geneid | 81609 |
---|---|
ensemblid | ENSG00000143376.14 |
hgncid | 20073 |
symbol | SNX27 |
name | sorting nexin 27 |
refseq_nuc | NM_001330723.2 |
refseq_prot | NP_001317652.1 |
ensembl_nuc | ENST00000458013.7 |
ensembl_prot | ENSP00000400333.2 |
mane_status | MANE Select |
chr | chr1 |
start | 151612050 |
end | 151699080 |
strand | + |
ver | v1.2 |
region | chr1:151612050-151699080 |
region5000 | chr1:151607050-151704080 |
regionname0 | SNX27_chr1_151612050_151699080 |
regionname5000 | SNX27_chr1_151607050_151704080 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 541 | 359 | 94 | 56 | 159 | 12 | 36 | 119 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0002 | 0/0 | 541 | 6 | 0 | 0 | 6 | 0 | 0 | 6 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0003 | 0/0 | 500 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1626 | 353 | 89 | 56 | 158 | 12 | 36 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
c0002 | 0/0 | 1626 | 6 | 0 | 0 | 6 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
c0003 | 0/0 | 1626 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
c0004 | 0/0 | 1626 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
c0005 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
c0006 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
c0007 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 4808 | 14 | 0 | 0 | 13 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0002 | 0/0 | 4821 | 13 | 0 | 0 | 13 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0003 | 0/0 | 4808 | 11 | 2 | 3 | 1 | 1 | 4 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0004 | 1/0 | 4816 | 11 | 3 | 3 | 0 | 2 | 2 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0005 | 0/0 | 4812 | 8 | 1 | 2 | 2 | 0 | 3 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0006 | 0/0 | 4819 | 8 | 0 | 0 | 8 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0007 | 0/0 | 4823 | 7 | 1 | 3 | 2 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0008 | 0/0 | 4826 | 7 | 0 | 2 | 3 | 0 | 2 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0009 | 0/0 | 4827 | 6 | 2 | 0 | 2 | 1 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0010 | 0/0 | 4819 | 6 | 2 | 3 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0011 | 0/0 | 4824 | 6 | 1 | 2 | 3 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0012 | 0/0 | 4823 | 5 | 5 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0013 | 0/0 | 4808 | 5 | 0 | 0 | 5 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0014 | 0/0 | 4835 | 5 | 1 | 1 | 1 | 2 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0015 | 0/0 | 4817 | 5 | 0 | 1 | 4 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0016 | 0/0 | 4809 | 5 | 2 | 2 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0017 | 0/0 | 4813 | 5 | 0 | 2 | 2 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0018 | 0/0 | 4817 | 5 | 1 | 0 | 3 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0019 | 0/0 | 4820 | 5 | 3 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0020 | 0/0 | 4822 | 5 | 0 | 1 | 4 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0021 | 0/0 | 4813 | 4 | 0 | 1 | 3 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0022 | 0/0 | 4824 | 4 | 2 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0023 | 0/0 | 4828 | 4 | 4 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0024 | 0/0 | 4812 | 3 | 3 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0025 | 0/0 | 4796 | 3 | 0 | 3 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0026 | 0/0 | 4812 | 3 | 0 | 0 | 3 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0027 | 0/0 | 4812 | 3 | 0 | 2 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0028 | 0/0 | 4820 | 3 | 1 | 0 | 1 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0029 | 0/0 | 4835 | 3 | 0 | 1 | 1 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0030 | 0/0 | 4831 | 3 | 0 | 1 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0031 | 0/0 | 4829 | 3 | 0 | 0 | 3 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0032 | 0/0 | 4825 | 3 | 0 | 1 | 1 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0033 | 0/0 | 4824 | 3 | 0 | 0 | 1 | 0 | 2 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0034 | 0/0 | 4828 | 3 | 0 | 1 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0035 | 0/0 | 4806 | 3 | 3 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0036 | 0/0 | 4830 | 3 | 0 | 0 | 2 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0037 | 0/0 | 4826 | 3 | 0 | 0 | 3 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0038 | 0/0 | 4828 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0039 | 0/0 | 4820 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0040 | 0/0 | 4832 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0041 | 0/0 | 4808 | 2 | 0 | 2 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0042 | 0/0 | 4809 | 2 | 0 | 0 | 1 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0043 | 0/0 | 4812 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0044 | 0/0 | 4836 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0045 | 0/0 | 4808 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0046 | 0/0 | 4812 | 2 | 0 | 2 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0047 | 0/0 | 4816 | 2 | 0 | 2 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0048 | 0/0 | 4827 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0049 | 0/0 | 4836 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0050 | 0/0 | 4828 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0051 | 0/0 | 4843 | 2 | 0 | 0 | 1 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0052 | 0/0 | 4844 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0053 | 0/0 | 4839 | 2 | 0 | 1 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0054 | 0/0 | 4824 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0055 | 0/0 | 4809 | 2 | 0 | 0 | 1 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0056 | 0/0 | 4809 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0057 | 0/0 | 4805 | 2 | 1 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0058 | 0/0 | 4833 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0059 | 0/0 | 4832 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0060 | 0/0 | 4828 | 2 | 0 | 0 | 1 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0061 | 0/0 | 4813 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0062 | 0/0 | 4821 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0063 | 0/0 | 4818 | 2 | 0 | 0 | 0 | 0 | 2 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0064 | 0/0 | 4834 | 2 | 0 | 2 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0065 | 0/0 | 4829 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0066 | 0/0 | 4813 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0067 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0068 | 0/0 | 4808 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0069 | 0/0 | 4816 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0070 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0071 | 0/0 | 4808 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0072 | 0/0 | 4817 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0073 | 0/0 | 4807 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0074 | 0/0 | 4811 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0075 | 0/0 | 4815 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0076 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0077 | 0/0 | 4822 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0078 | 0/0 | 4826 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0079 | 0/0 | 4808 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0080 | 0/0 | 4823 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0081 | 0/0 | 4820 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0082 | 0/0 | 4804 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0083 | 0/0 | 4813 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0084 | 0/0 | 4816 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0085 | 0/0 | 4816 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0086 | 0/0 | 4820 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0087 | 0/0 | 4821 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0088 | 0/0 | 4828 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0089 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0090 | 0/0 | 4816 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0091 | 0/0 | 4820 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0092 | 0/0 | 4832 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0093 | 0/0 | 4824 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0094 | 0/0 | 4804 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0095 | 0/0 | 4836 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0096 | 0/0 | 4832 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0097 | 0/0 | 4832 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0098 | 0/0 | 4819 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0099 | 0/0 | 4820 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0100 | 0/0 | 4823 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0101 | 0/1 | 4831 | 1 | 0 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0102 | 0/0 | 4815 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0103 | 0/0 | 4823 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0104 | 0/0 | 4823 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0105 | 0/0 | 4827 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0106 | 0/0 | 4848 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0107 | 0/0 | 4839 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0108 | 0/0 | 4840 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0109 | 0/0 | 4823 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0110 | 0/0 | 4827 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0111 | 0/0 | 4827 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0112 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0113 | 0/0 | 4817 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0114 | 0/0 | 4809 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0115 | 0/0 | 4813 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0116 | 0/0 | 4821 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0117 | 0/0 | 4829 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0118 | 0/0 | 4833 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0119 | 0/0 | 4829 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0120 | 0/0 | 4841 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0121 | 0/0 | 4812 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0122 | 0/0 | 4812 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0123 | 0/0 | 4816 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0124 | 0/0 | 4824 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0125 | 0/0 | 4836 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0126 | 0/0 | 4820 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0127 | 0/0 | 4828 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0128 | 0/0 | 4824 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0129 | 0/0 | 4832 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0130 | 0/0 | 4820 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0131 | 0/0 | 4836 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0132 | 0/0 | 4834 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0133 | 0/0 | 4806 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0134 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0135 | 0/0 | 4822 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0136 | 0/0 | 4834 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0137 | 0/0 | 4817 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0138 | 0/0 | 4825 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0139 | 0/0 | 4833 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0140 | 0/0 | 4835 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0141 | 0/0 | 4822 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0142 | 0/0 | 4803 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0143 | 0/0 | 4819 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0144 | 0/0 | 4813 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0145 | 0/0 | 4805 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0146 | 0/0 | 4817 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0147 | 0/0 | 4818 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0148 | 0/0 | 4822 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0149 | 0/0 | 4818 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0150 | 0/0 | 4794 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0151 | 0/0 | 4798 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0152 | 0/0 | 4802 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0153 | 0/0 | 4822 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0154 | 0/0 | 4810 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0155 | 0/0 | 4815 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0156 | 0/0 | 4827 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0157 | 0/0 | 4826 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0158 | 0/0 | 4819 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0159 | 0/0 | 4831 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0160 | 0/0 | 4814 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0161 | 0/0 | 4834 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0162 | 0/0 | 4827 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0163 | 0/0 | 4823 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0164 | 0/0 | 4822 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0165 | 0/0 | 4827 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0166 | 0/0 | 4819 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0167 | 0/0 | 4815 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0168 | 0/0 | 4827 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0169 | 0/0 | 4828 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0170 | 0/0 | 4820 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0171 | 0/0 | 4831 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0172 | 0/0 | 4801 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0173 | 0/0 | 4817 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0174 | 0/0 | 4823 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0175 | 0/0 | 4821 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0176 | 0/0 | 4822 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0177 | 0/0 | 4821 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0178 | 0/0 | 4825 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
t0179 | 0/0 | 4827 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0003 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0203 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1626 | 353 | 89 | 56 | 158 | 12 | 36 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0003 | 0/0 | 1626 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0004 | 0/0 | 1626 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0006 | 0/0 | 1626 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0007 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0002c0002 | 0/0 | 1626 | 6 | 0 | 0 | 6 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0003c0005 | 0/0 | 1626 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 6433 | 13 | 0 | 0 | 12 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0002 | 0/0 | 6446 | 13 | 0 | 0 | 13 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0003 | 0/0 | 6433 | 11 | 2 | 3 | 1 | 1 | 4 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0004 | 1/0 | 6441 | 11 | 3 | 3 | 0 | 2 | 2 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0005 | 0/0 | 6437 | 8 | 1 | 2 | 2 | 0 | 3 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0006 | 0/0 | 6444 | 4 | 0 | 0 | 4 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0007 | 0/0 | 6448 | 7 | 1 | 3 | 2 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0008 | 0/0 | 6451 | 7 | 0 | 2 | 3 | 0 | 2 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0009 | 0/0 | 6452 | 6 | 2 | 0 | 2 | 1 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0010 | 0/0 | 6444 | 6 | 2 | 3 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0011 | 0/0 | 6449 | 6 | 1 | 2 | 3 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0012 | 0/0 | 6448 | 5 | 5 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0013 | 0/0 | 6433 | 5 | 0 | 0 | 5 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0014 | 0/0 | 6460 | 5 | 1 | 1 | 1 | 2 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0015 | 0/0 | 6442 | 5 | 0 | 1 | 4 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0016 | 0/0 | 6434 | 5 | 2 | 2 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0017 | 0/0 | 6438 | 5 | 0 | 2 | 2 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0018 | 0/0 | 6442 | 4 | 1 | 0 | 2 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0019 | 0/0 | 6445 | 5 | 3 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0020 | 0/0 | 6447 | 5 | 0 | 1 | 4 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0021 | 0/0 | 6438 | 4 | 0 | 1 | 3 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0022 | 0/0 | 6449 | 4 | 2 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0023 | 0/0 | 6453 | 4 | 4 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0024 | 0/0 | 6437 | 3 | 3 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0025 | 0/0 | 6421 | 3 | 0 | 3 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0026 | 0/0 | 6437 | 3 | 0 | 0 | 3 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0027 | 0/0 | 6437 | 3 | 0 | 2 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0028 | 0/0 | 6445 | 3 | 1 | 0 | 1 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0029 | 0/0 | 6460 | 3 | 0 | 1 | 1 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0030 | 0/0 | 6456 | 3 | 0 | 1 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0031 | 0/0 | 6454 | 3 | 0 | 0 | 3 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0032 | 0/0 | 6450 | 3 | 0 | 1 | 1 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0033 | 0/0 | 6449 | 3 | 0 | 0 | 1 | 0 | 2 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0034 | 0/0 | 6453 | 3 | 0 | 1 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0035 | 0/0 | 6431 | 3 | 3 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0036 | 0/0 | 6455 | 3 | 0 | 0 | 2 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0037 | 0/0 | 6451 | 3 | 0 | 0 | 3 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0039 | 0/0 | 6445 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0040 | 0/0 | 6457 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0041 | 0/0 | 6433 | 2 | 0 | 2 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0042 | 0/0 | 6434 | 2 | 0 | 0 | 1 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0043 | 0/0 | 6437 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0044 | 0/0 | 6461 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0045 | 0/0 | 6433 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0046 | 0/0 | 6437 | 2 | 0 | 2 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0047 | 0/0 | 6441 | 2 | 0 | 2 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0049 | 0/0 | 6461 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0050 | 0/0 | 6453 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0051 | 0/0 | 6468 | 2 | 0 | 0 | 1 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0052 | 0/0 | 6469 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0053 | 0/0 | 6464 | 2 | 0 | 1 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0054 | 0/0 | 6449 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0055 | 0/0 | 6434 | 2 | 0 | 0 | 1 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0056 | 0/0 | 6434 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0057 | 0/0 | 6430 | 2 | 1 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0058 | 0/0 | 6458 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0059 | 0/0 | 6457 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0060 | 0/0 | 6453 | 2 | 0 | 0 | 1 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0062 | 0/0 | 6446 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0063 | 0/0 | 6443 | 2 | 0 | 0 | 0 | 0 | 2 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0064 | 0/0 | 6459 | 2 | 0 | 2 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0065 | 0/0 | 6454 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0066 | 0/0 | 6438 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0067 | 0/0 | 6449 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0068 | 0/0 | 6433 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0069 | 0/0 | 6441 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0070 | 0/0 | 6449 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0071 | 0/0 | 6433 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0072 | 0/0 | 6442 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0073 | 0/0 | 6432 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0074 | 0/0 | 6436 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0075 | 0/0 | 6440 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0076 | 0/0 | 6443 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0077 | 0/0 | 6447 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0078 | 0/0 | 6451 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0079 | 0/0 | 6433 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0080 | 0/0 | 6448 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0081 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0082 | 0/0 | 6429 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0083 | 0/0 | 6438 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0084 | 0/0 | 6441 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0085 | 0/0 | 6441 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0086 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0087 | 0/0 | 6446 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0088 | 0/0 | 6453 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0089 | 0/0 | 6449 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0090 | 0/0 | 6441 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0091 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0092 | 0/0 | 6457 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0093 | 0/0 | 6449 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0094 | 0/0 | 6429 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0095 | 0/0 | 6461 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0096 | 0/0 | 6457 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0098 | 0/0 | 6444 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0099 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0100 | 0/0 | 6448 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0101 | 0/1 | 6456 | 1 | 0 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0102 | 0/0 | 6440 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0103 | 0/0 | 6448 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0104 | 0/0 | 6448 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0105 | 0/0 | 6452 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0106 | 0/0 | 6473 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0107 | 0/0 | 6464 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0108 | 0/0 | 6465 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0109 | 0/0 | 6448 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0110 | 0/0 | 6452 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0111 | 0/0 | 6452 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0112 | 0/0 | 6456 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0113 | 0/0 | 6442 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0114 | 0/0 | 6434 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0115 | 0/0 | 6438 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0116 | 0/0 | 6446 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0117 | 0/0 | 6454 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0118 | 0/0 | 6458 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0119 | 0/0 | 6454 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0120 | 0/0 | 6466 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0121 | 0/0 | 6437 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0122 | 0/0 | 6437 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0123 | 0/0 | 6441 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0124 | 0/0 | 6449 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0125 | 0/0 | 6461 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0126 | 0/0 | 6445 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0127 | 0/0 | 6453 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0128 | 0/0 | 6449 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0129 | 0/0 | 6457 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0130 | 0/0 | 6445 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0131 | 0/0 | 6461 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0132 | 0/0 | 6459 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0133 | 0/0 | 6431 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0134 | 0/0 | 6443 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0135 | 0/0 | 6447 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0136 | 0/0 | 6459 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0137 | 0/0 | 6442 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0138 | 0/0 | 6450 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0139 | 0/0 | 6458 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0140 | 0/0 | 6460 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0141 | 0/0 | 6447 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0142 | 0/0 | 6428 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0143 | 0/0 | 6444 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0144 | 0/0 | 6438 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0145 | 0/0 | 6430 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0146 | 0/0 | 6442 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0147 | 0/0 | 6443 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0148 | 0/0 | 6447 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0149 | 0/0 | 6443 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0150 | 0/0 | 6419 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0151 | 0/0 | 6423 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0152 | 0/0 | 6427 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0153 | 0/0 | 6447 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0154 | 0/0 | 6435 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0155 | 0/0 | 6440 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0156 | 0/0 | 6452 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0157 | 0/0 | 6451 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0158 | 0/0 | 6444 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0159 | 0/0 | 6456 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0160 | 0/0 | 6439 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0161 | 0/0 | 6459 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0162 | 0/0 | 6452 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0163 | 0/0 | 6448 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0164 | 0/0 | 6447 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0165 | 0/0 | 6452 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0166 | 0/0 | 6444 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0167 | 0/0 | 6440 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0168 | 0/0 | 6452 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0169 | 0/0 | 6453 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0170 | 0/0 | 6445 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0171 | 0/0 | 6456 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0172 | 0/0 | 6426 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0173 | 0/0 | 6442 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0174 | 0/0 | 6448 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0175 | 0/0 | 6446 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0176 | 0/0 | 6447 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0177 | 0/0 | 6446 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0178 | 0/0 | 6450 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0001t0179 | 0/0 | 6452 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0003t0061 | 0/0 | 6438 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0004t0038 | 0/0 | 6453 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0006t0097 | 0/0 | 6457 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0001c0007t0001 | 0/0 | 6433 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0002c0002t0006 | 0/0 | 6444 | 4 | 0 | 0 | 4 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0002c0002t0048 | 0/0 | 6452 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
a0003c0005t0018 | 0/0 | 6442 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | copy fasta | chr1 | 151607050 | 151704080 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0010 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0006 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0098 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0100 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0003g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0077 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0167 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0004g0342 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0005g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0006g0001 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0006g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0006g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0007g0214 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0007g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0007g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0007g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0007g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0007g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0007g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0008g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0008g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0008g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0008g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0008g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0008g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0008g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0009g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0009g0196 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0009g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0009g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0009g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0009g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0010g0221 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0010g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0010g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0010g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0010g0280 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0010g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0011g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0011g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0011g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0011g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0011g0266 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0011g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0012g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0012g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0012g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0012g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0012g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0013g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0013g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0013g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0013g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0013g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0014g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0014g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0014g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0014g0246 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0014g0248 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0015g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0015g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0015g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0015g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0015g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0016g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0016g0169 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0016g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0016g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0016g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0017g0297 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0017g0303 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0017g0322 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0017g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0017g0326 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0018g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0018g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0018g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0018g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0019g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0019g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0019g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0019g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0019g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0020g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0020g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0020g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0020g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0020g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0021g0143 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0021g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0021g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0021g0340 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0022g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0022g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0022g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0022g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0023g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0023g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0023g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0023g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0024g0354 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0024g0355 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0024g0356 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0025g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0025g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0025g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0026g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0026g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0026g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0027g0343 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0027g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0027g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0028g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0028g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0028g0319 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0029g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0029g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0029g0273 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0030g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0030g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0030g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0031g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0031g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0031g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0032g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0032g0299 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0032g0301 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0033g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0033g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0033g0254 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0034g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0034g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0034g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0035g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0035g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0035g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0036g0035 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0036g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0036g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0037g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0037g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0037g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0039g0005 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0040g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0040g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0041g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0041g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0042g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0042g0151 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0043g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0043g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0044g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0044g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0045g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0045g0332 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0046g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0046g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0047g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0047g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0049g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0049g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0050g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0050g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0051g0215 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0051g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0052g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0052g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0053g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0053g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0054g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0054g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0055g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0055g0124 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0056g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0056g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0057g0294 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0057g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0058g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0059g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0059g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0060g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0060g0261 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0062g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0062g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0063g0055 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0063g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0064g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0064g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0065g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0065g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0066g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0067g0361 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0068g0351 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0069g0352 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0070g0353 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0071g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0072g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0073g0344 