geneid | 79989 |
---|---|
ensemblid | ENSG00000105948.13 |
hgncid | 21882 |
symbol | IFT56 |
name | intraflagellar transport 56 |
refseq_nuc | NM_024926.4 |
refseq_prot | NP_079202.2 |
ensembl_nuc | ENST00000464848.5 |
ensembl_prot | ENSP00000419279.1 |
mane_status | MANE Select |
chr | chr7 |
start | 139133778 |
end | 139191986 |
strand | + |
ver | v1.2 |
region | chr7:139133778-139191986 |
region5000 | chr7:139128778-139196986 |
regionname0 | IFT56_chr7_139133778_139191986 |
regionname5000 | IFT56_chr7_139128778_139196986 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 554 | 327 | 88 | 40 | 151 | 8 | 38 | 115 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0002 | 0/0 | 554 | 2 | 0 | 0 | 2 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0003 | 0/0 | 554 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1665 | 286 | 73 | 39 | 127 | 8 | 37 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
c0002 | 0/0 | 1665 | 34 | 12 | 1 | 21 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
c0003 | 0/0 | 1665 | 4 | 3 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
c0004 | 0/0 | 1665 | 3 | 0 | 0 | 3 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
c0005 | 0/0 | 1665 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
c0006 | 0/0 | 1665 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 2632 | 107 | 37 | 12 | 44 | 1 | 13 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0002 | 0/1 | 2635 | 85 | 11 | 14 | 40 | 4 | 15 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0003 | 0/0 | 2632 | 65 | 7 | 2 | 48 | 1 | 7 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0004 | 0/0 | 2635 | 22 | 0 | 1 | 21 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0005 | 0/0 | 2635 | 14 | 13 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0006 | 0/0 | 2632 | 6 | 0 | 4 | 0 | 1 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0007 | 0/0 | 2629 | 6 | 6 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0008 | 1/0 | 2635 | 6 | 1 | 3 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0009 | 0/0 | 2635 | 3 | 0 | 2 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0010 | 0/0 | 2632 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0011 | 0/0 | 2632 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0012 | 0/0 | 2635 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0013 | 0/0 | 2635 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0014 | 0/0 | 2632 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0015 | 0/0 | 2629 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0016 | 0/0 | 2635 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0017 | 0/0 | 2635 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0018 | 0/0 | 2635 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0019 | 0/0 | 2635 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0020 | 0/0 | 2632 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
t0021 | 0/0 | 2632 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 10 | 1 | 1 | 5 | 1 | 2 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0002 | 0/0 | 9 | 0 | 0 | 9 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0003 | 0/0 | 6 | 0 | 2 | 0 | 0 | 4 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0005 | 0/0 | 5 | 2 | 0 | 2 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0006 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0008 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0017 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0020 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0248 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0251 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1665 | 286 | 73 | 39 | 127 | 8 | 37 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0002 | 0/0 | 1665 | 34 | 12 | 1 | 21 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0003 | 0/0 | 1665 | 4 | 3 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0004 | 0/0 | 1665 | 3 | 0 | 0 | 3 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0002c0005 | 0/0 | 1665 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0003c0006 | 0/0 | 1665 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 4296 | 97 | 32 | 12 | 39 | 1 | 13 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0001t0002 | 0/1 | 4299 | 85 | 11 | 14 | 40 | 4 | 15 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0001t0003 | 0/0 | 4296 | 64 | 7 | 2 | 47 | 1 | 7 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0001t0005 | 0/0 | 4299 | 9 | 8 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0001t0006 | 0/0 | 4296 | 6 | 0 | 4 | 0 | 1 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0001t0007 | 0/0 | 4293 | 6 | 6 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0001t0008 | 1/0 | 4299 | 6 | 1 | 3 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0001t0009 | 0/0 | 4299 | 3 | 0 | 2 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0001t0010 | 0/0 | 4296 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0001t0012 | 0/0 | 4299 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0001t0014 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0001t0015 | 0/0 | 4293 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0001t0016 | 0/0 | 4299 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0001t0018 | 0/0 | 4299 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0001t0019 | 0/0 | 4299 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0001t0021 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0002t0001 | 0/0 | 4296 | 5 | 5 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0002t0004 | 0/0 | 4299 | 22 | 0 | 1 | 21 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0002t0005 | 0/0 | 4299 | 5 | 5 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0002t0011 | 0/0 | 4296 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0003t0013 | 0/0 | 4299 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0003t0017 | 0/0 | 4299 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0003t0020 | 0/0 | 4296 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0001c0004t0001 | 0/0 | 4296 | 3 | 0 | 0 | 3 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0002c0005t0001 | 0/0 | 4296 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
a0003c0006t0003 | 0/0 | 4296 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | copy fasta | chr7 | 139128778 | 139196986 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 8 | 0 | 0 | 8 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0005 | 0/0 | 4 | 2 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0007 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0012 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0013 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0016 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0019 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0089 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0091 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0001 | 0/0 | 9 | 1 | 0 | 5 | 1 | 2 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0003 | 0/0 | 6 | 0 | 2 | 0 | 0 | 4 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0004 | 0/0 | 6 | 0 | 0 | 6 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0023 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0024 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0026 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0204 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0214 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0216 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0222 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0251 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0256 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0266 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0002g0273 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0006 | 0/0 | 4 | 0 | 0 | 3 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0008 | 0/0 | 3 | 1 | 1 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0009 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0022 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0025 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0226 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0229 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0233 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0234 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0265 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0267 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0003g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0005g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0005g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0006g0005 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0006g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0006g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0006g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0006g0063 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0006g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0007g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0007g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0007g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0007g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0007g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0007g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0008g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0008g0161 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0008g0207 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0008g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0008g0248 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0008g0261 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0009g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0009g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0009g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0010g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0010g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0012g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0012g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0014g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0015g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0016g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0018g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0019g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0001t0021g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0001g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0001g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0010 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0040 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0043 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0045 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0004g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0005g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0005g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0005g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0005g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0005g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0011g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0002t0011g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0003t0013g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0003t0013g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0003t0017g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0003t0020g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0004t0001g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0004t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0001c0004t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0002c0005t0001g0002 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0002c0005t0001g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
a0003c0006t0003g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0008 | g0207 | EUR | GBR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00140 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | GBR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00323 | hp1 | a0001 | c0001 | t0002 | g0204 | EUR | FIN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00323 | hp2 | a0001 | c0001 | t0003 | g0229 | EUR | FIN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0110 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00438 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00438 | hp2 | a0001 | c0001 | t0003 | g0269 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00544 | hp1 | a0001 | c0001 | t0001 | g0068 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00544 | hp2 | a0002 | c0005 | t0001 | g0108 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00597 | hp1 | a0001 | c0001 | t0003 | g0190 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00597 | hp2 | a0001 | c0001 | t0002 | g0209 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00609 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00609 | hp2 | a0002 | c0005 | t0001 | g0002 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00621 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00642 | hp1 | a0001 | c0001 | t0006 | g0061 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00642 | hp2 | a0001 | c0001 | t0002 | g0177 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00673 | hp1 | a0001 | c0001 | t0002 | g0021 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0005 | EAS | CHS | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01070 | hp1 | a0001 | c0001 | t0006 | g0070 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01070 | hp2 | a0001 | c0001 | t0002 | g0157 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0085 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0013 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0205 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01099 | hp1 | a0001 | c0001 | t0006 | g0062 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0020 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01106 | hp1 | a0001 | c0001 | t0002 | g0158 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01106 | hp2 | a0001 | c0001 | t0008 | g0001 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01175 | hp1 | a0001 | c0001 | t0002 | g0171 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01175 | hp2 | a0001 | c0001 | t0006 | g0059 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01243 | hp1 | a0001 | c0001 | t0009 | g0168 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01243 | hp2 | a0001 | c0001 | t0001 | g0091 | AMR | PUR | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01256 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01256 | hp2 | a0001 | c0001 | t0002 | g0162 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01358 | hp1 | a0001 | c0001 | t0002 | g0188 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01358 | hp2 | a0001 | c0001 | t0008 | g0161 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01361 | hp1 | a0001 | c0001 | t0009 | g0169 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01361 | hp2 | a0001 | c0001 | t0003 | g0008 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0167 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01891 | hp1 | a0001 | c0001 | t0003 | g0191 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01891 | hp2 | a0001 | c0001 | t0021 | g0046 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01928 | hp1 | a0001 | c0001 | t0002 | g0163 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0079 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01934 | hp1 | a0001 | c0001 | t0002 | g0003 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01943 | hp1 | a0001 | c0001 | t0001 | g0018 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01943 | hp2 | a0001 | c0001 | t0005 | g0050 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0166 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0084 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0164 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0124 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02015 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02015 | hp2 | a0001 | c0002 | t0004 | g0043 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02027 | hp1 | a0001 | c0001 | t0001 | g0089 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0183 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02040 | hp1 | a0001 | c0001 | t0003 | g0253 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0219 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02055 | hp1 | a0001 | c0001 | t0003 | g0194 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0058 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0081 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02056 | hp2 | a0001 | c0001 | t0003 | g0271 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02071 | hp1 | a0001 | c0002 | t0004 | g0041 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02074 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02074 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02083 | hp1 | a0001 | c0001 | t0003 | g0239 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02083 | hp2 | a0001 | c0001 | t0002 | g0023 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02129 | hp2 | a0001 | c0001 | t0002 | g0266 | EAS | KHV | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02145 | hp1 | a0001 | c0001 | t0005 | g0048 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0198 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02148 | hp1 | a0001 | c0001 | t0002 | g0214 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02148 | hp2 | a0001 | c0001 | t0003 | g0230 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | CDX | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02155 | hp2 | a0001 | c0001 | t0003 | g0265 | EAS | CDX | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0267 | EAS | CDX | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | CDX | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02257 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02257 | hp2 | a0001 | c0001 | t0007 | g0150 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02258 | hp1 | a0001 | c0002 | t0005 | g0136 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0195 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0013 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02280 | hp2 | a0001 | c0003 | t0013 | g0129 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02300 | hp1 | a0001 | c0002 | t0004 | g0040 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02300 | hp2 | a0001 | c0001 | t0008 | g0221 | AMR | PEL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02451 | hp2 | a0001 | c0001 | t0002 | g0249 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02572 | hp1 | a0001 | c0002 | t0011 | g0139 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02572 | hp2 | a0001 | c0002 | t0001 | g0144 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02602 | hp1 | a0001 | c0001 | t0002 | g0256 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0140 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0116 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02615 | hp2 | a0001 | c0003 | t0020 | g0131 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0047 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02622 | hp2 | a0001 | c0001 | t0012 | g0146 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0072 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02630 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02647 | hp1 | a0001 | c0001 | t0002 | g0196 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0213 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0257 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0067 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02723 | hp2 | a0001 | c0001 | t0007 | g0156 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0071 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02818 | hp1 | a0001 | c0002 | t0001 | g0142 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02818 | hp2 | a0001 | c0001 | t0007 | g0149 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02886 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02886 | hp2 | a0001 | c0001 | t0005 | g0053 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02895 | hp1 | a0001 | c0001 | t0002 | g0222 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02896 | hp1 | a0001 | c0001 | t0005 | g0056 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02896 | hp2 | a0001 | c0001 | t0001 | g0005 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0019 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02897 | hp2 | a0001 | c0001 | t0005 | g0054 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02922 | hp1 | a0001 | c0001 | t0015 | g0148 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0017 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02965 | hp2 | a0001 | c0002 | t0001 | g0143 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03017 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03041 | hp1 | a0001 | c0002 | t0005 | g0133 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03041 | hp2 | a0001 | c0001 | t0007 | g0151 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03098 | hp1 | a0001 | c0003 | t0013 | g0128 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03098 | hp2 | a0001 | c0002 | t0001 | g0141 