Item | Value |
---|---|
geneid | 1213 |
ensemblid | ENSG00000141367.13 |
hgncid | 2092 |
symbol | CLTC |
name | clathrin heavy chain |
refseq_nuc | NM_004859.4 |
refseq_prot | NP_004850.1 |
ensembl_nuc | ENST00000269122.8 |
ensembl_prot | ENSP00000269122.3 |
mane_status | MANE Select |
chr | chr17 |
start | 59619895 |
end | 59696956 |
strand | + |
ver | v1.2 |
region | chr17:59619895-59696956 |
region5000 | chr17:59614895-59701956 |
regionname0 | CLTC_chr17_59619895_59696956 |
regionname5000 | CLTC_chr17_59614895_59701956 |
chapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 5028 | 254 | 86 | 35 | 91 | 4 | 36 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 | |
c0002 | 0/0 | 5028 | 4 | 0 | 4 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 | |
c0003 | 0/0 | 5028 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 | |
c0004 | 0/0 | 5028 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 3345 | 105 | 28 | 20 | 38 | 2 | 16 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
t0002 | 0/0 | 3341 | 70 | 3 | 7 | 43 | 1 | 16 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
t0003 | 1/0 | 3342 | 27 | 9 | 8 | 6 | 1 | 2 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
t0004 | 0/0 | 3345 | 17 | 16 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
t0005 | 0/0 | 3348 | 11 | 9 | 1 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
t0006 | 0/0 | 3345 | 9 | 9 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
t0007 | 0/0 | 3345 | 8 | 8 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
t0008 | 0/0 | 3342 | 3 | 3 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
t0009 | 0/0 | 3345 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
t0010 | 0/0 | 3345 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
t0011 | 0/0 | 3345 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
t0012 | 0/0 | 3345 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
t0013 | 0/0 | 3345 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
t0014 | 0/0 | 3341 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
t0015 | 0/0 | 3345 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
t0016 | 0/0 | 3341 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
t0017 | 0/0 | 3345 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
t0018 | 0/0 | 3341 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 11 | 0 | 0 | 9 | 0 | 2 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0002 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0010 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0208 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
achapid | grch38/chm13v2 | alen | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 5028 | 254 | 86 | 35 | 91 | 4 | 36 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 | |
a0001c0002 | 0/0 | 5028 | 4 | 0 | 4 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 | |
a0001c0004 | 0/0 | 5028 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 | |
a0002c0003 | 0/0 | 5028 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 8372 | 103 | 28 | 19 | 37 | 2 | 16 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0001t0002 | 0/0 | 8368 | 66 | 3 | 3 | 43 | 1 | 16 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0001t0003 | 1/0 | 8369 | 27 | 9 | 8 | 6 | 1 | 2 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0001t0004 | 0/0 | 8372 | 17 | 16 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0001t0005 | 0/0 | 8375 | 11 | 9 | 1 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0001t0006 | 0/0 | 8372 | 9 | 9 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0001t0007 | 0/0 | 8372 | 8 | 8 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0001t0008 | 0/0 | 8369 | 3 | 3 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0001t0009 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0001t0010 | 0/0 | 8372 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0001t0011 | 0/0 | 8372 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0001t0012 | 0/0 | 8372 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0001t0013 | 0/0 | 8372 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0001t0014 | 0/0 | 8368 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0001t0015 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0001t0016 | 0/0 | 8368 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0001t0017 | 0/0 | 8372 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0001t0018 | 0/0 | 8368 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0002t0002 | 0/0 | 8368 | 4 | 0 | 4 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0001c0004t0001 | 0/0 | 8372 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
a0002c0003t0001 | 0/0 | 8372 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | copy fasta | chr17 | 59614895 | 59701956 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 4 | 0 | 1 | 2 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 1 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0111 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0121 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0190 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0193 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0201 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0207 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0208 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0213 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0219 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0227 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0231 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0001g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0001 | 0/0 | 11 | 0 | 0 | 9 | 0 | 2 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0007 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0008 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0009 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0130 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0132 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0136 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0142 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0144 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0145 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0146 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0147 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0150 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0002g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0005 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0014 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0016 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0019 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0030 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0031 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0034 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0037 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0004g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0004g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0004g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0004g0070 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0004g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0004g0072 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0004g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0004g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0004g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0004g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0004g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0004g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0004g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0004g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0004g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0004g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0004g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0005g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0005g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0005g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0005g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0005g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0005g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0005g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0005g0046 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0006g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0006g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0006g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0006g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0006g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0006g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0006g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0006g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0006g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0007g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0007g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0007g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0007g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0007g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0007g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0007g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0007g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0008g0003 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0009g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0010g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0011g0228 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0012g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0013g0180 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0014g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0015g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0016g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0017g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0001t0018g0158 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0002t0002g0004 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0002t0002g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0001c0004t0001g0191 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
a0002c0003t0001g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00140 | hp1 | a0001 | c0001 | t0001 | g0010 | EUR | GBR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG00140 | hp2 | a0001 | c0001 | t0003 | g0034 | EUR | GBR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0194 | EAS | CHS | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG00408 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | CHS | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG00423 | hp1 | a0001 | c0001 | t0001 | g0206 | EAS | CHS | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG00423 | hp2 | a0001 | c0001 | t0002 | g0169 | EAS | CHS | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG00544 | hp1 | a0001 | c0001 | t0002 | g0160 | EAS | CHS | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG00544 | hp2 | a0001 | c0001 | t0001 | g0010 | EAS | CHS | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG00621 | hp1 | a0001 | c0001 | t0002 | g0175 | EAS | CHS | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG00621 | hp2 | a0001 | c0001 | t0001 | g0195 | EAS | CHS | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0151 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0215 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0101 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG00738 | hp2 | a0001 | c0001 | t0002 | g0152 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0179 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01099 | hp2 | a0001 | c0001 | t0001 | g0118 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0227 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01109 | hp2 | a0001 | c0001 | t0005 | g0042 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01168 | hp1 | a0001 | c0002 | t0002 | g0128 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0022 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01169 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01169 | hp2 | a0001 | c0001 | t0013 | g0180 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0201 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01243 | hp2 | a0001 | c0001 | t0004 | g0073 | AMR | PUR | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01255 | hp1 | a0001 | c0001 | t0003 | g0021 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0229 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0177 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01257 | hp2 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01258 | hp1 | a0001 | c0001 | t0003 | g0014 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0104 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01433 | hp1 | a0001 | c0004 | t0001 | g0191 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0185 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0117 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01891 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01891 | hp2 | a0001 | c0001 | t0004 | g0078 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0114 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01934 | hp2 | a0001 | c0001 | t0003 | g0030 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0116 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01952 | hp2 | a0001 | c0001 | t0003 | g0032 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01975 | hp1 | a0001 | c0001 | t0003 | g0031 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01975 | hp2 | a0001 | c0001 | t0002 | g0132 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01978 | hp1 | a0001 | c0001 | t0001 | g0097 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0192 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0193 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01981 | hp2 | a0001 | c0001 | t0018 | g0158 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02004 | hp1 | a0001 | c0001 | t0012 | g0221 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02004 | hp2 | a0001 | c0001 | t0003 | g0033 | AMR | PEL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0102 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0174 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0019 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02027 | hp2 | a0001 | c0001 | t0002 | g0172 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0173 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02040 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02055 | hp1 | a0001 | c0001 | t0001 | g0233 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0108 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02129 | hp1 | a0001 | c0001 | t0002 | g0170 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02129 | hp2 | a0001 | c0001 | t0001 | g0012 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0200 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02135 | hp2 | a0001 | c0001 | t0002 | g0168 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02155 | hp1 | a0001 | c0001 | t0014 | g0131 | EAS | CDX | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02155 | hp2 | a0001 | c0001 | t0001 | g0218 | EAS | CDX | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02257 | hp1 | a0001 | c0001 | t0006 | g0060 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02257 | hp2 | a0001 | c0001 | t0003 | g0016 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02280 | hp1 | a0001 | c0001 | t0001 | g0186 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02280 | hp2 | a0001 | c0001 | t0004 | g0072 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02451 | hp1 | a0001 | c0001 | t0004 | g0068 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0232 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02523 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02523 | hp2 | a0001 | c0001 | t0001 | g0199 | EAS | KHV | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02572 | hp1 | a0001 | c0001 | t0006 | g0064 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0023 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0190 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0144 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02615 | hp1 | a0001 | c0001 | t0005 | g0046 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02615 | hp2 | a0001 | c0001 | t0003 | g0018 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0112 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02630 | hp2 | a0001 | c0001 | t0004 | g0075 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02647 | hp1 | a0001 | c0001 | t0006 | g0066 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02647 | hp2 | a0001 | c0001 | t0004 | g0079 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0178 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0090 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02698 | hp2 | a0001 | c0001 | t0002 | g0145 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02717 | hp1 | a0001 | c0001 | t0001 | g0089 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02717 | hp2 | a0001 | c0001 | t0004 | g0076 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0231 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0146 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02735 | hp2 | a0001 | c0001 | t0011 | g0228 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0183 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0129 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02809 | hp1 | a0001 | c0001 | t0007 | g0051 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02809 | hp2 | a0001 | c0001 | t0006 | g0061 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02818 | hp1 | a0001 | c0001 | t0004 | g0071 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0109 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0119 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02886 | hp2 | a0001 | c0001 | t0001 | g0105 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02895 | hp1 | a0001 | c0001 | t0001 | g0088 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02895 | hp2 | a0001 | c0001 | t0006 | g0065 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02896 | hp1 | a0001 | c0001 | t0007 | g0054 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02896 | hp2 | a0001 | c0001 | t0005 | g0048 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0092 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02965 | hp2 | a0001 | c0001 | t0005 | g0044 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03041 | hp1 | a0001 | c0001 | t0003 | g0027 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03041 | hp2 | a0001 | c0001 | t0005 | g0045 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03098 | hp1 | a0001 | c0001 | t0001 | g0093 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03098 | hp2 | a0001 | c0001 | t0004 | g0074 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03130 | hp1 | a0001 | c0001 | t0001 | g0124 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03130 | hp2 | a0001 | c0001 | t0006 | g0056 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03139 | hp2 | a0001 | c0001 | t0003 | g0020 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03195 | hp1 | a0001 | c0001 | t0007 | g0057 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0006 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03209 | hp1 | a0001 | c0001 | t0007 | g0055 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03209 | hp2 | a0001 | c0001 | t0004 | g0069 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03225 | hp1 | a0001 | c0001 | t0003 | g0025 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03225 | hp2 | a0001 | c0001 | t0003 | g0024 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03239 | hp1 | a0001 | c0001 | t0003 | g0026 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0211 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03453 | hp1 | a0001 | c0001 | t0010 | g0015 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03453 | hp2 | a0001 | c0001 | t0005 | g0041 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03486 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03486 | hp2 | a0001 | c0001 | t0005 | g0043 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03491 | hp1 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03491 | hp2 | a0001 | c0001 | t0001 | g0182 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0207 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03492 | hp2 | a0001 | c0001 | t0002 | g0007 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03516 | hp1 | a0001 | c0001 | t0005 | g0049 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0121 | AFR | ESN | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03540 | hp1 | a0001 | c0001 | t0008 | g0003 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03540 | hp2 | a0001 | c0001 | t0004 | g0077 | AFR | GWD | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0166 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03579 | hp2 | a0001 | c0001 | t0006 | g0063 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0013 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03654 | hp2 | a0001 | c0001 | t0002 | g0142 | SAS | PJL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0150 | SAS | STU | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03688 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0111 | SAS | BEB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03834 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | BEB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0103 | SAS | BEB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | BEB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03942 | hp1 | a0001 | c0001 | t0001 | g0212 | SAS | BEB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03942 | hp2 | a0001 | c0001 | t0002 | g0148 | SAS | BEB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0220 | SAS | STU | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0153 | SAS | STU | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG04184 | hp1 | a0001 | c0001 | t0001 | g0213 | SAS | BEB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG04184 | hp2 | a0001 | c0001 | t0003 | g0005 | SAS | BEB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG04199 | hp1 | a0001 | c0001 | t0017 | g0085 | SAS | STU | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG04199 | hp2 | a0001 | c0001 | t0002 | g0136 | SAS | STU | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG04204 | hp1 | a0001 | c0001 | t0002 | g0135 | SAS | STU | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0217 | SAS | STU | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18522 | hp1 | a0001 | c0001 | t0005 | g0040 | AFR | YRI | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0143 | AFR | YRI | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18906 | hp1 | a0001 | c0001 | t0001 | g0110 | AFR | YRI | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18906 | hp2 | a0001 | c0001 | t0005 | g0047 | AFR | YRI | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0133 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0189 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18945 | hp2 | a0001 | c0001 | t0003 | g0036 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18950 | hp1 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0098 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18952 | hp2 | a0001 | c0001 | t0001 | g0203 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0196 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18956 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18961 | hp2 | a0001 | c0001 | t0003 | g0005 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18962 | hp1 | a0001 | c0001 | t0001 | g0106 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18962 | hp2 | a0001 | c0001 | t0002 | g0176 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18963 | hp1 | a0001 | c0001 | t0001 | g0210 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18963 | hp2 | a0001 | c0001 | t0002 | g0009 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18964 | hp1 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18967 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0113 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18972 | hp1 | a0001 | c0001 | t0002 | g0154 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18972 | hp2 | a0001 | c0001 | t0009 | g0209 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0214 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18978 | hp1 | a0001 | c0001 | t0002 | g0120 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18978 | hp2 | a0001 | c0001 | t0005 | g0039 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18979 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0225 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18982 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18983 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18983 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18985 | hp1 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0159 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18991 | hp1 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18991 | hp2 | a0001 | c0001 | t0002 | g0134 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18992 | hp1 | a0001 | c0001 | t0002 | g0157 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18992 | hp2 | a0001 | c0001 | t0001 | g0107 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0163 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18993 | hp2 | a0001 | c0001 | t0003 | g0035 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19000 | hp1 | a0001 | c0001 | t0015 | g0184 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19000 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19005 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0126 | AFR | LWK | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19030 | hp2 | a0001 | c0001 | t0007 | g0230 | AFR | LWK | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19043 | hp1 | a0001 | c0001 | t0004 | g0081 | AFR | LWK | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19043 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | LWK | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0139 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19056 | hp2 | a0002 | c0003 | t0001 | g0099 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0127 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0222 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19060 | hp1 | a0001 | c0001 | t0002 | g0141 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19060 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19062 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19062 | hp2 | a0001 | c0001 | t0016 | g0156 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19075 | hp2 | a0001 | c0001 | t0002 | g0122 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19077 | hp1 | a0001 | c0001 | t0001 | g0223 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0008 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19081 | hp2 | a0001 | c0001 | t0001 | g0204 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19083 | hp1 | a0001 | c0001 | t0002 | g0067 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19083 | hp2 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19084 | hp2 | a0001 | c0001 | t0002 | g0140 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0202 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19085 | hp2 | a0001 | c0001 | t0002 | g0138 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19086 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0224 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19088 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19240 | hp1 | a0001 | c0001 | t0007 | g0052 | AFR | YRI | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA19240 | hp2 | a0001 | c0001 | t0006 | g0062 | AFR | YRI | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0086 | AFR | ASW | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA20129 | hp2 | a0001 | c0001 | t0003 | g0017 | AFR | ASW | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA20752 | hp1 | a0001 | c0001 | t0002 | g0147 | EUR | TSI | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA20752 | hp2 | a0001 | c0001 | t0001 | g0219 | EUR | TSI | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0205 | SAS | GIH | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA20905 | hp2 | a0001 | c0001 | t0002 | g0130 | SAS | GIH | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01123 | hp1 | a0001 | c0002 | t0002 | g0004 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02109 | hp1 | a0001 | c0001 | t0001 | g0187 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0123 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02486 | hp1 | a0001 | c0001 | t0003 | g0038 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02486 | hp2 | a0001 | c0001 | t0004 | g0082 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02559 | hp1 | a0001 | c0001 | t0004 | g0083 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG02559 | hp2 | a0001 | c0001 | t0008 | g0003 | AFR | ACB | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03471 | hp1 | a0001 | c0001 | t0007 | g0050 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG03471 | hp2 | a0001 | c0001 | t0004 | g0058 | AFR | MSL | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0125 | AFR | USA | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
HG06807 | hp2 | a0001 | c0001 | t0004 | g0070 | AFR | USA | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0226 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA18955 | hp2 | a0001 | c0001 | t0002 | g0149 | EAS | JPT | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA20300 | hp1 | a0001 | c0001 | t0006 | g0059 | AFR | USA | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0155 | AFR | USA | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA21309 | hp1 | a0001 | c0001 | t0004 | g0080 | AFR | LWK | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
NA21309 | hp2 | a0001 | c0001 | t0007 | g0053 | AFR | LWK | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0208 | REF | REF | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0037 | REF | REF | CLTC_chr17_59614895_59701956 | CLTC | chr17 | 59614895 | 59701956 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:59674745 | T | A | 1 | a0002 | 1 | NA19056.hp2 | missense_variant | MODERATE | c.2463T>A | p.Asp821Glu | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/32 | 2700/8369 | 2463/5028 | 821/1675 | chr17 | 59674745 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:59644320 | C | T | 1 | a0001c0002 | 4 | HG01123.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
synonymous_variant | LOW | c.87C>T | p.Thr29Thr | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/32 | 324/8369 | 87/5028 | 29/1675 | chr17 | 59644320 | ||
chr17:59681658 | G | A | 1 | a0001c0004 | 1 | HG01433.hp1 | synonymous_variant | LOW | c.3261G>A | p.Glu1087Glu | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 21/32 | 3498/8369 | 3261/5028 | 1087/1675 | chr17 | 59681658 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:59619898 | C | A | 1 | a0001c0001t0009 | 1 | NA18972.hp2 | 5_prime_UTR_variant | MODIFIER | c.-234C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/32 | 234 | chr17 | 59619898 | |||||
chr17:59620006 | C | T | 1 | a0001c0001t0018 | 1 | HG01981.hp2 | 5_prime_UTR_variant | MODIFIER | c.-126C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/32 | 126 | chr17 | 59620006 | |||||
chr17:59620041 | C | A | 1 | a0001c0001t0010 | 1 | HG03453.hp1 | 5_prime_UTR_variant | MODIFIER | c.-91C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/32 | 91 | chr17 | 59620041 | |||||
chr17:59694430 | G | A | 1 | a0001c0001t0011 | 1 | HG02735.hp2 | 3_prime_UTR_variant | MODIFIER | c.*578G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 578 | chr17 | 59694430 | |||||
chr17:59694463 | A | G | 1 | a0001c0001t0017 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*611A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 611 | chr17 | 59694463 | |||||
chr17:59694538 | T | A | 1 | a0001c0001t0012 | 1 | HG02004.hp1 | 3_prime_UTR_variant | MODIFIER | c.*686T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 686 | chr17 | 59694538 | |||||
chr17:59695229 | A | G | 1 | a0001c0001t0016 | 1 | NA19062.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1377A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1377 | chr17 | 59695229 | |||||
chr17:59695452 | T | C | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1600T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1600 | chr17 | 59695452 | |||||
chr17:59695453 | C | T | 9 | a0001c0001t0001a0001c0001t0009a0001c0001t0011others(6): Show | 111 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
3_prime_UTR_variant | MODIFIER | c.*1601C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1601 | chr17 | 59695453 | |||||
chr17:59695456 | G | T | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1604G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1604 | chr17 | 59695456 | |||||
chr17:59695470 | A | G | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1618A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1618 | chr17 | 59695470 | |||||
chr17:59695475 | G | T | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1623G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1623 | chr17 | 59695475 | |||||
chr17:59695482 | C | A | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1630C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1630 | chr17 | 59695482 | |||||
chr17:59695484 | T | G | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1632T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1632 | chr17 | 59695484 | |||||
chr17:59695486 | T | C | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1634T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1634 | chr17 | 59695486 | |||||
chr17:59695487 | C | T | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1635C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1635 | chr17 | 59695487 | |||||
chr17:59695488 | T | G | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1636T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1636 | chr17 | 59695488 | |||||
chr17:59695493 | A | C | 1 | a0001c0001t0013 | 1 | HG01169.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1641A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1641 | chr17 | 59695493 | |||||
chr17:59695552 | G | A | 1 | a0001c0001t0008 | 3 | HG01891.hp1 HG02559.hp2 HG03540.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1700G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1700 | chr17 | 59695552 | |||||
chr17:59695672 | CAAAA | C | 5 | a0001c0001t0002a0001c0001t0014a0001c0001t0016others(2): Show | 73 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*1824_*1827delAAAA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1824 | INFO_REALIGN_3_PRIME | chr17 | 59695672 | ||||
chr17:59695735 | A | G | 1 | a0001c0001t0007 | 8 | HG02809.hp1 HG02896.hp1 HG03195.hp1 others(5): Show |
3_prime_UTR_variant | MODIFIER | c.*1883A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1883 | chr17 | 59695735 | |||||
chr17:59695842 | AAAT | A | 18 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(15): Show | 219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*1998_*2000delATA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1998 | INFO_REALIGN_3_PRIME | chr17 | 59695842 | ||||
chr17:59695850 | A | G | 1 | a0001c0001t0014 | 1 | HG02155.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1998A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 1998 | chr17 | 59695850 | |||||
chr17:59696001 | T | C | 1 | a0001c0001t0015 | 1 | NA19000.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2149T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 2149 | chr17 | 59696001 | |||||
chr17:59696475 | G | A | 2 | a0001c0001t0006a0001c0001t0007 | 17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2623G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 2623 | chr17 | 59696475 | |||||
chr17:59696525 | T | TAAAGAA | 19 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(16): Show | 230 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(227): Show |
3_prime_UTR_variant | MODIFIER | c.*2676_*2677insGAAA others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 32/32 | 2677 | INFO_REALIGN_3_PRIME | chr17 | 59696525 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr17:59620477 | C | T | 1 | a0001c0001t0003g0014 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.42+304C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59620477 | ||||||
chr17:59620785 | A | G | 3 | a0001c0001t0001g0231a0001c0001t0001g0232a0001c0001t0001g0233 | 3 | HG02055.hp1 HG02451.hp2 HG02723.hp2 |
intron_variant | MODIFIER | c.42+612A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59620785 | ||||||
chr17:59620847 | C | G | 195 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(192): Show | 218 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.42+674C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59620847 | ||||||
chr17:59621375 | G | A | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(193): Show | 219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.42+1202G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59621375 | ||||||