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0074g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0075g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0076g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0077g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0078g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0079g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0080g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0081g0009 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0082g0123 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0083g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0084g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0085g0346 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0086g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0087g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0088g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0089g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0090g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0091g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0092g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0093g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0094g0336 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0095g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0096g0333 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0098g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0099g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0100g0247 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0101g0203 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0102g0341 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0103g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0104g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0105g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0106g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0107g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0108g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0109g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0110g0256 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0111g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0112g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0113g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0114g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0115g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0116g0327 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0117g0304 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0118g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0119g0003 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0120g0335 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0121g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0122g0231 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0123g0339 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0124g0275 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0125g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0126g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0127g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0128g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0129g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0130g0267 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0131g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0132g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0133g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0134g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0135g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0136g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0137g0338 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0138g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0139g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0140g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0141g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0142g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0143g0359 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0144g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0145g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0146g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0147g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0148g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0149g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0150g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0151g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0152g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0153g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0154g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0155g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0156g0360 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0157g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0158g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0159g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0160g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0161g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0162g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0163g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0164g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0165g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0166g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0167g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0168g0037 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0169g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0170g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0171g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0172g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0173g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0174g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0175g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0176g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0177g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0178g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0001t0179g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0003t0061g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0003t0061g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0004t0038g0350 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0004t0038g0357 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0006t0097g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0001c0007t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0002c0002t0006g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0002c0002t0006g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0002c0002t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0002c0002t0048g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0002c0002t0048g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
a0003c0005t0018g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0004 | g0167 | EUR | GBR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00099 | hp2 | a0001 | c0001 | t0028 | g0144 | EUR | GBR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00280 | hp1 | a0001 | c0001 | t0042 | g0151 | EUR | FIN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00280 | hp2 | a0001 | c0001 | t0014 | g0246 | EUR | FIN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00323 | hp1 | a0001 | c0001 | t0051 | g0215 | EUR | FIN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00323 | hp2 | a0001 | c0001 | t0016 | g0169 | EUR | FIN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00408 | hp1 | a0001 | c0001 | t0086 | g0131 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00408 | hp2 | a0001 | c0001 | t0173 | g0046 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00423 | hp1 | a0001 | c0001 | t0037 | g0043 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00423 | hp2 | a0001 | c0001 | t0118 | g0311 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00438 | hp1 | a0001 | c0001 | t0011 | g0264 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00438 | hp2 | a0001 | c0001 | t0128 | g0226 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00544 | hp1 | a0001 | c0001 | t0021 | g0340 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00544 | hp2 | a0001 | c0001 | t0155 | g0070 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00597 | hp1 | a0001 | c0001 | t0002 | g0058 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00597 | hp2 | a0001 | c0001 | t0015 | g0312 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0056 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00639 | hp1 | a0001 | c0001 | t0124 | g0275 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00639 | hp2 | a0001 | c0001 | t0016 | g0181 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00642 | hp1 | a0001 | c0001 | t0122 | g0231 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00642 | hp2 | a0001 | c0001 | t0025 | g0185 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00673 | hp1 | a0001 | c0001 | t0029 | g0205 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00673 | hp2 | a0001 | c0001 | t0002 | g0052 | EAS | CHS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00735 | hp1 | a0001 | c0001 | t0007 | g0255 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00735 | hp2 | a0001 | c0001 | t0027 | g0348 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00738 | hp1 | a0001 | c0001 | t0021 | g0143 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00738 | hp2 | a0001 | c0001 | t0007 | g0216 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00741 | hp1 | a0001 | c0001 | t0041 | g0345 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG00741 | hp2 | a0001 | c0001 | t0169 | g0075 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01071 | hp1 | a0001 | c0001 | t0020 | g0048 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01071 | hp2 | a0001 | c0001 | t0004 | g0159 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01074 | hp1 | a0001 | c0001 | t0046 | g0192 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01074 | hp2 | a0001 | c0001 | t0003 | g0141 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01081 | hp1 | a0001 | c0001 | t0017 | g0303 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01081 | hp2 | a0001 | c0001 | t0053 | g0245 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01099 | hp1 | a0001 | c0001 | t0011 | g0266 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01099 | hp2 | a0001 | c0001 | t0016 | g0168 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01167 | hp1 | a0001 | c0001 | t0010 | g0240 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01167 | hp2 | a0001 | c0001 | t0085 | g0346 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01168 | hp1 | a0001 | c0001 | t0103 | g0274 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01168 | hp2 | a0001 | c0001 | t0075 | g0165 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01175 | hp1 | a0001 | c0001 | t0109 | g0007 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01175 | hp2 | a0001 | c0001 | t0032 | g0299 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01192 | hp1 | a0001 | c0001 | t0017 | g0326 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0150 | AMR | PUR | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01255 | hp1 | a0001 | c0001 | t0064 | g0047 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01255 | hp2 | a0001 | c0001 | t0004 | g0158 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01256 | hp1 | a0001 | c0001 | t0025 | g0128 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01256 | hp2 | a0001 | c0001 | t0064 | g0026 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01257 | hp1 | a0001 | c0001 | t0047 | g0191 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0156 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01258 | hp1 | a0001 | c0001 | t0025 | g0135 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01258 | hp2 | a0001 | c0001 | t0047 | g0193 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01261 | hp1 | a0001 | c0001 | t0010 | g0227 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01261 | hp2 | a0001 | c0001 | t0003 | g0142 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01346 | hp1 | a0001 | c0001 | t0157 | g0050 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01346 | hp2 | a0001 | c0001 | t0030 | g0198 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01358 | hp1 | a0001 | c0001 | t0015 | g0157 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01358 | hp2 | a0001 | c0001 | t0010 | g0229 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01433 | hp1 | a0001 | c0001 | t0034 | g0241 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01433 | hp2 | a0001 | c0001 | t0008 | g0049 | AMR | CLM | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01515 | hp1 | a0001 | c0001 | t0009 | g0196 | EUR | IBS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01515 | hp2 | a0001 | c0001 | t0004 | g0166 | EUR | IBS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01516 | hp1 | a0001 | c0001 | t0014 | g0248 | EUR | IBS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01516 | hp2 | a0001 | c0001 | t0017 | g0297 | EUR | IBS | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01884 | hp1 | a0001 | c0001 | t0003 | g0111 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01884 | hp2 | a0001 | c0001 | t0024 | g0354 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01934 | hp1 | a0001 | c0001 | t0003 | g0098 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01934 | hp2 | a0001 | c0001 | t0087 | g0179 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01975 | hp1 | a0001 | c0001 | t0041 | g0161 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01975 | hp2 | a0001 | c0001 | t0072 | g0349 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01978 | hp1 | a0001 | c0001 | t0027 | g0347 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG01978 | hp2 | a0001 | c0001 | t0014 | g0212 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02004 | hp1 | a0001 | c0001 | t0011 | g0265 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02004 | hp2 | a0001 | c0001 | t0046 | g0190 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02015 | hp1 | a0001 | c0001 | t0005 | g0147 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02015 | hp2 | a0001 | c0001 | t0111 | g0222 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02040 | hp1 | a0001 | c0001 | t0134 | g0309 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02040 | hp2 | a0001 | c0001 | t0079 | g0155 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02055 | hp1 | a0001 | c0001 | t0018 | g0315 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02055 | hp2 | a0001 | c0001 | t0016 | g0324 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02056 | hp1 | a0001 | c0001 | t0057 | g0294 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02056 | hp2 | a0001 | c0001 | t0014 | g0209 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02071 | hp1 | a0001 | c0001 | t0018 | g0298 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02071 | hp2 | a0001 | c0001 | t0175 | g0041 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02074 | hp1 | a0001 | c0001 | t0062 | g0095 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0153 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02080 | hp1 | a0001 | c0001 | t0002 | g0068 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02080 | hp2 | a0001 | c0001 | t0071 | g0152 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0030 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02083 | hp2 | a0001 | c0001 | t0177 | g0088 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02129 | hp1 | a0001 | c0001 | t0015 | g0329 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02129 | hp2 | a0001 | c0001 | t0081 | g0009 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02132 | hp1 | a0001 | c0001 | t0026 | g0133 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02132 | hp2 | a0001 | c0001 | t0032 | g0293 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02145 | hp1 | a0001 | c0001 | t0165 | g0014 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02145 | hp2 | a0001 | c0001 | t0120 | g0335 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02148 | hp1 | a0001 | c0001 | t0007 | g0228 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02148 | hp2 | a0001 | c0001 | t0171 | g0072 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02155 | hp1 | a0001 | c0001 | t0121 | g0268 | EAS | CDX | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02155 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | CDX | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02165 | hp1 | a0001 | c0001 | t0066 | g0089 | EAS | CDX | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02165 | hp2 | a0001 | c0001 | t0007 | g0233 | EAS | CDX | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02257 | hp1 | a0001 | c0001 | t0170 | g0091 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02257 | hp2 | a0001 | c0001 | t0069 | g0352 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02258 | hp1 | a0001 | c0001 | t0127 | g0084 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02258 | hp2 | a0001 | c0001 | t0012 | g0104 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02273 | hp1 | a0001 | c0001 | t0029 | g0273 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02273 | hp2 | a0001 | c0001 | t0008 | g0025 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02280 | hp1 | a0001 | c0001 | t0012 | g0109 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02280 | hp2 | a0001 | c0001 | t0141 | g0013 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02300 | hp1 | a0001 | c0001 | t0161 | g0054 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02300 | hp2 | a0001 | c0001 | t0005 | g0164 | AMR | PEL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02451 | hp1 | a0001 | c0001 | t0156 | g0360 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02451 | hp2 | a0001 | c0001 | t0142 | g0023 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02523 | hp2 | a0001 | c0001 | t0007 | g0220 | EAS | KHV | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02572 | hp1 | a0001 | c0001 | t0144 | g0011 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02572 | hp2 | a0001 | c0001 | t0024 | g0356 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02602 | hp1 | a0001 | c0001 | t0008 | g0071 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02602 | hp2 | a0001 | c0001 | t0004 | g0184 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02615 | hp1 | a0001 | c0001 | t0070 | g0353 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02615 | hp2 | a0001 | c0001 | t0094 | g0336 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02622 | hp1 | a0001 | c0001 | t0110 | g0256 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02622 | hp2 | a0001 | c0001 | t0105 | g0082 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02647 | hp1 | a0001 | c0001 | t0012 | g0110 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02647 | hp2 | a0001 | c0001 | t0139 | g0259 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02698 | hp1 | a0001 | c0001 | t0074 | g0146 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02698 | hp2 | a0001 | c0001 | t0154 | g0090 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02717 | hp1 | a0001 | c0001 | t0143 | g0359 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02717 | hp2 | a0001 | c0004 | t0038 | g0350 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02723 | hp1 | a0001 | c0001 | t0023 | g0286 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02723 | hp2 | a0001 | c0001 | t0067 | g0361 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02735 | hp1 | a0001 | c0001 | t0032 | g0301 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02735 | hp2 | a0001 | c0001 | t0009 | g0008 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0100 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02738 | hp2 | a0001 | c0001 | t0123 | g0339 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02809 | hp1 | a0001 | c0001 | t0023 | g0331 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02809 | hp2 | a0001 | c0001 | t0011 | g0276 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02818 | hp1 | a0001 | c0001 | t0162 | g0080 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02818 | hp2 | a0001 | c0001 | t0024 | g0355 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02886 | hp1 | a0001 | c0001 | t0010 | g0280 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02886 | hp2 | a0001 | c0001 | t0014 | g0194 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02895 | hp1 | a0001 | c0001 | t0035 | g0020 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02895 | hp2 | a0001 | c0003 | t0061 | g0097 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02896 | hp1 | a0001 | c0001 | t0073 | g0344 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02896 | hp2 | a0001 | c0001 | t0145 | g0018 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02922 | hp1 | a0001 | c0001 | t0068 | g0351 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02922 | hp2 | a0001 | c0001 | t0004 | g0342 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02965 | hp1 | a0001 | c0001 | t0150 | g0012 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02965 | hp2 | a0001 | c0001 | t0096 | g0333 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02970 | hp1 | a0001 | c0001 | t0077 | g0200 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02970 | hp2 | a0001 | c0004 | t0038 | g0357 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02976 | hp1 | a0001 | c0001 | t0149 | g0015 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02976 | hp2 | a0001 | c0001 | t0080 | g0108 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03041 | hp1 | a0001 | c0001 | t0016 | g0287 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03041 | hp2 | a0001 | c0001 | t0152 | g0019 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03098 | hp1 | a0001 | c0001 | t0039 | g0005 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03098 | hp2 | a0001 | c0001 | t0140 | g0093 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03130 | hp1 | a0001 | c0001 | t0163 | g0094 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03130 | hp2 | a0001 | c0001 | t0045 | g0288 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03139 | hp1 | a0001 | c0001 | t0093 | g0281 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03139 | hp2 | a0001 | c0001 | t0104 | g0081 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03195 | hp1 | a0001 | c0001 | t0004 | g0317 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03195 | hp2 | a0001 | c0001 | t0138 | g0086 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03209 | hp1 | a0001 | c0001 | t0119 | g0003 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03209 | hp2 | a0001 | c0001 | t0028 | g0319 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03225 | hp1 | a0001 | c0001 | t0039 | g0005 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03225 | hp2 | a0001 | c0001 | t0132 | g0195 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03239 | hp1 | a0001 | c0001 | t0100 | g0247 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0139 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03453 | hp1 | a0001 | c0001 | t0092 | g0283 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03453 | hp2 | a0001 | c0001 | t0095 | g0334 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03486 | hp1 | a0001 | c0001 | t0035 | g0021 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03486 | hp2 | a0001 | c0001 | t0023 | g0003 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03491 | hp1 | a0001 | c0001 | t0001 | g0127 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03491 | hp2 | a0001 | c0001 | t0018 | g0295 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03492 | hp1 | a0001 | c0001 | t0007 | g0214 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03492 | hp2 | a0001 | c0001 | t0055 | g0124 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03516 | hp1 | a0001 | c0001 | t0019 | g0279 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03516 | hp2 | a0001 | c0001 | t0004 | g0316 | AFR | ESN | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03540 | hp1 | a0001 | c0001 | t0091 | g0282 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03540 | hp2 | a0001 | c0001 | t0151 | g0017 | AFR | GWD | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03579 | hp1 | a0001 | c0001 | t0022 | g0320 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03579 | hp2 | a0001 | c0001 | t0054 | g0107 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03654 | hp1 | a0001 | c0001 | t0153 | g0031 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03654 | hp2 | a0001 | c0001 | t0005 | g0140 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03688 | hp1 | a0001 | c0001 | t0063 | g0066 | SAS | STU | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03688 | hp2 | a0001 | c0001 | t0005 | g0148 | SAS | STU | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03704 | hp1 | a0001 | c0001 | t0027 | g0343 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03704 | hp2 | a0001 | c0001 | t0063 | g0055 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0145 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03710 | hp2 | a0001 | c0001 | t0115 | g0290 | SAS | PJL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03831 | hp1 | a0001 | c0001 | t0003 | g0116 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03831 | hp2 | a0001 | c0001 | t0167 | g0074 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03834 | hp1 | a0001 | c0001 | t0029 | g0244 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03834 | hp2 | a0001 | c0001 | t0003 | g0149 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03927 | hp1 | a0001 | c0001 | t0060 | g0261 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03927 | hp2 | a0001 | c0001 | t0008 | g0044 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03942 | hp1 | a0001 | c0001 | t0005 | g0154 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03942 | hp2 | a0001 | c0001 | t0036 | g0035 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG04115 | hp1 | a0001 | c0001 | t0137 | g0338 | SAS | STU | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG04115 | hp2 | a0001 | c0001 | t0033 | g0254 | SAS | STU | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG04184 | hp1 | a0001 | c0001 | t0168 | g0037 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG04184 | hp2 | a0001 | c0001 | t0033 | g0213 | SAS | BEB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18522 | hp1 | a0001 | c0001 | t0148 | g0016 | AFR | YRI | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18522 | hp2 | a0001 | c0001 | t0158 | g0076 | AFR | YRI | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18612 | hp1 | a0001 | c0001 | t0017 | g0322 | EAS | CHB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18612 | hp2 | a0001 | c0001 | t0021 | g0162 | EAS | CHB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18906 | hp1 | a0001 | c0001 | t0078 | g0199 | AFR | YRI | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0318 | AFR | YRI | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18939 | hp1 | a0001 | c0001 | t0013 | g0174 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18939 | hp2 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18940 | hp1 | a0001 | c0001 | t0030 | g0258 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18940 | hp2 | a0001 | c0001 | t0015 | g0296 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18941 | hp1 | a0002 | c0002 | t0048 | g0219 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18941 | hp2 | a0001 | c0001 | t0011 | g0243 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18942 | hp1 | a0001 | c0001 | t0065 | g0085 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18942 | hp2 | a0001 | c0001 | t0009 | g0232 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18943 | hp1 | a0001 | c0001 | t0001 | g0117 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18943 | hp2 | a0001 | c0001 | t0018 | g0292 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18944 | hp1 | a0001 | c0001 | t0178 | g0032 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18944 | hp2 | a0001 | c0001 | t0013 | g0183 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18946 | hp1 | a0001 | c0001 | t0036 | g0059 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18946 | hp2 | a0001 | c0001 | t0099 | g0101 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18947 | hp1 | a0001 | c0001 | t0084 | g0138 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18947 | hp2 | a0002 | c0002 | t0006 | g0002 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18948 | hp1 | a0001 | c0001 | t0112 | g0208 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18948 | hp2 | a0001 | c0001 | t0031 | g0305 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18949 | hp1 | a0001 | c0001 | t0034 | g0211 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18949 | hp2 | a0001 | c0001 | t0008 | g0051 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18950 | hp1 | a0001 | c0001 | t0107 | g0271 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18950 | hp2 | a0001 | c0001 | t0135 | g0330 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18951 | hp1 | a0001 | c0001 | t0006 | g0189 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18951 | hp2 | a0001 | c0001 | t0060 | g0260 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18953 | hp1 | a0001 | c0001 | t0026 | g0137 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18953 | hp2 | a0001 | c0001 | t0031 | g0307 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18954 | hp1 | a0002 | c0002 | t0006 | g0197 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18954 | hp2 | a0001 | c0001 | t0043 | g0176 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18960 | hp1 | a0001 | c0001 | t0058 | g0004 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18960 | hp2 | a0001 | c0001 | t0053 | g0230 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18961 | hp1 | a0001 | c0001 | t0125 | g0204 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18961 | hp2 | a0001 | c0001 | t0043 | g0177 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18962 | hp1 | a0001 | c0001 | t0008 | g0027 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18962 | hp2 | a0001 | c0001 | t0052 | g0235 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18963 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18963 | hp2 | a0001 | c0001 | t0034 | g0225 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18965 | hp1 | a0001 | c0001 | t0174 | g0039 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18965 | hp2 | a0001 | c0001 | t0058 | g0004 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18966 | hp1 | a0001 | c0007 | t0001 | g0134 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18966 | hp2 | a0001 | c0001 | t0049 | g0236 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18967 | hp1 | a0001 | c0001 | t0056 | g0178 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18967 | hp2 | a0001 | c0001 | t0059 | g0251 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18971 | hp1 | a0001 | c0001 | t0050 | g0207 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0010 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18972 | hp2 | a0001 | c0001 | t0116 | g0327 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18973 | hp1 | a0001 | c0001 | t0015 | g0289 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18973 | hp2 | a0001 | c0001 | t0033 | g0223 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18975 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18975 | hp2 | a0001 | c0001 | t0065 | g0061 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18979 | hp1 | a0001 | c0001 | t0052 | g0238 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18979 | hp2 | a0001 | c0001 | t0083 | g0126 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18980 | hp1 | a0001 | c0001 | t0098 | g0187 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18980 | hp2 | a0001 | c0001 | t0017 | g0323 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18982 | hp1 | a0001 | c0001 | t0114 | g0310 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18982 | hp2 | a0001 | c0001 | t0160 | g0067 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18983 | hp1 | a0001 | c0001 | t0013 | g0175 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18983 | hp2 | a0001 | c0001 | t0131 | g0242 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18984 | hp1 | a0001 | c0001 | t0020 | g0063 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18984 | hp2 | a0001 | c0001 | t0051 | g0272 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18985 | hp1 | a0001 | c0001 | t0019 | g0269 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18985 | hp2 | a0001 | c0001 | t0037 | g0024 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18986 | hp1 | a0001 | c0001 | t0106 | g0239 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18986 | hp2 | a0001 | c0001 | t0089 | g0300 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18988 | hp2 | a0001 | c0001 | t0020 | g0040 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18991 | hp1 | a0001 | c0001 | t0147 | g0079 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18991 | hp2 | a0002 | c0002 | t0006 | g0250 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18992 | hp1 | a0001 | c0001 | t0059 | g0206 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18992 | hp2 | a0001 | c0001 | t0055 | g0115 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18997 | hp1 | a0003 | c0005 | t0018 | g0325 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18997 | hp2 | a0001 | c0001 | t0006 | g0188 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18998 | hp1 | a0001 | c0001 | t0009 | g0224 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18998 | hp2 | a0001 | c0001 | t0172 | g0060 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18999 | hp1 | a0001 | c0001 | t0030 | g0210 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18999 | hp2 | a0001 | c0001 | t0037 | g0045 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19000 | hp2 | a0001 | c0001 | t0036 | g0092 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19001 | hp1 | a0001 | c0001 | t0062 | g0028 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19001 | hp2 | a0001 | c0001 | t0108 | g0201 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19003 | hp1 | a0001 | c0001 | t0002 | g0057 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19003 | hp2 | a0001 | c0001 | t0010 | g0358 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0119 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19004 | hp2 | a0002 | c0002 | t0006 | g0002 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0136 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19005 | hp2 | a0001 | c0001 | t0040 | g0252 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19009 | hp1 | a0002 | c0002 | t0048 | g0218 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19009 | hp2 | a0001 | c0001 | t0013 | g0171 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19011 | hp1 | a0001 | c0001 | t0056 | g0173 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19011 | hp2 | a0001 | c0001 | t0159 | g0069 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19012 | hp1 | a0001 | c0001 | t0044 | g0302 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19012 | hp2 | a0001 | c0001 | t0044 | g0160 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19030 | hp1 | a0001 | c0001 | t0035 | g0022 | AFR | LWK | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19030 | hp2 | a0001 | c0001 | t0133 | g0313 | AFR | LWK | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19043 | hp1 | a0001 | c0001 | t0012 | g0106 | AFR | LWK | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19043 | hp2 | a0001 | c0001 | t0102 | g0341 | AFR | LWK | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19057 | hp1 | a0001 | c0001 | t0001 | g0121 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19057 | hp2 | a0001 | c0001 | t0019 | g0263 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19058 | hp1 | a0001 | c0001 | t0013 | g0182 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19058 | hp2 | a0001 | c0001 | t0020 | g0053 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19060 | hp1 | a0001 | c0001 | t0176 | g0087 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19060 | hp2 | a0001 | c0001 | t0021 | g0163 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19062 | hp1 | a0001 | c0001 | t0026 | g0114 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19062 | hp2 | a0001 | c0001 | t0164 | g0062 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19064 | hp1 | a0001 | c0001 | t0006 | g0001 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19066 | hp1 | a0001 | c0001 | t0028 | g0170 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19066 | hp2 | a0001 | c0001 | t0031 | g0306 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19067 | hp1 | a0001 | c0001 | t0166 | g0034 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19067 | hp2 | a0001 | c0001 | t0042 | g0112 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19068 | hp1 | a0001 | c0001 | t0020 | g0042 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19068 | hp2 | a0001 | c0001 | t0005 | g0328 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19070 | hp1 | a0001 | c0001 | t0088 | g0180 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19070 | hp2 | a0001 | c0001 | t0011 | g0262 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19074 | hp1 | a0001 | c0001 | t0022 | g0172 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19074 | hp2 | a0001 | c0001 | t0022 | g0291 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19080 | hp1 | a0001 | c0001 | t0049 | g0237 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19080 | hp2 | a0001 | c0001 | t0146 | g0078 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19081 | hp1 | a0001 | c0001 | t0050 | g0234 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19081 | hp2 | a0001 | c0001 | t0002 | g0029 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19083 | hp1 | a0001 | c0001 | t0126 | g0270 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19084 | hp2 | a0001 | c0001 | t0040 | g0249 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19087 | hp2 | a0001 | c0001 | t0136 | g0308 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19091 | hp1 | a0001 | c0001 | t0179 | g0257 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19240 | hp1 | a0001 | c0001 | t0009 | g0202 | AFR | YRI | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA19240 | hp2 | a0001 | c0001 | t0019 | g0278 | AFR | YRI | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA20129 | hp1 | a0001 | c0001 | t0009 | g0217 | AFR | ASW | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA20129 | hp2 | a0001 | c0001 | t0022 | g0321 | AFR | ASW | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA20752 | hp1 | a0001 | c0001 | t0003 | g0099 | EUR | TSI | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA20752 | hp2 | a0001 | c0001 | t0130 | g0267 | EUR | TSI | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA20905 | hp1 | a0001 | c0001 | t0082 | g0123 | SAS | GIH | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA20905 | hp2 | a0001 | c0001 | t0117 | g0304 | SAS | GIH | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02109 | hp1 | a0001 | c0001 | t0012 | g0102 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02109 | hp2 | a0001 | c0006 | t0097 | g0337 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02486 | hp1 | a0001 | c0001 | t0019 | g0277 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02486 | hp2 | a0001 | c0001 | t0023 | g0284 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02559 | hp1 | a0001 | c0001 | t0007 | g0253 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG02559 | hp2 | a0001 | c0001 | t0054 | g0105 | AFR | ACB | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03471 | hp1 | a0001 | c0001 | t0090 | g0285 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG03471 | hp2 | a0001 | c0001 | t0045 | g0332 | AFR | MSL | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG06807 | hp1 | a0001 | c0001 | t0129 | g0083 | AFR | USA | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
HG06807 | hp2 | a0001 | c0001 | t0057 | g0314 | AFR | USA | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18955 | hp1 | a0001 | c0001 | t0076 | g0186 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA18955 | hp2 | a0001 | c0001 | t0008 | g0064 | EAS | JPT | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA20300 | hp1 | a0001 | c0001 | t0010 | g0221 | AFR | USA | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA20300 | hp2 | a0001 | c0001 | t0113 | g0103 | AFR | USA | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA21309 | hp1 | a0001 | c0003 | t0061 | g0096 | AFR | LWK | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
