geneid | 57231 |
---|---|
ensemblid | ENSG00000135317.14 |
hgncid | 14977 |
symbol | SNX14 |
name | sorting nexin 14 |
refseq_nuc | NM_153816.6 |
refseq_prot | NP_722523.1 |
ensembl_nuc | ENST00000314673.8 |
ensembl_prot | ENSP00000313121.3 |
mane_status | MANE Select |
chr | chr6 |
start | 85505496 |
end | 85593858 |
strand | - |
ver | v1.2 |
region | chr6:85505496-85593858 |
region5000 | chr6:85500496-85598858 |
regionname0 | SNX14_chr6_85505496_85593858 |
regionname5000 | SNX14_chr6_85500496_85598858 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/0 | 946 | 354 | 89 | 56 | 164 | 10 | 34 | 128 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
a0002 | 0/1 | 946 | 5 | 0 | 2 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
a0003 | 0/0 | 946 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/0 | 2841 | 347 | 84 | 56 | 163 | 9 | 34 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
c0002 | 0/1 | 2841 | 5 | 0 | 2 | 0 | 2 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
c0003 | 0/0 | 2841 | 4 | 4 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
c0004 | 0/0 | 2841 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
c0005 | 0/0 | 2841 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
c0006 | 0/0 | 2841 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
c0007 | 0/0 | 2841 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 612 | 350 | 83 | 58 | 161 | 12 | 34 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
t0002 | 0/0 | 612 | 4 | 4 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
t0003 | 0/0 | 612 | 2 | 0 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
t0004 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
t0005 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
t0006 | 0/0 | 612 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
t0007 | 0/0 | 612 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0334 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/0 | 2841 | 347 | 84 | 56 | 163 | 9 | 34 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
a0001c0003 | 0/0 | 2841 | 4 | 4 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
a0001c0004 | 0/0 | 2841 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
a0001c0005 | 0/0 | 2841 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
a0001c0007 | 0/0 | 2841 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
a0002c0002 | 0/1 | 2841 | 5 | 0 | 2 | 0 | 2 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
a0003c0006 | 0/0 | 2841 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 3452 | 343 | 83 | 56 | 160 | 9 | 34 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
a0001c0001t0003 | 0/0 | 3452 | 2 | 0 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
a0001c0001t0004 | 0/0 | 3452 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
a0001c0001t0007 | 0/0 | 3452 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
a0001c0003t0002 | 0/0 | 3452 | 4 | 4 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
a0001c0004t0001 | 0/0 | 3452 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
a0001c0005t0005 | 0/0 | 3452 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
a0001c0007t0001 | 0/0 | 3452 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
a0002c0002t0001 | 0/1 | 3452 | 5 | 0 | 2 | 0 | 2 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
a0003c0006t0006 | 0/0 | 3452 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | copy fasta | chr6 | 85500496 | 85598858 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0004 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0005 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0007 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0012 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0031 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0037 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0164 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0175 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0231 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0232 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0236 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0257 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0274 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0275 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0281 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0282 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0283 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0310 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0316 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0320 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0323 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0324 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0325 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0326 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0327 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0329 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0331 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0332 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0333 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0336 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0337 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0338 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0340 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0343 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0003g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0003g0314 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0004g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0001t0007g0349 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0003t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0003t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0003t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0003t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0004t0001g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0005t0005g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0001c0007t0001g0348 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0002c0002t0001g0010 | 0/0 | 2 | 0 | 0 | 0 | 2 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0002c0002t0001g0298 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0002c0002t0001g0305 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0002c0002t0001g0334 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
a0003c0006t0006g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0001 | g0319 | EUR | GBR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00099 | hp2 | a0001 | c0007 | t0001 | g0348 | EUR | GBR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00280 | hp1 | a0001 | c0001 | t0001 | g0340 | EUR | FIN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0166 | EUR | FIN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0204 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0280 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0326 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0142 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00597 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00609 | hp1 | a0001 | c0001 | t0003 | g0301 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00609 | hp2 | a0001 | c0001 | t0001 | g0135 | EAS | CHS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0150 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0068 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00735 | hp2 | a0001 | c0001 | t0001 | g0230 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG00741 | hp2 | a0001 | c0001 | t0001 | g0341 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01069 | hp1 | a0001 | c0001 | t0001 | g0037 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0126 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01070 | hp2 | a0001 | c0001 | t0001 | g0267 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01071 | hp1 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0038 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0165 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0159 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0347 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0274 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01168 | hp1 | a0002 | c0002 | t0001 | g0298 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01168 | hp2 | a0001 | c0001 | t0001 | g0232 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01169 | hp1 | a0002 | c0002 | t0001 | g0305 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0072 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0178 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0310 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0168 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0122 | AMR | PUR | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0115 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0041 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0025 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0180 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01257 | hp2 | a0001 | c0001 | t0001 | g0345 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01258 | hp1 | a0001 | c0001 | t0001 | g0026 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0004 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0175 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01358 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0198 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0032 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0065 | AMR | CLM | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01515 | hp1 | a0002 | c0002 | t0001 | g0010 | EUR | IBS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0139 | EUR | IBS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0172 | EUR | IBS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01516 | hp2 | a0001 | c0001 | t0001 | g0177 | EUR | IBS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01517 | hp1 | a0002 | c0002 | t0001 | g0010 | EUR | IBS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01517 | hp2 | a0001 | c0001 | t0001 | g0173 | EUR | IBS | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0225 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0018 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0248 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0043 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0036 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0158 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0271 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0044 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0119 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0071 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0058 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0315 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02027 | hp2 | a0001 | c0001 | t0001 | g0141 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0224 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0027 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0084 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0331 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0260 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02074 | hp2 | a0001 | c0001 | t0001 | g0090 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0130 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0333 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02132 | hp1 | a0001 | c0001 | t0001 | g0328 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02132 | hp2 | a0001 | c0001 | t0001 | g0134 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0179 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0220 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02145 | hp1 | a0001 | c0001 | t0001 | g0028 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02145 | hp2 | a0001 | c0001 | t0001 | g0055 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02148 | hp1 | a0001 | c0001 | t0001 | g0147 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0105 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0129 | EAS | CDX | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0343 | EAS | CDX | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0181 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02257 | hp2 | a0001 | c0001 | t0001 | g0182 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02258 | hp1 | a0001 | c0001 | t0001 | g0251 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02258 | hp2 | a0001 | c0001 | t0001 | g0258 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0108 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02280 | hp2 | a0001 | c0001 | t0001 | g0273 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0076 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0123 | AMR | PEL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0138 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0062 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0238 | EAS | KHV | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0097 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02615 | hp2 | a0001 | c0001 | t0001 | g0250 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02622 | hp2 | a0001 | c0001 | t0001 | g0249 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0192 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0188 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0053 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0057 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0286 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02698 | hp2 | a0001 | c0001 | t0001 | g0031 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0183 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0136 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0094 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02735 | hp1 | a0001 | c0001 | t0001 | g0030 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0170 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02809 | hp2 | a0001 | c0001 | t0001 | g0096 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02818 | hp1 | a0001 | c0003 | t0002 | g0033 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0234 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0013 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0285 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0050 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0282 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0199 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0284 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0275 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0035 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0022 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02970 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02970 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02976 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02976 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0195 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0332 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03041 | hp1 | a0001 | c0003 | t0002 | g0052 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0020 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0235 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03098 | hp2 | a0001 | c0001 | t0001 | g0281 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03130 | hp2 | a0003 | c0006 | t0006 | g0047 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03195 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0233 | AFR | ESN | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03209 | hp1 | a0001 | c0003 | t0002 | g0051 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0056 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03225 | hp1 | a0001 | c0001 | t0001 | g0277 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0021 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0253 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03453 | hp2 | a0001 | c0003 | t0002 | g0034 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03486 | hp2 | a0001 | c0001 | t0001 | g0045 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0236 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0089 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03540 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0015 | AFR | GWD | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0190 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0095 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0081 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0193 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03669 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0104 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0075 | SAS | STU | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | STU | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0295 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0240 | SAS | PJL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0231 | SAS | BEB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0294 | SAS | BEB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0117 | SAS | BEB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | BEB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | BEB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | BEB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0091 | SAS | STU | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0269 | SAS | STU | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0287 | SAS | BEB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0029 | SAS | BEB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0112 | SAS | STU | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0077 | SAS | STU | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0110 | SAS | STU | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0074 | SAS | STU | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | YRI | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0283 | AFR | YRI | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | CHB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0219 | EAS | CHB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0309 | EAS | CHB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0254 | EAS | CHB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18906 | hp1 | a0001 | c0001 | t0004 | g0011 | AFR | YRI | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0272 | AFR | YRI | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0201 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18941 | hp2 | a0001 | c0001 | t0001 | g0102 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0293 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0312 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18947 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0256 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0317 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0042 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0245 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0229 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18956 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0207 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18959 | hp2 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18961 | hp1 | a0001 | c0001 | t0001 | g0263 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0144 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0221 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0125 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0318 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18966 | hp1 | a0001 | c0004 | t0001 | g0243 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0265 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18969 | hp2 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18970 | hp1 | a0001 | c0001 | t0001 | g0006 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0329 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0086 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0323 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18972 | hp1 | a0001 | c0001 | t0001 | g0040 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18972 | hp2 | a0001 | c0001 | t0001 | g0342 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18973 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18975 | hp1 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0306 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18977 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0137 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18981 | hp1 | a0001 | c0001 | t0003 | g0314 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0228 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0146 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0316 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18984 | hp2 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18985 | hp1 | a0001 | c0001 | t0001 | g0346 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18985 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0325 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18990 | hp1 | a0001 | c0001 | t0001 | g0266 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18991 | hp2 | a0001 | c0001 | t0007 | g0349 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0336 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18993 | hp1 | a0001 | c0001 | t0001 | g0338 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18994 | hp1 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0149 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18995 | hp1 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18998 | hp1 | a0001 | c0001 | t0001 | g0289 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0131 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0321 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19003 | hp1 | a0001 | c0001 | t0001 | g0320 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0111 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19005 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0313 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19006 | hp2 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19007 | hp1 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0085 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0299 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0039 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0330 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0191 | AFR | LWK | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0049 | AFR | LWK | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | LWK | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0259 | AFR | LWK | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0297 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19055 | hp2 | a0001 | c0001 | t0001 | g0239 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0082 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19059 | hp1 | a0001 | c0001 | t0001 | g0344 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19059 | hp2 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0152 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0153 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19064 | hp1 | a0001 | c0001 | t0001 | g0009 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0244 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19065 | hp1 | a0001 | c0001 | t0001 | g0063 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19065 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0241 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0303 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0311 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19074 | hp1 | a0001 | c0001 | t0001 | g0133 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19074 | hp2 | a0001 | c0001 | t0001 | g0339 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19075 | hp2 | a0001 | c0001 | t0001 | g0255 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19076 | hp1 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0324 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19077 | hp2 | a0001 | c0001 | t0001 | g0246 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19079 | hp1 | a0001 | c0001 | t0001 | g0268 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19079 | hp2 | a0001 | c0001 | t0001 | g0128 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0143 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0302 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0213 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0080 | EAS | JPT | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0054 | AFR | YRI | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0257 | AFR | YRI | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA20752 | hp1 | a0001 | c0001 | t0001 | g0163 | EUR | TSI | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0335 | EUR | TSI | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0327 | SAS | GIH | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA20905 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | GIH | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0046 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02486 | hp2 | a0001 | c0001 | t0001 | g0247 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0252 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG02559 | hp2 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03471 | hp1 | a0001 | c0005 | t0005 | g0024 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0014 | AFR | MSL | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0061 | AFR | USA | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0337 | AFR | USA | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0109 | AFR | USA | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