chr17:59621459 | C | T | 10 | a0001c0001t0005g0040a0001c0001t0005g0041a0001c0001t0005g0042others(7): Show | 10 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+1286C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59621459 | ||||||
chr17:59621481 | G | T | 1 | a0001c0001t0007g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.42+1308G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59621481 | ||||||
chr17:59621659 | C | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(174): Show | 200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.42+1486C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59621659 | ||||||
chr17:59621853 | T | C | 1 | a0001c0001t0002g0067 | 1 | NA19083.hp1 | intron_variant | MODIFIER | c.42+1680T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59621853 | ||||||
chr17:59621868 | C | G | 58 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(55): Show | 65 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.42+1695C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59621868 | ||||||
chr17:59621970 | G | A | 9 | a0001c0001t0006g0056a0001c0001t0007g0050a0001c0001t0007g0051others(6): Show | 9 | HG02809.hp1 HG02896.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.42+1797G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59621970 | ||||||
chr17:59622476 | C | A | 16 | a0001c0001t0004g0068a0001c0001t0004g0069a0001c0001t0004g0070others(13): Show | 16 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.42+2303C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622476 | ||||||
chr17:59622524 | T | C | 18 | a0001c0001t0004g0058a0001c0001t0006g0056a0001c0001t0006g0059others(15): Show | 18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.42+2351T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622524 | ||||||
chr17:59622627 | A | G | 206 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(203): Show | 229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.42+2454A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622627 | ||||||
chr17:59622651 | G | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0177 | 3 | HG00140.hp1 HG00544.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.42+2478G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622651 | ||||||
chr17:59622696 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.42+2523A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622696 | ||||||
chr17:59622735 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.42+2562A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622735 | ||||||
chr17:59622876 | G | A | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0013g0180 | 3 | HG01099.hp1 HG01169.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.42+2703G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622876 | ||||||
chr17:59622895 | T | C | 1 | a0001c0001t0010g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.42+2722T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622895 | ||||||
chr17:59622926 | G | A | 177 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(174): Show | 200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.42+2753G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622926 | ||||||
chr17:59622996 | A | G | 1 | a0001c0001t0007g0057 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.42+2823A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59622996 | ||||||
chr17:59623220 | G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.42+3047G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59623220 | ||||||
chr17:59623351 | T | G | 1 | a0001c0001t0001g0178 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.42+3178T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59623351 | ||||||
chr17:59623530 | G | A | 1 | a0001c0001t0001g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.42+3357G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59623530 | ||||||
chr17:59623792 | C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.42+3619C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59623792 | ||||||
chr17:59623888 | C | T | 1 | a0001c0001t0011g0228 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.42+3715C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59623888 | ||||||
chr17:59623945 | T | C | 6 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | HG02698.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.42+3772T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59623945 | ||||||
chr17:59624041 | C | T | 5 | a0001c0001t0002g0172a0001c0001t0002g0173a0001c0001t0002g0174others(2): Show | 5 | HG00621.hp1 HG02015.hp2 HG02027.hp2 others(2): Show |
intron_variant | MODIFIER | c.42+3868C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59624041 | ||||||
chr17:59624369 | A | G | 1 | a0001c0001t0002g0171 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.42+4196A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59624369 | ||||||
chr17:59624454 | C | CT | 18 | a0001c0001t0001g0084a0001c0001t0001g0121a0001c0001t0002g0122others(15): Show | 18 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(15): Show |
intron_variant | MODIFIER | c.42+4306dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59624454 | |||||
chr17:59624454 | C | CTT | 7 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(4): Show | 7 | HG01168.hp1 HG02109.hp2 HG02559.hp1 others(4): Show |
intron_variant | MODIFIER | c.42+4305_42+4306dup others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59624454 | |||||
chr17:59624454 | C | CTTT | 29 | a0001c0001t0002g0007a0001c0001t0002g0129a0001c0001t0002g0130others(26): Show | 32 | HG00639.hp1 HG00738.hp2 HG01123.hp1 others(29): Show |
intron_variant | MODIFIER | c.42+4304_42+4306dup others(3): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59624454 | |||||
chr17:59624454 | C | CTTTT | 23 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(20): Show | 35 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(32): Show |
intron_variant | MODIFIER | c.42+4303_42+4306dup others(4): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59624454 | |||||
chr17:59624454 | CT | C | 91 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 98 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.42+4306delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59624454 | |||||
chr17:59624454 | CTTT | C | 14 | a0001c0001t0004g0058a0001c0001t0006g0059a0001c0001t0006g0060others(11): Show | 14 | HG02257.hp1 HG02572.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.42+4304_42+4306del others(3): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59624454 | |||||
chr17:59624473 | T | G | 59 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(56): Show | 66 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(63): Show |
intron_variant | MODIFIER | c.42+4300T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59624473 | ||||||
chr17:59624567 | C | T | 1 | a0001c0001t0001g0112 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.42+4394C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59624567 | ||||||
chr17:59624787 | A | T | 1 | a0001c0001t0002g0122 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.42+4614A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59624787 | ||||||
chr17:59624789 | G | A | 1 | a0001c0001t0002g0122 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.42+4616G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59624789 | ||||||
chr17:59624790 | T | G | 1 | a0001c0001t0002g0122 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.42+4617T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59624790 | ||||||
chr17:59625110 | T | G | 1 | a0001c0001t0002g0129 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.42+4937T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625110 | ||||||
chr17:59625213 | A | G | 1 | a0001c0001t0001g0111 | 1 | HG03834.hp1 | intron_variant | MODIFIER | c.42+5040A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625213 | ||||||
chr17:59625231 | C | A | 1 | a0001c0001t0002g0122 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.42+5058C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625231 | ||||||
chr17:59625254 | G | A | 1 | a0001c0001t0003g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.42+5081G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625254 | ||||||
chr17:59625385 | G | A | 206 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(203): Show | 229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.42+5212G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625385 | ||||||
chr17:59625481 | C | T | 1 | a0001c0001t0003g0038 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.42+5308C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625481 | ||||||
chr17:59625492 | T | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(100): Show | 111 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.42+5319T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625492 | ||||||
chr17:59625513 | A | G | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG02055.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.42+5340A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625513 | ||||||
chr17:59625643 | C | T | 1 | a0001c0001t0006g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.42+5470C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625643 | ||||||
chr17:59625781 | C | T | 4 | a0001c0001t0005g0047a0001c0001t0005g0048a0001c0001t0005g0049others(1): Show | 4 | HG02896.hp2 HG03453.hp1 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+5608C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625781 | ||||||
chr17:59625835 | C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.42+5662C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625835 | ||||||
chr17:59625989 | A | C | 1 | a0001c0001t0001g0226 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.42+5816A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625989 | ||||||
chr17:59625999 | A | T | 1 | a0001c0001t0001g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.42+5826A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59625999 | ||||||
chr17:59626171 | A | G | 1 | a0001c0001t0011g0228 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.42+5998A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59626171 | ||||||
chr17:59626314 | A | T | 1 | a0001c0001t0004g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.42+6141A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59626314 | ||||||
chr17:59626732 | G | A | 1 | a0001c0001t0003g0021 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.42+6559G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59626732 | ||||||
chr17:59626907 | T | G | 1 | a0001c0001t0004g0058 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.42+6734T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59626907 | ||||||
chr17:59626908 | G | C | 1 | a0001c0001t0001g0181 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.42+6735G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59626908 | ||||||
chr17:59627073 | AT | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.42+6908delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59627073 | |||||
chr17:59627119 | T | C | 1 | a0001c0001t0003g0022 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.42+6946T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59627119 | ||||||
chr17:59627123 | A | T | 1 | a0001c0001t0003g0005 | 2 | HG04184.hp2 NA18961.hp2 |
intron_variant | MODIFIER | c.42+6950A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59627123 | ||||||
chr17:59627453 | C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.42+7280C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59627453 | ||||||
chr17:59627577 | T | C | 17 | a0001c0001t0006g0056a0001c0001t0006g0059a0001c0001t0006g0060others(14): Show | 17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.42+7404T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59627577 | ||||||
chr17:59627664 | A | C | 1 | a0001c0001t0001g0107 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.42+7491A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59627664 | ||||||
chr17:59627991 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.42+7818A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59627991 | ||||||
chr17:59628344 | A | G | 1 | a0001c0001t0001g0224 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.42+8171A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59628344 | ||||||
chr17:59628510 | A | G | 1 | a0001c0001t0001g0225 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.42+8337A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59628510 | ||||||
chr17:59628913 | C | T | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | NA19057.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.42+8740C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59628913 | ||||||
chr17:59628942 | G | A | 1 | a0001c0001t0002g0130 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.42+8769G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59628942 | ||||||
chr17:59628960 | C | A | 1 | a0001c0001t0014g0131 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.42+8787C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59628960 | ||||||
chr17:59629083 | CTT | C | 5 | a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0108others(2): Show | 5 | HG02055.hp2 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.42+8912_42+8913del others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59629083 | |||||
chr17:59629518 | A | AT | 76 | a0001c0001t0001g0084a0001c0001t0001g0094a0001c0001t0001g0123others(73): Show | 89 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(86): Show |
intron_variant | MODIFIER | c.42+9365dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59629518 | |||||
chr17:59629518 | A | ATT | 110 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(107): Show | 119 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(116): Show |
intron_variant | MODIFIER | c.42+9364_42+9365dup others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59629518 | |||||
chr17:59629518 | AT | A | 8 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(5): Show | 8 | HG01168.hp2 HG02257.hp2 HG02486.hp1 others(5): Show |
intron_variant | MODIFIER | c.42+9365delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59629518 | |||||
chr17:59629899 | C | T | 1 | a0001c0001t0006g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.42+9726C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59629899 | ||||||
chr17:59630092 | C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.42+9919C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59630092 | ||||||
chr17:59630151 | C | A | 1 | a0001c0001t0007g0050 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.42+9978C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59630151 | ||||||
chr17:59630200 | C | T | 1 | a0001c0001t0012g0221 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.42+10027C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59630200 | ||||||
chr17:59630392 | A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.42+10219A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59630392 | ||||||
chr17:59630568 | C | A | 17 | a0001c0001t0006g0056a0001c0001t0006g0059a0001c0001t0006g0060others(14): Show | 17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.42+10395C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59630568 | ||||||
chr17:59630582 | C | G | 3 | a0001c0001t0006g0063a0001c0001t0006g0064a0001c0001t0006g0065 | 3 | HG02572.hp1 HG02895.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.42+10409C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59630582 | ||||||
chr17:59630826 | A | G | 1 | a0001c0001t0001g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.42+10653A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59630826 | ||||||
chr17:59630873 | G | A | 10 | a0001c0001t0005g0040a0001c0001t0005g0041a0001c0001t0005g0042others(7): Show | 10 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.42+10700G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59630873 | ||||||
chr17:59631237 | T | G | 2 | a0001c0001t0003g0019a0001c0001t0003g0026 | 2 | HG02027.hp1 HG03239.hp1 |
intron_variant | MODIFIER | c.42+11064T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59631237 | ||||||
chr17:59631384 | A | T | 18 | a0001c0001t0004g0058a0001c0001t0006g0056a0001c0001t0006g0059others(15): Show | 18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.42+11211A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59631384 | ||||||
chr17:59631450 | A | G | 1 | a0001c0001t0002g0153 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.42+11277A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59631450 | ||||||
chr17:59631578 | T | G | 206 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(203): Show | 229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.42+11405T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59631578 | ||||||
chr17:59631711 | C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.42+11538C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59631711 | ||||||
chr17:59631778 | C | G | 2 | a0001c0001t0001g0108a0001c0001t0001g0110 | 2 | HG02055.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.42+11605C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59631778 | ||||||
chr17:59631969 | C | CA | 107 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(104): Show | 115 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(112): Show |
intron_variant | MODIFIER | c.42+11812dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59631969 | |||||
chr17:59631969 | CA | C | 11 | a0001c0001t0002g0176a0001c0001t0005g0040a0001c0001t0005g0041others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.42+11812delA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59631969 | |||||
chr17:59632007 | C | A | 1 | a0001c0001t0003g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.42+11834C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632007 | ||||||
chr17:59632087 | G | A | 1 | a0001c0001t0001g0011 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.42+11914G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632087 | ||||||
chr17:59632158 | G | A | 17 | a0001c0001t0006g0056a0001c0001t0006g0059a0001c0001t0006g0060others(14): Show | 17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.42+11985G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632158 | ||||||
chr17:59632161 | G | A | 1 | a0001c0001t0006g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.42+11988G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632161 | ||||||
chr17:59632224 | T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(174): Show | 200 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.42+12051T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632224 | ||||||
chr17:59632224 | T | G | 1 | a0001c0001t0002g0167 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.42+12051T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632224 | ||||||
