geneid | 160857 |
---|---|
ensemblid | ENSG00000151773.13 |
hgncid | 26478 |
symbol | CCDC122 |
name | coiled-coil domain containing 122 |
refseq_nuc | NM_144974.5 |
refseq_prot | NP_659411.2 |
ensembl_nuc | ENST00000444614.8 |
ensembl_prot | ENSP00000407763.2 |
mane_status | MANE Select |
chr | chr13 |
start | 43836352 |
end | 43879740 |
strand | - |
ver | v1.2 |
region | chr13:43836352-43879740 |
region5000 | chr13:43831352-43884740 |
regionname0 | CCDC122_chr13_43836352_43879740 |
regionname5000 | CCDC122_chr13_43831352_43884740 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 273 | 391 | 88 | 64 | 191 | 10 | 36 | 156 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0002 | 0/0 | 273 | 30 | 1 | 2 | 20 | 0 | 7 | 12 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0003 | 0/0 | 273 | 11 | 0 | 0 | 11 | 0 | 0 | 11 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0004 | 0/0 | 273 | 7 | 0 | 2 | 0 | 2 | 3 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0005 | 0/0 | 273 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0006 | 0/0 | 250 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0007 | 0/0 | 273 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 822 | 353 | 73 | 60 | 175 | 8 | 35 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
c0002 | 0/0 | 822 | 38 | 15 | 4 | 16 | 2 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
c0003 | 0/0 | 822 | 30 | 1 | 2 | 20 | 0 | 7 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
c0004 | 0/0 | 822 | 11 | 0 | 0 | 11 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
c0005 | 0/0 | 822 | 7 | 0 | 2 | 0 | 2 | 3 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
c0006 | 0/0 | 822 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
c0007 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
c0008 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/1 | 1239 | 135 | 30 | 19 | 65 | 3 | 17 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0002 | 0/0 | 1239 | 51 | 2 | 13 | 23 | 3 | 10 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0003 | 1/0 | 1238 | 51 | 8 | 9 | 32 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0004 | 0/0 | 1239 | 27 | 0 | 3 | 23 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0005 | 0/0 | 1240 | 25 | 5 | 3 | 14 | 2 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0006 | 0/0 | 1239 | 22 | 0 | 0 | 16 | 0 | 6 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0007 | 0/0 | 1239 | 19 | 0 | 5 | 12 | 0 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0008 | 0/0 | 1240 | 18 | 6 | 1 | 7 | 1 | 3 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0009 | 0/0 | 1238 | 18 | 10 | 4 | 0 | 1 | 3 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0010 | 0/0 | 1238 | 9 | 7 | 2 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0011 | 0/0 | 1239 | 9 | 0 | 0 | 9 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0012 | 0/0 | 1240 | 7 | 0 | 3 | 3 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0013 | 0/0 | 1238 | 7 | 6 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0014 | 0/0 | 1240 | 5 | 4 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0015 | 0/0 | 1240 | 4 | 0 | 1 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0016 | 0/0 | 1240 | 4 | 4 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0017 | 0/0 | 1239 | 4 | 1 | 1 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0018 | 0/0 | 1239 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0019 | 0/0 | 1238 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0020 | 0/0 | 1238 | 2 | 0 | 0 | 1 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0021 | 0/0 | 1240 | 2 | 1 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0022 | 0/0 | 1238 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0023 | 0/0 | 1240 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0024 | 0/0 | 1240 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0025 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0026 | 0/0 | 1239 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0027 | 0/0 | 1240 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0028 | 0/0 | 1570 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0029 | 0/0 | 1239 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0030 | 0/0 | 1239 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0031 | 0/0 | 1238 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0032 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0033 | 0/0 | 1238 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0034 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0035 | 0/0 | 1238 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
t0036 | 0/0 | 1239 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 26 | 0 | 6 | 12 | 3 | 5 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0002 | 0/0 | 20 | 2 | 3 | 9 | 0 | 6 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0003 | 0/0 | 16 | 1 | 3 | 12 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0004 | 0/0 | 8 | 0 | 0 | 6 | 1 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0005 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0007 | 0/0 | 6 | 0 | 2 | 0 | 2 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0008 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0009 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0015 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0018 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0022 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0031 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0055 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0058 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0060 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0061 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0062 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0063 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0064 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 822 | 353 | 73 | 60 | 175 | 8 | 35 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0002 | 0/0 | 822 | 38 | 15 | 4 | 16 | 2 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0002c0003 | 0/0 | 822 | 30 | 1 | 2 | 20 | 0 | 7 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0003c0004 | 0/0 | 822 | 11 | 0 | 0 | 11 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0004c0005 | 0/0 | 822 | 7 | 0 | 2 | 0 | 2 | 3 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0005c0007 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0006c0006 | 0/0 | 822 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0007c0008 | 0/0 | 822 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/1 | 2060 | 100 | 28 | 15 | 47 | 1 | 8 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0002 | 0/0 | 2060 | 50 | 2 | 13 | 22 | 3 | 10 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0003 | 1/0 | 2059 | 51 | 8 | 9 | 32 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0004 | 0/0 | 2060 | 27 | 0 | 3 | 23 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0006 | 0/0 | 2060 | 22 | 0 | 0 | 16 | 0 | 6 