NA20300 | hp2 | a0001 | c0001 | t0001 | g0279 | AFR | USA | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
homoSapiens_chm13v2 | hp1 | a0002 | c0002 | t0001 | g0334 | REF | REF | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0164 | REF | REF | SNX14_chr6_85500496_85598858 | SNX14 | chr6 | 85500496 | 85598858 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:85547145
|
C | A | 1 | a0003 | 1 | HG03130.hp2 | missense_variant | MODERATE | c.1075G>T | p.Ala359Ser | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/29 | 1215/3452 | 1075/2841 | 359/946 | chr6 | 85547145 | ||
chr6:85547511
|
T | G | 1 | a0002 | 5 | HG01168.hp1 HG01169.hp1 HG01515.hp1 others(2): Show |
missense_variant | MODERATE | c.907A>C | p.Ser303Arg | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 10/29 | 1047/3452 | 907/2841 | 303/946 | chr6 | 85547511 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:85514095
|
C | T | 1 | a0001c0003 | 4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
synonymous_variant | LOW | c.2532G>A | p.Leu844Leu | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 25/29 | 2672/3452 | 2532/2841 | 844/946 | chr6 | 85514095 | ||
chr6:85565365
|
A | G | 1 | a0001c0005 | 1 | HG03471.hp1 | synonymous_variant | LOW | c.516T>C | p.Phe172Phe | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/29 | 656/3452 | 516/2841 | 172/946 | chr6 | 85565365 | ||
chr6:85572158
|
C | T | 1 | a0001c0004 | 1 | NA18966.hp1 | synonymous_variant | LOW | c.396G>A | p.Lys132Lys | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/29 | 536/3452 | 396/2841 | 132/946 | chr6 | 85572158 | ||
chr6:85593710
|
G | A | 1 | a0001c0007 | 1 | HG00099.hp2 | synonymous_variant | LOW | c.9C>T | p.Pro3Pro | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/29 | 149/3452 | 9/2841 | 3/946 | chr6 | 85593710 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:85505625
|
T | C | 1 | a0001c0001t0003 | 2 | HG00609.hp1 NA18981.hp1 |
3_prime_UTR_variant | MODIFIER | c.*342A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 29/29 | 342 | chr6 | 85505625 | |||||
chr6:85505630
|
A | C | 1 | a0001c0005t0005 | 1 | HG03471.hp1 | 3_prime_UTR_variant | MODIFIER | c.*337T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 29/29 | 337 | chr6 | 85505630 | |||||
chr6:85505762
|
G | A | 1 | a0001c0003t0002 | 4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*205C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 29/29 | 205 | chr6 | 85505762 | |||||
chr6:85505953
|
C | A | 1 | a0003c0006t0006 | 1 | HG03130.hp2 | 3_prime_UTR_variant | MODIFIER | c.*14G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 29/29 | 14 | chr6 | 85505953 | |||||
chr6:85593825
|
G | A | 1 | a0001c0001t0007 | 1 | NA18991.hp2 | 5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-107C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/29 | chr6 | 85593825 | ||||||
chr6:85593829
|
C | T | 1 | a0001c0001t0004 | 1 | NA18906.hp1 | 5_prime_UTR_variant | MODIFIER | c.-111G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/29 | 111 | chr6 | 85593829 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:85506048
|
G | A | 9 | a0001c0001t0001g0069a0001c0001t0001g0168a0001c0001t0001g0169others(6): Show | 9 | HG01175.hp1 HG01243.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2803-43C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506048 | ||||||
chr6:85506054
|
T | C | 1 | a0003c0006t0006g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2803-49A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506054 | ||||||
chr6:85506126
|
T | C | 1 | a0001c0001t0001g0339 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.2803-121A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506126 | ||||||
chr6:85506179
|
C | T | 69 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0040others(66): Show | 70 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(67): Show |
intron_variant | MODIFIER | c.2803-174G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506179 | ||||||
chr6:85506198
|
T | C | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2803-193A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506198 | ||||||
chr6:85506320
|
A | AT | 11 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057others(8): Show | 11 | HG02109.hp1 HG02280.hp2 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.2803-316dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506320 | ||||||
chr6:85506320
|
AT | A | 31 | a0001c0001t0001g0120a0001c0001t0001g0187a0001c0001t0001g0188others(28): Show | 31 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.2803-316delA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506320 | ||||||
chr6:85506374
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2803-369A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506374 | ||||||
chr6:85506419
|
C | T | 1 | a0001c0001t0001g0283 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.2803-414G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506419 | ||||||
chr6:85506450
|
G | A | 1 | a0001c0001t0001g0080 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.2803-445C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506450 | ||||||
chr6:85506518
|
G | A | 1 | a0001c0001t0001g0143 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.2803-513C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506518 | ||||||
chr6:85506563
|
G | A | 2 | a0001c0001t0001g0144a0001c0001t0001g0148 | 2 | NA18961.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.2803-558C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506563 | ||||||
chr6:85506598
|
G | A | 1 | a0001c0001t0001g0028 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.2803-593C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506598 | ||||||
chr6:85506674
|
G | A | 1 | a0001c0001t0001g0345 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.2802+559C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506674 | ||||||
chr6:85506899
|
C | T | 7 | a0001c0001t0001g0049a0001c0001t0001g0187a0001c0001t0001g0188others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2802+334G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506899 | ||||||
chr6:85506907
|
A | G | 27 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0001t0001g0259others(24): Show | 27 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.2802+326T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506907 | ||||||
chr6:85506928
|
G | A | 1 | a0001c0001t0001g0210 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.2802+305C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85506928 | ||||||
chr6:85507166
|
C | A | 1 | a0001c0001t0001g0186 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2802+67G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 28/28 | chr6 | 85507166 | ||||||
chr6:85507361
|
A | G | 8 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(5): Show | 9 | HG01884.hp2 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2746-72T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 27/28 | chr6 | 85507361 | ||||||
chr6:85507372
|
T | C | 8 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(5): Show | 9 | HG01884.hp2 HG02559.hp1 HG02647.hp1 others(6): Show |
intron_variant | MODIFIER | c.2746-83A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 27/28 | chr6 | 85507372 | ||||||
chr6:85507730
|
G | T | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.2745+238C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 27/28 | chr6 | 85507730 | ||||||
chr6:85507742
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2745+226T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 27/28 | chr6 | 85507742 | ||||||
chr6:85507797
|
T | A | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2745+171A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 27/28 | chr6 | 85507797 | ||||||
chr6:85507884
|
T | C | 1 | a0001c0001t0001g0343 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.2745+84A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 27/28 | chr6 | 85507884 | ||||||
chr6:85507915
|
C | A | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2745+53G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 27/28 | chr6 | 85507915 | ||||||
chr6:85507915
|
C | T | 4 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 4 | HG02647.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2745+53G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 27/28 | chr6 | 85507915 | ||||||
chr6:85508098
|
T | G | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2654-39A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508098 | ||||||
chr6:85508320
|
T | TA | 16 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0018others(13): Show | 17 | HG01884.hp2 HG02148.hp2 HG02622.hp2 others(14): Show |
intron_variant | MODIFIER | c.2654-262dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508320 | ||||||
chr6:85508534
|
T | C | 1 | a0001c0001t0001g0063 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.2654-475A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508534 | ||||||
chr6:85508549
|
T | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.2654-490A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508549 | ||||||
chr6:85508638
|
G | C | 1 | a0001c0001t0001g0322 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2654-579C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508638 | ||||||
chr6:85508642
|
C | CAAACCAA others(3): Show |
1 | a0001c0001t0001g0322 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.2654-584_2654-583i others(12): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508642 | ||||||
chr6:85508696
|
A | G | 1 | a0001c0001t0001g0165 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.2654-637T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508696 | ||||||
chr6:85508711
|
A | G | 1 | a0001c0001t0001g0300 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.2654-652T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508711 | ||||||
chr6:85508716
|
G | C | 1 | a0001c0001t0001g0327 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2654-657C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508716 | ||||||
chr6:85508772
|
A | G | 1 | a0001c0001t0001g0331 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.2654-713T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508772 | ||||||
chr6:85508927
|
C | G | 4 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 4 | HG02647.hp2 HG03130.hp2 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.2654-868G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508927 | ||||||
chr6:85508959
|
G | A | 1 | a0001c0001t0001g0207 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.2654-900C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85508959 | ||||||
chr6:85509032
|
T | C | 2 | a0001c0001t0001g0176a0001c0001t0001g0347 | 2 | HG01069.hp2 HG01106.hp1 |
intron_variant | MODIFIER | c.2654-973A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85509032 | ||||||
chr6:85509336
|
T | TA | 31 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(28): Show | 31 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.2654-1278dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85509336 | ||||||
chr6:85509452
|
C | G | 1 | a0001c0001t0001g0139 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.2654-1393G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85509452 | ||||||
chr6:85509494
|
T | TTCTG | 231 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(228): Show | 237 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(234): Show |
intron_variant | MODIFIER | c.2654-1439_2654-143 others(8): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85509494 | ||||||
chr6:85509598
|
T | C | 4 | a0001c0001t0001g0253a0001c0001t0001g0257a0001c0001t0001g0273others(1): Show | 4 | HG02280.hp2 HG03225.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2654-1539A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85509598 | ||||||
chr6:85509769
|
A | G | 8 | a0001c0001t0001g0049a0001c0001t0001g0187a0001c0001t0001g0188others(5): Show | 8 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(5): Show |
intron_variant | MODIFIER | c.2654-1710T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85509769 | ||||||
chr6:85509841
|
C | T | 28 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0001t0001g0259others(25): Show | 28 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.2654-1782G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85509841 | ||||||
chr6:85510021
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2654-1962A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85510021 | ||||||
chr6:85510090
|
T | G | 1 | a0001c0001t0001g0136 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2654-2031A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85510090 | ||||||
chr6:85510379
|
T | G | 11 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0049others(8): Show | 11 | HG02109.hp1 HG02145.hp2 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.2654-2320A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85510379 | ||||||
chr6:85510534
|
G | A | 1 | a0001c0001t0001g0029 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.2654-2475C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85510534 | ||||||
chr6:85510645
|
G | A | 9 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(6): Show | 9 | HG00741.hp1 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2654-2586C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85510645 | ||||||
chr6:85510666
|
T | C | 1 | a0001c0001t0001g0208 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.2654-2607A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85510666 | ||||||
chr6:85510728
|
C | G | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2654-2669G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85510728 | ||||||
chr6:85510795
|
T | C | 1 | a0001c0001t0001g0082 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2654-2736A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85510795 | ||||||
chr6:85510823
|
T | C | 9 | a0001c0001t0001g0069a0001c0001t0001g0168a0001c0001t0001g0169others(6): Show | 9 | HG01175.hp1 HG01243.hp1 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.2654-2764A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85510823 | ||||||
chr6:85511000
|
T | C | 25 | a0001c0001t0001g0009a0001c0001t0001g0290a0001c0001t0001g0291others(22): Show | 26 | HG02027.hp1 HG02083.hp2 HG02523.hp1 others(23): Show |
intron_variant | MODIFIER | c.2653+2800A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511000 | ||||||
chr6:85511005
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2653+2795C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511005 | ||||||
chr6:85511189
|
AT | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2653+2610delA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511189 | ||||||
chr6:85511210
|
C | T | 25 | a0001c0001t0001g0008a0001c0001t0001g0041a0001c0001t0001g0042others(22): Show | 26 | HG00423.hp1 HG01255.hp2 HG01928.hp1 others(23): Show |
intron_variant | MODIFIER | c.2653+2590G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511210 | ||||||
chr6:85511402
|
A | G | 1 | a0001c0001t0001g0264 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.2653+2398T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511402 | ||||||
chr6:85511536
|
G | A | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2653+2264C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511536 | ||||||
chr6:85511603
|
A | G | 9 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(6): Show | 9 | HG00741.hp1 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.2653+2197T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511603 | ||||||
chr6:85511749
|
T | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG02451.hp2 HG02886.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.2653+2051A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511749 | ||||||
chr6:85511768
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2653+2032G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511768 | ||||||
chr6:85511795
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2653+2005C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511795 | ||||||
chr6:85511854
|
A | C | 81 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(78): Show | 84 | HG00408.hp2 HG00423.hp1 HG00735.hp1 others(81): Show |
intron_variant | MODIFIER | c.2653+1946T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511854 | ||||||
chr6:85511868
|
A | T | 158 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(155): Show | 164 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(161): Show |
intron_variant | MODIFIER | c.2653+1932T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511868 | ||||||
chr6:85511969
|
AG | A | 13 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0045others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02818.hp1 others(10): Show |
intron_variant | MODIFIER | c.2653+1830delC | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511969 | ||||||
chr6:85511984
|
T | G | 1 | a0001c0001t0001g0016 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2653+1816A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85511984 | ||||||
chr6:85512034
|
C | G | 6 | a0001c0001t0001g0014a0001c0001t0001g0056a0001c0001t0001g0057others(3): Show | 6 | HG02615.hp1 HG02647.hp2 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.2653+1766G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512034 | ||||||
chr6:85512049
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2653+1751A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512049 | ||||||
chr6:85512053
|
C | T | 207 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0013others(204): Show | 209 | HG00280.hp2 HG00408.hp2 HG00597.hp1 others(206): Show |
intron_variant | MODIFIER | c.2653+1747G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512053 | ||||||
chr6:85512215
|
G | A | 6 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0182others(3): Show | 6 | HG02257.hp2 HG02717.hp2 HG02809.hp1 others(3): Show |
intron_variant | MODIFIER | c.2653+1585C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512215 | ||||||
chr6:85512225
|
A | G | 58 | a0001c0001t0001g0040a0001c0001t0001g0041a0001c0001t0001g0042others(55): Show | 58 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(55): Show |
intron_variant | MODIFIER | c.2653+1575T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512225 | ||||||
chr6:85512230
|
G | A | 4 | a0001c0003t0002g0033a0001c0003t0002g0034a0001c0003t0002g0051others(1): Show | 4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.2653+1570C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512230 | ||||||
chr6:85512308
|
T | G | 4 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0217others(1): Show | 4 | HG01358.hp2 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.2653+1492A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512308 | ||||||
chr6:85512350
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.2653+1450C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512350 | ||||||
chr6:85512420
|
G | A | 1 | a0001c0001t0001g0071 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.2653+1380C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512420 | ||||||
chr6:85512557
|
G | C | 1 | a0001c0001t0001g0181 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2653+1243C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512557 | ||||||
chr6:85512621
|
CA | C | 255 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(252): Show | 262 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(259): Show |
intron_variant | MODIFIER | c.2653+1178delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512621 | ||||||
chr6:85512621
|
CAA | C | 7 | a0001c0001t0001g0017a0001c0001t0001g0037a0001c0001t0001g0136others(4): Show | 7 | HG01069.hp1 HG01168.hp2 HG01515.hp2 others(4): Show |
intron_variant | MODIFIER | c.2653+1177_2653+117 others(6): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512621 | ||||||
chr6:85512645
|
G | T | 1 | a0001c0001t0001g0344 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.2653+1155C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512645 | ||||||
chr6:85512660
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2653+1140C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512660 | ||||||
chr6:85512673
|
T | C | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2653+1127A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512673 | ||||||
chr6:85512884
|
T | C | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.2653+916A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85512884 | ||||||
chr6:85513079
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.2653+721G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513079 | ||||||
chr6:85513202
|
C | T | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062 | 3 | HG02451.hp2 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2653+598G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513202 | ||||||
chr6:85513309
|
A | G | 1 | a0001c0001t0001g0221 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.2653+491T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513309 | ||||||
chr6:85513500
|
G | A | 1 | a0001c0001t0001g0161 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.2653+300C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513500 | ||||||
chr6:85513558
|
T | A | 1 | a0001c0001t0001g0137 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2653+242A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513558 | ||||||
chr6:85513574
|
G | GAATGCCC others(21): Show |
1 | a0001c0001t0001g0137 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2653+225_2653+226i others(30): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513574 | ||||||
chr6:85513595
|
G | A | 8 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(5): Show | 8 | HG01884.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2653+205C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513595 | ||||||
chr6:85513598
|
T | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2653+202A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513598 | ||||||
chr6:85513737
|
T | C | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.2653+63A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513737 | ||||||
chr6:85513753
|
C | T | 13 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0036others(10): Show | 15 | HG00735.hp1 HG01106.hp2 HG01255.hp1 others(12): Show |
intron_variant | MODIFIER | c.2653+47G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513753 | ||||||
chr6:85513754
|
G | A | 1 | a0001c0001t0001g0281 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.2653+46C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 26/28 | chr6 | 85513754 | ||||||
chr6:85513914
|
A | G | 1 | a0001c0001t0001g0120 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.2558-19T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 25/28 | chr6 | 85513914 | ||||||
chr6:85514335
|
T | G | 159 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(156): Show | 165 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(162): Show |
intron_variant | MODIFIER | c.2393-101A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 24/28 | chr6 | 85514335 | ||||||