chr17:59632225 | G | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 98 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.43-12051G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632225 | ||||||
chr17:59632346 | C | T | 1 | a0001c0001t0003g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.43-11930C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632346 | ||||||
chr17:59632367 | C | CA | 168 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(165): Show | 191 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(188): Show |
intron_variant | MODIFIER | c.43-11893dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59632367 | |||||
chr17:59632367 | C | CAA | 7 | a0001c0001t0001g0183a0001c0001t0001g0185a0001c0001t0001g0186others(4): Show | 7 | HG01109.hp1 HG01433.hp2 HG02135.hp2 others(4): Show |
intron_variant | MODIFIER | c.43-11894_43-11893d others(4): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59632367 | |||||
chr17:59632453 | G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.43-11823G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632453 | ||||||
chr17:59632734 | C | G | 1 | a0001c0001t0003g0026 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.43-11542C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59632734 | ||||||
chr17:59633028 | TTGTCATT others(13): Show |
T | 103 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(100): Show | 111 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.43-11218_43-11199d others(22): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59633028 | |||||
chr17:59633258 | A | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-11018A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59633258 | ||||||
chr17:59633319 | C | T | 1 | a0001c0001t0007g0055 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.43-10957C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59633319 | ||||||
chr17:59633398 | C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-10878C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59633398 | ||||||
chr17:59633584 | C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.43-10692C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59633584 | ||||||
chr17:59633670 | TA | T | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(193): Show | 219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.43-10604delA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59633670 | |||||
chr17:59634321 | C | T | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG02055.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.43-9955C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59634321 | ||||||
chr17:59634338 | G | T | 17 | a0001c0001t0006g0056a0001c0001t0006g0059a0001c0001t0006g0060others(14): Show | 17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.43-9938G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59634338 | ||||||
chr17:59634531 | G | T | 17 | a0001c0001t0006g0056a0001c0001t0006g0059a0001c0001t0006g0060others(14): Show | 17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.43-9745G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59634531 | ||||||
chr17:59634642 | C | A | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(193): Show | 219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.43-9634C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59634642 | ||||||
chr17:59634682 | CTA | C | 18 | a0001c0001t0004g0058a0001c0001t0006g0056a0001c0001t0006g0059others(15): Show | 18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-9590_43-9589del others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59634682 | |||||
chr17:59634762 | A | G | 1 | a0001c0001t0003g0019 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.43-9514A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59634762 | ||||||
chr17:59634828 | G | A | 1 | a0001c0001t0004g0070 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.43-9448G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59634828 | ||||||
chr17:59634966 | G | A | 1 | a0001c0001t0001g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.43-9310G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59634966 | ||||||
chr17:59635098 | GACCTATT others(83): Show |
G | 1 | a0001c0001t0004g0058 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.43-9177_43-9088del others(90): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59635098 | ||||||
chr17:59635189 | G | C | 1 | a0001c0001t0004g0058 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.43-9087G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59635189 | ||||||
chr17:59635488 | T | A | 3 | a0001c0001t0001g0183a0001c0001t0001g0188a0001c0001t0001g0219 | 3 | HG01261.hp2 HG02738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.43-8788T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59635488 | ||||||
chr17:59635727 | A | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.43-8549A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59635727 | ||||||
chr17:59635751 | A | G | 18 | a0001c0001t0004g0058a0001c0001t0006g0056a0001c0001t0006g0059others(15): Show | 18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-8525A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59635751 | ||||||
chr17:59635851 | G | A | 8 | a0001c0001t0001g0189a0001c0001t0001g0190a0001c0001t0001g0192others(5): Show | 8 | HG01433.hp1 HG01978.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-8425G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59635851 | ||||||
chr17:59635919 | A | G | 99 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(96): Show | 107 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.43-8357A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59635919 | ||||||
chr17:59636134 | C | CA | 10 | a0001c0001t0001g0095a0001c0001t0001g0096a0001c0001t0001g0097others(7): Show | 10 | HG00408.hp1 HG01978.hp1 HG04199.hp1 others(7): Show |
intron_variant | MODIFIER | c.43-8128dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59636134 | |||||
chr17:59636159 | C | G | 1 | a0001c0001t0001g0218 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.43-8117C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59636159 | ||||||
chr17:59636511 | G | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 98 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.43-7765G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59636511 | ||||||
chr17:59636517 | G | A | 1 | a0001c0001t0001g0185 | 1 | HG01433.hp2 | intron_variant | MODIFIER | c.43-7759G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59636517 | ||||||
chr17:59636788 | G | A | 3 | a0001c0001t0001g0012a0001c0001t0001g0195a0001c0001t0001g0196 | 4 | HG00621.hp2 HG02040.hp2 HG02129.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-7488G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59636788 | ||||||
chr17:59636855 | C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-7421C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59636855 | ||||||
chr17:59636932 | C | CT | 17 | a0001c0001t0001g0193a0001c0001t0002g0129a0001c0001t0002g0175others(14): Show | 17 | HG00621.hp1 HG01891.hp2 HG01981.hp1 others(14): Show |
intron_variant | MODIFIER | c.43-7323dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59636932 | |||||
chr17:59636932 | CT | C | 41 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(38): Show | 41 | HG00738.hp1 HG01934.hp1 HG01978.hp1 others(38): Show |
intron_variant | MODIFIER | c.43-7323delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59636932 | |||||
chr17:59636970 | T | C | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(193): Show | 219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.43-7306T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59636970 | ||||||
chr17:59637361 | C | T | 2 | a0001c0002t0002g0004a0001c0002t0002g0128 | 4 | HG01123.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-6915C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59637361 | ||||||
chr17:59637389 | T | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.43-6887T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59637389 | ||||||
chr17:59637554 | T | TA | 6 | a0001c0001t0001g0199a0001c0001t0002g0122a0001c0001t0002g0129others(3): Show | 6 | HG02523.hp2 HG02738.hp2 HG03098.hp2 others(3): Show |
intron_variant | MODIFIER | c.43-6706dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59637554 | |||||
chr17:59637588 | T | C | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(193): Show | 219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.43-6688T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59637588 | ||||||
chr17:59637633 | T | C | 18 | a0001c0001t0004g0058a0001c0001t0006g0056a0001c0001t0006g0059others(15): Show | 18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-6643T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59637633 | ||||||
chr17:59637698 | C | CA | 20 | a0001c0001t0003g0024a0001c0001t0003g0025a0001c0001t0003g0027others(17): Show | 20 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(17): Show |
intron_variant | MODIFIER | c.43-6560dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59637698 | |||||
chr17:59637698 | CA | C | 170 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(167): Show | 193 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(190): Show |
intron_variant | MODIFIER | c.43-6560delA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59637698 | |||||
chr17:59637899 | G | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.43-6377G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59637899 | ||||||
chr17:59637984 | CT | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-6289delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59637984 | |||||
chr17:59637986 | T | TA | 92 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(89): Show | 99 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(96): Show |
intron_variant | MODIFIER | c.43-6290_43-6289ins others(1): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59637986 | ||||||
chr17:59637987 | T | A | 209 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(206): Show | 233 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(230): Show |
intron_variant | MODIFIER | c.43-6289T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59637987 | ||||||
chr17:59638040 | A | T | 18 | a0001c0001t0004g0058a0001c0001t0006g0056a0001c0001t0006g0059others(15): Show | 18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-6236A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59638040 | ||||||
chr17:59638239 | G | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-6037G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59638239 | ||||||
chr17:59638507 | TGGC | T | 216 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(213): Show | 241 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.43-5765_43-5763del others(3): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59638507 | |||||
chr17:59638550 | C | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 98 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.43-5726C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59638550 | ||||||
chr17:59638792 | C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.43-5484C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59638792 | ||||||
chr17:59638808 | G | A | 1 | a0001c0001t0004g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.43-5468G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59638808 | ||||||
chr17:59639349 | G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.43-4927G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59639349 | ||||||
chr17:59639803 | T | TA | 201 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(198): Show | 224 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(221): Show |
intron_variant | MODIFIER | c.43-4458dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59639803 | |||||
chr17:59639822 | G | A | 1 | a0001c0001t0014g0131 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.43-4454G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59639822 | ||||||
chr17:59639971 | A | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-4305A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59639971 | ||||||
chr17:59640129 | A | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-4147A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59640129 | ||||||
chr17:59640135 | A | G | 7 | a0001c0001t0007g0050a0001c0001t0007g0051a0001c0001t0007g0052others(4): Show | 7 | HG02809.hp1 HG02896.hp1 HG03195.hp1 others(4): Show |
intron_variant | MODIFIER | c.43-4141A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59640135 | ||||||
chr17:59640376 | C | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.43-3900C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59640376 | ||||||
chr17:59640402 | C | CT | 33 | a0001c0001t0001g0006a0001c0001t0001g0092a0001c0001t0001g0093others(30): Show | 34 | HG00639.hp2 HG01099.hp2 HG01884.hp1 others(31): Show |
intron_variant | MODIFIER | c.43-3860dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59640402 | |||||
chr17:59640550 | C | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 98 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.43-3726C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59640550 | ||||||
chr17:59640714 | T | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-3562T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59640714 | ||||||
chr17:59640838 | C | T | 1 | a0001c0001t0001g0090 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.43-3438C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59640838 | ||||||
chr17:59640916 | C | T | 1 | a0001c0001t0001g0091 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.43-3360C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59640916 | ||||||
chr17:59641075 | TGCCACTG others(475): Show |
T | 1 | a0001c0001t0001g0011 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.43-3193_43-2712del | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641075 | |||||
chr17:59641117 | C | CA | 16 | a0001c0001t0002g0137a0001c0001t0004g0068a0001c0001t0004g0069others(13): Show | 16 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.43-3148dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641117 | |||||
chr17:59641117 | C | CAA | 87 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0012others(84): Show | 93 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(90): Show |
intron_variant | MODIFIER | c.43-3149_43-3148dup others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641117 | |||||
chr17:59641398 | C | T | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-2878C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59641398 | ||||||
chr17:59641475 | C | G | 18 | a0001c0001t0004g0058a0001c0001t0006g0056a0001c0001t0006g0059others(15): Show | 18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-2801C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59641475 | ||||||
chr17:59641603 | C | CA | 24 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(21): Show | 25 | HG01109.hp1 HG01255.hp2 HG01256.hp2 others(22): Show |
intron_variant | MODIFIER | c.43-2649dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641603 | |||||
chr17:59641603 | C | CAA | 90 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(87): Show | 97 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(94): Show |
intron_variant | MODIFIER | c.43-2650_43-2649dup others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641603 | |||||
chr17:59641603 | C | CAAA | 48 | a0001c0001t0001g0113a0001c0001t0001g0195a0001c0001t0001g0220others(45): Show | 63 | HG00408.hp2 HG00544.hp1 HG00621.hp1 others(60): Show |
intron_variant | MODIFIER | c.43-2651_43-2649dup others(3): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641603 | |||||
chr17:59641603 | C | CAAAA | 16 | a0001c0001t0001g0108a0001c0001t0001g0110a0001c0001t0001g0233others(13): Show | 16 | HG00423.hp2 HG02027.hp2 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.43-2652_43-2649dup others(4): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641603 | |||||
chr17:59641603 | CAAAAAAA others(4): Show |
C | 2 | a0001c0001t0001g0092a0001c0001t0001g0093 | 2 | HG02965.hp1 HG03098.hp1 |
intron_variant | MODIFIER | c.43-2659_43-2649del others(11): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641603 | |||||
chr17:59641943 | C | T | 1 | a0001c0001t0008g0003 | 3 | HG01891.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.43-2333C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59641943 | ||||||
chr17:59641992 | C | T | 1 | a0001c0001t0006g0064 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.43-2284C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59641992 | ||||||
chr17:59641999 | G | GT | 15 | a0001c0001t0001g0126a0001c0001t0006g0056a0001c0001t0006g0059others(12): Show | 15 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(12): Show |
intron_variant | MODIFIER | c.43-2253dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641999 | |||||
chr17:59641999 | GT | G | 29 | a0001c0001t0001g0225a0001c0001t0002g0122a0001c0001t0003g0014others(26): Show | 32 | HG00140.hp2 HG01168.hp2 HG01255.hp1 others(29): Show |
intron_variant | MODIFIER | c.43-2253delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641999 | |||||
chr17:59641999 | GTTT | G | 8 | a0001c0001t0005g0041a0001c0001t0005g0042a0001c0001t0005g0043others(5): Show | 8 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(5): Show |
intron_variant | MODIFIER | c.43-2255_43-2253del others(3): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59641999 | |||||
chr17:59642004 | T | TG | 11 | a0001c0001t0001g0090a0001c0001t0001g0091a0001c0001t0001g0103others(8): Show | 12 | HG00738.hp2 HG01884.hp1 HG01884.hp2 others(9): Show |
intron_variant | MODIFIER | c.43-2272_43-2271ins others(1): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642004 | ||||||
chr17:59642005 | T | G | 160 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(157): Show | 182 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(179): Show |
intron_variant | MODIFIER | c.43-2271T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642005 | ||||||
chr17:59642006 | T | G | 5 | a0001c0001t0001g0225a0001c0001t0002g0122a0001c0001t0004g0070others(2): Show | 5 | HG03453.hp1 HG06807.hp2 NA18982.hp1 others(2): Show |
intron_variant | MODIFIER | c.43-2270T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642006 | ||||||
chr17:59642011 | T | G | 2 | a0001c0001t0004g0076a0001c0001t0004g0083 | 2 | HG02559.hp1 HG02717.hp2 |
intron_variant | MODIFIER | c.43-2265T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642011 | ||||||
chr17:59642012 | T | G | 1 | a0001c0001t0001g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.43-2264T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642012 | ||||||