NA21309 | hp2 | a0001 | c0001 | t0003 | g0006 | AFR | LWK | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0101 | g0203 | REF | REF | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0077 | REF | REF | SNX27_chr1_151607050_151704080 | SNX27 | chr1 | 151607050 | 151704080 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:151660833
|
A | G | 1 | a0002 | 6 | NA18941.hp1 NA18947.hp2 NA18954.hp1 others(3): Show |
missense_variant | MODERATE | c.772A>G | p.Met258Val | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 4/12 | 924/6441 | 772/1626 | 258/541 | chr1 | 151660833 | ||
chr1:151693022
|
A | T | 1 | a0003 | 1 | NA18997.hp1 | stop_gained | HIGH | c.1501A>T | p.Lys501* | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 10/12 | 1653/6441 | 1501/1626 | 501/541 | chr1 | 151693022 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:151612219
|
G | A | 1 | a0001c0003 | 2 | HG02895.hp2 NA21309.hp1 |
synonymous_variant | LOW | c.18G>A | p.Gly6Gly | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/12 | 170/6441 | 18/1626 | 6/541 | chr1 | 151612219 | ||
chr1:151662183
|
C | T | 1 | a0001c0007 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.819C>T | p.Ser273Ser | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/12 | 971/6441 | 819/1626 | 273/541 | chr1 | 151662183 | ||
chr1:151666010
|
T | C | 1 | a0001c0004 | 2 | HG02717.hp2 HG02970.hp2 |
splice_region_variant&synonymous_variant | LOW | c.984T>C | p.Phe328Phe | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/12 | 1136/6441 | 984/1626 | 328/541 | chr1 | 151666010 | ||
chr1:151683361
|
C | T | 1 | a0001c0006 | 1 | HG02109.hp2 | synonymous_variant | LOW | c.1155C>T | p.Val385Val | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/12 | 1307/6441 | 1155/1626 | 385/541 | chr1 | 151683361 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:151612124
|
G | A | 1 | a0001c0001t0066 | 1 | HG02165.hp1 | 5_prime_UTR_variant | MODIFIER | c.-78G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/12 | 78 | chr1 | 151612124 | |||||
chr1:151612151
|
G | A | 1 | a0001c0001t0067 | 1 | HG02723.hp2 | 5_prime_UTR_variant | MODIFIER | c.-51G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/12 | 51 | chr1 | 151612151 | |||||
chr1:151694519
|
T | TA | 6 | a0001c0001t0024a0001c0001t0039a0001c0001t0068others(3): Show | 10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*105dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 106 | INFO_REALIGN_3_PRIME | chr1 | 151694519 | ||||
chr1:151694718
|
C | T | 1 | a0001c0001t0179 | 1 | NA19091.hp1 | 3_prime_UTR_variant | MODIFIER | c.*301C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 301 | chr1 | 151694718 | |||||
chr1:151694941
|
T | C | 1 | a0001c0001t0040 | 2 | NA19005.hp2 NA19084.hp2 |
3_prime_UTR_variant | MODIFIER | c.*524T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 524 | chr1 | 151694941 | |||||
chr1:151694948
|
G | A | 1 | a0001c0001t0071 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*531G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 531 | chr1 | 151694948 | |||||
chr1:151695136
|
G | A | 1 | a0001c0001t0072 | 1 | HG01975.hp2 | 3_prime_UTR_variant | MODIFIER | c.*719G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 719 | chr1 | 151695136 | |||||
chr1:151695242
|
A | G | 50 | a0001c0001t0002a0001c0001t0008a0001c0001t0020others(47): Show | 83 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(80): Show |
3_prime_UTR_variant | MODIFIER | c.*825A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 825 | chr1 | 151695242 | |||||
chr1:151695353
|
T | C | 1 | a0001c0001t0141 | 1 | HG02280.hp2 | 3_prime_UTR_variant | MODIFIER | c.*936T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 936 | chr1 | 151695353 | |||||
chr1:151695410
|
C | CT | 55 | a0001c0001t0008a0001c0001t0011a0001c0001t0015others(52): Show | 108 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(105): Show |
3_prime_UTR_variant | MODIFIER | c.*1019dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1020 | INFO_REALIGN_3_PRIME | chr1 | 151695410 | ||||
chr1:151695410
|
C | CTT | 14 | a0001c0001t0132a0001c0001t0133a0001c0001t0134others(11): Show | 14 | HG00741.hp2 HG02040.hp1 HG02148.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*1018_*1019dupTT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1020 | INFO_REALIGN_3_PRIME | chr1 | 151695410 | ||||
chr1:151695410
|
C | CTTTT | 11 | a0001c0001t0002a0001c0001t0037a0001c0001t0065others(8): Show | 26 | HG00408.hp2 HG00423.hp1 HG00597.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1016_*1019dupTTTT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1020 | INFO_REALIGN_3_PRIME | chr1 | 151695410 | ||||
chr1:151695410
|
CT | C | 10 | a0001c0001t0067a0001c0001t0073a0001c0001t0074others(7): Show | 11 | HG01168.hp2 HG02572.hp1 HG02698.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1019delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1019 | INFO_REALIGN_3_PRIME | chr1 | 151695410 | ||||
chr1:151695410
|
CTTTTTTT others(4): Show |
C | 2 | a0001c0001t0142a0001c0001t0143 | 2 | HG02451.hp2 HG02717.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1009_*1019delTTTT others(7): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1009 | INFO_REALIGN_3_PRIME | chr1 | 151695410 | ||||
chr1:151695449
|
C | G | 6 | a0001c0001t0035a0001c0001t0145a0001c0001t0150others(3): Show | 9 | HG02895.hp1 HG02895.hp2 HG02896.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1032C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1032 | chr1 | 151695449 | |||||
chr1:151695460
|
G | A | 1 | a0001c0001t0153 | 1 | HG03654.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1043G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1043 | chr1 | 151695460 | |||||
chr1:151695605
|
T | G | 39 | a0001c0001t0002a0001c0001t0008a0001c0001t0020others(36): Show | 69 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(66): Show |
3_prime_UTR_variant | MODIFIER | c.*1188T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1188 | chr1 | 151695605 | |||||
chr1:151695658
|
C | G | 2 | a0001c0001t0077a0001c0001t0078 | 2 | HG02970.hp1 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1241C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1241 | chr1 | 151695658 | |||||
chr1:151695819
|
A | C | 113 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(110): Show | 204 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*1402A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1402 | chr1 | 151695819 | |||||
chr1:151696003
|
A | G | 6 | a0001c0001t0045a0001c0001t0094a0001c0001t0095others(3): Show | 7 | HG02109.hp2 HG02145.hp2 HG02615.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1586A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1586 | chr1 | 151696003 | |||||
chr1:151696063
|
A | G | 5 | a0001c0001t0035a0001c0001t0145a0001c0001t0150others(2): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1646A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1646 | chr1 | 151696063 | |||||
chr1:151696097
|
T | C | 1 | a0001c0001t0079 | 1 | HG02040.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1680T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1680 | chr1 | 151696097 | |||||
chr1:151696219
|
C | T | 6 | a0001c0001t0023a0001c0001t0090a0001c0001t0091others(3): Show | 9 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*1802C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1802 | chr1 | 151696219 | |||||
chr1:151696258
|
G | A | 1 | a0001c0001t0098 | 1 | NA18980.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1841G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1841 | chr1 | 151696258 | |||||
chr1:151696371
|
T | A | 6 | a0001c0001t0012a0001c0001t0054a0001c0001t0080others(3): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1954T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 1954 | chr1 | 151696371 | |||||
chr1:151696461
|
T | TTTTC | 14 | a0001c0001t0020a0001c0001t0028a0001c0001t0037others(11): Show | 23 | HG00099.hp2 HG00408.hp1 HG00423.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2085_*2088dupTTTC | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696461 | ||||
chr1:151696461
|
T | TTTTCTTT others(1): Show |
12 | a0001c0001t0008a0001c0001t0022a0001c0001t0032others(9): Show | 25 | HG00741.hp2 HG01175.hp2 HG01433.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*2081_*2088dupTTTC others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696461 | ||||
chr1:151696461
|
T | TTTTCTTT others(5): Show |
6 | a0001c0001t0031a0001c0001t0036a0001c0001t0088others(3): Show | 10 | HG02148.hp2 HG02717.hp1 HG03942.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2077_*2088dupTTTC others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696461 | ||||
chr1:151696461
|
T | TTTTCTTT others(9): Show |
5 | a0001c0001t0058a0001c0001t0064a0001c0001t0118others(2): Show | 7 | HG00423.hp2 HG01255.hp1 HG01256.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2073_*2088dupTTTC others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696461 | ||||
chr1:151696461
|
T | TTTTCTTT others(13): Show |
1 | a0001c0001t0044 | 2 | NA19012.hp1 NA19012.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2069_*2088dupTTTC others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696461 | ||||
chr1:151696461
|
TTTTC | T | 14 | a0001c0001t0005a0001c0001t0013a0001c0001t0021others(11): Show | 34 | HG00408.hp2 HG00544.hp1 HG00544.hp2 others(31): Show |
3_prime_UTR_variant | MODIFIER | c.*2085_*2088delTTTC | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2085 | INFO_REALIGN_3_PRIME | chr1 | 151696461 | ||||
chr1:151696461
|
TTTTCTTT others(1): Show |
T | 11 | a0001c0001t0001a0001c0001t0003a0001c0001t0041others(8): Show | 36 | HG00280.hp1 HG00609.hp2 HG00741.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*2081_*2088delTTTC others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2081 | INFO_REALIGN_3_PRIME | chr1 | 151696461 | ||||
chr1:151696461
|
TTTTCTTT others(5): Show |
T | 1 | a0001c0001t0082 | 1 | NA20905.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2077_*2088delTTTC others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2077 | INFO_REALIGN_3_PRIME | chr1 | 151696461 | ||||
chr1:151696461
|
TTTTCTTT others(13): Show |
T | 1 | a0001c0001t0025 | 3 | HG00642.hp2 HG01256.hp1 HG01258.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2069_*2088delTTTC others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2069 | INFO_REALIGN_3_PRIME | chr1 | 151696461 | ||||
chr1:151696471
|
T | C | 1 | a0001c0001t0144 | 1 | HG02572.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2054T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2054 | chr1 | 151696471 | |||||
chr1:151696486
|
TTTCTTTC others(13): Show |
T | 1 | a0001c0001t0172 | 1 | NA18998.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2077_*2096delTTTC others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2077 | INFO_REALIGN_3_PRIME | chr1 | 151696486 | ||||
chr1:151696490
|
T | G | 2 | a0001c0001t0046a0001c0001t0047 | 4 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2073T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2073 | chr1 | 151696490 | |||||
chr1:151696490
|
T | TTTCTTTC others(1): Show |
5 | a0001c0001t0006a0001c0001t0076a0001c0001t0098others(2): Show | 11 | NA18946.hp2 NA18947.hp2 NA18951.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2080_*2081insGTTC others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2081 | INFO_REALIGN_3_PRIME | chr1 | 151696490 | ||||
chr1:151696490
|
T | TTTCTTTC others(9): Show |
1 | a0002c0002t0048 | 2 | NA18941.hp1 NA19009.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2080_*2081insGTTC others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2081 | INFO_REALIGN_3_PRIME | chr1 | 151696490 | ||||
chr1:151696494
|
T | G | 4 | a0001c0001t0012a0001c0001t0054a0001c0001t0113others(1): Show | 9 | HG02109.hp1 HG02155.hp1 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2077T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2077 | chr1 | 151696494 | |||||
chr1:151696494
|
TTTCTTTC others(5): Show |
T | 3 | a0001c0001t0057a0001c0001t0094a0001c0001t0133 | 4 | HG02056.hp1 HG02615.hp2 HG06807.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2085_*2096delTTTC others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2085 | INFO_REALIGN_3_PRIME | chr1 | 151696494 | ||||
chr1:151696498
|
T | G | 14 | a0001c0001t0006a0001c0001t0046a0001c0001t0047others(11): Show | 23 | HG00642.hp1 HG01074.hp1 HG01257.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*2081T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2081 | chr1 | 151696498 | |||||
chr1:151696498
|
T | TTTCG | 4 | a0001c0001t0019a0001c0001t0102a0001c0001t0141others(1): Show | 8 | HG02280.hp2 HG02486.hp1 HG03516.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2084_*2085insGTTC | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2085 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | ||||
chr1:151696498
|
T | TTTCGTTC others(5): Show |
4 | a0001c0001t0007a0001c0001t0033a0001c0001t0077others(1): Show | 12 | HG00735.hp1 HG00738.hp2 HG02148.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2084_*2085insGTTC others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2085 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | ||||
chr1:151696498
|
T | TTTCGTTC others(13): Show |
1 | a0001c0001t0101 | 1 | homoSapiens_chm13v2.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2084_*2085insGTTC others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2085 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | ||||
chr1:151696498
|
T | TTTCTTTC others(1): Show |
4 | a0001c0001t0010a0001c0001t0126a0001c0001t0156others(1): Show | 9 | HG01167.hp1 HG01261.hp1 HG01346.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2105_*2112dupGTTC others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2113 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | ||||
chr1:151696498
|
T | TTTCTTTC others(9): Show |
4 | a0001c0001t0009a0001c0001t0034a0001c0001t0050others(1): Show | 12 | HG01433.hp1 HG01515.hp1 HG02735.hp2 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*2097_*2112dupGTTC others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2113 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | ||||
chr1:151696498
|
T | TTTCTTTC others(17): Show |
3 | a0001c0001t0029a0001c0001t0049a0001c0001t0125 | 6 | HG00673.hp1 HG02273.hp1 HG03834.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2089_*2112dupGTTC others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2113 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | ||||
chr1:151696498
|
T | TTTCTTTC others(5): Show |
7 | a0001c0001t0023a0001c0001t0060a0001c0001t0109others(4): Show | 11 | HG00438.hp2 HG01175.hp1 HG02486.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | ||||
chr1:151696498
|
T | TTTCTTTC others(13): Show |
6 | a0001c0001t0030a0001c0001t0040a0001c0001t0059others(3): Show | 10 | HG01346.hp2 HG03098.hp2 HG03453.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | ||||
chr1:151696498
|
T | TTTCTTTC others(21): Show |
2 | a0001c0001t0107a0001c0001t0108 | 2 | NA18950.hp1 NA19001.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(24): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | ||||
chr1:151696498
|
T | TTTCTTTC others(29): Show |
1 | a0001c0001t0106 | 1 | NA18986.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(32): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | ||||
chr1:151696498
|
T | TTTCTTTC others(9): Show |
6 | a0001c0001t0092a0001c0001t0096a0001c0001t0110others(3): Show | 7 | HG02015.hp2 HG02300.hp1 HG02622.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | ||||
chr1:151696498
|
T | TTTCTTTC others(17): Show |
3 | a0001c0001t0014a0001c0001t0120a0001c0001t0131 | 7 | HG00280.hp2 HG01516.hp1 HG01978.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | ||||
chr1:151696498
|
T | TTTCTTTC others(25): Show |
2 | a0001c0001t0051a0001c0001t0052 | 4 | HG00323.hp1 NA18962.hp2 NA18979.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(28): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | ||||
chr1:151696498
|
T | TTTCTTTC others(13): Show |
1 | a0001c0001t0112 | 1 | NA18948.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | ||||
chr1:151696498
|
T | TTTCTTTC others(21): Show |
1 | a0001c0001t0053 | 2 | HG01081.hp2 NA18960.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(24): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | ||||
chr1:151696498
|
TTTCTTTC others(1): Show |
T | 2 | a0001c0001t0016a0001c0001t0045 | 7 | HG00323.hp2 HG00639.hp2 HG01099.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2105_*2112delGTTC others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2105 | INFO_REALIGN_3_PRIME | chr1 | 151696498 | ||||
chr1:151696502
|
T | G | 4 | a0001c0001t0012a0001c0001t0054a0001c0001t0113others(1): Show | 9 | HG02109.hp1 HG02155.hp1 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2085T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2085 | chr1 | 151696502 | |||||
chr1:151696502
|
TTTCG | T | 4 | a0001c0001t0017a0001c0001t0142a0001c0001t0160others(1): Show | 8 | HG01081.hp1 HG01192.hp1 HG01516.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2089_*2092delGTTC | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696502 | ||||
chr1:151696502
|
TTTCGTTC others(5): Show |
T | 2 | a0001c0001t0035a0001c0001t0145 | 4 | HG02895.hp1 HG02896.hp2 HG03486.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*2089_*2100delGTTC others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696502 | ||||
chr1:151696502
|
TTTCGTTC others(13): Show |
T | 1 | a0001c0001t0151 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2089_*2108delGTTC others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | INFO_REALIGN_3_PRIME | chr1 | 151696502 | ||||
chr1:151696505
|
C | CTTTCTTT others(9): Show |
1 | a0001c0001t0139 | 1 | HG02647.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2088_*2089insTTTC others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | chr1 | 151696505 | |||||
chr1:151696506
|
G | T | 17 | a0001c0001t0012a0001c0001t0018a0001c0001t0032others(14): Show | 27 | HG00423.hp2 HG01175.hp2 HG02055.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*2089G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2089 | chr1 | 151696506 | |||||
chr1:151696506
|
GTTCTTTC others(17): Show |
G | 1 | a0001c0001t0150 | 1 | HG02965.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2097_*2120delGTTC others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2097 | INFO_REALIGN_3_PRIME | chr1 | 151696506 | ||||
chr1:151696510
|
T | G | 4 | a0001c0001t0012a0001c0001t0054a0001c0001t0113others(1): Show | 9 | HG02109.hp1 HG02155.hp1 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2093T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2093 | chr1 | 151696510 | |||||
chr1:151696514
|
G | A | 2 | a0001c0001t0103a0001c0001t0124 | 2 | HG00639.hp1 HG01168.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2097G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2097 | chr1 | 151696514 | |||||
chr1:151696514
|
G | T | 4 | a0001c0001t0012a0001c0001t0054a0001c0001t0113others(1): Show | 9 | HG02109.hp1 HG02155.hp1 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2097G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2097 | chr1 | 151696514 | |||||
chr1:151696514
|
GTTCTTTC others(9): Show |
G | 1 | a0001c0001t0152 | 1 | HG03041.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2105_*2120delGTTC others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2105 | INFO_REALIGN_3_PRIME | chr1 | 151696514 | ||||
chr1:151696518
|
T | G | 4 | a0001c0001t0012a0001c0001t0054a0001c0001t0113others(1): Show | 9 | HG02109.hp1 HG02155.hp1 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2101T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2101 | chr1 | 151696518 | |||||
chr1:151696522
|
G | GTTCT | 9 | a0001c0001t0019a0001c0001t0060a0001c0001t0069others(6): Show | 14 | HG02129.hp2 HG02257.hp2 HG02486.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*2126_*2129dupTTCT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2130 | INFO_REALIGN_3_PRIME | chr1 | 151696522 | ||||
chr1:151696522
|
G | GTTCTTTC others(5): Show |
6 | a0001c0001t0011a0001c0001t0070a0001c0001t0103others(3): Show | 11 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*2112_*2113insGTTC others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2113 | INFO_REALIGN_3_PRIME | chr1 | 151696522 | ||||
chr1:151696522
|
G | GTTCTTTC others(9): Show |
3 | a0001c0001t0078a0001c0001t0105a0001c0001t0127 | 3 | HG02258.hp1 HG02622.hp2 NA18906.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2112_*2113insGTTC others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2113 | INFO_REALIGN_3_PRIME | chr1 | 151696522 | ||||
chr1:151696522
|
G | T | 14 | a0001c0001t0012a0001c0001t0031a0001c0001t0035others(11): Show | 24 | HG02109.hp1 HG02155.hp1 HG02258.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*2105G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2105 | chr1 | 151696522 | |||||
chr1:151696522
|
GTTCT | G | 3 | a0001c0001t0013a0001c0001t0043a0001c0001t0056 | 9 | NA18939.hp1 NA18944.hp2 NA18954.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2126_*2129delTTCT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2126 | INFO_REALIGN_3_PRIME | chr1 | 151696522 | ||||
chr1:151696526
|
T | G | 1 | a0001c0001t0100 | 1 | HG03239.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2109T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2109 | chr1 | 151696526 | |||||
chr1:151696530
|
T | G | 47 | a0001c0001t0002a0001c0001t0008a0001c0001t0020others(44): Show | 80 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(77): Show |
3_prime_UTR_variant | MODIFIER | c.*2113T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2113 | chr1 | 151696530 | |||||
chr1:151696651
|
G | GT | 6 | a0001c0001t0021a0001c0001t0042a0001c0001t0067others(3): Show | 10 | HG00280.hp1 HG00544.hp1 HG00738.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*2252dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2253 | INFO_REALIGN_3_PRIME | chr1 | 151696651 | ||||
chr1:151696651
|
GTTTT | G | 8 | a0001c0001t0040a0001c0001t0046a0001c0001t0049others(5): Show | 13 | HG01074.hp1 HG02004.hp2 NA18946.hp2 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*2249_*2252delTTTT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2249 | INFO_REALIGN_3_PRIME | chr1 | 151696651 | ||||
chr1:151696651
|
GTTTTT | G | 54 | a0001c0001t0006a0001c0001t0007a0001c0001t0009others(51): Show | 106 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(103): Show |
3_prime_UTR_variant | MODIFIER | c.*2248_*2252delTTTT others(1): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2248 | INFO_REALIGN_3_PRIME | chr1 | 151696651 | ||||
chr1:151696668
|
T | TTTTC | 43 | a0001c0001t0002a0001c0001t0008a0001c0001t0020others(40): Show | 74 | HG00408.hp2 HG00597.hp1 HG00609.hp1 others(71): Show |
3_prime_UTR_variant | MODIFIER | c.*2252_*2253insTTCT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2253 | INFO_REALIGN_3_PRIME | chr1 | 151696668 | ||||
chr1:151696668
|
T | TTTTTC | 6 | a0001c0001t0037a0001c0001t0147a0001c0001t0155others(3): Show | 8 | HG00423.hp1 HG00544.hp2 HG00741.hp2 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2252_*2253insTTTC others(1): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2253 | INFO_REALIGN_3_PRIME | chr1 | 151696668 | ||||
chr1:151696669
|
T | TTTTTTTC | 3 | a0001c0001t0012a0001c0001t0054a0001c0001t0080 | 8 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*2252_*2253insTTTT others(3): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2253 | chr1 | 151696669 | |||||
chr1:151696683
|
T | C | 1 | a0001c0001t0140 | 1 | HG03098.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2266T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2266 | chr1 | 151696683 | |||||
chr1:151696688
|
C | T | 4 | a0001c0001t0027a0001c0001t0041a0001c0001t0073others(1): Show | 7 | HG00735.hp2 HG00741.hp1 HG01167.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2271C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2271 | chr1 | 151696688 | |||||
chr1:151696966
|
C | T | 113 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(110): Show | 204 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*2549C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2549 | chr1 | 151696966 | |||||
chr1:151697079
|
C | A | 57 | a0001c0001t0006a0001c0001t0007a0001c0001t0009others(54): Show | 111 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*2662C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2662 | chr1 | 151697079 | |||||
chr1:151697215
|
T | G | 2 | a0001c0001t0163a0001c0001t0170 | 2 | HG02257.hp1 HG03130.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2798T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2798 | chr1 | 151697215 | |||||
chr1:151697225
|
TA | T | 32 | a0001c0001t0002a0001c0001t0008a0001c0001t0020others(29): Show | 62 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*2811delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 2811 | INFO_REALIGN_3_PRIME | chr1 | 151697225 | ||||
chr1:151697521
|
C | A | 119 | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(116): Show | 215 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*3104C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 3104 | chr1 | 151697521 | |||||
chr1:151697614
|
G | A | 1 | a0001c0001t0081 | 1 | HG02129.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3197G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 3197 | chr1 | 151697614 | |||||
chr1:151697912
|
G | A | 1 | a0001c0001t0110 | 1 | HG02622.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3495G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 3495 | chr1 | 151697912 | |||||
chr1:151698114
|
CAG | C | 49 | a0001c0001t0002a0001c0001t0008a0001c0001t0020others(46): Show | 82 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*3698_*3699delAG | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 3698 | chr1 | 151698114 | |||||
chr1:151698123
|
A | C | 1 | a0001c0001t0175 | 1 | HG02071.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3706A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 3706 | chr1 | 151698123 | |||||
chr1:151698210
|
C | G | 4 | a0001c0001t0156a0001c0001t0158a0001c0001t0163others(1): Show | 4 | HG02257.hp1 HG02451.hp1 HG03130.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3793C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 3793 | chr1 | 151698210 | |||||
chr1:151698377
|
C | T | 5 | a0001c0001t0035a0001c0001t0145a0001c0001t0150others(2): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3960C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 3960 | chr1 | 151698377 | |||||
chr1:151698751
|
G | A | 43 | a0001c0001t0002a0001c0001t0008a0001c0001t0020others(40): Show | 73 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*4334G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 4334 | chr1 | 151698751 | |||||
chr1:151698879
|
T | C | 7 | a0001c0001t0001a0001c0001t0026a0001c0001t0055others(4): Show | 22 | HG00408.hp1 HG00609.hp2 HG02132.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*4462T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 12/12 | 4462 | chr1 | 151698879 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:151612549
|
G | A | 1 | a0001c0001t0003g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.311+37G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151612549 | ||||||
chr1:151612774
|
C | G | 1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.311+262C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151612774 | ||||||
chr1:151612841
|
T | G | 1 | a0001c0001t0109g0007 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.311+329T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151612841 | ||||||
chr1:151612890
|
G | A | 1 | a0001c0001t0009g0008 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.311+378G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151612890 | ||||||
chr1:151612981
|
C | G | 2 | a0001c0001t0143g0359a0001c0001t0156g0360 | 2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.311+469C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151612981 | ||||||
chr1:151613067
|
C | T | 1 | a0001c0001t0010g0358 | 1 | NA19003.hp2 | intron_variant | MODIFIER | c.311+555C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151613067 | ||||||
chr1:151613332
|
C | T | 9 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(6): Show | 10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.311+820C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151613332 | ||||||
chr1:151613742
|
C | T | 7 | a0001c0001t0027g0343a0001c0001t0027g0347a0001c0001t0027g0348others(4): Show | 7 | HG00735.hp2 HG00741.hp1 HG01167.hp2 others(4): Show |
intron_variant | MODIFIER | c.311+1230C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151613742 | ||||||
chr1:151613852
|
G | C | 2 | a0001c0001t0002g0010a0001c0001t0081g0009 | 2 | HG02129.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.311+1340G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151613852 | ||||||
chr1:151613895
|
T | C | 1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.311+1383T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151613895 | ||||||
chr1:151613898
|
C | T | 1 | a0001c0001t0004g0342 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.311+1386C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151613898 | ||||||
chr1:151613919
|
C | T | 1 | a0001c0001t0102g0341 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.311+1407C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151613919 | ||||||
chr1:151613948
|
A | AATTTT | 273 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(270): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.311+1438_311+1442d others(7): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151613948 | |||||
chr1:151614064
|
T | C | 9 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(6): Show | 10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.311+1552T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151614064 | ||||||
chr1:151614178
|
A | G | 2 | a0001c0003t0061g0096a0001c0003t0061g0097 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.311+1666A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151614178 | ||||||
chr1:151614442
|
G | C | 2 | a0001c0003t0061g0096a0001c0003t0061g0097 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.311+1930G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151614442 | ||||||
chr1:151614564
|
C | T | 1 | a0001c0001t0021g0340 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.311+2052C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151614564 | ||||||
chr1:151614709
|
T | G | 3 | a0001c0001t0003g0098a0001c0001t0003g0099a0001c0001t0003g0100 | 3 | HG01934.hp1 HG02738.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.311+2197T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151614709 | ||||||
chr1:151614772
|
A | C | 2 | a0001c0001t0123g0339a0001c0001t0137g0338 | 2 | HG02738.hp2 HG04115.hp1 |
intron_variant | MODIFIER | c.311+2260A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151614772 | ||||||
chr1:151615327
|
G | C | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.311+2815G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151615327 | ||||||
chr1:151615404
|
G | A | 1 | a0001c0001t0143g0359 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.311+2892G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151615404 | ||||||
chr1:151615437
|
T | C | 1 | a0001c0001t0099g0101 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.311+2925T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151615437 | ||||||
chr1:151615773
|
G | A | 9 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(6): Show | 9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.311+3261G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151615773 | ||||||
chr1:151615803
|
T | A | 286 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(283): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.311+3291T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151615803 | ||||||
chr1:151616151
|
G | A | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.311+3639G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151616151 | ||||||
chr1:151616259
|
G | A | 87 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(84): Show | 87 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(84): Show |
intron_variant | MODIFIER | c.311+3747G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151616259 | ||||||
chr1:151616339
|
A | G | 148 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.311+3827A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151616339 | ||||||
chr1:151616441
|
T | A | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.311+3929T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151616441 | ||||||
chr1:151616678
|
A | G | 2 | a0001c0001t0010g0280a0001c0001t0102g0341 | 2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.311+4166A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151616678 | ||||||
chr1:151616887
|
G | A | 5 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(2): Show | 6 | NA18951.hp1 NA18955.hp1 NA18975.hp1 others(3): Show |
intron_variant | MODIFIER | c.311+4375G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151616887 | ||||||
chr1:151616938
|
C | T | 2 | a0001c0003t0061g0096a0001c0003t0061g0097 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.311+4426C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151616938 | ||||||
chr1:151617219
|
C | A | 2 | a0001c0003t0061g0096a0001c0003t0061g0097 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.311+4707C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617219 | ||||||
chr1:151617263
|
T | TTTTA | 25 | a0001c0001t0011g0276a0001c0001t0019g0277a0001c0001t0019g0278others(22): Show | 25 | HG00639.hp1 HG00642.hp2 HG01168.hp1 others(22): Show |
intron_variant | MODIFIER | c.311+4780_311+4783d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151617263 | |||||
chr1:151617263
|
TTTTA | T | 6 | a0001c0001t0046g0190a0001c0001t0046g0192a0001c0001t0047g0191others(3): Show | 6 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.311+4780_311+4783d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151617263 | |||||
chr1:151617364
|
C | T | 1 | a0001c0001t0142g0023 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.311+4852C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617364 | ||||||
chr1:151617371
|
C | A | 1 | a0001c0001t0003g0111 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.311+4859C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617371 | ||||||
chr1:151617373
|
G | C | 1 | a0001c0001t0014g0194 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.311+4861G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617373 | ||||||
chr1:151617535
|
C | T | 1 | a0001c0004t0038g0357 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.311+5023C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617535 | ||||||
chr1:151617589
|
G | T | 3 | a0001c0001t0005g0328a0001c0001t0015g0329a0001c0001t0135g0330 | 3 | HG02129.hp1 NA18950.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.311+5077G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617589 | ||||||
chr1:151617730
|
A | G | 1 | a0001c0001t0004g0184 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.311+5218A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617730 | ||||||
chr1:151617803
|
T | C | 2 | a0001c0001t0143g0359a0001c0001t0156g0360 | 2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.311+5291T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617803 | ||||||
chr1:151617834
|
G | A | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.311+5322G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617834 | ||||||
chr1:151617878
|
G | GT | 9 | a0001c0001t0013g0182a0001c0001t0013g0183a0001c0001t0036g0092others(6): Show | 9 | HG02083.hp2 HG02165.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.311+5389dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151617878 | |||||
chr1:151617878
|
GT | G | 33 | a0001c0001t0003g0100a0001c0001t0004g0156a0001c0001t0004g0158others(30): Show | 33 | HG00099.hp1 HG00323.hp2 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.311+5389delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151617878 | |||||
chr1:151617878
|
GTT | G | 129 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(126): Show | 130 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(127): Show |
intron_variant | MODIFIER | c.311+5388_311+5389d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151617878 | |||||
chr1:151617878
|
GTTT | G | 100 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(97): Show | 103 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(100): Show |
intron_variant | MODIFIER | c.311+5387_311+5389d others(5): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151617878 | |||||
chr1:151617878
|
GTTTT | G | 13 | a0001c0001t0009g0196a0001c0001t0012g0102a0001c0001t0012g0104others(10): Show | 13 | HG01515.hp1 HG02109.hp1 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.311+5386_311+5389d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151617878 | |||||
chr1:151617880
|
T | A | 1 | a0001c0001t0042g0112 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.311+5368T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617880 | ||||||
chr1:151617887
|
T | G | 9 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(6): Show | 10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.311+5375T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617887 | ||||||
chr1:151617889
|
T | G | 9 | a0001c0001t0023g0003a0001c0001t0023g0284a0001c0001t0023g0286others(6): Show | 9 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.311+5377T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617889 | ||||||
chr1:151617967
|
C | G | 5 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.311+5455C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151617967 | ||||||
chr1:151618131
|
G | T | 4 | a0001c0001t0141g0013a0001c0001t0148g0016a0001c0001t0149g0015others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.311+5619G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151618131 | ||||||
chr1:151618177
|
A | G | 7 | a0001c0001t0045g0288a0001c0001t0045g0332a0001c0001t0094g0336others(4): Show | 7 | HG02109.hp2 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.311+5665A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151618177 | ||||||
chr1:151618258
|
A | G | 16 | a0001c0001t0023g0003a0001c0001t0023g0284a0001c0001t0023g0286others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.311+5746A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151618258 | ||||||
chr1:151618473
|
CT | C | 5 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.311+5962delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151618473 | ||||||
chr1:151618564
|
A | G | 1 | a0001c0001t0126g0270 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.311+6052A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151618564 | ||||||
chr1:151618588
|
G | A | 1 | a0001c0001t0030g0198 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.311+6076G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151618588 | ||||||
chr1:151618885
|
C | T | 1 | a0001c0001t0023g0331 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.311+6373C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151618885 | ||||||
chr1:151618935
|
G | C | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.311+6423G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151618935 | ||||||
chr1:151619011
|
C | CA | 7 | a0001c0001t0001g0113a0001c0001t0003g0116a0001c0001t0026g0114others(4): Show | 7 | HG00609.hp2 HG02129.hp2 HG03831.hp1 others(4): Show |
intron_variant | MODIFIER | c.311+6511dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151619011 | |||||
chr1:151619011
|
CA | C | 108 | a0001c0001t0003g0099a0001c0001t0006g0001a0001c0001t0006g0188others(105): Show | 111 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(108): Show |
intron_variant | MODIFIER | c.311+6511delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151619011 | |||||
chr1:151619158
|
T | A | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.311+6646T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151619158 | ||||||
chr1:151619295
|
C | G | 2 | a0001c0001t0017g0322a0001c0001t0017g0323 | 2 | NA18612.hp1 NA18980.hp2 |
intron_variant | MODIFIER | c.311+6783C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151619295 | ||||||