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0082 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03130 | hp2 | a0001 | c0001 | t0008 | g0261 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03139 | hp1 | a0001 | c0001 | t0010 | g0155 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03139 | hp2 | a0001 | c0001 | t0012 | g0147 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03195 | hp1 | a0001 | c0002 | t0005 | g0135 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03195 | hp2 | a0001 | c0001 | t0005 | g0075 | AFR | ESN | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03209 | hp1 | a0001 | c0001 | t0001 | g0130 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03209 | hp2 | a0001 | c0001 | t0005 | g0049 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03225 | hp1 | a0001 | c0001 | t0007 | g0153 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0111 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0092 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03239 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0060 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03453 | hp2 | a0001 | c0001 | t0014 | g0017 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03486 | hp1 | a0001 | c0001 | t0003 | g0192 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03486 | hp2 | a0001 | c0001 | t0019 | g0175 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03490 | hp1 | a0001 | c0001 | t0003 | g0243 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0026 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0226 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03492 | hp2 | a0001 | c0001 | t0003 | g0006 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03540 | hp1 | a0001 | c0001 | t0005 | g0051 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0176 | AFR | GWD | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03579 | hp1 | a0001 | c0001 | t0007 | g0152 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03579 | hp2 | a0001 | c0001 | t0001 | g0117 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03669 | hp1 | a0001 | c0001 | t0002 | g0003 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03669 | hp2 | a0001 | c0001 | t0006 | g0063 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03704 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0011 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03710 | hp1 | a0001 | c0001 | t0003 | g0244 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03710 | hp2 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0119 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03831 | hp2 | a0001 | c0001 | t0002 | g0182 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03834 | hp1 | a0001 | c0003 | t0017 | g0088 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0189 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0008 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03942 | hp1 | a0001 | c0001 | t0003 | g0233 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03942 | hp2 | a0001 | c0001 | t0001 | g0090 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0066 | SAS | STU | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG04115 | hp2 | a0001 | c0001 | t0003 | g0234 | SAS | STU | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG04184 | hp1 | a0001 | c0001 | t0002 | g0165 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG04184 | hp2 | a0001 | c0001 | t0001 | g0078 | SAS | BEB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG04199 | hp1 | a0001 | c0001 | t0001 | g0080 | SAS | STU | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0178 | SAS | STU | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0064 | SAS | STU | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG04204 | hp2 | a0001 | c0001 | t0009 | g0170 | SAS | STU | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18522 | hp1 | a0001 | c0001 | t0001 | g0076 | AFR | YRI | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | YRI | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18612 | hp1 | a0001 | c0002 | t0004 | g0034 | EAS | CHB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0210 | EAS | CHB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18747 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | CHB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0238 | EAS | CHB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18939 | hp1 | a0001 | c0001 | t0003 | g0264 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18939 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18940 | hp1 | a0001 | c0002 | t0004 | g0038 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0241 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18941 | hp1 | a0001 | c0001 | t0003 | g0237 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18944 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0246 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18946 | hp2 | a0001 | c0002 | t0004 | g0045 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18947 | hp2 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18948 | hp1 | a0001 | c0001 | t0001 | g0101 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18948 | hp2 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18950 | hp1 | a0001 | c0001 | t0003 | g0232 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0112 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18951 | hp1 | a0001 | c0001 | t0001 | g0007 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18951 | hp2 | a0003 | c0006 | t0003 | g0268 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18952 | hp1 | a0001 | c0001 | t0003 | g0263 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18952 | hp2 | a0001 | c0001 | t0002 | g0212 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18953 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18953 | hp2 | a0001 | c0001 | t0003 | g0199 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18956 | hp1 | a0001 | c0001 | t0018 | g0103 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18956 | hp2 | a0001 | c0002 | t0004 | g0037 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18960 | hp1 | a0001 | c0001 | t0002 | g0273 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18960 | hp2 | a0001 | c0001 | t0003 | g0224 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18961 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18961 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0197 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18964 | hp2 | a0001 | c0002 | t0004 | g0039 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18965 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18965 | hp2 | a0001 | c0001 | t0003 | g0242 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18966 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18966 | hp2 | a0001 | c0001 | t0003 | g0231 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18967 | hp1 | a0001 | c0001 | t0001 | g0115 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18967 | hp2 | a0001 | c0001 | t0003 | g0235 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18968 | hp2 | a0001 | c0002 | t0004 | g0031 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0272 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18970 | hp2 | a0001 | c0001 | t0001 | g0069 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18971 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18972 | hp2 | a0001 | c0001 | t0003 | g0228 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18975 | hp1 | a0001 | c0001 | t0003 | g0173 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18975 | hp2 | a0001 | c0002 | t0004 | g0032 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0200 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18977 | hp2 | a0001 | c0002 | t0004 | g0028 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18979 | hp1 | a0001 | c0001 | t0002 | g0217 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18979 | hp2 | a0001 | c0001 | t0003 | g0227 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18981 | hp2 | a0001 | c0001 | t0002 | g0211 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18983 | hp1 | a0001 | c0002 | t0004 | g0035 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18983 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18984 | hp1 | a0001 | c0002 | t0004 | g0030 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18984 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18986 | hp1 | a0001 | c0002 | t0004 | g0029 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0223 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18987 | hp1 | a0001 | c0001 | t0002 | g0206 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18987 | hp2 | a0001 | c0002 | t0004 | g0010 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18989 | hp1 | a0001 | c0001 | t0002 | g0220 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18989 | hp2 | a0001 | c0001 | t0001 | g0083 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18990 | hp1 | a0001 | c0001 | t0003 | g0262 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18990 | hp2 | a0001 | c0002 | t0004 | g0159 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18991 | hp2 | a0001 | c0001 | t0003 | g0172 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18992 | hp1 | a0001 | c0001 | t0003 | g0260 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18993 | hp1 | a0001 | c0001 | t0003 | g0025 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18993 | hp2 | a0001 | c0002 | t0004 | g0027 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18994 | hp1 | a0001 | c0001 | t0003 | g0203 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18994 | hp2 | a0001 | c0001 | t0001 | g0123 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18995 | hp1 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18995 | hp2 | a0001 | c0001 | t0001 | g0099 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0215 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18998 | hp2 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18999 | hp1 | a0001 | c0002 | t0004 | g0042 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0109 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0255 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19000 | hp2 | a0001 | c0001 | t0003 | g0252 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0006 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19003 | hp1 | a0001 | c0004 | t0001 | g0086 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19003 | hp2 | a0001 | c0001 | t0003 | g0245 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19004 | hp2 | a0001 | c0002 | t0004 | g0036 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19005 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19005 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19006 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19006 | hp2 | a0001 | c0001 | t0003 | g0184 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19010 | hp1 | a0001 | c0004 | t0001 | g0104 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19010 | hp2 | a0001 | c0001 | t0003 | g0254 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19011 | hp1 | a0001 | c0001 | t0003 | g0009 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19012 | hp2 | a0001 | c0001 | t0002 | g0021 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0096 | AFR | LWK | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19030 | hp2 | a0001 | c0001 | t0002 | g0202 | AFR | LWK | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19043 | hp1 | a0001 | c0001 | t0003 | g0193 | AFR | LWK | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0012 | AFR | LWK | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19056 | hp1 | a0001 | c0002 | t0004 | g0033 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19060 | hp2 | a0001 | c0001 | t0003 | g0225 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19072 | hp1 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19072 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19074 | hp2 | a0001 | c0002 | t0004 | g0044 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19076 | hp1 | a0001 | c0004 | t0001 | g0114 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19076 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19090 | hp1 | a0001 | c0001 | t0002 | g0208 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19240 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | YRI | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA19240 | hp2 | a0001 | c0002 | t0005 | g0134 | AFR | YRI | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0016 | AFR | ASW | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA20129 | hp2 | a0001 | c0002 | t0001 | g0145 | AFR | ASW | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | TSI | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA20752 | hp2 | a0001 | c0001 | t0006 | g0005 | EUR | TSI | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0216 | EUR | TSI | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0186 | EUR | TSI | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01123 | hp1 | a0001 | c0001 | t0016 | g0020 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0014 | AMR | CLM | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02109 | hp1 | a0001 | c0001 | t0010 | g0154 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0127 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0094 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02486 | hp2 | a0001 | c0002 | t0005 | g0137 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02559 | hp1 | a0001 | c0001 | t0003 | g0187 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0180 | AFR | ACB | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03471 | hp1 | a0001 | c0001 | t0001 | g0077 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0181 | AFR | MSL | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG06807 | hp1 | a0001 | c0001 | t0005 | g0055 | AFR | USA | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
HG06807 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | USA | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18955 | hp1 | a0001 | c0001 | t0003 | g0247 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA18955 | hp2 | a0001 | c0001 | t0003 | g0022 | EAS | JPT | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | USA | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA20300 | hp2 | a0001 | c0001 | t0003 | g0008 | AFR | USA | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
NA21309 | hp2 | a0001 | c0002 | t0011 | g0138 | AFR | LWK | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0251 | REF | REF | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0008 | g0248 | REF | REF | IFT56_chr7_139128778_139196986 | IFT56 | chr7 | 139128778 | 139196986 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:139137853
|
C | T | 1 | a0002 | 2 | HG00544.hp2 HG00609.hp2 |
missense_variant | MODERATE | c.148C>T | p.Arg50Cys | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/18 | 228/4299 | 148/1665 | 50/554 | chr7 | 139137853 | ||
chr7:139165228
|
C | T | 1 | a0003 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.889C>T | p.Arg297Cys | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/18 | 969/4299 | 889/1665 | 297/554 | chr7 | 139165228 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:139134699
|
C | T | 1 | a0001c0002 | 34 | HG02015.hp2 HG02071.hp1 HG02258.hp1 others(31): Show |
synonymous_variant | LOW | c.48C>T | p.His16His | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/18 | 128/4299 | 48/1665 | 16/554 | chr7 | 139134699 | ||
chr7:139178556
|
C | G | 1 | a0001c0004 | 3 | NA19003.hp1 NA19010.hp1 NA19076.hp1 |
synonymous_variant | LOW | c.1200C>G | p.Ala400Ala | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/18 | 1280/4299 | 1200/1665 | 400/554 | chr7 | 139178556 | ||
chr7:139189342
|
C | T | 1 | a0001c0003 | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
synonymous_variant | LOW | c.1575C>T | p.Leu525Leu | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 1655/4299 | 1575/1665 | 525/554 | chr7 | 139189342 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:139189445
|
G | A | 1 | a0001c0002t0004 | 22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*13G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 13 | chr7 | 139189445 | |||||
chr7:139189670
|
C | G | 2 | a0001c0001t0003a0003c0006t0003 | 65 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(62): Show |
3_prime_UTR_variant | MODIFIER | c.*238C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 238 | chr7 | 139189670 | |||||
chr7:139189975
|
G | C | 6 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(3): Show | 114 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*543G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 543 | chr7 | 139189975 | |||||
chr7:139190071
|
G | T | 1 | a0001c0001t0021 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*639G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 639 | chr7 | 139190071 | |||||
chr7:139190106
|
T | C | 6 | a0001c0001t0001a0001c0001t0006a0001c0001t0014others(3): Show | 114 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(111): Show |
3_prime_UTR_variant | MODIFIER | c.*674T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 674 | chr7 | 139190106 | |||||
chr7:139190221
|
AGTTTTT | A | 2 | a0001c0001t0007a0001c0001t0015 | 7 | HG02257.hp2 HG02723.hp2 HG02818.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*793_*798delTTTGTT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 793 | INFO_REALIGN_3_PRIME | chr7 | 139190221 | ||||
chr7:139190222
|
GTTT | G | 3 | a0001c0001t0010a0001c0001t0021a0001c0002t0011 | 5 | HG01891.hp2 HG02109.hp1 HG02572.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*793_*795delTTT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 793 | INFO_REALIGN_3_PRIME | chr7 | 139190222 | ||||
chr7:139190225
|
T | G | 2 | a0001c0001t0005a0001c0002t0005 | 14 | HG01943.hp2 HG02145.hp1 HG02258.hp1 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*793T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 793 | chr7 | 139190225 | |||||
chr7:139190225
|
TTTG | T | 9 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(6): Show | 180 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(177): Show |
3_prime_UTR_variant | MODIFIER | c.*826_*828delGTT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 826 | INFO_REALIGN_3_PRIME | chr7 | 139190225 | ||||
chr7:139190243
|
G | T | 1 | a0001c0001t0021 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*811G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 811 | chr7 | 139190243 | |||||
chr7:139190313
|
T | G | 4 | a0001c0001t0007a0001c0001t0010a0001c0001t0015others(1): Show | 10 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*881T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 881 | chr7 | 139190313 | |||||
chr7:139190391
|
A | G | 2 | a0001c0003t0013a0001c0003t0020 | 3 | HG02280.hp2 HG02615.hp2 HG03098.hp1 |
3_prime_UTR_variant | MODIFIER | c.*959A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 959 | chr7 | 139190391 | |||||
chr7:139190401
|
G | A | 25 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | 324 | HG00140.hp2 HG00323.hp1 HG00323.hp2 others(321): Show |
3_prime_UTR_variant | MODIFIER | c.*969G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 969 | chr7 | 139190401 | |||||
chr7:139190944
|
G | A | 1 | a0001c0001t0015 | 1 | HG02922.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1512G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 1512 | chr7 | 139190944 | |||||
chr7:139191144
|
A | T | 1 | a0001c0001t0019 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1712A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 1712 | chr7 | 139191144 | |||||
chr7:139191239
|
T | C | 1 | a0001c0001t0012 | 2 | HG02622.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*1807T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 1807 | chr7 | 139191239 | |||||
chr7:139191586
|
A | G | 1 | a0001c0001t0006 | 6 | HG00642.hp1 HG01070.hp1 HG01099.hp1 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*2154A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 2154 | chr7 | 139191586 | |||||
chr7:139191603
|
C | G | 1 | a0001c0001t0021 | 1 | HG01891.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2171C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 2171 | chr7 | 139191603 | |||||
chr7:139191603
|
C | T | 1 | a0001c0001t0018 | 1 | NA18956.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2171C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 2171 | chr7 | 139191603 | |||||
chr7:139191613
|
C | T | 1 | a0001c0001t0014 | 1 | HG03453.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2181C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 2181 | chr7 | 139191613 | |||||
chr7:139191718
|
A | G | 1 | a0001c0001t0009 | 3 | HG01243.hp1 HG01361.hp1 HG04204.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2286A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 2286 | chr7 | 139191718 | |||||
chr7:139191740
|
G | C | 1 | a0001c0001t0016 | 1 | HG01123.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2308G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 2308 | chr7 | 139191740 | |||||
chr7:139191762
|
T | C | 3 | a0001c0001t0007a0001c0001t0010a0001c0001t0015 | 9 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*2330T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 2330 | chr7 | 139191762 | |||||
