geneid | 64089 |
---|---|
ensemblid | ENSG00000104497.15 |
hgncid | 14980 |
symbol | SNX16 |
name | sorting nexin 16 |
refseq_nuc | NM_152836.3 |
refseq_prot | NP_690049.1 |
ensembl_nuc | ENST00000345957.9 |
ensembl_prot | ENSP00000322652.4 |
mane_status | MANE Select |
chr | chr8 |
start | 81799583 |
end | 81842185 |
strand | - |
ver | v1.2 |
region | chr8:81799583-81842185 |
region5000 | chr8:81794583-81847185 |
regionname0 | SNX16_chr8_81799583_81842185 |
regionname5000 | SNX16_chr8_81794583_81847185 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000 | 0/0 | 0 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001 | 1/1 | 344 | 299 | 77 | 69 | 95 | 10 | 46 | 70 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0002 | 0/0 | 344 | 3 | 3 | 0 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0003 | 0/0 | 344 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0004 | 0/0 | 120 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1035 | 230 | 75 | 51 | 61 | 7 | 34 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
c0002 | 0/0 | 1035 | 68 | 2 | 18 | 33 | 3 | 12 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
c0003 | 0/0 | 1035 | 3 | 3 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
c0004 | 0/0 | 1035 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
c0005 | 0/0 | 1035 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
c0006 | 0/0 | 1035 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
c0007 | 0/0 | 1015 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2077 | 77 | 41 | 18 | 3 | 4 | 11 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
t0002 | 0/1 | 2075 | 69 | 4 | 17 | 34 | 1 | 12 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
t0003 | 0/0 | 2077 | 67 | 2 | 18 | 32 | 3 | 12 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
t0004 | 0/0 | 2077 | 45 | 5 | 10 | 23 | 1 | 6 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
t0005 | 0/0 | 2077 | 15 | 5 | 5 | 0 | 1 | 4 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
t0006 | 0/0 | 2077 | 14 | 13 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
t0007 | 0/0 | 2077 | 7 | 7 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
t0008 | 0/0 | 2077 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
t0009 | 0/0 | 2077 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
t0010 | 1/0 | 2075 | 1 | 0 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
t0011 | 0/0 | 2077 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
t0012 | 0/0 | 2077 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
t0013 | 0/0 | 2075 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
t0014 | 0/0 | 2077 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
t0015 | 0/0 | 2075 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
t0016 | 0/0 | 2075 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
t0017 | 0/0 | 2075 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 12 | 9 | 0 | 2 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0002 | 0/0 | 11 | 0 | 2 | 9 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0003 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0005 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0006 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0007 | 0/0 | 5 | 2 | 1 | 1 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0008 | 0/0 | 4 | 2 | 1 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0009 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0012 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0013 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0021 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0030 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0033 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0006 | 0/0 | 1035 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0001 | 1/1 | 1035 | 230 | 75 | 51 | 61 | 7 | 34 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0002 | 0/0 | 1035 | 68 | 2 | 18 | 33 | 3 | 12 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0005 | 0/0 | 1035 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0002c0003 | 0/0 | 1035 | 3 | 3 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0003c0004 | 0/0 | 1035 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0004c0007 | 0/0 | 1015 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0006t0002 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0001t0001 | 0/0 | 3111 | 77 | 41 | 18 | 3 | 4 | 11 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0001t0002 | 0/1 | 3109 | 68 | 4 | 17 | 33 | 1 | 12 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0001t0004 | 0/0 | 3111 | 42 | 3 | 10 | 22 | 1 | 6 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0001t0005 | 0/0 | 3111 | 15 | 5 | 5 | 0 | 1 | 4 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0001t0006 | 0/0 | 3111 | 13 | 13 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0001t0007 | 0/0 | 3111 | 4 | 4 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0001t0008 | 0/0 | 3111 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0001t0009 | 0/0 | 3111 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0001t0010 | 1/0 | 3109 | 1 | 0 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0001t0012 | 0/0 | 3111 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0001t0013 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0001t0014 | 0/0 | 3111 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0001t0015 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0001t0016 | 0/0 | 3109 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0001t0017 | 0/0 | 3109 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0002t0003 | 0/0 | 3111 | 67 | 2 | 18 | 32 | 3 | 12 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0002t0011 | 0/0 | 3111 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0001c0005t0004 | 0/0 | 3111 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0002c0003t0007 | 0/0 | 3111 | 3 | 3 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0003c0004t0004 | 0/0 | 3111 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
a0004c0007t0006 | 0/0 | 3091 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | copy fasta | chr8 | 81794583 | 81847185 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0000c0006t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0001 | 0/0 | 12 | 9 | 0 | 2 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0004 | 0/0 | 6 | 6 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0005 | 0/0 | 5 | 0 | 4 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0008 | 0/0 | 4 | 2 | 1 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0009 | 0/0 | 3 | 0 | 1 | 0 | 0 | 2 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0010 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0017 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0019 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0021 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0022 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0049 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0060 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0002 | 0/0 | 11 | 0 | 2 | 9 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0007 | 0/0 | 5 | 2 | 1 | 1 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0031 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0143 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0150 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0165 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0196 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0002g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0006 | 0/0 | 5 | 0 | 4 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0015 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0026 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0027 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0131 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0133 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0138 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0139 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0004g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0005g0029 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0005g0030 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0005g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0005g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0005g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0005g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0005g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0005g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0005g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0005g0162 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0005g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0005g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0005g0194 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0006g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0006g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0006g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0006g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0006g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0006g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0006g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0006g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0006g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0006g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0006g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0006g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0007g0032 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0007g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0007g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0008g0020 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0009g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0009g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0010g0033 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0012g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0013g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0014g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0015g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0016g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0001t0017g0224 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0003 | 0/0 | 7 | 0 | 1 | 6 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0011 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0012 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0013 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0014 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0023 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0087 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0089 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0094 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0095 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0102 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0003g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0002t0011g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0001c0005t0004g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0002c0003t0007g0028 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0002c0003t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0003c0004t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0003c0004t0004g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
a0004c0007t0006g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0062 | EUR | GBR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0164 | EUR | GBR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00140 | hp1 | a0001 | c0002 | t0003 | g0093 | EUR | GBR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00140 | hp2 | a0001 | c0002 | t0003 | g0094 | EUR | GBR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00280 | hp1 | a0001 | c0001 | t0004 | g0138 | EUR | FIN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0043 | EUR | FIN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00423 | hp1 | a0001 | c0002 | t0003 | g0076 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00423 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00438 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00438 | hp2 | a0001 | c0001 | t0002 | g0204 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00558 | hp1 | a0000 | c0006 | t0002 | g0206 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00558 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00609 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00639 | hp1 | a0001 | c0002 | t0003 | g0023 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00639 | hp2 | a0001 | c0001 | t0005 | g0029 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00642 | hp1 | a0001 | c0001 | t0002 | g0173 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00642 | hp2 | a0001 | c0002 | t0003 | g0105 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00673 | hp1 | a0001 | c0002 | t0003 | g0101 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00673 | hp2 | a0001 | c0005 | t0004 | g0126 | EAS | CHS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00733 | hp1 | a0001 | c0001 | t0002 | g0203 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00733 | hp2 | a0001 | c0001 | t0014 | g0198 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0065 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00735 | hp2 | a0001 | c0002 | t0003 | g0090 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00738 | hp1 | a0001 | c0002 | t0003 | g0100 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00738 | hp2 | a0001 | c0001 | t0005 | g0146 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00741 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0182 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01069 | hp1 | a0001 | c0001 | t0002 | g0147 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0057 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01070 | hp2 | a0001 | c0002 | t0003 | g0084 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01071 | hp2 | a0001 | c0002 | t0003 | g0012 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0170 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01074 | hp2 | a0001 | c0002 | t0003 | g0012 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0019 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0044 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01099 | hp1 | a0001 | c0002 | t0003 | g0003 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0133 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01106 | hp1 | a0001 | c0001 | t0005 | g0194 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01106 | hp2 | a0001 | c0001 | t0002 | g0172 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0061 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01109 | hp2 | a0001 | c0002 | t0003 | g0075 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01168 | hp1 | a0001 | c0002 | t0003 | g0072 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0017 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01169 | hp2 | a0004 | c0007 | t0006 | g0214 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0211 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01175 | hp2 | a0001 | c0001 | t0002 | g0212 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01192 | hp1 | a0001 | c0001 | t0005 | g0156 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01192 | hp2 | a0001 | c0002 | t0003 | g0097 | AMR | PUR | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01255 | hp1 | a0001 | c0001 | t0005 | g0155 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01255 | hp2 | a0001 | c0001 | t0002 | g0161 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01256 | hp1 | a0001 | c0002 | t0003 | g0110 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01256 | hp2 | a0001 | c0002 | t0003 | g0014 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01257 | hp2 | a0001 | c0001 | t0004 | g0132 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01258 | hp2 | a0001 | c0002 | t0003 | g0014 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0026 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0008 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01346 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01346 | hp2 | a0001 | c0001 | t0002 | g0148 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01496 | hp1 | a0001 | c0002 | t0003 | g0096 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01496 | hp2 | a0001 | c0001 | t0002 | g0002 | AMR | CLM | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01515 | hp1 | a0001 | c0002 | t0003 | g0095 | EUR | IBS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0008 | EUR | IBS | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01884 | hp1 | a0001 | c0001 | t0004 | g0134 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01884 | hp2 | a0001 | c0001 | t0006 | g0184 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01891 | hp1 | a0001 | c0002 | t0003 | g0103 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0036 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01928 | hp1 | a0001 | c0001 | t0004 | g0139 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01928 | hp2 | a0001 | c0002 | t0003 | g0014 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0202 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01934 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01943 | hp1 | a0001 | c0001 | t0002 | g0002 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01943 | hp2 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0196 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01978 | hp1 | a0001 | c0001 | t0004 | g0006 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01978 | hp2 | a0001 | c0002 | t0003 | g0109 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0120 