chr1:151619308
|
T | C | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.311+6796T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151619308 | ||||||
chr1:151619753
|
T | G | 1 | a0001c0001t0069g0352 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.311+7241T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151619753 | ||||||
chr1:151620212
|
G | A | 1 | a0001c0001t0002g0029 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.311+7700G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151620212 | ||||||
chr1:151620231
|
A | G | 1 | a0001c0001t0042g0112 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.311+7719A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151620231 | ||||||
chr1:151620422
|
T | C | 1 | a0001c0003t0061g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.311+7910T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151620422 | ||||||
chr1:151620425
|
T | C | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.311+7913T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151620425 | ||||||
chr1:151620512
|
G | GT | 112 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(109): Show | 115 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.311+8001dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151620512 | |||||
chr1:151620694
|
C | CT | 103 | a0001c0001t0001g0113a0001c0001t0001g0118a0001c0001t0001g0119others(100): Show | 103 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(100): Show |
intron_variant | MODIFIER | c.311+8195dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151620694 | |||||
chr1:151620694
|
C | CTT | 112 | a0001c0001t0004g0184a0001c0001t0005g0154a0001c0001t0006g0001others(109): Show | 115 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.311+8194_311+8195d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151620694 | |||||
chr1:151620758
|
C | T | 5 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0029g0244others(2): Show | 5 | HG00280.hp2 HG01081.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.311+8246C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151620758 | ||||||
chr1:151620804
|
C | T | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.311+8292C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151620804 | ||||||
chr1:151620983
|
C | T | 20 | a0001c0001t0011g0243a0001c0001t0011g0262a0001c0001t0011g0264others(17): Show | 20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.311+8471C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151620983 | ||||||
chr1:151621039
|
G | A | 1 | a0001c0001t0015g0289 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.311+8527G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151621039 | ||||||
chr1:151621068
|
A | G | 1 | a0001c0001t0140g0093 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.311+8556A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151621068 | ||||||
chr1:151621196
|
A | C | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.311+8684A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151621196 | ||||||
chr1:151621737
|
T | G | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.311+9225T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151621737 | ||||||
chr1:151621807
|
G | C | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.311+9295G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151621807 | ||||||
chr1:151622052
|
C | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | NA19000.hp1 NA19004.hp1 |
intron_variant | MODIFIER | c.311+9540C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151622052 | ||||||
chr1:151622078
|
A | G | 1 | a0001c0001t0139g0259 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.311+9566A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151622078 | ||||||
chr1:151622335
|
A | T | 3 | a0001c0001t0018g0315a0001c0001t0057g0314a0001c0001t0133g0313 | 3 | HG02055.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.311+9823A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151622335 | ||||||
chr1:151622499
|
T | G | 2 | a0001c0001t0009g0202a0001c0001t0014g0194 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.311+9987T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151622499 | ||||||
chr1:151622589
|
A | G | 1 | a0001c0001t0003g0153 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.311+10077A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151622589 | ||||||
chr1:151622744
|
A | G | 7 | a0001c0001t0104g0081a0001c0001t0105g0082a0001c0001t0127g0084others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.311+10232A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151622744 | ||||||
chr1:151622859
|
G | A | 1 | a0001c0001t0095g0334 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.311+10347G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151622859 | ||||||
chr1:151623153
|
T | A | 338 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(335): Show | 342 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(339): Show |
intron_variant | MODIFIER | c.311+10641T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623153 | ||||||
chr1:151623155
|
T | A | 13 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(10): Show | 13 | HG02004.hp2 HG02129.hp2 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.311+10643T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623155 | ||||||
chr1:151623181
|
G | A | 5 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0120others(2): Show | 5 | NA18971.hp2 NA19000.hp1 NA19004.hp1 others(2): Show |
intron_variant | MODIFIER | c.311+10669G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623181 | ||||||
chr1:151623224
|
T | C | 3 | a0001c0001t0018g0315a0001c0001t0057g0314a0001c0001t0133g0313 | 3 | HG02055.hp1 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.311+10712T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623224 | ||||||
chr1:151623265
|
C | T | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.311+10753C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623265 | ||||||
chr1:151623292
|
C | T | 1 | a0001c0001t0167g0074 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.311+10780C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623292 | ||||||
chr1:151623308
|
T | A | 1 | a0001c0001t0093g0281 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.311+10796T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623308 | ||||||
chr1:151623319
|
T | G | 16 | a0001c0001t0023g0003a0001c0001t0023g0284a0001c0001t0023g0286others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.311+10807T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623319 | ||||||
chr1:151623430
|
G | A | 20 | a0001c0001t0011g0243a0001c0001t0011g0262a0001c0001t0011g0264others(17): Show | 20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.311+10918G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623430 | ||||||
chr1:151623691
|
C | T | 1 | a0001c0001t0015g0312 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.311+11179C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623691 | ||||||
chr1:151623692
|
G | A | 1 | a0001c0001t0002g0030 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.311+11180G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623692 | ||||||
chr1:151623725
|
C | T | 1 | a0001c0001t0002g0073 | 1 | NA18963.hp1 | intron_variant | MODIFIER | c.311+11213C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623725 | ||||||
chr1:151623948
|
T | C | 1 | a0001c0001t0016g0324 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.311+11436T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623948 | ||||||
chr1:151623953
|
T | A | 2 | a0001c0001t0148g0016a0001c0001t0165g0014 | 2 | HG02145.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.311+11441T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623953 | ||||||
chr1:151623954
|
A | T | 273 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(270): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.311+11442A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151623954 | ||||||
chr1:151624219
|
G | C | 4 | a0001c0001t0010g0280a0001c0001t0077g0200a0001c0001t0078g0199others(1): Show | 4 | HG02886.hp1 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.311+11707G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624219 | ||||||
chr1:151624231
|
G | A | 1 | a0001c0001t0115g0290 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.311+11719G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624231 | ||||||
chr1:151624245
|
A | C | 9 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(6): Show | 10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.311+11733A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624245 | ||||||
chr1:151624409
|
T | TTA | 41 | a0001c0001t0001g0119a0001c0001t0002g0033a0001c0001t0004g0342others(38): Show | 41 | HG00438.hp1 HG00639.hp1 HG00673.hp1 others(38): Show |
intron_variant | MODIFIER | c.311+11919_311+1192 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151624409 | |||||
chr1:151624409
|
T | TTATA | 45 | a0001c0001t0005g0328a0001c0001t0010g0280a0001c0001t0011g0243others(42): Show | 47 | HG00423.hp2 HG00597.hp2 HG01081.hp1 others(44): Show |
intron_variant | MODIFIER | c.311+11917_311+1192 others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151624409 | |||||
chr1:151624409
|
T | TTATATA | 3 | a0001c0001t0017g0322a0001c0001t0057g0294a0001c0001t0060g0260 | 3 | HG02056.hp1 NA18612.hp1 NA18951.hp2 |
intron_variant | MODIFIER | c.311+11915_311+1192 others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151624409 | |||||
chr1:151624409
|
T | TTATATAT others(1): Show |
3 | a0001c0001t0018g0292a0001c0001t0022g0291a0001c0001t0032g0293 | 3 | HG02132.hp2 NA18943.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.311+11913_311+1192 others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151624409 | |||||
chr1:151624409
|
T | TTATATAT others(3): Show |
4 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(1): Show | 4 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(1): Show |
intron_variant | MODIFIER | c.311+11911_311+1192 others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151624409 | |||||
chr1:151624409
|
T | TTATATAT others(5): Show |
2 | a0001c0001t0070g0353a0001c0001t0137g0338 | 2 | HG02615.hp1 HG04115.hp1 |
intron_variant | MODIFIER | c.311+11909_311+1192 others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151624409 | |||||
chr1:151624409
|
TTA | T | 78 | a0001c0001t0003g0006a0001c0001t0003g0098a0001c0001t0003g0099others(75): Show | 78 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(75): Show |
intron_variant | MODIFIER | c.311+11919_311+1192 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151624409 | |||||
chr1:151624431
|
A | G | 3 | a0001c0001t0003g0100a0001c0001t0028g0170a0001c0001t0067g0361 | 3 | HG02723.hp2 HG02738.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.311+11919A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624431 | ||||||
chr1:151624433
|
G | A | 6 | a0001c0001t0001g0118a0001c0001t0003g0100a0001c0001t0028g0170others(3): Show | 6 | HG02723.hp2 HG02738.hp1 HG02738.hp2 others(3): Show |
intron_variant | MODIFIER | c.311+11921G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624433 | ||||||
chr1:151624434
|
TA | T | 3 | a0001c0001t0003g0100a0001c0001t0028g0170a0001c0001t0067g0361 | 3 | HG02723.hp2 HG02738.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.311+11923delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624434 | ||||||
chr1:151624435
|
A | AT | 12 | a0001c0001t0018g0315a0001c0001t0019g0269a0001c0001t0035g0022others(9): Show | 12 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(9): Show |
intron_variant | MODIFIER | c.311+11937dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151624435 | |||||
chr1:151624435
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0123g0339 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.311+11924_311+1192 others(17): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151624435 | |||||
chr1:151624512
|
A | G | 1 | a0001c0001t0032g0293 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.311+12000A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624512 | ||||||
chr1:151624618
|
G | A | 78 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(75): Show | 80 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.311+12106G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624618 | ||||||
chr1:151624683
|
C | T | 1 | a0001c0001t0071g0152 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.311+12171C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624683 | ||||||
chr1:151624744
|
T | C | 1 | a0001c0001t0022g0291 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.311+12232T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151624744 | ||||||
chr1:151625003
|
T | C | 1 | a0001c0001t0141g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.311+12491T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625003 | ||||||
chr1:151625169
|
G | A | 1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.311+12657G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625169 | ||||||
chr1:151625184
|
G | C | 90 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.311+12672G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625184 | ||||||
chr1:151625185
|
T | C | 132 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(129): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.311+12673T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625185 | ||||||
chr1:151625220
|
G | C | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.311+12708G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625220 | ||||||
chr1:151625276
|
G | A | 1 | a0001c0001t0149g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.311+12764G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625276 | ||||||
chr1:151625277
|
C | G | 1 | a0001c0001t0149g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.311+12765C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625277 | ||||||
chr1:151625277
|
C | T | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.311+12765C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625277 | ||||||
chr1:151625278
|
G | T | 1 | a0001c0001t0149g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.311+12766G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625278 | ||||||
chr1:151625279
|
G | A | 1 | a0001c0001t0149g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.311+12767G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625279 | ||||||
chr1:151625287
|
C | G | 148 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.311+12775C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625287 | ||||||
chr1:151625463
|
G | A | 2 | a0001c0003t0061g0096a0001c0003t0061g0097 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.311+12951G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625463 | ||||||
chr1:151625515
|
A | G | 20 | a0001c0001t0011g0243a0001c0001t0011g0262a0001c0001t0011g0264others(17): Show | 20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.311+13003A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625515 | ||||||
chr1:151625708
|
C | T | 1 | a0001c0001t0132g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.312-13180C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151625708 | ||||||
chr1:151625784
|
C | CA | 34 | a0001c0001t0001g0118a0001c0001t0007g0214a0001c0001t0007g0253others(31): Show | 34 | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(31): Show |
intron_variant | MODIFIER | c.312-13087dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151625784 | |||||
chr1:151625846
|
G | GC | 3 | a0001c0001t0029g0205a0001c0001t0059g0251a0001c0001t0125g0204 | 3 | HG00673.hp1 NA18961.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.312-13041dupC | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151625846 | |||||
chr1:151626019
|
C | T | 2 | a0001c0001t0143g0359a0001c0001t0156g0360 | 2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.312-12869C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151626019 | ||||||
chr1:151626204
|
G | C | 1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.312-12684G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151626204 | ||||||
chr1:151626265
|
CT | C | 21 | a0001c0001t0011g0243a0001c0001t0011g0262a0001c0001t0011g0264others(18): Show | 21 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.312-12611delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151626265 | |||||
chr1:151626277
|
TG | T | 8 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(5): Show | 8 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.312-12610delG | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151626277 | ||||||
chr1:151626278
|
G | T | 4 | a0001c0001t0012g0110a0001c0001t0067g0361a0001c0001t0132g0195others(1): Show | 4 | HG02647.hp1 HG02723.hp2 HG03225.hp2 others(1): Show |
intron_variant | MODIFIER | c.312-12610G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151626278 | ||||||
chr1:151626283
|
T | C | 9 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(6): Show | 9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.312-12605T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151626283 | ||||||
chr1:151626479
|
T | G | 1 | a0001c0001t0022g0291 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.312-12409T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151626479 | ||||||
chr1:151626607
|
C | T | 78 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(75): Show | 80 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.312-12281C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151626607 | ||||||
chr1:151626680
|
C | T | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.312-12208C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151626680 | ||||||
chr1:151626699
|
C | CTAAA | 4 | a0001c0001t0129g0083a0001c0001t0144g0011a0001c0003t0061g0096others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.312-12163_312-1216 others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151626699 | |||||
chr1:151626699
|
C | CTAAATAA others(5): Show |
9 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(6): Show | 10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.312-12171_312-1216 others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151626699 | |||||
chr1:151626699
|
CTAAATAA others(1): Show |
C | 78 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(75): Show | 80 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.312-12167_312-1216 others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151626699 | |||||
chr1:151626791
|
G | T | 90 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.312-12097G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151626791 | ||||||
chr1:151627087
|
C | T | 1 | a0001c0001t0131g0242 | 1 | NA18983.hp2 | intron_variant | MODIFIER | c.312-11801C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151627087 | ||||||
chr1:151627396
|
G | T | 1 | a0001c0001t0012g0109 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.312-11492G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151627396 | ||||||
chr1:151627643
|
G | A | 2 | a0001c0001t0077g0200a0001c0001t0078g0199 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.312-11245G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151627643 | ||||||
chr1:151627719
|
C | T | 2 | a0001c0003t0061g0096a0001c0003t0061g0097 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.312-11169C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151627719 | ||||||
chr1:151627741
|
TGTTCTAT others(3): Show |
T | 90 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.312-11138_312-1112 others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151627741 | |||||
chr1:151627890
|
C | A | 1 | a0001c0001t0022g0291 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.312-10998C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151627890 | ||||||
chr1:151627890
|
C | T | 1 | a0001c0001t0165g0014 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.312-10998C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151627890 | ||||||
chr1:151627965
|
G | A | 273 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(270): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.312-10923G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151627965 | ||||||
chr1:151628006
|
G | GT | 12 | a0001c0001t0005g0154a0001c0001t0008g0071a0001c0001t0032g0299others(9): Show | 12 | HG00280.hp1 HG00544.hp2 HG01175.hp2 others(9): Show |
intron_variant | MODIFIER | c.312-10863dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151628006 | |||||
chr1:151628006
|
GT | G | 104 | a0001c0001t0002g0036a0001c0001t0004g0317a0001c0001t0006g0001others(101): Show | 107 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(104): Show |
intron_variant | MODIFIER | c.312-10863delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151628006 | |||||
chr1:151628151
|
C | T | 2 | a0001c0003t0061g0096a0001c0003t0061g0097 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.312-10737C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628151 | ||||||
chr1:151628155
|
C | T | 1 | a0001c0001t0011g0276 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.312-10733C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628155 | ||||||
chr1:151628264
|
A | G | 1 | a0001c0001t0132g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.312-10624A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628264 | ||||||
chr1:151628302
|
C | T | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.312-10586C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628302 | ||||||
chr1:151628347
|
A | G | 4 | a0001c0001t0014g0246a0001c0001t0014g0248a0001c0001t0053g0245others(1): Show | 4 | HG00280.hp2 HG01081.hp2 HG01516.hp1 others(1): Show |
intron_variant | MODIFIER | c.312-10541A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628347 | ||||||
chr1:151628578
|
T | C | 1 | a0001c0001t0060g0261 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.312-10310T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628578 | ||||||
chr1:151628579
|
A | G | 2 | a0001c0001t0018g0298a0001c0001t0118g0311 | 2 | HG00423.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.312-10309A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628579 | ||||||
chr1:151628596
|
C | T | 9 | a0001c0001t0023g0003a0001c0001t0023g0284a0001c0001t0023g0286others(6): Show | 9 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.312-10292C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628596 | ||||||
chr1:151628655
|
T | G | 1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.312-10233T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628655 | ||||||
chr1:151628669
|
G | T | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.312-10219G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628669 | ||||||
chr1:151628751
|
A | G | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.312-10137A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151628751 | ||||||
chr1:151628925
|
GTT | G | 3 | a0001c0001t0045g0288a0001c0001t0045g0332a0001c0001t0094g0336 | 3 | HG02615.hp2 HG03130.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.312-9960_312-9959d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151628925 | |||||
chr1:151629083
|
CT | C | 9 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(6): Show | 9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.312-9801delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629083 | |||||
chr1:151629203
|
T | C | 1 | a0001c0001t0132g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.312-9685T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629203 | ||||||
chr1:151629211
|
T | TTGTACTA others(2727): Show |
1 | a0001c0001t0012g0110 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.312-9664_312-9663i others(2736): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629211 | |||||
chr1:151629211
|
T | TTGTACTA others(2726): Show |
2 | a0001c0001t0012g0102a0001c0001t0080g0108 | 2 | HG02109.hp1 HG02976.hp2 |
intron_variant | MODIFIER | c.312-9664_312-9663i others(2735): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629211 | |||||
chr1:151629211
|
T | TTGTACTA others(2727): Show |
3 | a0001c0001t0012g0104a0001c0001t0012g0109a0001c0001t0113g0103 | 3 | HG02258.hp2 HG02280.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.312-9664_312-9663i others(2736): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629211 | |||||
chr1:151629211
|
T | TTGTACTA others(2726): Show |
2 | a0001c0001t0012g0106a0001c0001t0054g0105 | 2 | HG02559.hp2 NA19043.hp1 |
intron_variant | MODIFIER | c.312-9664_312-9663i others(2735): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629211 | |||||
chr1:151629211
|
T | TTGTACTA others(2727): Show |
1 | a0001c0001t0054g0107 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.312-9664_312-9663i others(2736): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629211 | |||||
chr1:151629256
|
A | G | 148 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.312-9632A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629256 | ||||||
chr1:151629385
|
C | T | 1 | a0001c0001t0004g0167 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.312-9503C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629385 | ||||||
chr1:151629402
|
C | T | 1 | a0001c0001t0034g0241 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.312-9486C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629402 | ||||||
chr1:151629451
|
G | A | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.312-9437G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629451 | ||||||
chr1:151629453
|
A | G | 78 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(75): Show | 80 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.312-9435A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629453 | ||||||
chr1:151629458
|
T | TAC | 23 | a0001c0001t0004g0342a0001c0001t0011g0243a0001c0001t0011g0262others(20): Show | 23 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(20): Show |
intron_variant | MODIFIER | c.312-9429_312-9428d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629458 | |||||
chr1:151629478
|
C | CAT | 19 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(16): Show | 19 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.312-9410_312-9409i others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629478 | ||||||
chr1:151629478
|
C | CGT | 261 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.312-9409_312-9408d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629478 | |||||
chr1:151629496
|
C | T | 112 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(109): Show | 115 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.312-9392C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629496 | ||||||
chr1:151629509
|
A | G | 1 | a0001c0001t0010g0240 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.312-9379A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629509 | ||||||
chr1:151629539
|
A | G | 90 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.312-9349A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629539 | ||||||
chr1:151629585
|
A | G | 1 | a0001c0001t0095g0334 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.312-9303A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629585 | ||||||
chr1:151629586
|
A | AT | 19 | a0001c0001t0002g0073a0001c0001t0003g0116a0001c0001t0005g0150others(16): Show | 19 | HG01192.hp2 HG02109.hp1 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.312-9287dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629586 | |||||
chr1:151629686
|
C | CGATTCTC others(7): Show |
1 | a0001c0001t0159g0069 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.312-9201_312-9188d others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151629686 | |||||
chr1:151629711
|
G | A | 1 | a0001c0001t0015g0296 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.312-9177G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629711 | ||||||
chr1:151629897
|
A | T | 107 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(104): Show | 107 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(104): Show |
intron_variant | MODIFIER | c.312-8991A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629897 | ||||||
chr1:151629899
|
A | T | 160 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(157): Show | 161 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(158): Show |
intron_variant | MODIFIER | c.312-8989A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151629899 | ||||||
chr1:151630030
|
G | A | 1 | a0001c0001t0013g0174 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.312-8858G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630030 | ||||||
chr1:151630110
|
C | CA | 114 | a0001c0001t0006g0001a0001c0001t0006g0189a0001c0001t0007g0214others(111): Show | 117 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(114): Show |
intron_variant | MODIFIER | c.312-8765dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151630110 | |||||
chr1:151630171
|
A | G | 286 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(283): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.312-8717A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630171 | ||||||
chr1:151630215
|
G | A | 1 | a0001c0001t0168g0037 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.312-8673G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630215 | ||||||
chr1:151630276
|
A | T | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.312-8612A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630276 | ||||||
chr1:151630298
|
T | G | 9 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(6): Show | 9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.312-8590T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630298 | ||||||
chr1:151630371
|
A | G | 1 | a0001c0001t0141g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.312-8517A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630371 | ||||||
chr1:151630711
|
A | G | 286 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(283): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.312-8177A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630711 | ||||||
chr1:151630755
|
C | T | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.312-8133C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630755 | ||||||
chr1:151630761
|
C | T | 78 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(75): Show | 80 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.312-8127C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630761 | ||||||
chr1:151630784
|
A | G | 9 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(6): Show | 10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.312-8104A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630784 | ||||||
chr1:151630860
|
C | T | 56 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(53): Show | 56 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(53): Show |
intron_variant | MODIFIER | c.312-8028C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630860 | ||||||
chr1:151630896
|
G | A | 1 | a0001c0001t0059g0206 | 1 | NA18992.hp1 | intron_variant | MODIFIER | c.312-7992G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630896 | ||||||
chr1:151630957
|
G | A | 9 | a0001c0001t0007g0216a0001c0001t0007g0253a0001c0001t0007g0255others(6): Show | 9 | HG00323.hp1 HG00735.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.312-7931G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151630957 | ||||||
chr1:151631027
|
G | A | 1 | a0001c0001t0060g0260 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.312-7861G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151631027 | ||||||
chr1:151631136
|
A | G | 10 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(7): Show | 10 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.312-7752A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151631136 | ||||||
chr1:151631197
|
TTCTAGTA | T | 5 | a0002c0002t0006g0002a0002c0002t0006g0197a0002c0002t0006g0250others(2): Show | 6 | NA18941.hp1 NA18947.hp2 NA18954.hp1 others(3): Show |
intron_variant | MODIFIER | c.312-7690_312-7684d others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151631197 | ||||||
chr1:151631284
|
T | A | 1 | a0001c0001t0004g0139 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.312-7604T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151631284 | ||||||
chr1:151631343
|
G | T | 20 | a0001c0001t0011g0243a0001c0001t0011g0262a0001c0001t0011g0264others(17): Show | 20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.312-7545G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151631343 | ||||||
chr1:151631461
|
A | G | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.312-7427A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151631461 | ||||||
chr1:151631512
|
G | T | 1 | a0001c0001t0162g0080 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.312-7376G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151631512 | ||||||
chr1:151631705
|
G | T | 2 | a0001c0001t0004g0166a0001c0001t0075g0165 | 2 | HG01168.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.312-7183G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151631705 | ||||||
chr1:151632024
|
A | G | 78 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(75): Show | 80 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.312-6864A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151632024 | ||||||
chr1:151632154
|
C | T | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.312-6734C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151632154 | ||||||
chr1:151632322
|
T | TTC | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.312-6566_312-6565i others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151632322 | ||||||
chr1:151632411
|
T | C | 272 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(269): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.312-6477T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151632411 | ||||||
chr1:151632502
|
A | G | 1 | a0001c0001t0114g0310 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.312-6386A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151632502 | ||||||
chr1:151632788
|
C | CTTTTCAC others(3): Show |
1 | a0001c0001t0062g0028 | 1 | NA19001.hp1 | intron_variant | MODIFIER | c.312-6099_312-6090d others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151632788 | |||||
chr1:151632810
|
C | A | 1 | a0001c0001t0095g0334 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.312-6078C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151632810 | ||||||
chr1:151632833
|
G | A | 1 | a0001c0001t0051g0215 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.312-6055G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151632833 | ||||||
chr1:151633052
|
C | T | 1 | a0001c0001t0132g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.312-5836C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633052 | ||||||
chr1:151633083
|
A | G | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.312-5805A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633083 | ||||||
chr1:151633086
|
A | G | 1 | a0001c0001t0134g0309 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.312-5802A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633086 | ||||||
chr1:151633161
|
C | T | 1 | a0001c0001t0068g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.312-5727C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633161 | ||||||
chr1:151633164
|
G | T | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.312-5724G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633164 | ||||||
chr1:151633215
|
A | G | 2 | a0001c0001t0077g0200a0001c0001t0078g0199 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.312-5673A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633215 | ||||||
chr1:151633372
|
C | T | 1 | a0001c0001t0015g0296 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.312-5516C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633372 | ||||||
chr1:151633399
|
G | A | 3 | a0001c0001t0004g0156a0001c0001t0004g0158a0001c0001t0015g0157 | 3 | HG01255.hp2 HG01257.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.312-5489G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633399 | ||||||
chr1:151633557
|
CCA | C | 132 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(129): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.312-5328_312-5327d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151633557 | |||||
chr1:151633644
|
CA | C | 17 | a0001c0001t0011g0243a0001c0001t0011g0262a0001c0001t0011g0264others(14): Show | 17 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(14): Show |
intron_variant | MODIFIER | c.312-5242delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151633644 | |||||
chr1:151633725
|
C | T | 1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.312-5163C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633725 | ||||||
chr1:151633901
|
T | A | 286 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(283): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.312-4987T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633901 | ||||||
chr1:151633929
|
G | A | 285 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(282): Show | 289 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(286): Show |
intron_variant | MODIFIER | c.312-4959G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633929 | ||||||
chr1:151633966
|
A | G | 273 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(270): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.312-4922A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633966 | ||||||
chr1:151633972
|
G | GT | 8 | a0001c0001t0002g0068a0001c0001t0003g0098a0001c0001t0003g0100others(5): Show | 8 | HG01934.hp1 HG02080.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.312-4904dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151633972 | |||||
chr1:151633974
|
T | G | 1 | a0001c0006t0097g0337 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.312-4914T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151633974 | ||||||
chr1:151634092
|
A | G | 1 | a0001c0001t0023g0284 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.312-4796A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151634092 | ||||||
chr1:151634435
|
A | G | 273 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(270): Show | 277 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
intron_variant | MODIFIER | c.312-4453A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151634435 | ||||||
chr1:151634601
|
T | C | 1 | a0001c0001t0003g0099 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.312-4287T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151634601 | ||||||
chr1:151634670
|
G | C | 9 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(6): Show | 9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.312-4218G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151634670 | ||||||
chr1:151634994
|
C | T | 2 | a0001c0001t0009g0202a0001c0001t0014g0194 | 2 | HG02886.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.312-3894C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151634994 | ||||||
chr1:151635292
|
C | A | 1 | a0001c0001t0005g0140 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.312-3596C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151635292 | ||||||
chr1:151635576
|
C | G | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.312-3312C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151635576 | ||||||
chr1:151635620
|
A | G | 112 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(109): Show | 115 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.312-3268A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151635620 | ||||||
chr1:151635721
|
A | G | 2 | a0001c0001t0022g0320a0001c0001t0022g0321 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.312-3167A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151635721 | ||||||
chr1:151635733
|
G | C | 1 | a0001c0001t0019g0277 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.312-3155G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151635733 | ||||||
chr1:151635954
|
C | T | 1 | a0001c0001t0042g0112 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.312-2934C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151635954 | ||||||
chr1:151635966
|
A | C | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.312-2922A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151635966 | ||||||
chr1:151636083
|
G | A | 1 | a0001c0001t0079g0155 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.312-2805G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151636083 | ||||||
chr1:151636115
|
C | A | 2 | a0001c0001t0003g0111a0001c0001t0082g0123 | 2 | HG01884.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.312-2773C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151636115 | ||||||