chr6:85514748
|
A | G | 1 | a0001c0003t0002g0051 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.2269-119T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85514748 | ||||||
chr6:85514794
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2269-165G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85514794 | ||||||
chr6:85514796
|
G | A | 4 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0049others(1): Show | 4 | HG02145.hp2 HG02486.hp1 HG02922.hp2 others(1): Show |
intron_variant | MODIFIER | c.2269-167C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85514796 | ||||||
chr6:85515021
|
T | C | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2269-392A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515021 | ||||||
chr6:85515068
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2269-439G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515068 | ||||||
chr6:85515177
|
G | A | 28 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(25): Show | 28 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.2269-548C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515177 | ||||||
chr6:85515216
|
G | A | 4 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 4 | HG02647.hp2 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.2269-587C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515216 | ||||||
chr6:85515234
|
T | G | 1 | a0001c0001t0001g0302 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.2269-605A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515234 | ||||||
chr6:85515250
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2269-621C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515250 | ||||||
chr6:85515262
|
C | CA | 44 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0027others(41): Show | 44 | HG00642.hp1 HG01070.hp1 HG01071.hp1 others(41): Show |
intron_variant | MODIFIER | c.2269-634dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515262 | ||||||
chr6:85515262
|
C | CAA | 32 | a0001c0001t0001g0002a0001c0001t0001g0048a0001c0001t0001g0050others(29): Show | 33 | HG00544.hp2 HG01109.hp1 HG01168.hp2 others(30): Show |
intron_variant | MODIFIER | c.2269-635_2269-634d others(4): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515262 | ||||||
chr6:85515262
|
C | CAAA | 32 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0040others(29): Show | 33 | HG00408.hp2 HG00735.hp2 HG01255.hp2 others(30): Show |
intron_variant | MODIFIER | c.2269-636_2269-634d others(5): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515262 | ||||||
chr6:85515262
|
C | CAAAA | 12 | a0001c0001t0001g0043a0001c0001t0001g0201a0001c0001t0001g0203others(9): Show | 12 | HG00423.hp1 HG01928.hp1 HG02135.hp2 others(9): Show |
intron_variant | MODIFIER | c.2269-637_2269-634d others(6): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515262 | ||||||
chr6:85515262
|
CA | C | 8 | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0045others(5): Show | 8 | HG01975.hp2 HG02109.hp2 HG02615.hp1 others(5): Show |
intron_variant | MODIFIER | c.2269-634delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515262 | ||||||
chr6:85515268
|
A | AC | 8 | a0001c0001t0001g0259a0001c0001t0001g0274a0001c0001t0001g0279others(5): Show | 8 | HG01109.hp2 HG02818.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.2269-640_2269-639i others(3): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515268 | ||||||
chr6:85515273
|
A | AC | 23 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(20): Show | 23 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(20): Show |
intron_variant | MODIFIER | c.2269-645_2269-644i others(3): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515273 | ||||||
chr6:85515273
|
A | C | 8 | a0001c0001t0001g0259a0001c0001t0001g0274a0001c0001t0001g0279others(5): Show | 8 | HG01109.hp2 HG02818.hp1 HG03041.hp1 others(5): Show |
intron_variant | MODIFIER | c.2269-644T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515273 | ||||||
chr6:85515278
|
A | C | 5 | a0001c0001t0001g0272a0001c0003t0002g0033a0001c0003t0002g0034others(2): Show | 5 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.2269-649T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515278 | ||||||
chr6:85515342
|
G | A | 68 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0040others(65): Show | 69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.2269-713C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515342 | ||||||
chr6:85515551
|
G | A | 1 | a0001c0001t0001g0310 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.2269-922C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515551 | ||||||
chr6:85515575
|
T | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0055 | 3 | HG02145.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.2269-946A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515575 | ||||||
chr6:85515897
|
A | G | 1 | a0001c0001t0001g0112 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.2269-1268T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515897 | ||||||
chr6:85515953
|
G | A | 47 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 51 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.2269-1324C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85515953 | ||||||
chr6:85516021
|
T | C | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.2269-1392A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516021 | ||||||
chr6:85516061
|
T | C | 1 | a0001c0001t0001g0031 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.2269-1432A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516061 | ||||||
chr6:85516414
|
T | C | 1 | a0001c0001t0001g0058 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.2268+1342A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516414 | ||||||
chr6:85516508
|
A | C | 1 | a0001c0001t0004g0011 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2268+1248T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516508 | ||||||
chr6:85516584
|
A | G | 1 | a0001c0001t0001g0134 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2268+1172T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516584 | ||||||
chr6:85516585
|
TTATAGGC others(2): Show |
T | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235 | 3 | HG02818.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2268+1162_2268+117 others(13): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516585 | ||||||
chr6:85516630
|
A | ACC | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2268+1125_2268+112 others(6): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516630 | ||||||
chr6:85516632
|
C | CT | 36 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(33): Show | 36 | HG00423.hp1 HG01496.hp1 HG01515.hp2 others(33): Show |
intron_variant | MODIFIER | c.2268+1123dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516632 | ||||||
chr6:85516632
|
C | T | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.2268+1124G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516632 | ||||||
chr6:85516632
|
CTTTT | C | 31 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(28): Show | 31 | HG00423.hp2 HG01070.hp2 HG01109.hp2 others(28): Show |
intron_variant | MODIFIER | c.2268+1120_2268+112 others(8): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516632 | ||||||
chr6:85516632
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2268+1110_2268+112 others(18): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516632 | ||||||
chr6:85516763
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2268+993C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516763 | ||||||
chr6:85516897
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2268+859G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85516897 | ||||||
chr6:85517175
|
A | T | 1 | a0001c0001t0001g0330 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.2268+581T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85517175 | ||||||
chr6:85517265
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2268+491G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85517265 | ||||||
chr6:85517426
|
C | A | 1 | a0001c0001t0001g0068 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.2268+330G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85517426 | ||||||
chr6:85517516
|
A | T | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2268+240T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85517516 | ||||||
chr6:85517725
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.2268+31G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 23/28 | chr6 | 85517725 | ||||||
chr6:85518161
|
A | G | 8 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(5): Show | 8 | HG01884.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2108-113T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85518161 | ||||||
chr6:85518174
|
T | C | 1 | a0001c0001t0001g0211 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.2108-126A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85518174 | ||||||
chr6:85518314
|
A | G | 1 | a0001c0001t0001g0292 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.2108-266T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85518314 | ||||||
chr6:85518391
|
G | A | 187 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(184): Show | 192 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.2108-343C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85518391 | ||||||
chr6:85518442
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2108-394C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85518442 | ||||||
chr6:85518763
|
A | G | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.2108-715T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85518763 | ||||||
chr6:85518787
|
T | C | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062 | 3 | HG02451.hp2 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.2108-739A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85518787 | ||||||
chr6:85518953
|
G | A | 1 | a0001c0001t0001g0095 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2108-905C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85518953 | ||||||
chr6:85519002
|
G | C | 1 | a0001c0001t0001g0095 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.2108-954C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519002 | ||||||
chr6:85519023
|
A | G | 28 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(25): Show | 28 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.2108-975T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519023 | ||||||
chr6:85519123
|
A | G | 1 | a0001c0001t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.2108-1075T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519123 | ||||||
chr6:85519371
|
C | T | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2108-1323G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519371 | ||||||
chr6:85519471
|
T | G | 1 | a0003c0006t0006g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2108-1423A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519471 | ||||||
chr6:85519482
|
G | T | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2108-1434C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519482 | ||||||
chr6:85519491
|
G | A | 47 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 51 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.2108-1443C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519491 | ||||||
chr6:85519502
|
CCTGTAGT others(24): Show |
C | 1 | a0001c0001t0001g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.2108-1485_2108-145 others(35): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519502 | ||||||
chr6:85519561
|
T | C | 2 | a0001c0001t0001g0002a0001c0001t0001g0050 | 3 | HG02895.hp2 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2108-1513A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519561 | ||||||
chr6:85519595
|
G | T | 2 | a0001c0001t0001g0053a0001c0001t0001g0054 | 2 | HG02647.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.2108-1547C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519595 | ||||||
chr6:85519651
|
C | A | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.2108-1603G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519651 | ||||||
chr6:85519712
|
T | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.2108-1664A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519712 | ||||||
chr6:85519794
|
G | A | 32 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.2108-1746C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519794 | ||||||
chr6:85519862
|
C | T | 68 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0040others(65): Show | 69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.2108-1814G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519862 | ||||||
chr6:85519885
|
A | C | 2 | a0001c0001t0001g0239a0001c0004t0001g0243 | 2 | NA18966.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.2108-1837T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519885 | ||||||
chr6:85519889
|
C | CA | 5 | a0001c0001t0001g0015a0001c0001t0001g0198a0001c0001t0001g0199others(2): Show | 5 | HG01358.hp2 HG02896.hp2 HG02970.hp2 others(2): Show |
intron_variant | MODIFIER | c.2108-1842dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519889 | ||||||
chr6:85519933
|
T | C | 8 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(5): Show | 8 | HG01884.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.2108-1885A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519933 | ||||||
chr6:85519962
|
A | G | 15 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0288others(12): Show | 17 | HG00597.hp2 HG00609.hp1 HG01106.hp1 others(14): Show |
intron_variant | MODIFIER | c.2108-1914T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85519962 | ||||||
chr6:85520015
|
C | CAGT | 12 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(9): Show | 12 | HG02647.hp2 HG02886.hp1 HG02965.hp1 others(9): Show |
intron_variant | MODIFIER | c.2108-1970_2108-196 others(7): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85520015 | ||||||
chr6:85520120
|
G | A | 1 | a0001c0001t0001g0236 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.2108-2072C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85520120 | ||||||
chr6:85520211
|
T | A | 1 | a0001c0001t0001g0134 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.2108-2163A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85520211 | ||||||
chr6:85520545
|
A | G | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.2108-2497T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85520545 | ||||||
chr6:85520748
|
C | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0053others(2): Show | 6 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2108-2700G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85520748 | ||||||
chr6:85520808
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2108-2760T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85520808 | ||||||
chr6:85521254
|
G | T | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2108-3206C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85521254 | ||||||
chr6:85521347
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2108-3299C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85521347 | ||||||
chr6:85521444
|
G | A | 1 | a0001c0001t0001g0154 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2108-3396C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85521444 | ||||||
chr6:85521495
|
T | A | 2 | a0001c0001t0001g0046a0001c0001t0001g0055 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.2108-3447A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85521495 | ||||||
chr6:85521561
|
A | G | 1 | a0001c0001t0001g0083 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.2108-3513T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85521561 | ||||||
chr6:85521646
|
A | C | 1 | a0001c0001t0004g0011 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2108-3598T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85521646 | ||||||
chr6:85521782
|
T | C | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0182others(4): Show | 7 | HG02257.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2108-3734A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85521782 | ||||||
chr6:85521800
|
C | A | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.2108-3752G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85521800 | ||||||
chr6:85521897
|
C | T | 5 | a0001c0001t0001g0140a0001c0001t0001g0152a0001c0001t0001g0155others(2): Show | 5 | HG03471.hp1 NA18967.hp1 NA18977.hp1 others(2): Show |
intron_variant | MODIFIER | c.2108-3849G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85521897 | ||||||
chr6:85522003
|
T | A | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.2108-3955A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522003 | ||||||
chr6:85522136
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2107+3990C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522136 | ||||||
chr6:85522369
|
G | A | 1 | a0001c0001t0001g0093 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2107+3757C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522369 | ||||||
chr6:85522401
|
G | A | 1 | a0001c0001t0001g0186 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2107+3725C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522401 | ||||||
chr6:85522515
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0053others(2): Show | 6 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.2107+3611C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522515 | ||||||
chr6:85522645
|
T | A | 1 | a0001c0001t0001g0268 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2107+3481A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522645 | ||||||
chr6:85522714
|
A | G | 3 | a0001c0001t0001g0035a0001c0001t0001g0098a0001c0001t0001g0099 | 3 | HG02280.hp1 HG02922.hp1 NA19043.hp1 |
intron_variant | MODIFIER | c.2107+3412T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522714 | ||||||
chr6:85522825
|
A | G | 32 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.2107+3301T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522825 | ||||||
chr6:85522836
|
A | G | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.2107+3290T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522836 | ||||||
chr6:85522908
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2107+3218A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522908 | ||||||
chr6:85522916
|
C | T | 1 | a0001c0001t0001g0278 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.2107+3210G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522916 | ||||||
chr6:85522940
|
A | G | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2107+3186T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522940 | ||||||
chr6:85522992
|
G | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2107+3134C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85522992 | ||||||
chr6:85523001
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2107+3125C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85523001 | ||||||
chr6:85523100
|
T | C | 1 | a0001c0001t0001g0297 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.2107+3026A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85523100 | ||||||
chr6:85523679
|
T | C | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.2107+2447A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85523679 | ||||||
chr6:85523846
|
G | A | 7 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0293others(4): Show | 9 | NA18944.hp1 NA18952.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.2107+2280C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85523846 | ||||||
chr6:85523949
|
T | C | 4 | a0001c0001t0001g0325a0001c0001t0001g0326a0001c0001t0001g0328others(1): Show | 4 | HG00544.hp2 HG02132.hp1 HG02155.hp2 others(1): Show |
intron_variant | MODIFIER | c.2107+2177A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85523949 | ||||||
chr6:85524071
|
A | C | 71 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0040others(68): Show | 72 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(69): Show |
intron_variant | MODIFIER | c.2107+2055T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524071 | ||||||
chr6:85524117
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.2107+2009C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524117 | ||||||
chr6:85524190
|
A | AAAAG | 9 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(6): Show | 9 | HG02109.hp1 HG02129.hp1 HG02559.hp1 others(6): Show |
intron_variant | MODIFIER | c.2107+1932_2107+193 others(8): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524190 | ||||||
chr6:85524190
|
AAAAGAAA others(1): Show |
A | 4 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.2107+1928_2107+193 others(12): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524190 | ||||||
chr6:85524255
|
T | C | 1 | a0001c0001t0001g0234 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2107+1871A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524255 | ||||||
chr6:85524261
|
C | G | 1 | a0001c0001t0001g0230 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2107+1865G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524261 | ||||||
chr6:85524352
|
A | G | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.2107+1774T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524352 | ||||||
chr6:85524666
|
C | T | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.2107+1460G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524666 | ||||||
chr6:85524698
|
C | A | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.2107+1428G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524698 | ||||||
chr6:85524754
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.2107+1372T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524754 | ||||||
chr6:85524785
|
G | GA | 12 | a0001c0001t0001g0028a0001c0001t0001g0055a0001c0001t0001g0060others(9): Show | 12 | HG00423.hp2 HG02074.hp1 HG02145.hp1 others(9): Show |
intron_variant | MODIFIER | c.2107+1340dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524785 | ||||||
chr6:85524785
|
GA | G | 78 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(75): Show | 79 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(76): Show |
intron_variant | MODIFIER | c.2107+1340delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524785 | ||||||
chr6:85524956
|
T | A | 1 | a0001c0001t0001g0230 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.2107+1170A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85524956 | ||||||
chr6:85525047
|
A | G | 1 | a0001c0001t0001g0247 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.2107+1079T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525047 | ||||||
chr6:85525117
|
C | T | 42 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(39): Show | 42 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.2107+1009G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525117 | ||||||
chr6:85525170
|
A | C | 3 | a0001c0001t0001g0122a0001c0001t0001g0136a0001c0001t0001g0181 | 3 | HG01243.hp2 HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.2107+956T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525170 | ||||||
chr6:85525257
|
C | A | 6 | a0001c0001t0001g0070a0001c0001t0001g0071a0001c0001t0001g0072others(3): Show | 6 | HG01169.hp2 HG01261.hp1 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.2107+869G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525257 | ||||||
chr6:85525286
|
T | C | 1 | a0001c0001t0001g0268 | 1 | NA19079.hp1 | intron_variant | MODIFIER | c.2107+840A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525286 | ||||||
chr6:85525370
|
A | G | 68 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0040others(65): Show | 69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.2107+756T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525370 | ||||||
chr6:85525401
|
A | G | 5 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057others(2): Show | 5 | HG02647.hp2 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.2107+725T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525401 | ||||||
chr6:85525434
|
T | C | 2 | a0001c0001t0001g0327a0001c0001t0001g0337 | 2 | HG06807.hp2 NA20905.hp1 |
intron_variant | MODIFIER | c.2107+692A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525434 | ||||||
chr6:85525663
|
C | T | 1 | a0001c0001t0001g0223 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.2107+463G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525663 | ||||||
chr6:85525693
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.2107+433A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525693 | ||||||
chr6:85525989
|