chr7:139191862
|
T | G | 1 | a0001c0003t0017 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2430T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 2430 | chr7 | 139191862 | |||||
chr7:139191894
|
G | A | 1 | a0001c0001t0012 | 2 | HG02622.hp2 HG03139.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2462G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 18/18 | 2462 | chr7 | 139191894 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr7:139133886
|
G | A | 21 | a0001c0001t0021g0046a0001c0002t0004g0010a0001c0002t0004g0027others(18): Show | 22 | HG01891.hp2 HG02015.hp2 HG02071.hp1 others(19): Show |
intron_variant | MODIFIER | c.3+26G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 1/17 | chr7 | 139133886 | ||||||
chr7:139133998
|
G | A | 135 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(132): Show | 154 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(151): Show |
intron_variant | MODIFIER | c.3+138G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 1/17 | chr7 | 139133998 | ||||||
chr7:139134122
|
C | A | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.3+262C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 1/17 | chr7 | 139134122 | ||||||
chr7:139134188
|
C | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(133): Show | 155 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(152): Show |
intron_variant | MODIFIER | c.3+328C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 1/17 | chr7 | 139134188 | ||||||
chr7:139134273
|
AT | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0011others(135): Show | 157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.4-366delT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr7 | 139134273 | |||||
chr7:139134395
|
C | T | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.4-260C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 1/17 | chr7 | 139134395 | ||||||
chr7:139134416
|
G | A | 9 | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0005g0049others(6): Show | 9 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.4-239G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 1/17 | chr7 | 139134416 | ||||||
chr7:139134545
|
G | T | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.4-110G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 1/17 | chr7 | 139134545 | ||||||
chr7:139134856
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.141+64G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139134856 | ||||||
chr7:139134864
|
T | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.141+72T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139134864 | ||||||
chr7:139134955
|
G | A | 1 | a0001c0001t0005g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.141+163G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139134955 | ||||||
chr7:139134997
|
T | G | 2 | a0001c0001t0007g0149a0001c0001t0015g0148 | 2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.141+205T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139134997 | ||||||
chr7:139135050
|
A | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(134): Show | 158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.141+258A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135050 | ||||||
chr7:139135082
|
C | T | 1 | a0001c0001t0002g0273 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.141+290C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135082 | ||||||
chr7:139135211
|
G | A | 7 | a0001c0001t0002g0003a0001c0001t0002g0162a0001c0001t0002g0163others(4): Show | 12 | HG01256.hp2 HG01258.hp1 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.141+419G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135211 | ||||||
chr7:139135273
|
G | A | 1 | a0001c0001t0002g0167 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.141+481G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135273 | ||||||
chr7:139135277
|
C | CA | 22 | a0001c0001t0002g0020a0001c0001t0002g0021a0001c0001t0002g0171others(19): Show | 23 | HG00642.hp2 HG00673.hp1 HG01099.hp2 others(20): Show |
intron_variant | MODIFIER | c.141+506dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139135277 | |||||
chr7:139135277
|
CA | C | 7 | a0001c0001t0002g0259a0001c0001t0003g0260a0001c0001t0003g0262others(4): Show | 7 | HG02155.hp2 HG03130.hp2 NA18939.hp1 others(4): Show |
intron_variant | MODIFIER | c.141+506delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139135277 | |||||
chr7:139135277
|
CAA | C | 7 | a0001c0001t0003g0009a0001c0001t0003g0267a0001c0001t0003g0269others(4): Show | 9 | HG00438.hp2 HG02056.hp2 HG02165.hp1 others(6): Show |
intron_variant | MODIFIER | c.141+505_141+506del others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139135277 | |||||
chr7:139135293
|
A | C | 1 | a0001c0001t0001g0132 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.141+501A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135293 | ||||||
chr7:139135294
|
A | C | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.141+502A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135294 | ||||||
chr7:139135294
|
AAAAAC | A | 64 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0013others(61): Show | 79 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.141+513_141+517del others(5): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139135294 | |||||
chr7:139135295
|
AAAAC | A | 42 | a0001c0001t0001g0012a0001c0001t0001g0076a0001c0001t0001g0077others(39): Show | 44 | HG01074.hp1 HG01928.hp2 HG01952.hp2 others(41): Show |
intron_variant | MODIFIER | c.141+507_141+510del others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139135295 | |||||
chr7:139135298
|
A | C | 1 | a0001c0001t0002g0266 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.141+506A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135298 | ||||||
chr7:139135298
|
AC | A | 25 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0064others(22): Show | 29 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(26): Show |
intron_variant | MODIFIER | c.141+507delC | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135298 | ||||||
chr7:139135299
|
C | A | 10 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0060others(7): Show | 10 | HG00642.hp1 HG01099.hp1 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.141+507C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135299 | ||||||
chr7:139135299
|
CAAA | C | 3 | a0001c0002t0001g0141a0001c0002t0004g0027a0001c0002t0004g0028 | 3 | HG03098.hp2 NA18977.hp2 NA18993.hp2 |
intron_variant | MODIFIER | c.141+509_141+511del others(3): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139135299 | |||||
chr7:139135301
|
A | C | 2 | a0001c0001t0007g0149a0001c0001t0015g0148 | 2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.141+509A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135301 | ||||||
chr7:139135302
|
A | C | 29 | a0001c0002t0001g0142a0001c0002t0001g0143a0001c0002t0001g0144others(26): Show | 30 | HG02015.hp2 HG02071.hp1 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.141+510A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135302 | ||||||
chr7:139135318
|
T | C | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.141+526T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135318 | ||||||
chr7:139135322
|
G | A | 9 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(6): Show | 9 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.141+530G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135322 | ||||||
chr7:139135424
|
T | C | 1 | a0001c0001t0002g0162 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.141+632T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135424 | ||||||
chr7:139135499
|
G | A | 68 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(65): Show | 84 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.141+707G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135499 | ||||||
chr7:139135678
|
T | A | 1 | a0001c0001t0002g0186 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.141+886T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139135678 | ||||||
chr7:139135915
|
C | CT | 104 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(101): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.141+1133dupT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139135915 | |||||
chr7:139136074
|
C | A | 10 | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0005g0049others(7): Show | 10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.141+1282C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139136074 | ||||||
chr7:139136326
|
C | A | 1 | a0001c0001t0003g0187 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.142-1521C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139136326 | ||||||
chr7:139136432
|
C | T | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-1415C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139136432 | ||||||
chr7:139136637
|
TTG | T | 10 | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0005g0049others(7): Show | 10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.142-1197_142-1196d others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139136637 | |||||
chr7:139136676
|
C | T | 1 | a0001c0001t0021g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.142-1171C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139136676 | ||||||
chr7:139136794
|
C | T | 5 | a0001c0001t0002g0185a0001c0001t0002g0255a0001c0001t0002g0256others(2): Show | 5 | HG02165.hp2 HG02602.hp1 HG02698.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-1053C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139136794 | ||||||
chr7:139136856
|
G | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(134): Show | 158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.142-991G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139136856 | ||||||
chr7:139137065
|
C | T | 5 | a0001c0001t0003g0183a0001c0001t0003g0184a0001c0001t0003g0252others(2): Show | 5 | HG02027.hp2 HG02040.hp1 NA19000.hp2 others(2): Show |
intron_variant | MODIFIER | c.142-782C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139137065 | ||||||
chr7:139137484
|
C | T | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.142-363C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139137484 | ||||||
chr7:139137758
|
T | TGTTC | 148 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(145): Show | 175 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(172): Show |
intron_variant | MODIFIER | c.142-87_142-86insTC others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr7 | 139137758 | |||||
chr7:139137797
|
G | A | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.142-50G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 2/17 | chr7 | 139137797 | ||||||
chr7:139137989
|
A | G | 28 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0002t0001g0141others(25): Show | 29 | HG02015.hp2 HG02071.hp1 HG02109.hp2 others(26): Show |
intron_variant | MODIFIER | c.234+50A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139137989 | ||||||
chr7:139138016
|
A | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.234+77A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138016 | ||||||
chr7:139138149
|
A | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(61): Show | 80 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.234+210A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138149 | ||||||
chr7:139138185
|
A | T | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.234+246A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138185 | ||||||
chr7:139138485
|
C | T | 10 | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0005g0049others(7): Show | 10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.234+546C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138485 | ||||||
chr7:139138503
|
C | T | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.234+564C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138503 | ||||||
chr7:139138523
|
T | C | 5 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0002t0001g0143others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.234+584T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138523 | ||||||
chr7:139138533
|
G | A | 1 | a0001c0001t0002g0188 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.234+594G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138533 | ||||||
chr7:139138567
|
C | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.234+628C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138567 | ||||||
chr7:139138811
|
C | CT | 104 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(101): Show | 124 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(121): Show |
intron_variant | MODIFIER | c.234+889dupT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 139138811 | |||||
chr7:139138811
|
C | CTT | 25 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0002t0001g0141others(22): Show | 26 | HG02015.hp2 HG02071.hp1 HG02109.hp2 others(23): Show |
intron_variant | MODIFIER | c.234+888_234+889dup others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr7 | 139138811 | |||||
chr7:139138874
|
G | A | 2 | a0001c0001t0002g0026a0001c0001t0002g0182 | 3 | HG02735.hp1 HG03491.hp1 HG03831.hp2 |
intron_variant | MODIFIER | c.234+935G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138874 | ||||||
chr7:139138972
|
G | A | 1 | a0001c0001t0007g0151 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.235-918G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139138972 | ||||||
chr7:139139034
|
G | A | 10 | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0005g0049others(7): Show | 10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.235-856G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139034 | ||||||
chr7:139139089
|
G | A | 2 | a0001c0001t0001g0057a0001c0001t0001g0064 | 2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.235-801G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139089 | ||||||
chr7:139139091
|
C | T | 1 | a0001c0001t0001g0125 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.235-799C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139091 | ||||||
chr7:139139166
|
G | C | 148 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(145): Show | 169 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(166): Show |
intron_variant | MODIFIER | c.235-724G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139166 | ||||||
chr7:139139299
|
C | T | 1 | a0001c0001t0001g0124 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.235-591C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139299 | ||||||
chr7:139139403
|
A | T | 22 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0057others(19): Show | 26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.235-487A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139403 | ||||||
chr7:139139627
|
C | A | 1 | a0001c0001t0002g0189 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.235-263C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139627 | ||||||
chr7:139139658
|
T | C | 2 | a0001c0001t0007g0149a0001c0001t0015g0148 | 2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.235-232T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139658 | ||||||
chr7:139139692
|
G | T | 1 | a0001c0003t0017g0088 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.235-198G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139692 | ||||||
chr7:139139700
|
T | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(134): Show | 158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.235-190T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 3/17 | chr7 | 139139700 | ||||||
chr7:139140096
|
GA | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(134): Show | 158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.349+102delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140096 | |||||
chr7:139140103
|
A | G | 27 | a0001c0001t0012g0146a0001c0001t0012g0147a0001c0002t0001g0141others(24): Show | 28 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(25): Show |
intron_variant | MODIFIER | c.349+99A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140103 | ||||||
chr7:139140128
|
A | G | 28 | a0001c0001t0012g0146a0001c0001t0012g0147a0001c0002t0001g0141others(25): Show | 29 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(26): Show |
intron_variant | MODIFIER | c.349+124A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140128 | ||||||
chr7:139140162
|
G | GTAAC | 10 | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0005g0049others(7): Show | 10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+161_349+164dup others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140162 | |||||
chr7:139140243
|
G | A | 1 | a0001c0001t0003g0190 | 1 | HG00597.hp1 | intron_variant | MODIFIER | c.349+239G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140243 | ||||||
chr7:139140440
|
G | C | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.349+436G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140440 | ||||||
chr7:139140458
|
T | TTAAAAA | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(144): Show | 168 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.349+457_349+458ins others(6): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140458 | |||||
chr7:139140462
|
G | A | 1 | a0001c0002t0005g0134 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.349+458G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140462 | ||||||
chr7:139140699
|
C | T | 22 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0057others(19): Show | 26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.349+695C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140699 | ||||||
chr7:139140700
|
G | A | 66 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(63): Show | 82 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.349+696G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140700 | ||||||
chr7:139140731
|
C | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(127): Show | 151 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.349+727C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140731 | ||||||
chr7:139140775
|
C | CA | 125 | a0001c0001t0001g0052a0001c0001t0001g0130a0001c0001t0002g0001others(122): Show | 156 | HG00140.hp1 HG00323.hp1 HG00323.hp2 others(153): Show |
intron_variant | MODIFIER | c.349+794dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140775 | |||||
chr7:139140775
|
C | CAA | 29 | a0001c0001t0001g0074a0001c0001t0002g0163a0001c0001t0002g0164others(26): Show | 29 | HG01175.hp1 HG01891.hp2 HG01928.hp1 others(26): Show |
intron_variant | MODIFIER | c.349+793_349+794dup others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140775 | |||||
chr7:139140775
|
C | CAAA | 39 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0057others(36): Show | 44 | HG00408.hp1 HG00544.hp1 HG00642.hp1 others(41): Show |
intron_variant | MODIFIER | c.349+792_349+794dup others(3): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140775 | |||||
chr7:139140775
|
C | CAAAA | 7 | a0001c0001t0001g0058a0001c0001t0001g0065a0001c0001t0001g0132others(4): Show | 7 | HG00438.hp1 HG01175.hp2 HG01891.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+791_349+794dup others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140775 | |||||
chr7:139140775
|
CAA | C | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+793_349+794del others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140775 | |||||
chr7:139140775
|
CAAAAAAA | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(63): Show | 82 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.349+788_349+794del others(7): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140775 | |||||
chr7:139140832
|
G | A | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.349+828G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140832 | ||||||
chr7:139140948
|
A | G | 10 | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0005g0049others(7): Show | 10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.349+944A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140948 | ||||||
chr7:139140951
|
C | CTTTTTTT others(2685): Show |
1 | a0001c0001t0001g0052 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.349+959_349+960ins others(2692): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140951 | |||||
chr7:139140951
|
C | CTTTTTTT others(2687): Show |
1 | a0001c0001t0005g0075 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.349+960_349+961ins others(2694): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140951 | |||||
chr7:139140951
|
C | CTTTTTTT others(2686): Show |
1 | a0001c0001t0005g0051 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.349+960_349+961ins others(2693): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140951 | |||||
chr7:139140951
|
C | CTTTTTTT others(2688): Show |
1 | a0001c0001t0005g0049 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.349+960_349+961ins others(2695): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140951 | |||||
chr7:139140951
|
C | CTTTTTTT others(2687): Show |
1 | a0001c0001t0005g0048 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.349+960_349+961ins others(2694): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140951 | |||||
chr7:139140951
|
C | CTTTTTTT others(2687): Show |
3 | a0001c0001t0005g0053a0001c0001t0005g0054a0001c0001t0005g0056 | 3 | HG02886.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.349+960_349+961ins others(2694): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140951 | |||||