chr1:151636247
|
G | A | 9 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(6): Show | 9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.312-2641G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151636247 | ||||||
chr1:151636342
|
C | T | 6 | a0001c0001t0004g0316a0001c0001t0004g0317a0001c0001t0005g0318others(3): Show | 6 | HG03195.hp1 HG03209.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.312-2546C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151636342 | ||||||
chr1:151636345
|
AGGCTGGA others(7): Show |
A | 6 | a0001c0001t0013g0171a0001c0001t0013g0174a0001c0001t0013g0175others(3): Show | 6 | NA18939.hp1 NA18944.hp2 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.312-2539_312-2526d others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151636345 | |||||
chr1:151636546
|
T | C | 282 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(279): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.312-2342T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151636546 | ||||||
chr1:151636636
|
T | G | 1 | a0001c0001t0145g0018 | 1 | HG02896.hp2 | intron_variant | MODIFIER | c.312-2252T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151636636 | ||||||
chr1:151636666
|
T | TA | 25 | a0001c0001t0002g0038a0001c0001t0002g0068a0001c0001t0012g0102others(22): Show | 25 | HG02071.hp2 HG02074.hp1 HG02080.hp1 others(22): Show |
intron_variant | MODIFIER | c.312-2198dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151636666 | |||||
chr1:151636666
|
T | TAA | 15 | a0001c0001t0017g0297a0001c0001t0024g0354a0001c0001t0024g0355others(12): Show | 16 | HG01516.hp2 HG01884.hp2 HG02145.hp1 others(13): Show |
intron_variant | MODIFIER | c.312-2199_312-2198d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151636666 | |||||
chr1:151636666
|
TA | T | 226 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0119others(223): Show | 229 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(226): Show |
intron_variant | MODIFIER | c.312-2198delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151636666 | |||||
chr1:151636716
|
CCTAGGGA others(6): Show |
C | 9 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(6): Show | 9 | HG02895.hp1 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.312-2171_312-2159d others(15): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151636716 | ||||||
chr1:151637149
|
TC | T | 78 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(75): Show | 80 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.312-1738delC | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637149 | ||||||
chr1:151637153
|
G | GT | 6 | a0001c0001t0045g0288a0001c0001t0094g0336a0001c0001t0095g0334others(3): Show | 6 | HG02109.hp2 HG02145.hp2 HG02572.hp1 others(3): Show |
intron_variant | MODIFIER | c.312-1727dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151637153 | |||||
chr1:151637153
|
G | GTTT | 6 | a0001c0001t0023g0284a0001c0001t0023g0286a0001c0001t0090g0285others(3): Show | 6 | HG02486.hp2 HG02723.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.312-1729_312-1727d others(5): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151637153 | |||||
chr1:151637160
|
TTG | T | 81 | a0001c0001t0001g0113a0001c0001t0001g0120a0001c0001t0001g0121others(78): Show | 82 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(79): Show |
intron_variant | MODIFIER | c.312-1726_312-1725d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151637160 | |||||
chr1:151637161
|
TG | T | 49 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(46): Show | 49 | HG00280.hp1 HG00423.hp2 HG00735.hp2 others(46): Show |
intron_variant | MODIFIER | c.312-1726delG | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637161 | ||||||
chr1:151637162
|
G | T | 22 | a0001c0001t0005g0164a0001c0001t0007g0255a0001c0001t0023g0003others(19): Show | 22 | HG00735.hp1 HG02056.hp1 HG02109.hp2 others(19): Show |
intron_variant | MODIFIER | c.312-1726G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637162 | ||||||
chr1:151637163
|
T | G | 6 | a0001c0001t0007g0255a0001c0001t0040g0249a0001c0001t0040g0252others(3): Show | 6 | HG00735.hp1 NA18946.hp2 NA18971.hp1 others(3): Show |
intron_variant | MODIFIER | c.312-1725T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637163 | ||||||
chr1:151637168
|
T | G | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.312-1720T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637168 | ||||||
chr1:151637168
|
TTG | T | 9 | a0001c0001t0012g0102a0001c0001t0012g0106a0001c0001t0012g0109others(6): Show | 9 | HG02109.hp1 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.312-1718_312-1717d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151637168 | |||||
chr1:151637169
|
TG | T | 118 | a0001c0001t0006g0001a0001c0001t0006g0189a0001c0001t0007g0214others(115): Show | 121 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.312-1718delG | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637169 | ||||||
chr1:151637170
|
G | T | 158 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(155): Show | 159 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(156): Show |
intron_variant | MODIFIER | c.312-1718G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637170 | ||||||
chr1:151637173
|
T | G | 102 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(99): Show | 104 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(101): Show |
intron_variant | MODIFIER | c.312-1715T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637173 | ||||||
chr1:151637210
|
G | A | 3 | a0002c0002t0006g0002a0002c0002t0006g0197a0002c0002t0006g0250 | 4 | NA18947.hp2 NA18954.hp1 NA18991.hp2 others(1): Show |
intron_variant | MODIFIER | c.312-1678G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637210 | ||||||
chr1:151637281
|
C | T | 3 | a0001c0001t0148g0016a0001c0001t0149g0015a0001c0001t0165g0014 | 3 | HG02145.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.312-1607C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637281 | ||||||
chr1:151637412
|
T | C | 1 | a0001c0001t0093g0281 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.312-1476T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637412 | ||||||
chr1:151637697
|
G | A | 2 | a0001c0001t0057g0314a0001c0001t0133g0313 | 2 | HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.312-1191G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151637697 | ||||||
chr1:151638413
|
GTCTC | G | 5 | a0001c0001t0003g0153a0001c0001t0025g0128a0001c0001t0025g0135others(2): Show | 5 | HG00642.hp2 HG01256.hp1 HG01258.hp1 others(2): Show |
intron_variant | MODIFIER | c.312-473_312-470del others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr1 | 151638413 | |||||
chr1:151638494
|
A | G | 1 | a0001c0001t0021g0340 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.312-394A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151638494 | ||||||
chr1:151638590
|
T | C | 1 | a0001c0001t0132g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.312-298T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151638590 | ||||||
chr1:151638714
|
A | G | 1 | a0001c0007t0001g0134 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.312-174A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 1/11 | chr1 | 151638714 | ||||||
chr1:151639349
|
TTAGA | T | 78 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(75): Show | 80 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.543+234_543+237del others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151639349 | |||||
chr1:151639472
|
G | C | 78 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(75): Show | 80 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.543+353G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151639472 | ||||||
chr1:151639478
|
G | T | 1 | a0001c0001t0132g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.543+359G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151639478 | ||||||
chr1:151639525
|
A | T | 2 | a0001c0003t0061g0096a0001c0003t0061g0097 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.543+406A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151639525 | ||||||
chr1:151639631
|
A | G | 1 | a0001c0001t0132g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.543+512A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151639631 | ||||||
chr1:151639689
|
C | T | 1 | a0001c0001t0063g0066 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.543+570C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151639689 | ||||||
chr1:151639898
|
T | G | 1 | a0001c0001t0020g0042 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.543+779T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151639898 | ||||||
chr1:151639911
|
A | G | 6 | a0001c0001t0004g0316a0001c0001t0004g0317a0001c0001t0005g0318others(3): Show | 6 | HG03195.hp1 HG03209.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+792A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151639911 | ||||||
chr1:151639997
|
G | A | 1 | a0001c0001t0177g0088 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.543+878G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151639997 | ||||||
chr1:151640226
|
T | G | 1 | a0001c0001t0037g0043 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.543+1107T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151640226 | ||||||
chr1:151640400
|
C | T | 2 | a0001c0001t0029g0205a0001c0001t0125g0204 | 2 | HG00673.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.543+1281C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151640400 | ||||||
chr1:151640522
|
G | A | 3 | a0001c0001t0018g0292a0001c0001t0022g0291a0001c0001t0032g0293 | 3 | HG02132.hp2 NA18943.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.543+1403G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151640522 | ||||||
chr1:151640550
|
T | G | 2 | a0001c0001t0007g0220a0001c0001t0034g0211 | 2 | HG02523.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.543+1431T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151640550 | ||||||
chr1:151640699
|
C | A | 2 | a0001c0001t0077g0200a0001c0001t0078g0199 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.543+1580C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151640699 | ||||||
chr1:151640869
|
C | G | 1 | a0001c0001t0139g0259 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.543+1750C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151640869 | ||||||
chr1:151641012
|
A | G | 6 | a0001c0001t0049g0236a0001c0001t0049g0237a0001c0001t0052g0235others(3): Show | 6 | NA18962.hp2 NA18966.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.543+1893A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641012 | ||||||
chr1:151641013
|
CATT | C | 6 | a0001c0001t0004g0316a0001c0001t0004g0317a0001c0001t0005g0318others(3): Show | 6 | HG03195.hp1 HG03209.hp2 HG03516.hp2 others(3): Show |
intron_variant | MODIFIER | c.543+1895_543+1897d others(5): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641013 | ||||||
chr1:151641016
|
T | G | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.543+1897T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641016 | ||||||
chr1:151641171
|
A | G | 1 | a0001c0001t0016g0168 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.543+2052A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641171 | ||||||
chr1:151641301
|
C | A | 1 | a0001c0001t0034g0241 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.543+2182C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641301 | ||||||
chr1:151641331
|
T | A | 1 | a0001c0001t0126g0270 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.543+2212T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641331 | ||||||
chr1:151641504
|
T | C | 2 | a0001c0001t0004g0316a0001c0001t0005g0318 | 2 | HG03516.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.543+2385T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641504 | ||||||
chr1:151641555
|
G | T | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+2436G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641555 | ||||||
chr1:151641598
|
G | GAT | 16 | a0001c0001t0003g0099a0001c0001t0003g0100a0001c0001t0004g0316others(13): Show | 16 | HG00735.hp2 HG00741.hp2 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.543+2510_543+2511d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
G | GATAT | 22 | a0001c0001t0002g0065a0001c0001t0003g0098a0001c0001t0003g0111others(19): Show | 22 | HG00099.hp1 HG01168.hp2 HG01515.hp2 others(19): Show |
intron_variant | MODIFIER | c.543+2508_543+2511d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
G | GATATAT | 35 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(32): Show | 35 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(32): Show |
intron_variant | MODIFIER | c.543+2506_543+2511d others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
G | GATATATA others(1): Show |
25 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0129others(22): Show | 25 | HG01074.hp2 HG02015.hp1 HG02083.hp1 others(22): Show |
intron_variant | MODIFIER | c.543+2504_543+2511d others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
G | GATATATA others(3): Show |
23 | a0001c0001t0002g0036a0001c0001t0002g0058a0001c0001t0005g0154others(20): Show | 24 | HG00544.hp1 HG00597.hp1 HG01256.hp2 others(21): Show |
intron_variant | MODIFIER | c.543+2502_543+2511d others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
G | GATATATA others(5): Show |
14 | a0001c0001t0002g0029a0001c0001t0002g0056a0001c0001t0002g0057others(11): Show | 14 | HG00423.hp1 HG00609.hp1 HG01192.hp2 others(11): Show |
intron_variant | MODIFIER | c.543+2500_543+2511d others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
G | GATATATA others(7): Show |
19 | a0001c0001t0004g0139a0001c0001t0004g0158a0001c0001t0005g0328others(16): Show | 19 | HG01175.hp2 HG01255.hp2 HG01358.hp1 others(16): Show |
intron_variant | MODIFIER | c.543+2498_543+2511d others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
G | GATATATA others(9): Show |
20 | a0001c0001t0002g0052a0001c0001t0004g0156a0001c0001t0008g0025others(17): Show | 20 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(17): Show |
intron_variant | MODIFIER | c.543+2496_543+2511d others(18): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
G | GATATATA others(11): Show |
15 | a0001c0001t0002g0038a0001c0001t0015g0289a0001c0001t0015g0296others(12): Show | 15 | HG01255.hp1 HG01516.hp2 HG02040.hp1 others(12): Show |
intron_variant | MODIFIER | c.543+2494_543+2511d others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
G | GATATATA others(13): Show |
13 | a0001c0001t0008g0044a0001c0001t0008g0071a0001c0001t0017g0322others(10): Show | 13 | HG00408.hp2 HG02056.hp1 HG02602.hp1 others(10): Show |
intron_variant | MODIFIER | c.543+2492_543+2511d others(22): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
G | GATATATA others(15): Show |
4 | a0001c0001t0020g0042a0001c0001t0036g0092a0001c0001t0078g0199others(1): Show | 4 | HG03654.hp1 NA18906.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+2490_543+2511d others(24): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
G | GATATATA others(17): Show |
3 | a0001c0001t0044g0302a0001c0001t0063g0066a0001c0001t0138g0086 | 3 | HG03195.hp2 HG03688.hp1 NA19012.hp1 |
intron_variant | MODIFIER | c.543+2488_543+2511d others(26): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
G | GATATATA others(19): Show |
2 | a0001c0001t0002g0010a0001c0001t0104g0081 | 2 | HG03139.hp2 NA18972.hp1 |
intron_variant | MODIFIER | c.543+2486_543+2511d others(28): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
G | GATATATA others(21): Show |
1 | a0001c0001t0155g0070 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.543+2484_543+2511d others(30): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
GAT | G | 11 | a0001c0001t0002g0073a0001c0001t0011g0243a0001c0001t0011g0262others(8): Show | 11 | HG02280.hp2 HG02735.hp1 HG02809.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+2510_543+2511d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
GATAT | G | 28 | a0001c0001t0010g0221a0001c0001t0011g0264a0001c0001t0012g0102others(25): Show | 28 | HG00438.hp1 HG00639.hp1 HG01168.hp1 others(25): Show |
intron_variant | MODIFIER | c.543+2508_543+2511d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
GATATAT | G | 4 | a0001c0001t0050g0207a0001c0001t0101g0203a0001c0001t0110g0256others(1): Show | 4 | HG02622.hp1 NA18971.hp1 NA18983.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+2506_543+2511d others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
GATATATA others(1): Show |
G | 78 | a0001c0001t0006g0001a0001c0001t0006g0189a0001c0001t0007g0214others(75): Show | 81 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.543+2504_543+2511d others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
GATATATA others(3): Show |
G | 1 | a0001c0001t0006g0188 | 1 | NA18997.hp2 | intron_variant | MODIFIER | c.543+2502_543+2511d others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
GATATATA others(5): Show |
G | 1 | a0001c0001t0023g0284 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.543+2500_543+2511d others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641598
|
GATATATA others(7): Show |
G | 15 | a0001c0001t0023g0003a0001c0001t0023g0286a0001c0001t0023g0331others(12): Show | 15 | HG02109.hp2 HG02145.hp2 HG02615.hp2 others(12): Show |
intron_variant | MODIFIER | c.543+2498_543+2511d others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641598 | |||||
chr1:151641631
|
C | A | 3 | a0001c0001t0068g0351a0001c0004t0038g0350a0001c0004t0038g0357 | 3 | HG02717.hp2 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.543+2512C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641631 | ||||||
chr1:151641647
|
A | C | 148 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.543+2528A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641647 | ||||||
chr1:151641656
|
G | A | 1 | a0001c0001t0149g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.543+2537G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641656 | ||||||
chr1:151641661
|
A | T | 1 | a0001c0001t0149g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.543+2542A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641661 | ||||||
chr1:151641682
|
C | A | 62 | a0001c0001t0002g0010a0001c0001t0002g0029a0001c0001t0002g0030others(59): Show | 62 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.543+2563C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641682 | ||||||
chr1:151641694
|
T | G | 283 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(280): Show | 287 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(284): Show |
intron_variant | MODIFIER | c.543+2575T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641694 | ||||||
chr1:151641773
|
ATATC | A | 148 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.543+2656_543+2659d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641773 | |||||
chr1:151641775
|
ATC | A | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+2658_543+2659d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641775 | |||||
chr1:151641800
|
ATATAGAT others(81): Show |
A | 1 | a0001c0001t0132g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.543+2706_543+2793d others(90): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641800 | |||||
chr1:151641821
|
A | G | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG01099.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.543+2702A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641821 | ||||||
chr1:151641825
|
G | A | 272 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(269): Show | 276 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(273): Show |
intron_variant | MODIFIER | c.543+2706G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641825 | ||||||
chr1:151641845
|
A | AGATATAT others(21): Show |
1 | a0001c0001t0162g0080 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.543+2757_543+2784d others(30): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641845 | |||||
chr1:151641873
|
TGATATAT others(23): Show |
T | 1 | a0001c0001t0141g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.543+2826_543+2855d others(32): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641873 | |||||
chr1:151641881
|
ATATC | A | 9 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(6): Show | 9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+2763_543+2766d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641881 | ||||||
chr1:151641918
|
CTATAGAT others(55): Show |
C | 1 | a0001c0001t0016g0181 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.543+2829_543+2890d others(64): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641918 | |||||
chr1:151641931
|
TGAGATAT others(25): Show |
T | 1 | a0001c0001t0068g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.543+2815_543+2846d others(34): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641931 | |||||
chr1:151641948
|
C | A | 10 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(7): Show | 10 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.543+2829C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641948 | ||||||
chr1:151641948
|
CTATAGAT others(25): Show |
C | 4 | a0001c0001t0059g0206a0001c0001t0089g0300a0001c0001t0111g0222others(1): Show | 4 | HG02015.hp2 NA18948.hp1 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.543+2856_543+2887d others(34): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641948 | |||||
chr1:151641964
|
G | T | 1 | a0001c0001t0149g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.543+2845G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641964 | ||||||
chr1:151641964
|
GAT | G | 261 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(258): Show | 265 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(262): Show |
intron_variant | MODIFIER | c.543+2856_543+2857d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641964 | |||||
chr1:151641966
|
T | TATATATA others(21): Show |
1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.543+2855_543+2856i others(30): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641966 | |||||
chr1:151641966
|
T | TATATATA others(81): Show |
1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.543+2855_543+2856i others(90): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641966 | |||||
chr1:151641966
|
T | TATATATA others(21): Show |
3 | a0001c0001t0003g0141a0001c0001t0072g0349a0001c0001t0073g0344 | 3 | HG01074.hp2 HG01975.hp2 HG02896.hp1 |
intron_variant | MODIFIER | c.543+2855_543+2856i others(30): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641966 | |||||
chr1:151641966
|
T | TATATATA others(51): Show |
1 | a0001c0001t0032g0293 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.543+2855_543+2856i others(60): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151641966 | |||||
chr1:151641980
|
A | C | 152 | a0001c0001t0003g0099a0001c0001t0003g0145a0001c0001t0003g0149others(149): Show | 156 | HG00280.hp2 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.543+2861A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151641980 | ||||||
chr1:151642010
|
A | C | 1 | a0001c0001t0068g0351 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.543+2891A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642010 | ||||||
chr1:151642094
|
C | T | 3 | a0001c0001t0019g0277a0001c0001t0019g0278a0001c0001t0019g0279 | 3 | HG02486.hp1 HG03516.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.543+2975C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642094 | ||||||
chr1:151642095
|
G | A | 10 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(7): Show | 10 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.543+2976G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642095 | ||||||
chr1:151642100
|
G | A | 1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.543+2981G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642100 | ||||||
chr1:151642456
|
C | T | 1 | a0001c0001t0141g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.543+3337C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642456 | ||||||
chr1:151642481
|
T | G | 2 | a0001c0003t0061g0096a0001c0003t0061g0097 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.543+3362T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642481 | ||||||
chr1:151642677
|
C | T | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.543+3558C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642677 | ||||||
chr1:151642679
|
C | G | 9 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(6): Show | 9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+3560C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642679 | ||||||
chr1:151642831
|
G | A | 78 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(75): Show | 80 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.543+3712G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642831 | ||||||
chr1:151642919
|
C | T | 90 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.543+3800C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642919 | ||||||
chr1:151642929
|
C | T | 3 | a0001c0001t0059g0206a0001c0001t0111g0222a0001c0001t0112g0208 | 3 | HG02015.hp2 NA18948.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.543+3810C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642929 | ||||||
chr1:151642932
|
G | A | 1 | a0001c0001t0166g0034 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.543+3813G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642932 | ||||||
chr1:151642954
|
G | GTTTTA | 8 | a0001c0001t0003g0142a0001c0001t0003g0145a0001c0001t0003g0149others(5): Show | 8 | HG01261.hp2 HG02145.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.543+3855_543+3859d others(7): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151642954 | |||||
chr1:151642986
|
G | A | 1 | a0001c0001t0002g0058 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.543+3867G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151642986 | ||||||
chr1:151643183
|
G | A | 1 | a0001c0001t0057g0294 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.543+4064G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643183 | ||||||
chr1:151643210
|
C | T | 148 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.543+4091C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643210 | ||||||
chr1:151643264
|
T | TTTTA | 49 | a0001c0001t0007g0214a0001c0001t0007g0216a0001c0001t0007g0233others(46): Show | 49 | HG00323.hp1 HG00735.hp1 HG00738.hp2 others(46): Show |
intron_variant | MODIFIER | c.543+4189_543+4192d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151643264 | |||||
chr1:151643264
|
T | TTTTATTT others(1): Show |
48 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(45): Show | 51 | HG00280.hp2 HG00438.hp1 HG00639.hp1 others(48): Show |
intron_variant | MODIFIER | c.543+4185_543+4192d others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151643264 | |||||
chr1:151643264
|
T | TTTTATTT others(5): Show |
20 | a0001c0001t0007g0220a0001c0001t0009g0224a0001c0001t0010g0227others(17): Show | 20 | HG00438.hp2 HG00673.hp1 HG01261.hp1 others(17): Show |
intron_variant | MODIFIER | c.543+4181_543+4192d others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151643264 | |||||
chr1:151643264
|
T | TTTTATTT others(9): Show |
4 | a0001c0001t0011g0266a0001c0001t0019g0263a0001c0001t0099g0101others(1): Show | 4 | HG01099.hp1 NA18946.hp2 NA18961.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+4177_543+4192d others(18): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151643264 | |||||
chr1:151643264
|
TTTTA | T | 15 | a0001c0001t0002g0038a0001c0001t0010g0280a0001c0001t0023g0284others(12): Show | 15 | HG00408.hp2 HG00642.hp2 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.543+4189_543+4192d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151643264 | |||||
chr1:151643264
|
TTTTATTT others(1): Show |
T | 65 | a0001c0001t0001g0117a0001c0001t0001g0118a0001c0001t0001g0119others(62): Show | 65 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(62): Show |
intron_variant | MODIFIER | c.543+4185_543+4192d others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151643264 | |||||
chr1:151643264
|
TTTTATTT others(5): Show |
T | 76 | a0001c0001t0001g0113a0001c0001t0003g0006a0001c0001t0003g0098others(73): Show | 77 | HG00323.hp2 HG00423.hp2 HG00544.hp1 others(74): Show |
intron_variant | MODIFIER | c.543+4181_543+4192d others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151643264 | |||||
chr1:151643544
|
C | T | 1 | a0001c0001t0035g0020 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.543+4425C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643544 | ||||||
chr1:151643619
|
A | G | 1 | a0001c0001t0173g0046 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.543+4500A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643619 | ||||||
chr1:151643629
|
C | T | 2 | a0001c0001t0004g0166a0001c0001t0075g0165 | 2 | HG01168.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.543+4510C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643629 | ||||||
chr1:151643638
|
A | G | 1 | a0001c0001t0002g0057 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.543+4519A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643638 | ||||||
chr1:151643656
|
T | G | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+4537T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643656 | ||||||
chr1:151643662
|
T | A | 9 | a0001c0001t0023g0003a0001c0001t0023g0284a0001c0001t0023g0286others(6): Show | 9 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+4543T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643662 | ||||||
chr1:151643663
|
T | A | 16 | a0001c0001t0023g0003a0001c0001t0023g0284a0001c0001t0023g0286others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.543+4544T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643663 | ||||||
chr1:151643804
|
G | T | 9 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(6): Show | 9 | HG02895.hp1 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.543+4685G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643804 | ||||||
chr1:151643812
|
C | T | 1 | a0001c0001t0132g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.543+4693C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643812 | ||||||
chr1:151643822
|
G | A | 9 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(6): Show | 9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+4703G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151643822 | ||||||
chr1:151644200
|
T | C | 1 | a0001c0001t0027g0343 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.543+5081T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151644200 | ||||||
chr1:151644232
|
C | A | 1 | a0001c0001t0003g0006 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.543+5113C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151644232 | ||||||
chr1:151644588
|
C | T | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.543+5469C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151644588 | ||||||
chr1:151644645
|
T | C | 91 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(88): Show | 91 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(88): Show |
intron_variant | MODIFIER | c.543+5526T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151644645 | ||||||
chr1:151644859
|
C | T | 1 | a0001c0001t0101g0203 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.543+5740C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151644859 | ||||||
chr1:151644865
|
A | G | 1 | a0001c0001t0104g0081 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.543+5746A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151644865 | ||||||
chr1:151644916
|
A | G | 62 | a0001c0001t0002g0010a0001c0001t0002g0029a0001c0001t0002g0030others(59): Show | 62 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.543+5797A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151644916 | ||||||
chr1:151645064
|
T | C | 3 | a0001c0001t0148g0016a0001c0001t0149g0015a0001c0001t0165g0014 | 3 | HG02145.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.543+5945T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151645064 | ||||||
chr1:151645090
|
G | GACC | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.543+5973_543+5975d others(5): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151645090 | |||||
chr1:151645279
|
T | C | 5 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(2): Show | 5 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(2): Show |
intron_variant | MODIFIER | c.543+6160T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151645279 | ||||||
chr1:151645511
|
C | A | 2 | a0001c0001t0059g0206a0001c0001t0112g0208 | 2 | NA18948.hp1 NA18992.hp1 |
intron_variant | MODIFIER | c.543+6392C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151645511 | ||||||
chr1:151645601
|
T | G | 1 | a0001c0001t0099g0101 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.543+6482T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151645601 | ||||||
chr1:151645913
|
G | C | 1 | a0001c0001t0141g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.543+6794G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151645913 | ||||||
chr1:151645952
|
A | G | 1 | a0001c0001t0034g0241 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.543+6833A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151645952 | ||||||
chr1:151646197
|
C | T | 2 | a0001c0001t0143g0359a0001c0001t0156g0360 | 2 | HG02451.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.543+7078C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151646197 | ||||||
chr1:151646210
|
C | T | 9 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(6): Show | 9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.543+7091C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151646210 | ||||||
chr1:151646211
|
G | A | 2 | a0001c0001t0081g0009a0001c0001t0141g0013 | 2 | HG02129.hp2 HG02280.hp2 |
intron_variant | MODIFIER | c.543+7092G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151646211 | ||||||
chr1:151646312
|
A | G | 4 | a0001c0001t0010g0280a0001c0001t0077g0200a0001c0001t0078g0199others(1): Show | 4 | HG02886.hp1 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+7193A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151646312 | ||||||
chr1:151646843
|
G | C | 1 | a0001c0006t0097g0337 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.543+7724G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151646843 | ||||||
chr1:151646882
|
G | GAC | 196 | a0001c0001t0002g0029a0001c0001t0002g0030a0001c0001t0002g0033others(193): Show | 198 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.543+7783_543+7784d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151646882 | |||||
chr1:151646882
|
G | GACAC | 114 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(111): Show | 115 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.543+7781_543+7784d others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151646882 | |||||
chr1:151646882
|
G | GACACAC | 40 | a0001c0001t0005g0140a0001c0001t0005g0328a0001c0001t0015g0289others(37): Show | 41 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.543+7779_543+7784d others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151646882 | |||||
chr1:151646882
|
G | GACACACA others(1): Show |
4 | a0001c0001t0016g0324a0001c0001t0057g0314a0001c0001t0114g0310others(1): Show | 4 | HG02055.hp2 HG06807.hp2 NA18982.hp1 others(1): Show |
intron_variant | MODIFIER | c.543+7777_543+7784d others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151646882 | |||||
chr1:151647079
|
A | G | 1 | a0001c0001t0071g0152 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.543+7960A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151647079 | ||||||
chr1:151647132
|
C | CT | 258 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(255): Show | 261 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(258): Show |
intron_variant | MODIFIER | c.543+8030dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151647132 | |||||
chr1:151647237
|
G | A | 1 | a0001c0001t0039g0005 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.543+8118G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151647237 | ||||||
chr1:151647292
|
C | T | 21 | a0001c0001t0011g0243a0001c0001t0011g0262a0001c0001t0011g0264others(18): Show | 21 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.543+8173C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151647292 | ||||||
chr1:151647439
|
C | G | 1 | a0001c0001t0009g0008 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.543+8320C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151647439 | ||||||
chr1:151647598
|
T | G | 42 | a0001c0001t0004g0342a0001c0001t0005g0328a0001c0001t0015g0289others(39): Show | 43 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.543+8479T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151647598 | ||||||
chr1:151647682
|
G | C | 2 | a0001c0001t0002g0033a0001c0001t0178g0032 | 2 | NA18939.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.543+8563G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151647682 | ||||||
chr1:151647758
|
G | T | 20 | a0001c0001t0011g0243a0001c0001t0011g0262a0001c0001t0011g0264others(17): Show | 20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.543+8639G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151647758 | ||||||
chr1:151647795
|
T | C | 1 | a0001c0001t0141g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.543+8676T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151647795 | ||||||
chr1:151647923
|
A | T | 1 | a0001c0001t0026g0114 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.543+8804A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151647923 | ||||||
chr1:151647992
|
T | TA | 10 | a0001c0001t0015g0296a0001c0001t0035g0020a0001c0001t0035g0021others(7): Show | 10 | HG02056.hp1 HG02895.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.543+8884dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151647992 | |||||
chr1:151648059
|
T | G | 1 | a0001c0001t0026g0114 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.543+8940T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648059 | ||||||
chr1:151648060
|
G | T | 1 | a0001c0001t0026g0114 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.543+8941G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648060 | ||||||
chr1:151648119
|
A | G | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.543+9000A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648119 | ||||||
chr1:151648133
|
C | T | 1 | a0001c0001t0004g0342 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.543+9014C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648133 | ||||||
chr1:151648200
|
C | T | 1 | a0001c0001t0139g0259 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.543+9081C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648200 | ||||||
chr1:151648254
|
C | T | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.543+9135C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648254 | ||||||
chr1:151648432
|
T | C | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.543+9313T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648432 | ||||||
chr1:151648481
|
G | A | 1 | a0001c0001t0016g0324 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.543+9362G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648481 | ||||||
chr1:151648482
|
C | T | 2 | a0001c0003t0061g0096a0001c0003t0061g0097 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.543+9363C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648482 | ||||||
chr1:151648568
|
A | C | 12 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(9): Show | 12 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(9): Show |
intron_variant | MODIFIER | c.543+9449A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648568 | ||||||
chr1:151648658
|
A | G | 2 | a0001c0003t0061g0096a0001c0003t0061g0097 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.543+9539A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648658 | ||||||
chr1:151648693
|
A | G | 2 | a0001c0001t0009g0224a0001c0001t0034g0225 | 2 | NA18963.hp2 NA18998.hp1 |
intron_variant | MODIFIER | c.544-9542A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648693 | ||||||
chr1:151648698
|
C | T | 1 | a0001c0001t0114g0310 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.544-9537C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648698 | ||||||
chr1:151648740
|
A | C | 148 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.544-9495A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648740 | ||||||
chr1:151648744
|
TA | T | 147 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(144): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.544-9490delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648744 | ||||||
chr1:151648745
|