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02004 | hp1 | a0001 | c0002 | t0003 | g0089 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0009 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02015 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02015 | hp2 | a0001 | c0002 | t0011 | g0083 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02055 | hp1 | a0001 | c0001 | t0009 | g0041 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02055 | hp2 | a0001 | c0001 | t0006 | g0186 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02074 | hp1 | a0001 | c0001 | t0004 | g0127 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02074 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02080 | hp1 | a0001 | c0002 | t0003 | g0023 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02080 | hp2 | a0001 | c0001 | t0016 | g0220 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02083 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02083 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02132 | hp1 | a0001 | c0002 | t0003 | g0107 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02132 | hp2 | a0001 | c0001 | t0004 | g0123 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02135 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02135 | hp2 | a0001 | c0002 | t0003 | g0108 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02145 | hp2 | a0001 | c0001 | t0006 | g0210 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02257 | hp2 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0051 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02273 | hp1 | a0001 | c0001 | t0002 | g0180 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02273 | hp2 | a0001 | c0001 | t0004 | g0121 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02280 | hp1 | a0001 | c0001 | t0005 | g0030 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02293 | hp1 | a0001 | c0001 | t0002 | g0201 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0005 | AMR | PEL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0007 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0022 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02523 | hp1 | a0001 | c0001 | t0004 | g0124 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | KHV | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0021 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02572 | hp2 | a0002 | c0003 | t0007 | g0028 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02602 | hp1 | a0001 | c0001 | t0004 | g0131 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02602 | hp2 | a0001 | c0002 | t0003 | g0013 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02615 | hp1 | a0001 | c0001 | t0006 | g0183 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0037 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0010 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0064 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02630 | hp2 | a0001 | c0001 | t0006 | g0192 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02647 | hp1 | a0001 | c0002 | t0003 | g0077 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02683 | hp1 | a0001 | c0002 | t0003 | g0102 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02683 | hp2 | a0001 | c0002 | t0003 | g0013 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02698 | hp1 | a0001 | c0002 | t0003 | g0088 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0021 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02717 | hp1 | a0001 | c0001 | t0004 | g0026 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02717 | hp2 | a0001 | c0001 | t0006 | g0189 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02723 | hp1 | a0001 | c0001 | t0012 | g0142 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02723 | hp2 | a0001 | c0001 | t0006 | g0190 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0216 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0039 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0209 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02738 | hp2 | a0001 | c0001 | t0001 | g0049 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02809 | hp1 | a0001 | c0001 | t0006 | g0160 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0058 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02818 | hp2 | a0002 | c0003 | t0007 | g0028 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02895 | hp2 | a0001 | c0001 | t0005 | g0029 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02922 | hp1 | a0001 | c0001 | t0005 | g0152 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0047 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0066 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02970 | hp2 | a0001 | c0001 | t0006 | g0187 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0053 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03017 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0046 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03041 | hp1 | a0001 | c0001 | t0005 | g0163 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0035 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03098 | hp1 | a0001 | c0001 | t0004 | g0114 | AFR | MSL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0001 | AFR | MSL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0059 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03130 | hp2 | a0001 | c0001 | t0001 | g0010 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0045 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03139 | hp2 | a0002 | c0003 | t0007 | g0153 | AFR | ESN | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03239 | hp1 | a0001 | c0001 | t0004 | g0129 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0143 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03486 | hp1 | a0003 | c0004 | t0004 | g0115 | AFR | MSL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03486 | hp2 | a0001 | c0001 | t0006 | g0188 | AFR | MSL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03490 | hp1 | a0001 | c0001 | t0005 | g0030 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03490 | hp2 | a0001 | c0001 | t0004 | g0027 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03492 | hp1 | a0001 | c0001 | t0004 | g0027 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03540 | hp2 | a0001 | c0001 | t0007 | g0032 | AFR | GWD | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0050 | AFR | MSL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0067 | AFR | MSL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03654 | hp1 | a0001 | c0001 | t0002 | g0169 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03654 | hp2 | a0001 | c0002 | t0003 | g0082 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03669 | hp1 | a0001 | c0001 | t0005 | g0157 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03669 | hp2 | a0001 | c0002 | t0003 | g0104 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03688 | hp1 | a0001 | c0002 | t0003 | g0087 | SAS | STU | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0167 | SAS | STU | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03704 | hp1 | a0001 | c0001 | t0017 | g0224 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03704 | hp2 | a0001 | c0002 | t0003 | g0099 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03710 | hp1 | a0001 | c0001 | t0002 | g0168 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03710 | hp2 | a0001 | c0001 | t0005 | g0158 | SAS | PJL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0040 | SAS | BEB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | BEB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03834 | hp1 | a0001 | c0001 | t0005 | g0159 | SAS | BEB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0001 | SAS | BEB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0054 | SAS | BEB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03927 | hp2 | a0001 | c0001 | t0004 | g0140 | SAS | BEB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03942 | hp1 | a0001 | c0001 | t0004 | g0130 | SAS | BEB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0195 | SAS | BEB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0175 | SAS | STU | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG04199 | hp2 | a0001 | c0002 | t0003 | g0106 | SAS | STU | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0060 | SAS | STU | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG04204 | hp2 | a0001 | c0002 | t0003 | g0013 | SAS | STU | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG04228 | hp1 | a0001 | c0002 | t0003 | g0092 | SAS | STU | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0038 | SAS | STU | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | YRI | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | CHB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18747 | hp2 | a0001 | c0001 | t0004 | g0128 | EAS | CHB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18906 | hp1 | a0003 | c0004 | t0004 | g0116 | AFR | YRI | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | YRI | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18939 | hp1 | a0001 | c0001 | t0004 | g0122 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18939 | hp2 | a0001 | c0002 | t0003 | g0071 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18941 | hp1 | a0001 | c0001 | t0004 | g0228 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18944 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18944 | hp2 | a0001 | c0001 | t0004 | g0111 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18946 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18947 | hp1 | a0001 | c0001 | t0013 | g0199 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18947 | hp2 | a0001 | c0001 | t0004 | g0135 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18950 | hp2 | a0001 | c0001 | t0004 | g0113 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18951 | hp1 | a0001 | c0002 | t0003 | g0079 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18951 | hp2 | a0001 | c0001 | t0004 | g0125 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18952 | hp2 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18957 | hp1 | a0001 | c0002 | t0003 | g0081 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18957 | hp2 | a0001 | c0001 | t0002 | g0222 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18960 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18960 | hp2 | a0001 | c0002 | t0003 | g0074 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18964 | hp2 | a0001 | c0002 | t0003 | g0012 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18965 | hp2 | a0001 | c0002 | t0003 | g0024 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18970 | hp1 | a0001 | c0002 | t0003 | g0024 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18971 | hp1 | a0001 | c0002 | t0003 | g0078 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0007 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18980 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18980 | hp2 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18983 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0136 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18984 | hp1 | a0001 | c0001 | t0004 | g0112 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0221 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18985 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18992 | hp1 | a0001 | c0001 | t0004 | g0006 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18998 | hp1 | a0001 | c0002 | t0003 | g0073 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0151 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19000 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19000 | hp2 | a0001 | c0001 | t0004 | g0141 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19002 | hp1 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19004 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19007 | hp2 | a0001 | c0002 | t0003 | g0098 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19012 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19012 | hp2 | a0001 | c0002 | t0003 | g0025 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19030 | hp1 | a0001 | c0001 | t0007 | g0218 | AFR | LWK | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0034 | AFR | LWK | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19043 | hp2 | a0001 | c0001 | t0007 | g0217 | AFR | LWK | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19056 | hp1 | a0001 | c0002 | t0003 | g0070 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19058 | hp2 | a0001 | c0002 | t0003 | g0091 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19062 | hp1 | a0001 | c0002 | t0003 | g0069 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19062 | hp2 | a0001 | c0001 | t0002 | g0225 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19063 | hp1 | a0001 | c0001 | t0015 | g0226 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19063 | hp2 | a0001 | c0002 | t0003 | g0068 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19065 | hp1 | a0001 | c0002 | t0003 | g0003 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19065 | hp2 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19079 | hp2 | a0001 | c0002 | t0003 | g0086 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19084 | hp1 | a0001 | c0001 | t0002 | g0002 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19084 | hp2 | a0001 | c0002 | t0003 | g0011 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19085 | hp1 | a0001 | c0001 | t0004 | g0227 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0205 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19088 | hp2 | a0001 | c0002 | t0003 | g0080 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19091 | hp1 | a0001 | c0001 | t0002 | g0219 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19091 | hp2 | a0001 | c0001 | t0004 | g0137 | EAS | JPT | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19240 | hp1 | a0001 | c0001 | t0008 | g0020 | AFR | YRI | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0165 | AFR | YRI | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | ASW | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0004 | AFR | ASW | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA20805 | hp1 | a0001 | c0001 | t0001 | g0005 | EUR | TSI | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA20805 | hp2 | a0001 | c0001 | t0005 | g0162 | EUR | TSI | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA20905 | hp1 | a0001 | c0001 | t0002 | g0176 | SAS | GIH | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA20905 | hp2 | a0001 | c0002 | t0003 | g0085 | SAS | GIH | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0004 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG02109 | hp2 | a0001 | c0001 | t0006 | g0191 | AFR | ACB | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03471 | hp1 | a0001 | c0001 | t0005 | g0177 | AFR | MSL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG03471 | hp2 | a0001 | c0001 | t0009 | g0042 | AFR | MSL | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG06807 | hp1 | a0001 | c0001 | t0006 | g0185 | AFR | USA | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
HG06807 | hp2 | a0001 | c0001 | t0006 | g0193 | AFR | USA | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | USA | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0207 | AFR | USA | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0001 | AFR | LWK | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
NA21309 | hp2 | a0001 | c0001 | t0007 | g0032 | AFR | LWK | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0150 | REF | REF | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0010 | g0033 | REF | REF | SNX16_chr8_81794583_81847185 | SNX16 | chr8 | 81794583 | 81847185 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:81801499
|
A | G | 1 | a0000 | 1 | HG00558.hp1 | stop_lost | HIGH | c.1033T>C | p.Ter345Glnext*? | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1193/3109 | 1033/1035 | 345/344 | chr8 | 81801499 | ||
chr8:81839610
|
ACAGTAAA others(14): Show |
A | 1 | a0004 | 1 | HG01169.hp2 | frameshift_variant&splice_donor_variant&splice_region_variant&intron_variant | HIGH | c.356_375+1delAAGAAA others(15): Show |
p.Glu119fs | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/8 | 356/1035 | 119/344 | chr8 | 81839610 | |||
chr8:81839694
|
G | A | 1 | a0002 | 3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
missense_variant | MODERATE | c.293C>T | p.Pro98Leu | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/8 | 453/3109 | 293/1035 | 98/344 | chr8 | 81839694 | ||
chr8:81839722
|
T | C | 1 | a0003 | 2 | HG03486.hp1 NA18906.hp1 |
missense_variant | MODERATE | c.265A>G | p.Arg89Gly | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/8 | 425/3109 | 265/1035 | 89/344 | chr8 | 81839722 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:81803109
|
A | C | 1 | a0001c0005 | 1 | HG00673.hp2 | synonymous_variant | LOW | c.801T>G | p.Thr267Thr | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 6/8 | 961/3109 | 801/1035 | 267/344 | chr8 | 81803109 | ||
chr8:81815334
|
T | C | 1 | a0001c0002 | 68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
synonymous_variant | LOW | c.672A>G | p.Glu224Glu | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/8 | 832/3109 | 672/1035 | 224/344 | chr8 | 81815334 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:81799615
|
T | A | 1 | a0001c0001t0009 | 2 | HG02055.hp1 HG03471.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1882A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1882 | chr8 | 81799615 | |||||
chr8:81799692
|
A | C | 1 | a0001c0001t0014 | 1 | HG00733.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1805T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1805 | chr8 | 81799692 | |||||
chr8:81799768