chr7:139140951
|
C | CTTTTTTT others(2687): Show |
1 | a0001c0001t0005g0050 | 1 | HG01943.hp2 | intron_variant | MODIFIER | c.349+960_349+961ins others(2694): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140951 | |||||
chr7:139140951
|
C | CTTTTTTT others(2687): Show |
1 | a0001c0001t0005g0055 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.349+960_349+961ins others(2694): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140951 | |||||
chr7:139140951
|
CT | C | 22 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0057others(19): Show | 26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.349+961delT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139140951 | |||||
chr7:139140965
|
T | C | 3 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135 | 3 | HG03041.hp1 HG03195.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.349+961T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140965 | ||||||
chr7:139140966
|
A | T | 5 | a0001c0001t0001g0130a0001c0003t0013g0128a0001c0003t0013g0129others(2): Show | 5 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.349+962A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139140966 | ||||||
chr7:139141183
|
C | T | 1 | a0001c0001t0001g0019 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.350-1073C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141183 | ||||||
chr7:139141191
|
G | A | 1 | a0001c0001t0002g0174 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.350-1065G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141191 | ||||||
chr7:139141193
|
G | A | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-1063G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141193 | ||||||
chr7:139141218
|
G | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(134): Show | 158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.350-1038G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141218 | ||||||
chr7:139141256
|
GA | G | 11 | a0001c0001t0002g0250a0001c0001t0007g0149a0001c0001t0007g0150others(8): Show | 11 | HG01891.hp2 HG02109.hp1 HG02257.hp2 others(8): Show |
intron_variant | MODIFIER | c.350-984delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139141256 | |||||
chr7:139141256
|
GAA | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(134): Show | 158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.350-985_350-984del others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr7 | 139141256 | |||||
chr7:139141265
|
A | G | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.350-991A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141265 | ||||||
chr7:139141275
|
CAG | C | 3 | a0001c0001t0003g0245a0001c0001t0003g0246a0001c0001t0003g0247 | 3 | NA18944.hp2 NA18955.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.350-980_350-979del others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141275 | ||||||
chr7:139141407
|
C | A | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(144): Show | 168 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.350-849C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141407 | ||||||
chr7:139141467
|
G | T | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.350-789G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141467 | ||||||
chr7:139141499
|
A | C | 10 | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0005g0049others(7): Show | 10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.350-757A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141499 | ||||||
chr7:139141558
|
G | A | 66 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(63): Show | 82 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.350-698G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141558 | ||||||
chr7:139141764
|
G | A | 1 | a0001c0001t0021g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.350-492G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141764 | ||||||
chr7:139141951
|
C | T | 9 | a0001c0002t0004g0029a0001c0002t0004g0030a0001c0002t0004g0031others(6): Show | 9 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(6): Show |
intron_variant | MODIFIER | c.350-305C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139141951 | ||||||
chr7:139142167
|
G | A | 105 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(102): Show | 125 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(122): Show |
intron_variant | MODIFIER | c.350-89G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 4/17 | chr7 | 139142167 | ||||||
chr7:139142489
|
C | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.399+184C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139142489 | ||||||
chr7:139142552
|
T | TG | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.399+249dupG | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 139142552 | |||||
chr7:139142567
|
C | T | 22 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0057others(19): Show | 26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.399+262C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139142567 | ||||||
chr7:139142781
|
G | A | 66 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(63): Show | 82 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.399+476G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139142781 | ||||||
chr7:139142862
|
A | G | 1 | a0001c0001t0021g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.399+557A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139142862 | ||||||
chr7:139142944
|
T | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.399+639T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139142944 | ||||||
chr7:139143084
|
G | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.399+779G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139143084 | ||||||
chr7:139143171
|
C | T | 1 | a0001c0001t0001g0123 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.399+866C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139143171 | ||||||
chr7:139143426
|
CAT | C | 10 | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0005g0049others(7): Show | 10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.399+1126_399+1127d others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 139143426 | |||||
chr7:139143689
|
A | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.399+1384A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139143689 | ||||||
chr7:139143719
|
A | T | 10 | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0005g0049others(7): Show | 10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.399+1414A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139143719 | ||||||
chr7:139143751
|
C | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.399+1446C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139143751 | ||||||
chr7:139143805
|
A | C | 22 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0057others(19): Show | 26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.399+1500A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139143805 | ||||||
chr7:139143842
|
T | C | 2 | a0001c0001t0003g0022a0001c0001t0003g0260 | 3 | NA18955.hp2 NA18992.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.399+1537T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139143842 | ||||||
chr7:139143944
|
C | G | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.399+1639C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139143944 | ||||||
chr7:139143995
|
A | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(133): Show | 157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.399+1690A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139143995 | ||||||
chr7:139144037
|
T | C | 5 | a0001c0001t0001g0130a0001c0003t0013g0128a0001c0003t0013g0129others(2): Show | 5 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.399+1732T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139144037 | ||||||
chr7:139144187
|
G | C | 7 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0002t0001g0141others(4): Show | 7 | HG02109.hp2 HG02572.hp2 HG02818.hp1 others(4): Show |
intron_variant | MODIFIER | c.399+1882G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139144187 | ||||||
chr7:139144350
|
A | C | 1 | a0001c0002t0001g0145 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.399+2045A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139144350 | ||||||
chr7:139144360
|
T | C | 3 | a0001c0001t0001g0012a0001c0001t0001g0076a0001c0001t0001g0077 | 4 | HG03471.hp1 NA18522.hp1 NA18522.hp2 others(1): Show |
intron_variant | MODIFIER | c.399+2055T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139144360 | ||||||
chr7:139144379
|
T | G | 1 | a0001c0002t0004g0029 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.399+2074T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139144379 | ||||||
chr7:139144597
|
A | ATATG | 24 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0057others(21): Show | 28 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(25): Show |
intron_variant | MODIFIER | c.399+2311_399+2314d others(6): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 139144597 | |||||
chr7:139144699
|
A | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.399+2394A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139144699 | ||||||
chr7:139144719
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.399+2414C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139144719 | ||||||
chr7:139144741
|
C | T | 1 | a0001c0001t0003g0265 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.400-2404C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139144741 | ||||||
chr7:139145016
|
A | C | 2 | a0001c0001t0003g0243a0001c0001t0003g0244 | 2 | HG03490.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.400-2129A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145016 | ||||||
chr7:139145295
|
T | C | 2 | a0001c0001t0002g0256a0001c0001t0002g0257 | 2 | HG02602.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.400-1850T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145295 | ||||||
chr7:139145332
|
G | A | 1 | a0001c0001t0019g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.400-1813G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145332 | ||||||
chr7:139145380
|
GTCT | G | 63 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(60): Show | 79 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(76): Show |
intron_variant | MODIFIER | c.400-1762_400-1760d others(5): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 139145380 | |||||
chr7:139145461
|
G | A | 9 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(6): Show | 9 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.400-1684G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145461 | ||||||
chr7:139145470
|
G | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(134): Show | 158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.400-1675G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145470 | ||||||
chr7:139145510
|
T | C | 35 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0002t0001g0141others(32): Show | 36 | HG02015.hp2 HG02071.hp1 HG02109.hp2 others(33): Show |
intron_variant | MODIFIER | c.400-1635T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145510 | ||||||
chr7:139145583
|
C | G | 5 | a0001c0001t0001g0130a0001c0003t0013g0128a0001c0003t0013g0129others(2): Show | 5 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.400-1562C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145583 | ||||||
chr7:139145585
|
C | T | 1 | a0001c0001t0005g0051 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.400-1560C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145585 | ||||||
chr7:139145586
|
A | G | 132 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(129): Show | 153 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.400-1559A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145586 | ||||||
chr7:139145691
|
T | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(134): Show | 158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.400-1454T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139145691 | ||||||
chr7:139146161
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0021g0046 | 2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.400-984A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139146161 | ||||||
chr7:139146537
|
G | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(127): Show | 151 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.400-608G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139146537 | ||||||
chr7:139146735
|
C | T | 22 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0057others(19): Show | 26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.400-410C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139146735 | ||||||
chr7:139146766
|
C | CA | 115 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(112): Show | 140 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(137): Show |
intron_variant | MODIFIER | c.400-361dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 139146766 | |||||
chr7:139146766
|
C | CAA | 33 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0127others(30): Show | 34 | HG02015.hp2 HG02071.hp1 HG02109.hp2 others(31): Show |
intron_variant | MODIFIER | c.400-362_400-361dup others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 139146766 | |||||
chr7:139146766
|
CA | C | 13 | a0001c0001t0002g0174a0001c0001t0003g0195a0001c0001t0003g0242others(10): Show | 13 | HG02109.hp1 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.400-361delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | INFO_REALIGN_3_PRIME | chr7 | 139146766 | |||||
chr7:139146961
|
C | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(134): Show | 158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.400-184C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139146961 | ||||||
chr7:139146976
|
C | A | 2 | a0001c0001t0005g0051a0001c0001t0005g0075 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.400-169C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139146976 | ||||||
chr7:139147080
|
A | G | 5 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(2): Show | 5 | HG01891.hp1 HG02055.hp1 HG02258.hp2 others(2): Show |
intron_variant | MODIFIER | c.400-65A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 5/17 | chr7 | 139147080 | ||||||
chr7:139147361
|
T | A | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.545+71T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 6/17 | chr7 | 139147361 | ||||||
chr7:139147455
|
T | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.545+165T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 6/17 | chr7 | 139147455 | ||||||
chr7:139147721
|
G | A | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.545+431G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 6/17 | chr7 | 139147721 | ||||||
chr7:139147892
|
C | T | 10 | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0005g0049others(7): Show | 10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.546-314C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 6/17 | chr7 | 139147892 | ||||||
chr7:139148190
|
T | C | 22 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0057others(19): Show | 26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.546-16T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 6/17 | chr7 | 139148190 | ||||||
chr7:139148660
|
C | T | 1 | a0001c0001t0001g0085 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.717+283C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139148660 | ||||||
chr7:139148691
|
A | G | 214 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(211): Show | 244 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(241): Show |
intron_variant | MODIFIER | c.717+314A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139148691 | ||||||
chr7:139148817
|
G | C | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+440G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139148817 | ||||||
chr7:139148818
|
G | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.717+441G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139148818 | ||||||
chr7:139148822
|
G | A | 10 | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0005g0049others(7): Show | 10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.717+445G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139148822 | ||||||
chr7:139148887
|
C | T | 2 | a0001c0002t0005g0133a0001c0002t0005g0135 | 2 | HG03041.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.717+510C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139148887 | ||||||
chr7:139149133
|
A | G | 1 | a0001c0002t0011g0139 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.717+756A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149133 | ||||||
chr7:139149135
|
C | T | 7 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(4): Show | 7 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.717+758C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149135 | ||||||
chr7:139149191
|
G | A | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+814G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149191 | ||||||
chr7:139149230
|
G | A | 10 | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0005g0049others(7): Show | 10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.717+853G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149230 | ||||||
chr7:139149304
|
C | CA | 92 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(89): Show | 112 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(109): Show |
intron_variant | MODIFIER | c.717+943dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139149304 | |||||
chr7:139149304
|
CA | C | 10 | a0001c0001t0001g0126a0001c0001t0001g0127a0001c0001t0002g0223others(7): Show | 10 | HG02109.hp2 HG02572.hp2 HG02622.hp2 others(7): Show |
intron_variant | MODIFIER | c.717+943delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139149304 | |||||
chr7:139149304
|
CAA | C | 20 | a0001c0002t0004g0010a0001c0002t0004g0027a0001c0002t0004g0028others(17): Show | 21 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(18): Show |
intron_variant | MODIFIER | c.717+942_717+943del others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139149304 | |||||
chr7:139149458
|
C | A | 1 | a0001c0001t0002g0188 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.717+1081C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149458 | ||||||
chr7:139149563
|
T | A | 1 | a0001c0001t0001g0090 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.717+1186T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149563 | ||||||
chr7:139149584
|
C | G | 20 | a0001c0002t0004g0010a0001c0002t0004g0027a0001c0002t0004g0028others(17): Show | 21 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(18): Show |
intron_variant | MODIFIER | c.717+1207C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149584 | ||||||
chr7:139149765
|
G | A | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.717+1388G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149765 | ||||||
chr7:139149779
|
C | T | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+1402C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149779 | ||||||
chr7:139149884
|
A | G | 10 | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0005g0049others(7): Show | 10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.717+1507A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149884 | ||||||
chr7:139149906
|
A | G | 29 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0057others(26): Show | 33 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(30): Show |
intron_variant | MODIFIER | c.717+1529A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139149906 | ||||||
chr7:139150564
|
A | G | 1 | a0001c0001t0007g0149 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.717+2187A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139150564 | ||||||
chr7:139150596
|
G | A | 1 | a0001c0001t0021g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.717+2219G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139150596 | ||||||
chr7:139150734
|
A | G | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.717+2357A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139150734 | ||||||
chr7:139150769
|
G | A | 1 | a0001c0001t0021g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.717+2392G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139150769 | ||||||
chr7:139151141
|
A | G | 22 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0057others(19): Show | 26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.717+2764A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139151141 | ||||||
chr7:139151148
|
G | T | 1 | a0001c0003t0020g0131 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.717+2771G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139151148 | ||||||
chr7:139151602
|
T | C | 2 | a0001c0001t0001g0076a0001c0001t0021g0046 | 2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.717+3225T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139151602 | ||||||
chr7:139151629
|
A | G | 1 | a0001c0001t0002g0222 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.717+3252A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139151629 | ||||||
chr7:139151731
|
G | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.717+3354G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139151731 | ||||||
chr7:139151804
|