chr17:59642013 | T | G | 2 | a0001c0001t0001g0084a0001c0001t0001g0098 | 2 | HG02723.hp1 NA18950.hp2 |
intron_variant | MODIFIER | c.43-2263T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642013 | ||||||
chr17:59642207 | A | C | 18 | a0001c0001t0004g0058a0001c0001t0006g0056a0001c0001t0006g0059others(15): Show | 18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-2069A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642207 | ||||||
chr17:59642208 | A | G | 1 | a0001c0001t0001g0208 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.43-2068A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642208 | ||||||
chr17:59642440 | G | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.43-1836G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642440 | ||||||
chr17:59642441 | C | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.43-1835C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642441 | ||||||
chr17:59642520 | A | C | 206 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(203): Show | 229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.43-1756A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642520 | ||||||
chr17:59642702 | A | G | 1 | a0001c0001t0003g0023 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.43-1574A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59642702 | ||||||
chr17:59643099 | G | C | 1 | a0001c0001t0001g0227 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.43-1177G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59643099 | ||||||
chr17:59643129 | T | TGG | 8 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0111others(5): Show | 8 | HG02630.hp1 HG02698.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.43-1144_43-1143dup others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59643129 | |||||
chr17:59643132 | G | GGGGTGTG others(3): Show |
1 | a0001c0001t0002g0142 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.43-1143_43-1142ins others(10): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59643132 | |||||
chr17:59643132 | G | GGT | 8 | a0001c0001t0002g0007a0001c0001t0002g0120a0001c0001t0002g0157others(5): Show | 11 | HG01891.hp1 HG02559.hp2 HG03139.hp2 others(8): Show |
intron_variant | MODIFIER | c.43-1109_43-1108dup others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59643132 | |||||
chr17:59643132 | G | GGTGT | 21 | a0001c0001t0002g0127a0001c0001t0002g0143a0001c0001t0003g0019others(18): Show | 21 | HG01109.hp2 HG01243.hp2 HG01891.hp2 others(18): Show |
intron_variant | MODIFIER | c.43-1111_43-1108dup others(4): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59643132 | |||||
chr17:59643132 | G | GGTGTGT | 55 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0009others(52): Show | 70 | HG00423.hp2 HG00544.hp1 HG01123.hp1 others(67): Show |
intron_variant | MODIFIER | c.43-1113_43-1108dup others(6): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59643132 | |||||
chr17:59643132 | G | GGTGTGTG others(1): Show |
18 | a0001c0001t0002g0067a0001c0001t0002g0136a0001c0001t0002g0140others(15): Show | 18 | HG00408.hp2 HG00621.hp1 HG00639.hp1 others(15): Show |
intron_variant | MODIFIER | c.43-1115_43-1108dup others(8): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59643132 | |||||
chr17:59643132 | G | GGTGTGTG others(3): Show |
4 | a0001c0001t0002g0152a0001c0001t0002g0166a0001c0001t0005g0044others(1): Show | 4 | HG00738.hp2 HG02965.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-1117_43-1108dup others(10): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59643132 | |||||
chr17:59643132 | G | GGTGTGTG others(5): Show |
2 | a0001c0001t0005g0046a0001c0001t0007g0055 | 2 | HG02615.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.43-1119_43-1108dup others(12): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59643132 | |||||
chr17:59643132 | GGT | G | 16 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(13): Show | 17 | HG01099.hp2 HG01168.hp2 HG01884.hp1 others(14): Show |
intron_variant | MODIFIER | c.43-1109_43-1108del others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | INFO_REALIGN_3_PRIME | chr17 | 59643132 | |||||
chr17:59643134 | T | G | 64 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(61): Show | 70 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(67): Show |
intron_variant | MODIFIER | c.43-1142T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59643134 | ||||||
chr17:59643136 | T | G | 1 | a0001c0001t0001g0231 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.43-1140T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59643136 | ||||||
chr17:59643138 | T | G | 1 | a0001c0001t0001g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.43-1138T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59643138 | ||||||
chr17:59643380 | G | A | 1 | a0001c0001t0001g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.43-896G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59643380 | ||||||
chr17:59643516 | A | G | 1 | a0001c0001t0001g0206 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.43-760A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59643516 | ||||||
chr17:59643780 | T | C | 1 | a0001c0001t0001g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.43-496T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59643780 | ||||||
chr17:59644175 | T | C | 4 | a0001c0001t0002g0127a0001c0001t0002g0138a0001c0001t0002g0140others(1): Show | 4 | NA19057.hp1 NA19060.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.43-101T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 1/31 | chr17 | 59644175 | ||||||
chr17:59644529 | G | T | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+46G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59644529 | ||||||
chr17:59644535 | T | G | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.250+52T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59644535 | ||||||
chr17:59644546 | T | G | 4 | a0001c0001t0001g0123a0001c0001t0001g0126a0001c0001t0001g0207others(1): Show | 4 | HG02109.hp2 HG02280.hp2 HG03492.hp1 others(1): Show |
intron_variant | MODIFIER | c.250+63T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59644546 | ||||||
chr17:59644546 | T | TTTTG | 172 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(169): Show | 195 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.250+79_250+82dupGT others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr17 | 59644546 | |||||
chr17:59644550 | G | T | 16 | a0001c0001t0006g0056a0001c0001t0006g0059a0001c0001t0006g0060others(13): Show | 16 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.250+67G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59644550 | ||||||
chr17:59644624 | C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.250+141C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59644624 | ||||||
chr17:59644641 | C | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.250+158C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59644641 | ||||||
chr17:59645386 | G | C | 1 | a0001c0001t0002g0163 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.250+903G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59645386 | ||||||
chr17:59645864 | C | CT | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.250+1383dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr17 | 59645864 | |||||
chr17:59645912 | G | A | 75 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(72): Show | 90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.250+1429G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59645912 | ||||||
chr17:59645940 | A | G | 1 | a0001c0001t0001g0199 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.250+1457A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59645940 | ||||||
chr17:59646514 | T | C | 1 | a0001c0001t0003g0029 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.251-884T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59646514 | ||||||
chr17:59646548 | T | A | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.251-850T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59646548 | ||||||
chr17:59646740 | C | T | 1 | a0001c0001t0001g0189 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.251-658C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59646740 | ||||||
chr17:59646980 | C | A | 1 | a0001c0001t0002g0007 | 2 | HG03491.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.251-418C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59646980 | ||||||
chr17:59647180 | A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.251-218A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59647180 | ||||||
chr17:59647222 | G | C | 1 | a0001c0001t0001g0212 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.251-176G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 2/31 | chr17 | 59647222 | ||||||
chr17:59647682 | T | G | 206 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(203): Show | 229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.519+16T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 3/31 | chr17 | 59647682 | ||||||
chr17:59647853 | C | T | 1 | a0001c0001t0016g0156 | 1 | NA19062.hp2 | intron_variant | MODIFIER | c.519+187C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 3/31 | chr17 | 59647853 | ||||||
chr17:59648120 | G | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.520-120G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 3/31 | chr17 | 59648120 | ||||||
chr17:59648923 | G | C | 1 | a0001c0001t0001g0092 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.681+522G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59648923 | ||||||
chr17:59648994 | T | C | 17 | a0001c0001t0004g0068a0001c0001t0004g0069a0001c0001t0004g0070others(14): Show | 17 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.681+593T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59648994 | ||||||
chr17:59649330 | C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.681+929C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59649330 | ||||||
chr17:59649888 | G | GC | 206 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(203): Show | 229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.682-1314dupC | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 59649888 | |||||
chr17:59649929 | A | G | 1 | a0001c0001t0004g0083 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.682-1274A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59649929 | ||||||
chr17:59650275 | A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.682-928A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59650275 | ||||||
chr17:59650313 | T | A | 1 | a0001c0001t0001g0093 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.682-890T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59650313 | ||||||
chr17:59650430 | C | T | 3 | a0001c0001t0002g0139a0001c0001t0002g0149a0001c0001t0002g0154 | 3 | NA18955.hp2 NA18972.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.682-773C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59650430 | ||||||
chr17:59650483 | C | CT | 11 | a0001c0001t0001g0084a0001c0001t0001g0125a0001c0001t0001g0206others(8): Show | 11 | HG00423.hp1 HG01243.hp2 HG02723.hp1 others(8): Show |
intron_variant | MODIFIER | c.682-698dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 59650483 | |||||
chr17:59650483 | CT | C | 58 | a0001c0001t0001g0226a0001c0001t0002g0001a0001c0001t0002g0007others(55): Show | 73 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.682-698delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr17 | 59650483 | |||||
chr17:59650513 | A | G | 17 | a0001c0001t0006g0056a0001c0001t0006g0059a0001c0001t0006g0060others(14): Show | 17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.682-690A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59650513 | ||||||
chr17:59650555 | C | G | 1 | a0001c0001t0002g0151 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.682-648C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59650555 | ||||||
chr17:59650983 | C | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 98 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.682-220C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59650983 | ||||||
chr17:59651106 | A | G | 1 | a0001c0001t0003g0020 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.682-97A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 4/31 | chr17 | 59651106 | ||||||
chr17:59651458 | A | G | 2 | a0001c0001t0001g0205a0001c0001t0001g0220 | 2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.795+142A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59651458 | ||||||
chr17:59651654 | A | G | 2 | a0001c0001t0006g0061a0001c0001t0006g0066 | 2 | HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.795+338A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59651654 | ||||||
chr17:59651655 | T | A | 1 | a0001c0001t0001g0187 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.795+339T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59651655 | ||||||
chr17:59651656 | A | G | 1 | a0001c0001t0008g0003 | 3 | HG01891.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.795+340A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59651656 | ||||||
chr17:59651690 | A | C | 1 | a0001c0001t0001g0199 | 1 | HG02523.hp2 | intron_variant | MODIFIER | c.795+374A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59651690 | ||||||
chr17:59652148 | G | C | 1 | a0001c0001t0001g0105 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.795+832G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59652148 | ||||||
chr17:59652195 | G | A | 3 | a0001c0001t0001g0185a0001c0001t0001g0186a0001c0001t0001g0227 | 3 | HG01109.hp1 HG01433.hp2 HG02280.hp1 |
intron_variant | MODIFIER | c.795+879G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59652195 | ||||||
chr17:59652224 | T | C | 3 | a0001c0001t0001g0178a0001c0001t0001g0179a0001c0001t0013g0180 | 3 | HG01099.hp1 HG01169.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.795+908T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59652224 | ||||||
chr17:59652483 | T | C | 1 | a0001c0001t0001g0196 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.795+1167T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59652483 | ||||||
chr17:59652496 | C | T | 1 | a0001c0001t0003g0026 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.795+1180C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59652496 | ||||||
chr17:59652588 | C | T | 3 | a0001c0001t0002g0139a0001c0001t0002g0149a0001c0001t0002g0154 | 3 | NA18955.hp2 NA18972.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.795+1272C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59652588 | ||||||
chr17:59652678 | T | G | 17 | a0001c0001t0006g0056a0001c0001t0006g0059a0001c0001t0006g0060others(14): Show | 17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.795+1362T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59652678 | ||||||
chr17:59652828 | A | G | 104 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(101): Show | 112 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.795+1512A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59652828 | ||||||
chr17:59652896 | G | A | 1 | a0001c0001t0001g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.795+1580G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59652896 | ||||||
chr17:59653070 | C | T | 1 | a0001c0001t0003g0034 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.795+1754C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59653070 | ||||||
chr17:59653166 | T | C | 3 | a0001c0001t0006g0060a0001c0001t0006g0061a0001c0001t0006g0066 | 3 | HG02257.hp1 HG02647.hp1 HG02809.hp2 |
intron_variant | MODIFIER | c.795+1850T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59653166 | ||||||
chr17:59653171 | GTTTA | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.795+1875_795+1878d others(6): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr17 | 59653171 | |||||
chr17:59653196 | A | T | 1 | a0001c0001t0002g0147 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.795+1880A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59653196 | ||||||
chr17:59653204 | T | A | 99 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(96): Show | 107 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(104): Show |
intron_variant | MODIFIER | c.795+1888T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59653204 | ||||||
chr17:59653256 | C | T | 10 | a0001c0001t0005g0040a0001c0001t0005g0041a0001c0001t0005g0042others(7): Show | 10 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.795+1940C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59653256 | ||||||
chr17:59653294 | C | T | 1 | a0001c0001t0007g0230 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.795+1978C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59653294 | ||||||
chr17:59653444 | C | T | 75 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(72): Show | 90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.795+2128C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59653444 | ||||||
chr17:59653852 | A | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.796-2002A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59653852 | ||||||
chr17:59653961 | T | C | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(193): Show | 219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.796-1893T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59653961 | ||||||
chr17:59654206 | C | T | 10 | a0001c0001t0005g0040a0001c0001t0005g0041a0001c0001t0005g0042others(7): Show | 10 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.796-1648C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59654206 | ||||||
chr17:59654236 | C | T | 1 | a0001c0001t0007g0055 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.796-1618C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59654236 | ||||||
chr17:59654408 | CCTCAAGT others(296): Show |
C | 1 | a0001c0001t0001g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.796-1441_796-1139d others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr17 | 59654408 | |||||
chr17:59654503 | C | T | 18 | a0001c0001t0004g0058a0001c0001t0006g0056a0001c0001t0006g0059others(15): Show | 18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.796-1351C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59654503 | ||||||
chr17:59654566 | C | T | 10 | a0001c0001t0003g0016a0001c0001t0003g0017a0001c0001t0003g0018others(7): Show | 12 | HG01168.hp2 HG01891.hp1 HG02027.hp1 others(9): Show |
intron_variant | MODIFIER | c.796-1288C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59654566 | ||||||
chr17:59654624 | T | C | 193 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(190): Show | 216 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(213): Show |
intron_variant | MODIFIER | c.796-1230T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59654624 | ||||||