G | A | 1 | a0001c0001t0001g0244 | 1 | NA19064.hp2 | intron_variant | MODIFIER | c.2107+137C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 21/28 | chr6 | 85525989 | ||||||
chr6:85526284
|
G | T | 1 | a0001c0001t0001g0123 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.1996-47C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85526284 | ||||||
chr6:85526396
|
T | C | 1 | a0001c0001t0001g0227 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1996-159A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85526396 | ||||||
chr6:85526438
|
G | A | 2 | a0001c0001t0001g0195a0001c0001t0001g0200 | 2 | HG03017.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.1996-201C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85526438 | ||||||
chr6:85526470
|
C | A | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 199 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1996-233G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85526470 | ||||||
chr6:85526508
|
C | T | 1 | a0001c0001t0001g0251 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1996-271G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85526508 | ||||||
chr6:85526685
|
G | A | 1 | a0001c0001t0001g0109 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.1996-448C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85526685 | ||||||
chr6:85526793
|
G | C | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1996-556C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85526793 | ||||||
chr6:85526797
|
C | A | 1 | a0001c0001t0001g0235 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.1996-560G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85526797 | ||||||
chr6:85526898
|
G | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1996-661C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85526898 | ||||||
chr6:85527034
|
G | A | 2 | a0001c0001t0001g0017a0001c0001t0001g0018 | 2 | HG01884.hp2 HG02109.hp2 |
intron_variant | MODIFIER | c.1996-797C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527034 | ||||||
chr6:85527395
|
A | G | 2 | a0001c0003t0002g0033a0001c0003t0002g0051 | 2 | HG02818.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1995+867T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527395 | ||||||
chr6:85527397
|
A | AT | 188 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(185): Show | 191 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(188): Show |
intron_variant | MODIFIER | c.1995+864dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527397 | ||||||
chr6:85527398
|
T | TA | 94 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(91): Show | 98 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(95): Show |
intron_variant | MODIFIER | c.1995+863_1995+864i others(3): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527398 | ||||||
chr6:85527399
|
T | A | 1 | a0001c0001t0001g0328 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.1995+863A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527399 | ||||||
chr6:85527400
|
T | A | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1995+862A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527400 | ||||||
chr6:85527477
|
G | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0055 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.1995+785C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527477 | ||||||
chr6:85527556
|
T | C | 8 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(5): Show | 8 | HG01884.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1995+706A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527556 | ||||||
chr6:85527576
|
A | C | 1 | a0003c0006t0006g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1995+686T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527576 | ||||||
chr6:85527638
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1995+624A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527638 | ||||||
chr6:85527652
|
A | C | 5 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(2): Show | 5 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(2): Show |
intron_variant | MODIFIER | c.1995+610T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527652 | ||||||
chr6:85527705
|
A | G | 1 | a0001c0001t0001g0111 | 1 | NA19005.hp1 | intron_variant | MODIFIER | c.1995+557T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527705 | ||||||
chr6:85527962
|
T | C | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1995+300A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85527962 | ||||||
chr6:85528079
|
A | G | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.1995+183T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85528079 | ||||||
chr6:85528081
|
G | A | 3 | a0001c0001t0001g0049a0001c0001t0001g0187a0001c0001t0001g0188 | 3 | HG02559.hp2 HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.1995+181C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85528081 | ||||||
chr6:85528143
|
A | G | 2 | a0001c0001t0001g0037a0001c0001t0001g0038 | 2 | HG01069.hp1 HG01071.hp2 |
intron_variant | MODIFIER | c.1995+119T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 20/28 | chr6 | 85528143 | ||||||
chr6:85528384
|
G | T | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1895-22C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85528384 | ||||||
chr6:85528749
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0053others(1): Show | 5 | HG02647.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1895-387A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85528749 | ||||||
chr6:85528831
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1895-469G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85528831 | ||||||
chr6:85528914
|
TG | T | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1895-553delC | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85528914 | ||||||
chr6:85528947
|
G | A | 1 | a0001c0001t0001g0115 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.1895-585C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85528947 | ||||||
chr6:85528991
|
G | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1895-629C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85528991 | ||||||
chr6:85529053
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1895-691T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85529053 | ||||||
chr6:85529086
|
C | A | 1 | a0001c0001t0001g0204 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.1895-724G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85529086 | ||||||
chr6:85529233
|
C | T | 1 | a0001c0004t0001g0243 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.1895-871G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85529233 | ||||||
chr6:85529568
|
G | C | 1 | a0001c0001t0001g0332 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.1894+624C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85529568 | ||||||
chr6:85529575
|
A | G | 1 | a0003c0006t0006g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1894+617T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85529575 | ||||||
chr6:85530149
|
C | T | 4 | a0001c0003t0002g0033a0001c0003t0002g0034a0001c0003t0002g0051others(1): Show | 4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1894+43G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 19/28 | chr6 | 85530149 | ||||||
chr6:85530290
|
C | T | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0240 | 3 | HG03492.hp1 HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1811-15G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85530290 | ||||||
chr6:85530348
|
T | C | 1 | a0001c0001t0001g0338 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1811-73A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85530348 | ||||||
chr6:85530429
|
G | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1811-154C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85530429 | ||||||
chr6:85530504
|
G | C | 67 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0040others(64): Show | 68 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.1811-229C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85530504 | ||||||
chr6:85530555
|
G | T | 1 | a0001c0001t0001g0070 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.1811-280C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85530555 | ||||||
chr6:85530601
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1811-326G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85530601 | ||||||
chr6:85530644
|
C | CA | 23 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(20): Show | 24 | HG01070.hp1 HG01071.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.1811-370dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85530644 | ||||||
chr6:85530910
|
G | GT | 68 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0040others(65): Show | 69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.1811-636dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85530910 | ||||||
chr6:85531233
|
A | G | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.1811-958T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85531233 | ||||||
chr6:85531460
|
A | G | 1 | a0001c0001t0001g0230 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.1811-1185T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85531460 | ||||||
chr6:85531720
|
A | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01433.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.1811-1445T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85531720 | ||||||
chr6:85531795
|
G | T | 1 | a0001c0001t0001g0084 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1811-1520C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85531795 | ||||||
chr6:85531875
|
A | T | 1 | a0001c0001t0001g0177 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1811-1600T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85531875 | ||||||
chr6:85531883
|
C | T | 1 | a0001c0001t0001g0110 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1811-1608G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85531883 | ||||||
chr6:85532033
|
G | GA | 250 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(247): Show | 257 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(254): Show |
intron_variant | MODIFIER | c.1810+1565dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85532033 | ||||||
chr6:85532117
|
T | C | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1810+1482A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85532117 | ||||||
chr6:85532176
|
T | C | 262 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(259): Show | 268 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(265): Show |
intron_variant | MODIFIER | c.1810+1423A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85532176 | ||||||
chr6:85532300
|
T | A | 1 | a0001c0001t0001g0107 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.1810+1299A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85532300 | ||||||
chr6:85532593
|
A | C | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1810+1006T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85532593 | ||||||
chr6:85532700
|
C | T | 1 | a0001c0001t0001g0347 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1810+899G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85532700 | ||||||
chr6:85532713
|
T | TAATTTGA others(330): Show |
1 | a0001c0001t0001g0240 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.1810+885_1810+886i others(339): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85532713 | ||||||
chr6:85533233
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0053others(1): Show | 5 | HG02647.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1810+366G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85533233 | ||||||
chr6:85533250
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1810+349A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85533250 | ||||||
chr6:85533265
|
T | A | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1810+334A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85533265 | ||||||
chr6:85533345
|
T | C | 3 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1810+254A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85533345 | ||||||
chr6:85533496
|
A | G | 1 | a0001c0001t0001g0200 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1810+103T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 18/28 | chr6 | 85533496 | ||||||
chr6:85533869
|
A | G | 1 | a0001c0001t0001g0157 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1609-69T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85533869 | ||||||
chr6:85534036
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1609-236G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534036 | ||||||
chr6:85534138
|
C | G | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1609-338G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534138 | ||||||
chr6:85534186
|
C | T | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1609-386G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534186 | ||||||
chr6:85534189
|
G | T | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1609-389C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534189 | ||||||
chr6:85534317
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0053others(2): Show | 6 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.1609-517A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534317 | ||||||
chr6:85534469
|
G | A | 1 | a0001c0001t0001g0278 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1609-669C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534469 | ||||||
chr6:85534785
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1609-985A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534785 | ||||||
chr6:85534831
|
G | GT | 145 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(142): Show | 151 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.1609-1032dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534831 | ||||||
chr6:85534831
|
G | GTT | 187 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(184): Show | 192 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(189): Show |
intron_variant | MODIFIER | c.1609-1033_1609-103 others(6): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534831 | ||||||
chr6:85534831
|
G | GTTT | 13 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(10): Show | 13 | HG00741.hp1 HG01496.hp1 HG01884.hp2 others(10): Show |
intron_variant | MODIFIER | c.1609-1034_1609-103 others(7): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534831 | ||||||
chr6:85534849
|
A | T | 3 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251 | 3 | HG02258.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1609-1049T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534849 | ||||||
chr6:85534913
|
T | C | 1 | a0003c0006t0006g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1609-1113A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534913 | ||||||
chr6:85534937
|
A | G | 1 | a0001c0001t0001g0136 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.1609-1137T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85534937 | ||||||
chr6:85535012
|
C | T | 1 | a0001c0001t0001g0318 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.1609-1212G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535012 | ||||||
chr6:85535028
|
C | CT | 32 | a0001c0001t0001g0049a0001c0001t0001g0256a0001c0001t0001g0257others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.1609-1229dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535028 | ||||||
chr6:85535028
|
CT | C | 155 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(152): Show | 160 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(157): Show |
intron_variant | MODIFIER | c.1609-1229delA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535028 | ||||||
chr6:85535031
|
T | C | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1609-1231A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535031 | ||||||
chr6:85535130
|
C | G | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 199 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1609-1330G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535130 | ||||||
chr6:85535252
|
C | A | 1 | a0001c0001t0001g0200 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.1609-1452G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535252 | ||||||
chr6:85535497
|
C | T | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 199 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1608+1295G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535497 | ||||||
chr6:85535500
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.1608+1292G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535500 | ||||||
chr6:85535537
|
G | A | 1 | a0001c0001t0001g0016 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1608+1255C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535537 | ||||||
chr6:85535589
|
A | G | 1 | a0001c0001t0001g0340 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.1608+1203T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535589 | ||||||
chr6:85535604
|
C | CA | 76 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0041others(73): Show | 78 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(75): Show |
intron_variant | MODIFIER | c.1608+1187dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535604 | ||||||
chr6:85535604
|
C | CAA | 6 | a0001c0001t0001g0015a0001c0001t0001g0040a0001c0001t0001g0045others(3): Show | 6 | HG02135.hp2 HG03453.hp1 HG03486.hp2 others(3): Show |
intron_variant | MODIFIER | c.1608+1186_1608+118 others(6): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535604 | ||||||
chr6:85535604
|
CA | C | 169 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(166): Show | 173 | HG00280.hp2 HG00408.hp1 HG00423.hp2 others(170): Show |
intron_variant | MODIFIER | c.1608+1187delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535604 | ||||||
chr6:85535604
|
CAA | C | 26 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0017others(23): Show | 26 | HG00099.hp2 HG01070.hp2 HG01256.hp1 others(23): Show |
intron_variant | MODIFIER | c.1608+1186_1608+118 others(6): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535604 | ||||||
chr6:85535873
|
C | T | 1 | a0001c0007t0001g0348 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1608+919G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535873 | ||||||
chr6:85535908
|
G | A | 1 | a0001c0001t0001g0238 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.1608+884C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535908 | ||||||
chr6:85535999
|
A | C | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1608+793T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85535999 | ||||||
chr6:85536092
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1608+700G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85536092 | ||||||
chr6:85536267
|
T | C | 1 | a0001c0001t0001g0213 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.1608+525A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85536267 | ||||||
chr6:85536287
|
A | G | 1 | a0001c0001t0001g0330 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.1608+505T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85536287 | ||||||
chr6:85536682
|
A | G | 3 | a0001c0001t0001g0122a0001c0001t0001g0136a0001c0001t0001g0181 | 3 | HG01243.hp2 HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.1608+110T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 17/28 | chr6 | 85536682 | ||||||
chr6:85536991
|
C | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1476-67G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85536991 | ||||||
chr6:85536998
|
T | TA | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.1476-75dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85536998 | ||||||
chr6:85537073
|
G | C | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1476-149C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85537073 | ||||||
chr6:85537212
|
A | C | 1 | a0001c0001t0001g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1476-288T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85537212 | ||||||
chr6:85537349
|
G | GA | 7 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057others(4): Show | 7 | HG02257.hp2 HG02615.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.1476-426dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85537349 | ||||||
chr6:85537579
|
A | G | 1 | a0001c0001t0001g0122 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1476-655T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85537579 | ||||||
chr6:85537706
|
T | C | 1 | a0003c0006t0006g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1476-782A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85537706 | ||||||
chr6:85537927
|
G | C | 9 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(6): Show | 9 | HG00741.hp1 HG01256.hp1 HG01258.hp1 others(6): Show |
intron_variant | MODIFIER | c.1475+911C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85537927 | ||||||
chr6:85537934
|
T | G | 1 | a0001c0001t0001g0197 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.1475+904A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85537934 | ||||||
chr6:85537962
|
C | A | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1475+876G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85537962 | ||||||
chr6:85537988
|
T | C | 1 | a0001c0007t0001g0348 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.1475+850A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85537988 | ||||||
chr6:85538041
|
T | C | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 199 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.1475+797A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538041 | ||||||
chr6:85538081
|
T | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.1475+757A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538081 | ||||||
chr6:85538155
|
T | C | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1475+683A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538155 | ||||||
chr6:85538224
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1475+614C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538224 | ||||||
chr6:85538269
|
G | GT | 12 | a0001c0001t0001g0069a0001c0001t0001g0091a0001c0001t0001g0168others(9): Show | 12 | HG00099.hp2 HG01069.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.1475+568dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538269 | ||||||
chr6:85538329
|
A | T | 1 | a0001c0001t0007g0349 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.1475+509T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538329 | ||||||
chr6:85538330
|
C | A | 2 | a0001c0001t0001g0230a0001c0001t0001g0232 | 2 | HG00735.hp2 HG01168.hp2 |
intron_variant | MODIFIER | c.1475+508G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538330 | ||||||
chr6:85538448
|
A | G | 1 | a0001c0001t0001g0074 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.1475+390T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538448 | ||||||
chr6:85538459
|
G | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1475+379C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538459 | ||||||
chr6:85538491
|
A | T | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.1475+347T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538491 | ||||||
chr6:85538582
|
A | G | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.1475+256T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538582 | ||||||
chr6:85538667
|
T | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1475+171A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538667 | ||||||
chr6:85538742
|
T | C | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.1475+96A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 16/28 | chr6 | 85538742 | ||||||
chr6:85539128
|
G | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1449-264C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539128 | ||||||
chr6:85539353
|
G | C | 3 | a0001c0001t0001g0105a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG01975.hp2 HG02004.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.1449-489C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539353 | ||||||
chr6:85539385
|
A | T | 1 | a0001c0001t0001g0169 | 1 | HG01993.hp1 | intron_variant | MODIFIER | c.1449-521T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539385 | ||||||
chr6:85539560
|
A | G | 2 | a0001c0001t0001g0315a0001c0001t0001g0316 | 2 | HG02027.hp1 NA18983.hp2 |
intron_variant | MODIFIER | c.1449-696T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539560 | ||||||
chr6:85539935
|
T | TTTTTA | 24 | a0001c0001t0001g0015a0001c0001t0001g0017a0001c0001t0001g0046others(21): Show | 24 | HG00597.hp2 HG00609.hp1 HG00642.hp2 others(21): Show |