|
C | T | 1 | a0001c0001t0008 | 2 | HG03540.hp1 NA19240.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1729G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1729 | chr8 | 81799768 | |||||
chr8:81799918
|
A | G | 11 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(8): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
3_prime_UTR_variant | MODIFIER | c.*1579T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1579 | chr8 | 81799918 | |||||
chr8:81799962
|
T | C | 1 | a0001c0001t0016 | 1 | HG02080.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1535A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1535 | chr8 | 81799962 | |||||
chr8:81799999
|
C | T | 1 | a0001c0001t0015 | 1 | NA19063.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1498G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1498 | chr8 | 81799999 | |||||
chr8:81800007
|
C | CAA | 15 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(12): Show | 232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
3_prime_UTR_variant | MODIFIER | c.*1489_*1490insTT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1489 | chr8 | 81800007 | |||||
chr8:81800090
|
A | G | 2 | a0001c0001t0005a0001c0001t0014 | 16 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*1407T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1407 | chr8 | 81800090 | |||||
chr8:81800190
|
C | T | 1 | a0001c0001t0013 | 1 | NA18947.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1307G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1307 | chr8 | 81800190 | |||||
chr8:81800213
|
C | T | 1 | a0001c0002t0011 | 1 | HG02015.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1284G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 1284 | chr8 | 81800213 | |||||
chr8:81800694
|
A | C | 3 | a0001c0001t0001a0001c0001t0008a0001c0001t0009 | 81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
3_prime_UTR_variant | MODIFIER | c.*803T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 803 | chr8 | 81800694 | |||||
chr8:81800891
|
G | C | 3 | a0001c0001t0004a0001c0005t0004a0003c0004t0004 | 45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
3_prime_UTR_variant | MODIFIER | c.*606C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 606 | chr8 | 81800891 | |||||
chr8:81800988
|
G | A | 2 | a0001c0002t0003a0001c0002t0011 | 68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
3_prime_UTR_variant | MODIFIER | c.*509C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 509 | chr8 | 81800988 | |||||
chr8:81801169
|
C | A | 1 | a0001c0001t0012 | 1 | HG02723.hp1 | 3_prime_UTR_variant | MODIFIER | c.*328G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 328 | chr8 | 81801169 | |||||
chr8:81801460
|
T | C | 1 | a0001c0001t0017 | 1 | HG03704.hp1 | 3_prime_UTR_variant | MODIFIER | c.*37A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 8/8 | 37 | chr8 | 81801460 | |||||
chr8:81840056
|
A | G | 6 | a0001c0001t0004a0001c0001t0012a0001c0002t0003others(3): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
5_prime_UTR_variant | MODIFIER | c.-70T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/8 | 70 | chr8 | 81840056 | |||||
chr8:81842130
|
C | A | 18 | a0000c0006t0002a0001c0001t0002a0001c0001t0004others(15): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
5_prime_UTR_variant | MODIFIER | c.-105G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/8 | 2144 | chr8 | 81842130 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr8:81801597
|
C | CA | 51 | a0001c0001t0012g0142a0001c0002t0003g0003a0001c0002t0003g0011others(48): Show | 69 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(66): Show |
splice_region_variant&intron_variant | LOW | c.939-5dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81801597 | ||||||
chr8:81801597
|
C | CAA | 36 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(33): Show | 44 | HG00280.hp1 HG00423.hp2 HG01099.hp2 others(41): Show |
splice_region_variant&intron_variant | LOW | c.939-6_939-5dupTT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81801597 | ||||||
chr8:81801647
|
A | G | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.939-54T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81801647 | ||||||
chr8:81801695
|
A | AGAGT | 165 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(162): Show | 228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.939-103_939-102ins others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81801695 | ||||||
chr8:81801783
|
G | A | 1 | a0001c0001t0004g0133 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.939-190C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81801783 | ||||||
chr8:81801787
|
G | C | 36 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(33): Show | 63 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.939-194C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81801787 | ||||||
chr8:81801924
|
T | C | 2 | a0001c0001t0004g0113a0001c0001t0004g0141 | 2 | NA18950.hp2 NA19000.hp2 |
intron_variant | MODIFIER | c.939-331A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81801924 | ||||||
chr8:81802089
|
T | TA | 3 | a0001c0001t0007g0032a0001c0001t0007g0217a0001c0001t0007g0218 | 4 | HG03540.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.938+290dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81802089 | ||||||
chr8:81802092
|
A | G | 51 | a0001c0002t0003g0003a0001c0002t0003g0011a0001c0002t0003g0012others(48): Show | 68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.938+288T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81802092 | ||||||
chr8:81802103
|
A | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.938+277T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81802103 | ||||||
chr8:81802186
|
T | A | 2 | a0003c0004t0004g0115a0003c0004t0004g0116 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.938+194A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81802186 | ||||||
chr8:81802246
|
A | G | 1 | a0001c0001t0007g0218 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.938+134T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81802246 | ||||||
chr8:81802262
|
C | A | 2 | a0001c0001t0001g0039a0001c0001t0001g0040 | 2 | HG02735.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.938+118G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81802262 | ||||||
chr8:81802344
|
C | G | 2 | a0001c0001t0004g0026a0001c0001t0004g0114 | 3 | HG01261.hp1 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.938+36G>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 7/7 | chr8 | 81802344 | ||||||
chr8:81802685
|
T | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.819-186A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 6/7 | chr8 | 81802685 | ||||||
chr8:81802823
|
T | A | 51 | a0001c0002t0003g0003a0001c0002t0003g0011a0001c0002t0003g0012others(48): Show | 68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.818+269A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 6/7 | chr8 | 81802823 | ||||||
chr8:81802918
|
T | C | 37 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(34): Show | 45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.818+174A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 6/7 | chr8 | 81802918 | ||||||
chr8:81802976
|
GC | G | 35 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0027others(32): Show | 42 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.818+115delG | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 6/7 | chr8 | 81802976 | ||||||
chr8:81802990
|
G | A | 6 | a0001c0001t0004g0006a0001c0001t0004g0120a0001c0001t0004g0121others(3): Show | 10 | HG01928.hp1 HG01934.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.818+102C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 6/7 | chr8 | 81802990 | ||||||
chr8:81803380
|
C | A | 1 | a0001c0001t0002g0167 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.682-152G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81803380 | ||||||
chr8:81803516
|
T | C | 1 | a0001c0002t0003g0071 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.682-288A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81803516 | ||||||
chr8:81803561
|
A | G | 1 | a0001c0002t0003g0069 | 1 | NA19062.hp1 | intron_variant | MODIFIER | c.682-333T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81803561 | ||||||
chr8:81803617
|
C | T | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-389G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81803617 | ||||||
chr8:81803900
|
T | C | 2 | a0002c0003t0007g0028a0002c0003t0007g0153 | 3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.682-672A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81803900 | ||||||
chr8:81803931
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0050 | 4 | HG02257.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-703T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81803931 | ||||||
chr8:81803963
|
A | AAT | 37 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(34): Show | 45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.682-737_682-736dup others(2): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81803963 | ||||||
chr8:81804029
|
C | T | 1 | a0001c0001t0002g0150 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.682-801G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804029 | ||||||
chr8:81804033
|
G | T | 1 | a0001c0001t0001g0047 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.682-805C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804033 | ||||||
chr8:81804194
|
GAAAC | G | 6 | a0001c0001t0004g0006a0001c0001t0004g0120a0001c0001t0004g0121others(3): Show | 10 | HG01928.hp1 HG01934.hp2 HG01943.hp2 others(7): Show |
intron_variant | MODIFIER | c.682-970_682-967del others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804194 | ||||||
chr8:81804334
|
A | T | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-1106T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804334 | ||||||
chr8:81804578
|
T | G | 35 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(32): Show | 62 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(59): Show |
intron_variant | MODIFIER | c.682-1350A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804578 | ||||||
chr8:81804661
|
A | G | 1 | a0001c0002t0003g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.682-1433T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804661 | ||||||
chr8:81804671
|
C | T | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-1443G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804671 | ||||||
chr8:81804748
|
A | G | 2 | a0002c0003t0007g0028a0002c0003t0007g0153 | 3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.682-1520T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804748 | ||||||
chr8:81804802
|
C | T | 1 | a0001c0001t0001g0034 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.682-1574G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804802 | ||||||
chr8:81804965
|
G | A | 1 | a0001c0001t0001g0066 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.682-1737C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81804965 | ||||||
chr8:81805023
|
T | TA | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-1796_682-1795i others(3): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805023 | ||||||
chr8:81805087
|
G | A | 1 | a0001c0001t0006g0183 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.682-1859C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805087 | ||||||
chr8:81805215
|
A | T | 2 | a0001c0001t0004g0135a0001c0001t0004g0136 | 2 | NA18947.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.682-1987T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805215 | ||||||
chr8:81805218
|
A | G | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.682-1990T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805218 | ||||||
chr8:81805435
|
A | C | 1 | a0001c0002t0003g0080 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.682-2207T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805435 | ||||||
chr8:81805440
|
A | G | 1 | a0001c0001t0002g0171 | 1 | HG00609.hp1 | intron_variant | MODIFIER | c.682-2212T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805440 | ||||||
chr8:81805458
|
C | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0050 | 4 | HG02257.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-2230G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805458 | ||||||
chr8:81805541
|
G | T | 1 | a0001c0001t0004g0129 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.682-2313C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805541 | ||||||
chr8:81805790
|
G | A | 1 | a0001c0002t0003g0071 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.682-2562C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805790 | ||||||
chr8:81805791
|
A | G | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-2563T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805791 | ||||||
chr8:81805793
|
G | T | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-2565C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805793 | ||||||
chr8:81805808
|
A | C | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-2580T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805808 | ||||||
chr8:81805853
|
G | A | 1 | a0001c0001t0002g0175 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.682-2625C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805853 | ||||||
chr8:81805872
|
A | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.682-2644T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805872 | ||||||
chr8:81805904
|
G | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0050 | 4 | HG02257.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-2676C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805904 | ||||||
chr8:81805915
|
T | C | 1 | a0001c0001t0002g0148 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.682-2687A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805915 | ||||||
chr8:81805919
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0050 | 4 | HG02257.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-2691G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805919 | ||||||
chr8:81805921
|
C | CA | 37 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(34): Show | 45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.682-2694dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81805921 | ||||||
chr8:81806102
|
T | G | 1 | a0001c0001t0002g0143 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.682-2874A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81806102 | ||||||
chr8:81806429
|
G | A | 2 | a0002c0003t0007g0028a0002c0003t0007g0153 | 3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.682-3201C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81806429 | ||||||
chr8:81806495
|
T | C | 3 | a0001c0001t0007g0032a0001c0001t0007g0217a0001c0001t0007g0218 | 4 | HG03540.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-3267A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81806495 | ||||||
chr8:81806619
|
T | G | 1 | a0001c0002t0003g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.682-3391A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81806619 | ||||||
chr8:81806765
|
T | A | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-3537A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81806765 | ||||||
chr8:81806771
|
A | G | 2 | a0001c0001t0002g0143a0001c0001t0002g0164 | 2 | HG00099.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.682-3543T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81806771 | ||||||
chr8:81806787
|
AAACT | A | 2 | a0002c0003t0007g0028a0002c0003t0007g0153 | 3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.682-3563_682-3560d others(6): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81806787 | ||||||
chr8:81806903
|
C | A | 2 | a0001c0002t0003g0078a0001c0002t0003g0081 | 2 | NA18957.hp1 NA18971.hp1 |
intron_variant | MODIFIER | c.682-3675G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81806903 | ||||||
chr8:81806951
|
TA | T | 36 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(33): Show | 63 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(60): Show |
intron_variant | MODIFIER | c.682-3724delT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81806951 | ||||||
chr8:81807056
|
T | C | 1 | a0001c0002t0011g0083 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.682-3828A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807056 | ||||||
chr8:81807066
|
A | G | 1 | a0001c0002t0003g0072 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.682-3838T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807066 | ||||||
chr8:81807348
|
G | A | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-4120C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807348 | ||||||
chr8:81807374
|
C | A | 1 | a0001c0001t0001g0049 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.682-4146G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807374 | ||||||
chr8:81807378
|
A | G | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-4150T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807378 | ||||||
chr8:81807427
|
G | A | 29 | a0001c0002t0003g0011a0001c0002t0003g0012a0001c0002t0003g0014others(26): Show | 36 | HG00140.hp1 HG00423.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.682-4199C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807427 | ||||||
chr8:81807501
|
A | G | 8 | a0001c0001t0006g0184a0001c0001t0006g0185a0001c0001t0006g0186others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.682-4273T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807501 | ||||||
chr8:81807518
|
C | CA | 57 | a0001c0001t0001g0010a0001c0001t0001g0050a0001c0001t0001g0052others(54): Show | 66 | HG00280.hp1 HG00423.hp1 HG00423.hp2 others(63): Show |
intron_variant | MODIFIER | c.682-4291dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807518 | ||||||
chr8:81807518
|