chr17:59654655 | G | A | 1 | a0001c0001t0001g0102 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.796-1199G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59654655 | ||||||
chr17:59654732 | C | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0188a0001c0001t0001g0219 | 3 | HG01261.hp2 HG02738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.796-1122C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59654732 | ||||||
chr17:59654919 | A | C | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(193): Show | 219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.796-935A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59654919 | ||||||
chr17:59655224 | C | T | 75 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(72): Show | 90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.796-630C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59655224 | ||||||
chr17:59655232 | G | T | 17 | a0001c0001t0004g0068a0001c0001t0004g0069a0001c0001t0004g0070others(14): Show | 17 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.796-622G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59655232 | ||||||
chr17:59655412 | G | A | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(193): Show | 219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.796-442G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59655412 | ||||||
chr17:59655553 | G | A | 76 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(73): Show | 91 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(88): Show |
intron_variant | MODIFIER | c.796-301G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59655553 | ||||||
chr17:59655565 | C | CT | 75 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(72): Show | 90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.796-288dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr17 | 59655565 | |||||
chr17:59655596 | C | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.796-258C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59655596 | ||||||
chr17:59655648 | T | C | 1 | a0001c0001t0002g0150 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.796-206T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 5/31 | chr17 | 59655648 | ||||||
chr17:59656076 | T | C | 1 | a0001c0001t0005g0041 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.969+49T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656076 | ||||||
chr17:59656118 | T | A | 206 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(203): Show | 229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.969+91T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656118 | ||||||
chr17:59656262 | A | G | 1 | a0001c0001t0010g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.969+235A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656262 | ||||||
chr17:59656270 | A | T | 1 | a0001c0001t0003g0018 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.969+243A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656270 | ||||||
chr17:59656399 | T | TC | 206 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(203): Show | 229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.969+372_969+373ins others(1): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656399 | ||||||
chr17:59656437 | A | G | 98 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(95): Show | 106 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.969+410A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656437 | ||||||
chr17:59656545 | G | A | 1 | a0001c0001t0001g0091 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.969+518G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656545 | ||||||
chr17:59656666 | A | AT | 15 | a0001c0001t0004g0068a0001c0001t0004g0069a0001c0001t0004g0073others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02451.hp1 others(12): Show |
intron_variant | MODIFIER | c.969+661dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr17 | 59656666 | |||||
chr17:59656666 | AT | A | 143 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(140): Show | 167 | HG00140.hp1 HG00408.hp2 HG00423.hp1 others(164): Show |
intron_variant | MODIFIER | c.969+661delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr17 | 59656666 | |||||
chr17:59656670 | T | C | 1 | a0001c0001t0001g0194 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.969+643T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656670 | ||||||
chr17:59656688 | T | C | 1 | a0001c0001t0003g0030 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.969+661T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656688 | ||||||
chr17:59656705 | G | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(100): Show | 111 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.969+678G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656705 | ||||||
chr17:59656719 | G | A | 1 | a0001c0001t0004g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.969+692G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656719 | ||||||
chr17:59656963 | C | T | 1 | a0001c0001t0001g0213 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.969+936C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59656963 | ||||||
chr17:59657200 | G | A | 1 | a0001c0001t0001g0118 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.969+1173G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59657200 | ||||||
chr17:59657203 | G | T | 3 | a0001c0001t0003g0022a0001c0001t0003g0023a0001c0001t0003g0024 | 3 | HG01168.hp2 HG02572.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.969+1176G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59657203 | ||||||
chr17:59657299 | T | C | 216 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(213): Show | 241 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.969+1272T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59657299 | ||||||
chr17:59657324 | G | A | 1 | a0001c0001t0001g0232 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.969+1297G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59657324 | ||||||
chr17:59657329 | G | A | 75 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(72): Show | 90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.969+1302G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59657329 | ||||||
chr17:59657678 | G | C | 1 | a0001c0001t0001g0233 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.969+1651G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59657678 | ||||||
chr17:59657767 | C | CA | 5 | a0001c0001t0001g0095a0001c0001t0001g0183a0001c0001t0002g0144others(2): Show | 5 | HG02602.hp2 HG02738.hp1 HG06807.hp2 others(2): Show |
intron_variant | MODIFIER | c.969+1757dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr17 | 59657767 | |||||
chr17:59657767 | CA | C | 5 | a0001c0001t0001g0111a0001c0001t0001g0118a0001c0001t0001g0225others(2): Show | 5 | HG01099.hp2 HG02965.hp2 HG03834.hp1 others(2): Show |
intron_variant | MODIFIER | c.969+1757delA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr17 | 59657767 | |||||
chr17:59657798 | G | T | 1 | a0001c0001t0001g0203 | 1 | NA18952.hp2 | intron_variant | MODIFIER | c.969+1771G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59657798 | ||||||
chr17:59657804 | A | G | 1 | a0001c0001t0001g0202 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.969+1777A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59657804 | ||||||
chr17:59657974 | G | A | 1 | a0001c0001t0003g0031 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.969+1947G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59657974 | ||||||
chr17:59658204 | A | G | 103 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(100): Show | 111 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.969+2177A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59658204 | ||||||
chr17:59658275 | C | T | 1 | a0001c0001t0001g0202 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.970-2116C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59658275 | ||||||
chr17:59658323 | C | T | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.970-2068C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59658323 | ||||||
chr17:59658376 | C | T | 1 | a0001c0001t0001g0093 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.970-2015C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59658376 | ||||||
chr17:59658624 | T | C | 2 | a0001c0001t0001g0205a0001c0001t0001g0220 | 2 | HG04115.hp1 NA20905.hp1 |
intron_variant | MODIFIER | c.970-1767T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59658624 | ||||||
chr17:59658965 | T | C | 216 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(213): Show | 241 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.970-1426T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59658965 | ||||||
chr17:59658996 | T | C | 1 | a0001c0001t0001g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.970-1395T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59658996 | ||||||
chr17:59659304 | A | G | 1 | a0001c0001t0001g0126 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.970-1087A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59659304 | ||||||
chr17:59659429 | ATTTTTAT | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.970-950_970-944del others(7): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr17 | 59659429 | |||||
chr17:59659453 | AT | A | 6 | a0001c0001t0001g0097a0001c0001t0001g0126a0001c0001t0001g0192others(3): Show | 6 | HG00544.hp1 HG01978.hp1 HG01978.hp2 others(3): Show |
intron_variant | MODIFIER | c.970-923delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr17 | 59659453 | |||||
chr17:59659453 | ATT | A | 172 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(169): Show | 195 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(192): Show |
intron_variant | MODIFIER | c.970-924_970-923del others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr17 | 59659453 | |||||
chr17:59659473 | CAG | C | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.970-915_970-914del others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr17 | 59659473 | |||||
chr17:59659619 | A | T | 1 | a0001c0001t0001g0116 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.970-772A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59659619 | ||||||
chr17:59659649 | C | A | 1 | a0001c0001t0006g0062 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.970-742C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59659649 | ||||||
chr17:59659762 | C | T | 1 | a0001c0001t0010g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.970-629C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59659762 | ||||||
chr17:59659877 | A | C | 1 | a0001c0001t0002g0151 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.970-514A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59659877 | ||||||
chr17:59660002 | A | C | 75 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(72): Show | 90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.970-389A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59660002 | ||||||
chr17:59660136 | G | A | 1 | a0001c0001t0001g0204 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.970-255G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 6/31 | chr17 | 59660136 | ||||||
chr17:59660627 | C | T | 10 | a0001c0001t0005g0040a0001c0001t0005g0041a0001c0001t0005g0042others(7): Show | 10 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.1167+39C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 7/31 | chr17 | 59660627 | ||||||
chr17:59661066 | CTTAAT | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.1168-371_1168-367d others(7): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr17 | 59661066 | |||||
chr17:59661179 | AT | A | 18 | a0001c0001t0001g0084a0001c0001t0006g0056a0001c0001t0006g0059others(15): Show | 18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.1168-251delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr17 | 59661179 | |||||
chr17:59661231 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1168-212A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 7/31 | chr17 | 59661231 | ||||||
chr17:59661283 | C | T | 58 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(55): Show | 73 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1168-160C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 7/31 | chr17 | 59661283 | ||||||
chr17:59661376 | C | G | 3 | a0001c0001t0001g0108a0001c0001t0001g0109a0001c0001t0001g0110 | 3 | HG02055.hp2 HG02818.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.1168-67C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 7/31 | chr17 | 59661376 | ||||||
chr17:59661384 | G | A | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1168-59G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 7/31 | chr17 | 59661384 | ||||||
chr17:59661712 | A | G | 1 | a0001c0001t0004g0080 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1368+69A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59661712 | ||||||
chr17:59661906 | C | T | 91 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 98 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.1368+263C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59661906 | ||||||
chr17:59662018 | A | C | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1368+375A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59662018 | ||||||
chr17:59662060 | A | G | 4 | a0001c0001t0002g0127a0001c0001t0002g0138a0001c0001t0002g0140others(1): Show | 4 | NA19057.hp1 NA19060.hp1 NA19084.hp2 others(1): Show |
intron_variant | MODIFIER | c.1368+417A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59662060 | ||||||
chr17:59662714 | C | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(100): Show | 111 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.1368+1071C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59662714 | ||||||
chr17:59662831 | T | A | 17 | a0001c0001t0004g0068a0001c0001t0004g0069a0001c0001t0004g0070others(14): Show | 17 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.1369-1011T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59662831 | ||||||
chr17:59662902 | T | C | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(193): Show | 219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.1369-940T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59662902 | ||||||
chr17:59663161 | A | T | 1 | a0001c0001t0001g0194 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.1369-681A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59663161 | ||||||
chr17:59663393 | A | C | 1 | a0001c0001t0001g0214 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1369-449A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59663393 | ||||||
chr17:59663558 | C | A | 2 | a0001c0001t0001g0010a0001c0001t0001g0177 | 3 | HG00140.hp1 HG00544.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.1369-284C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59663558 | ||||||
chr17:59663694 | A | G | 1 | a0001c0001t0001g0211 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.1369-148A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 8/31 | chr17 | 59663694 | ||||||
chr17:59664132 | T | A | 1 | a0001c0001t0007g0055 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1521+138T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 9/31 | chr17 | 59664132 | ||||||
chr17:59664425 | T | C | 58 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(55): Show | 73 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1522-362T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 9/31 | chr17 | 59664425 | ||||||
chr17:59664450 | C | T | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.1522-337C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 9/31 | chr17 | 59664450 | ||||||
chr17:59664550 | C | CA | 5 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(2): Show | 5 | HG01934.hp2 HG01952.hp2 HG01975.hp1 others(2): Show |
intron_variant | MODIFIER | c.1522-220dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr17 | 59664550 | |||||
chr17:59664550 | CA | C | 98 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(95): Show | 106 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(103): Show |
intron_variant | MODIFIER | c.1522-220delA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr17 | 59664550 | |||||
chr17:59664562 | AAAAAAG | A | 71 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(68): Show | 86 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(83): Show |
intron_variant | MODIFIER | c.1522-220_1522-215d others(8): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr17 | 59664562 | |||||
chr17:59664563 | AAAAAG | A | 5 | a0001c0001t0002g0129a0001c0001t0002g0144a0001c0001t0006g0063others(2): Show | 5 | HG02572.hp1 HG02602.hp2 HG02738.hp2 others(2): Show |
intron_variant | MODIFIER | c.1522-204_1522-200d others(7): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr17 | 59664563 | |||||
chr17:59665096 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1644+187A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 10/31 | chr17 | 59665096 | ||||||
chr17:59665190 | A | T | 1 | a0001c0001t0004g0082 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1644+281A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 10/31 | chr17 | 59665190 | ||||||
chr17:59665226 | GA | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.1644+329delA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 10/31 | INFO_REALIGN_3_PRIME | chr17 | 59665226 | |||||
chr17:59665249 | C | G | 1 | a0001c0001t0001g0201 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.1644+340C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 10/31 | chr17 | 59665249 | ||||||
chr17:59665335 | G | A | 1 | a0001c0001t0001g0190 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1644+426G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 10/31 | chr17 | 59665335 | ||||||
chr17:59665475 | A | G | 58 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(55): Show | 73 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.1644+566A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 10/31 | chr17 | 59665475 | ||||||
chr17:59665766 | G | A | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1645-337G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 10/31 | chr17 | 59665766 | ||||||
chr17:59666290 | T | C | 3 | a0001c0001t0001g0192a0001c0001t0001g0193a0001c0004t0001g0191 | 3 | HG01433.hp1 HG01978.hp2 HG01981.hp1 |
intron_variant | MODIFIER | c.1782+50T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 11/31 | chr17 | 59666290 | ||||||
chr17:59666330 | G | A | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(193): Show | 219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.1782+90G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 11/31 | chr17 | 59666330 | ||||||
chr17:59666372 | C | A | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.1783-108C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 11/31 | chr17 | 59666372 | ||||||
