g0170 | 3 | HG02818.hp1 HG03516.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.1415-3068A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77757760 | ||||||
chr13:77757907
|
T | A | 11 | a0001c0001t0002g0031a0001c0001t0002g0073a0001c0001t0002g0074others(8): Show | 11 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1415-2921T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77757907 | ||||||
chr13:77758087
|
C | T | 8 | a0001c0001t0002g0006a0001c0001t0002g0063a0001c0001t0002g0064others(5): Show | 9 | HG01099.hp1 HG02257.hp1 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.1415-2741C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77758087 | ||||||
chr13:77758140
|
G | A | 2 | a0001c0001t0004g0112a0001c0001t0004g0114 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1415-2688G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77758140 | ||||||
chr13:77758185
|
T | C | 2 | a0001c0001t0001g0094a0001c0001t0001g0100 | 2 | HG00642.hp2 HG01123.hp2 |
intron_variant | MODIFIER | c.1415-2643T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77758185 | ||||||
chr13:77758278
|
G | GT | 15 | a0001c0001t0001g0093a0001c0001t0002g0177a0001c0001t0002g0233others(12): Show | 15 | HG00558.hp1 HG00741.hp1 HG01070.hp1 others(12): Show |
intron_variant | MODIFIER | c.1415-2542dupT | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | INFO_REALIGN_3_PRIME | chr13 | 77758278 | |||||
chr13:77758421
|
G | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0018others(127): Show | 137 | HG00140.hp1 HG00280.hp2 HG00438.hp2 others(134): Show |
intron_variant | MODIFIER | c.1415-2407G>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77758421 | ||||||
chr13:77758810
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1415-2018G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77758810 | ||||||
chr13:77758960
|
A | G | 1 | a0001c0001t0001g0206 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.1415-1868A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77758960 | ||||||
chr13:77758976
|
A | C | 1 | a0001c0001t0001g0027 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1415-1852A>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77758976 | ||||||
chr13:77759116
|
T | G | 2 | a0001c0001t0002g0133a0001c0001t0002g0135 | 2 | HG01070.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.1415-1712T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77759116 | ||||||
chr13:77759485
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1415-1343A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77759485 | ||||||
chr13:77759803
|
A | G | 35 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0008others(32): Show | 39 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(36): Show |
intron_variant | MODIFIER | c.1415-1025A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77759803 | ||||||
chr13:77759835
|
T | C | 1 | a0001c0001t0007g0155 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1415-993T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77759835 | ||||||
chr13:77760082
|
T | G | 108 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0028others(105): Show | 113 | HG00280.hp2 HG00438.hp2 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.1415-746T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77760082 | ||||||
chr13:77760088
|
G | C | 7 | a0001c0001t0001g0002a0001c0001t0001g0022a0001c0001t0001g0036others(4): Show | 8 | HG01168.hp1 HG01243.hp2 HG01433.hp1 others(5): Show |
intron_variant | MODIFIER | c.1415-740G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77760088 | ||||||
chr13:77760183
|
T | C | 9 | a0001c0001t0002g0006a0001c0001t0002g0063a0001c0001t0002g0064others(6): Show | 10 | HG01099.hp1 HG02257.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1415-645T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77760183 | ||||||
chr13:77760188
|
C | A | 4 | a0001c0001t0001g0014a0001c0001t0001g0191a0001c0001t0001g0192others(1): Show | 5 | HG00741.hp2 HG02257.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1415-640C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77760188 | ||||||
chr13:77760439
|
A | G | 1 | a0001c0001t0001g0202 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.1415-389A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 5/6 | chr13 | 77760439 | ||||||
chr13:77761121
|
G | A | 1 | a0001c0001t0002g0031 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1697+11G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77761121 | ||||||
chr13:77761173
|
C | T | 11 | a0001c0001t0001g0021a0001c0001t0001g0023a0001c0001t0001g0024others(8): Show | 11 | HG00558.hp2 HG02080.hp2 NA18612.hp1 others(8): Show |
intron_variant | MODIFIER | c.1697+63C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77761173 | ||||||
chr13:77761483
|
C | T | 2 | a0001c0001t0004g0112a0001c0001t0004g0114 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1697+373C>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77761483 | ||||||
chr13:77761948
|
A | G | 1 | a0001c0001t0002g0006 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1697+838A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77761948 | ||||||
chr13:77761969
|
G | A | 11 | a0001c0001t0002g0031a0001c0001t0002g0073a0001c0001t0002g0074others(8): Show | 11 | HG02486.hp2 HG02630.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.1697+859G>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77761969 | ||||||
chr13:77762211
|
T | C | 1 | a0001c0001t0001g0100 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.1698-934T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77762211 | ||||||
chr13:77762277
|
T | A | 1 | a0001c0001t0001g0179 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1698-868T>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77762277 | ||||||
chr13:77762283
|
C | A | 1 | a0001c0001t0002g0006 | 2 | HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.1698-862C>A | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77762283 | ||||||
chr13:77762405
|
A | T | 5 | a0001c0001t0001g0015a0001c0001t0001g0236a0001c0001t0001g0237others(2): Show | 6 | HG00280.hp1 HG01069.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.1698-740A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77762405 | ||||||
chr13:77762426
|
T | G | 1 | a0001c0001t0001g0018 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.1698-719T>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77762426 | ||||||
chr13:77762689
|
T | C | 2 | a0001c0001t0004g0112a0001c0001t0004g0114 | 2 | HG01109.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1698-456T>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77762689 | ||||||
chr13:77762911
|
A | T | 1 | a0001c0001t0007g0155 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.1698-234A>T | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77762911 | ||||||
chr13:77763018
|
G | C | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1698-127G>C | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77763018 | ||||||
chr13:77763059
|
A | G | 5 | a0001c0001t0003g0010a0001c0001t0003g0146a0001c0001t0003g0147others(2): Show | 6 | HG00735.hp1 HG02647.hp2 HG02717.hp2 others(3): Show |
intron_variant | MODIFIER | c.1698-86A>G | SLAIN1 | ENSG00000139737.23 | transcript | ENST00000418532.6 | protein_coding | 6/6 | chr13 | 77763059 |