C | CAA | 17 | a0001c0001t0001g0004a0001c0001t0001g0059a0001c0001t0001g0064others(14): Show | 26 | HG01928.hp1 HG01934.hp2 HG01943.hp2 others(23): Show |
intron_variant | MODIFIER | c.682-4292_682-4291d others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807518 | ||||||
chr8:81807518
|
C | CAAA | 8 | a0001c0001t0001g0034a0001c0001t0001g0051a0001c0001t0001g0066others(5): Show | 8 | HG01255.hp1 HG01993.hp1 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.682-4293_682-4291d others(5): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807518 | ||||||
chr8:81807518
|
C | CAAAA | 5 | a0001c0001t0005g0030a0001c0001t0005g0146a0001c0001t0005g0156others(2): Show | 6 | HG00733.hp2 HG00738.hp2 HG01192.hp1 others(3): Show |
intron_variant | MODIFIER | c.682-4294_682-4291d others(6): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807518 | ||||||
chr8:81807518
|
CA | C | 7 | a0001c0001t0002g0174a0001c0001t0002g0222a0001c0001t0006g0184others(4): Show | 7 | HG01884.hp2 HG02717.hp2 HG02970.hp2 others(4): Show |
intron_variant | MODIFIER | c.682-4291delT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807518 | ||||||
chr8:81807518
|
CAAAAAA | C | 33 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(30): Show | 59 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(56): Show |
intron_variant | MODIFIER | c.682-4296_682-4291d others(8): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807518 | ||||||
chr8:81807518
|
CAAAAAAA others(8): Show |
C | 2 | a0002c0003t0007g0028a0002c0003t0007g0153 | 3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.682-4305_682-4291d others(17): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807518 | ||||||
chr8:81807573
|
G | A | 1 | a0001c0001t0001g0005 | 5 | HG01952.hp2 HG01975.hp1 HG01993.hp2 others(2): Show |
intron_variant | MODIFIER | c.682-4345C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807573 | ||||||
chr8:81807587
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.682-4359T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807587 | ||||||
chr8:81807872
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.682-4644A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807872 | ||||||
chr8:81807921
|
C | T | 35 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0027others(32): Show | 42 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.682-4693G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807921 | ||||||
chr8:81807930
|
C | T | 1 | a0001c0001t0001g0055 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.682-4702G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807930 | ||||||
chr8:81807962
|
C | T | 1 | a0001c0002t0003g0082 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.682-4734G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81807962 | ||||||
chr8:81808116
|
C | A | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-4888G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808116 | ||||||
chr8:81808169
|
T | C | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-4941A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808169 | ||||||
chr8:81808362
|
G | A | 1 | a0001c0001t0001g0063 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.682-5134C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808362 | ||||||
chr8:81808373
|
C | A | 1 | a0001c0001t0013g0199 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.682-5145G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808373 | ||||||
chr8:81808465
|
G | A | 45 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(42): Show | 78 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(75): Show |
intron_variant | MODIFIER | c.682-5237C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808465 | ||||||
chr8:81808490
|
T | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0050 | 4 | HG02257.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-5262A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808490 | ||||||
chr8:81808525
|
G | A | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-5297C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808525 | ||||||
chr8:81808636
|
A | G | 35 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0027others(32): Show | 42 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.682-5408T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808636 | ||||||
chr8:81808668
|
C | T | 37 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(34): Show | 45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.682-5440G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808668 | ||||||
chr8:81808689
|
G | A | 2 | a0001c0001t0004g0026a0001c0001t0004g0114 | 3 | HG01261.hp1 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.682-5461C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808689 | ||||||
chr8:81808810
|
G | C | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-5582C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81808810 | ||||||
chr8:81809068
|
T | A | 1 | a0001c0001t0005g0158 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.682-5840A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809068 | ||||||
chr8:81809125
|
G | C | 3 | a0001c0001t0007g0032a0001c0001t0007g0217a0001c0001t0007g0218 | 4 | HG03540.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.682-5897C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809125 | ||||||
chr8:81809155
|
C | A | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.682-5927G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809155 | ||||||
chr8:81809333
|
T | C | 2 | a0001c0001t0004g0026a0001c0001t0004g0114 | 3 | HG01261.hp1 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.681+5992A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809333 | ||||||
chr8:81809356
|
T | C | 88 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(85): Show | 113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.681+5969A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809356 | ||||||
chr8:81809433
|
T | C | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.681+5892A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809433 | ||||||
chr8:81809439
|
T | TA | 88 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(85): Show | 113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.681+5885dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809439 | ||||||
chr8:81809454
|
C | A | 1 | a0001c0002t0003g0110 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.681+5871G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809454 | ||||||
chr8:81809587
|
C | T | 2 | a0001c0001t0005g0152a0001c0001t0005g0163 | 2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.681+5738G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809587 | ||||||
chr8:81809615
|
G | A | 4 | a0001c0001t0006g0183a0001c0001t0006g0191a0001c0001t0006g0192others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+5710C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809615 | ||||||
chr8:81809700
|
T | G | 1 | a0001c0001t0001g0061 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.681+5625A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809700 | ||||||
chr8:81809794
|
G | A | 2 | a0001c0001t0002g0147a0001c0001t0002g0165 | 2 | HG01069.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.681+5531C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809794 | ||||||
chr8:81809851
|
T | C | 1 | a0001c0001t0002g0172 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.681+5474A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809851 | ||||||
chr8:81809899
|
A | G | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.681+5426T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809899 | ||||||
chr8:81809926
|
T | G | 1 | a0001c0001t0004g0137 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.681+5399A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81809926 | ||||||
chr8:81810148
|
G | A | 1 | a0001c0001t0001g0065 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.681+5177C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810148 | ||||||
chr8:81810309
|
C | T | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.681+5016G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810309 | ||||||
chr8:81810401
|
T | C | 1 | a0001c0001t0001g0037 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.681+4924A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810401 | ||||||
chr8:81810475
|
T | C | 1 | a0001c0001t0001g0059 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.681+4850A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810475 | ||||||
chr8:81810486
|
T | A | 1 | a0001c0001t0002g0173 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.681+4839A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810486 | ||||||
chr8:81810508
|
G | A | 1 | a0001c0001t0002g0219 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.681+4817C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810508 | ||||||
chr8:81810548
|
T | G | 1 | a0001c0002t0003g0101 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.681+4777A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810548 | ||||||
chr8:81810582
|
T | C | 5 | a0001c0001t0004g0026a0001c0001t0006g0183a0001c0001t0006g0191others(2): Show | 6 | HG01261.hp1 HG02109.hp2 HG02615.hp1 others(3): Show |
intron_variant | MODIFIER | c.681+4743A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810582 | ||||||
chr8:81810634
|
G | A | 1 | a0001c0001t0004g0026 | 2 | HG01261.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.681+4691C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810634 | ||||||
chr8:81810727
|
C | T | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.681+4598G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810727 | ||||||
chr8:81810759
|
T | C | 138 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.681+4566A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810759 | ||||||
chr8:81810817
|
C | T | 37 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(34): Show | 45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.681+4508G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810817 | ||||||
chr8:81810876
|
A | C | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.681+4449T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810876 | ||||||
chr8:81810949
|
C | T | 2 | a0001c0001t0001g0010a0001c0001t0001g0050 | 4 | HG02257.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+4376G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81810949 | ||||||
chr8:81811045
|
C | G | 4 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0064others(1): Show | 9 | HG02109.hp1 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.681+4280G>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811045 | ||||||
chr8:81811093
|
T | C | 1 | a0001c0001t0001g0051 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.681+4232A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811093 | ||||||
chr8:81811101
|
T | G | 1 | a0001c0001t0001g0017 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.681+4224A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811101 | ||||||
chr8:81811173
|
C | T | 1 | a0001c0001t0002g0204 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.681+4152G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811173 | ||||||
chr8:81811308
|
A | G | 1 | a0001c0001t0001g0060 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.681+4017T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811308 | ||||||
chr8:81811439
|
T | C | 2 | a0001c0001t0002g0143a0001c0001t0002g0164 | 2 | HG00099.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.681+3886A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811439 | ||||||
chr8:81811574
|
TGAG | T | 3 | a0001c0001t0006g0187a0001c0001t0006g0188a0001c0001t0006g0210 | 3 | HG02145.hp2 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.681+3748_681+3750d others(5): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811574 | ||||||
chr8:81811620
|
G | A | 1 | a0001c0001t0006g0190 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.681+3705C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811620 | ||||||
chr8:81811634
|
C | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.681+3691G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811634 | ||||||
chr8:81811727
|
T | C | 1 | a0001c0001t0001g0061 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.681+3598A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811727 | ||||||
chr8:81811756
|
T | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.681+3569A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811756 | ||||||
chr8:81811821
|
T | C | 1 | a0001c0002t0003g0072 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.681+3504A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811821 | ||||||
chr8:81811912
|
A | G | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.681+3413T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81811912 | ||||||
chr8:81812056
|
G | C | 1 | a0001c0001t0009g0042 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.681+3269C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81812056 | ||||||
chr8:81812091
|
T | C | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.681+3234A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81812091 | ||||||
chr8:81812194
|
A | G | 51 | a0001c0002t0003g0003a0001c0002t0003g0011a0001c0002t0003g0012others(48): Show | 68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.681+3131T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81812194 | ||||||
chr8:81812296
|
A | T | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.681+3029T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81812296 | ||||||
chr8:81812727
|
C | T | 88 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0027others(85): Show | 112 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(109): Show |
intron_variant | MODIFIER | c.681+2598G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81812727 | ||||||
chr8:81812806
|
A | G | 1 | a0001c0001t0001g0059 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.681+2519T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81812806 | ||||||
chr8:81812899
|
T | C | 1 | a0001c0001t0016g0220 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.681+2426A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81812899 | ||||||
chr8:81812944
|
T | A | 2 | a0001c0001t0002g0174a0001c0001t0002g0197 | 2 | NA18964.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.681+2381A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81812944 | ||||||
chr8:81812993
|
G | T | 1 | a0001c0001t0004g0130 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.681+2332C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81812993 | ||||||
chr8:81813238
|
A | AAC | 2 | a0001c0001t0004g0026a0001c0001t0004g0114 | 3 | HG01261.hp1 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.681+2085_681+2086d others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813238 | ||||||
chr8:81813342
|
C | T | 29 | a0001c0002t0003g0011a0001c0002t0003g0012a0001c0002t0003g0014others(26): Show | 36 | HG00140.hp1 HG00423.hp1 HG00639.hp1 others(33): Show |
intron_variant | MODIFIER | c.681+1983G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813342 | ||||||
chr8:81813416
|
C | A | 2 | a0001c0001t0001g0008a0001c0001t0001g0044 | 5 | HG01081.hp2 HG01261.hp2 HG01515.hp2 others(2): Show |
intron_variant | MODIFIER | c.681+1909G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813416 | ||||||
chr8:81813529
|
AAG | A | 88 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(85): Show | 113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.681+1794_681+1795d others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813529 | ||||||
chr8:81813631
|
G | A | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.681+1694C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813631 | ||||||
chr8:81813648
|
T | G | 4 | a0001c0001t0006g0183a0001c0001t0006g0191a0001c0001t0006g0192others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.681+1677A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813648 | ||||||
chr8:81813671
|
C | T | 11 | a0001c0002t0003g0003a0001c0002t0003g0024a0001c0002t0003g0068others(8): Show | 18 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.681+1654G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813671 | ||||||
chr8:81813678
|
T | C | 2 | a0002c0003t0007g0028a0002c0003t0007g0153 | 3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.681+1647A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813678 | ||||||
chr8:81813895
|
GGCTAT | G | 16 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0146others(13): Show | 18 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.681+1425_681+1429d others(7): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813895 | ||||||
chr8:81813905
|
C | T | 51 | a0001c0002t0003g0003a0001c0002t0003g0011a0001c0002t0003g0012others(48): Show | 68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.681+1420G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81813905 | ||||||
chr8:81814140
|
C | T | 3 | a0001c0001t0004g0117a0001c0001t0004g0125a0001c0001t0004g0140 | 3 | HG03927.hp2 NA18951.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.681+1185G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81814140 | ||||||
chr8:81814250
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.681+1075T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81814250 | ||||||
chr8:81814447
|
G | A | 138 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(135): Show | 198 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(195): Show |
intron_variant | MODIFIER | c.681+878C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81814447 | ||||||
chr8:81814497
|
G | A | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.681+828C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81814497 | ||||||
chr8:81814913
|