intron_variant | MODIFIER | c.1449-1076_1449-107 others(9): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | ||||||
chr6:85539935
|
T | TTTTTATT others(3): Show |
14 | a0001c0001t0001g0035a0001c0001t0001g0055a0001c0001t0001g0056others(11): Show | 14 | HG02083.hp1 HG02109.hp1 HG02145.hp2 others(11): Show |
intron_variant | MODIFIER | c.1449-1081_1449-107 others(14): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | ||||||
chr6:85539935
|
T | TTTTTATT others(8): Show |
15 | a0001c0001t0001g0045a0001c0001t0001g0049a0001c0001t0001g0053others(12): Show | 15 | HG00609.hp2 HG01081.hp1 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1449-1086_1449-107 others(19): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | ||||||
chr6:85539935
|
T | TTTTTATT others(13): Show |
31 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0014others(28): Show | 33 | HG00099.hp2 HG00280.hp2 HG01070.hp1 others(30): Show |
intron_variant | MODIFIER | c.1449-1091_1449-107 others(24): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | ||||||
chr6:85539935
|
T | TTTTTATT others(18): Show |
72 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0013others(69): Show | 74 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.1449-1096_1449-107 others(29): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | ||||||
chr6:85539935
|
T | TTTTTATT others(23): Show |
17 | a0001c0001t0001g0005a0001c0001t0001g0025a0001c0001t0001g0026others(14): Show | 18 | HG01175.hp1 HG01243.hp1 HG01256.hp1 others(15): Show |
intron_variant | MODIFIER | c.1449-1101_1449-107 others(34): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | ||||||
chr6:85539935
|
T | TTTTTATT others(28): Show |
6 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0132others(3): Show | 7 | HG01516.hp1 HG01517.hp2 HG02040.hp1 others(4): Show |
intron_variant | MODIFIER | c.1449-1106_1449-107 others(39): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | ||||||
chr6:85539935
|
T | TTTTTATT others(33): Show |
1 | a0001c0001t0001g0134 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.1449-1111_1449-107 others(44): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | ||||||
chr6:85539935
|
TTTTTA | T | 5 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(2): Show | 5 | HG01358.hp2 HG02615.hp1 HG02717.hp1 others(2): Show |
intron_variant | MODIFIER | c.1449-1076_1449-107 others(9): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | ||||||
chr6:85539935
|
TTTTTATT others(3): Show |
T | 43 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(40): Show | 43 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.1449-1081_1449-107 others(14): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539935 | ||||||
chr6:85539976
|
T | TTTTATTT others(8): Show |
1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1449-1113_1449-111 others(19): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539976 | ||||||
chr6:85539989
|
G | A | 1 | a0001c0001t0001g0219 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1449-1125C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85539989 | ||||||
chr6:85540116
|
C | T | 1 | a0001c0001t0001g0260 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.1449-1252G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540116 | ||||||
chr6:85540253
|
C | T | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.1449-1389G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540253 | ||||||
chr6:85540254
|
G | A | 1 | a0001c0001t0001g0116 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.1449-1390C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540254 | ||||||
chr6:85540338
|
C | A | 1 | a0001c0001t0001g0331 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1449-1474G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540338 | ||||||
chr6:85540342
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1449-1478C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540342 | ||||||
chr6:85540383
|
G | A | 1 | a0001c0001t0001g0102 | 1 | NA18941.hp2 | intron_variant | MODIFIER | c.1449-1519C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540383 | ||||||
chr6:85540479
|
A | G | 3 | a0001c0001t0001g0313a0001c0001t0003g0301a0001c0001t0003g0314 | 3 | HG00609.hp1 NA18981.hp1 NA19006.hp1 |
intron_variant | MODIFIER | c.1448+1506T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540479 | ||||||
chr6:85540609
|
C | T | 7 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0182others(4): Show | 7 | HG02257.hp2 HG02717.hp2 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.1448+1376G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540609 | ||||||
chr6:85540707
|
G | C | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1448+1278C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540707 | ||||||
chr6:85540712
|
G | A | 32 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.1448+1273C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540712 | ||||||
chr6:85540804
|
T | C | 1 | a0001c0001t0001g0157 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1448+1181A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540804 | ||||||
chr6:85540805
|
C | T | 1 | a0001c0001t0001g0163 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1448+1180G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540805 | ||||||
chr6:85540896
|
T | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0240 | 2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.1448+1089A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540896 | ||||||
chr6:85540996
|
C | CT | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02647.hp2 others(6): Show |
intron_variant | MODIFIER | c.1448+988dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540996 | ||||||
chr6:85540996
|
CT | C | 7 | a0001c0001t0001g0126a0001c0001t0001g0176a0001c0001t0001g0281others(4): Show | 7 | HG01069.hp2 HG01070.hp1 HG02698.hp1 others(4): Show |
intron_variant | MODIFIER | c.1448+988delA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85540996 | ||||||
chr6:85541070
|
T | C | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG00280.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.1448+915A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85541070 | ||||||
chr6:85541405
|
T | C | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.1448+580A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85541405 | ||||||
chr6:85541600
|
G | T | 1 | a0001c0001t0004g0011 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.1448+385C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 15/28 | chr6 | 85541600 | ||||||
chr6:85542445
|
A | G | 3 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251 | 3 | HG02258.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.1390-402T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 14/28 | chr6 | 85542445 | ||||||
chr6:85542488
|
G | A | 1 | a0001c0001t0001g0094 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.1390-445C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 14/28 | chr6 | 85542488 | ||||||
chr6:85542605
|
G | A | 1 | a0001c0001t0001g0117 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1390-562C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 14/28 | chr6 | 85542605 | ||||||
chr6:85542636
|
C | T | 36 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0038others(33): Show | 37 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(34): Show |
intron_variant | MODIFIER | c.1389+546G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 14/28 | chr6 | 85542636 | ||||||
chr6:85542673
|
C | T | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1389+509G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 14/28 | chr6 | 85542673 | ||||||
chr6:85542690
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1389+492C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 14/28 | chr6 | 85542690 | ||||||
chr6:85542732
|
G | A | 2 | a0001c0001t0001g0253a0001c0001t0001g0337 | 2 | HG03453.hp1 HG06807.hp2 |
intron_variant | MODIFIER | c.1389+450C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 14/28 | chr6 | 85542732 | ||||||
chr6:85542956
|
T | C | 68 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0040others(65): Show | 69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.1389+226A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 14/28 | chr6 | 85542956 | ||||||
chr6:85543023
|
C | T | 4 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0053others(1): Show | 5 | HG02647.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1389+159G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 14/28 | chr6 | 85543023 | ||||||
chr6:85543879
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.1109-119G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85543879 | ||||||
chr6:85543883
|
T | C | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1109-123A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85543883 | ||||||
chr6:85544370
|
G | A | 1 | a0001c0001t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.1109-610C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85544370 | ||||||
chr6:85544546
|
C | G | 1 | a0001c0001t0001g0310 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1109-786G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85544546 | ||||||
chr6:85544588
|
C | T | 37 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0038others(34): Show | 38 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.1109-828G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85544588 | ||||||
chr6:85544685
|
C | T | 1 | a0001c0001t0001g0046 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.1109-925G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85544685 | ||||||
chr6:85544744
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1109-984T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85544744 | ||||||
chr6:85544804
|
T | C | 47 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 51 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.1109-1044A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85544804 | ||||||
chr6:85544832
|
T | C | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1109-1072A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85544832 | ||||||
chr6:85544969
|
G | C | 1 | a0001c0001t0001g0338 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1109-1209C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85544969 | ||||||
chr6:85545123
|
C | G | 1 | a0001c0001t0001g0093 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1109-1363G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545123 | ||||||
chr6:85545351
|
A | T | 1 | a0001c0001t0001g0246 | 1 | NA19077.hp2 | intron_variant | MODIFIER | c.1109-1591T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545351 | ||||||
chr6:85545435
|
CAGAT | C | 9 | a0001c0001t0001g0256a0001c0001t0001g0260a0001c0001t0001g0261others(6): Show | 9 | HG00423.hp2 HG00544.hp1 HG02074.hp1 others(6): Show |
intron_variant | MODIFIER | c.1108+1673_1108+167 others(8): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545435 | ||||||
chr6:85545644
|
T | C | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.1108+1468A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545644 | ||||||
chr6:85545769
|
C | T | 2 | a0001c0001t0001g0196a0001c0001t0001g0206 | 2 | HG00408.hp2 HG02129.hp1 |
intron_variant | MODIFIER | c.1108+1343G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545769 | ||||||
chr6:85545831
|
G | A | 1 | a0001c0001t0001g0333 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.1108+1281C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545831 | ||||||
chr6:85545937
|
C | G | 1 | a0001c0001t0001g0297 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1108+1175G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545937 | ||||||
chr6:85545939
|
T | C | 1 | a0001c0001t0001g0297 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1108+1173A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545939 | ||||||
chr6:85545940
|
C | T | 1 | a0001c0001t0001g0297 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.1108+1172G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545940 | ||||||
chr6:85545943
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.1108+1169C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85545943 | ||||||
chr6:85546095
|
A | G | 1 | a0001c0001t0001g0205 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.1108+1017T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546095 | ||||||
chr6:85546181
|
G | A | 8 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(5): Show | 8 | HG01884.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.1108+931C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546181 | ||||||
chr6:85546191
|
A | G | 2 | a0001c0001t0001g0016a0001c0001t0001g0018 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1108+921T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546191 | ||||||
chr6:85546340
|
A | T | 1 | a0001c0001t0001g0045 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1108+772T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546340 | ||||||
chr6:85546502
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.1108+610C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546502 | ||||||
chr6:85546526
|
T | A | 1 | a0001c0001t0001g0193 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1108+586A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546526 | ||||||
chr6:85546689
|
G | A | 2 | a0001c0001t0001g0016a0001c0001t0001g0018 | 2 | HG01884.hp2 HG03195.hp1 |
intron_variant | MODIFIER | c.1108+423C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546689 | ||||||
chr6:85546732
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.1108+380C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546732 | ||||||
chr6:85546753
|
G | A | 1 | a0001c0001t0001g0214 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.1108+359C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546753 | ||||||
chr6:85546965
|
C | CA | 48 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(45): Show | 48 | HG00544.hp1 HG01070.hp2 HG01109.hp2 others(45): Show |
intron_variant | MODIFIER | c.1108+146dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85546965 | ||||||
chr6:85547065
|
T | G | 2 | a0001c0001t0001g0019a0001c0001t0001g0020 | 2 | HG02886.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.1108+47A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 12/28 | chr6 | 85547065 | ||||||
chr6:85547231
|
A | T | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | splice_region_variant&intron_variant | LOW | c.994-5T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 11/28 | chr6 | 85547231 | ||||||
chr6:85547817
|
C | A | 145 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(142): Show | 150 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.868-267G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 9/28 | chr6 | 85547817 | ||||||
chr6:85548072
|
G | A | 3 | a0001c0001t0001g0105a0001c0001t0001g0118a0001c0001t0001g0119 | 3 | HG01975.hp2 HG02004.hp2 HG02148.hp2 |
intron_variant | MODIFIER | c.867+229C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 9/28 | chr6 | 85548072 | ||||||
chr6:85548088
|
G | A | 1 | a0001c0001t0001g0343 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.867+213C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 9/28 | chr6 | 85548088 | ||||||
chr6:85548156
|
A | C | 32 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.867+145T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 9/28 | chr6 | 85548156 | ||||||
chr6:85548787
|
T | A | 6 | a0001c0001t0001g0256a0001c0001t0001g0263a0001c0001t0001g0264others(3): Show | 6 | HG00544.hp1 NA18948.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.792-411A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85548787 | ||||||
chr6:85548839
|
T | C | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.792-463A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85548839 | ||||||
chr6:85548896
|
G | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.792-520C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85548896 | ||||||
chr6:85548982
|
A | C | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0135 | 3 | HG00609.hp2 HG02155.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.792-606T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85548982 | ||||||
chr6:85548988
|
AG | A | 279 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(276): Show | 286 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(283): Show |
intron_variant | MODIFIER | c.792-613delC | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85548988 | ||||||
chr6:85548989
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.792-613C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85548989 | ||||||
chr6:85548993
|
G | A | 10 | a0001c0001t0001g0069a0001c0001t0001g0168a0001c0001t0001g0169others(7): Show | 10 | HG01175.hp1 HG01243.hp1 HG01261.hp1 others(7): Show |
intron_variant | MODIFIER | c.792-617C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85548993 | ||||||
chr6:85549118
|
C | T | 32 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.791+605G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85549118 | ||||||
chr6:85549310
|
T | A | 1 | a0001c0001t0001g0180 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.791+413A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85549310 | ||||||
chr6:85549424
|
A | G | 3 | a0001c0001t0001g0236a0001c0001t0001g0237a0001c0001t0001g0240 | 3 | HG03492.hp1 HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.791+299T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85549424 | ||||||
chr6:85549487
|
A | G | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.791+236T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85549487 | ||||||
chr6:85549595
|
A | T | 4 | a0001c0001t0001g0198a0001c0001t0001g0199a0001c0001t0001g0217others(1): Show | 4 | HG01358.hp2 HG02896.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.791+128T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85549595 | ||||||
chr6:85549627
|
A | G | 1 | a0001c0001t0001g0231 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.791+96T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 8/28 | chr6 | 85549627 | ||||||
chr6:85550067
|
C | A | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.635-188G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85550067 | ||||||
chr6:85550438
|
A | C | 2 | a0001c0001t0001g0274a0001c0001t0001g0279 | 2 | HG01109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.635-559T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85550438 | ||||||
chr6:85550644
|
G | A | 1 | a0001c0001t0001g0291 | 1 | NA18984.hp2 | intron_variant | MODIFIER | c.635-765C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85550644 | ||||||
chr6:85550788
|
C | CT | 10 | a0001c0001t0001g0256a0001c0001t0001g0260a0001c0001t0001g0263others(7): Show | 10 | HG00609.hp1 HG02074.hp1 NA18946.hp1 others(7): Show |
intron_variant | MODIFIER | c.635-910dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85550788 | ||||||
chr6:85551038
|
C | T | 32 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.635-1159G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85551038 | ||||||
chr6:85551103
|
G | T | 6 | a0001c0001t0001g0256a0001c0001t0001g0263a0001c0001t0001g0264others(3): Show | 6 | HG00544.hp1 NA18948.hp1 NA18961.hp1 others(3): Show |
intron_variant | MODIFIER | c.635-1224C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85551103 | ||||||
chr6:85551172
|
T | A | 1 | a0001c0001t0001g0335 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.635-1293A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85551172 | ||||||
chr6:85551414
|
C | A | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.635-1535G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85551414 | ||||||
chr6:85551513
|
T | C | 3 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0178 | 3 | HG01175.hp1 HG01516.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.635-1634A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85551513 | ||||||
chr6:85551563
|
T | C | 1 | a0001c0001t0001g0036 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.635-1684A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85551563 | ||||||
chr6:85551668
|
C | T | 68 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0040others(65): Show | 69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.635-1789G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85551668 | ||||||
chr6:85551924
|
T | C | 1 | a0001c0001t0001g0014 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.635-2045A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85551924 | ||||||
chr6:85551949
|
A | G | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.635-2070T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85551949 | ||||||
chr6:85552031
|
T | G | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01433.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.635-2152A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552031 | ||||||
chr6:85552032
|
C | CT | 100 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0016others(97): Show | 101 | HG00408.hp2 HG00597.hp1 HG00642.hp1 others(98): Show |
intron_variant | MODIFIER | c.635-2154dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552032 | ||||||
chr6:85552032
|
C | CTT | 9 | a0001c0001t0001g0141a0001c0001t0001g0143a0001c0001t0001g0144others(6): Show | 9 | HG00423.hp1 HG02027.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.635-2155_635-2154d others(4): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552032 | ||||||
chr6:85552032
|
CT | C | 15 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0045others(12): Show | 17 | HG00099.hp2 HG00735.hp1 HG01069.hp2 others(14): Show |
intron_variant | MODIFIER | c.635-2154delA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552032 | ||||||
chr6:85552119
|
C | T | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG01928.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.635-2240G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552119 | ||||||
chr6:85552152
|
T | C | 3 | a0001c0001t0001g0260a0001c0001t0001g0261a0001c0001t0001g0262 | 3 | HG00423.hp2 HG02074.hp1 NA18965.hp1 |
intron_variant | MODIFIER | c.635-2273A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552152 | ||||||
chr6:85552194
|
A | G | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 356 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(353): Show |
intron_variant | MODIFIER | c.635-2315T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552194 | ||||||
chr6:85552288
|
G | A | 5 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(2): Show | 5 | HG01256.hp1 HG01258.hp1 HG02055.hp2 others(2): Show |
intron_variant | MODIFIER | c.635-2409C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552288 | ||||||
chr6:85552534
|
A | C | 2 | a0001c0001t0001g0311a0001c0001t0001g0312 | 2 | NA18946.hp1 NA19068.hp2 |
intron_variant | MODIFIER | c.635-2655T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552534 | ||||||
chr6:85552591
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0053others(2): Show | 6 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.635-2712A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85552591 | ||||||
chr6:85553009
|
A | G | 68 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0040others(65): Show | 69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.635-3130T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553009 | ||||||
chr6:85553090
|
G | T | 1 | a0001c0001t0001g0070 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.635-3211C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553090 | ||||||
chr6:85553491
|
A | C | 1 | a0001c0001t0001g0231 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.635-3612T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553491 | ||||||
chr6:85553587
|
A | G | 3 | a0001c0001t0001g0122a0001c0001t0001g0136a0001c0001t0001g0181 | 3 | HG01243.hp2 HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.635-3708T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553587 | ||||||
chr6:85553593
|
G | C | 1 | a0001c0001t0001g0289 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.635-3714C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553593 | ||||||
chr6:85553647
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.635-3768C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553647 | ||||||
chr6:85553786
|
C | CA | 158 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(155): Show | 163 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.635-3908dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553786 | ||||||
chr6:85553830
|