A | T | 1 | a0001c0001t0026g0114 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.544-9490A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648745 | ||||||
chr1:151648870
|
G | A | 9 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(6): Show | 10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.544-9365G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151648870 | ||||||
chr1:151649058
|
G | A | 4 | a0001c0001t0046g0190a0001c0001t0046g0192a0001c0001t0047g0191others(1): Show | 4 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-9177G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649058 | ||||||
chr1:151649061
|
C | T | 1 | a0001c0001t0008g0025 | 1 | HG02273.hp2 | intron_variant | MODIFIER | c.544-9174C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649061 | ||||||
chr1:151649086
|
C | T | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-9149C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649086 | ||||||
chr1:151649195
|
C | T | 9 | a0001c0001t0023g0003a0001c0001t0023g0284a0001c0001t0023g0286others(6): Show | 9 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.544-9040C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649195 | ||||||
chr1:151649196
|
G | A | 132 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(129): Show | 133 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(130): Show |
intron_variant | MODIFIER | c.544-9039G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649196 | ||||||
chr1:151649317
|
A | G | 2 | a0001c0001t0044g0160a0001c0001t0088g0180 | 2 | NA19012.hp2 NA19070.hp1 |
intron_variant | MODIFIER | c.544-8918A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649317 | ||||||
chr1:151649341
|
G | C | 1 | a0001c0001t0091g0282 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.544-8894G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649341 | ||||||
chr1:151649579
|
T | C | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-8656T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649579 | ||||||
chr1:151649644
|
G | A | 40 | a0001c0001t0005g0328a0001c0001t0015g0289a0001c0001t0015g0296others(37): Show | 41 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.544-8591G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649644 | ||||||
chr1:151649813
|
C | A | 78 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(75): Show | 80 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.544-8422C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649813 | ||||||
chr1:151649835
|
A | G | 1 | a0001c0001t0139g0259 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.544-8400A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151649835 | ||||||
chr1:151650053
|
A | C | 149 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(146): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.544-8182A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650053 | ||||||
chr1:151650135
|
A | T | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-8100A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650135 | ||||||
chr1:151650285
|
C | G | 1 | a0001c0001t0074g0146 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.544-7950C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650285 | ||||||
chr1:151650292
|
A | G | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.544-7943A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650292 | ||||||
chr1:151650595
|
T | C | 1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.544-7640T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650595 | ||||||
chr1:151650602
|
T | A | 3 | a0001c0001t0148g0016a0001c0001t0149g0015a0001c0001t0165g0014 | 3 | HG02145.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.544-7633T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650602 | ||||||
chr1:151650603
|
T | A | 13 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(10): Show | 13 | HG02040.hp1 HG02145.hp1 HG02895.hp1 others(10): Show |
intron_variant | MODIFIER | c.544-7632T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650603 | ||||||
chr1:151650604
|
A | T | 18 | a0001c0001t0022g0172a0001c0001t0023g0003a0001c0001t0023g0284others(15): Show | 18 | HG02109.hp2 HG02145.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.544-7631A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650604 | ||||||
chr1:151650654
|
G | C | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-7581G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650654 | ||||||
chr1:151650730
|
T | G | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.544-7505T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650730 | ||||||
chr1:151650746
|
C | T | 1 | a0001c0001t0074g0146 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.544-7489C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650746 | ||||||
chr1:151650747
|
GGCCTTCC others(3): Show |
G | 1 | a0001c0001t0141g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.544-7486_544-7477d others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151650747 | |||||
chr1:151650773
|
G | C | 10 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(7): Show | 10 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.544-7462G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650773 | ||||||
chr1:151650808
|
C | G | 1 | a0001c0001t0018g0295 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.544-7427C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650808 | ||||||
chr1:151650886
|
C | T | 2 | a0001c0001t0020g0040a0001c0001t0020g0053 | 2 | NA18988.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.544-7349C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650886 | ||||||
chr1:151650905
|
C | T | 112 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(109): Show | 115 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.544-7330C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650905 | ||||||
chr1:151650979
|
G | T | 2 | a0001c0001t0002g0033a0001c0001t0178g0032 | 2 | NA18939.hp2 NA18944.hp1 |
intron_variant | MODIFIER | c.544-7256G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151650979 | ||||||
chr1:151651010
|
C | T | 8 | a0001c0001t0005g0150a0001c0001t0027g0343a0001c0001t0027g0347others(5): Show | 8 | HG00735.hp2 HG00741.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.544-7225C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651010 | ||||||
chr1:151651015
|
A | C | 1 | a0001c0001t0071g0152 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.544-7220A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651015 | ||||||
chr1:151651130
|
C | T | 1 | a0001c0001t0139g0259 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.544-7105C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651130 | ||||||
chr1:151651136
|
G | C | 2 | a0001c0001t0008g0044a0001c0001t0155g0070 | 2 | HG00544.hp2 HG03927.hp2 |
intron_variant | MODIFIER | c.544-7099G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651136 | ||||||
chr1:151651153
|
G | A | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.544-7082G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651153 | ||||||
chr1:151651199
|
C | T | 78 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(75): Show | 80 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.544-7036C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651199 | ||||||
chr1:151651203
|
C | G | 1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.544-7032C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651203 | ||||||
chr1:151651203
|
C | T | 4 | a0001c0001t0003g0099a0001c0001t0143g0359a0001c0001t0144g0011others(1): Show | 4 | HG02451.hp1 HG02572.hp1 HG02717.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-7032C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651203 | ||||||
chr1:151651225
|
G | C | 1 | a0001c0001t0162g0080 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.544-7010G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651225 | ||||||
chr1:151651241
|
G | C | 357 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(354): Show | 361 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(358): Show |
intron_variant | MODIFIER | c.544-6994G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651241 | ||||||
chr1:151651278
|
G | T | 9 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(6): Show | 9 | HG02895.hp1 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.544-6957G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651278 | ||||||
chr1:151651319
|
GGGCGGGG others(43): Show |
G | 1 | a0001c0001t0012g0102 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.544-6880_544-6831d others(52): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151651319 | |||||
chr1:151651360
|
C | T | 1 | a0001c0001t0121g0268 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.544-6875C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651360 | ||||||
chr1:151651388
|
C | A | 1 | a0001c0001t0101g0203 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.544-6847C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651388 | ||||||
chr1:151651402
|
G | C | 1 | a0001c0001t0018g0295 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.544-6833G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651402 | ||||||
chr1:151651427
|
C | T | 1 | a0001c0001t0139g0259 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.544-6808C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651427 | ||||||
chr1:151651491
|
G | A | 1 | a0001c0001t0027g0347 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.544-6744G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651491 | ||||||
chr1:151651569
|
G | A | 2 | a0001c0001t0132g0195a0001c0001t0164g0062 | 2 | HG03225.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.544-6666G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651569 | ||||||
chr1:151651571
|
G | A | 78 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(75): Show | 80 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.544-6664G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651571 | ||||||
chr1:151651610
|
C | T | 1 | a0001c0001t0039g0005 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.544-6625C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651610 | ||||||
chr1:151651650
|
C | A | 4 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(1): Show | 4 | HG02895.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.544-6585C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651650 | ||||||
chr1:151651776
|
C | T | 1 | a0001c0001t0003g0098 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.544-6459C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651776 | ||||||
chr1:151651777
|
G | A | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-6458G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651777 | ||||||
chr1:151651794
|
C | CG | 24 | a0001c0001t0001g0120a0001c0001t0002g0010a0001c0001t0004g0316others(21): Show | 24 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(21): Show |
intron_variant | MODIFIER | c.544-6437dupG | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151651794 | |||||
chr1:151651807
|
G | A | 1 | a0001c0001t0053g0230 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.544-6428G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651807 | ||||||
chr1:151651825
|
C | T | 1 | a0001c0001t0149g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.544-6410C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651825 | ||||||
chr1:151651851
|
G | A | 1 | a0001c0001t0057g0314 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.544-6384G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651851 | ||||||
chr1:151651901
|
G | A | 3 | a0001c0001t0148g0016a0001c0001t0149g0015a0001c0001t0165g0014 | 3 | HG02145.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.544-6334G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651901 | ||||||
chr1:151651945
|
A | G | 3 | a0001c0001t0148g0016a0001c0001t0149g0015a0001c0001t0165g0014 | 3 | HG02145.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.544-6290A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651945 | ||||||
chr1:151651954
|
C | T | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-6281C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651954 | ||||||
chr1:151651957
|
G | C | 264 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(261): Show | 267 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(264): Show |
intron_variant | MODIFIER | c.544-6278G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651957 | ||||||
chr1:151651957
|
G | T | 9 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(6): Show | 10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.544-6278G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651957 | ||||||
chr1:151651983
|
T | C | 1 | a0001c0001t0030g0258 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.544-6252T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651983 | ||||||
chr1:151651993
|
G | A | 1 | a0001c0001t0030g0258 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.544-6242G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151651993 | ||||||
chr1:151652007
|
T | C | 1 | a0001c0001t0030g0258 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.544-6228T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652007 | ||||||
chr1:151652021
|
G | A | 1 | a0001c0001t0030g0258 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.544-6214G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652021 | ||||||
chr1:151652028
|
C | T | 4 | a0001c0001t0009g0217a0001c0001t0045g0288a0001c0001t0045g0332others(1): Show | 4 | HG02615.hp2 HG03130.hp2 HG03471.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-6207C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652028 | ||||||
chr1:151652037
|
C | CAAAAAAA others(5): Show |
1 | a0001c0001t0030g0258 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.544-6194_544-6193i others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652037 | |||||
chr1:151652045
|
G | C | 1 | a0001c0001t0030g0258 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.544-6190G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652045 | ||||||
chr1:151652051
|
T | C | 1 | a0001c0001t0030g0258 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.544-6184T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652051 | ||||||
chr1:151652055
|
G | A | 1 | a0001c0001t0005g0140 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.544-6180G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652055 | ||||||
chr1:151652056
|
C | T | 1 | a0001c0001t0124g0275 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.544-6179C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652056 | ||||||
chr1:151652063
|
A | C | 1 | a0001c0001t0030g0258 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.544-6172A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652063 | ||||||
chr1:151652065
|
C | G | 3 | a0001c0001t0004g0156a0001c0001t0004g0158a0001c0001t0015g0157 | 3 | HG01255.hp2 HG01257.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.544-6170C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652065 | ||||||
chr1:151652073
|
C | T | 1 | a0001c0001t0023g0284 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.544-6162C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652073 | ||||||
chr1:151652205
|
G | GGGGAGA | 115 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(112): Show | 116 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(113): Show |
intron_variant | MODIFIER | c.544-5993_544-5988d others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652205 | |||||
chr1:151652205
|
G | GGGGAGAG others(5): Show |
84 | a0001c0001t0006g0001a0001c0001t0006g0189a0001c0001t0007g0214others(81): Show | 86 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.544-5999_544-5988d others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652205 | |||||
chr1:151652205
|
G | GGGGAGAG others(11): Show |
9 | a0001c0001t0006g0188a0001c0001t0009g0202a0001c0001t0034g0241others(6): Show | 9 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(6): Show |
intron_variant | MODIFIER | c.544-6005_544-5988d others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652205 | |||||
chr1:151652205
|
G | GGGGAGAG others(17): Show |
1 | a0001c0001t0052g0235 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.544-6011_544-5988d others(26): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652205 | |||||
chr1:151652205
|
GGGGAGA | G | 9 | a0001c0001t0003g0099a0001c0001t0035g0020a0001c0001t0035g0021others(6): Show | 9 | HG02280.hp2 HG02895.hp1 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.544-5993_544-5988d others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652205 | |||||
chr1:151652205
|
GGGGAGAG others(5): Show |
G | 2 | a0001c0001t0078g0199a0001c0001t0132g0195 | 2 | HG03225.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.544-5999_544-5988d others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652205 | |||||
chr1:151652205
|
GGGGAGAG others(11): Show |
G | 9 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(6): Show | 9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.544-6005_544-5988d others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652205 | |||||
chr1:151652206
|
G | GGGAGAGG others(35): Show |
1 | a0001c0001t0175g0041 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.544-6009_544-5968d others(44): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652206 | |||||
chr1:151652207
|
G | A | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.544-6028G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652207 | ||||||
chr1:151652211
|
A | AGGGAGAG others(16): Show |
2 | a0001c0001t0010g0280a0001c0001t0102g0341 | 2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.544-6006_544-6005i others(25): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652211 | |||||
chr1:151652212
|
GGGAGAGG others(29): Show |
G | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-6003_544-5968d others(38): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652212 | |||||
chr1:151652236
|
G | GGGAGAGG others(5): Show |
1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.544-5987_544-5976d others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652236 | |||||
chr1:151652242
|
G | GGGAGAGG others(23): Show |
1 | a0001c0001t0117g0304 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.544-5988_544-5987i others(32): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652242 | |||||
chr1:151652248
|
C | G | 1 | a0001c0001t0153g0031 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.544-5987C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652248 | ||||||
chr1:151652395
|
T | C | 1 | a0001c0001t0005g0328 | 1 | NA19068.hp2 | intron_variant | MODIFIER | c.544-5840T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652395 | ||||||
chr1:151652403
|
C | CT | 33 | a0001c0001t0001g0118a0001c0001t0002g0052a0001c0001t0002g0073others(30): Show | 33 | HG00544.hp2 HG00673.hp2 HG00741.hp1 others(30): Show |
intron_variant | MODIFIER | c.544-5812dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652403 | |||||
chr1:151652510
|
G | A | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-5725G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652510 | ||||||
chr1:151652618
|
G | A | 1 | a0001c0001t0004g0184 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.544-5617G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652618 | ||||||
chr1:151652682
|
A | G | 1 | a0001c0001t0162g0080 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.544-5553A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652682 | ||||||
chr1:151652842
|
G | T | 1 | a0001c0001t0063g0066 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.544-5393G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652842 | ||||||
chr1:151652868
|
A | G | 2 | a0001c0001t0077g0200a0001c0001t0078g0199 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.544-5367A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652868 | ||||||
chr1:151652921
|
G | C | 1 | a0001c0001t0106g0239 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.544-5314G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652921 | ||||||
chr1:151652927
|
CT | C | 243 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(240): Show | 247 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(244): Show |
intron_variant | MODIFIER | c.544-5291delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151652927 | |||||
chr1:151652991
|
G | C | 9 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(6): Show | 10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.544-5244G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151652991 | ||||||
chr1:151653014
|
G | A | 2 | a0001c0001t0009g0232a0001c0001t0053g0230 | 2 | NA18942.hp2 NA18960.hp2 |
intron_variant | MODIFIER | c.544-5221G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653014 | ||||||
chr1:151653057
|
A | G | 1 | a0001c0001t0078g0199 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.544-5178A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653057 | ||||||
chr1:151653083
|
A | G | 1 | a0001c0001t0040g0249 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.544-5152A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653083 | ||||||
chr1:151653106
|
T | C | 148 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.544-5129T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653106 | ||||||
chr1:151653127
|
A | T | 2 | a0001c0003t0061g0096a0001c0003t0061g0097 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.544-5108A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653127 | ||||||
chr1:151653172
|
C | T | 1 | a0001c0001t0035g0021 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.544-5063C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653172 | ||||||
chr1:151653215
|
C | T | 3 | a0001c0001t0008g0051a0001c0001t0159g0069a0001c0001t0166g0034 | 3 | NA18949.hp2 NA19011.hp2 NA19067.hp1 |
intron_variant | MODIFIER | c.544-5020C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653215 | ||||||
chr1:151653232
|
T | G | 282 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(279): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.544-5003T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653232 | ||||||
chr1:151653266
|
TTTG | T | 20 | a0001c0001t0011g0243a0001c0001t0011g0262a0001c0001t0011g0264others(17): Show | 20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.544-4966_544-4964d others(5): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151653266 | |||||
chr1:151653313
|
A | G | 1 | a0001c0001t0020g0042 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.544-4922A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653313 | ||||||
chr1:151653434
|
C | T | 1 | a0001c0001t0015g0289 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.544-4801C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653434 | ||||||
chr1:151653439
|
G | A | 1 | a0001c0001t0078g0199 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.544-4796G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653439 | ||||||
chr1:151653636
|
G | C | 1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.544-4599G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653636 | ||||||
chr1:151653683
|
A | G | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-4552A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653683 | ||||||
chr1:151653750
|
G | A | 6 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(3): Show | 7 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.544-4485G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653750 | ||||||
chr1:151653768
|
G | A | 1 | a0001c0001t0165g0014 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.544-4467G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653768 | ||||||
chr1:151653827
|
GTTTTTTT others(8): Show |
G | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-4399_544-4385d others(17): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151653827 | |||||
chr1:151653836
|
G | GT | 217 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(214): Show | 221 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(218): Show |
intron_variant | MODIFIER | c.544-4384dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151653836 | |||||
chr1:151653896
|
G | A | 282 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(279): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.544-4339G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653896 | ||||||
chr1:151653920
|
C | T | 2 | a0001c0001t0003g0098a0001c0001t0003g0100 | 2 | HG01934.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.544-4315C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653920 | ||||||
chr1:151653934
|
GT | G | 6 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(3): Show | 6 | HG02895.hp1 HG02965.hp1 HG03041.hp2 others(3): Show |
intron_variant | MODIFIER | c.544-4300delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151653934 | ||||||
chr1:151654294
|
T | C | 1 | a0001c0001t0030g0198 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.544-3941T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151654294 | ||||||
chr1:151654355
|
T | G | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-3880T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151654355 | ||||||
chr1:151654406
|
C | G | 1 | a0001c0001t0072g0349 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.544-3829C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151654406 | ||||||
chr1:151654407
|
G | A | 1 | a0001c0001t0020g0063 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.544-3828G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151654407 | ||||||
chr1:151654637
|
A | G | 20 | a0001c0001t0011g0243a0001c0001t0011g0262a0001c0001t0011g0264others(17): Show | 20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.544-3598A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151654637 | ||||||
chr1:151654771
|
G | C | 1 | a0001c0001t0084g0138 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.544-3464G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151654771 | ||||||
chr1:151654834
|
G | A | 1 | a0001c0001t0003g0098 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.544-3401G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151654834 | ||||||
chr1:151654855
|
T | A | 1 | a0001c0001t0096g0333 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.544-3380T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151654855 | ||||||
chr1:151654942
|
C | T | 2 | a0001c0001t0077g0200a0001c0001t0078g0199 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.544-3293C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151654942 | ||||||
chr1:151655068
|
G | A | 1 | a0001c0001t0062g0095 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.544-3167G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655068 | ||||||
chr1:151655094
|
T | C | 20 | a0001c0001t0011g0243a0001c0001t0011g0262a0001c0001t0011g0264others(17): Show | 20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.544-3141T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655094 | ||||||
chr1:151655128
|
A | G | 90 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.544-3107A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655128 | ||||||
chr1:151655397
|
G | A | 28 | a0001c0001t0003g0006a0001c0001t0004g0156a0001c0001t0004g0158others(25): Show | 28 | HG00099.hp1 HG00544.hp1 HG01071.hp2 others(25): Show |
intron_variant | MODIFIER | c.544-2838G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655397 | ||||||
chr1:151655682
|
G | C | 1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.544-2553G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655682 | ||||||
chr1:151655686
|
C | A | 4 | a0001c0001t0008g0049a0001c0001t0020g0048a0001c0001t0064g0047others(1): Show | 4 | HG01071.hp1 HG01255.hp1 HG01433.hp2 others(1): Show |
intron_variant | MODIFIER | c.544-2549C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655686 | ||||||
chr1:151655714
|
C | T | 1 | a0001c0001t0003g0116 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.544-2521C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655714 | ||||||
chr1:151655754
|
C | T | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-2481C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655754 | ||||||
chr1:151655776
|
A | G | 286 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(283): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.544-2459A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655776 | ||||||
chr1:151655824
|
T | C | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.544-2411T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151655824 | ||||||
chr1:151656009
|
C | G | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.544-2226C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656009 | ||||||
chr1:151656050
|
C | T | 1 | a0001c0001t0118g0311 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.544-2185C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656050 | ||||||
chr1:151656066
|
A | G | 147 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(144): Show | 148 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(145): Show |
intron_variant | MODIFIER | c.544-2169A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656066 | ||||||
chr1:151656094
|
G | C | 1 | a0001c0001t0141g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.544-2141G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656094 | ||||||
chr1:151656110
|
C | G | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.544-2125C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656110 | ||||||
chr1:151656147
|
C | T | 1 | a0001c0001t0017g0297 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.544-2088C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656147 | ||||||
chr1:151656223
|
C | CA | 109 | a0001c0001t0001g0113a0001c0001t0004g0342a0001c0001t0006g0001others(106): Show | 112 | HG00280.hp2 HG00438.hp2 HG00609.hp2 others(109): Show |
intron_variant | MODIFIER | c.544-1992dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151656223 | |||||
chr1:151656223
|
C | CAA | 12 | a0001c0001t0002g0033a0001c0001t0010g0280a0001c0001t0011g0264others(9): Show | 12 | HG00438.hp1 HG01175.hp1 HG01433.hp1 others(9): Show |
intron_variant | MODIFIER | c.544-1993_544-1992d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151656223 | |||||
chr1:151656223
|
CA | C | 10 | a0001c0001t0015g0312a0001c0001t0027g0343a0001c0001t0027g0347others(7): Show | 10 | HG00597.hp2 HG00735.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.544-1992delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151656223 | |||||
chr1:151656313
|
G | T | 1 | a0001c0001t0041g0345 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.544-1922G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656313 | ||||||
chr1:151656362
|
G | A | 1 | a0001c0001t0001g0113 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.544-1873G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656362 | ||||||
chr1:151656814
|
T | C | 3 | a0001c0001t0068g0351a0001c0004t0038g0350a0001c0004t0038g0357 | 3 | HG02717.hp2 HG02922.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.544-1421T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656814 | ||||||
chr1:151656972
|
T | C | 3 | a0001c0001t0016g0324a0001c0001t0057g0314a0001c0001t0133g0313 | 3 | HG02055.hp2 HG06807.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.544-1263T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151656972 | ||||||
chr1:151657067
|
G | A | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.544-1168G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657067 | ||||||
chr1:151657184
|
G | GT | 5 | a0001c0001t0022g0172a0001c0001t0028g0170a0001c0001t0044g0160others(2): Show | 5 | HG01934.hp2 NA19012.hp2 NA19066.hp1 others(2): Show |
intron_variant | MODIFIER | c.544-1044dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151657184 | |||||
chr1:151657225
|
G | A | 9 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(6): Show | 10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.544-1010G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657225 | ||||||
chr1:151657278
|
A | G | 3 | a0001c0001t0004g0166a0001c0001t0004g0167a0001c0001t0075g0165 | 3 | HG00099.hp1 HG01168.hp2 HG01515.hp2 |
intron_variant | MODIFIER | c.544-957A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657278 | ||||||
chr1:151657482
|
A | G | 71 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(68): Show | 73 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(70): Show |
intron_variant | MODIFIER | c.544-753A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657482 | ||||||
chr1:151657534
|
C | A | 1 | a0001c0001t0133g0313 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.544-701C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657534 | ||||||
chr1:151657534
|
C | T | 148 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.544-701C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657534 | ||||||
chr1:151657535
|
G | T | 1 | a0001c0001t0004g0139 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.544-700G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657535 | ||||||
chr1:151657637
|
CTT | C | 3 | a0001c0001t0029g0205a0001c0001t0059g0251a0001c0001t0125g0204 | 3 | HG00673.hp1 NA18961.hp1 NA18967.hp2 |
intron_variant | MODIFIER | c.544-595_544-594del others(2): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr1 | 151657637 | |||||
chr1:151657654
|
A | T | 1 | a0001c0001t0002g0010 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.544-581A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657654 | ||||||
chr1:151657655
|
T | A | 1 | a0001c0001t0002g0010 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.544-580T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657655 | ||||||
chr1:151657759
|
G | A | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.544-476G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657759 | ||||||
chr1:151657943
|
A | G | 9 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(6): Show | 9 | HG02895.hp1 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.544-292A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657943 | ||||||
chr1:151657971
|
A | C | 1 | a0001c0001t0156g0360 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.544-264A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657971 | ||||||
chr1:151657981
|
A | G | 1 | a0001c0003t0061g0096 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.544-254A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657981 | ||||||
chr1:151657994
|
C | G | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.544-241C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 2/11 | chr1 | 151657994 | ||||||
chr1:151658662
|
GT | G | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.736+240delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 151658662 | |||||
chr1:151658725
|
C | T | 113 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(110): Show | 116 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.736+298C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151658725 | ||||||
chr1:151658759
|
A | G | 1 | a0001c0001t0005g0150 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.736+332A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151658759 | ||||||
chr1:151658833
|
T | C | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.736+406T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151658833 | ||||||
chr1:151658859
|
AT | A | 360 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(357): Show | 364 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(361): Show |
intron_variant | MODIFIER | c.736+438delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 151658859 | |||||
chr1:151658945
|
A | G | 90 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.736+518A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151658945 | ||||||
chr1:151659049
|
A | G | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.736+622A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151659049 | ||||||
chr1:151659099
|
G | A | 1 | a0001c0001t0132g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.736+672G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151659099 | ||||||
chr1:151659216
|
C | A | 113 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(110): Show | 116 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(113): Show |
intron_variant | MODIFIER | c.736+789C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151659216 | ||||||
chr1:151659236
|
T | TTTTTG | 3 | a0001c0001t0035g0021a0001c0001t0035g0022a0001c0001t0152g0019 | 3 | HG03041.hp2 HG03486.hp1 NA19030.hp1 |
intron_variant | MODIFIER | c.736+835_736+839dup others(5): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 151659236 | |||||
chr1:151659236
|
TTTTTGTT others(3): Show |
T | 2 | a0002c0002t0048g0218a0002c0002t0048g0219 | 2 | NA18941.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.736+830_736+839del others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 151659236 | |||||
chr1:151659321
|
C | T | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.736+894C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151659321 | ||||||
chr1:151659394
|
C | T | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.736+967C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151659394 | ||||||
chr1:151659881
|
T | G | 2 | a0001c0001t0001g0113a0001c0001t0055g0115 | 2 | HG00609.hp2 NA18992.hp2 |
intron_variant | MODIFIER | c.737-917T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151659881 | ||||||
chr1:151659926
|
G | A | 1 | a0001c0001t0005g0150 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.737-872G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151659926 | ||||||
chr1:151660170
|
T | C | 131 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(128): Show | 132 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
intron_variant | MODIFIER | c.737-628T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151660170 | ||||||
chr1:151660234
|
C | T | 7 | a0001c0001t0045g0288a0001c0001t0045g0332a0001c0001t0094g0336others(4): Show | 7 | HG02109.hp2 HG02145.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.737-564C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151660234 | ||||||
chr1:151660240
|
G | GT | 9 | a0001c0001t0002g0010a0001c0001t0003g0100a0001c0001t0004g0158others(6): Show | 9 | HG01255.hp2 HG02257.hp2 HG02738.hp1 others(6): Show |
intron_variant | MODIFIER | c.737-541dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 151660240 | |||||
chr1:151660256
|
T | C | 2 | a0001c0001t0010g0280a0001c0001t0102g0341 | 2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.737-542T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151660256 | ||||||
chr1:151660452
|
C | G | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.737-346C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151660452 | ||||||
chr1:151660611
|
T | C | 2 | a0001c0001t0011g0265a0001c0001t0011g0266 | 2 | HG01099.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.737-187T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151660611 | ||||||
chr1:151660651
|
C | CCA | 4 | a0001c0001t0046g0190a0001c0001t0046g0192a0001c0001t0047g0191others(1): Show | 4 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.737-146_737-145dup others(2): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr1 | 151660651 | |||||
chr1:151660711
|
G | T | 1 | a0001c0001t0132g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.737-87G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 3/11 | chr1 | 151660711 | ||||||
chr1:151661435
|
C | A | 9 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(6): Show | 10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.801+573C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 4/11 | chr1 | 151661435 | ||||||
chr1:151661529
|
C | T | 3 | a0001c0001t0018g0292a0001c0001t0022g0291a0001c0001t0032g0293 | 3 | HG02132.hp2 NA18943.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.802-637C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 4/11 | chr1 | 151661529 | ||||||
chr1:151661671
|
A | C | 6 | a0001c0001t0010g0221a0001c0001t0010g0227a0001c0001t0010g0229others(3): Show | 6 | HG00642.hp1 HG01167.hp1 HG01175.hp1 others(3): Show |
intron_variant | MODIFIER | c.802-495A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 4/11 | chr1 | 151661671 | ||||||
chr1:151661778
|
G | T | 2 | a0001c0003t0061g0096a0001c0003t0061g0097 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.802-388G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 4/11 | chr1 | 151661778 | ||||||
chr1:151662030
|
G | C | 1 | a0001c0001t0020g0048 | 1 | HG01071.hp1 | intron_variant | MODIFIER | c.802-136G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 4/11 | chr1 | 151662030 | ||||||
chr1:151662036
|
A | AT | 146 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(143): Show | 147 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(144): Show |