C | T | 16 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0146others(13): Show | 18 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.681+412G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81814913 | ||||||
chr8:81814966
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.681+359A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81814966 | ||||||
chr8:81815061
|
T | C | 1 | a0002c0003t0007g0153 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.681+264A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81815061 | ||||||
chr8:81815074
|
A | C | 1 | a0001c0001t0001g0045 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.681+251T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81815074 | ||||||
chr8:81815094
|
T | C | 33 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0027others(30): Show | 40 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.681+231A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81815094 | ||||||
chr8:81815122
|
T | G | 1 | a0001c0002t0003g0096 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.681+203A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81815122 | ||||||
chr8:81815142
|
G | C | 1 | a0002c0003t0007g0153 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.681+183C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81815142 | ||||||
chr8:81815280
|
C | T | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.681+45G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81815280 | ||||||
chr8:81815285
|
A | T | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.681+40T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 5/7 | chr8 | 81815285 | ||||||
chr8:81815405
|
GA | G | 37 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(34): Show | 45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.612-12delT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81815405 | ||||||
chr8:81815598
|
A | G | 1 | a0001c0002t0003g0102 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.612-204T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81815598 | ||||||
chr8:81815789
|
T | G | 141 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(138): Show | 202 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(199): Show |
intron_variant | MODIFIER | c.612-395A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81815789 | ||||||
chr8:81815879
|
T | C | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.612-485A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81815879 | ||||||
chr8:81816068
|
T | A | 88 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(85): Show | 113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.612-674A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816068 | ||||||
chr8:81816089
|
C | A | 3 | a0001c0001t0007g0032a0001c0001t0007g0217a0001c0001t0007g0218 | 4 | HG03540.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.612-695G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816089 | ||||||
chr8:81816181
|
C | CTTTTT | 50 | a0001c0002t0003g0003a0001c0002t0003g0011a0001c0002t0003g0012others(47): Show | 67 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(64): Show |
intron_variant | MODIFIER | c.612-792_612-788dup others(5): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816181 | ||||||
chr8:81816181
|
C | CTTTTTT | 12 | a0001c0001t0004g0026a0001c0001t0004g0027a0001c0001t0004g0113others(9): Show | 14 | HG00280.hp1 HG01099.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.612-793_612-788dup others(6): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816181 | ||||||
chr8:81816181
|
C | CTTTTTTT | 23 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0111others(20): Show | 29 | HG00423.hp2 HG00673.hp2 HG01928.hp1 others(26): Show |
intron_variant | MODIFIER | c.612-794_612-788dup others(7): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816181 | ||||||
chr8:81816181
|
C | T | 1 | a0001c0001t0004g0140 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.612-787G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816181 | ||||||
chr8:81816186
|
T | C | 1 | a0001c0001t0002g0221 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.612-792A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816186 | ||||||
chr8:81816303
|
C | A | 37 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(34): Show | 64 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.612-909G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816303 | ||||||
chr8:81816731
|
C | T | 2 | a0001c0001t0001g0019a0001c0001t0001g0035 | 3 | HG01081.hp1 HG03041.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.612-1337G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816731 | ||||||
chr8:81816848
|
C | T | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.612-1454G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816848 | ||||||
chr8:81816975
|
A | G | 171 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(168): Show | 234 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(231): Show |
intron_variant | MODIFIER | c.612-1581T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81816975 | ||||||
chr8:81817139
|
C | T | 4 | a0001c0001t0006g0183a0001c0001t0006g0191a0001c0001t0006g0192others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.612-1745G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81817139 | ||||||
chr8:81817253
|
C | G | 1 | a0001c0001t0001g0050 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.612-1859G>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81817253 | ||||||
chr8:81817296
|
A | G | 1 | a0001c0002t0003g0087 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.612-1902T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81817296 | ||||||
chr8:81817355
|
G | A | 1 | a0001c0001t0017g0224 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.612-1961C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81817355 | ||||||
chr8:81817439
|
C | A | 2 | a0002c0003t0007g0028a0002c0003t0007g0153 | 3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.612-2045G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81817439 | ||||||
chr8:81817563
|
C | A | 1 | a0002c0003t0007g0153 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.612-2169G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81817563 | ||||||
chr8:81817720
|
C | T | 5 | a0001c0001t0002g0167a0001c0001t0002g0168a0001c0001t0002g0170others(2): Show | 5 | HG00741.hp2 HG01074.hp1 HG01175.hp1 others(2): Show |
intron_variant | MODIFIER | c.612-2326G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81817720 | ||||||
chr8:81817721
|
A | G | 1 | a0002c0003t0007g0153 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.612-2327T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81817721 | ||||||
chr8:81818042
|
T | C | 2 | a0002c0003t0007g0028a0002c0003t0007g0153 | 3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.612-2648A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818042 | ||||||
chr8:81818050
|
C | A | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.612-2656G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818050 | ||||||
chr8:81818051
|
C | A | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.612-2657G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818051 | ||||||
chr8:81818052
|
T | A | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.612-2658A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818052 | ||||||
chr8:81818059
|
T | A | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.612-2665A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818059 | ||||||
chr8:81818060
|
T | A | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.612-2666A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818060 | ||||||
chr8:81818086
|
G | T | 1 | a0001c0001t0002g0195 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.612-2692C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818086 | ||||||
chr8:81818657
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.612-3263A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818657 | ||||||
chr8:81818680
|
T | C | 165 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(162): Show | 228 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(225): Show |
intron_variant | MODIFIER | c.612-3286A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818680 | ||||||
chr8:81818704
|
G | A | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.612-3310C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818704 | ||||||
chr8:81818789
|
C | T | 1 | a0001c0001t0001g0044 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.612-3395G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818789 | ||||||
chr8:81818922
|
T | C | 157 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(154): Show | 220 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(217): Show |
intron_variant | MODIFIER | c.612-3528A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81818922 | ||||||
chr8:81819171
|
C | T | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.612-3777G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81819171 | ||||||
chr8:81819242
|
G | A | 136 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.612-3848C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81819242 | ||||||
chr8:81819569
|
G | T | 1 | a0001c0001t0001g0022 | 2 | HG01346.hp1 HG02451.hp2 |
intron_variant | MODIFIER | c.612-4175C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81819569 | ||||||
chr8:81819714
|
ATC | A | 2 | a0002c0003t0007g0028a0002c0003t0007g0153 | 3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.611+4076_611+4077d others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81819714 | ||||||
chr8:81819764
|
C | T | 1 | a0001c0001t0001g0018 | 2 | HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.611+4028G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81819764 | ||||||
chr8:81819778
|
T | C | 1 | a0001c0001t0004g0134 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.611+4014A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81819778 | ||||||
chr8:81820231
|
AT | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.611+3560delA | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820231 | ||||||
chr8:81820233
|
T | A | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.611+3559A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820233 | ||||||
chr8:81820256
|
T | TA | 18 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0146others(15): Show | 21 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(18): Show |
intron_variant | MODIFIER | c.611+3535dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820256 | ||||||
chr8:81820280
|
C | A | 169 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(166): Show | 232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.611+3512G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820280 | ||||||
chr8:81820370
|
T | C | 2 | a0001c0001t0001g0010a0001c0001t0001g0050 | 4 | HG02257.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+3422A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820370 | ||||||
chr8:81820476
|
A | G | 4 | a0001c0001t0006g0183a0001c0001t0006g0191a0001c0001t0006g0192others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+3316T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820476 | ||||||
chr8:81820487
|
G | C | 1 | a0004c0007t0006g0214 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.611+3305C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820487 | ||||||
chr8:81820505
|
C | G | 37 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(34): Show | 45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.611+3287G>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820505 | ||||||
chr8:81820590
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3202A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820590 | ||||||
chr8:81820594
|
C | A | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3198G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820594 | ||||||
chr8:81820596
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3196A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820596 | ||||||
chr8:81820602
|
T | G | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3190A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820602 | ||||||
chr8:81820603
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3189A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820603 | ||||||
chr8:81820607
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3185A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820607 | ||||||
chr8:81820608
|
G | C | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3184C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820608 | ||||||
chr8:81820608
|
G | T | 88 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(85): Show | 113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.611+3184C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820608 | ||||||
chr8:81820610
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3182A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820610 | ||||||
chr8:81820611
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3181A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820611 | ||||||
chr8:81820613
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3179A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820613 | ||||||
chr8:81820614
|
G | T | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3178C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820614 | ||||||
chr8:81820616
|
C | A | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3176G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820616 | ||||||
chr8:81820618
|
T | C | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3174A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820618 | ||||||
chr8:81820619
|
A | T | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3173T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820619 | ||||||
chr8:81820622
|
T | A | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3170A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820622 | ||||||
chr8:81820623
|
C | G | 1 | a0001c0001t0001g0043 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.611+3169G>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820623 | ||||||
chr8:81820814
|
G | A | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.611+2978C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820814 | ||||||
chr8:81820905
|
C | T | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.611+2887G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81820905 | ||||||
chr8:81821004
|
A | G | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.611+2788T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821004 | ||||||
chr8:81821132
|
C | T | 37 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(34): Show | 45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.611+2660G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821132 | ||||||
chr8:81821134
|
A | C | 2 | a0003c0004t0004g0115a0003c0004t0004g0116 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.611+2658T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821134 | ||||||
chr8:81821160
|
A | T | 11 | a0001c0002t0003g0003a0001c0002t0003g0024a0001c0002t0003g0068others(8): Show | 18 | HG00558.hp2 HG00609.hp2 HG00673.hp1 others(15): Show |
intron_variant | MODIFIER | c.611+2632T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821160 | ||||||
chr8:81821352
|
T | C | 1 | a0001c0002t0003g0085 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.611+2440A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821352 | ||||||
chr8:81821369
|
G | T | 16 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0146others(13): Show | 18 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.611+2423C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821369 | ||||||
chr8:81821428
|
G | A | 51 | a0001c0002t0003g0003a0001c0002t0003g0011a0001c0002t0003g0012others(48): Show | 68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.611+2364C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821428 | ||||||
chr8:81821512
|
A | T | 2 | a0001c0001t0002g0222a0001c0001t0002g0225 | 2 | NA18957.hp2 NA19062.hp2 |
intron_variant | MODIFIER | c.611+2280T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821512 | ||||||
chr8:81821866
|
T | C | 1 | a0001c0001t0005g0159 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.611+1926A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821866 | ||||||
chr8:81821896
|
T | G | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.611+1896A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81821896 | ||||||
chr8:81822007
|
C | G | 8 | a0001c0001t0006g0184a0001c0001t0006g0185a0001c0001t0006g0186others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.611+1785G>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822007 | ||||||
chr8:81822031
|
T | C | 2 | a0001c0001t0002g0203a0001c0001t0002g0212 | 2 | HG00733.hp1 HG01175.hp2 |
intron_variant | MODIFIER | c.611+1761A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822031 | ||||||
chr8:81822080
|
G | GAA | 24 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0111others(21): Show | 30 | HG00423.hp2 HG00673.hp2 HG01099.hp2 others(27): Show |
intron_variant | MODIFIER | c.611+1710_611+1711d others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822080 | ||||||
chr8:81822083
|
C | T | 4 | a0001c0001t0006g0183a0001c0001t0006g0191a0001c0001t0006g0192others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+1709G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822083 | ||||||
chr8:81822422
|
A | G | 136 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(133): Show | 195 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(192): Show |
intron_variant | MODIFIER | c.611+1370T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822422 | ||||||
chr8:81822668
|