chr17:59666417 | G | A | 2 | a0001c0001t0002g0155a0001c0001t0018g0158 | 2 | HG01981.hp2 NA20300.hp2 |
intron_variant | MODIFIER | c.1783-63G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 11/31 | chr17 | 59666417 | ||||||
chr17:59666455 | A | G | 1 | a0001c0001t0001g0098 | 1 | NA18950.hp2 | intron_variant | MODIFIER | c.1783-25A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 11/31 | chr17 | 59666455 | ||||||
chr17:59667051 | G | A | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(193): Show | 219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.2128+74G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59667051 | ||||||
chr17:59667085 | A | C | 1 | a0001c0001t0003g0035 | 1 | NA18993.hp2 | intron_variant | MODIFIER | c.2128+108A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59667085 | ||||||
chr17:59667145 | T | G | 2 | a0001c0001t0005g0040a0001c0001t0005g0045 | 2 | HG03041.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.2128+168T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59667145 | ||||||
chr17:59667289 | A | G | 1 | a0001c0001t0003g0036 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.2128+312A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59667289 | ||||||
chr17:59667302 | G | A | 1 | a0001c0001t0004g0058 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.2128+325G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59667302 | ||||||
chr17:59667313 | C | T | 216 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(213): Show | 241 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.2128+336C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59667313 | ||||||
chr17:59667409 | G | A | 1 | a0001c0001t0001g0216 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.2128+432G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59667409 | ||||||
chr17:59668196 | A | C | 1 | a0001c0001t0001g0226 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.2129-581A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59668196 | ||||||
chr17:59668288 | G | C | 1 | a0001c0001t0001g0214 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.2129-489G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59668288 | ||||||
chr17:59668511 | C | T | 16 | a0001c0001t0004g0068a0001c0001t0004g0069a0001c0001t0004g0070others(13): Show | 16 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(13): Show |
intron_variant | MODIFIER | c.2129-266C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59668511 | ||||||
chr17:59668581 | G | T | 1 | a0001c0001t0002g0167 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2129-196G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59668581 | ||||||
chr17:59668652 | C | T | 2 | a0001c0001t0001g0207a0001c0001t0001g0215 | 2 | HG00639.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2129-125C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59668652 | ||||||
chr17:59668746 | A | G | 75 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(72): Show | 90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.2129-31A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 13/31 | chr17 | 59668746 | ||||||
chr17:59669692 | C | G | 6 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(3): Show | 6 | HG02698.hp1 HG02717.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.2292+752C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59669692 | ||||||
chr17:59669724 | C | CTA | 80 | a0001c0001t0001g0084a0001c0001t0001g0123a0001c0001t0001g0124others(77): Show | 95 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(92): Show |
intron_variant | MODIFIER | c.2292+797_2292+798d others(4): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59669724 | |||||
chr17:59669737 | T | TATAA | 91 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 98 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.2292+798_2292+799i others(6): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59669737 | |||||
chr17:59669737 | T | TATATAA | 6 | a0001c0001t0001g0006a0001c0001t0001g0116a0001c0001t0001g0117others(3): Show | 7 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(4): Show |
intron_variant | MODIFIER | c.2292+798_2292+799i others(8): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59669737 | |||||
chr17:59669737 | T | TATATATA others(3): Show |
1 | a0001c0001t0001g0115 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2292+798_2292+799i others(12): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59669737 | |||||
chr17:59670059 | C | G | 2 | a0001c0001t0001g0010a0001c0001t0001g0177 | 3 | HG00140.hp1 HG00544.hp2 HG01256.hp2 |
intron_variant | MODIFIER | c.2292+1119C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59670059 | ||||||
chr17:59670178 | T | G | 58 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(55): Show | 73 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.2292+1238T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59670178 | ||||||
chr17:59670223 | A | C | 5 | a0001c0001t0003g0005a0001c0001t0003g0028a0001c0001t0003g0029others(2): Show | 6 | HG04184.hp2 NA18945.hp2 NA18961.hp2 others(3): Show |
intron_variant | MODIFIER | c.2292+1283A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59670223 | ||||||
chr17:59670277 | GT | G | 154 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(151): Show | 177 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(174): Show |
intron_variant | MODIFIER | c.2292+1348delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59670277 | |||||
chr17:59670282 | TTTTTTTG | T | 22 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(19): Show | 22 | HG00738.hp1 HG01261.hp1 HG01934.hp1 others(19): Show |
intron_variant | MODIFIER | c.2292+1348_2292+135 others(11): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59670282 | |||||
chr17:59670295 | C | G | 23 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0088others(20): Show | 23 | HG00738.hp1 HG01261.hp1 HG01934.hp1 others(20): Show |
intron_variant | MODIFIER | c.2292+1355C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59670295 | ||||||
chr17:59670784 | C | T | 1 | a0001c0001t0006g0062 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.2292+1844C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59670784 | ||||||
chr17:59670926 | T | C | 1 | a0001c0001t0006g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.2292+1986T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59670926 | ||||||
chr17:59670964 | T | G | 3 | a0001c0001t0001g0086a0001c0001t0001g0090a0001c0001t0017g0085 | 3 | HG02698.hp1 HG04199.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.2292+2024T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59670964 | ||||||
chr17:59671049 | C | T | 17 | a0001c0001t0006g0056a0001c0001t0006g0059a0001c0001t0006g0060others(14): Show | 17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.2292+2109C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59671049 | ||||||
chr17:59671158 | T | C | 1 | a0001c0001t0002g0008 | 2 | NA18964.hp1 NA19077.hp2 |
intron_variant | MODIFIER | c.2292+2218T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59671158 | ||||||
chr17:59671161 | A | G | 75 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(72): Show | 90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.2292+2221A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59671161 | ||||||
chr17:59671226 | C | T | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(193): Show | 219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.2292+2286C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59671226 | ||||||
chr17:59671333 | G | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2293-2314G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59671333 | ||||||
chr17:59671394 | A | C | 1 | a0001c0001t0003g0026 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.2293-2253A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59671394 | ||||||
chr17:59671795 | A | G | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | NA19057.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2293-1852A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59671795 | ||||||
chr17:59672450 | CTT | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.2293-1192_2293-119 others(6): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59672450 | |||||
chr17:59672488 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2293-1159C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59672488 | ||||||
chr17:59672674 | T | A | 1 | a0001c0001t0001g0123 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.2293-973T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59672674 | ||||||
chr17:59673076 | G | GATATCTT others(6): Show |
1 | a0002c0003t0001g0099 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2293-569_2293-557d others(15): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59673076 | |||||
chr17:59673099 | GT | G | 175 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(172): Show | 198 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(195): Show |
intron_variant | MODIFIER | c.2293-537delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59673099 | |||||
chr17:59673110 | T | C | 1 | a0001c0001t0005g0041 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2293-537T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59673110 | ||||||
chr17:59673178 | A | T | 1 | a0002c0003t0001g0099 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2293-469A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59673178 | ||||||
chr17:59673180 | T | A | 1 | a0002c0003t0001g0099 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2293-467T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59673180 | ||||||
chr17:59673188 | T | C | 1 | a0001c0001t0006g0059 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.2293-459T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59673188 | ||||||
chr17:59673439 | T | A | 1 | a0001c0001t0001g0205 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2293-208T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59673439 | ||||||
chr17:59673514 | ATTCT | A | 2 | a0001c0001t0001g0189a0001c0001t0015g0184 | 2 | NA18945.hp1 NA19000.hp1 |
intron_variant | MODIFIER | c.2293-126_2293-123d others(6): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr17 | 59673514 | |||||
chr17:59673621 | T | C | 216 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(213): Show | 241 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(238): Show |
intron_variant | MODIFIER | c.2293-26T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 14/31 | chr17 | 59673621 | ||||||
chr17:59673843 | T | A | 1 | a0002c0003t0001g0099 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2418+71T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59673843 | ||||||
chr17:59673860 | C | G | 1 | a0001c0001t0001g0102 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.2418+88C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59673860 | ||||||
chr17:59673861 | A | C | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2418+89A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59673861 | ||||||
chr17:59673930 | G | C | 1 | a0001c0001t0002g0129 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.2418+158G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59673930 | ||||||
chr17:59674062 | C | T | 1 | a0001c0001t0001g0196 | 1 | NA18956.hp1 | intron_variant | MODIFIER | c.2418+290C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59674062 | ||||||
chr17:59674093 | C | G | 1 | a0001c0001t0003g0027 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.2418+321C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59674093 | ||||||
chr17:59674101 | G | A | 1 | a0002c0003t0001g0099 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2418+329G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59674101 | ||||||
chr17:59674103 | A | T | 1 | a0002c0003t0001g0099 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2418+331A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59674103 | ||||||
chr17:59674104 | T | G | 1 | a0002c0003t0001g0099 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2418+332T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59674104 | ||||||
chr17:59674132 | C | T | 10 | a0001c0001t0005g0040a0001c0001t0005g0041a0001c0001t0005g0042others(7): Show | 10 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(7): Show |
intron_variant | MODIFIER | c.2418+360C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 15/31 | chr17 | 59674132 | ||||||
chr17:59674898 | A | G | 2 | a0001c0001t0001g0207a0001c0001t0001g0215 | 2 | HG00639.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.2561+55A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/31 | chr17 | 59674898 | ||||||
chr17:59674910 | A | G | 1 | a0001c0001t0001g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.2561+67A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/31 | chr17 | 59674910 | ||||||
chr17:59674935 | T | A | 1 | a0002c0003t0001g0099 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.2561+92T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/31 | chr17 | 59674935 | ||||||
chr17:59675107 | A | G | 1 | a0001c0001t0002g0167 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.2561+264A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/31 | chr17 | 59675107 | ||||||
chr17:59675126 | A | G | 9 | a0001c0001t0006g0056a0001c0001t0007g0050a0001c0001t0007g0051others(6): Show | 9 | HG02809.hp1 HG02896.hp1 HG03130.hp2 others(6): Show |
intron_variant | MODIFIER | c.2561+283A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/31 | chr17 | 59675126 | ||||||
chr17:59675417 | G | A | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2561+574G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/31 | chr17 | 59675417 | ||||||
chr17:59675508 | C | T | 3 | a0001c0001t0001g0183a0001c0001t0001g0188a0001c0001t0001g0219 | 3 | HG01261.hp2 HG02738.hp1 NA20752.hp2 |
intron_variant | MODIFIER | c.2561+665C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/31 | chr17 | 59675508 | ||||||
chr17:59675758 | A | G | 7 | a0001c0001t0001g0197a0001c0001t0001g0200a0001c0001t0001g0202others(4): Show | 7 | HG02004.hp1 HG02135.hp1 NA18952.hp2 others(4): Show |
intron_variant | MODIFIER | c.2561+915A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/31 | chr17 | 59675758 | ||||||
chr17:59675915 | G | A | 1 | a0001c0001t0003g0032 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.2562-1039G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 16/31 | chr17 | 59675915 | ||||||
chr17:59677230 | A | G | 75 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(72): Show | 90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.2796+42A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59677230 | ||||||
chr17:59677435 | T | TA | 9 | a0001c0001t0001g0094a0001c0001t0001g0095a0001c0001t0001g0097others(6): Show | 9 | HG00738.hp1 HG01261.hp1 HG01934.hp1 others(6): Show |
intron_variant | MODIFIER | c.2796+248dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr17 | 59677435 | |||||
chr17:59677603 | G | C | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2796+415G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59677603 | ||||||
chr17:59677833 | A | G | 1 | a0001c0001t0005g0049 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2796+645A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59677833 | ||||||
chr17:59678049 | A | G | 1 | a0001c0001t0010g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.2796+861A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59678049 | ||||||
chr17:59678219 | A | G | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.2796+1031A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59678219 | ||||||
chr17:59678382 | C | CTT | 58 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(55): Show | 73 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.2797-1014_2797-101 others(6): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr17 | 59678382 | |||||
chr17:59678825 | C | T | 17 | a0001c0001t0006g0056a0001c0001t0006g0059a0001c0001t0006g0060others(14): Show | 17 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(14): Show |
intron_variant | MODIFIER | c.2797-572C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59678825 | ||||||
chr17:59678858 | TG | T | 232 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(229): Show | 259 | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(256): Show |
intron_variant | MODIFIER | c.2797-533delG | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr17 | 59678858 | |||||
chr17:59678957 | G | A | 103 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(100): Show | 111 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.2797-440G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59678957 | ||||||
chr17:59679129 | C | T | 1 | a0001c0001t0001g0084 | 1 | HG02723.hp1 | intron_variant | MODIFIER | c.2797-268C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59679129 | ||||||
chr17:59679165 | A | C | 1 | a0001c0001t0001g0089 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.2797-232A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59679165 | ||||||
chr17:59679290 | G | C | 2 | a0001c0001t0001g0222a0001c0001t0001g0223 | 2 | NA19057.hp2 NA19077.hp1 |
intron_variant | MODIFIER | c.2797-107G>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59679290 | ||||||
chr17:59679388 | C | T | 4 | a0001c0001t0001g0123a0001c0001t0001g0124a0001c0001t0001g0125others(1): Show | 4 | HG02109.hp2 HG03130.hp1 HG06807.hp1 others(1): Show |
intron_variant | MODIFIER | c.2797-9C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 17/31 | chr17 | 59679388 | ||||||
chr17:59679939 | C | A | 1 | a0001c0001t0002g0151 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.2919+420C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 18/31 | chr17 | 59679939 | ||||||
chr17:59679962 | G | A | 1 | a0001c0001t0001g0193 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.2919+443G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 18/31 | chr17 | 59679962 | ||||||
chr17:59680003 | C | T | 2 | a0001c0001t0001g0183a0001c0001t0001g0218 | 2 | HG02155.hp2 HG02738.hp1 |
intron_variant | MODIFIER | c.2919+484C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 18/31 | chr17 | 59680003 | ||||||
chr17:59680328 | T | A | 91 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(88): Show | 98 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(95): Show |
intron_variant | MODIFIER | c.2920-584T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 18/31 | chr17 | 59680328 | ||||||
chr17:59680563 | A | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.2920-349A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 18/31 | chr17 | 59680563 | ||||||
chr17:59680719 | A | C | 75 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(72): Show | 90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.2920-193A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 18/31 | chr17 | 59680719 | ||||||