G | A | 1 | a0001c0001t0002g0204 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.717+3427G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139151804 | ||||||
chr7:139151870
|
T | C | 1 | a0001c0001t0001g0091 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.717+3493T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139151870 | ||||||
chr7:139152017
|
C | T | 1 | a0001c0002t0011g0138 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.717+3640C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139152017 | ||||||
chr7:139152061
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA18991.hp1 | intron_variant | MODIFIER | c.717+3684C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139152061 | ||||||
chr7:139152268
|
A | C | 2 | a0001c0001t0003g0203a0001c0001t0003g0241 | 2 | NA18940.hp2 NA18994.hp1 |
intron_variant | MODIFIER | c.717+3891A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139152268 | ||||||
chr7:139152420
|
C | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(127): Show | 151 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(148): Show |
intron_variant | MODIFIER | c.717+4043C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139152420 | ||||||
chr7:139152781
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(133): Show | 157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.717+4404G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139152781 | ||||||
chr7:139152878
|
G | A | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(144): Show | 168 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.717+4501G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139152878 | ||||||
chr7:139153097
|
C | T | 8 | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0005g0049others(5): Show | 8 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.717+4720C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153097 | ||||||
chr7:139153151
|
G | GA | 143 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(140): Show | 164 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(161): Show |
intron_variant | MODIFIER | c.717+4788dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139153151 | |||||
chr7:139153207
|
T | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.717+4830T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153207 | ||||||
chr7:139153446
|
C | CA | 134 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(131): Show | 153 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(150): Show |
intron_variant | MODIFIER | c.717+5083dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139153446 | |||||
chr7:139153446
|
C | T | 1 | a0001c0001t0008g0261 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.717+5069C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153446 | ||||||
chr7:139153549
|
C | A | 1 | a0001c0001t0003g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.717+5172C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153549 | ||||||
chr7:139153708
|
C | G | 1 | a0001c0001t0008g0221 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.717+5331C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153708 | ||||||
chr7:139153743
|
A | G | 1 | a0001c0001t0003g0194 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.717+5366A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153743 | ||||||
chr7:139153781
|
G | A | 27 | a0001c0001t0012g0146a0001c0001t0012g0147a0001c0002t0001g0141others(24): Show | 28 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(25): Show |
intron_variant | MODIFIER | c.717+5404G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153781 | ||||||
chr7:139153878
|
A | G | 27 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0057others(24): Show | 31 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.717+5501A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153878 | ||||||
chr7:139153881
|
G | A | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+5504G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153881 | ||||||
chr7:139153933
|
G | A | 1 | a0001c0001t0003g0267 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.717+5556G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139153933 | ||||||
chr7:139154340
|
A | G | 1 | a0001c0001t0007g0156 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.717+5963A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154340 | ||||||
chr7:139154353
|
C | CT | 75 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0052others(72): Show | 80 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(77): Show |
intron_variant | MODIFIER | c.717+5990dupT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139154353 | |||||
chr7:139154353
|
CT | C | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.717+5990delT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139154353 | |||||
chr7:139154392
|
G | A | 1 | a0001c0001t0002g0177 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.717+6015G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154392 | ||||||
chr7:139154411
|
T | C | 1 | a0001c0002t0004g0039 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.717+6034T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154411 | ||||||
chr7:139154665
|
C | A | 1 | a0001c0001t0002g0186 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.718-6283C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154665 | ||||||
chr7:139154680
|
C | A | 13 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0018others(10): Show | 16 | HG00140.hp2 HG01074.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.718-6268C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154680 | ||||||
chr7:139154686
|
C | T | 10 | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0005g0049others(7): Show | 10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.718-6262C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154686 | ||||||
chr7:139154819
|
G | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.718-6129G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154819 | ||||||
chr7:139154830
|
A | G | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-6118A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154830 | ||||||
chr7:139154966
|
G | GTTTTTTT | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-5977_718-5976i others(9): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139154966 | |||||
chr7:139154972
|
C | T | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-5976C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154972 | ||||||
chr7:139154973
|
C | T | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-5975C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139154973 | ||||||
chr7:139155095
|
C | T | 1 | a0001c0002t0004g0044 | 1 | NA19074.hp2 | intron_variant | MODIFIER | c.718-5853C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139155095 | ||||||
chr7:139155316
|
C | T | 137 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(134): Show | 158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.718-5632C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139155316 | ||||||
chr7:139155457
|
T | G | 1 | a0001c0001t0021g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.718-5491T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139155457 | ||||||
chr7:139155525
|
A | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(134): Show | 158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.718-5423A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139155525 | ||||||
chr7:139155532
|
A | G | 2 | a0001c0001t0003g0184a0001c0001t0003g0254 | 2 | NA19006.hp2 NA19010.hp2 |
intron_variant | MODIFIER | c.718-5416A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139155532 | ||||||
chr7:139155751
|
T | C | 1 | a0001c0001t0002g0205 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.718-5197T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139155751 | ||||||
chr7:139155773
|
G | A | 6 | a0001c0001t0003g0203a0001c0001t0003g0225a0001c0001t0003g0241others(3): Show | 6 | NA18940.hp2 NA18944.hp2 NA18955.hp1 others(3): Show |
intron_variant | MODIFIER | c.718-5175G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139155773 | ||||||
chr7:139155773
|
G | T | 136 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(133): Show | 157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.718-5175G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139155773 | ||||||
chr7:139156362
|
C | T | 1 | a0001c0001t0002g0220 | 1 | NA18989.hp1 | intron_variant | MODIFIER | c.718-4586C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139156362 | ||||||
chr7:139156389
|
CT | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(134): Show | 158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.718-4549delT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139156389 | |||||
chr7:139156423
|
T | C | 27 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0057others(24): Show | 31 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.718-4525T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139156423 | ||||||
chr7:139156463
|
A | G | 2 | a0001c0001t0001g0091a0001c0001t0001g0117 | 2 | HG01243.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.718-4485A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139156463 | ||||||
chr7:139156499
|
C | T | 27 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0057others(24): Show | 31 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(28): Show |
intron_variant | MODIFIER | c.718-4449C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139156499 | ||||||
chr7:139156611
|
C | A | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(126): Show | 150 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.718-4337C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139156611 | ||||||
chr7:139156784
|
A | T | 5 | a0001c0001t0003g0172a0001c0001t0003g0173a0001c0001t0003g0236others(2): Show | 5 | NA18939.hp1 NA18941.hp1 NA18975.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-4164A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139156784 | ||||||
chr7:139156845
|
C | T | 1 | a0001c0001t0012g0147 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.718-4103C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139156845 | ||||||
chr7:139156982
|
C | A | 1 | a0001c0001t0001g0067 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.718-3966C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139156982 | ||||||
chr7:139157058
|
G | A | 137 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(134): Show | 158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.718-3890G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139157058 | ||||||
chr7:139157139
|
C | CT | 127 | a0001c0001t0001g0066a0001c0001t0001g0072a0001c0001t0001g0073others(124): Show | 158 | HG00323.hp1 HG00323.hp2 HG00438.hp2 others(155): Show |
intron_variant | MODIFIER | c.718-3785dupT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139157139 | |||||
chr7:139157139
|
CTT | C | 16 | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0005g0049others(13): Show | 16 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.718-3786_718-3785d others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139157139 | |||||
chr7:139157139
|
CTTT | C | 29 | a0001c0002t0001g0145a0001c0002t0004g0010a0001c0002t0004g0027others(26): Show | 30 | HG02015.hp2 HG02071.hp1 HG02258.hp1 others(27): Show |
intron_variant | MODIFIER | c.718-3787_718-3785d others(5): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139157139 | |||||
chr7:139157139
|
CTTTTTTT others(2): Show |
C | 64 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(61): Show | 80 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.718-3793_718-3785d others(11): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139157139 | |||||
chr7:139157139
|
CTTTTTTT others(3): Show |
C | 1 | a0001c0001t0001g0093 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.718-3794_718-3785d others(12): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139157139 | |||||
chr7:139157139
|
CTTTTTTT others(7): Show |
C | 5 | a0001c0001t0001g0130a0001c0003t0013g0128a0001c0003t0013g0129others(2): Show | 5 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(2): Show |
intron_variant | MODIFIER | c.718-3798_718-3785d others(16): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139157139 | |||||
chr7:139157146
|
T | C | 4 | a0001c0001t0001g0052a0001c0001t0005g0053a0001c0001t0005g0054others(1): Show | 4 | HG02257.hp1 HG02886.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.718-3802T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139157146 | ||||||
chr7:139157249
|
C | T | 1 | a0001c0002t0004g0043 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.718-3699C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139157249 | ||||||
chr7:139157290
|
A | G | 137 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(134): Show | 158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.718-3658A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139157290 | ||||||
chr7:139157306
|
C | T | 1 | a0001c0001t0001g0089 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.718-3642C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139157306 | ||||||
chr7:139157495
|
A | AT | 91 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(88): Show | 106 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(103): Show |
intron_variant | MODIFIER | c.718-3430dupT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139157495 | |||||
chr7:139157495
|
A | ATT | 11 | a0001c0001t0001g0047a0001c0001t0001g0078a0001c0001t0001g0079others(8): Show | 11 | HG01928.hp2 HG01952.hp2 HG02109.hp2 others(8): Show |
intron_variant | MODIFIER | c.718-3431_718-3430d others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139157495 | |||||
chr7:139157495
|
AT | A | 27 | a0001c0001t0002g0157a0001c0001t0002g0206a0001c0001t0002g0209others(24): Show | 28 | HG00597.hp2 HG01070.hp2 HG02071.hp1 others(25): Show |
intron_variant | MODIFIER | c.718-3430delT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139157495 | |||||
chr7:139157734
|
G | A | 1 | a0001c0003t0013g0129 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.718-3214G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139157734 | ||||||
chr7:139157769
|
A | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.718-3179A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139157769 | ||||||
chr7:139157819
|
T | C | 1 | a0001c0001t0001g0089 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.718-3129T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139157819 | ||||||
chr7:139157949
|
G | A | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-2999G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139157949 | ||||||
chr7:139158114
|
C | T | 4 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0002t0001g0143others(1): Show | 4 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.718-2834C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139158114 | ||||||
chr7:139158270
|
C | T | 1 | a0001c0001t0001g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.718-2678C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139158270 | ||||||
chr7:139158271
|
G | A | 9 | a0001c0001t0012g0146a0001c0001t0012g0147a0001c0002t0005g0133others(6): Show | 9 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(6): Show |
intron_variant | MODIFIER | c.718-2677G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139158271 | ||||||
chr7:139158313
|
C | CAAAAAAA others(4): Show |
4 | a0001c0001t0005g0048a0001c0001t0005g0049a0001c0001t0005g0050others(1): Show | 4 | HG01943.hp2 HG02145.hp1 HG03209.hp2 others(1): Show |
intron_variant | MODIFIER | c.718-2633_718-2623d others(13): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139158313 | |||||
chr7:139158313
|
C | CAAAAAAA others(5): Show |
36 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0052others(33): Show | 40 | HG00408.hp1 HG00438.hp1 HG00673.hp2 others(37): Show |
intron_variant | MODIFIER | c.718-2634_718-2623d others(14): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139158313 | |||||
chr7:139158313
|
C | CAAAAAAA others(6): Show |
24 | a0001c0001t0001g0057a0001c0001t0001g0058a0001c0001t0001g0060others(21): Show | 25 | HG00544.hp1 HG00642.hp1 HG02055.hp2 others(22): Show |
intron_variant | MODIFIER | c.718-2623_718-2622i others(15): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139158313 | |||||
chr7:139158313
|
C | CAAAAAAA others(7): Show |
4 | a0001c0002t0004g0027a0001c0002t0004g0033a0001c0002t0004g0040others(1): Show | 4 | HG02258.hp1 HG02300.hp1 NA18993.hp2 others(1): Show |
intron_variant | MODIFIER | c.718-2623_718-2622i others(16): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139158313 | |||||
chr7:139158313
|
C | CAAAAAAA others(8): Show |
7 | a0001c0001t0001g0091a0001c0001t0001g0113a0001c0001t0001g0116others(4): Show | 7 | HG01243.hp2 HG02280.hp2 HG02615.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-2623_718-2622i others(17): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139158313 | |||||
chr7:139158313
|
C | CAAAAAAA others(9): Show |
37 | a0001c0001t0001g0002a0001c0001t0001g0012a0001c0001t0001g0013others(34): Show | 51 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(48): Show |
intron_variant | MODIFIER | c.718-2623_718-2622i others(18): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139158313 | |||||
chr7:139158313
|
C | CAAAAAAA others(10): Show |
24 | a0001c0001t0001g0007a0001c0001t0001g0047a0001c0001t0001g0077others(21): Show | 26 | HG00621.hp1 HG01952.hp2 HG02027.hp1 others(23): Show |
intron_variant | MODIFIER | c.718-2623_718-2622i others(19): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139158313 | |||||
chr7:139158313
|
C | CAAAAAAA others(11): Show |
1 | a0001c0001t0001g0078 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.718-2623_718-2622i others(20): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139158313 | |||||
chr7:139158391
|
T | C | 2 | a0001c0002t0011g0138a0001c0002t0011g0139 | 2 | HG02572.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.718-2557T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139158391 | ||||||
chr7:139158783
|
G | A | 5 | a0001c0001t0002g0176a0001c0001t0002g0181a0001c0001t0002g0196others(2): Show | 5 | HG02647.hp1 HG02886.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.718-2165G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139158783 | ||||||
chr7:139158787
|
A | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.718-2161A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139158787 | ||||||
chr7:139158833
|
G | C | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-2115G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139158833 | ||||||
chr7:139158871
|
G | A | 8 | a0001c0001t0002g0174a0001c0002t0005g0133a0001c0002t0005g0134others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.718-2077G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139158871 | ||||||
chr7:139158941
|
G | A | 2 | a0001c0001t0001g0094a0001c0001t0002g0163 | 2 | HG01928.hp1 HG02486.hp1 |
intron_variant | MODIFIER | c.718-2007G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139158941 | ||||||
chr7:139159149
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0021g0046 | 2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.718-1799A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139159149 | ||||||
chr7:139159201
|
G | A | 22 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0057others(19): Show | 26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.718-1747G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139159201 | ||||||
chr7:139159222
|
A | T | 21 | a0001c0002t0004g0010a0001c0002t0004g0027a0001c0002t0004g0028others(18): Show | 22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.718-1726A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139159222 | ||||||
chr7:139159417
|
G | A | 120 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(117): Show | 141 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(138): Show |
intron_variant | MODIFIER | c.718-1531G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139159417 | ||||||
chr7:139159501
|
G | A | 7 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(4): Show | 7 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.718-1447G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139159501 | ||||||
chr7:139159956
|
C | T | 1 | a0001c0001t0021g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.718-992C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139159956 | ||||||
chr7:139159981
|
G | A | 9 | a0001c0001t0001g0058a0001c0001t0001g0060a0001c0001t0001g0067others(6): Show | 9 | HG02055.hp2 HG02280.hp2 HG02615.hp2 others(6): Show |
intron_variant | MODIFIER | c.718-967G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139159981 | ||||||
chr7:139160017
|
A | G | 1 | a0001c0001t0001g0052 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.718-931A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139160017 | ||||||
chr7:139160123
|
A | T | 7 | a0001c0001t0003g0203a0001c0001t0003g0225a0001c0001t0003g0232others(4): Show | 7 | NA18940.hp2 NA18944.hp2 NA18950.hp1 others(4): Show |
intron_variant | MODIFIER | c.718-825A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139160123 | ||||||
chr7:139160433
|
C | CT | 22 | a0001c0001t0007g0149a0001c0002t0004g0010a0001c0002t0004g0027others(19): Show | 23 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(20): Show |
intron_variant | MODIFIER | c.718-498dupT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139160433 | |||||