T | C | 1 | a0001c0001t0001g0097 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.635-3951A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553830 | ||||||
chr6:85553837
|
T | C | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.635-3958A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553837 | ||||||
chr6:85553911
|
C | G | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.635-4032G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553911 | ||||||
chr6:85553918
|
T | C | 1 | a0001c0001t0001g0260 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.635-4039A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85553918 | ||||||
chr6:85554050
|
G | C | 1 | a0001c0001t0001g0120 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.634+3926C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85554050 | ||||||
chr6:85554210
|
T | C | 2 | a0001c0001t0001g0043a0001c0001t0001g0044 | 2 | HG01928.hp1 HG01975.hp1 |
intron_variant | MODIFIER | c.634+3766A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85554210 | ||||||
chr6:85554222
|
T | TTA | 11 | a0001c0001t0001g0083a0001c0001t0001g0180a0001c0001t0001g0224others(8): Show | 11 | HG01256.hp2 HG01884.hp1 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.634+3752_634+3753d others(4): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85554222 | ||||||
chr6:85554297
|
T | TACACACA others(15): Show |
7 | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0293others(4): Show | 9 | NA18944.hp1 NA18952.hp1 NA18968.hp1 others(6): Show |
intron_variant | MODIFIER | c.634+3657_634+3678d others(24): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85554297 | ||||||
chr6:85554367
|
C | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01433.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.634+3609G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85554367 | ||||||
chr6:85554656
|
T | G | 194 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(191): Show | 199 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(196): Show |
intron_variant | MODIFIER | c.634+3320A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85554656 | ||||||
chr6:85554683
|
T | G | 1 | a0001c0001t0001g0139 | 1 | HG01515.hp2 | intron_variant | MODIFIER | c.634+3293A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85554683 | ||||||
chr6:85554964
|
GCACATGC others(3): Show |
G | 1 | a0001c0001t0001g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.634+3002_634+3011d others(12): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85554964 | ||||||
chr6:85555335
|
T | C | 2 | a0001c0001t0001g0182a0001c0001t0001g0185 | 2 | HG02257.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.634+2641A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85555335 | ||||||
chr6:85555367
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.634+2609C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85555367 | ||||||
chr6:85555484
|
G | A | 1 | a0001c0001t0001g0216 | 1 | NA18990.hp2 | intron_variant | MODIFIER | c.634+2492C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85555484 | ||||||
chr6:85555646
|
T | C | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.634+2330A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85555646 | ||||||
chr6:85555755
|
C | A | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.634+2221G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85555755 | ||||||
chr6:85555994
|
A | AT | 3 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0055 | 3 | HG02145.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.634+1981dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85555994 | ||||||
chr6:85556114
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.634+1862C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85556114 | ||||||
chr6:85556227
|
G | A | 2 | a0001c0001t0001g0217a0001c0001t0001g0218 | 2 | HG02970.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.634+1749C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85556227 | ||||||
chr6:85556310
|
T | C | 2 | a0001c0001t0001g0274a0001c0001t0001g0279 | 2 | HG01109.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.634+1666A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85556310 | ||||||
chr6:85556410
|
A | T | 1 | a0001c0003t0002g0033 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.634+1566T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85556410 | ||||||
chr6:85556411
|
A | T | 31 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(28): Show | 31 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(28): Show |
intron_variant | MODIFIER | c.634+1565T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85556411 | ||||||
chr6:85556415
|
G | T | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.634+1561C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85556415 | ||||||
chr6:85556472
|
C | CT | 240 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(237): Show | 247 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(244): Show |
intron_variant | MODIFIER | c.634+1503dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85556472 | ||||||
chr6:85556764
|
T | G | 32 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.634+1212A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85556764 | ||||||
chr6:85556933
|
C | T | 42 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(39): Show | 42 | HG00099.hp2 HG00280.hp2 HG00642.hp2 others(39): Show |
intron_variant | MODIFIER | c.634+1043G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85556933 | ||||||
chr6:85557216
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0053others(1): Show | 5 | HG02647.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.634+760C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85557216 | ||||||
chr6:85557396
|
G | A | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.634+580C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85557396 | ||||||
chr6:85557409
|
T | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01433.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.634+567A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85557409 | ||||||
chr6:85557661
|
C | T | 1 | a0001c0001t0001g0264 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.634+315G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85557661 | ||||||
chr6:85557691
|
A | T | 1 | a0001c0001t0001g0309 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.634+285T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 7/28 | chr6 | 85557691 | ||||||
chr6:85558072
|
C | T | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.550-12G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558072 | ||||||
chr6:85558302
|
A | G | 1 | a0001c0001t0001g0280 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.550-242T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558302 | ||||||
chr6:85558325
|
G | T | 1 | a0001c0001t0001g0266 | 1 | NA18990.hp1 | intron_variant | MODIFIER | c.550-265C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558325 | ||||||
chr6:85558408
|
A | G | 4 | a0001c0003t0002g0033a0001c0003t0002g0034a0001c0003t0002g0051others(1): Show | 4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.550-348T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558408 | ||||||
chr6:85558430
|
C | A | 1 | a0001c0001t0001g0219 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.550-370G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558430 | ||||||
chr6:85558535
|
C | T | 1 | a0001c0001t0001g0258 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.550-475G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558535 | ||||||
chr6:85558555
|
G | A | 10 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(7): Show | 11 | HG00609.hp2 HG02040.hp1 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.550-495C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558555 | ||||||
chr6:85558588
|
G | T | 2 | a0001c0001t0001g0002a0001c0001t0001g0050 | 3 | HG02895.hp2 HG02965.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.550-528C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558588 | ||||||
chr6:85558606
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.550-546G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558606 | ||||||
chr6:85558618
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.550-558G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558618 | ||||||
chr6:85558653
|
G | A | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.550-593C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558653 | ||||||
chr6:85558936
|
GA | G | 281 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(278): Show | 288 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(285): Show |
intron_variant | MODIFIER | c.550-877delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85558936 | ||||||
chr6:85559008
|
G | A | 10 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.550-948C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85559008 | ||||||
chr6:85559321
|
C | T | 47 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(44): Show | 51 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(48): Show |
intron_variant | MODIFIER | c.550-1261G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85559321 | ||||||
chr6:85559374
|
A | G | 2 | a0001c0001t0001g0237a0001c0001t0001g0240 | 2 | HG03704.hp2 HG03942.hp1 |
intron_variant | MODIFIER | c.550-1314T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85559374 | ||||||
chr6:85559413
|
A | T | 2 | a0001c0001t0001g0141a0001c0001t0001g0142 | 2 | HG00597.hp1 HG02027.hp2 |
intron_variant | MODIFIER | c.550-1353T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85559413 | ||||||
chr6:85559437
|
T | C | 1 | a0001c0001t0001g0220 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.550-1377A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85559437 | ||||||
chr6:85559475
|
A | G | 1 | a0001c0001t0001g0087 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.550-1415T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85559475 | ||||||
chr6:85559654
|
T | A | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.550-1594A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85559654 | ||||||
chr6:85559694
|
G | A | 1 | a0001c0001t0001g0344 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.550-1634C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85559694 | ||||||
chr6:85559913
|
G | A | 1 | a0001c0001t0001g0134 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.550-1853C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85559913 | ||||||
chr6:85560201
|
T | C | 1 | a0001c0001t0001g0200 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.550-2141A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85560201 | ||||||
chr6:85560494
|
G | A | 11 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(8): Show | 11 | HG00099.hp2 HG01069.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.550-2434C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85560494 | ||||||
chr6:85560803
|
G | A | 5 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0049others(2): Show | 5 | HG02145.hp2 HG02486.hp1 HG02559.hp1 others(2): Show |
intron_variant | MODIFIER | c.550-2743C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85560803 | ||||||
chr6:85560818
|
G | C | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.550-2758C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85560818 | ||||||
chr6:85561033
|
TA | T | 7 | a0001c0001t0001g0016a0001c0001t0001g0240a0001c0001t0001g0254others(4): Show | 7 | HG02523.hp1 HG02895.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.550-2974delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85561033 | ||||||
chr6:85561052
|
G | C | 1 | a0001c0001t0001g0073 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.550-2992C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85561052 | ||||||
chr6:85561240
|
C | T | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.550-3180G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85561240 | ||||||
chr6:85561471
|
A | G | 3 | a0001c0001t0001g0104a0001c0001t0001g0121a0001c0001t0001g0126 | 3 | HG01070.hp1 HG01071.hp1 HG03669.hp2 |
intron_variant | MODIFIER | c.550-3411T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85561471 | ||||||
chr6:85561472
|
A | C | 2 | a0001c0001t0001g0092a0001c0001t0001g0255 | 2 | NA19006.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.550-3412T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85561472 | ||||||
chr6:85561711
|
G | A | 3 | a0001c0001t0001g0067a0001c0001t0001g0085a0001c0001t0001g0086 | 3 | NA18959.hp2 NA18971.hp1 NA19007.hp2 |
intron_variant | MODIFIER | c.549+3621C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85561711 | ||||||
chr6:85561808
|
T | G | 72 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0015others(69): Show | 74 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(71): Show |
intron_variant | MODIFIER | c.549+3524A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85561808 | ||||||
chr6:85561818
|
CTTTTTTG | C | 8 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0100others(5): Show | 8 | HG02257.hp2 HG02717.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.549+3507_549+3513d others(9): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85561818 | ||||||
chr6:85561825
|
G | GT | 13 | a0001c0001t0001g0028a0001c0001t0001g0045a0001c0001t0001g0049others(10): Show | 13 | HG01109.hp2 HG01243.hp1 HG01358.hp1 others(10): Show |
intron_variant | MODIFIER | c.549+3506dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85561825 | ||||||
chr6:85562103
|
G | A | 26 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(23): Show | 26 | HG00423.hp2 HG01070.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.549+3229C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562103 | ||||||
chr6:85562118
|
T | A | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.549+3214A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562118 | ||||||
chr6:85562193
|
G | A | 7 | a0001c0001t0001g0239a0001c0001t0001g0241a0001c0001t0001g0242others(4): Show | 7 | NA18952.hp2 NA18966.hp1 NA19055.hp2 others(4): Show |
intron_variant | MODIFIER | c.549+3139C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562193 | ||||||
chr6:85562454
|
G | A | 5 | a0001c0001t0001g0094a0001c0001t0001g0182a0001c0001t0001g0184others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG02809.hp1 others(2): Show |
intron_variant | MODIFIER | c.549+2878C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562454 | ||||||
chr6:85562582
|
C | CT | 193 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0008others(190): Show | 196 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(193): Show |
intron_variant | MODIFIER | c.549+2749dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562582 | ||||||
chr6:85562582
|
C | CTT | 29 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0020others(26): Show | 29 | HG00642.hp2 HG01243.hp1 HG01884.hp2 others(26): Show |
intron_variant | MODIFIER | c.549+2748_549+2749d others(4): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562582 | ||||||
chr6:85562582
|
CTTT | C | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG01168.hp2 HG02109.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.549+2747_549+2749d others(5): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562582 | ||||||
chr6:85562582
|
CTTTTTTT | C | 44 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(41): Show | 48 | HG00609.hp2 HG00735.hp1 HG01070.hp1 others(45): Show |
intron_variant | MODIFIER | c.549+2743_549+2749d others(9): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562582 | ||||||
chr6:85562606
|
A | C | 5 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057others(2): Show | 5 | HG02647.hp2 HG03130.hp2 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.549+2726T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562606 | ||||||
chr6:85562658
|
C | T | 26 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0259others(23): Show | 26 | HG00423.hp2 HG01070.hp2 HG01109.hp2 others(23): Show |
intron_variant | MODIFIER | c.549+2674G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562658 | ||||||
chr6:85562755
|
A | G | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.549+2577T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562755 | ||||||
chr6:85562857
|
T | C | 1 | a0001c0003t0002g0051 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.549+2475A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562857 | ||||||
chr6:85562920
|
C | T | 2 | a0001c0001t0001g0025a0001c0001t0001g0026 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.549+2412G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85562920 | ||||||
chr6:85563297
|
A | G | 1 | a0003c0006t0006g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.549+2035T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85563297 | ||||||
chr6:85563541
|
G | A | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.549+1791C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85563541 | ||||||
chr6:85563626
|
C | T | 1 | a0001c0001t0001g0226 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.549+1706G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85563626 | ||||||
chr6:85563627
|
G | T | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.549+1705C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85563627 | ||||||
chr6:85563682
|
C | A | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.549+1650G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85563682 | ||||||
chr6:85563684
|
C | T | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.549+1648G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85563684 | ||||||
chr6:85563920
|
C | A | 4 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0191others(1): Show | 4 | HG02109.hp1 HG02630.hp1 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.549+1412G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85563920 | ||||||
chr6:85564039
|
A | G | 282 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(279): Show | 289 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(286): Show |
intron_variant | MODIFIER | c.549+1293T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564039 | ||||||
chr6:85564341
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.549+991G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564341 | ||||||
chr6:85564614
|
G | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0055 | 3 | HG02145.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.549+718C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564614 | ||||||
chr6:85564737
|
C | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.549+595G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564737 | ||||||
chr6:85564807
|
G | A | 78 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0015others(75): Show | 80 | HG00408.hp2 HG00423.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.549+525C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564807 | ||||||
chr6:85564849
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.549+483G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564849 | ||||||
chr6:85564921
|
G | A | 1 | a0001c0001t0001g0222 | 1 | NA19076.hp1 | intron_variant | MODIFIER | c.549+411C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564921 | ||||||
chr6:85564947
|
C | T | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.549+385G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564947 | ||||||
chr6:85564951
|
T | C | 2 | a0001c0003t0002g0034a0001c0003t0002g0052 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.549+381A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564951 | ||||||
chr6:85564987
|
T | TA | 16 | a0001c0001t0001g0191a0001c0001t0001g0257a0001c0001t0001g0258others(13): Show | 16 | HG00423.hp2 HG01109.hp2 HG01891.hp2 others(13): Show |
intron_variant | MODIFIER | c.549+344dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85564987 | ||||||
chr6:85565063
|
G | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.549+269C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85565063 | ||||||
chr6:85565111
|
T | TAACA | 195 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(192): Show | 200 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(197): Show |
intron_variant | MODIFIER | c.549+220_549+221ins others(4): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 6/28 | chr6 | 85565111 | ||||||
chr6:85565663
|
A | T | 1 | a0001c0001t0001g0048 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.462-244T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85565663 | ||||||
chr6:85565762
|
C | G | 1 | a0001c0001t0001g0269 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.462-343G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85565762 | ||||||
chr6:85565771
|
T | G | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.462-352A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85565771 | ||||||
chr6:85566031
|
T | C | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.462-612A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566031 | ||||||
chr6:85566178
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.462-759C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566178 | ||||||
chr6:85566239
|
C | G | 1 | a0001c0001t0001g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.462-820G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566239 | ||||||
chr6:85566298
|
C | G | 1 | a0001c0001t0001g0228 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.462-879G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566298 | ||||||
chr6:85566448
|
A | G | 4 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0053others(1): Show | 5 | HG02647.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.462-1029T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566448 | ||||||
chr6:85566570
|
C | T | 32 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.461+964G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566570 | ||||||
chr6:85566653
|
G | A | 21 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(18): Show | 21 | HG00735.hp2 HG01168.hp2 HG02818.hp2 others(18): Show |
intron_variant | MODIFIER | c.461+881C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566653 | ||||||
chr6:85566729
|
A | G | 1 | a0001c0001t0001g0236 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.461+805T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566729 | ||||||
chr6:85566748
|
T | A | 2 | a0001c0001t0001g0074a0001c0001t0001g0075 | 2 | HG03688.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.461+786A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566748 | ||||||
chr6:85566748
|
T | C | 4 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0053others(1): Show | 5 | HG02647.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.461+786A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566748 | ||||||
chr6:85566916
|
T | C | 1 | a0001c0001t0001g0135 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.461+618A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566916 | ||||||
chr6:85566950
|
G | A | 1 | a0001c0001t0001g0087 | 1 | NA18975.hp1 | intron_variant | MODIFIER | c.461+584C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566950 | ||||||
chr6:85566986
|
A | G | 28 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(25): Show | 28 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.461+548T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85566986 | ||||||
chr6:85567123
|
C | T | 28 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(25): Show | 28 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.461+411G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85567123 | ||||||
chr6:85567135
|
A | G | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG00280.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.461+399T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85567135 | ||||||
chr6:85567351
|
CA | C | 67 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0040others(64): Show | 68 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(65): Show |
intron_variant | MODIFIER | c.461+182delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85567351 | ||||||
chr6:85567402
|
T | C | 3 | a0001c0001t0001g0233a0001c0001t0001g0234a0001c0001t0001g0235 | 3 | HG02818.hp2 HG03098.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.461+132A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85567402 | ||||||
chr6:85567437
|
A | G | 2 | a0002c0002t0001g0298a0002c0002t0001g0305 | 2 | HG01168.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.461+97T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 5/28 | chr6 | 85567437 | ||||||
chr6:85567654
|