chr17:59681149 | A | G | 1 | a0001c0001t0006g0056 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.3065+92A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 19/31 | chr17 | 59681149 | ||||||
chr17:59681185 | C | T | 1 | a0001c0001t0001g0190 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.3066-110C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 19/31 | chr17 | 59681185 | ||||||
chr17:59682061 | C | T | 1 | a0001c0001t0003g0019 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.3443-210C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 21/31 | chr17 | 59682061 | ||||||
chr17:59682591 | A | C | 1 | a0001c0001t0002g0144 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3601-38A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 22/31 | chr17 | 59682591 | ||||||
chr17:59683018 | T | C | 18 | a0001c0001t0004g0058a0001c0001t0006g0056a0001c0001t0006g0059others(15): Show | 18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
splice_region_variant&intron_variant | LOW | c.3873+4T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 24/31 | chr17 | 59683018 | ||||||
chr17:59683089 | G | A | 2 | a0001c0001t0003g0025a0001c0001t0003g0027 | 2 | HG03041.hp1 HG03225.hp1 |
splice_region_variant&intron_variant | LOW | c.3874-6G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 24/31 | chr17 | 59683089 | ||||||
chr17:59683811 | G | A | 1 | a0001c0001t0001g0200 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.4323+55G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 27/31 | chr17 | 59683811 | ||||||
chr17:59684023 | CAT | C | 58 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(55): Show | 73 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(70): Show |
intron_variant | MODIFIER | c.4434+40_4434+41del others(2): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | INFO_REALIGN_3_PRIME | chr17 | 59684023 | |||||
chr17:59684257 | T | C | 1 | a0001c0001t0010g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4434+272T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | chr17 | 59684257 | ||||||
chr17:59684261 | T | C | 1 | a0001c0001t0004g0058 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.4434+276T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | chr17 | 59684261 | ||||||
chr17:59684361 | T | C | 2 | a0001c0001t0001g0124a0001c0001t0001g0125 | 2 | HG03130.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4434+376T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | chr17 | 59684361 | ||||||
chr17:59684662 | C | T | 57 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(54): Show | 72 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(69): Show |
intron_variant | MODIFIER | c.4435-394C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | chr17 | 59684662 | ||||||
chr17:59684672 | G | A | 1 | a0001c0001t0001g0207 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.4435-384G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | chr17 | 59684672 | ||||||
chr17:59684801 | C | T | 103 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(100): Show | 111 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(108): Show |
intron_variant | MODIFIER | c.4435-255C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | chr17 | 59684801 | ||||||
chr17:59684806 | C | CAA | 16 | a0001c0001t0006g0056a0001c0001t0006g0059a0001c0001t0006g0060others(13): Show | 16 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(13): Show |
intron_variant | MODIFIER | c.4435-242_4435-241d others(4): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | INFO_REALIGN_3_PRIME | chr17 | 59684806 | |||||
chr17:59684806 | C | CAAA | 96 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(93): Show | 104 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(101): Show |
intron_variant | MODIFIER | c.4435-243_4435-241d others(5): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | INFO_REALIGN_3_PRIME | chr17 | 59684806 | |||||
chr17:59684806 | C | CAAAA | 7 | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0113others(4): Show | 7 | HG01168.hp1 HG01243.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.4435-244_4435-241d others(6): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | INFO_REALIGN_3_PRIME | chr17 | 59684806 | |||||
chr17:59684806 | C | CAAAAA | 70 | a0001c0001t0001g0093a0001c0001t0001g0216a0001c0001t0002g0001others(67): Show | 85 | HG00408.hp2 HG00423.hp2 HG00639.hp1 others(82): Show |
intron_variant | MODIFIER | c.4435-245_4435-241d others(7): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | INFO_REALIGN_3_PRIME | chr17 | 59684806 | |||||
chr17:59684806 | C | CAAAAAA | 6 | a0001c0001t0002g0129a0001c0001t0002g0153a0001c0001t0002g0160others(3): Show | 6 | HG00544.hp1 HG00621.hp1 HG02027.hp2 others(3): Show |
intron_variant | MODIFIER | c.4435-246_4435-241d others(8): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | INFO_REALIGN_3_PRIME | chr17 | 59684806 | |||||
chr17:59684816 | G | A | 206 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(203): Show | 229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.4435-240G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | chr17 | 59684816 | ||||||
chr17:59684858 | A | G | 1 | a0001c0001t0006g0062 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.4435-198A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 28/31 | chr17 | 59684858 | ||||||
chr17:59685288 | TTATAATC | T | 2 | a0001c0001t0003g0025a0001c0001t0003g0027 | 2 | HG03041.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.4605+68_4605+74del others(7): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 29/31 | INFO_REALIGN_3_PRIME | chr17 | 59685288 | |||||
chr17:59685510 | T | C | 75 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(72): Show | 90 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(87): Show |
intron_variant | MODIFIER | c.4606-77T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 29/31 | chr17 | 59685510 | ||||||
chr17:59685949 | T | A | 1 | a0001c0001t0005g0041 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.4827+141T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59685949 | ||||||
chr17:59686094 | T | G | 1 | a0001c0001t0004g0068 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.4827+286T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59686094 | ||||||
chr17:59686116 | G | A | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(193): Show | 219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.4827+308G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59686116 | ||||||
chr17:59686192 | G | A | 1 | a0001c0001t0001g0182 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.4827+384G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59686192 | ||||||
chr17:59686332 | TATAAC | T | 56 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(53): Show | 71 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(68): Show |
intron_variant | MODIFIER | c.4827+527_4827+531d others(7): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr17 | 59686332 | |||||
chr17:59686415 | C | G | 7 | a0001c0001t0001g0006a0001c0001t0001g0115a0001c0001t0001g0116others(4): Show | 8 | HG01099.hp2 HG01884.hp1 HG01952.hp1 others(5): Show |
intron_variant | MODIFIER | c.4827+607C>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59686415 | ||||||
chr17:59686632 | A | C | 1 | a0001c0001t0001g0216 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.4827+824A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59686632 | ||||||
chr17:59686633 | C | A | 1 | a0001c0001t0001g0216 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.4827+825C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59686633 | ||||||
chr17:59686648 | A | G | 1 | a0001c0001t0010g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4827+840A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59686648 | ||||||
chr17:59686769 | T | C | 1 | a0001c0001t0004g0077 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.4827+961T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59686769 | ||||||
chr17:59686817 | T | G | 197 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(194): Show | 220 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(217): Show |
intron_variant | MODIFIER | c.4827+1009T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59686817 | ||||||
chr17:59687487 | G | GT | 16 | a0001c0001t0001g0094a0001c0001t0001g0103a0001c0001t0001g0196others(13): Show | 16 | HG01109.hp2 HG01243.hp1 HG01975.hp2 others(13): Show |
intron_variant | MODIFIER | c.4827+1692dupT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | INFO_REALIGN_3_PRIME | chr17 | 59687487 | |||||
chr17:59687825 | C | T | 1 | a0001c0001t0008g0003 | 3 | HG01891.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4827+2017C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59687825 | ||||||
chr17:59688241 | T | C | 1 | a0001c0001t0002g0140 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.4828-2395T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59688241 | ||||||
chr17:59688347 | C | T | 206 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(203): Show | 229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.4828-2289C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59688347 | ||||||
chr17:59688646 | C | T | 1 | a0001c0001t0005g0045 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.4828-1990C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59688646 | ||||||
chr17:59689299 | C | T | 1 | a0001c0001t0010g0015 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.4828-1337C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59689299 | ||||||
chr17:59689384 | A | C | 18 | a0001c0001t0004g0058a0001c0001t0006g0056a0001c0001t0006g0059others(15): Show | 18 | HG02257.hp1 HG02572.hp1 HG02647.hp1 others(15): Show |
intron_variant | MODIFIER | c.4828-1252A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59689384 | ||||||
chr17:59689614 | T | C | 104 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(101): Show | 112 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(109): Show |
intron_variant | MODIFIER | c.4828-1022T>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59689614 | ||||||
chr17:59689924 | C | A | 178 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(175): Show | 201 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(198): Show |
intron_variant | MODIFIER | c.4828-712C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59689924 | ||||||
chr17:59690062 | A | G | 1 | a0001c0001t0001g0088 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.4828-574A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59690062 | ||||||
chr17:59690288 | C | T | 1 | a0001c0001t0002g0152 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.4828-348C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59690288 | ||||||
chr17:59690289 | A | G | 196 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(193): Show | 219 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(216): Show |
intron_variant | MODIFIER | c.4828-347A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59690289 | ||||||
chr17:59690322 | C | T | 1 | a0001c0001t0001g0107 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.4828-314C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59690322 | ||||||
chr17:59690348 | G | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0126 | 2 | HG02109.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.4828-288G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 30/31 | chr17 | 59690348 | ||||||
chr17:59690802 | A | G | 1 | a0001c0001t0001g0102 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.4903+91A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59690802 | ||||||
chr17:59691352 | C | T | 1 | a0001c0001t0001g0229 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.4903+641C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59691352 | ||||||
chr17:59691623 | T | TA | 15 | a0001c0001t0003g0038a0001c0001t0004g0068a0001c0001t0004g0069others(12): Show | 15 | HG01243.hp2 HG01891.hp2 HG02280.hp2 others(12): Show |
intron_variant | MODIFIER | c.4903+922dupA | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 59691623 | |||||
chr17:59691623 | T | TAA | 51 | a0001c0001t0002g0001a0001c0001t0002g0007a0001c0001t0002g0008others(48): Show | 66 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(63): Show |
intron_variant | MODIFIER | c.4903+921_4903+922d others(4): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 59691623 | |||||
chr17:59691632 | A | AAT | 11 | a0001c0001t0001g0092a0001c0001t0001g0124a0001c0001t0001g0125others(8): Show | 11 | HG01981.hp2 HG02027.hp2 HG02486.hp2 others(8): Show |
intron_variant | MODIFIER | c.4903+937_4903+938d others(4): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 59691632 | |||||
chr17:59691632 | A | T | 14 | a0001c0001t0001g0012a0001c0001t0001g0088a0001c0001t0001g0093others(11): Show | 15 | HG00621.hp2 HG00639.hp2 HG02040.hp2 others(12): Show |
intron_variant | MODIFIER | c.4903+921A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59691632 | ||||||
chr17:59691633 | AT | A | 1 | a0001c0001t0008g0003 | 3 | HG01891.hp1 HG02559.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.4903+923delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59691633 | ||||||
chr17:59691634 | T | A | 26 | a0001c0001t0001g0100a0001c0001t0001g0204a0001c0001t0002g0139others(23): Show | 26 | HG00423.hp2 HG01109.hp2 HG01168.hp2 others(23): Show |
intron_variant | MODIFIER | c.4903+923T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59691634 | ||||||
chr17:59691636 | T | A | 1 | a0001c0001t0014g0131 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.4903+925T>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59691636 | ||||||
chr17:59691837 | A | G | 77 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0002g0001others(74): Show | 92 | HG00408.hp2 HG00423.hp2 HG00544.hp1 others(89): Show |
intron_variant | MODIFIER | c.4903+1126A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59691837 | ||||||
chr17:59692122 | T | G | 11 | a0001c0001t0004g0077a0001c0001t0005g0040a0001c0001t0005g0041others(8): Show | 11 | HG01109.hp2 HG02615.hp1 HG02896.hp2 others(8): Show |
intron_variant | MODIFIER | c.4903+1411T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692122 | ||||||
chr17:59692171 | G | A | 2 | a0001c0002t0002g0004a0001c0002t0002g0128 | 4 | HG01123.hp1 HG01168.hp1 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.4903+1460G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692171 | ||||||
chr17:59692292 | C | T | 1 | a0001c0001t0003g0033 | 1 | HG02004.hp2 | intron_variant | MODIFIER | c.4904-1436C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692292 | ||||||
chr17:59692307 | C | A | 14 | a0001c0001t0004g0058a0001c0001t0006g0056a0001c0001t0006g0060others(11): Show | 14 | HG02257.hp1 HG02647.hp1 HG02809.hp1 others(11): Show |
intron_variant | MODIFIER | c.4904-1421C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692307 | ||||||
chr17:59692308 | C | T | 4 | a0001c0001t0006g0059a0001c0001t0006g0063a0001c0001t0006g0064others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG03579.hp2 others(1): Show |
intron_variant | MODIFIER | c.4904-1420C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692308 | ||||||
chr17:59692323 | T | TAATAA | 206 | a0001c0001t0001g0002a0001c0001t0001g0006a0001c0001t0001g0010others(203): Show | 229 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(226): Show |
intron_variant | MODIFIER | c.4904-1403_4904-139 others(9): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 59692323 | |||||
chr17:59692328 | AACTGGTT others(3): Show |
A | 1 | a0001c0001t0013g0180 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4904-1398_4904-138 others(14): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 59692328 | |||||
chr17:59692346 | A | C | 1 | a0001c0001t0013g0180 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4904-1382A>C | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692346 | ||||||
chr17:59692348 | T | G | 1 | a0001c0001t0013g0180 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4904-1380T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692348 | ||||||
chr17:59692349 | T | G | 1 | a0001c0001t0013g0180 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4904-1379T>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692349 | ||||||
chr17:59692350 | G | T | 1 | a0001c0001t0013g0180 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.4904-1378G>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692350 | ||||||
chr17:59692637 | A | G | 77 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(74): Show | 84 | HG00140.hp1 HG00408.hp1 HG00423.hp1 others(81): Show |
intron_variant | MODIFIER | c.4904-1091A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692637 | ||||||
chr17:59692890 | G | A | 1 | a0001c0001t0001g0213 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.4904-838G>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692890 | ||||||
chr17:59692927 | C | A | 2 | a0001c0001t0002g0164a0001c0001t0002g0171 | 2 | HG02523.hp1 NA18977.hp1 |
intron_variant | MODIFIER | c.4904-801C>A | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59692927 | ||||||
chr17:59693360 | CT | C | 41 | a0001c0001t0001g0006a0001c0001t0001g0084a0001c0001t0001g0115others(38): Show | 42 | HG01099.hp2 HG01109.hp2 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.4904-348delT | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 59693360 | |||||
chr17:59693360 | CTT | C | 138 | a0001c0001t0001g0002a0001c0001t0001g0010a0001c0001t0001g0011others(135): Show | 160 | HG00140.hp1 HG00408.hp1 HG00408.hp2 others(157): Show |
intron_variant | MODIFIER | c.4904-349_4904-348d others(4): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 59693360 | |||||
chr17:59693360 | CTTT | C | 9 | a0001c0001t0001g0088a0001c0001t0001g0106a0001c0001t0001g0182others(6): Show | 9 | HG02280.hp1 HG02735.hp1 HG02895.hp1 others(6): Show |
intron_variant | MODIFIER | c.4904-350_4904-348d others(5): Show |
CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | INFO_REALIGN_3_PRIME | chr17 | 59693360 | |||||
chr17:59693381 | A | T | 2 | a0001c0001t0004g0058a0001c0001t0010g0015 | 2 | HG03453.hp1 HG03471.hp2 |
intron_variant | MODIFIER | c.4904-347A>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59693381 | ||||||
chr17:59693460 | A | G | 1 | a0001c0001t0006g0063 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.4904-268A>G | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59693460 | ||||||
chr17:59693681 | C | T | 4 | a0001c0001t0003g0030a0001c0001t0003g0031a0001c0001t0003g0032others(1): Show | 4 | HG01934.hp2 HG01952.hp2 HG01975.hp1 others(1): Show |
intron_variant | MODIFIER | c.4904-47C>T | CLTC | ENSG00000141367.13 | transcript | ENST00000269122.8 | protein_coding | 31/31 | chr17 | 59693681 |