chr7:139160433
|
CT | C | 111 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(108): Show | 131 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(128): Show |
intron_variant | MODIFIER | c.718-498delT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | INFO_REALIGN_3_PRIME | chr7 | 139160433 | |||||
chr7:139160618
|
A | G | 182 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(179): Show | 210 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.718-330A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139160618 | ||||||
chr7:139160657
|
C | T | 1 | a0001c0001t0001g0071 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.718-291C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139160657 | ||||||
chr7:139160683
|
G | A | 1 | a0001c0001t0001g0102 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.718-265G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139160683 | ||||||
chr7:139160732
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0021g0046 | 2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.718-216G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139160732 | ||||||
chr7:139160742
|
A | T | 1 | a0001c0002t0001g0142 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.718-206A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 7/17 | chr7 | 139160742 | ||||||
chr7:139161186
|
T | A | 28 | a0001c0001t0012g0146a0001c0001t0012g0147a0001c0002t0001g0141others(25): Show | 29 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(26): Show |
intron_variant | MODIFIER | c.792+164T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139161186 | ||||||
chr7:139161510
|
T | C | 10 | a0001c0001t0001g0052a0001c0001t0005g0048a0001c0001t0005g0049others(7): Show | 10 | HG01943.hp2 HG02145.hp1 HG02257.hp1 others(7): Show |
intron_variant | MODIFIER | c.792+488T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139161510 | ||||||
chr7:139161603
|
G | T | 1 | a0001c0001t0002g0273 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.792+581G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139161603 | ||||||
chr7:139161731
|
A | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(61): Show | 80 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.792+709A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139161731 | ||||||
chr7:139161743
|
T | C | 21 | a0001c0002t0004g0010a0001c0002t0004g0027a0001c0002t0004g0028others(18): Show | 22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.792+721T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139161743 | ||||||
chr7:139161826
|
A | C | 23 | a0001c0001t0012g0146a0001c0001t0012g0147a0001c0002t0004g0010others(20): Show | 24 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(21): Show |
intron_variant | MODIFIER | c.792+804A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139161826 | ||||||
chr7:139162145
|
A | G | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.792+1123A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139162145 | ||||||
chr7:139162454
|
C | G | 1 | a0001c0002t0004g0010 | 2 | NA18939.hp2 NA18987.hp2 |
intron_variant | MODIFIER | c.792+1432C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139162454 | ||||||
chr7:139162627
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(133): Show | 157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.792+1605G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139162627 | ||||||
chr7:139162730
|
G | A | 1 | a0001c0001t0002g0158 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.792+1708G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139162730 | ||||||
chr7:139162749
|
A | G | 22 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0057others(19): Show | 26 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(23): Show |
intron_variant | MODIFIER | c.792+1727A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139162749 | ||||||
chr7:139162972
|
A | G | 1 | a0001c0001t0001g0127 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.792+1950A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139162972 | ||||||
chr7:139162984
|
G | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0160 | 4 | HG00621.hp1 NA18747.hp1 NA18951.hp1 others(1): Show |
intron_variant | MODIFIER | c.792+1962G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139162984 | ||||||
chr7:139163111
|
G | A | 23 | a0001c0001t0012g0146a0001c0001t0012g0147a0001c0002t0004g0010others(20): Show | 24 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(21): Show |
intron_variant | MODIFIER | c.793-2021G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139163111 | ||||||
chr7:139163141
|
G | A | 1 | a0001c0001t0003g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.793-1991G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139163141 | ||||||
chr7:139163296
|
C | T | 2 | a0001c0001t0001g0057a0001c0001t0001g0064 | 2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.793-1836C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139163296 | ||||||
chr7:139163329
|
G | A | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.793-1803G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139163329 | ||||||
chr7:139163340
|
T | TA | 5 | a0001c0001t0001g0016a0001c0001t0001g0087a0001c0001t0001g0093others(2): Show | 6 | HG02451.hp1 HG02630.hp2 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.793-1777dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | INFO_REALIGN_3_PRIME | chr7 | 139163340 | |||||
chr7:139163673
|
A | G | 1 | a0001c0002t0001g0145 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.793-1459A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139163673 | ||||||
chr7:139163856
|
A | G | 23 | a0001c0001t0012g0146a0001c0001t0012g0147a0001c0002t0004g0010others(20): Show | 24 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(21): Show |
intron_variant | MODIFIER | c.793-1276A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139163856 | ||||||
chr7:139163967
|
T | G | 1 | a0001c0002t0001g0145 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.793-1165T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139163967 | ||||||
chr7:139164054
|
T | C | 8 | a0001c0001t0003g0192a0001c0002t0005g0133a0001c0002t0005g0134others(5): Show | 8 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(5): Show |
intron_variant | MODIFIER | c.793-1078T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139164054 | ||||||
chr7:139164055
|
G | A | 5 | a0001c0001t0002g0176a0001c0001t0002g0181a0001c0001t0002g0196others(2): Show | 5 | HG02647.hp1 HG02886.hp1 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.793-1077G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139164055 | ||||||
chr7:139164470
|
G | C | 1 | a0001c0002t0004g0028 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.793-662G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139164470 | ||||||
chr7:139164537
|
G | T | 21 | a0001c0002t0004g0010a0001c0002t0004g0027a0001c0002t0004g0028others(18): Show | 22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.793-595G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139164537 | ||||||
chr7:139164575
|
C | T | 2 | a0001c0001t0003g0239a0001c0001t0003g0240 | 2 | HG02074.hp2 HG02083.hp1 |
intron_variant | MODIFIER | c.793-557C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139164575 | ||||||
chr7:139164796
|
G | T | 21 | a0001c0002t0004g0010a0001c0002t0004g0027a0001c0002t0004g0028others(18): Show | 22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.793-336G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139164796 | ||||||
chr7:139164939
|
G | A | 1 | a0001c0001t0003g0233 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.793-193G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139164939 | ||||||
chr7:139165053
|
T | C | 21 | a0001c0002t0004g0010a0001c0002t0004g0027a0001c0002t0004g0028others(18): Show | 22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.793-79T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 8/17 | chr7 | 139165053 | ||||||
chr7:139165275
|
T | A | 2 | a0001c0001t0002g0250a0001c0001t0002g0266 | 2 | HG02129.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.895+41T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139165275 | ||||||
chr7:139165579
|
A | G | 2 | a0001c0001t0010g0154a0001c0001t0010g0155 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.895+345A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139165579 | ||||||
chr7:139165903
|
A | G | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.895+669A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139165903 | ||||||
chr7:139166034
|
C | T | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(144): Show | 168 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.895+800C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139166034 | ||||||
chr7:139166168
|
G | C | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.896-672G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139166168 | ||||||
chr7:139166221
|
G | A | 65 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(62): Show | 81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.896-619G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139166221 | ||||||
chr7:139166248
|
G | A | 131 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(128): Show | 152 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(149): Show |
intron_variant | MODIFIER | c.896-592G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139166248 | ||||||
chr7:139166419
|
A | C | 21 | a0001c0002t0004g0010a0001c0002t0004g0027a0001c0002t0004g0028others(18): Show | 22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.896-421A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139166419 | ||||||
chr7:139166517
|
AAT | A | 51 | a0001c0001t0002g0250a0001c0001t0005g0048a0001c0001t0005g0049others(48): Show | 52 | HG01943.hp2 HG02015.hp2 HG02071.hp1 others(49): Show |
intron_variant | MODIFIER | c.896-310_896-309del others(2): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 139166517 | |||||
chr7:139166517
|
AATAT | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(85): Show | 108 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.896-312_896-309del others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | INFO_REALIGN_3_PRIME | chr7 | 139166517 | |||||
chr7:139166556
|
TG | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(62): Show | 81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.896-283delG | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139166556 | ||||||
chr7:139166633
|
C | T | 2 | a0001c0001t0002g0180a0001c0001t0002g0216 | 2 | HG02559.hp2 NA20805.hp1 |
intron_variant | MODIFIER | c.896-207C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139166633 | ||||||
chr7:139166681
|
A | G | 12 | a0001c0001t0003g0191a0001c0001t0003g0192a0001c0001t0003g0193others(9): Show | 12 | HG01891.hp1 HG02055.hp1 HG02258.hp1 others(9): Show |
intron_variant | MODIFIER | c.896-159A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139166681 | ||||||
chr7:139166775
|
G | C | 2 | a0001c0001t0002g0250a0001c0001t0002g0266 | 2 | HG02129.hp2 NA19075.hp2 |
intron_variant | MODIFIER | c.896-65G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 9/17 | chr7 | 139166775 | ||||||
chr7:139166968
|
G | T | 1 | a0001c0001t0002g0177 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.951+73G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139166968 | ||||||
chr7:139166969
|
T | A | 1 | a0001c0001t0002g0177 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.951+74T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139166969 | ||||||
chr7:139167029
|
A | G | 1 | a0001c0001t0001g0047 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.951+134A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167029 | ||||||
chr7:139167426
|
G | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.951+531G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167426 | ||||||
chr7:139167605
|
T | A | 21 | a0001c0002t0004g0010a0001c0002t0004g0027a0001c0002t0004g0028others(18): Show | 22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.951+710T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167605 | ||||||
chr7:139167703
|
C | T | 95 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(92): Show | 115 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.952-641C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167703 | ||||||
chr7:139167767
|
C | T | 5 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0002t0001g0143others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.952-577C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167767 | ||||||
chr7:139167839
|
G | C | 1 | a0001c0003t0017g0088 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.952-505G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167839 | ||||||
chr7:139167876
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0021g0046 | 2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.952-468G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167876 | ||||||
chr7:139167887
|
G | A | 1 | a0001c0002t0001g0145 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.952-457G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167887 | ||||||
chr7:139167940
|
CA | C | 139 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(136): Show | 160 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.952-389delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr7 | 139167940 | |||||
chr7:139167980
|
G | T | 21 | a0001c0002t0004g0010a0001c0002t0004g0027a0001c0002t0004g0028others(18): Show | 22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.952-364G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167980 | ||||||
chr7:139167984
|
T | C | 1 | a0001c0001t0003g0239 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.952-360T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139167984 | ||||||
chr7:139168112
|
T | C | 1 | a0001c0001t0006g0061 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.952-232T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139168112 | ||||||
chr7:139168149
|
T | C | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.952-195T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139168149 | ||||||
chr7:139168217
|
C | T | 2 | a0001c0001t0003g0022a0001c0001t0003g0260 | 3 | NA18955.hp2 NA18992.hp1 NA19005.hp2 |
intron_variant | MODIFIER | c.952-127C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139168217 | ||||||
chr7:139168285
|
T | G | 1 | a0001c0001t0001g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.952-59T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 10/17 | chr7 | 139168285 | ||||||
chr7:139168569
|
C | CA | 14 | a0001c0001t0002g0003a0001c0001t0002g0026a0001c0001t0002g0162others(11): Show | 20 | HG00140.hp1 HG01256.hp2 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.1005+184dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 139168569 | |||||
chr7:139168569
|
CA | C | 129 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(126): Show | 150 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(147): Show |
intron_variant | MODIFIER | c.1005+184delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 11/17 | INFO_REALIGN_3_PRIME | chr7 | 139168569 | |||||
chr7:139168581
|
AC | A | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1005+185delC | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 11/17 | chr7 | 139168581 | ||||||
chr7:139168582
|
C | A | 1 | a0001c0001t0003g0270 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.1005+185C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 11/17 | chr7 | 139168582 | ||||||
chr7:139168754
|
A | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1005+357A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 11/17 | chr7 | 139168754 | ||||||
chr7:139168981
|
G | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1006-308G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 11/17 | chr7 | 139168981 | ||||||
chr7:139169208
|
C | A | 1 | a0001c0001t0008g0221 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.1006-81C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 11/17 | chr7 | 139169208 | ||||||
chr7:139169687
|
C | T | 2 | a0001c0001t0002g0256a0001c0001t0002g0257 | 2 | HG02602.hp1 HG02698.hp2 |
intron_variant | MODIFIER | c.1069+335C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139169687 | ||||||
chr7:139169757
|
T | G | 22 | a0001c0002t0004g0010a0001c0002t0004g0027a0001c0002t0004g0028others(19): Show | 23 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(20): Show |
intron_variant | MODIFIER | c.1069+405T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139169757 | ||||||
chr7:139169933
|
G | C | 3 | a0001c0001t0002g0023a0001c0001t0002g0210a0001c0001t0002g0211 | 4 | HG00609.hp1 HG02083.hp2 NA18612.hp2 others(1): Show |
intron_variant | MODIFIER | c.1069+581G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139169933 | ||||||
chr7:139169988
|
T | C | 213 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(210): Show | 243 | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(240): Show |
intron_variant | MODIFIER | c.1069+636T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139169988 | ||||||
chr7:139170463
|
A | G | 11 | a0001c0001t0002g0004a0001c0001t0002g0023a0001c0001t0002g0024others(8): Show | 18 | HG00609.hp1 HG00621.hp2 HG02083.hp2 others(15): Show |
intron_variant | MODIFIER | c.1069+1111A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139170463 | ||||||
chr7:139170547
|
C | T | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1069+1195C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139170547 | ||||||
chr7:139170564
|
TG | T | 29 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0015others(26): Show | 39 | HG00408.hp2 HG00544.hp2 HG00609.hp2 others(36): Show |
intron_variant | MODIFIER | c.1069+1215delG | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139170564 | |||||
chr7:139170706
|
A | C | 3 | a0001c0001t0009g0168a0001c0001t0009g0169a0001c0001t0009g0170 | 3 | HG01243.hp1 HG01361.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1069+1354A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139170706 | ||||||
chr7:139170930
|
T | A | 1 | a0001c0001t0001g0089 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1069+1578T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139170930 | ||||||
chr7:139171034
|
T | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1069+1682T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139171034 | ||||||
chr7:139171083
|
A | G | 95 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(92): Show | 115 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(112): Show |
intron_variant | MODIFIER | c.1069+1731A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139171083 | ||||||
chr7:139171487
|
C | T | 1 | a0001c0001t0005g0075 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.1069+2135C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139171487 | ||||||
chr7:139171549
|
T | A | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1069+2197T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139171549 | ||||||
chr7:139171588
|
A | G | 2 | a0001c0001t0001g0076a0001c0001t0021g0046 | 2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1069+2236A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139171588 | ||||||
chr7:139171684
|
C | T | 2 | a0001c0001t0001g0011a0001c0001t0001g0073 | 3 | HG03017.hp1 HG03704.hp2 HG03710.hp2 |
intron_variant | MODIFIER | c.1069+2332C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139171684 | ||||||
chr7:139171803
|
G | A | 1 | a0001c0001t0012g0146 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.1069+2451G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139171803 | ||||||
chr7:139171907
|
G | C | 2 | a0001c0001t0001g0076a0001c0001t0021g0046 | 2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1069+2555G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139171907 | ||||||
chr7:139172079
|
C | A | 2 | a0001c0001t0007g0149a0001c0001t0015g0148 | 2 | HG02818.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1069+2727C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172079 | ||||||
chr7:139172144
|
AATT | A | 33 | a0001c0001t0001g0057a0001c0001t0012g0146a0001c0001t0012g0147others(30): Show | 34 | HG02015.hp2 HG02071.hp1 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.1069+2794_1069+279 others(7): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139172144 | |||||
chr7:139172144
|
AATTAC | A | 10 | a0001c0001t0001g0110a0001c0001t0005g0048a0001c0001t0005g0049others(7): Show | 10 | HG00408.hp2 HG01943.hp2 HG02145.hp1 others(7): Show |
intron_variant | MODIFIER | c.1069+2793_1069+279 others(9): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172144 | ||||||
chr7:139172145
|
ATTAC | A | 95 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(92): Show | 115 | HG00140.hp2 HG00408.hp1 HG00438.hp1 others(112): Show |
intron_variant | MODIFIER | c.1069+2797_1069+280 others(8): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139172145 | |||||
chr7:139172149
|
C | A | 33 | a0001c0001t0001g0057a0001c0001t0012g0146a0001c0001t0012g0147others(30): Show | 34 | HG02015.hp2 HG02071.hp1 HG02258.hp1 others(31): Show |
intron_variant | MODIFIER | c.1069+2797C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172149 | ||||||
chr7:139172236
|
C | T | 1 | a0001c0001t0005g0051 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1069+2884C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172236 | ||||||