intron_variant | MODIFIER | c.802-123dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 4/11 | INFO_REALIGN_3_PRIME | chr1 | 151662036 | |||||
chr1:151662047
|
G | A | 1 | a0001c0001t0129g0083 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.802-119G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 4/11 | chr1 | 151662047 | ||||||
chr1:151662327
|
G | A | 84 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.906+57G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662327 | ||||||
chr1:151662354
|
G | A | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.906+84G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662354 | ||||||
chr1:151662378
|
C | T | 1 | a0001c0001t0113g0103 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.906+108C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662378 | ||||||
chr1:151662547
|
A | G | 1 | a0001c0001t0034g0241 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.906+277A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662547 | ||||||
chr1:151662552
|
C | T | 1 | a0001c0001t0016g0287 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.906+282C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662552 | ||||||
chr1:151662672
|
A | G | 2 | a0001c0001t0029g0205a0001c0001t0125g0204 | 2 | HG00673.hp1 NA18961.hp1 |
intron_variant | MODIFIER | c.906+402A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662672 | ||||||
chr1:151662706
|
A | C | 1 | a0001c0001t0034g0241 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.906+436A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662706 | ||||||
chr1:151662735
|
G | A | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.906+465G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662735 | ||||||
chr1:151662900
|
C | G | 2 | a0001c0003t0061g0096a0001c0003t0061g0097 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.906+630C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662900 | ||||||
chr1:151662901
|
G | A | 7 | a0001c0001t0016g0287a0001c0001t0017g0303a0001c0001t0017g0326others(4): Show | 7 | HG01081.hp1 HG01192.hp1 HG02055.hp1 others(4): Show |
intron_variant | MODIFIER | c.906+631G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151662901 | ||||||
chr1:151662914
|
T | TTTTTCTT others(318): Show |
1 | a0001c0001t0003g0116 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.906+653_906+654ins others(325): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 151662914 | |||||
chr1:151663152
|
A | AT | 8 | a0001c0001t0002g0068a0001c0001t0004g0342a0001c0001t0018g0315others(5): Show | 8 | HG01175.hp1 HG02055.hp1 HG02080.hp1 others(5): Show |
intron_variant | MODIFIER | c.906+898dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 151663152 | |||||
chr1:151663214
|
G | A | 1 | a0001c0001t0049g0237 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.906+944G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663214 | ||||||
chr1:151663295
|
C | T | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.906+1025C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663295 | ||||||
chr1:151663307
|
C | T | 2 | a0001c0001t0010g0280a0001c0001t0102g0341 | 2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.906+1037C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663307 | ||||||
chr1:151663312
|
G | A | 1 | a0001c0001t0132g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.906+1042G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663312 | ||||||
chr1:151663367
|
G | T | 2 | a0001c0001t0007g0214a0001c0001t0033g0213 | 2 | HG03492.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.906+1097G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663367 | ||||||
chr1:151663400
|
T | C | 79 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(76): Show | 81 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(78): Show |
intron_variant | MODIFIER | c.906+1130T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663400 | ||||||
chr1:151663444
|
C | T | 1 | a0001c0001t0012g0106 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.906+1174C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663444 | ||||||
chr1:151663487
|
T | C | 1 | a0001c0001t0035g0022 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.906+1217T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663487 | ||||||
chr1:151663766
|
A | G | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.906+1496A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663766 | ||||||
chr1:151663792
|
T | C | 9 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(6): Show | 10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.906+1522T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151663792 | ||||||
chr1:151664122
|
C | T | 282 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(279): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.907-1811C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664122 | ||||||
chr1:151664138
|
T | C | 1 | a0001c0001t0090g0285 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.907-1795T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664138 | ||||||
chr1:151664204
|
A | T | 2 | a0001c0001t0077g0200a0001c0001t0078g0199 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.907-1729A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664204 | ||||||
chr1:151664208
|
A | ATAT | 286 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(283): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.907-1723_907-1721d others(5): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 151664208 | |||||
chr1:151664261
|
GTC | G | 20 | a0001c0001t0011g0243a0001c0001t0011g0262a0001c0001t0011g0264others(17): Show | 20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.907-1669_907-1668d others(4): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr1 | 151664261 | |||||
chr1:151664338
|
G | A | 1 | a0001c0001t0141g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.907-1595G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664338 | ||||||
chr1:151664427
|
A | T | 4 | a0001c0001t0010g0280a0001c0001t0077g0200a0001c0001t0078g0199others(1): Show | 4 | HG02886.hp1 HG02970.hp1 NA18906.hp1 others(1): Show |
intron_variant | MODIFIER | c.907-1506A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664427 | ||||||
chr1:151664458
|
C | T | 1 | a0001c0001t0163g0094 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.907-1475C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664458 | ||||||
chr1:151664470
|
A | G | 16 | a0001c0001t0023g0003a0001c0001t0023g0284a0001c0001t0023g0286others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.907-1463A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664470 | ||||||
chr1:151664539
|
G | A | 1 | a0001c0001t0149g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.907-1394G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664539 | ||||||
chr1:151664589
|
C | T | 21 | a0001c0001t0011g0243a0001c0001t0011g0262a0001c0001t0011g0264others(18): Show | 21 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(18): Show |
intron_variant | MODIFIER | c.907-1344C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664589 | ||||||
chr1:151664611
|
G | T | 2 | a0001c0001t0077g0200a0001c0001t0078g0199 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.907-1322G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664611 | ||||||
chr1:151664674
|
C | T | 282 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(279): Show | 286 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(283): Show |
intron_variant | MODIFIER | c.907-1259C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664674 | ||||||
chr1:151664715
|
A | G | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.907-1218A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664715 | ||||||
chr1:151664858
|
T | G | 1 | a0001c0001t0139g0259 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.907-1075T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151664858 | ||||||
chr1:151665062
|
G | C | 1 | a0001c0001t0105g0082 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.907-871G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151665062 | ||||||
chr1:151665314
|
A | G | 1 | a0001c0001t0141g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.907-619A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151665314 | ||||||
chr1:151665422
|
A | C | 1 | a0001c0001t0002g0010 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.907-511A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151665422 | ||||||
chr1:151665523
|
G | A | 1 | a0001c0001t0141g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.907-410G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151665523 | ||||||
chr1:151665595
|
G | A | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.907-338G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151665595 | ||||||
chr1:151665715
|
A | G | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.907-218A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 5/11 | chr1 | 151665715 | ||||||
chr1:151666327
|
A | G | 2 | a0001c0003t0061g0096a0001c0003t0061g0097 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.985+316A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151666327 | ||||||
chr1:151666490
|
T | C | 1 | a0001c0001t0013g0174 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.985+479T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151666490 | ||||||
chr1:151666588
|
T | C | 5 | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0136others(2): Show | 5 | NA18947.hp1 NA18953.hp1 NA18988.hp1 others(2): Show |
intron_variant | MODIFIER | c.985+577T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151666588 | ||||||
chr1:151667017
|
C | G | 1 | a0001c0001t0110g0256 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.985+1006C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667017 | ||||||
chr1:151667025
|
G | A | 2 | a0001c0001t0010g0280a0001c0001t0102g0341 | 2 | HG02886.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.985+1014G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667025 | ||||||
chr1:151667052
|
G | A | 1 | a0001c0001t0003g0098 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.985+1041G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667052 | ||||||
chr1:151667247
|
C | CA | 6 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(3): Show | 7 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(4): Show |
intron_variant | MODIFIER | c.986-1213dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667247 | |||||
chr1:151667247
|
C | CAAAAAAA others(1): Show |
36 | a0001c0001t0005g0328a0001c0001t0013g0174a0001c0001t0015g0289others(33): Show | 37 | HG00423.hp2 HG00597.hp2 HG00639.hp2 others(34): Show |
intron_variant | MODIFIER | c.986-1220_986-1213d others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667247 | |||||
chr1:151667247
|
C | CAAAAAAA others(2): Show |
60 | a0001c0001t0004g0156a0001c0001t0004g0158a0001c0001t0004g0159others(57): Show | 60 | HG00099.hp1 HG00323.hp1 HG00544.hp1 others(57): Show |
intron_variant | MODIFIER | c.986-1221_986-1213d others(11): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667247 | |||||
chr1:151667247
|
C | CAAAAAAA others(3): Show |
138 | a0001c0001t0001g0113a0001c0001t0001g0118a0001c0001t0001g0119others(135): Show | 139 | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
intron_variant | MODIFIER | c.986-1222_986-1213d others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667247 | |||||
chr1:151667247
|
C | CAAAAAAA others(4): Show |
80 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0002g0038others(77): Show | 81 | HG00408.hp2 HG00544.hp2 HG00639.hp1 others(78): Show |
intron_variant | MODIFIER | c.986-1223_986-1213d others(13): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667247 | |||||
chr1:151667247
|
C | CAAAAAAA others(5): Show |
27 | a0001c0001t0001g0132a0001c0001t0002g0029a0001c0001t0002g0030others(24): Show | 27 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(24): Show |
intron_variant | MODIFIER | c.986-1224_986-1213d others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667247 | |||||
chr1:151667247
|
C | CAAAAAAA others(6): Show |
1 | a0001c0001t0002g0010 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.986-1213_986-1212i others(15): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667247 | |||||
chr1:151667250
|
A | AAAAAAAA others(1): Show |
10 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(7): Show | 10 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.986-1215_986-1214i others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667250 | |||||
chr1:151667386
|
G | C | 358 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(355): Show | 362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.986-1086G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667386 | ||||||
chr1:151667396
|
T | G | 1 | a0001c0001t0005g0150 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.986-1076T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667396 | ||||||
chr1:151667548
|
G | A | 1 | a0001c0001t0074g0146 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-924G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667548 | ||||||
chr1:151667563
|
C | T | 2 | a0001c0001t0074g0146a0001c0001t0081g0009 | 2 | HG02129.hp2 HG02698.hp1 |
intron_variant | MODIFIER | c.986-909C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667563 | ||||||
chr1:151667574
|
C | T | 1 | a0001c0001t0074g0146 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-898C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667574 | ||||||
chr1:151667591
|
C | T | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.986-881C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667591 | ||||||
chr1:151667592
|
G | A | 1 | a0001c0001t0074g0146 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-880G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667592 | ||||||
chr1:151667596
|
CG | C | 89 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(86): Show | 89 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(86): Show |
intron_variant | MODIFIER | c.986-873delG | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667596 | |||||
chr1:151667600
|
C | T | 1 | a0001c0001t0074g0146 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-872C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667600 | ||||||
chr1:151667632
|
C | T | 1 | a0001c0001t0074g0146 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-840C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667632 | ||||||
chr1:151667639
|
A | C | 1 | a0001c0001t0074g0146 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-833A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667639 | ||||||
chr1:151667641
|
C | T | 1 | a0001c0001t0074g0146 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-831C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667641 | ||||||
chr1:151667652
|
C | T | 1 | a0001c0001t0074g0146 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-820C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667652 | ||||||
chr1:151667687
|
C | A | 1 | a0001c0001t0074g0146 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-785C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667687 | ||||||
chr1:151667688
|
G | A | 26 | a0001c0001t0002g0010a0001c0001t0002g0029a0001c0001t0002g0030others(23): Show | 26 | HG00423.hp1 HG00597.hp1 HG00609.hp1 others(23): Show |
intron_variant | MODIFIER | c.986-784G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667688 | ||||||
chr1:151667689
|
T | A | 1 | a0001c0001t0074g0146 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-783T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667689 | ||||||
chr1:151667690
|
A | G | 1 | a0001c0001t0074g0146 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-782A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667690 | ||||||
chr1:151667696
|
G | A | 1 | a0001c0001t0074g0146 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.986-776G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667696 | ||||||
chr1:151667738
|
A | C | 1 | a0001c0001t0141g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.986-734A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667738 | ||||||
chr1:151667756
|
G | A | 9 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(6): Show | 9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.986-716G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151667756 | ||||||
chr1:151667826
|
C | CA | 11 | a0001c0001t0002g0038a0001c0001t0008g0071a0001c0001t0011g0243others(8): Show | 11 | HG02004.hp1 HG02074.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.986-621dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667826 | |||||
chr1:151667826
|
CA | C | 78 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(75): Show | 80 | HG00280.hp2 HG00642.hp1 HG00673.hp1 others(77): Show |
intron_variant | MODIFIER | c.986-621delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667826 | |||||
chr1:151667826
|
CAA | C | 35 | a0001c0001t0001g0129a0001c0001t0001g0132a0001c0001t0004g0184others(32): Show | 35 | HG00323.hp1 HG00408.hp1 HG01433.hp1 others(32): Show |
intron_variant | MODIFIER | c.986-622_986-621del others(2): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667826 | |||||
chr1:151667826
|
CAAA | C | 128 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(125): Show | 129 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(126): Show |
intron_variant | MODIFIER | c.986-623_986-621del others(3): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr1 | 151667826 | |||||
chr1:151668170
|
T | C | 4 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(1): Show | 4 | HG02895.hp1 HG03041.hp2 HG03486.hp1 others(1): Show |
intron_variant | MODIFIER | c.986-302T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151668170 | ||||||
chr1:151668314
|
G | A | 1 | a0001c0001t0032g0301 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.986-158G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151668314 | ||||||
chr1:151668452
|
G | C | 2 | a0001c0001t0007g0214a0001c0001t0033g0213 | 2 | HG03492.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.986-20G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 6/11 | chr1 | 151668452 | ||||||
chr1:151669282
|
A | C | 1 | a0001c0001t0008g0071 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1149+647A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151669282 | ||||||
chr1:151669459
|
C | T | 1 | a0001c0001t0039g0005 | 2 | HG03098.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.1149+824C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151669459 | ||||||
chr1:151669517
|
C | T | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1149+882C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151669517 | ||||||
chr1:151669701
|
G | A | 1 | a0001c0001t0070g0353 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1149+1066G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151669701 | ||||||
chr1:151669841
|
A | G | 295 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(292): Show | 299 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(296): Show |
intron_variant | MODIFIER | c.1149+1206A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151669841 | ||||||
chr1:151670092
|
TG | T | 5 | a0001c0001t0023g0003a0001c0001t0023g0286a0001c0001t0023g0331others(2): Show | 5 | HG02723.hp1 HG02809.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1149+1460delG | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151670092 | |||||
chr1:151670369
|
A | C | 1 | a0001c0001t0044g0302 | 1 | NA19012.hp1 | intron_variant | MODIFIER | c.1149+1734A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151670369 | ||||||
chr1:151670431
|
C | T | 1 | a0001c0001t0004g0317 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1149+1796C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151670431 | ||||||
chr1:151670512
|
C | T | 1 | a0001c0001t0083g0126 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.1149+1877C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151670512 | ||||||
chr1:151670674
|
C | G | 9 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(6): Show | 9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1149+2039C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151670674 | ||||||
chr1:151670798
|
A | G | 1 | a0001c0001t0036g0035 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1149+2163A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151670798 | ||||||
chr1:151670869
|
T | C | 7 | a0001c0001t0003g0141a0001c0001t0004g0184a0001c0001t0005g0147others(4): Show | 7 | HG00099.hp2 HG00738.hp1 HG01074.hp2 others(4): Show |
intron_variant | MODIFIER | c.1149+2234T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151670869 | ||||||
chr1:151670885
|
T | C | 286 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(283): Show | 290 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(287): Show |
intron_variant | MODIFIER | c.1149+2250T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151670885 | ||||||
chr1:151670902
|
A | G | 149 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(146): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1149+2267A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151670902 | ||||||
chr1:151671058
|
A | G | 1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1149+2423A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151671058 | ||||||
chr1:151671236
|
C | CT | 8 | a0001c0001t0012g0110a0001c0001t0019g0277a0001c0001t0052g0238others(5): Show | 8 | HG02145.hp1 HG02280.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.1149+2617dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151671236 | |||||
chr1:151671236
|
C | CTT | 5 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(2): Show | 6 | HG01884.hp2 HG02572.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.1149+2616_1149+261 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151671236 | |||||
chr1:151671236
|
CT | C | 40 | a0001c0001t0005g0328a0001c0001t0015g0289a0001c0001t0015g0312others(37): Show | 41 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(38): Show |
intron_variant | MODIFIER | c.1149+2617delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151671236 | |||||
chr1:151671255
|
A | G | 1 | a0001c0001t0179g0257 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1149+2620A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151671255 | ||||||
chr1:151671297
|
G | A | 1 | a0001c0001t0149g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1149+2662G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151671297 | ||||||
chr1:151671609
|
G | A | 1 | a0001c0001t0117g0304 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1149+2974G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151671609 | ||||||
chr1:151671817
|
C | G | 4 | a0001c0001t0016g0287a0001c0001t0017g0303a0001c0001t0017g0326others(1): Show | 4 | HG01081.hp1 HG01192.hp1 HG02055.hp1 others(1): Show |
intron_variant | MODIFIER | c.1149+3182C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151671817 | ||||||
chr1:151671883
|
C | T | 1 | a0001c0001t0141g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1149+3248C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151671883 | ||||||
chr1:151671900
|
C | T | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1149+3265C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151671900 | ||||||
chr1:151671929
|
A | G | 9 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(6): Show | 10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1149+3294A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151671929 | ||||||
chr1:151671961
|
T | G | 358 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(355): Show | 362 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(359): Show |
intron_variant | MODIFIER | c.1149+3326T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151671961 | ||||||
chr1:151672462
|
A | G | 2 | a0001c0001t0004g0159a0001c0001t0005g0164 | 2 | HG01071.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.1149+3827A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151672462 | ||||||
chr1:151672574
|
A | T | 1 | a0001c0001t0114g0310 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.1149+3939A>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151672574 | ||||||
chr1:151672730
|
T | C | 9 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(6): Show | 9 | HG02895.hp1 HG02895.hp2 HG02896.hp2 others(6): Show |
intron_variant | MODIFIER | c.1149+4095T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151672730 | ||||||
chr1:151672867
|
C | CT | 7 | a0001c0001t0016g0168a0001c0001t0016g0169a0001c0001t0016g0181others(4): Show | 7 | HG00323.hp2 HG00639.hp2 HG01099.hp2 others(4): Show |
intron_variant | MODIFIER | c.1149+4242dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151672867 | |||||
chr1:151672877
|
T | C | 1 | a0001c0001t0141g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1149+4242T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151672877 | ||||||
chr1:151673181
|
T | C | 1 | a0001c0001t0132g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1149+4546T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151673181 | ||||||
chr1:151673442
|
A | G | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1149+4807A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151673442 | ||||||
chr1:151674210
|
G | GT | 10 | a0001c0001t0010g0280a0001c0001t0024g0354a0001c0001t0024g0355others(7): Show | 11 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(8): Show |
intron_variant | MODIFIER | c.1149+5576dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151674210 | |||||
chr1:151674472
|
T | C | 148 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(145): Show | 149 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(146): Show |
intron_variant | MODIFIER | c.1149+5837T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151674472 | ||||||
chr1:151674531
|
T | C | 90 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1149+5896T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151674531 | ||||||
chr1:151674637
|
G | A | 1 | a0001c0001t0115g0290 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.1149+6002G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151674637 | ||||||
chr1:151674714
|
G | A | 2 | a0001c0003t0061g0096a0001c0003t0061g0097 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1149+6079G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151674714 | ||||||
chr1:151674926
|
T | C | 3 | a0001c0001t0007g0228a0001c0001t0014g0212a0001c0001t0029g0273 | 3 | HG01978.hp2 HG02148.hp1 HG02273.hp1 |
intron_variant | MODIFIER | c.1149+6291T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151674926 | ||||||
chr1:151674975
|
C | T | 2 | a0001c0003t0061g0096a0001c0003t0061g0097 | 2 | HG02895.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1149+6340C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151674975 | ||||||
chr1:151674976
|
G | A | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1149+6341G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151674976 | ||||||
chr1:151674982
|
G | A | 16 | a0001c0001t0023g0003a0001c0001t0023g0284a0001c0001t0023g0286others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1149+6347G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151674982 | ||||||
chr1:151675101
|
A | G | 9 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(6): Show | 10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1149+6466A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675101 | ||||||
chr1:151675409
|
CATAGTTA others(23): Show |
C | 1 | a0001c0001t0020g0040 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1149+6775_1149+680 others(34): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675409 | ||||||
chr1:151675422
|
C | T | 149 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(146): Show | 150 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(147): Show |
intron_variant | MODIFIER | c.1149+6787C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675422 | ||||||
chr1:151675508
|
A | G | 1 | a0001c0001t0064g0026 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.1149+6873A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675508 | ||||||
chr1:151675576
|
G | C | 1 | a0001c0001t0149g0015 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.1149+6941G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675576 | ||||||
chr1:151675626
|
A | G | 10 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(7): Show | 10 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1149+6991A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675626 | ||||||
chr1:151675716
|
ATGATGCT others(12): Show |
A | 1 | a0001c0001t0050g0234 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1149+7084_1149+710 others(23): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675716 | |||||
chr1:151675798
|
C | G | 1 | a0001c0001t0065g0061 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1149+7163C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675798 | ||||||
chr1:151675810
|
C | CT | 37 | a0001c0001t0001g0119a0001c0001t0001g0125a0001c0001t0001g0127others(34): Show | 37 | HG00280.hp1 HG01074.hp2 HG01167.hp2 others(34): Show |
intron_variant | MODIFIER | c.1149+7210dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | |||||
chr1:151675810
|
C | CTT | 23 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(20): Show | 23 | HG00099.hp1 HG00099.hp2 HG00609.hp2 others(20): Show |
intron_variant | MODIFIER | c.1149+7209_1149+721 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | |||||
chr1:151675810
|
C | CTTT | 14 | a0001c0001t0001g0121a0001c0001t0003g0006a0001c0001t0005g0154others(11): Show | 14 | HG00735.hp2 HG01168.hp2 HG01934.hp2 others(11): Show |
intron_variant | MODIFIER | c.1149+7208_1149+721 others(7): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | |||||
chr1:151675810
|
CT | C | 6 | a0001c0001t0004g0317a0001c0001t0005g0318a0001c0001t0021g0162others(3): Show | 6 | HG02258.hp1 HG02622.hp2 HG03195.hp1 others(3): Show |
intron_variant | MODIFIER | c.1149+7210delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | |||||
chr1:151675810
|
CTT | C | 9 | a0001c0001t0016g0324a0001c0001t0032g0299a0001c0001t0068g0351others(6): Show | 9 | HG01175.hp2 HG02055.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.1149+7209_1149+721 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | |||||
chr1:151675810
|
CTTT | C | 9 | a0001c0001t0015g0289a0001c0001t0015g0312a0001c0001t0016g0168others(6): Show | 9 | HG00323.hp2 HG00597.hp2 HG00639.hp2 others(6): Show |
intron_variant | MODIFIER | c.1149+7208_1149+721 others(7): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | |||||
chr1:151675810
|
CTTTT | C | 35 | a0001c0001t0004g0342a0001c0001t0015g0296a0001c0001t0015g0329others(32): Show | 36 | HG00423.hp2 HG01081.hp1 HG01192.hp1 others(33): Show |
intron_variant | MODIFIER | c.1149+7207_1149+721 others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | |||||
chr1:151675810
|
CTTTTT | C | 41 | a0001c0001t0005g0328a0001c0001t0007g0253a0001c0001t0011g0243others(38): Show | 42 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(39): Show |
intron_variant | MODIFIER | c.1149+7206_1149+721 others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | |||||
chr1:151675810
|
CTTTTTT | C | 24 | a0001c0001t0007g0255a0001c0001t0010g0221a0001c0001t0011g0276others(21): Show | 24 | HG00280.hp2 HG00438.hp2 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1149+7205_1149+721 others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | |||||
chr1:151675810
|
CTTTTTTT | C | 58 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(55): Show | 60 | HG00323.hp1 HG00642.hp1 HG00673.hp1 others(57): Show |
intron_variant | MODIFIER | c.1149+7204_1149+721 others(11): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | |||||
chr1:151675810
|
CTTTTTTT others(1): Show |
C | 10 | a0001c0001t0007g0233a0001c0001t0010g0280a0001c0001t0033g0223others(7): Show | 10 | HG01257.hp1 HG02165.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.1149+7203_1149+721 others(12): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | |||||
chr1:151675810
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0001t0012g0110 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.1149+7197_1149+721 others(18): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | |||||
chr1:151675810
|
CTTTTTTT others(9): Show |
C | 60 | a0001c0001t0002g0010a0001c0001t0002g0029a0001c0001t0002g0030others(57): Show | 60 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(57): Show |
intron_variant | MODIFIER | c.1149+7195_1149+721 others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | |||||
chr1:151675810
|
CTTTTTTT others(10): Show |
C | 7 | a0001c0001t0002g0033a0001c0001t0008g0051a0001c0001t0026g0133others(4): Show | 7 | HG00408.hp1 HG02132.hp1 HG02970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1149+7194_1149+721 others(21): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | |||||
chr1:151675810
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1149+7193_1149+721 others(22): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | |||||
chr1:151675810
|
CTTTTTTT others(12): Show |
C | 1 | a0001c0001t0003g0099 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1149+7192_1149+721 others(23): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151675810 | |||||
chr1:151675818
|
T | C | 3 | a0001c0001t0148g0016a0001c0001t0149g0015a0001c0001t0165g0014 | 3 | HG02145.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1149+7183T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675818 | ||||||
chr1:151675821
|
T | C | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1149+7186T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675821 | ||||||
chr1:151675830
|
T | C | 1 | a0001c0001t0147g0079 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.1149+7195T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151675830 | ||||||
chr1:151676006
|
T | A | 77 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(74): Show | 79 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(76): Show |
intron_variant | MODIFIER | c.1150-7350T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151676006 | ||||||
chr1:151676068
|
G | T | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150-7288G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151676068 | ||||||
chr1:151676101
|
G | T | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1150-7255G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151676101 | ||||||
chr1:151676171
|
G | C | 9 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(6): Show | 10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1150-7185G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151676171 | ||||||
chr1:151676270
|
ATTTTTTT others(3): Show |
A | 1 | a0001c0001t0002g0057 | 1 | NA19003.hp1 | intron_variant | MODIFIER | c.1150-7042_1150-703 others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(4): Show |
A | 4 | a0001c0001t0013g0183a0001c0001t0077g0200a0001c0001t0143g0359others(1): Show | 4 | HG02451.hp1 HG02717.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150-7043_1150-703 others(15): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(5): Show |
A | 5 | a0001c0001t0002g0030a0001c0001t0013g0175a0001c0001t0020g0042others(2): Show | 5 | HG02083.hp1 HG02083.hp2 NA18983.hp1 others(2): Show |
intron_variant | MODIFIER | c.1150-7044_1150-703 others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(6): Show |
A | 9 | a0001c0001t0037g0024a0001c0001t0037g0043a0001c0001t0065g0085others(6): Show | 9 | HG00423.hp1 HG02071.hp2 HG02738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1150-7045_1150-703 others(17): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(7): Show |
A | 10 | a0001c0001t0002g0010a0001c0001t0002g0052a0001c0001t0002g0073others(7): Show | 10 | HG00673.hp2 HG01099.hp1 HG02004.hp1 others(7): Show |
intron_variant | MODIFIER | c.1150-7046_1150-703 others(18): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(8): Show |
A | 13 | a0001c0001t0011g0264a0001c0001t0011g0276a0001c0001t0018g0295others(10): Show | 13 | HG00438.hp1 HG00639.hp1 HG00642.hp2 others(10): Show |
intron_variant | MODIFIER | c.1150-7047_1150-703 others(19): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(9): Show |
A | 32 | a0001c0001t0001g0113a0001c0001t0003g0100a0001c0001t0003g0142others(29): Show | 32 | HG00280.hp1 HG00408.hp1 HG00544.hp1 others(29): Show |
intron_variant | MODIFIER | c.1150-7048_1150-703 others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(10): Show |
A | 62 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0002g0038others(59): Show | 63 | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(60): Show |
intron_variant | MODIFIER | c.1150-7049_1150-703 others(21): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(11): Show |
A | 42 | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0129others(39): Show | 42 | HG00408.hp2 HG00597.hp2 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.1150-7050_1150-703 others(22): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(12): Show |
A | 6 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0122others(3): Show | 6 | HG02922.hp2 HG03491.hp1 HG03704.hp2 others(3): Show |
intron_variant | MODIFIER | c.1150-7051_1150-703 others(23): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(14): Show |
A | 3 | a0001c0001t0063g0066a0001c0001t0120g0335a0001c0001t0171g0072 | 3 | HG02145.hp2 HG02148.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.1150-7053_1150-703 others(25): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(15): Show |
A | 9 | a0001c0001t0008g0049a0001c0001t0020g0048a0001c0001t0036g0059others(6): Show | 9 | HG01071.hp1 HG01255.hp1 HG01433.hp2 others(6): Show |
intron_variant | MODIFIER | c.1150-7054_1150-703 others(26): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(16): Show |
A | 9 | a0001c0001t0012g0104a0001c0001t0012g0106a0001c0001t0012g0109others(6): Show | 9 | HG02258.hp2 HG02280.hp1 HG02559.hp2 others(6): Show |
intron_variant | MODIFIER | c.1150-7055_1150-703 others(27): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(17): Show |
A | 19 | a0001c0001t0012g0102a0001c0001t0023g0003a0001c0001t0023g0284others(16): Show | 19 | HG01884.hp2 HG02109.hp1 HG02257.hp2 others(16): Show |
intron_variant | MODIFIER | c.1150-7056_1150-703 others(28): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(18): Show |
A | 3 | a0001c0001t0130g0267a0001c0001t0144g0011a0001c0001t0154g0090 | 3 | HG02572.hp1 HG02698.hp2 NA20752.hp2 |
intron_variant | MODIFIER | c.1150-7057_1150-703 others(29): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(19): Show |
A | 6 | a0001c0001t0010g0280a0001c0001t0039g0005a0001c0001t0102g0341others(3): Show | 7 | HG02886.hp1 HG02895.hp2 HG03098.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150-7058_1150-703 others(30): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(21): Show |
A | 6 | a0001c0001t0104g0081a0001c0001t0127g0084a0001c0001t0129g0083others(3): Show | 6 | HG02258.hp1 HG02647.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.1150-7060_1150-703 others(32): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(22): Show |
A | 5 | a0001c0001t0002g0065a0001c0001t0068g0351a0001c0001t0105g0082others(2): Show | 5 | HG02155.hp2 HG02622.hp2 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.1150-7061_1150-703 others(33): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(23): Show |
A | 1 | a0001c0001t0004g0139 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1150-7062_1150-703 others(34): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(24): Show |
A | 1 | a0001c0001t0020g0053 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.1150-7063_1150-703 others(35): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(25): Show |
A | 4 | a0001c0001t0011g0243a0001c0001t0011g0262a0001c0001t0060g0260others(1): Show | 4 | HG03927.hp1 NA18941.hp2 NA18951.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-7064_1150-703 others(36): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(26): Show |
A | 2 | a0001c0001t0006g0188a0001c0001t0052g0238 | 2 | NA18979.hp1 NA18997.hp2 |
intron_variant | MODIFIER | c.1150-7065_1150-703 others(37): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(27): Show |
A | 72 | a0001c0001t0006g0001a0001c0001t0006g0189a0001c0001t0007g0214others(69): Show | 74 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(71): Show |
intron_variant | MODIFIER | c.1150-7066_1150-703 others(38): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676270
|
ATTTTTTT others(28): Show |
A | 4 | a0001c0001t0007g0255a0001c0001t0078g0199a0001c0001t0098g0187others(1): Show | 4 | HG00735.hp1 NA18906.hp1 NA18948.hp1 others(1): Show |