T | C | 1 | a0003c0006t0006g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.418-77A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85567654 | ||||||
chr6:85567679
|
A | G | 1 | a0001c0001t0001g0182 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.418-102T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85567679 | ||||||
chr6:85567704
|
G | A | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.418-127C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85567704 | ||||||
chr6:85567874
|
T | C | 1 | a0001c0001t0001g0057 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.418-297A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85567874 | ||||||
chr6:85567900
|
T | C | 2 | a0001c0001t0001g0121a0001c0001t0001g0126 | 2 | HG01070.hp1 HG01071.hp1 |
intron_variant | MODIFIER | c.418-323A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85567900 | ||||||
chr6:85567957
|
T | C | 7 | a0001c0001t0001g0037a0001c0001t0001g0038a0001c0001t0001g0138others(4): Show | 7 | HG01069.hp1 HG01071.hp2 HG01081.hp2 others(4): Show |
intron_variant | MODIFIER | c.418-380A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85567957 | ||||||
chr6:85568102
|
A | AAAAATTC others(7): Show |
9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.418-539_418-526dup others(14): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568102 | ||||||
chr6:85568225
|
C | T | 1 | a0001c0001t0001g0100 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.418-648G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568225 | ||||||
chr6:85568464
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.418-887C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568464 | ||||||
chr6:85568548
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.418-971G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568548 | ||||||
chr6:85568575
|
A | G | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.418-998T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568575 | ||||||
chr6:85568585
|
C | T | 1 | a0001c0001t0001g0304 | 1 | NA19065.hp2 | intron_variant | MODIFIER | c.418-1008G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568585 | ||||||
chr6:85568586
|
G | A | 1 | a0001c0001t0001g0269 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.418-1009C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568586 | ||||||
chr6:85568698
|
A | G | 1 | a0001c0001t0001g0245 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.418-1121T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568698 | ||||||
chr6:85568729
|
T | C | 1 | a0001c0001t0001g0186 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.418-1152A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568729 | ||||||
chr6:85568973
|
T | C | 199 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(196): Show | 204 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.418-1396A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568973 | ||||||
chr6:85568974
|
T | C | 1 | a0001c0001t0001g0076 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.418-1397A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85568974 | ||||||
chr6:85569006
|
C | T | 1 | a0001c0001t0001g0227 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.418-1429G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85569006 | ||||||
chr6:85569037
|
C | T | 1 | a0001c0001t0001g0127 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.418-1460G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85569037 | ||||||
chr6:85569103
|
T | C | 3 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251 | 3 | HG02258.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.418-1526A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85569103 | ||||||
chr6:85569408
|
C | T | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.418-1831G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85569408 | ||||||
chr6:85569409
|
A | T | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.418-1832T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85569409 | ||||||
chr6:85569523
|
G | A | 2 | a0001c0003t0002g0034a0001c0003t0002g0052 | 2 | HG03041.hp1 HG03453.hp2 |
intron_variant | MODIFIER | c.418-1946C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85569523 | ||||||
chr6:85569699
|
T | C | 3 | a0001c0001t0001g0122a0001c0001t0001g0136a0001c0001t0001g0181 | 3 | HG01243.hp2 HG02257.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.418-2122A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85569699 | ||||||
chr6:85569755
|
C | T | 2 | a0001c0001t0001g0165a0001c0001t0001g0166 | 2 | HG00280.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.418-2178G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85569755 | ||||||
chr6:85569786
|
T | C | 1 | a0001c0001t0001g0292 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.418-2209A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85569786 | ||||||
chr6:85570019
|
C | T | 122 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(119): Show | 126 | HG00099.hp2 HG00280.hp2 HG00609.hp2 others(123): Show |
intron_variant | MODIFIER | c.417+2118G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570019 | ||||||
chr6:85570333
|
TG | T | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 206 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.417+1803delC | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570333 | ||||||
chr6:85570416
|
T | C | 1 | a0001c0001t0001g0245 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.417+1721A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570416 | ||||||
chr6:85570537
|
T | C | 1 | a0001c0001t0001g0088 | 1 | NA18973.hp1 | intron_variant | MODIFIER | c.417+1600A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570537 | ||||||
chr6:85570580
|
C | T | 3 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.417+1557G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570580 | ||||||
chr6:85570597
|
A | AT | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.417+1539dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570597 | ||||||
chr6:85570604
|
C | A | 1 | a0001c0001t0001g0259 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.417+1533G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570604 | ||||||
chr6:85570621
|
G | A | 1 | a0001c0001t0001g0187 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.417+1516C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570621 | ||||||
chr6:85570668
|
T | C | 2 | a0001c0001t0001g0123a0001c0001t0001g0124 | 2 | HG01433.hp2 HG02293.hp2 |
intron_variant | MODIFIER | c.417+1469A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570668 | ||||||
chr6:85570670
|
T | C | 2 | a0001c0001t0001g0224a0001c0001t0001g0225 | 2 | HG01884.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.417+1467A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570670 | ||||||
chr6:85570675
|
A | C | 1 | a0001c0001t0001g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.417+1462T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85570675 | ||||||
chr6:85571091
|
G | A | 3 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0055 | 3 | HG02145.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.417+1046C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571091 | ||||||
chr6:85571157
|
G | A | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 206 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.417+980C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571157 | ||||||
chr6:85571211
|
T | C | 1 | a0001c0001t0001g0125 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.417+926A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571211 | ||||||
chr6:85571216
|
C | T | 11 | a0001c0001t0001g0068a0001c0001t0001g0069a0001c0001t0001g0070others(8): Show | 11 | HG00642.hp2 HG01169.hp2 HG01261.hp2 others(8): Show |
intron_variant | MODIFIER | c.417+921G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571216 | ||||||
chr6:85571220
|
C | A | 1 | a0001c0001t0001g0044 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.417+917G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571220 | ||||||
chr6:85571232
|
C | T | 1 | a0001c0001t0001g0067 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.417+905G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571232 | ||||||
chr6:85571359
|
C | CA | 10 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0053others(7): Show | 11 | HG00544.hp1 HG02040.hp2 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.417+777dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571359 | ||||||
chr6:85571536
|
G | A | 1 | a0001c0001t0001g0226 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.417+601C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571536 | ||||||
chr6:85571742
|
C | T | 4 | a0001c0003t0002g0033a0001c0003t0002g0034a0001c0003t0002g0051others(1): Show | 4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.417+395G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571742 | ||||||
chr6:85571819
|
C | A | 1 | a0001c0001t0001g0270 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.417+318G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571819 | ||||||
chr6:85571864
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0053others(1): Show | 5 | HG02647.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.417+273C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85571864 | ||||||
chr6:85572058
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.417+79A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 4/28 | chr6 | 85572058 | ||||||
chr6:85572262
|
T | C | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.338+36A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 3/28 | chr6 | 85572262 | ||||||
chr6:85572542
|
A | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.262-168T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85572542 | ||||||
chr6:85572560
|
A | AAAATACC | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.262-193_262-187dup others(7): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85572560 | ||||||
chr6:85572725
|
G | A | 1 | a0001c0001t0001g0271 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.262-351C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85572725 | ||||||
chr6:85572740
|
T | A | 8 | a0001c0001t0001g0016a0001c0001t0001g0018a0001c0001t0001g0019others(5): Show | 8 | HG01884.hp2 HG02886.hp1 HG02965.hp1 others(5): Show |
intron_variant | MODIFIER | c.262-366A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85572740 | ||||||
chr6:85572865
|
G | A | 1 | a0001c0001t0001g0058 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.262-491C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85572865 | ||||||
chr6:85573060
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.262-686C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85573060 | ||||||
chr6:85573348
|
C | A | 1 | a0001c0001t0001g0055 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.261+910G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85573348 | ||||||
chr6:85573372
|
T | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0088 | 2 | NA18973.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.261+886A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85573372 | ||||||
chr6:85573798
|
A | G | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.261+460T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85573798 | ||||||
chr6:85573857
|
G | C | 201 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(198): Show | 206 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.261+401C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85573857 | ||||||
chr6:85574059
|
TATA | T | 151 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(148): Show | 156 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(153): Show |
intron_variant | MODIFIER | c.261+196_261+198del others(3): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85574059 | ||||||
chr6:85574080
|
T | C | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.261+178A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85574080 | ||||||
chr6:85574100
|
G | A | 3 | a0001c0001t0001g0227a0001c0001t0001g0247a0001c0001t0001g0248 | 3 | HG01109.hp1 HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.261+158C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85574100 | ||||||
chr6:85574119
|
C | A | 1 | a0001c0001t0001g0160 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.261+139G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85574119 | ||||||
chr6:85574119
|
C | CA | 241 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(238): Show | 249 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(246): Show |
intron_variant | MODIFIER | c.261+138dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85574119 | ||||||
chr6:85574119
|
C | CAA | 18 | a0001c0001t0001g0006a0001c0001t0001g0127a0001c0001t0001g0128others(15): Show | 19 | HG00609.hp2 HG02040.hp1 HG02080.hp2 others(16): Show |
intron_variant | MODIFIER | c.261+137_261+138dup others(2): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85574119 | ||||||
chr6:85574123
|
A | C | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.261+135T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85574123 | ||||||
chr6:85574131
|
AGAG | A | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.261+124_261+126del others(3): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 2/28 | chr6 | 85574131 | ||||||
chr6:85574383
|
AAAAT | A | 3 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0028 | 3 | HG01258.hp1 HG02055.hp2 HG02145.hp1 |
splice_region_variant&intron_variant | LOW | c.141-9_141-6delATTT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574383 | ||||||
chr6:85574437
|
C | T | 7 | a0001c0001t0001g0015a0001c0001t0001g0187a0001c0001t0001g0188others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-59G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574437 | ||||||
chr6:85574506
|
GATTA | G | 6 | a0001c0001t0001g0035a0001c0001t0001g0095a0001c0001t0001g0096others(3): Show | 6 | HG02280.hp1 HG02615.hp1 HG02809.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-132_141-129del others(4): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574506 | ||||||
chr6:85574583
|
A | C | 2 | a0001c0001t0001g0101a0001c0001t0001g0102 | 2 | NA18941.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.141-205T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574583 | ||||||
chr6:85574618
|
C | T | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.141-240G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574618 | ||||||
chr6:85574646
|
C | T | 1 | a0001c0001t0001g0029 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.141-268G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574646 | ||||||
chr6:85574794
|
TAGTCTCT others(52): Show |
T | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.141-475_141-417del others(59): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574794 | ||||||
chr6:85574885
|
C | T | 4 | a0001c0003t0002g0033a0001c0003t0002g0034a0001c0003t0002g0051others(1): Show | 4 | HG02818.hp1 HG03041.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-507G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574885 | ||||||
chr6:85574953
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.141-575C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574953 | ||||||
chr6:85574962
|
G | A | 9 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(6): Show | 9 | HG01175.hp1 HG01243.hp1 HG01261.hp1 others(6): Show |
intron_variant | MODIFIER | c.141-584C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85574962 | ||||||
chr6:85575108
|
C | T | 6 | a0001c0001t0001g0019a0001c0001t0001g0020a0001c0001t0001g0021others(3): Show | 6 | HG02886.hp1 HG02965.hp1 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-730G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85575108 | ||||||
chr6:85575138
|
TA | T | 4 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057others(1): Show | 4 | HG02647.hp2 HG03209.hp2 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.141-761delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85575138 | ||||||
chr6:85575236
|
A | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0053others(2): Show | 6 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-858T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85575236 | ||||||
chr6:85575741
|
G | A | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.141-1363C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85575741 | ||||||
chr6:85575867
|
T | G | 5 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0053others(2): Show | 6 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-1489A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85575867 | ||||||
chr6:85576258
|
T | C | 1 | a0001c0001t0001g0016 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.141-1880A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85576258 | ||||||
chr6:85576345
|
A | G | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.141-1967T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85576345 | ||||||
chr6:85576364
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.141-1986C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85576364 | ||||||
chr6:85576520
|
CA | C | 32 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.141-2143delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85576520 | ||||||
chr6:85576631
|
C | T | 2 | a0001c0001t0001g0138a0001c0001t0001g0163 | 2 | HG02451.hp1 NA20752.hp1 |
intron_variant | MODIFIER | c.141-2253G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85576631 | ||||||
chr6:85576849
|
T | C | 1 | a0001c0001t0001g0161 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.141-2471A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85576849 | ||||||
chr6:85576879
|
A | T | 1 | a0001c0001t0001g0040 | 1 | NA18972.hp1 | intron_variant | MODIFIER | c.141-2501T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85576879 | ||||||
chr6:85576944
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0065 | 3 | HG01257.hp1 HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.141-2566C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85576944 | ||||||
chr6:85576978
|
A | G | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.141-2600T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85576978 | ||||||
chr6:85577287
|
G | A | 1 | a0001c0001t0001g0280 | 1 | HG00544.hp1 | intron_variant | MODIFIER | c.141-2909C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85577287 | ||||||
chr6:85577411
|
C | A | 161 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(158): Show | 166 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(163): Show |
intron_variant | MODIFIER | c.141-3033G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85577411 | ||||||
chr6:85577711
|
T | C | 1 | a0001c0001t0001g0018 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.141-3333A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85577711 | ||||||
chr6:85578023
|
G | A | 1 | a0001c0001t0001g0200 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.141-3645C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85578023 | ||||||
chr6:85578150
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0053others(2): Show | 6 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.141-3772C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85578150 | ||||||
chr6:85578185
|
G | A | 1 | a0001c0001t0001g0227 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.141-3807C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85578185 | ||||||
chr6:85578330
|
T | C | 1 | a0003c0006t0006g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.141-3952A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85578330 | ||||||
chr6:85578641
|
T | C | 1 | a0001c0001t0001g0162 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.141-4263A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85578641 | ||||||
chr6:85578858
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.141-4480C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85578858 | ||||||
chr6:85578874
|
G | A | 4 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0053others(1): Show | 5 | HG02647.hp1 HG02895.hp2 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.141-4496C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85578874 | ||||||
chr6:85578995
|
G | A | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.141-4617C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85578995 | ||||||
chr6:85579080
|
G | A | 1 | a0001c0001t0001g0176 | 1 | HG01069.hp2 | intron_variant | MODIFIER | c.141-4702C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579080 | ||||||
chr6:85579203
|
T | A | 32 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.141-4825A>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579203 | ||||||
chr6:85579385
|
C | T | 1 | a0001c0001t0001g0056 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.141-5007G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579385 | ||||||
chr6:85579459
|
C | T | 3 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0055 | 3 | HG02145.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.141-5081G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579459 | ||||||
chr6:85579598
|
G | C | 7 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-5220C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579598 | ||||||
chr6:85579671
|
G | A | 1 | a0003c0006t0006g0047 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.141-5293C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579671 | ||||||
chr6:85579697
|
A | G | 345 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(342): Show | 356 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(353): Show |
intron_variant | MODIFIER | c.141-5319T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579697 | ||||||
chr6:85579705
|
G | A | 2 | a0001c0001t0001g0245a0001c0001t0001g0246 | 2 | NA18952.hp2 NA19077.hp2 |
intron_variant | MODIFIER | c.141-5327C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579705 | ||||||
chr6:85579739
|
C | T | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.141-5361G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579739 | ||||||
chr6:85579955
|
C | T | 214 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(211): Show | 220 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(217): Show |
intron_variant | MODIFIER | c.141-5577G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579955 | ||||||
chr6:85579972
|
C | A | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.141-5594G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85579972 | ||||||
chr6:85580028
|
G | A | 1 | a0001c0001t0001g0136 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.141-5650C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85580028 | ||||||
chr6:85580081
|
T | C | 1 | a0001c0001t0001g0228 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.141-5703A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85580081 | ||||||
chr6:85580294
|
G | A | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.141-5916C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85580294 | ||||||
chr6:85580462
|
A | G | 1 | a0001c0001t0001g0066 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.141-6084T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85580462 | ||||||
chr6:85580606
|
C | T | 14 | a0001c0001t0001g0256a0001c0001t0001g0260a0001c0001t0001g0261others(11): Show | 14 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(11): Show |
intron_variant | MODIFIER | c.141-6228G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85580606 | ||||||
chr6:85580648
|
A | G | 1 | a0001c0001t0001g0297 | 1 | NA19055.hp1 | intron_variant | MODIFIER | c.141-6270T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85580648 | ||||||
chr6:85580925
|
T | C | 1 | a0001c0001t0001g0163 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.141-6547A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85580925 | ||||||
chr6:85581275
|
G | A | 1 | a0001c0001t0001g0192 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.141-6897C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85581275 | ||||||
chr6:85581352
|
G | A | 10 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(7): Show | 10 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(7): Show |
intron_variant | MODIFIER | c.141-6974C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85581352 | ||||||
chr6:85581597
|
A | G | 3 | a0001c0001t0001g0287a0001c0001t0001g0294a0001c0001t0001g0295 | 3 | HG03704.hp1 HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.141-7219T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85581597 | ||||||
chr6:85581731
|