G | A | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.611+1124C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822668 | ||||||
chr8:81822755
|
C | T | 16 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0146others(13): Show | 18 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.611+1037G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822755 | ||||||
chr8:81822781
|
C | T | 16 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0146others(13): Show | 18 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.611+1011G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822781 | ||||||
chr8:81822789
|
C | T | 2 | a0001c0001t0009g0041a0001c0001t0009g0042 | 2 | HG02055.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.611+1003G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822789 | ||||||
chr8:81822816
|
A | T | 1 | a0001c0001t0002g0175 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.611+976T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822816 | ||||||
chr8:81822926
|
G | GTA | 3 | a0001c0001t0006g0187a0001c0001t0006g0188a0001c0001t0006g0210 | 3 | HG02145.hp2 HG02970.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.611+864_611+865dup others(2): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822926 | ||||||
chr8:81822926
|
GTA | G | 5 | a0001c0002t0003g0070a0001c0002t0003g0071a0001c0002t0003g0079others(2): Show | 5 | HG02132.hp1 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.611+864_611+865del others(2): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822926 | ||||||
chr8:81822935
|
T | TATAC | 125 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(122): Show | 181 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(178): Show |
intron_variant | MODIFIER | c.611+856_611+857ins others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822935 | ||||||
chr8:81822941
|
C | T | 1 | a0002c0003t0007g0153 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.611+851G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822941 | ||||||
chr8:81822947
|
C | CAT | 8 | a0001c0001t0002g0150a0001c0001t0002g0164a0001c0001t0002g0168others(5): Show | 8 | HG00099.hp2 HG03654.hp1 HG03710.hp1 others(5): Show |
intron_variant | MODIFIER | c.611+843_611+844dup others(2): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822947 | ||||||
chr8:81822947
|
C | T | 122 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(119): Show | 173 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(170): Show |
intron_variant | MODIFIER | c.611+845G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822947 | ||||||
chr8:81822947
|
CAT | C | 7 | a0001c0001t0002g0149a0001c0001t0002g0154a0001c0001t0002g0211others(4): Show | 7 | HG01175.hp1 HG02109.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.611+843_611+844del others(2): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822947 | ||||||
chr8:81822958
|
A | ATATG | 7 | a0001c0002t0003g0011a0001c0002t0003g0014a0001c0002t0003g0087others(4): Show | 11 | HG01192.hp2 HG01256.hp1 HG01256.hp2 others(8): Show |
intron_variant | MODIFIER | c.611+833_611+834ins others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822958 | ||||||
chr8:81822958
|
A | ATG | 69 | a0001c0001t0004g0015a0001c0001t0004g0026a0001c0001t0004g0027others(66): Show | 86 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(83): Show |
intron_variant | MODIFIER | c.611+833_611+834ins others(2): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822958 | ||||||
chr8:81822958
|
A | G | 1 | a0002c0003t0007g0153 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.611+834T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822958 | ||||||
chr8:81822960
|
A | ATATATG | 2 | a0001c0001t0001g0037a0002c0003t0007g0028 | 3 | HG02572.hp2 HG02615.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.611+831_611+832ins others(6): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822960 | ||||||
chr8:81822960
|
A | ATATG | 3 | a0001c0001t0001g0034a0001c0001t0001g0054a0001c0001t0009g0041 | 3 | HG02055.hp1 HG03927.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.611+831_611+832ins others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822960 | ||||||
chr8:81822960
|
A | ATG | 41 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(38): Show | 75 | HG00099.hp1 HG00280.hp2 HG01069.hp2 others(72): Show |
intron_variant | MODIFIER | c.611+831_611+832ins others(2): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822960 | ||||||
chr8:81822960
|
A | G | 1 | a0001c0001t0001g0065 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.611+832T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822960 | ||||||
chr8:81822962
|
A | ATATATAT others(13): Show |
2 | a0001c0001t0005g0152a0001c0001t0005g0163 | 2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.611+829_611+830ins others(20): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822962 | ||||||
chr8:81822962
|
A | G | 1 | a0001c0001t0002g0204 | 1 | HG00438.hp2 | intron_variant | MODIFIER | c.611+830T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822962 | ||||||
chr8:81822964
|
A | ACACATAT others(15): Show |
5 | a0001c0002t0003g0070a0001c0002t0003g0071a0001c0002t0003g0079others(2): Show | 5 | HG02132.hp1 NA18939.hp2 NA18951.hp1 others(2): Show |
intron_variant | MODIFIER | c.611+827_611+828ins others(22): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | ||||||
chr8:81822964
|
A | ATATATAT others(15): Show |
1 | a0001c0001t0006g0184 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.611+827_611+828ins others(22): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | ||||||
chr8:81822964
|
A | ATATATAT others(13): Show |
4 | a0001c0001t0005g0029a0001c0001t0005g0146a0001c0001t0005g0155others(1): Show | 5 | HG00639.hp2 HG00738.hp2 HG01192.hp1 others(2): Show |
intron_variant | MODIFIER | c.611+827_611+828ins others(20): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | ||||||
chr8:81822964
|
A | ATATATAT others(11): Show |
11 | a0001c0001t0005g0030a0001c0001t0005g0157a0001c0001t0005g0158others(8): Show | 12 | HG00733.hp2 HG01106.hp1 HG02055.hp2 others(9): Show |
intron_variant | MODIFIER | c.611+827_611+828ins others(18): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | ||||||
chr8:81822964
|
A | ATATATAT others(9): Show |
4 | a0001c0001t0005g0177a0001c0001t0006g0160a0001c0001t0006g0187others(1): Show | 4 | HG01169.hp2 HG02809.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+827_611+828ins others(16): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | ||||||
chr8:81822964
|
A | ATATATAT others(7): Show |
2 | a0001c0001t0006g0188a0001c0001t0006g0210 | 2 | HG02145.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.611+827_611+828ins others(14): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | ||||||
chr8:81822964
|
A | ATATATGT others(5): Show |
3 | a0001c0001t0007g0032a0001c0001t0007g0217a0001c0001t0007g0218 | 4 | HG03540.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+827_611+828ins others(12): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | ||||||
chr8:81822964
|
A | ATATGTAT others(3): Show |
1 | a0001c0002t0003g0104 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.611+827_611+828ins others(10): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | ||||||
chr8:81822964
|
A | ATGTATAT others(1): Show |
7 | a0001c0001t0004g0006a0001c0001t0004g0119a0001c0001t0004g0120others(4): Show | 11 | HG01928.hp1 HG01934.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.611+827_611+828ins others(8): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | ||||||
chr8:81822964
|
A | G | 77 | a0001c0001t0004g0015a0001c0001t0004g0026a0001c0001t0004g0027others(74): Show | 98 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(95): Show |
intron_variant | MODIFIER | c.611+828T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822964 | ||||||
chr8:81822966
|
A | ATATATAT others(7): Show |
1 | a0001c0001t0001g0059 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.611+825_611+826ins others(14): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822966 | ||||||
chr8:81822966
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 82 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(79): Show |
intron_variant | MODIFIER | c.611+826T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822966 | ||||||
chr8:81822977
|
C | T | 1 | a0001c0001t0002g0175 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.611+815G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822977 | ||||||
chr8:81822981
|
T | C | 1 | a0001c0001t0002g0175 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.611+811A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822981 | ||||||
chr8:81822984
|
G | A | 1 | a0001c0001t0002g0175 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.611+808C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822984 | ||||||
chr8:81822990
|
G | A | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.611+802C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81822990 | ||||||
chr8:81823012
|
C | T | 1 | a0001c0001t0002g0167 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.611+780G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81823012 | ||||||
chr8:81823224
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.611+568T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81823224 | ||||||
chr8:81823285
|
T | C | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.611+507A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81823285 | ||||||
chr8:81823404
|
A | G | 3 | a0001c0001t0007g0032a0001c0001t0007g0217a0001c0001t0007g0218 | 4 | HG03540.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.611+388T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81823404 | ||||||
chr8:81823442
|
C | T | 7 | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0017others(4): Show | 14 | HG01168.hp2 HG01169.hp1 HG01952.hp2 others(11): Show |
intron_variant | MODIFIER | c.611+350G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81823442 | ||||||
chr8:81823457
|
A | C | 1 | a0001c0001t0002g0175 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.611+335T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81823457 | ||||||
chr8:81823459
|
C | A | 1 | a0001c0001t0002g0175 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.611+333G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81823459 | ||||||
chr8:81823554
|
C | T | 16 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0146others(13): Show | 18 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.611+238G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 4/7 | chr8 | 81823554 | ||||||
chr8:81824140
|
T | A | 1 | a0001c0001t0006g0189 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.463-200A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824140 | ||||||
chr8:81824160
|
T | C | 2 | a0001c0001t0001g0022a0001c0001t0001g0054 | 3 | HG01346.hp1 HG02451.hp2 HG03927.hp1 |
intron_variant | MODIFIER | c.463-220A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824160 | ||||||
chr8:81824196
|
T | G | 1 | a0001c0001t0002g0175 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.463-256A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824196 | ||||||
chr8:81824255
|
T | A | 4 | a0001c0001t0006g0183a0001c0001t0006g0191a0001c0001t0006g0192others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.463-315A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824255 | ||||||
chr8:81824470
|
T | A | 1 | a0001c0001t0006g0190 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.463-530A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824470 | ||||||
chr8:81824471
|
T | A | 59 | a0001c0001t0006g0184a0001c0001t0006g0185a0001c0001t0006g0186others(56): Show | 76 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(73): Show |
intron_variant | MODIFIER | c.463-531A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824471 | ||||||
chr8:81824519
|
C | CT | 4 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0064others(1): Show | 9 | HG02109.hp1 HG02630.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.463-580dupA | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824519 | ||||||
chr8:81824534
|
TA | T | 4 | a0001c0001t0006g0183a0001c0001t0006g0191a0001c0001t0006g0192others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.463-595delT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824534 | ||||||
chr8:81824662
|
A | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0050 | 4 | HG02257.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.463-722T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824662 | ||||||
chr8:81824691
|
A | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.463-751T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81824691 | ||||||
chr8:81825098
|
T | G | 1 | a0001c0002t0003g0024 | 2 | NA18965.hp2 NA18970.hp1 |
intron_variant | MODIFIER | c.463-1158A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825098 | ||||||
chr8:81825128
|
C | T | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.463-1188G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825128 | ||||||
chr8:81825141
|
T | C | 1 | a0002c0003t0007g0028 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.463-1201A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825141 | ||||||
chr8:81825432
|
T | C | 1 | a0001c0002t0003g0087 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.463-1492A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825432 | ||||||
chr8:81825453
|
T | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0050 | 4 | HG02257.hp1 HG02622.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.463-1513A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825453 | ||||||
chr8:81825510
|
T | C | 169 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(166): Show | 232 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(229): Show |
intron_variant | MODIFIER | c.463-1570A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825510 | ||||||
chr8:81825536
|
A | G | 40 | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0008others(37): Show | 69 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(66): Show |
intron_variant | MODIFIER | c.463-1596T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825536 | ||||||
chr8:81825551
|
C | T | 37 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(34): Show | 45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.463-1611G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825551 | ||||||
chr8:81825624
|
G | C | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.463-1684C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825624 | ||||||
chr8:81825669
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.463-1729G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825669 | ||||||
chr8:81825804
|
T | C | 88 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(85): Show | 113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.463-1864A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825804 | ||||||
chr8:81825808
|
T | C | 1 | a0001c0002t0003g0088 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.463-1868A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825808 | ||||||
chr8:81825816
|
A | G | 1 | a0001c0001t0001g0038 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.463-1876T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81825816 | ||||||
chr8:81826031
|
TC | T | 88 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(85): Show | 113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.463-2092delG | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81826031 | ||||||
chr8:81826032
|
C | T | 1 | a0001c0001t0004g0135 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.463-2092G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81826032 | ||||||
chr8:81826327
|
A | G | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.463-2387T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81826327 | ||||||
chr8:81826572
|
C | G | 47 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 81 | HG00099.hp1 HG00280.hp2 HG00735.hp1 others(78): Show |
intron_variant | MODIFIER | c.463-2632G>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81826572 | ||||||
chr8:81826602
|
C | T | 1 | a0001c0001t0007g0217 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.463-2662G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81826602 | ||||||
chr8:81826894
|
C | T | 6 | a0001c0001t0002g0180a0001c0001t0002g0201a0001c0001t0002g0202others(3): Show | 6 | HG00733.hp1 HG01175.hp2 HG01934.hp1 others(3): Show |
intron_variant | MODIFIER | c.462+2536G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81826894 | ||||||
chr8:81827079
|
G | A | 1 | a0001c0002t0003g0075 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.462+2351C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81827079 | ||||||
chr8:81827222
|
C | T | 1 | a0001c0001t0004g0124 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.462+2208G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81827222 | ||||||
chr8:81827278
|
C | T | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.462+2152G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81827278 | ||||||
chr8:81827316
|
A | AT | 21 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0111others(18): Show | 27 | HG00423.hp2 HG00673.hp2 HG01928.hp1 others(24): Show |
intron_variant | MODIFIER | c.462+2113dupA | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81827316 | ||||||
chr8:81827424
|
A | G | 2 | a0002c0003t0007g0028a0002c0003t0007g0153 | 3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.462+2006T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81827424 | ||||||
chr8:81827555
|
T | G | 2 | a0001c0002t0003g0089a0001c0002t0003g0090 | 2 | HG00735.hp2 HG02004.hp1 |
intron_variant | MODIFIER | c.462+1875A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81827555 | ||||||
chr8:81827813
|
C | A | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.462+1617G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81827813 | ||||||