intron_variant | MODIFIER | c.1150-7067_1150-703 others(39): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676270 | |||||
chr1:151676287
|
T | C | 1 | a0001c0001t0036g0035 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1150-7069T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151676287 | ||||||
chr1:151676933
|
G | GGT | 12 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(9): Show | 12 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(9): Show |
intron_variant | MODIFIER | c.1150-6404_1150-640 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151676933 | |||||
chr1:151676954
|
A | G | 2 | a0001c0001t0021g0340a0001c0003t0061g0097 | 2 | HG00544.hp1 HG02895.hp2 |
intron_variant | MODIFIER | c.1150-6402A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151676954 | ||||||
chr1:151677003
|
A | G | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150-6353A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151677003 | ||||||
chr1:151677104
|
C | A | 1 | a0001c0001t0008g0064 | 1 | NA18955.hp2 | intron_variant | MODIFIER | c.1150-6252C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151677104 | ||||||
chr1:151677141
|
A | G | 7 | a0001c0001t0104g0081a0001c0001t0105g0082a0001c0001t0127g0084others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150-6215A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151677141 | ||||||
chr1:151677150
|
T | C | 3 | a0001c0001t0091g0282a0001c0001t0092g0283a0001c0001t0093g0281 | 3 | HG03139.hp1 HG03453.hp1 HG03540.hp1 |
intron_variant | MODIFIER | c.1150-6206T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151677150 | ||||||
chr1:151677740
|
G | A | 4 | a0001c0001t0002g0038a0001c0001t0062g0028a0001c0001t0146g0078others(1): Show | 4 | HG00408.hp2 NA19001.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-5616G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151677740 | ||||||
chr1:151677865
|
C | T | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150-5491C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151677865 | ||||||
chr1:151677991
|
G | A | 1 | a0001c0001t0052g0238 | 1 | NA18979.hp1 | intron_variant | MODIFIER | c.1150-5365G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151677991 | ||||||
chr1:151678039
|
T | C | 1 | a0001c0001t0065g0061 | 1 | NA18975.hp2 | intron_variant | MODIFIER | c.1150-5317T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678039 | ||||||
chr1:151678084
|
G | A | 4 | a0001c0001t0040g0249a0001c0001t0040g0252a0001c0001t0050g0207others(1): Show | 4 | NA18946.hp2 NA18971.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-5272G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678084 | ||||||
chr1:151678271
|
C | A | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1150-5085C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678271 | ||||||
chr1:151678289
|
T | G | 1 | a0001c0001t0009g0224 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1150-5067T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678289 | ||||||
chr1:151678352
|
A | G | 1 | a0001c0001t0164g0062 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.1150-5004A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678352 | ||||||
chr1:151678505
|
A | G | 1 | a0001c0001t0063g0055 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1150-4851A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678505 | ||||||
chr1:151678540
|
G | C | 1 | a0001c0001t0167g0074 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.1150-4816G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678540 | ||||||
chr1:151678704
|
A | AT | 84 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(81): Show | 84 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(81): Show |
intron_variant | MODIFIER | c.1150-4645dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151678704 | |||||
chr1:151678713
|
T | C | 1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1150-4643T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678713 | ||||||
chr1:151678782
|
C | T | 1 | a0001c0001t0163g0094 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1150-4574C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678782 | ||||||
chr1:151678825
|
T | C | 10 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(7): Show | 10 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1150-4531T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678825 | ||||||
chr1:151678989
|
T | C | 1 | a0001c0001t0154g0090 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1150-4367T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151678989 | ||||||
chr1:151679228
|
G | T | 9 | a0001c0001t0023g0003a0001c0001t0023g0284a0001c0001t0023g0286others(6): Show | 9 | HG02486.hp2 HG02723.hp1 HG02809.hp1 others(6): Show |
intron_variant | MODIFIER | c.1150-4128G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151679228 | ||||||
chr1:151679343
|
A | G | 1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1150-4013A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151679343 | ||||||
chr1:151679667
|
C | G | 1 | a0001c0001t0132g0195 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1150-3689C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151679667 | ||||||
chr1:151679737
|
G | A | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1150-3619G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151679737 | ||||||
chr1:151679793
|
G | A | 78 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(75): Show | 80 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.1150-3563G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151679793 | ||||||
chr1:151679976
|
G | A | 2 | a0001c0001t0077g0200a0001c0001t0078g0199 | 2 | HG02970.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.1150-3380G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151679976 | ||||||
chr1:151679985
|
C | T | 1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1150-3371C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151679985 | ||||||
chr1:151680016
|
A | G | 1 | a0001c0001t0050g0234 | 1 | NA19081.hp1 | intron_variant | MODIFIER | c.1150-3340A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151680016 | ||||||
chr1:151680053
|
T | C | 211 | a0001c0001t0002g0010a0001c0001t0002g0029a0001c0001t0002g0030others(208): Show | 214 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(211): Show |
intron_variant | MODIFIER | c.1150-3303T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151680053 | ||||||
chr1:151680152
|
CT | C | 139 | a0001c0001t0004g0342a0001c0001t0006g0001a0001c0001t0006g0188others(136): Show | 142 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(139): Show |
intron_variant | MODIFIER | c.1150-3187delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151680152 | |||||
chr1:151680152
|
CTT | C | 46 | a0001c0001t0005g0328a0001c0001t0010g0358a0001c0001t0015g0289others(43): Show | 47 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(44): Show |
intron_variant | MODIFIER | c.1150-3188_1150-318 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151680152 | |||||
chr1:151680183
|
G | A | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150-3173G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151680183 | ||||||
chr1:151680386
|
C | A | 3 | a0001c0001t0036g0059a0001c0001t0160g0067a0001c0001t0164g0062 | 3 | NA18946.hp1 NA18982.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.1150-2970C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151680386 | ||||||
chr1:151680435
|
C | T | 90 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(87): Show | 90 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(87): Show |
intron_variant | MODIFIER | c.1150-2921C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151680435 | ||||||
chr1:151680568
|
G | C | 1 | a0001c0001t0060g0260 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1150-2788G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151680568 | ||||||
chr1:151680786
|
C | G | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1150-2570C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151680786 | ||||||
chr1:151680836
|
A | C | 118 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(115): Show | 121 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1150-2520A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151680836 | ||||||
chr1:151680921
|
T | G | 5 | a0001c0001t0023g0003a0001c0001t0023g0286a0001c0001t0023g0331others(2): Show | 5 | HG02723.hp1 HG02809.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.1150-2435T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151680921 | ||||||
chr1:151681037
|
C | T | 1 | a0001c0001t0162g0080 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1150-2319C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151681037 | ||||||
chr1:151681105
|
C | T | 1 | a0001c0001t0009g0202 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1150-2251C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151681105 | ||||||
chr1:151681231
|
C | T | 355 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(352): Show | 359 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(356): Show |
intron_variant | MODIFIER | c.1150-2125C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151681231 | ||||||
chr1:151681235
|
C | CT | 19 | a0001c0001t0001g0129a0001c0001t0003g0006a0001c0001t0003g0142others(16): Show | 19 | HG00597.hp2 HG00673.hp1 HG00741.hp1 others(16): Show |
intron_variant | MODIFIER | c.1150-2097dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTT | 6 | a0001c0001t0011g0243a0001c0001t0011g0262a0001c0001t0057g0294others(3): Show | 6 | HG02056.hp1 HG02572.hp1 HG03927.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150-2098_1150-209 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTT | 6 | a0001c0001t0019g0277a0001c0001t0019g0279a0001c0001t0035g0021others(3): Show | 6 | HG02486.hp1 HG02896.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1150-2101_1150-209 others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0030g0198 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.1150-2106_1150-209 others(14): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(4): Show |
4 | a0001c0001t0007g0228a0001c0001t0046g0192a0001c0001t0047g0191others(1): Show | 4 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-2107_1150-209 others(15): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(5): Show |
1 | a0001c0001t0009g0224 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1150-2108_1150-209 others(16): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(6): Show |
3 | a0001c0001t0007g0233a0001c0001t0014g0194a0001c0001t0126g0270 | 3 | HG02165.hp2 HG02886.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1150-2109_1150-209 others(17): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(8): Show |
6 | a0001c0001t0011g0276a0001c0001t0060g0260a0001c0001t0103g0274others(3): Show | 6 | HG00639.hp1 HG01168.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.1150-2111_1150-209 others(19): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(9): Show |
3 | a0001c0001t0019g0263a0001c0001t0019g0269a0001c0001t0121g0268 | 3 | HG02155.hp1 NA18985.hp1 NA19057.hp2 |
intron_variant | MODIFIER | c.1150-2112_1150-209 others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(10): Show |
2 | a0001c0001t0011g0264a0001c0001t0011g0265 | 2 | HG00438.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.1150-2113_1150-209 others(21): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(12): Show |
5 | a0001c0001t0010g0358a0001c0001t0011g0266a0001c0001t0179g0257others(2): Show | 6 | HG01099.hp1 NA18947.hp2 NA18991.hp2 others(3): Show |
intron_variant | MODIFIER | c.1150-2115_1150-209 others(23): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(13): Show |
1 | a0002c0002t0006g0197 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1150-2116_1150-209 others(24): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(14): Show |
4 | a0001c0001t0104g0081a0001c0001t0123g0339a0001c0001t0127g0084others(1): Show | 4 | HG02258.hp1 HG02738.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-2117_1150-209 others(25): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(15): Show |
1 | a0001c0001t0140g0093 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1150-2118_1150-209 others(26): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(16): Show |
3 | a0001c0001t0029g0273a0002c0002t0048g0218a0002c0002t0048g0219 | 3 | HG02273.hp1 NA18941.hp1 NA19009.hp1 |
intron_variant | MODIFIER | c.1150-2119_1150-209 others(27): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(17): Show |
7 | a0001c0001t0006g0189a0001c0001t0007g0216a0001c0001t0007g0220others(4): Show | 7 | HG00738.hp2 HG02523.hp2 NA18949.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150-2120_1150-209 others(28): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(18): Show |
11 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0014g0246others(8): Show | 12 | HG00280.hp2 HG00438.hp2 HG01081.hp2 others(9): Show |
intron_variant | MODIFIER | c.1150-2097_1150-209 others(29): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(19): Show |
8 | a0001c0001t0014g0248a0001c0001t0030g0258a0001c0001t0052g0238others(5): Show | 8 | HG01516.hp1 HG03195.hp2 HG03239.hp1 others(5): Show |
intron_variant | MODIFIER | c.1150-2097_1150-209 others(30): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(21): Show |
1 | a0001c0001t0033g0223 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1150-2097_1150-209 others(32): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(22): Show |
2 | a0001c0001t0034g0225a0001c0001t0050g0207 | 2 | NA18963.hp2 NA18971.hp1 |
intron_variant | MODIFIER | c.1150-2097_1150-209 others(33): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(24): Show |
3 | a0001c0001t0009g0202a0001c0001t0014g0212a0001c0001t0033g0254 | 3 | HG01978.hp2 HG04115.hp2 NA19240.hp1 |
intron_variant | MODIFIER | c.1150-2097_1150-209 others(35): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(25): Show |
2 | a0001c0001t0009g0196a0001c0001t0034g0241 | 2 | HG01433.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.1150-2097_1150-209 others(36): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(28): Show |
1 | a0001c0001t0009g0217 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.1150-2097_1150-209 others(39): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(29): Show |
1 | a0001c0001t0030g0210 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1150-2097_1150-209 others(40): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(32): Show |
2 | a0001c0001t0053g0230a0001c0001t0059g0206 | 2 | NA18960.hp2 NA18992.hp1 |
intron_variant | MODIFIER | c.1150-2097_1150-209 others(43): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
C | CTTTTTTT others(33): Show |
1 | a0001c0001t0009g0232 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1150-2097_1150-209 others(44): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
CT | C | 17 | a0001c0001t0023g0003a0001c0001t0023g0284a0001c0001t0023g0286others(14): Show | 17 | HG00323.hp1 HG02109.hp2 HG02145.hp2 others(14): Show |
intron_variant | MODIFIER | c.1150-2097delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
CTT | C | 6 | a0001c0001t0049g0236a0001c0001t0050g0234a0001c0001t0052g0235others(3): Show | 6 | HG01175.hp1 NA18962.hp2 NA18966.hp2 others(3): Show |
intron_variant | MODIFIER | c.1150-2098_1150-209 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
CTTT | C | 8 | a0001c0001t0010g0221a0001c0001t0010g0227a0001c0001t0010g0229others(5): Show | 8 | HG00642.hp1 HG01167.hp1 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.1150-2099_1150-209 others(7): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
CTTTT | C | 22 | a0001c0001t0002g0068a0001c0001t0002g0073a0001c0001t0008g0027others(19): Show | 23 | HG01884.hp2 HG02080.hp1 HG02109.hp1 others(20): Show |
intron_variant | MODIFIER | c.1150-2100_1150-209 others(8): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681235
|
CTTTTT | C | 67 | a0001c0001t0002g0010a0001c0001t0002g0029a0001c0001t0002g0030others(64): Show | 67 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(64): Show |
intron_variant | MODIFIER | c.1150-2101_1150-209 others(9): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681235 | |||||
chr1:151681404
|
G | A | 2 | a0001c0001t0022g0172a0001c0001t0087g0179 | 2 | HG01934.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.1150-1952G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151681404 | ||||||
chr1:151681532
|
G | A | 4 | a0001c0001t0002g0038a0001c0001t0062g0028a0001c0001t0146g0078others(1): Show | 4 | HG00408.hp2 NA19001.hp1 NA19080.hp2 others(1): Show |
intron_variant | MODIFIER | c.1150-1824G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151681532 | ||||||
chr1:151681575
|
C | G | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1150-1781C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151681575 | ||||||
chr1:151681783
|
C | CTTTTTAG others(31): Show |
5 | a0001c0001t0008g0025a0001c0001t0064g0026a0001c0001t0157g0050others(2): Show | 5 | HG00741.hp2 HG01256.hp2 HG01346.hp1 others(2): Show |
intron_variant | MODIFIER | c.1150-1571_1150-153 others(42): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr1 | 151681783 | |||||
chr1:151681952
|
C | T | 1 | a0001c0001t0013g0182 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1150-1404C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151681952 | ||||||
chr1:151682313
|
T | G | 1 | a0001c0001t0110g0256 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.1150-1043T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682313 | ||||||
chr1:151682512
|
G | A | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1150-844G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682512 | ||||||
chr1:151682543
|
G | A | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1150-813G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682543 | ||||||
chr1:151682545
|
A | G | 7 | a0001c0001t0104g0081a0001c0001t0105g0082a0001c0001t0127g0084others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1150-811A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682545 | ||||||
chr1:151682886
|
T | C | 1 | a0001c0001t0015g0296 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1150-470T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682886 | ||||||
chr1:151682890
|
C | T | 1 | a0001c0001t0015g0296 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1150-466C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682890 | ||||||
chr1:151682891
|
T | A | 1 | a0001c0001t0015g0296 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1150-465T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682891 | ||||||
chr1:151682892
|
G | C | 1 | a0001c0001t0015g0296 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1150-464G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682892 | ||||||
chr1:151682893
|
G | A | 1 | a0001c0001t0015g0296 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1150-463G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682893 | ||||||
chr1:151682894
|
G | T | 1 | a0001c0001t0015g0296 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1150-462G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682894 | ||||||
chr1:151682895
|
C | A | 1 | a0001c0001t0015g0296 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1150-461C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682895 | ||||||
chr1:151682967
|
G | A | 1 | a0001c0001t0044g0160 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.1150-389G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151682967 | ||||||
chr1:151683051
|
C | A | 213 | a0001c0001t0002g0010a0001c0001t0002g0029a0001c0001t0002g0030others(210): Show | 216 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.1150-305C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151683051 | ||||||
chr1:151683151
|
A | G | 42 | a0001c0001t0004g0342a0001c0001t0005g0328a0001c0001t0015g0289others(39): Show | 43 | HG00323.hp2 HG00423.hp2 HG00597.hp2 others(40): Show |
intron_variant | MODIFIER | c.1150-205A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151683151 | ||||||
chr1:151683275
|
C | T | 27 | a0001c0001t0011g0243a0001c0001t0011g0262a0001c0001t0011g0264others(24): Show | 27 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(24): Show |
intron_variant | MODIFIER | c.1150-81C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 7/11 | chr1 | 151683275 | ||||||
chr1:151683594
|
C | T | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1239+149C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151683594 | ||||||
chr1:151683728
|
G | A | 1 | a0001c0001t0036g0092 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.1239+283G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151683728 | ||||||
chr1:151683850
|
A | G | 20 | a0001c0001t0011g0243a0001c0001t0011g0262a0001c0001t0011g0264others(17): Show | 20 | HG00438.hp1 HG00639.hp1 HG01099.hp1 others(17): Show |
intron_variant | MODIFIER | c.1239+405A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151683850 | ||||||
chr1:151683921
|
C | A | 9 | a0001c0001t0024g0354a0001c0001t0024g0355a0001c0001t0024g0356others(6): Show | 10 | HG01884.hp2 HG02257.hp2 HG02572.hp2 others(7): Show |
intron_variant | MODIFIER | c.1239+476C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151683921 | ||||||
chr1:151684299
|
C | G | 1 | a0001c0001t0137g0338 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.1239+854C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151684299 | ||||||
chr1:151684418
|
G | A | 62 | a0001c0001t0002g0010a0001c0001t0002g0029a0001c0001t0002g0030others(59): Show | 62 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(59): Show |
intron_variant | MODIFIER | c.1239+973G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151684418 | ||||||
chr1:151684598
|
T | C | 16 | a0001c0001t0023g0003a0001c0001t0023g0284a0001c0001t0023g0286others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1239+1153T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151684598 | ||||||
chr1:151684635
|
C | A | 82 | a0001c0001t0002g0010a0001c0001t0002g0029a0001c0001t0002g0030others(79): Show | 82 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.1239+1190C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151684635 | ||||||
chr1:151684934
|
G | A | 2 | a0001c0001t0007g0214a0001c0001t0033g0213 | 2 | HG03492.hp1 HG04184.hp2 |
intron_variant | MODIFIER | c.1239+1489G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151684934 | ||||||
chr1:151685190
|
T | A | 1 | a0001c0001t0141g0013 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1239+1745T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151685190 | ||||||
chr1:151685360
|
T | G | 1 | a0001c0001t0010g0280 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.1239+1915T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151685360 | ||||||
chr1:151685368
|
A | G | 2 | a0001c0001t0020g0040a0001c0001t0020g0053 | 2 | NA18988.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.1239+1923A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151685368 | ||||||
chr1:151685419
|
C | T | 1 | a0001c0001t0011g0264 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.1239+1974C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151685419 | ||||||
chr1:151685479
|
C | G | 1 | a0001c0001t0004g0167 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.1239+2034C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151685479 | ||||||
chr1:151685677
|
G | A | 10 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(7): Show | 10 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1239+2232G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151685677 | ||||||
chr1:151685786
|
AAGTAATA others(9): Show |
A | 1 | a0001c0001t0002g0038 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1239+2343_1239+235 others(20): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151685786 | |||||
chr1:151685792
|
T | G | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1239+2347T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151685792 | ||||||
chr1:151686067
|
G | A | 2 | a0001c0001t0027g0343a0001c0001t0027g0348 | 2 | HG00735.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1239+2622G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151686067 | ||||||
chr1:151686089
|
C | A | 1 | a0001c0001t0041g0345 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.1239+2644C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151686089 | ||||||
chr1:151686178
|
A | G | 16 | a0001c0001t0023g0003a0001c0001t0023g0284a0001c0001t0023g0286others(13): Show | 16 | HG02109.hp2 HG02145.hp2 HG02486.hp2 others(13): Show |
intron_variant | MODIFIER | c.1239+2733A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151686178 | ||||||
chr1:151686463
|
G | A | 8 | a0001c0001t0008g0025a0001c0001t0008g0051a0001c0001t0064g0026others(5): Show | 8 | HG00741.hp2 HG01256.hp2 HG01346.hp1 others(5): Show |
intron_variant | MODIFIER | c.1239+3018G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151686463 | ||||||
chr1:151686547
|
G | A | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1239+3102G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151686547 | ||||||
chr1:151686592
|
T | A | 1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1239+3147T>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151686592 | ||||||
chr1:151686595
|
A | G | 118 | a0001c0001t0006g0001a0001c0001t0006g0188a0001c0001t0006g0189others(115): Show | 121 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(118): Show |
intron_variant | MODIFIER | c.1239+3150A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151686595 | ||||||
chr1:151686890
|
T | C | 73 | a0001c0001t0002g0010a0001c0001t0002g0029a0001c0001t0002g0030others(70): Show | 73 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(70): Show |
intron_variant | MODIFIER | c.1239+3445T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151686890 | ||||||
chr1:151687311
|
G | A | 9 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(6): Show | 9 | HG02109.hp1 HG02258.hp2 HG02280.hp1 others(6): Show |
intron_variant | MODIFIER | c.1239+3866G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151687311 | ||||||
chr1:151687486
|
A | C | 1 | a0001c0001t0022g0291 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.1239+4041A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151687486 | ||||||
chr1:151687603
|
C | G | 7 | a0001c0001t0104g0081a0001c0001t0105g0082a0001c0001t0127g0084others(4): Show | 7 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1239+4158C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151687603 | ||||||
chr1:151687675
|
G | A | 4 | a0001c0001t0001g0117a0001c0001t0001g0125a0001c0001t0001g0132others(1): Show | 4 | NA18943.hp1 NA19062.hp1 NA19064.hp2 others(1): Show |
intron_variant | MODIFIER | c.1239+4230G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151687675 | ||||||
chr1:151687863
|
G | A | 1 | a0001c0001t0005g0140 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1239+4418G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151687863 | ||||||
chr1:151687902
|
C | G | 1 | a0001c0001t0056g0173 | 1 | NA19011.hp1 | intron_variant | MODIFIER | c.1239+4457C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151687902 | ||||||
chr1:151687945
|
C | CA | 9 | a0001c0001t0001g0130a0001c0001t0003g0006a0001c0001t0015g0296others(6): Show | 9 | HG02055.hp2 HG02109.hp2 HG06807.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240-4475dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151687945 | |||||
chr1:151687945
|
CA | C | 9 | a0001c0001t0053g0245a0001c0001t0067g0361a0001c0001t0077g0200others(6): Show | 9 | HG01081.hp2 HG02145.hp1 HG02280.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240-4475delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151687945 | |||||
chr1:151687945
|
CAA | C | 203 | a0001c0001t0002g0010a0001c0001t0002g0029a0001c0001t0002g0030others(200): Show | 206 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(203): Show |
intron_variant | MODIFIER | c.1240-4476_1240-447 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151687945 | |||||
chr1:151687960
|
A | C | 2 | a0001c0001t0007g0220a0001c0001t0034g0211 | 2 | HG02523.hp2 NA18949.hp1 |
intron_variant | MODIFIER | c.1240-4475A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151687960 | ||||||
chr1:151687971
|
C | CA | 90 | a0001c0001t0002g0033a0001c0001t0006g0001a0001c0001t0006g0188others(87): Show | 92 | HG00280.hp2 HG00323.hp1 HG00438.hp2 others(89): Show |
intron_variant | MODIFIER | c.1240-4453dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151687971 | |||||
chr1:151687979
|
A | G | 3 | a0001c0001t0148g0016a0001c0001t0149g0015a0001c0001t0165g0014 | 3 | HG02145.hp1 HG02976.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.1240-4456A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151687979 | ||||||
chr1:151688048
|
A | G | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240-4387A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151688048 | ||||||
chr1:151688139
|
A | G | 9 | a0001c0001t0007g0216a0001c0001t0007g0253a0001c0001t0007g0255others(6): Show | 9 | HG00323.hp1 HG00735.hp1 HG00738.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240-4296A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151688139 | ||||||
chr1:151688275
|
G | A | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1240-4160G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151688275 | ||||||
chr1:151688295
|
A | G | 1 | a0001c0001t0013g0171 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.1240-4140A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151688295 | ||||||
chr1:151688307
|
C | A | 1 | a0001c0001t0108g0201 | 1 | NA19001.hp2 | intron_variant | MODIFIER | c.1240-4128C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151688307 | ||||||
chr1:151688522
|
C | T | 2 | a0001c0001t0047g0191a0001c0001t0047g0193 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.1240-3913C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151688522 | ||||||
chr1:151688631
|
C | CA | 209 | a0001c0001t0001g0120a0001c0001t0002g0010a0001c0001t0002g0029others(206): Show | 212 | HG00280.hp2 HG00323.hp1 HG00408.hp2 others(209): Show |
intron_variant | MODIFIER | c.1240-3787dupA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151688631 | |||||
chr1:151688631
|
C | CAA | 9 | a0001c0001t0030g0210a0001c0001t0104g0081a0001c0001t0105g0082others(6): Show | 9 | HG02258.hp1 HG02622.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1240-3788_1240-378 others(6): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151688631 | |||||
chr1:151688917
|
C | A | 2 | a0001c0001t0009g0196a0001c0001t0009g0217 | 2 | HG01515.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1240-3518C>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151688917 | ||||||
chr1:151689107
|
C | G | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1240-3328C>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151689107 | ||||||
chr1:151689108
|
A | C | 3 | a0001c0001t0003g0142a0001c0001t0003g0145a0001c0001t0003g0149 | 3 | HG01261.hp2 HG03710.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.1240-3327A>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151689108 | ||||||
chr1:151689116
|
C | T | 8 | a0001c0001t0037g0024a0001c0001t0037g0043a0001c0001t0037g0045others(5): Show | 8 | HG00423.hp1 HG02071.hp2 HG02083.hp2 others(5): Show |
intron_variant | MODIFIER | c.1240-3319C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151689116 | ||||||
chr1:151689124
|
G | A | 4 | a0001c0001t0141g0013a0001c0001t0148g0016a0001c0001t0149g0015others(1): Show | 4 | HG02145.hp1 HG02280.hp2 HG02976.hp1 others(1): Show |
intron_variant | MODIFIER | c.1240-3311G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151689124 | ||||||
chr1:151689637
|
G | A | 94 | a0001c0001t0002g0010a0001c0001t0002g0029a0001c0001t0002g0030others(91): Show | 94 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(91): Show |
intron_variant | MODIFIER | c.1240-2798G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151689637 | ||||||
chr1:151689737
|
C | T | 1 | a0001c0001t0179g0257 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1240-2698C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151689737 | ||||||
chr1:151689762
|
A | G | 1 | a0001c0001t0077g0200 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1240-2673A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151689762 | ||||||
chr1:151689850
|
CT | C | 110 | a0001c0001t0002g0038a0001c0001t0006g0001a0001c0001t0006g0188others(107): Show | 112 | HG00280.hp2 HG00323.hp1 HG00438.hp1 others(109): Show |
intron_variant | MODIFIER | c.1240-2573delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151689850 | |||||
chr1:151689917
|
C | T | 2 | a0001c0001t0142g0023a0001c0001t0143g0359 | 2 | HG02451.hp2 HG02717.hp1 |
intron_variant | MODIFIER | c.1240-2518C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151689917 | ||||||
chr1:151690223
|
G | A | 1 | a0001c0001t0085g0346 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1240-2212G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151690223 | ||||||
chr1:151690337
|
C | T | 1 | a0001c0001t0073g0344 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1240-2098C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151690337 | ||||||
chr1:151690510
|
G | T | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1240-1925G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151690510 | ||||||
chr1:151690616
|
G | T | 1 | a0001c0001t0151g0017 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.1240-1819G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151690616 | ||||||
chr1:151690617
|
T | G | 1 | a0003c0005t0018g0325 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1240-1818T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151690617 | ||||||
chr1:151690638
|
G | A | 1 | a0001c0001t0034g0211 | 1 | NA18949.hp1 | intron_variant | MODIFIER | c.1240-1797G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151690638 | ||||||
chr1:151690662
|
G | A | 4 | a0001c0001t0046g0190a0001c0001t0046g0192a0001c0001t0047g0191others(1): Show | 4 | HG01074.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1240-1773G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151690662 | ||||||
chr1:151690677
|
G | A | 1 | a0001c0001t0130g0267 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.1240-1758G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151690677 | ||||||
chr1:151691157
|
C | T | 1 | a0001c0001t0081g0009 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1240-1278C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151691157 | ||||||
chr1:151691305
|
A | G | 82 | a0001c0001t0002g0010a0001c0001t0002g0029a0001c0001t0002g0030others(79): Show | 82 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.1240-1130A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151691305 | ||||||
chr1:151691356
|
A | G | 1 | a0001c0001t0009g0202 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.1240-1079A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151691356 | ||||||
chr1:151691387
|
G | A | 1 | a0001c0001t0144g0011 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1240-1048G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151691387 | ||||||
chr1:151691466
|
G | GT | 25 | a0001c0001t0001g0118a0001c0001t0002g0010a0001c0001t0002g0038others(22): Show | 25 | HG00544.hp2 HG00642.hp1 HG00673.hp2 others(22): Show |
intron_variant | MODIFIER | c.1240-951dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151691466 | |||||
chr1:151691875
|
T | C | 6 | a0001c0001t0049g0236a0001c0001t0049g0237a0001c0001t0052g0235others(3): Show | 6 | NA18962.hp2 NA18966.hp2 NA18979.hp1 others(3): Show |
intron_variant | MODIFIER | c.1240-560T>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151691875 | ||||||
chr1:151691966
|
G | A | 1 | a0001c0001t0067g0361 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1240-469G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151691966 | ||||||
chr1:151692402
|
C | T | 2 | a0001c0001t0003g0098a0001c0001t0003g0100 | 2 | HG01934.hp1 HG02738.hp1 |
intron_variant | MODIFIER | c.1240-33C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | chr1 | 151692402 | ||||||
chr1:151692406
|
C | CT | 85 | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0118others(82): Show | 85 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(82): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1240-3dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151692406 | |||||
chr1:151692406
|
C | CTT | 68 | a0001c0001t0001g0136a0001c0001t0003g0099a0001c0001t0003g0141others(65): Show | 70 | HG00323.hp1 HG00438.hp1 HG00438.hp2 others(67): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1240-4_1240-3dupTT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151692406 | |||||
chr1:151692406
|
C | CTTT | 14 | a0001c0001t0003g0145a0001c0001t0003g0149a0001c0001t0007g0228others(11): Show | 14 | HG00280.hp2 HG01081.hp2 HG01167.hp1 others(11): Show |
splice_acceptor_variant&intron_variant | HIGH | c.1240-5_1240-3dupTT others(1): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151692406 | |||||
chr1:151692406
|
CT | C | 21 | a0001c0001t0004g0166a0001c0001t0012g0102a0001c0001t0012g0104others(18): Show | 21 | HG01515.hp2 HG02109.hp1 HG02145.hp1 others(18): Show |
splice_region_variant&intron_variant | LOW | c.1240-3delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151692406 | |||||
chr1:151692406
|
CTT | C | 70 | a0001c0001t0002g0010a0001c0001t0002g0029a0001c0001t0002g0030others(67): Show | 70 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(67): Show |
splice_region_variant&intron_variant | LOW | c.1240-4_1240-3delTT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151692406 | |||||
chr1:151692406
|
CTTTTTTT others(4): Show |
C | 1 | a0001c0001t0005g0328 | 1 | NA19068.hp2 | splice_region_variant&intron_variant | LOW | c.1240-13_1240-3delT others(10): Show |
SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr1 | 151692406 | |||||
chr1:151692667
|
TA | T | 5 | a0001c0001t0022g0172a0001c0001t0044g0160a0001c0001t0044g0302others(2): Show | 5 | HG01934.hp2 NA19012.hp1 NA19012.hp2 others(2): Show |
intron_variant | MODIFIER | c.1389+84delA | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 9/11 | chr1 | 151692667 | ||||||
chr1:151692849
|
C | T | 11 | a0001c0001t0012g0102a0001c0001t0012g0104a0001c0001t0012g0106others(8): Show | 11 | HG02109.hp1 HG02129.hp2 HG02258.hp2 others(8): Show |
intron_variant | MODIFIER | c.1390-62C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 9/11 | chr1 | 151692849 | ||||||
chr1:151693078
|
G | T | 1 | a0003c0005t0018g0325 | 1 | NA18997.hp1 | intron_variant | MODIFIER | c.1518+39G>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 10/11 | chr1 | 151693078 | ||||||
chr1:151693086
|
G | GT | 74 | a0001c0001t0002g0010a0001c0001t0002g0029a0001c0001t0002g0030others(71): Show | 74 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.1518+57dupT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr1 | 151693086 | |||||
chr1:151693125
|
T | G | 2 | a0001c0001t0016g0287a0001c0001t0018g0315 | 2 | HG02055.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.1518+86T>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 10/11 | chr1 | 151693125 | ||||||
chr1:151693381
|
CT | C | 83 | a0001c0001t0002g0010a0001c0001t0002g0029a0001c0001t0002g0030others(80): Show | 83 | HG00408.hp2 HG00423.hp1 HG00544.hp2 others(80): Show |
intron_variant | MODIFIER | c.1519-42delT | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 10/11 | chr1 | 151693381 | ||||||
chr1:151693549
|
T | TG | 5 | a0001c0001t0040g0249a0001c0001t0040g0252a0001c0001t0050g0207others(2): Show | 5 | NA18946.hp2 NA18971.hp1 NA19005.hp2 others(2): Show |
intron_variant | MODIFIER | c.1578+68dupG | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 11/11 | INFO_REALIGN_3_PRIME | chr1 | 151693549 | |||||
chr1:151693659
|
G | C | 2 | a0001c0001t0022g0320a0001c0001t0022g0321 | 2 | HG03579.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1578+176G>C | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 11/11 | chr1 | 151693659 | ||||||
chr1:151693677
|
C | T | 1 | a0001c0001t0029g0273 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1578+194C>T | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 11/11 | chr1 | 151693677 | ||||||
chr1:151694036
|
A | G | 7 | a0001c0001t0035g0020a0001c0001t0035g0021a0001c0001t0035g0022others(4): Show | 7 | HG02895.hp1 HG02896.hp2 HG02965.hp1 others(4): Show |
intron_variant | MODIFIER | c.1579-334A>G | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 11/11 | chr1 | 151694036 | ||||||
chr1:151694325
|
G | A | 1 | a0001c0001t0066g0089 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.1579-45G>A | SNX27 | ENSG00000143376.14 | transcript | ENST00000458013.7 | protein_coding | 11/11 | chr1 | 151694325 |