T | C | 1 | a0001c0001t0001g0137 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.141-7353A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85581731 | ||||||
chr6:85581752
|
A | T | 3 | a0001c0001t0001g0288a0001c0001t0001g0289a0001c0001t0001g0296 | 3 | HG00597.hp2 NA18998.hp1 NA19060.hp2 |
intron_variant | MODIFIER | c.141-7374T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85581752 | ||||||
chr6:85582193
|
T | C | 32 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(29): Show | 32 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(29): Show |
intron_variant | MODIFIER | c.141-7815A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85582193 | ||||||
chr6:85582217
|
G | A | 152 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0005others(149): Show | 157 | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(154): Show |
intron_variant | MODIFIER | c.141-7839C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85582217 | ||||||
chr6:85582628
|
T | G | 3 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.141-8250A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85582628 | ||||||
chr6:85583007
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.141-8629C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583007 | ||||||
chr6:85583040
|
C | T | 1 | a0001c0001t0001g0230 | 1 | HG00735.hp2 | intron_variant | MODIFIER | c.141-8662G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583040 | ||||||
chr6:85583056
|
A | G | 3 | a0001c0001t0001g0258a0001c0001t0001g0259a0001c0001t0001g0281 | 3 | HG02258.hp2 HG03098.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.141-8678T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583056 | ||||||
chr6:85583069
|
C | T | 3 | a0001c0001t0001g0287a0001c0001t0001g0294a0001c0001t0001g0295 | 3 | HG03704.hp1 HG03831.hp2 HG04184.hp1 |
intron_variant | MODIFIER | c.141-8691G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583069 | ||||||
chr6:85583079
|
C | T | 7 | a0001c0001t0001g0035a0001c0001t0001g0095a0001c0001t0001g0096others(4): Show | 7 | HG02280.hp1 HG02615.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.141-8701G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583079 | ||||||
chr6:85583305
|
T | C | 1 | a0001c0001t0001g0237 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.141-8927A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583305 | ||||||
chr6:85583509
|
T | C | 37 | a0001c0001t0001g0007a0001c0001t0001g0037a0001c0001t0001g0038others(34): Show | 38 | HG00408.hp1 HG00597.hp1 HG00642.hp1 others(35): Show |
intron_variant | MODIFIER | c.141-9131A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583509 | ||||||
chr6:85583605
|
T | C | 1 | a0001c0001t0001g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.141-9227A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583605 | ||||||
chr6:85583777
|
G | C | 1 | a0001c0001t0001g0055 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.141-9399C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583777 | ||||||
chr6:85583783
|
G | C | 2 | a0001c0001t0001g0046a0001c0001t0001g0055 | 2 | HG02145.hp2 HG02486.hp1 |
intron_variant | MODIFIER | c.141-9405C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583783 | ||||||
chr6:85583802
|
C | A | 68 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0040others(65): Show | 69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.141-9424G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85583802 | ||||||
chr6:85584065
|
A | G | 4 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(1): Show | 4 | HG01256.hp1 HG01258.hp1 HG02055.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+9514T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85584065 | ||||||
chr6:85584175
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.140+9404A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85584175 | ||||||
chr6:85584330
|
C | T | 1 | a0001c0001t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.140+9249G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85584330 | ||||||
chr6:85584397
|
T | G | 1 | a0001c0001t0001g0239 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.140+9182A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85584397 | ||||||
chr6:85584400
|
G | A | 1 | a0001c0001t0001g0239 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.140+9179C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85584400 | ||||||
chr6:85584885
|
A | C | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.140+8694T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85584885 | ||||||
chr6:85585229
|
C | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(63): Show | 70 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.140+8350G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585229 | ||||||
chr6:85585292
|
G | A | 5 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0053others(2): Show | 6 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.140+8287C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585292 | ||||||
chr6:85585365
|
C | T | 2 | a0001c0001t0001g0187a0001c0001t0001g0188 | 2 | HG02559.hp2 HG02630.hp2 |
intron_variant | MODIFIER | c.140+8214G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585365 | ||||||
chr6:85585391
|
A | C | 3 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0055 | 3 | HG02145.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.140+8188T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585391 | ||||||
chr6:85585461
|
A | G | 1 | a0001c0001t0001g0345 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.140+8118T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585461 | ||||||
chr6:85585680
|
ACTAT | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(63): Show | 70 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.140+7895_140+7898d others(6): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585680 | ||||||
chr6:85585711
|
C | T | 290 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(287): Show | 301 | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(298): Show |
intron_variant | MODIFIER | c.140+7868G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585711 | ||||||
chr6:85585855
|
T | G | 1 | a0001c0001t0001g0091 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.140+7724A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585855 | ||||||
chr6:85585908
|
C | A | 11 | a0001c0001t0001g0168a0001c0001t0001g0169a0001c0001t0001g0170others(8): Show | 11 | HG00099.hp2 HG01069.hp2 HG01175.hp1 others(8): Show |
intron_variant | MODIFIER | c.140+7671G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585908 | ||||||
chr6:85585939
|
T | C | 3 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.140+7640A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585939 | ||||||
chr6:85585982
|
C | T | 1 | a0001c0001t0007g0349 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.140+7597G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585982 | ||||||
chr6:85585990
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.140+7589C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585990 | ||||||
chr6:85585990
|
G | GA | 8 | a0001c0001t0001g0059a0001c0001t0001g0177a0001c0001t0001g0178others(5): Show | 8 | HG00544.hp1 HG01175.hp1 HG01516.hp2 others(5): Show |
intron_variant | MODIFIER | c.140+7588dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585990 | ||||||
chr6:85585990
|
GA | G | 10 | a0001c0001t0001g0002a0001c0001t0001g0049a0001c0001t0001g0050others(7): Show | 11 | HG02559.hp1 HG02647.hp1 HG02723.hp2 others(8): Show |
intron_variant | MODIFIER | c.140+7588delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85585990 | ||||||
chr6:85586007
|
A | C | 1 | a0001c0001t0001g0019 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.140+7572T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85586007 | ||||||
chr6:85586140
|
C | A | 70 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(67): Show | 74 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(71): Show |
intron_variant | MODIFIER | c.140+7439G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85586140 | ||||||
chr6:85586274
|
G | C | 1 | a0001c0001t0001g0343 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.140+7305C>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85586274 | ||||||
chr6:85586315
|
G | A | 1 | a0001c0001t0001g0229 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.140+7264C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85586315 | ||||||
chr6:85586613
|
C | T | 1 | a0001c0001t0001g0293 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.140+6966G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85586613 | ||||||
chr6:85586662
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.140+6917G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85586662 | ||||||
chr6:85586728
|
G | A | 1 | a0001c0001t0001g0197 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.140+6851C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85586728 | ||||||
chr6:85587070
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(63): Show | 70 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.140+6509C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85587070 | ||||||
chr6:85587146
|
C | T | 1 | a0001c0001t0001g0049 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.140+6433G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85587146 | ||||||
chr6:85587207
|
CA | C | 148 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(145): Show | 154 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.140+6371delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85587207 | ||||||
chr6:85587364
|
T | C | 5 | a0001c0001t0001g0002a0001c0001t0001g0050a0001c0001t0001g0053others(2): Show | 6 | HG02559.hp1 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.140+6215A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85587364 | ||||||
chr6:85587659
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.140+5920C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85587659 | ||||||
chr6:85587762
|
TTAAA | T | 9 | a0001c0001t0001g0002a0001c0001t0001g0046a0001c0001t0001g0048others(6): Show | 10 | HG02145.hp2 HG02486.hp1 HG02559.hp1 others(7): Show |
intron_variant | MODIFIER | c.140+5813_140+5816d others(6): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85587762 | ||||||
chr6:85587839
|
A | G | 3 | a0001c0001t0001g0046a0001c0001t0001g0048a0001c0001t0001g0055 | 3 | HG02145.hp2 HG02486.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.140+5740T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85587839 | ||||||
chr6:85587908
|
C | G | 68 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0040others(65): Show | 69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.140+5671G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85587908 | ||||||
chr6:85588001
|
A | G | 29 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062others(26): Show | 29 | HG00642.hp2 HG01169.hp2 HG01261.hp2 others(26): Show |
intron_variant | MODIFIER | c.140+5578T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588001 | ||||||
chr6:85588345
|
A | G | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(193): Show | 202 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.140+5234T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588345 | ||||||
chr6:85588401
|
G | A | 1 | a0001c0001t0001g0179 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.140+5178C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588401 | ||||||
chr6:85588438
|
G | A | 1 | a0001c0001t0001g0032 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.140+5141C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588438 | ||||||
chr6:85588440
|
G | A | 2 | a0001c0001t0001g0015a0001c0001t0001g0253 | 2 | HG03453.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.140+5139C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588440 | ||||||
chr6:85588453
|
T | G | 1 | a0001c0001t0001g0016 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.140+5126A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588453 | ||||||
chr6:85588575
|
C | CTAAATAA others(1): Show |
10 | a0001c0001t0001g0045a0001c0001t0001g0187a0001c0001t0001g0188others(7): Show | 10 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(7): Show |
intron_variant | MODIFIER | c.140+4996_140+5003d others(10): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588575 | ||||||
chr6:85588575
|
C | CTAAATAA others(5): Show |
116 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0009others(113): Show | 121 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(118): Show |
intron_variant | MODIFIER | c.140+4992_140+5003d others(14): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588575 | ||||||
chr6:85588575
|
C | CTAAATAA others(9): Show |
36 | a0001c0001t0001g0002a0001c0001t0001g0016a0001c0001t0001g0017others(33): Show | 37 | HG00735.hp2 HG01168.hp2 HG01884.hp2 others(34): Show |
intron_variant | MODIFIER | c.140+4988_140+5003d others(18): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588575 | ||||||
chr6:85588575
|
C | CTAAATAA others(13): Show |
4 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0193others(1): Show | 4 | HG02647.hp1 HG03654.hp2 HG03688.hp2 others(1): Show |
intron_variant | MODIFIER | c.140+4984_140+5003d others(22): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588575 | ||||||
chr6:85588575
|
C | CTAAATAA others(17): Show |
1 | a0001c0001t0001g0195 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.140+4980_140+5003d others(26): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588575 | ||||||
chr6:85588780
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0065 | 3 | HG01257.hp1 HG01258.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.140+4799T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588780 | ||||||
chr6:85588799
|
T | C | 6 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195others(3): Show | 6 | HG03017.hp1 HG03492.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.140+4780A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85588799 | ||||||
chr6:85589051
|
C | T | 1 | a0001c0003t0002g0033 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.140+4528G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589051 | ||||||
chr6:85589052
|
G | A | 1 | a0001c0007t0001g0348 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.140+4527C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589052 | ||||||
chr6:85589139
|
C | T | 1 | a0001c0001t0001g0012 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.140+4440G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589139 | ||||||
chr6:85589143
|
G | A | 1 | a0001c0001t0001g0017 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.140+4436C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589143 | ||||||
chr6:85589225
|
C | CT | 10 | a0001c0001t0001g0040a0001c0001t0001g0046a0001c0001t0001g0055others(7): Show | 10 | HG01358.hp2 HG02129.hp1 HG02145.hp2 others(7): Show |
intron_variant | MODIFIER | c.140+4353dupA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589225 | ||||||
chr6:85589225
|
CT | C | 87 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(84): Show | 91 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(88): Show |
intron_variant | MODIFIER | c.140+4353delA | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589225 | ||||||
chr6:85589287
|
G | A | 1 | a0001c0001t0001g0055 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.140+4292C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589287 | ||||||
chr6:85589365
|
C | T | 1 | a0001c0001t0001g0198 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.140+4214G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589365 | ||||||
chr6:85589474
|
T | G | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062 | 3 | HG02451.hp2 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.140+4105A>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589474 | ||||||
chr6:85589475
|
C | T | 3 | a0001c0001t0001g0060a0001c0001t0001g0061a0001c0001t0001g0062 | 3 | HG02451.hp2 HG03486.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.140+4104G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589475 | ||||||
chr6:85589750
|
A | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0057 | 2 | HG02647.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.140+3829T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589750 | ||||||
chr6:85589808
|
A | G | 1 | a0001c0001t0001g0287 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.140+3771T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589808 | ||||||
chr6:85589981
|
G | A | 3 | a0001c0001t0001g0045a0001c0001t0001g0056a0001c0001t0001g0057 | 3 | HG02647.hp2 HG03209.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.140+3598C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85589981 | ||||||
chr6:85590078
|
A | T | 1 | a0001c0001t0001g0003 | 2 | HG00735.hp1 HG01106.hp2 |
intron_variant | MODIFIER | c.140+3501T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85590078 | ||||||
chr6:85590142
|
A | C | 1 | a0001c0001t0001g0197 | 1 | NA19007.hp1 | intron_variant | MODIFIER | c.140+3437T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85590142 | ||||||
chr6:85590230
|
A | G | 1 | a0001c0001t0001g0045 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.140+3349T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85590230 | ||||||
chr6:85590263
|
T | C | 1 | a0001c0001t0001g0344 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.140+3316A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85590263 | ||||||
chr6:85590440
|
C | A | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.140+3139G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85590440 | ||||||
chr6:85590569
|
C | T | 1 | a0001c0001t0001g0059 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.140+3010G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85590569 | ||||||
chr6:85590701
|
G | A | 6 | a0001c0001t0001g0241a0001c0001t0001g0242a0001c0001t0001g0244others(3): Show | 6 | NA18952.hp2 NA18966.hp1 NA19056.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+2878C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85590701 | ||||||
chr6:85590784
|
T | C | 2 | a0001c0001t0001g0247a0001c0001t0001g0248 | 2 | HG01891.hp1 HG02486.hp2 |
intron_variant | MODIFIER | c.140+2795A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85590784 | ||||||
chr6:85591026
|
C | T | 1 | a0001c0001t0001g0196 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.140+2553G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591026 | ||||||
chr6:85591070
|
T | C | 3 | a0001c0001t0001g0249a0001c0001t0001g0250a0001c0001t0001g0251 | 3 | HG02258.hp1 HG02615.hp2 HG02622.hp2 |
intron_variant | MODIFIER | c.140+2509A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591070 | ||||||
chr6:85591112
|
C | T | 3 | a0001c0001t0001g0193a0001c0001t0001g0194a0001c0001t0001g0195 | 3 | HG03017.hp1 HG03654.hp2 HG03688.hp2 |
intron_variant | MODIFIER | c.140+2467G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591112 | ||||||
chr6:85591133
|
A | G | 68 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0040others(65): Show | 69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.140+2446T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591133 | ||||||
chr6:85591220
|
CTG | C | 196 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(193): Show | 202 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(199): Show |
intron_variant | MODIFIER | c.140+2357_140+2358d others(4): Show |
SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591220 | ||||||
chr6:85591388
|
A | G | 1 | a0001c0001t0001g0256 | 1 | NA18948.hp1 | intron_variant | MODIFIER | c.140+2191T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591388 | ||||||
chr6:85591692
|
G | A | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.140+1887C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591692 | ||||||
chr6:85591707
|
T | C | 1 | a0001c0001t0001g0023 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.140+1872A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591707 | ||||||
chr6:85591887
|
C | T | 1 | a0001c0001t0001g0286 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.140+1692G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591887 | ||||||
chr6:85591896
|
C | G | 1 | a0001c0001t0001g0253 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.140+1683G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85591896 | ||||||
chr6:85592115
|
A | G | 1 | a0001c0001t0001g0252 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.140+1464T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592115 | ||||||
chr6:85592151
|
C | T | 1 | a0001c0001t0001g0058 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.140+1428G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592151 | ||||||
chr6:85592302
|
C | G | 68 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0040others(65): Show | 69 | HG00408.hp2 HG00423.hp1 HG00735.hp2 others(66): Show |
intron_variant | MODIFIER | c.140+1277G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592302 | ||||||
chr6:85592316
|
A | G | 190 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0008others(187): Show | 196 | HG00099.hp1 HG00280.hp1 HG00408.hp2 others(193): Show |
intron_variant | MODIFIER | c.140+1263T>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592316 | ||||||
chr6:85592619
|
T | C | 28 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0001g0258others(25): Show | 28 | HG00423.hp2 HG00544.hp1 HG01070.hp2 others(25): Show |
intron_variant | MODIFIER | c.140+960A>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592619 | ||||||
chr6:85592644
|
G | A | 6 | a0001c0001t0001g0187a0001c0001t0001g0188a0001c0001t0001g0189others(3): Show | 6 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(3): Show |
intron_variant | MODIFIER | c.140+935C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592644 | ||||||
chr6:85592742
|
C | A | 1 | a0001c0001t0001g0345 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.140+837G>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592742 | ||||||
chr6:85592803
|
A | C | 1 | a0001c0001t0001g0039 | 1 | NA19010.hp1 | intron_variant | MODIFIER | c.140+776T>G | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592803 | ||||||
chr6:85592825
|
T | TA | 101 | a0001c0001t0001g0008a0001c0001t0001g0015a0001c0001t0001g0018others(98): Show | 102 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(99): Show |
intron_variant | MODIFIER | c.140+753dupT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592825 | ||||||
chr6:85592825
|
TA | T | 71 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(68): Show | 75 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(72): Show |
intron_variant | MODIFIER | c.140+753delT | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592825 | ||||||
chr6:85592963
|
G | A | 2 | a0001c0001t0001g0284a0001c0001t0001g0285 | 2 | HG02895.hp1 HG02897.hp1 |
intron_variant | MODIFIER | c.140+616C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85592963 | ||||||
chr6:85593016
|
A | T | 8 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(5): Show | 8 | HG01256.hp1 HG01258.hp1 HG01496.hp1 others(5): Show |
intron_variant | MODIFIER | c.140+563T>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85593016 | ||||||
chr6:85593091
|
G | T | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.140+488C>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85593091 | ||||||
chr6:85593364
|
C | T | 1 | a0001c0005t0005g0024 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.140+215G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85593364 | ||||||
chr6:85593373
|
G | A | 66 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0012others(63): Show | 70 | HG00099.hp1 HG00280.hp1 HG00544.hp2 others(67): Show |
intron_variant | MODIFIER | c.140+206C>T | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85593373 | ||||||
chr6:85593426
|
C | G | 9 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(6): Show | 9 | HG01884.hp2 HG02109.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.140+153G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85593426 | ||||||
chr6:85593456
|
C | T | 1 | a0001c0001t0001g0015 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.140+123G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85593456 | ||||||
chr6:85593522
|
C | T | 2 | a0001c0001t0001g0013a0001c0001t0001g0014 | 2 | HG02886.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.140+57G>A | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85593522 | ||||||
chr6:85593567
|
C | G | 1 | a0001c0001t0001g0012 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.140+12G>C | SNX14 | ENSG00000135317.14 | transcript | ENST00000314673.8 | protein_coding | 1/28 | chr6 | 85593567 |