chr8:81827950
|
A | C | 1 | a0001c0001t0004g0114 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.462+1480T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81827950 | ||||||
chr8:81828091
|
T | C | 1 | a0001c0002t0003g0103 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.462+1339A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828091 | ||||||
chr8:81828267
|
A | C | 88 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(85): Show | 113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.462+1163T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828267 | ||||||
chr8:81828391
|
A | C | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.462+1039T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828391 | ||||||
chr8:81828502
|
G | A | 3 | a0001c0001t0001g0004a0001c0001t0001g0052a0001c0001t0001g0067 | 8 | HG02109.hp1 HG02895.hp1 HG02897.hp2 others(5): Show |
intron_variant | MODIFIER | c.462+928C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828502 | ||||||
chr8:81828707
|
T | C | 1 | a0001c0001t0005g0177 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.462+723A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828707 | ||||||
chr8:81828713
|
T | C | 4 | a0001c0001t0001g0022a0001c0001t0001g0053a0001c0001t0001g0054others(1): Show | 5 | HG00735.hp1 HG01346.hp1 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.462+717A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828713 | ||||||
chr8:81828765
|
T | C | 4 | a0001c0001t0006g0183a0001c0001t0006g0191a0001c0001t0006g0192others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.462+665A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828765 | ||||||
chr8:81828785
|
C | T | 37 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(34): Show | 45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.462+645G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828785 | ||||||
chr8:81828811
|
G | A | 2 | a0002c0003t0007g0028a0002c0003t0007g0153 | 3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.462+619C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828811 | ||||||
chr8:81828970
|
G | A | 1 | a0001c0001t0002g0180 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.462+460C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81828970 | ||||||
chr8:81829273
|
C | CTAAAAAT others(21): Show |
89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.462+156_462+157ins others(28): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81829273 | ||||||
chr8:81829341
|
C | CA | 180 | a0000c0006t0002g0206a0001c0001t0002g0002a0001c0001t0002g0007others(177): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.462+88dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 3/7 | chr8 | 81829341 | ||||||
chr8:81829716
|
A | G | 1 | a0001c0002t0003g0079 | 1 | NA18951.hp1 | intron_variant | MODIFIER | c.376-200T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81829716 | ||||||
chr8:81829720
|
A | G | 1 | a0001c0001t0002g0178 | 1 | NA18980.hp1 | intron_variant | MODIFIER | c.376-204T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81829720 | ||||||
chr8:81829758
|
T | G | 1 | a0001c0001t0002g0213 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.376-242A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81829758 | ||||||
chr8:81830008
|
G | C | 37 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(34): Show | 45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.376-492C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830008 | ||||||
chr8:81830053
|
G | C | 180 | a0000c0006t0002g0206a0001c0001t0002g0002a0001c0001t0002g0007others(177): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.376-537C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830053 | ||||||
chr8:81830094
|
C | CAGGATAT others(8): Show |
1 | a0004c0007t0006g0214 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.376-593_376-579dup others(15): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830094 | ||||||
chr8:81830334
|
C | T | 1 | a0001c0002t0003g0078 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.376-818G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830334 | ||||||
chr8:81830336
|
G | A | 1 | a0001c0001t0004g0123 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.376-820C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830336 | ||||||
chr8:81830370
|
A | C | 1 | a0001c0001t0001g0059 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.376-854T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830370 | ||||||
chr8:81830428
|
G | A | 35 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0027others(32): Show | 42 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(39): Show |
intron_variant | MODIFIER | c.376-912C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830428 | ||||||
chr8:81830438
|
G | A | 1 | a0001c0001t0002g0208 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.376-922C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830438 | ||||||
chr8:81830443
|
C | T | 2 | a0001c0001t0002g0147a0001c0001t0002g0165 | 2 | HG01069.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.376-927G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830443 | ||||||
chr8:81830465
|
G | A | 16 | a0001c0001t0005g0029a0001c0001t0005g0030a0001c0001t0005g0146others(13): Show | 18 | HG00639.hp2 HG00733.hp2 HG00738.hp2 others(15): Show |
intron_variant | MODIFIER | c.376-949C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830465 | ||||||
chr8:81830549
|
T | C | 5 | a0001c0001t0001g0036a0001c0001t0001g0055a0001c0001t0001g0056others(2): Show | 5 | HG01070.hp1 HG01891.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.376-1033A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830549 | ||||||
chr8:81830578
|
G | GT | 2 | a0001c0001t0001g0038a0001c0001t0007g0032 | 3 | HG03540.hp2 HG04228.hp2 NA21309.hp2 |
intron_variant | MODIFIER | c.376-1063dupA | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830578 | ||||||
chr8:81830579
|
TA | T | 111 | a0000c0006t0002g0206a0001c0001t0001g0037a0001c0001t0002g0002others(108): Show | 144 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(141): Show |
intron_variant | MODIFIER | c.376-1064delT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830579 | ||||||
chr8:81830579
|
TAA | T | 12 | a0001c0001t0002g0200a0001c0001t0002g0219a0001c0001t0006g0184others(9): Show | 12 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(9): Show |
intron_variant | MODIFIER | c.376-1065_376-1064d others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830579 | ||||||
chr8:81830591
|
A | G | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.376-1075T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830591 | ||||||
chr8:81830687
|
G | A | 1 | a0001c0002t0003g0095 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.376-1171C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830687 | ||||||
chr8:81830724
|
G | A | 180 | a0000c0006t0002g0206a0001c0001t0002g0002a0001c0001t0002g0007others(177): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.376-1208C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830724 | ||||||
chr8:81830785
|
C | A | 5 | a0001c0001t0001g0036a0001c0001t0001g0055a0001c0001t0001g0056others(2): Show | 5 | HG01070.hp1 HG01891.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.376-1269G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830785 | ||||||
chr8:81830980
|
T | A | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.376-1464A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81830980 | ||||||
chr8:81831122
|
G | C | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.376-1606C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831122 | ||||||
chr8:81831195
|
A | G | 1 | a0002c0003t0007g0028 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.376-1679T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831195 | ||||||
chr8:81831213
|
T | G | 1 | a0001c0001t0004g0134 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.376-1697A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831213 | ||||||
chr8:81831377
|
A | G | 1 | a0001c0001t0013g0199 | 1 | NA18947.hp1 | intron_variant | MODIFIER | c.376-1861T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831377 | ||||||
chr8:81831457
|
CTGAGGTG others(11): Show |
C | 1 | a0001c0001t0002g0154 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.376-1959_376-1942d others(20): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831457 | ||||||
chr8:81831523
|
C | T | 1 | a0001c0001t0004g0137 | 1 | NA19091.hp2 | intron_variant | MODIFIER | c.376-2007G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831523 | ||||||
chr8:81831693
|
C | CA | 9 | a0001c0001t0001g0059a0001c0001t0001g0060a0001c0001t0001g0061others(6): Show | 9 | HG00140.hp1 HG00140.hp2 HG01109.hp1 others(6): Show |
intron_variant | MODIFIER | c.376-2178dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831693 | ||||||
chr8:81831693
|
CA | C | 56 | a0001c0001t0002g0007a0001c0001t0002g0143a0001c0001t0002g0144others(53): Show | 62 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(59): Show |
intron_variant | MODIFIER | c.376-2178delT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831693 | ||||||
chr8:81831734
|
A | C | 8 | a0001c0001t0006g0184a0001c0001t0006g0185a0001c0001t0006g0186others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-2218T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831734 | ||||||
chr8:81831750
|
T | C | 1 | a0001c0001t0001g0034 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.376-2234A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831750 | ||||||
chr8:81831782
|
A | C | 1 | a0001c0001t0006g0184 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.376-2266T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831782 | ||||||
chr8:81831944
|
G | A | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.376-2428C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81831944 | ||||||
chr8:81832107
|
A | G | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.376-2591T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81832107 | ||||||
chr8:81832234
|
T | C | 1 | a0001c0001t0007g0217 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.376-2718A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81832234 | ||||||
chr8:81832602
|
C | A | 1 | a0001c0002t0003g0097 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.376-3086G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81832602 | ||||||
chr8:81832687
|
T | C | 1 | a0001c0001t0005g0029 | 2 | HG00639.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.376-3171A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81832687 | ||||||
chr8:81832794
|
T | C | 1 | a0001c0001t0002g0182 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.376-3278A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81832794 | ||||||
chr8:81832863
|
T | G | 2 | a0003c0004t0004g0115a0003c0004t0004g0116 | 2 | HG03486.hp1 NA18906.hp1 |
intron_variant | MODIFIER | c.376-3347A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81832863 | ||||||
chr8:81832939
|
C | T | 1 | a0001c0001t0002g0195 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.376-3423G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81832939 | ||||||
chr8:81833011
|
C | T | 2 | a0001c0001t0002g0147a0001c0001t0002g0165 | 2 | HG01069.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.376-3495G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833011 | ||||||
chr8:81833153
|
A | G | 2 | a0001c0001t0004g0026a0001c0001t0004g0114 | 3 | HG01261.hp1 HG02717.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.376-3637T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833153 | ||||||
chr8:81833157
|
T | C | 1 | a0001c0001t0001g0066 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.376-3641A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833157 | ||||||
chr8:81833171
|
T | C | 1 | a0001c0002t0003g0068 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.376-3655A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833171 | ||||||
chr8:81833172
|
C | CT | 86 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(83): Show | 111 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(108): Show |
intron_variant | MODIFIER | c.376-3657dupA | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833172 | ||||||
chr8:81833172
|
C | T | 1 | a0001c0002t0003g0068 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.376-3656G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833172 | ||||||
chr8:81833229
|
T | C | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.376-3713A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833229 | ||||||
chr8:81833330
|
A | G | 8 | a0001c0001t0006g0184a0001c0001t0006g0185a0001c0001t0006g0186others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-3814T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833330 | ||||||
chr8:81833399
|
T | TA | 90 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(87): Show | 115 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(112): Show |
intron_variant | MODIFIER | c.376-3884dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833399 | ||||||
chr8:81833407
|
T | A | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.376-3891A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833407 | ||||||
chr8:81833412
|
C | T | 1 | a0001c0001t0005g0029 | 2 | HG00639.hp2 HG02895.hp2 |
intron_variant | MODIFIER | c.376-3896G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833412 | ||||||
chr8:81833481
|
G | T | 1 | a0001c0002t0003g0076 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.376-3965C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833481 | ||||||
chr8:81833593
|
C | T | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.376-4077G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833593 | ||||||
chr8:81833636
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.376-4120T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833636 | ||||||
chr8:81833726
|
T | C | 1 | a0001c0001t0004g0112 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.376-4210A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833726 | ||||||
chr8:81833866
|
T | C | 1 | a0001c0001t0001g0062 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.376-4350A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833866 | ||||||
chr8:81833888
|
G | C | 90 | a0000c0006t0002g0206a0001c0001t0002g0002a0001c0001t0002g0007others(87): Show | 109 | HG00099.hp2 HG00438.hp1 HG00438.hp2 others(106): Show |
intron_variant | MODIFIER | c.376-4372C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833888 | ||||||
chr8:81833889
|
T | C | 1 | a0001c0001t0015g0226 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.376-4373A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833889 | ||||||
chr8:81833909
|
A | C | 1 | a0001c0001t0015g0226 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.376-4393T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833909 | ||||||
chr8:81833977
|
C | T | 1 | a0001c0001t0002g0166 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.376-4461G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81833977 | ||||||
chr8:81834020
|
C | T | 2 | a0002c0003t0007g0028a0002c0003t0007g0153 | 3 | HG02572.hp2 HG02818.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.376-4504G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834020 | ||||||
chr8:81834132
|
A | C | 36 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0027others(33): Show | 43 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(40): Show |
intron_variant | MODIFIER | c.376-4616T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834132 | ||||||
chr8:81834139
|
TGGTGGAA others(21): Show |
T | 1 | a0001c0002t0003g0068 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.376-4651_376-4624d others(30): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834139 | ||||||
chr8:81834201
|
C | G | 180 | a0000c0006t0002g0206a0001c0001t0001g0036a0001c0001t0002g0002others(177): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.376-4685G>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834201 | ||||||
chr8:81834317
|
T | C | 1 | a0001c0002t0003g0095 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.376-4801A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834317 | ||||||
chr8:81834370
|
C | T | 2 | a0001c0002t0003g0099a0001c0002t0003g0100 | 2 | HG00738.hp1 HG03704.hp2 |
intron_variant | MODIFIER | c.376-4854G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834370 | ||||||
chr8:81834462
|
T | G | 1 | a0001c0002t0003g0068 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.376-4946A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834462 | ||||||
chr8:81834495
|
C | T | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.376-4979G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834495 | ||||||
chr8:81834514
|
C | T | 8 | a0001c0001t0006g0184a0001c0001t0006g0185a0001c0001t0006g0186others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.376-4998G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834514 | ||||||
chr8:81834516
|
T | C | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.376-5000A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834516 | ||||||
chr8:81834524
|
C | G | 1 | a0004c0007t0006g0214 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.376-5008G>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834524 | ||||||
chr8:81834529
|
A | G | 2 | a0001c0001t0002g0147a0001c0001t0002g0165 | 2 | HG01069.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.376-5013T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834529 | ||||||
chr8:81834576
|
G | A | 4 | a0001c0002t0003g0014a0001c0002t0003g0096a0001c0002t0003g0097others(1): Show | 6 | HG01192.hp2 HG01256.hp2 HG01258.hp2 others(3): Show |
intron_variant | MODIFIER | c.375+5036C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834576 | ||||||