chr7:139172267
|
TTCCTGCC others(24): Show |
T | 1 | a0001c0001t0001g0065 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2916_1069+294 others(35): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172267 | ||||||
chr7:139172299
|
A | C | 1 | a0001c0001t0001g0065 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2947A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172299 | ||||||
chr7:139172302
|
T | A | 1 | a0001c0001t0001g0065 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2950T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172302 | ||||||
chr7:139172330
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2978G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172330 | ||||||
chr7:139172334
|
A | C | 1 | a0001c0001t0001g0065 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2982A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172334 | ||||||
chr7:139172335
|
C | A | 1 | a0001c0001t0001g0065 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2983C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172335 | ||||||
chr7:139172337
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2985A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172337 | ||||||
chr7:139172340
|
C | G | 3 | a0001c0004t0001g0086a0001c0004t0001g0104a0001c0004t0001g0114 | 3 | NA19003.hp1 NA19010.hp1 NA19076.hp1 |
intron_variant | MODIFIER | c.1069+2988C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172340 | ||||||
chr7:139172340
|
C | T | 1 | a0001c0001t0001g0065 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2988C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172340 | ||||||
chr7:139172341
|
C | G | 1 | a0001c0001t0001g0065 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2989C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172341 | ||||||
chr7:139172343
|
A | G | 1 | a0001c0001t0001g0065 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2991A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172343 | ||||||
chr7:139172344
|
A | T | 1 | a0001c0001t0001g0065 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2992A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172344 | ||||||
chr7:139172350
|
T | C | 1 | a0001c0001t0001g0065 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2998T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172350 | ||||||
chr7:139172351
|
A | T | 1 | a0001c0001t0001g0065 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+2999A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172351 | ||||||
chr7:139172375
|
G | A | 1 | a0001c0001t0001g0065 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+3023G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172375 | ||||||
chr7:139172381
|
C | CCTCTACA others(21): Show |
1 | a0001c0001t0001g0065 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.1069+3033_1069+303 others(32): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139172381 | |||||
chr7:139172463
|
C | T | 1 | a0001c0001t0001g0130 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1069+3111C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172463 | ||||||
chr7:139172527
|
G | A | 1 | a0001c0001t0002g0165 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.1069+3175G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172527 | ||||||
chr7:139172563
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(62): Show | 81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1069+3211C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172563 | ||||||
chr7:139172700
|
A | G | 1 | a0001c0001t0001g0081 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.1069+3348A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172700 | ||||||
chr7:139172747
|
C | T | 1 | a0001c0001t0005g0051 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.1069+3395C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139172747 | ||||||
chr7:139173024
|
G | T | 140 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(137): Show | 161 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(158): Show |
intron_variant | MODIFIER | c.1069+3672G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139173024 | ||||||
chr7:139173136
|
C | T | 1 | a0001c0001t0002g0204 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.1069+3784C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139173136 | ||||||
chr7:139173145
|
G | C | 1 | a0001c0001t0003g0239 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.1069+3793G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139173145 | ||||||
chr7:139173225
|
C | CT | 10 | a0001c0001t0001g0065a0001c0001t0001g0109a0001c0001t0002g0178others(7): Show | 10 | HG02451.hp2 HG02486.hp2 HG02895.hp1 others(7): Show |
intron_variant | MODIFIER | c.1069+3892dupT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139173225 | |||||
chr7:139173268
|
C | T | 3 | a0001c0001t0005g0053a0001c0001t0005g0054a0001c0001t0005g0056 | 3 | HG02886.hp2 HG02896.hp1 HG02897.hp2 |
intron_variant | MODIFIER | c.1069+3916C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139173268 | ||||||
chr7:139173330
|
C | T | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1069+3978C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139173330 | ||||||
chr7:139173464
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1069+4112G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139173464 | ||||||
chr7:139173524
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(62): Show | 81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1069+4172C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139173524 | ||||||
chr7:139173587
|
G | T | 9 | a0001c0001t0005g0048a0001c0001t0005g0049a0001c0001t0005g0050others(6): Show | 9 | HG01943.hp2 HG02145.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1069+4235G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139173587 | ||||||
chr7:139173665
|
G | C | 1 | a0001c0001t0002g0200 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.1069+4313G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139173665 | ||||||
chr7:139174011
|
A | C | 116 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(113): Show | 137 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(134): Show |
intron_variant | MODIFIER | c.1070-4203A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174011 | ||||||
chr7:139174092
|
G | A | 1 | a0001c0001t0002g0166 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1070-4122G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174092 | ||||||
chr7:139174109
|
G | A | 88 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(85): Show | 108 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1070-4105G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174109 | ||||||
chr7:139174277
|
C | T | 1 | a0001c0001t0001g0077 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1070-3937C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174277 | ||||||
chr7:139174385
|
G | A | 1 | a0001c0002t0004g0041 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1070-3829G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174385 | ||||||
chr7:139174403
|
A | G | 2 | a0001c0001t0005g0051a0001c0001t0005g0075 | 2 | HG03195.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1070-3811A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174403 | ||||||
chr7:139174421
|
A | T | 1 | a0001c0001t0001g0099 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.1070-3793A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174421 | ||||||
chr7:139174481
|
G | A | 2 | a0001c0001t0007g0150a0001c0001t0007g0156 | 2 | HG02257.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.1070-3733G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174481 | ||||||
chr7:139174560
|
ACAAT | A | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1070-3650_1070-364 others(8): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139174560 | |||||
chr7:139174565
|
C | A | 1 | a0001c0003t0017g0088 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.1070-3649C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174565 | ||||||
chr7:139174622
|
A | G | 2 | a0001c0001t0001g0126a0001c0001t0001g0127 | 2 | HG02109.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1070-3592A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174622 | ||||||
chr7:139174743
|
G | A | 2 | a0001c0001t0001g0081a0001c0001t0001g0099 | 2 | HG02056.hp1 NA18995.hp2 |
intron_variant | MODIFIER | c.1070-3471G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174743 | ||||||
chr7:139174743
|
G | C | 5 | a0001c0002t0004g0027a0001c0002t0004g0028a0001c0002t0004g0034others(2): Show | 5 | NA18612.hp1 NA18940.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.1070-3471G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174743 | ||||||
chr7:139174807
|
C | T | 2 | a0001c0001t0002g0185a0001c0001t0002g0255 | 2 | NA18947.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.1070-3407C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174807 | ||||||
chr7:139174864
|
T | C | 4 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0002t0001g0143others(1): Show | 4 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.1070-3350T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174864 | ||||||
chr7:139174984
|
A | G | 136 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(133): Show | 157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1070-3230A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139174984 | ||||||
chr7:139175037
|
AAAG | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(133): Show | 157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1070-3174_1070-317 others(7): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139175037 | |||||
chr7:139175069
|
G | A | 1 | a0001c0001t0001g0082 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1070-3145G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139175069 | ||||||
chr7:139175138
|
A | G | 65 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(62): Show | 81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1070-3076A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139175138 | ||||||
chr7:139175269
|
C | T | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1070-2945C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139175269 | ||||||
chr7:139176099
|
A | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1070-2115A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176099 | ||||||
chr7:139176109
|
G | A | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1070-2105G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176109 | ||||||
chr7:139176111
|
A | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1070-2103A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176111 | ||||||
chr7:139176170
|
T | C | 23 | a0001c0001t0012g0146a0001c0001t0012g0147a0001c0002t0004g0010others(20): Show | 24 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(21): Show |
intron_variant | MODIFIER | c.1070-2044T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176170 | ||||||
chr7:139176213
|
GT | G | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1070-1998delT | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139176213 | |||||
chr7:139176257
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(62): Show | 81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1070-1957C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176257 | ||||||
chr7:139176538
|
A | C | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1070-1676A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176538 | ||||||
chr7:139176696
|
T | C | 7 | a0001c0001t0007g0150a0001c0001t0007g0151a0001c0001t0007g0152others(4): Show | 7 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(4): Show |
intron_variant | MODIFIER | c.1070-1518T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176696 | ||||||
chr7:139176812
|
A | T | 4 | a0001c0001t0003g0022a0001c0001t0003g0025a0001c0001t0003g0242others(1): Show | 6 | NA18947.hp2 NA18955.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1070-1402A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176812 | ||||||
chr7:139176901
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1070-1313C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176901 | ||||||
chr7:139176949
|
G | A | 9 | a0001c0001t0005g0048a0001c0001t0005g0049a0001c0001t0005g0050others(6): Show | 9 | HG01943.hp2 HG02145.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1070-1265G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176949 | ||||||
chr7:139176969
|
C | T | 65 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(62): Show | 81 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(78): Show |
intron_variant | MODIFIER | c.1070-1245C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139176969 | ||||||
chr7:139177039
|
G | C | 2 | a0001c0002t0001g0143a0001c0002t0001g0144 | 2 | HG02572.hp2 HG02965.hp2 |
intron_variant | MODIFIER | c.1070-1175G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177039 | ||||||
chr7:139177041
|
G | A | 1 | a0001c0001t0001g0069 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.1070-1173G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177041 | ||||||
chr7:139177171
|
C | CA | 9 | a0001c0001t0005g0048a0001c0001t0005g0049a0001c0001t0005g0050others(6): Show | 9 | HG01943.hp2 HG02145.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1070-1030dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177171 | |||||
chr7:139177171
|
CA | C | 77 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(74): Show | 93 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(90): Show |
intron_variant | MODIFIER | c.1070-1030delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177171 | |||||
chr7:139177277
|
T | C | 2 | a0001c0001t0001g0076a0001c0001t0021g0046 | 2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1070-937T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177277 | ||||||
chr7:139177355
|
A | G | 100 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(97): Show | 120 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(117): Show |
intron_variant | MODIFIER | c.1070-859A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177355 | ||||||
chr7:139177482
|
A | C | 1 | a0001c0001t0007g0153 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1070-732A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177482 | ||||||
chr7:139177499
|
G | A | 5 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0002t0001g0143others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1070-715G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177499 | ||||||
chr7:139177611
|
A | AGTGT | 3 | a0001c0001t0012g0146a0001c0001t0012g0147a0001c0003t0017g0088 | 3 | HG02622.hp2 HG03139.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1070-586_1070-583d others(6): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177611 | |||||
chr7:139177611
|
A | AGTGTGT | 11 | a0001c0001t0001g0057a0001c0001t0001g0091a0001c0001t0001g0130others(8): Show | 11 | HG01243.hp2 HG02258.hp1 HG02280.hp2 others(8): Show |
intron_variant | MODIFIER | c.1070-588_1070-583d others(8): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177611 | |||||
chr7:139177611
|
A | AGTGTGTG others(1): Show |
78 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(75): Show | 95 | HG00408.hp1 HG00408.hp2 HG00438.hp1 others(92): Show |
intron_variant | MODIFIER | c.1070-590_1070-583d others(10): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177611 | |||||
chr7:139177611
|
A | AGTGTGTG others(3): Show |
30 | a0001c0001t0001g0013a0001c0001t0001g0078a0001c0001t0001g0089others(27): Show | 32 | HG00140.hp2 HG01074.hp2 HG01884.hp2 others(29): Show |
intron_variant | MODIFIER | c.1070-592_1070-583d others(12): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177611 | |||||
chr7:139177611
|
A | AGTGTGTG others(5): Show |
8 | a0001c0001t0005g0048a0001c0001t0005g0049a0001c0001t0005g0051others(5): Show | 8 | HG02145.hp1 HG02886.hp2 HG02896.hp1 others(5): Show |
intron_variant | MODIFIER | c.1070-594_1070-583d others(14): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177611 | |||||
chr7:139177611
|
A | AGTGTGTG others(7): Show |
6 | a0001c0001t0001g0014a0001c0001t0001g0018a0001c0001t0001g0079others(3): Show | 8 | HG01081.hp2 HG01123.hp2 HG01256.hp1 others(5): Show |
intron_variant | MODIFIER | c.1070-596_1070-583d others(16): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177611 | |||||
chr7:139177611
|
A | AGTTGTGT others(4): Show |
2 | a0001c0001t0001g0076a0001c0001t0021g0046 | 2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1070-601_1070-600i others(13): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177611 | |||||
chr7:139177632
|
A | G | 36 | a0001c0001t0005g0051a0001c0001t0005g0054a0001c0001t0005g0056others(33): Show | 37 | HG02015.hp2 HG02071.hp1 HG02280.hp2 others(34): Show |
intron_variant | MODIFIER | c.1070-582A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177632 | ||||||
chr7:139177634
|
A | G | 8 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0002t0001g0143others(5): Show | 8 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(5): Show |
intron_variant | MODIFIER | c.1070-580A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177634 | ||||||
chr7:139177656
|
A | T | 1 | a0001c0001t0003g0195 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.1070-558A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177656 | ||||||
chr7:139177686
|
AAAATT | A | 21 | a0001c0002t0004g0010a0001c0002t0004g0027a0001c0002t0004g0028others(18): Show | 22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.1070-524_1070-520d others(7): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | INFO_REALIGN_3_PRIME | chr7 | 139177686 | |||||
chr7:139177932
|
C | G | 1 | a0001c0001t0001g0077 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1070-282C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139177932 | ||||||
chr7:139178011
|
C | G | 2 | a0001c0001t0003g0199a0001c0001t0003g0231 | 2 | NA18953.hp2 NA18966.hp2 |
intron_variant | MODIFIER | c.1070-203C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139178011 | ||||||
chr7:139178084
|
A | G | 1 | a0001c0001t0019g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1070-130A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 12/17 | chr7 | 139178084 | ||||||
chr7:139178682
|
G | A | 2 | a0001c0001t0001g0106a0001c0001t0001g0107 | 2 | NA18946.hp1 NA19075.hp1 |
intron_variant | MODIFIER | c.1242+84G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | chr7 | 139178682 | ||||||
chr7:139178720
|
C | T | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1242+122C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | chr7 | 139178720 | ||||||
chr7:139178771
|
A | G | 1 | a0001c0002t0004g0041 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.1242+173A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | chr7 | 139178771 | ||||||
chr7:139178774
|
T | C | 1 | a0003c0006t0003g0268 | 1 | NA18951.hp2 | intron_variant | MODIFIER | c.1242+176T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | chr7 | 139178774 | ||||||
chr7:139178898
|
TA | T | 8 | a0001c0001t0001g0107a0001c0001t0001g0122a0001c0001t0002g0214others(5): Show | 10 | HG00323.hp2 HG01361.hp2 HG02148.hp1 others(7): Show |
intron_variant | MODIFIER | c.1242+312delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr7 | 139178898 | |||||
chr7:139178917
|
T | C | 1 | a0001c0001t0003g0229 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.1242+319T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | chr7 | 139178917 | ||||||
chr7:139179105
|
C | T | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1243-469C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | chr7 | 139179105 | ||||||
chr7:139179112
|
G | T | 1 | a0001c0001t0003g0265 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1243-462G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | chr7 | 139179112 | ||||||
chr7:139179176
|
G | C | 1 | a0002c0005t0001g0108 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.1243-398G>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | chr7 | 139179176 | ||||||
chr7:139179465
|
G | A | 2 | a0001c0001t0003g0233a0001c0001t0003g0234 | 2 | HG03942.hp1 HG04115.hp2 |
intron_variant | MODIFIER | c.1243-109G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 14/17 | chr7 | 139179465 | ||||||
chr7:139179883
|
C | G | 21 | a0001c0002t0004g0010a0001c0002t0004g0027a0001c0002t0004g0028others(18): Show | 22 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(19): Show |
intron_variant | MODIFIER | c.1312+240C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139179883 | ||||||
chr7:139179971
|
C | T | 1 | a0001c0002t0011g0139 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1312+328C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139179971 | ||||||
chr7:139180065
|
C | T | 1 | a0001c0001t0003g0244 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1312+422C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180065 | ||||||
chr7:139180134
|
G | A | 1 | a0001c0001t0001g0087 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.1312+491G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180134 | ||||||
chr7:139180162
|
C | T | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1312+519C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180162 | ||||||
chr7:139180221
|
C | T | 1 | a0001c0001t0019g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1312+578C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180221 | ||||||