chr8:81834582
|
G | A | 51 | a0001c0002t0003g0003a0001c0002t0003g0011a0001c0002t0003g0012others(48): Show | 68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.375+5030C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834582 | ||||||
chr8:81834641
|
A | T | 1 | a0001c0002t0003g0075 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.375+4971T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834641 | ||||||
chr8:81834953
|
A | C | 1 | a0001c0002t0003g0073 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.375+4659T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81834953 | ||||||
chr8:81835220
|
A | G | 1 | a0001c0001t0001g0034 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.375+4392T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81835220 | ||||||
chr8:81835282
|
G | A | 51 | a0001c0002t0003g0003a0001c0002t0003g0011a0001c0002t0003g0012others(48): Show | 68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.375+4330C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81835282 | ||||||
chr8:81835314
|
G | A | 1 | a0001c0001t0004g0026 | 2 | HG01261.hp1 HG02717.hp1 |
intron_variant | MODIFIER | c.375+4298C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81835314 | ||||||
chr8:81835495
|
T | C | 4 | a0001c0001t0006g0183a0001c0001t0006g0191a0001c0001t0006g0192others(1): Show | 4 | HG02109.hp2 HG02615.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.375+4117A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81835495 | ||||||
chr8:81835863
|
G | A | 2 | a0001c0002t0003g0025a0001c0002t0003g0098 | 3 | NA18980.hp2 NA19007.hp2 NA19012.hp2 |
intron_variant | MODIFIER | c.375+3749C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81835863 | ||||||
chr8:81835948
|
T | C | 180 | a0000c0006t0002g0206a0001c0001t0002g0002a0001c0001t0002g0007others(177): Show | 224 | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(221): Show |
intron_variant | MODIFIER | c.375+3664A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81835948 | ||||||
chr8:81836066
|
A | G | 8 | a0001c0001t0006g0184a0001c0001t0006g0185a0001c0001t0006g0186others(5): Show | 8 | HG01884.hp2 HG02055.hp2 HG02145.hp2 others(5): Show |
intron_variant | MODIFIER | c.375+3546T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836066 | ||||||
chr8:81836114
|
T | C | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.375+3498A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836114 | ||||||
chr8:81836172
|
C | A | 1 | a0001c0002t0003g0099 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.375+3440G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836172 | ||||||
chr8:81836202
|
A | T | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.375+3410T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836202 | ||||||
chr8:81836439
|
T | A | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.375+3173A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836439 | ||||||
chr8:81836457
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.375+3155A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836457 | ||||||
chr8:81836614
|
C | T | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.375+2998G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836614 | ||||||
chr8:81836615
|
G | A | 3 | a0001c0001t0007g0032a0001c0001t0007g0217a0001c0001t0007g0218 | 4 | HG03540.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.375+2997C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836615 | ||||||
chr8:81836635
|
T | G | 2 | a0001c0001t0005g0152a0001c0001t0005g0163 | 2 | HG02922.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.375+2977A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836635 | ||||||
chr8:81836661
|
T | C | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.375+2951A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836661 | ||||||
chr8:81836693
|
T | C | 88 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(85): Show | 113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.375+2919A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836693 | ||||||
chr8:81836836
|
T | C | 1 | a0004c0007t0006g0214 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.375+2776A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836836 | ||||||
chr8:81836898
|
A | G | 2 | a0001c0001t0002g0143a0001c0001t0002g0164 | 2 | HG00099.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.375+2714T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81836898 | ||||||
chr8:81837396
|
T | G | 1 | a0001c0001t0001g0064 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.375+2216A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81837396 | ||||||
chr8:81837528
|
C | T | 1 | a0001c0001t0001g0016 | 2 | HG01069.hp2 HG01071.hp1 |
intron_variant | MODIFIER | c.375+2084G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81837528 | ||||||
chr8:81837554
|
T | G | 1 | a0001c0002t0003g0108 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.375+2058A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81837554 | ||||||
chr8:81837739
|
C | T | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.375+1873G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81837739 | ||||||
chr8:81837822
|
A | G | 1 | a0002c0003t0007g0028 | 2 | HG02572.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.375+1790T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81837822 | ||||||
chr8:81837977
|
A | T | 7 | a0001c0001t0004g0006a0001c0001t0004g0119a0001c0001t0004g0120others(4): Show | 11 | HG01928.hp1 HG01934.hp2 HG01943.hp2 others(8): Show |
intron_variant | MODIFIER | c.375+1635T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81837977 | ||||||
chr8:81837993
|
T | C | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.375+1619A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81837993 | ||||||
chr8:81838332
|
G | A | 2 | a0001c0001t0004g0135a0001c0001t0004g0136 | 2 | NA18947.hp2 NA18983.hp2 |
intron_variant | MODIFIER | c.375+1280C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838332 | ||||||
chr8:81838414
|
T | A | 1 | a0001c0002t0003g0068 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.375+1198A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838414 | ||||||
chr8:81838414
|
T | C | 88 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(85): Show | 113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.375+1198A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838414 | ||||||
chr8:81838415
|
T | C | 1 | a0001c0002t0003g0068 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.375+1197A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838415 | ||||||
chr8:81838416
|
A | T | 1 | a0001c0002t0003g0068 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.375+1196T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838416 | ||||||
chr8:81838561
|
T | A | 1 | a0001c0001t0001g0064 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.375+1051A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838561 | ||||||
chr8:81838574
|
G | GA | 18 | a0001c0001t0002g0211a0001c0001t0002g0212a0001c0001t0002g0213others(15): Show | 18 | HG00280.hp1 HG00642.hp2 HG01175.hp1 others(15): Show |
intron_variant | MODIFIER | c.375+1037dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838574 | ||||||
chr8:81838574
|
GA | G | 18 | a0001c0001t0001g0035a0001c0001t0002g0161a0001c0001t0004g0119others(15): Show | 20 | HG00639.hp2 HG00738.hp2 HG01106.hp1 others(17): Show |
intron_variant | MODIFIER | c.375+1037delT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838574 | ||||||
chr8:81838663
|
C | A | 1 | a0001c0001t0002g0215 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.375+949G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838663 | ||||||
chr8:81838731
|
A | G | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.375+881T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838731 | ||||||
chr8:81838970
|
A | ATCCAAAC others(15): Show |
1 | a0001c0001t0006g0191 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.375+620_375+641dup others(22): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838970 | ||||||
chr8:81838982
|
CA | C | 4 | a0001c0001t0015g0226a0001c0001t0016g0220a0001c0002t0003g0069others(1): Show | 4 | HG02080.hp2 NA18998.hp1 NA19062.hp1 others(1): Show |
intron_variant | MODIFIER | c.375+629delT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81838982 | ||||||
chr8:81839223
|
C | T | 1 | a0001c0001t0012g0142 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.375+389G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81839223 | ||||||
chr8:81839225
|
A | T | 1 | a0001c0001t0002g0215 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.375+387T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81839225 | ||||||
chr8:81839355
|
T | C | 2 | a0001c0001t0006g0191a0001c0001t0006g0192 | 2 | HG02109.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.375+257A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81839355 | ||||||
chr8:81839400
|
A | T | 1 | a0001c0002t0003g0068 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.375+212T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81839400 | ||||||
chr8:81839435
|
A | T | 1 | a0001c0002t0003g0068 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.375+177T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81839435 | ||||||
chr8:81839587
|
T | G | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.375+25A>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 2/7 | chr8 | 81839587 | ||||||
chr8:81840100
|
A | G | 4 | a0001c0001t0004g0015a0001c0001t0004g0112a0001c0001t0004g0117others(1): Show | 6 | HG00423.hp2 NA18946.hp2 NA18984.hp1 others(3): Show |
intron_variant | MODIFIER | c.-96-18T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840100 | ||||||
chr8:81840195
|
T | C | 1 | a0001c0001t0004g0228 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-96-113A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840195 | ||||||
chr8:81840197
|
C | A | 1 | a0001c0001t0004g0228 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-96-115G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840197 | ||||||
chr8:81840542
|
T | A | 1 | a0001c0001t0015g0226 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-96-460A>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840542 | ||||||
chr8:81840544
|
A | C | 1 | a0001c0001t0015g0226 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-96-462T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840544 | ||||||
chr8:81840545
|
A | T | 1 | a0001c0001t0015g0226 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-96-463T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840545 | ||||||
chr8:81840548
|
T | C | 1 | a0001c0001t0015g0226 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-96-466A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840548 | ||||||
chr8:81840592
|
A | C | 1 | a0001c0001t0015g0226 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-96-510T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840592 | ||||||
chr8:81840604
|
G | A | 33 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0027others(30): Show | 40 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.-96-522C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840604 | ||||||
chr8:81840647
|
C | T | 2 | a0001c0001t0007g0032a0001c0001t0007g0218 | 3 | HG03540.hp2 NA19030.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.-96-565G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840647 | ||||||
chr8:81840666
|
CAAAT | C | 37 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(34): Show | 45 | HG00280.hp1 HG00423.hp2 HG00673.hp2 others(42): Show |
intron_variant | MODIFIER | c.-96-588_-96-585del others(4): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840666 | ||||||
chr8:81840870
|
G | T | 3 | a0001c0001t0007g0032a0001c0001t0007g0217a0001c0001t0007g0218 | 4 | HG03540.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-96-788C>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840870 | ||||||
chr8:81840953
|
CACA | C | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.-96-874_-96-872del others(3): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81840953 | ||||||
chr8:81841115
|
T | C | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.-97+1007A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841115 | ||||||
chr8:81841165
|
A | C | 1 | a0001c0001t0006g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-97+957T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841165 | ||||||
chr8:81841166
|
C | A | 1 | a0001c0001t0006g0193 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-97+956G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841166 | ||||||
chr8:81841197
|
CG | C | 3 | a0001c0001t0002g0154a0001c0001t0002g0215a0001c0001t0002g0225 | 3 | NA18747.hp1 NA18946.hp1 NA19062.hp2 |
intron_variant | MODIFIER | c.-97+924delC | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841197 | ||||||
chr8:81841341
|
C | CA | 55 | a0001c0001t0001g0065a0001c0001t0002g0007a0001c0001t0002g0145others(52): Show | 61 | HG00099.hp2 HG00609.hp1 HG00639.hp2 others(58): Show |
intron_variant | MODIFIER | c.-97+780dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841341 | ||||||
chr8:81841341
|
C | CAA | 31 | a0000c0006t0002g0206a0001c0001t0002g0002a0001c0001t0002g0031others(28): Show | 42 | HG00438.hp1 HG00438.hp2 HG00558.hp1 others(39): Show |
intron_variant | MODIFIER | c.-97+779_-97+780dup others(2): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841341 | ||||||
chr8:81841341
|
CA | C | 8 | a0001c0001t0001g0034a0001c0001t0004g0112a0001c0001t0004g0113others(5): Show | 8 | HG01168.hp1 NA18939.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.-97+780delT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841341 | ||||||
chr8:81841360
|
G | A | 1 | a0001c0001t0002g0216 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.-97+762C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841360 | ||||||
chr8:81841403
|
A | G | 2 | a0001c0001t0004g0111a0001c0001t0012g0142 | 2 | HG02723.hp1 NA18944.hp2 |
intron_variant | MODIFIER | c.-97+719T>C | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841403 | ||||||
chr8:81841459
|
C | T | 2 | a0001c0001t0002g0144a0001c0001t0002g0145 | 2 | HG03491.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.-97+663G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841459 | ||||||
chr8:81841481
|
G | A | 3 | a0001c0001t0007g0032a0001c0001t0007g0217a0001c0001t0007g0218 | 4 | HG03540.hp2 NA19030.hp1 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.-97+641C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841481 | ||||||
chr8:81841630
|
A | T | 1 | a0001c0002t0003g0068 | 1 | NA19063.hp2 | intron_variant | MODIFIER | c.-97+492T>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841630 | ||||||
chr8:81841654
|
A | C | 1 | a0001c0001t0015g0226 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-97+468T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841654 | ||||||
chr8:81841655
|
C | A | 1 | a0001c0001t0015g0226 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-97+467G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841655 | ||||||
chr8:81841655
|
C | CA | 15 | a0001c0001t0002g0219a0001c0001t0002g0221a0001c0001t0002g0222others(12): Show | 15 | HG01978.hp2 HG02080.hp2 HG02132.hp1 others(12): Show |
intron_variant | MODIFIER | c.-97+466dupT | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841655 | ||||||
chr8:81841739
|
C | A | 1 | a0001c0002t0003g0110 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.-97+383G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841739 | ||||||
chr8:81841788
|
C | T | 51 | a0001c0002t0003g0003a0001c0002t0003g0011a0001c0002t0003g0012others(48): Show | 68 | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(65): Show |
intron_variant | MODIFIER | c.-97+334G>A | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841788 | ||||||
chr8:81841791
|
GAGGAAAG others(18): Show |
G | 1 | a0001c0001t0002g0143 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.-97+306_-97+330del others(25): Show |
SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841791 | ||||||
chr8:81841851
|
C | A | 1 | a0001c0001t0001g0066 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-97+271G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841851 | ||||||
chr8:81841883
|
A | C | 88 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(85): Show | 113 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(110): Show |
intron_variant | MODIFIER | c.-97+239T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841883 | ||||||
chr8:81841905
|
A | C | 89 | a0001c0001t0004g0006a0001c0001t0004g0015a0001c0001t0004g0026others(86): Show | 114 | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(111): Show |
intron_variant | MODIFIER | c.-97+217T>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841905 | ||||||
chr8:81841917
|
G | C | 1 | a0001c0001t0015g0226 | 1 | NA19063.hp1 | intron_variant | MODIFIER | c.-97+205C>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841917 | ||||||
chr8:81841985
|
G | A | 1 | a0001c0001t0001g0067 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.-97+137C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841985 | ||||||
chr8:81841990
|
G | A | 1 | a0001c0001t0004g0227 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.-97+132C>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81841990 | ||||||
chr8:81842030
|
T | C | 227 | a0000c0006t0002g0206a0001c0001t0001g0001a0001c0001t0001g0004others(224): Show | 305 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(302): Show |
intron_variant | MODIFIER | c.-97+92A>G | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81842030 | ||||||
chr8:81842033
|
C | A | 1 | a0001c0001t0004g0228 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.-97+89G>T | SNX16 | ENSG00000104497.15 | transcript | ENST00000345957.9 | protein_coding | 1/7 | chr8 | 81842033 |