chr7:139180268
|
C | T | 2 | a0001c0001t0001g0085a0001c0001t0003g0025 | 3 | HG01074.hp1 NA18947.hp2 NA18993.hp1 |
intron_variant | MODIFIER | c.1312+625C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180268 | ||||||
chr7:139180362
|
C | T | 9 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(6): Show | 9 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1312+719C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180362 | ||||||
chr7:139180366
|
G | T | 1 | a0001c0001t0001g0117 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1312+723G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180366 | ||||||
chr7:139180446
|
A | G | 1 | a0001c0001t0002g0211 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.1313-646A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180446 | ||||||
chr7:139180587
|
A | G | 276 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(273): Show | 328 | HG00140.hp1 HG00140.hp2 HG00323.hp1 others(325): Show |
intron_variant | MODIFIER | c.1313-505A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180587 | ||||||
chr7:139180664
|
G | A | 1 | a0001c0001t0008g0207 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.1313-428G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180664 | ||||||
chr7:139180708
|
C | CA | 67 | a0001c0001t0001g0087a0001c0001t0001g0115a0001c0001t0002g0024others(64): Show | 77 | HG00323.hp2 HG00438.hp2 HG00597.hp1 others(74): Show |
intron_variant | MODIFIER | c.1313-371dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | INFO_REALIGN_3_PRIME | chr7 | 139180708 | |||||
chr7:139180731
|
T | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(134): Show | 158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1313-361T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180731 | ||||||
chr7:139180737
|
A | G | 138 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(135): Show | 159 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(156): Show |
intron_variant | MODIFIER | c.1313-355A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180737 | ||||||
chr7:139180794
|
C | T | 1 | a0001c0001t0003g0265 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.1313-298C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 15/17 | chr7 | 139180794 | ||||||
chr7:139181659
|
C | T | 4 | a0001c0001t0003g0022a0001c0001t0003g0025a0001c0001t0003g0242others(1): Show | 6 | NA18947.hp2 NA18955.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1419+461C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139181659 | ||||||
chr7:139182088
|
G | A | 1 | a0001c0001t0003g0224 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.1419+890G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139182088 | ||||||
chr7:139182106
|
G | A | 1 | a0001c0001t0021g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1419+908G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139182106 | ||||||
chr7:139182161
|
A | G | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1419+963A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139182161 | ||||||
chr7:139182179
|
A | T | 2 | a0001c0001t0002g0158a0001c0001t0005g0075 | 2 | HG01106.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1419+981A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139182179 | ||||||
chr7:139182187
|
C | T | 3 | a0001c0001t0012g0146a0001c0001t0012g0147a0001c0002t0001g0145 | 3 | HG02622.hp2 HG03139.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1419+989C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139182187 | ||||||
chr7:139182316
|
C | CA | 9 | a0001c0001t0005g0048a0001c0001t0005g0049a0001c0001t0005g0050others(6): Show | 9 | HG01943.hp2 HG02145.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1419+1125dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139182316 | |||||
chr7:139182713
|
T | C | 137 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(134): Show | 158 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(155): Show |
intron_variant | MODIFIER | c.1419+1515T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139182713 | ||||||
chr7:139183201
|
G | A | 5 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0002t0001g0143others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1419+2003G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139183201 | ||||||
chr7:139183215
|
GA | G | 13 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0018others(10): Show | 16 | HG00140.hp2 HG01074.hp2 HG01081.hp2 others(13): Show |
intron_variant | MODIFIER | c.1419+2019delA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139183215 | |||||
chr7:139183311
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(133): Show | 157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1419+2113G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139183311 | ||||||
chr7:139183325
|
T | C | 23 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0052others(20): Show | 27 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.1419+2127T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139183325 | ||||||
chr7:139183330
|
C | T | 1 | a0001c0001t0002g0273 | 1 | NA18960.hp1 | intron_variant | MODIFIER | c.1419+2132C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139183330 | ||||||
chr7:139183346
|
A | T | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1419+2148A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139183346 | ||||||
chr7:139183517
|
A | T | 1 | a0001c0001t0007g0152 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.1419+2319A>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139183517 | ||||||
chr7:139183594
|
G | A | 136 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(133): Show | 157 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(154): Show |
intron_variant | MODIFIER | c.1419+2396G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139183594 | ||||||
chr7:139183680
|
A | G | 23 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0052others(20): Show | 27 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.1419+2482A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139183680 | ||||||
chr7:139183931
|
A | C | 9 | a0001c0001t0005g0048a0001c0001t0005g0049a0001c0001t0005g0050others(6): Show | 9 | HG01943.hp2 HG02145.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.1419+2733A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139183931 | ||||||
chr7:139184066
|
G | A | 1 | a0001c0002t0004g0037 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.1419+2868G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184066 | ||||||
chr7:139184288
|
T | A | 15 | a0001c0002t0004g0029a0001c0002t0004g0030a0001c0002t0004g0031others(12): Show | 15 | HG02015.hp2 HG02071.hp1 HG02300.hp1 others(12): Show |
intron_variant | MODIFIER | c.1419+3090T>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184288 | ||||||
chr7:139184340
|
T | C | 7 | a0001c0001t0007g0149a0001c0001t0007g0151a0001c0001t0007g0152others(4): Show | 7 | HG01891.hp2 HG02109.hp1 HG02818.hp2 others(4): Show |
intron_variant | MODIFIER | c.1420-3066T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184340 | ||||||
chr7:139184501
|
TTA | T | 3 | a0001c0001t0007g0150a0001c0001t0007g0152a0001c0001t0007g0156 | 3 | HG02257.hp2 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1420-2903_1420-290 others(6): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139184501 | |||||
chr7:139184506
|
G | A | 3 | a0001c0001t0007g0150a0001c0001t0007g0152a0001c0001t0007g0156 | 3 | HG02257.hp2 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1420-2900G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184506 | ||||||
chr7:139184546
|
G | A | 1 | a0001c0001t0021g0046 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1420-2860G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184546 | ||||||
chr7:139184589
|
A | G | 23 | a0001c0001t0001g0007a0001c0001t0001g0160a0001c0002t0004g0010others(20): Show | 26 | HG00621.hp1 HG02015.hp2 HG02071.hp1 others(23): Show |
intron_variant | MODIFIER | c.1420-2817A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184589 | ||||||
chr7:139184636
|
C | T | 5 | a0001c0002t0001g0141a0001c0002t0001g0142a0001c0002t0001g0143others(2): Show | 5 | HG02572.hp2 HG02818.hp1 HG02965.hp2 others(2): Show |
intron_variant | MODIFIER | c.1420-2770C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184636 | ||||||
chr7:139184637
|
G | A | 1 | a0001c0001t0001g0089 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.1420-2769G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184637 | ||||||
chr7:139184776
|
C | T | 1 | a0001c0001t0003g0244 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.1420-2630C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184776 | ||||||
chr7:139184780
|
C | T | 89 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(86): Show | 109 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(106): Show |
intron_variant | MODIFIER | c.1420-2626C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184780 | ||||||
chr7:139184792
|
TGCCTGTA others(1366): Show |
T | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1420-2601_1420-122 others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139184792 | |||||
chr7:139184804
|
C | T | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-2602C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184804 | ||||||
chr7:139184819
|
C | T | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-2587C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184819 | ||||||
chr7:139184820
|
T | C | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-2586T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184820 | ||||||
chr7:139184829
|
C | T | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-2577C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184829 | ||||||
chr7:139184836
|
C | T | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-2570C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184836 | ||||||
chr7:139184837
|
A | G | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-2569A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184837 | ||||||
chr7:139184850
|
C | G | 6 | a0001c0001t0001g0066a0001c0001t0001g0071a0001c0003t0013g0128others(3): Show | 6 | HG02280.hp2 HG02615.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.1420-2556C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184850 | ||||||
chr7:139184864
|
T | C | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-2542T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184864 | ||||||
chr7:139184871
|
A | G | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-2535A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184871 | ||||||
chr7:139184993
|
G | A | 2 | a0001c0001t0010g0154a0001c0001t0010g0155 | 2 | HG02109.hp1 HG03139.hp1 |
intron_variant | MODIFIER | c.1420-2413G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139184993 | ||||||
chr7:139185018
|
C | T | 2 | a0001c0001t0003g0243a0001c0001t0003g0244 | 2 | HG03490.hp1 HG03710.hp1 |
intron_variant | MODIFIER | c.1420-2388C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139185018 | ||||||
chr7:139185053
|
C | CA | 88 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(85): Show | 108 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1420-2337dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139185053 | |||||
chr7:139185053
|
C | CAAA | 9 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(6): Show | 9 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1420-2339_1420-233 others(7): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139185053 | |||||
chr7:139185114
|
T | C | 5 | a0001c0001t0003g0009a0001c0001t0003g0262a0001c0001t0003g0269others(2): Show | 7 | HG00438.hp2 NA18961.hp1 NA18970.hp1 others(4): Show |
intron_variant | MODIFIER | c.1420-2292T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139185114 | ||||||
chr7:139185201
|
CAA | C | 90 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(87): Show | 110 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(107): Show |
intron_variant | MODIFIER | c.1420-2197_1420-219 others(6): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139185201 | |||||
chr7:139185242
|
T | C | 16 | a0001c0001t0005g0048a0001c0001t0005g0049a0001c0001t0005g0050others(13): Show | 16 | HG01943.hp2 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1420-2164T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139185242 | ||||||
chr7:139185243
|
G | A | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1420-2163G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139185243 | ||||||
chr7:139185298
|
C | T | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-2108C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139185298 | ||||||
chr7:139185406
|
T | C | 1 | a0001c0001t0019g0175 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1420-2000T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139185406 | ||||||
chr7:139185878
|
G | A | 2 | a0001c0001t0001g0076a0001c0001t0021g0046 | 2 | HG01891.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.1420-1528G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139185878 | ||||||
chr7:139186156
|
G | A | 23 | a0001c0001t0001g0005a0001c0001t0001g0011a0001c0001t0001g0052others(20): Show | 27 | HG00408.hp1 HG00438.hp1 HG00544.hp1 others(24): Show |
intron_variant | MODIFIER | c.1420-1250G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186156 | ||||||
chr7:139186361
|
G | A | 2 | a0001c0001t0012g0146a0001c0001t0012g0147 | 2 | HG02622.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.1420-1045G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186361 | ||||||
chr7:139186406
|
A | G | 1 | a0001c0001t0002g0210 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.1420-1000A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186406 | ||||||
chr7:139186532
|
C | T | 64 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(61): Show | 80 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(77): Show |
intron_variant | MODIFIER | c.1420-874C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186532 | ||||||
chr7:139186656
|
G | T | 4 | a0001c0001t0003g0022a0001c0001t0003g0025a0001c0001t0003g0242others(1): Show | 6 | NA18947.hp2 NA18955.hp2 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1420-750G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186656 | ||||||
chr7:139186676
|
A | G | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-730A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186676 | ||||||
chr7:139186816
|
C | T | 3 | a0001c0001t0007g0150a0001c0001t0007g0152a0001c0001t0007g0156 | 3 | HG02257.hp2 HG02723.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.1420-590C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186816 | ||||||
chr7:139186833
|
G | A | 1 | a0001c0001t0002g0213 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.1420-573G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186833 | ||||||
chr7:139186860
|
T | C | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(144): Show | 168 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.1420-546T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186860 | ||||||
chr7:139186864
|
A | G | 147 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(144): Show | 168 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(165): Show |
intron_variant | MODIFIER | c.1420-542A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186864 | ||||||
chr7:139186890
|
C | T | 1 | a0001c0001t0002g0186 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1420-516C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186890 | ||||||
chr7:139186891
|
G | A | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-515G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186891 | ||||||
chr7:139186955
|
G | A | 9 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(6): Show | 9 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1420-451G>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186955 | ||||||
chr7:139186983
|
A | G | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-423A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139186983 | ||||||
chr7:139187064
|
G | T | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1420-342G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139187064 | ||||||
chr7:139187075
|
T | C | 1 | a0001c0001t0002g0171 | 1 | HG01175.hp1 | intron_variant | MODIFIER | c.1420-331T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139187075 | ||||||
chr7:139187100
|
C | CA | 133 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(130): Show | 152 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(149): Show |
intron_variant | MODIFIER | c.1420-283dupA | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139187100 | |||||
chr7:139187100
|
C | CAA | 19 | a0001c0001t0001g0015a0001c0001t0001g0072a0001c0001t0001g0076others(16): Show | 20 | HG00408.hp2 HG01891.hp2 HG02015.hp2 others(17): Show |
intron_variant | MODIFIER | c.1420-284_1420-283d others(4): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139187100 | |||||
chr7:139187100
|
CAAAAAAA others(3): Show |
C | 1 | a0001c0001t0001g0115 | 1 | NA18967.hp1 | intron_variant | MODIFIER | c.1420-292_1420-283d others(12): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr7 | 139187100 | |||||
chr7:139187192
|
A | G | 88 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(85): Show | 108 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(105): Show |
intron_variant | MODIFIER | c.1420-214A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139187192 | ||||||
chr7:139187213
|
A | C | 1 | a0001c0001t0006g0059 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.1420-193A>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139187213 | ||||||
chr7:139187301
|
C | T | 16 | a0001c0001t0005g0048a0001c0001t0005g0049a0001c0001t0005g0050others(13): Show | 16 | HG01943.hp2 HG02145.hp1 HG02258.hp1 others(13): Show |
intron_variant | MODIFIER | c.1420-105C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139187301 | ||||||
chr7:139187321
|
T | C | 66 | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0012others(63): Show | 82 | HG00140.hp2 HG00408.hp2 HG00544.hp2 others(79): Show |
intron_variant | MODIFIER | c.1420-85T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 16/17 | chr7 | 139187321 | ||||||
chr7:139187548
|
A | G | 9 | a0001c0001t0007g0149a0001c0001t0007g0150a0001c0001t0007g0151others(6): Show | 9 | HG02109.hp1 HG02257.hp2 HG02723.hp2 others(6): Show |
intron_variant | MODIFIER | c.1553+9A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139187548 | ||||||
chr7:139187599
|
C | A | 146 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(143): Show | 167 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(164): Show |
intron_variant | MODIFIER | c.1553+60C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139187599 | ||||||
chr7:139187922
|
C | G | 1 | a0001c0002t0004g0040 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.1553+383C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139187922 | ||||||
chr7:139188097
|
C | T | 1 | a0001c0001t0002g0174 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1553+558C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139188097 | ||||||
chr7:139188098
|
T | C | 1 | a0001c0001t0002g0174 | 1 | NA19072.hp2 | intron_variant | MODIFIER | c.1553+559T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139188098 | ||||||
chr7:139188099
|
T | G | 1 | a0001c0001t0002g0177 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.1553+560T>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139188099 | ||||||
chr7:139188109
|
T | C | 93 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0007others(90): Show | 113 | HG00140.hp2 HG00408.hp1 HG00408.hp2 others(110): Show |
intron_variant | MODIFIER | c.1553+570T>C | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139188109 | ||||||
chr7:139188141
|
C | T | 7 | a0001c0001t0005g0048a0001c0001t0005g0049a0001c0001t0005g0050others(4): Show | 7 | HG01943.hp2 HG02145.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1553+602C>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139188141 | ||||||
chr7:139188147
|
C | G | 1 | a0001c0002t0001g0145 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1553+608C>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139188147 | ||||||
chr7:139188459
|
C | A | 1 | a0001c0001t0001g0097 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.1554-862C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139188459 | ||||||
chr7:139188900
|
C | A | 1 | a0001c0001t0001g0124 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.1554-421C>A | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139188900 | ||||||
chr7:139189028
|
G | T | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1554-293G>T | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139189028 | ||||||
chr7:139189190
|
A | G | 4 | a0001c0003t0013g0128a0001c0003t0013g0129a0001c0003t0017g0088others(1): Show | 4 | HG02280.hp2 HG02615.hp2 HG03098.hp1 others(1): Show |
intron_variant | MODIFIER | c.1554-131A>G | IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | chr7 | 139189190 | ||||||
chr7:139189255
|
GTTTAT | G | 7 | a0001c0002t0005g0133a0001c0002t0005g0134a0001c0002t0005g0135others(4): Show | 7 | HG02258.hp1 HG02486.hp2 HG02572.hp1 others(4): Show |
intron_variant | MODIFIER | c.1554-57_1554-53del others(5): Show |
IFT56 | ENSG00000105948.13 | transcript | ENST00000464848.5 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr7 | 139189255 |