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0007 | 0/0 | 2060 | 19 | 0 | 5 | 12 | 0 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0008 | 0/0 | 2061 | 15 | 6 | 1 | 5 | 1 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0009 | 0/0 | 2059 | 18 | 10 | 4 | 0 | 1 | 3 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0010 | 0/0 | 2059 | 9 | 7 | 2 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0012 | 0/0 | 2061 | 7 | 0 | 3 | 3 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0013 | 0/0 | 2059 | 7 | 6 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0015 | 0/0 | 2061 | 4 | 0 | 1 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0017 | 0/0 | 2060 | 4 | 1 | 1 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0018 | 0/0 | 2060 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0019 | 0/0 | 2059 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0020 | 0/0 | 2059 | 2 | 0 | 0 | 1 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0021 | 0/0 | 2061 | 2 | 1 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0022 | 0/0 | 2059 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0024 | 0/0 | 2061 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0025 | 0/0 | 2060 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0026 | 0/0 | 2060 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0028 | 0/0 | 2391 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0029 | 0/0 | 2060 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0030 | 0/0 | 2060 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0031 | 0/0 | 2059 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0001t0032 | 0/0 | 2060 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0002t0005 | 0/0 | 2061 | 25 | 5 | 3 | 14 | 2 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0002t0014 | 0/0 | 2061 | 5 | 4 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0002t0016 | 0/0 | 2061 | 4 | 4 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0002t0027 | 0/0 | 2061 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0002t0033 | 0/0 | 2059 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0002t0034 | 0/0 | 2060 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0001c0002t0035 | 0/0 | 2059 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0002c0003t0001 | 0/0 | 2060 | 27 | 1 | 2 | 18 | 0 | 6 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0002c0003t0008 | 0/0 | 2061 | 2 | 0 | 0 | 1 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0002c0003t0036 | 0/0 | 2060 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0003c0004t0011 | 0/0 | 2060 | 9 | 0 | 0 | 9 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0003c0004t0023 | 0/0 | 2061 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0004c0005t0001 | 0/0 | 2060 | 7 | 0 | 2 | 0 | 2 | 3 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0005c0007t0002 | 0/0 | 2060 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0006c0006t0001 | 0/0 | 2060 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
a0007c0008t0008 | 0/0 | 2061 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | copy fasta | chr13 | 43831352 | 43884740 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0002 | 0/0 | 20 | 2 | 3 | 9 | 0 | 6 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0003 | 0/0 | 16 | 1 | 3 | 12 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0008 | 0/0 | 6 | 1 | 0 | 5 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0023 | 0/0 | 3 | 3 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0024 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0025 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0048 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0050 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0052 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0055 | 0/0 | 2 | 0 | 1 | 0 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0148 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0152 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0158 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0185 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0204 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0001g0219 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0002g0001 | 0/0 | 26 | 0 | 6 | 12 | 3 | 5 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0002g0014 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0002g0019 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0002g0032 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0002g0033 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0002g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0002g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0002g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0002g0085 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0009 | 0/0 | 6 | 0 | 6 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0013 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0028 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0029 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0030 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0031 | 0/0 | 3 | 0 | 0 | 2 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0061 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0062 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0063 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0064 | 1/0 | 2 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0237 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0239 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0241 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0245 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0247 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0252 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0257 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0258 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0003g0259 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0004g0016 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0004g0017 | 0/0 | 4 | 0 | 0 | 4 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0004g0021 | 0/0 | 3 | 0 | 2 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0004g0037 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0004g0038 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0004g0039 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0004g0053 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0004g0114 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0004g0116 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0004g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0004g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0004g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0004g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0004g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0004g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0006g0010 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0006g0011 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0006g0022 | 0/0 | 3 | 0 | 0 | 0 | 0 | 3 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0006g0040 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0006g0041 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0006g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0006g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0006g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0006g0125 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0006g0126 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0007g0005 | 0/0 | 7 | 0 | 3 | 4 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0007g0015 | 0/0 | 4 | 0 | 0 | 2 | 0 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0007g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0007g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0007g0099 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0007g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0007g0102 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0007g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0007g0104 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0007g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0008g0049 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0008g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0008g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0008g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0008g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0008g0168 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0008g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0008g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0008g0199 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0008g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0008g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0008g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0008g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0009g0043 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0009g0044 | 0/0 | 2 | 0 | 0 | 0 | 1 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0009g0045 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0009g0046 | 0/0 | 2 | 1 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0009g0127 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0009g0128 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0009g0129 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0009g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0009g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0009g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0009g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0009g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0009g0137 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0009g0138 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0010g0020 | 0/0 | 3 | 2 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0010g0035 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0010g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0010g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0010g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0010g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0012g0036 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0012g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0012g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0012g0100 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0012g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0012g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0013g0034 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0013g0086 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0013g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0013g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0013g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0013g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0015g0054 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0015g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0015g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0017g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0017g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0017g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0017g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0018g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0018g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0018g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0019g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0019g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0020g0071 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0020g0084 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0021g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0021g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0022g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0022g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0024g0042 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0025g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0026g0066 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0028g0074 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0029g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0030g0213 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0031g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0001t0032g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0005g0004 | 0/0 | 8 | 0 | 0 | 6 | 1 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0005g0027 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0005g0058 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0005g0059 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0005g0060 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0005g0221 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0005g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0005g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0005g0227 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0005g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0005g0230 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0005g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0005g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0014g0056 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0014g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0014g0220 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0014g0223 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0016g0057 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0016g0224 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0016g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0027g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0033g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0034g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0001c0002t0035g0229 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0001g0012 | 0/0 | 5 | 0 | 0 | 5 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0001g0018 | 0/0 | 4 | 0 | 1 | 1 | 0 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0001g0026 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0001g0051 | 0/0 | 2 | 0 | 0 | 0 | 0 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0001g0112 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0001g0176 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0001g0177 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0001g0178 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0001g0181 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0001g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0001g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0008g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0008g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0002c0003t0036g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0003c0004t0011g0006 | 0/0 | 7 | 0 | 0 | 7 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0003c0004t0011g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0003c0004t0011g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0003c0004t0023g0047 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0004c0005t0001g0007 | 0/0 | 6 | 0 | 2 | 0 | 2 | 2 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0004c0005t0001g0160 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0005c0007t0002g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0006c0006t0001g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
a0007c0008t0008g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | GBR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0055 | EUR | GBR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00280 | hp1 | a0001 | c0001 | t0008 | g0199 | EUR | FIN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00280 | hp2 | a0001 | c0001 | t0002 | g0001 | EUR | FIN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00323 | hp1 | a0001 | c0001 | t0004 | g0116 | EUR | FIN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00323 | hp2 | a0004 | c0005 | t0001 | g0007 | EUR | FIN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00408 | hp1 | a0001 | c0001 | t0007 | g0107 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0024 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00423 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00438 | hp1 | a0002 | c0003 | t0001 | g0180 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00438 | hp2 | a0001 | c0001 | t0008 | g0210 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00558 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00558 | hp2 | a0001 | c0001 | t0003 | g0251 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00597 | hp2 | a0001 | c0001 | t0004 | g0021 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00609 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00609 | hp2 | a0002 | c0003 | t0001 | g0177 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00621 | hp1 | a0001 | c0001 | t0003 | g0252 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00621 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00639 | hp1 | a0001 | c0001 | t0002 | g0065 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00639 | hp2 | a0001 | c0001 | t0003 | g0254 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00642 | hp1 | a0001 | c0001 | t0029 | g0109 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00642 | hp2 | a0001 | c0001 | t0001 | g0202 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00673 | hp1 | a0002 | c0003 | t0001 | g0112 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00673 | hp2 | a0001 | c0002 | t0005 | g0004 | EAS | CHS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00735 | hp1 | a0001 | c0001 | t0015 | g0115 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00735 | hp2 | a0004 | c0005 | t0001 | g0007 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00738 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00738 | hp2 | a0001 | c0001 | t0009 | g0127 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00741 | hp1 | a0001 | c0002 | t0005 | g0221 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG00741 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01069 | hp1 | a0001 | c0002 | t0005 | g0058 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01069 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0079 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01081 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0204 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01099 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01099 | hp2 | a0001 | c0001 | t0004 | g0021 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01109 | hp1 | a0001 | c0001 | t0010 | g0092 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01109 | hp2 | a0001 | c0001 | t0012 | g0106 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01167 | hp1 | a0001 | c0001 | t0009 | g0043 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01167 | hp2 | a0001 | c0001 | t0004 | g0114 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01168 | hp1 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01168 | hp2 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0033 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01169 | hp2 | a0001 | c0001 | t0009 | g0043 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01192 | hp1 | a0001 | c0002 | t0005 | g0058 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0186 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01243 | hp1 | a0001 | c0001 | t0010 | g0020 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01243 | hp2 | a0001 | c0002 | t0014 | g0113 | AMR | PUR | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01256 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01256 | hp2 | a0001 | c0001 | t0007 | g0104 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0159 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01257 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01258 | hp1 | a0001 | c0001 | t0002 | g0001 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01258 | hp2 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01346 | hp1 | a0004 | c0005 | t0001 | g0007 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01346 | hp2 | a0001 | c0001 | t0017 | g0256 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01361 | hp1 | a0001 | c0001 | t0009 | g0046 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01361 | hp2 | a0001 | c0001 | t0008 | g0203 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01433 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01433 | hp2 | a0001 | c0001 | t0001 | g0055 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0238 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01496 | hp2 | a0001 | c0001 | t0028 | g0074 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01515 | hp1 | a0001 | c0002 | t0005 | g0060 | EUR | IBS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01515 | hp2 | a0001 | c0001 | t0020 | g0071 | EUR | IBS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01516 | hp1 | a0001 | c0001 | t0002 | g0001 | EUR | IBS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01516 | hp2 | a0001 | c0002 | t0005 | g0004 | EUR | IBS | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01884 | hp1 | a0001 | c0001 | t0001 | g0153 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0148 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01891 | hp1 | a0001 | c0002 | t0014 | g0223 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01891 | hp2 | a0001 | c0001 | t0001 | g0152 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01928 | hp2 | a0001 | c0001 | t0007 | g0101 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0255 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01943 | hp2 | a0001 | c0001 | t0007 | g0005 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01952 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01952 | hp2 | a0001 | c0001 | t0012 | g0036 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01978 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0156 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01993 | hp1 | a0001 | c0001 | t0012 | g0100 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01993 | hp2 | a0002 | c0003 | t0001 | g0174 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02004 | hp1 | a0001 | c0001 | t0002 | g0032 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02015 | hp1 | a0001 | c0001 | t0007 | g0099 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02015 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02027 | hp1 | a0001 | c0001 | t0003 | g0030 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02027 | hp2 | a0001 | c0001 | t0004 | g0193 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02055 | hp1 | a0001 | c0002 | t0005 | g0060 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02055 | hp2 | a0001 | c0001 | t0021 | g0080 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02056 | hp1 | a0001 | c0001 | t0012 | g0108 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02056 | hp2 | a0007 | c0008 | t0008 | g0214 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02071 | hp1 | a0002 | c0003 | t0008 | g0183 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02071 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02074 | hp1 | a0001 | c0002 | t0005 | g0228 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02074 | hp2 | a0002 | c0003 | t0001 | g0026 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02080 | hp1 | a0002 | c0003 | t0001 | g0190 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02083 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02083 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02132 | hp1 | a0001 | c0001 | t0004 | g0119 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02132 | hp2 | a0002 | c0003 | t0001 | g0176 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02135 | hp2 | a0001 | c0001 | t0003 | g0239 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02145 | hp1 | a0001 | c0001 | t0010 | g0091 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02145 | hp2 | a0001 | c0001 | t0009 | g0130 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02148 | hp1 | a0001 | c0001 | t0007 | g0005 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02155 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | CDX | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02155 | hp2 | a0001 | c0001 | t0008 | g0161 | EAS | CDX | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02165 | hp1 | a0001 | c0001 | t0003 | g0242 | EAS | CDX | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02165 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CDX | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02257 | hp1 | a0001 | c0001 | t0009 | g0045 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02257 | hp2 | a0001 | c0001 | t0010 | g0035 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02258 | hp1 | a0001 | c0002 | t0016 | g0057 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02258 | hp2 | a0001 | c0001 | t0003 | g0247 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02273 | hp2 | a0001 | c0001 | t0007 | g0005 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02280 | hp1 | a0001 | c0001 | t0013 | g0089 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02280 | hp2 | a0001 | c0002 | t0014 | g0220 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02293 | hp2 | a0001 | c0001 | t0002 | g0076 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02300 | hp1 | a0002 | c0003 | t0001 | g0018 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02300 | hp2 | a0001 | c0001 | t0030 | g0213 | AMR | PEL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02451 | hp1 | a0001 | c0001 | t0013 | g0088 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02451 | hp2 | a0001 | c0001 | t0001 | g0217 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0053 | EAS | KHV | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02572 | hp1 | a0001 | c0002 | t0016 | g0224 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02572 | hp2 | a0001 | c0001 | t0003 | g0241 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0067 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02615 | hp2 | a0001 | c0001 | t0018 | g0139 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0184 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02622 | hp2 | a0001 | c0002 | t0005 | g0059 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02630 | hp1 | a0001 | c0001 | t0009 | g0045 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02630 | hp2 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02647 | hp1 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02647 | hp2 | a0001 | c0001 | t0001 | g0144 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02683 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02683 | hp2 | a0004 | c0005 | t0001 | g0007 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02717 | hp1 | a0001 | c0002 | t0016 | g0235 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02717 | hp2 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02735 | hp2 | a0004 | c0005 | t0001 | g0007 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02738 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02738 | hp2 | a0001 | c0001 | t0006 | g0040 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02809 | hp1 | a0001 | c0001 | t0001 | g0171 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02809 | hp2 | a0006 | c0006 | t0001 | g0155 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02818 | hp1 | a0001 | c0001 | t0010 | g0020 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0052 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02886 | hp1 | a0001 | c0001 | t0009 | g0046 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02886 | hp2 | a0001 | c0002 | t0035 | g0229 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02895 | hp1 | a0001 | c0001 | t0003 | g0061 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02896 | hp1 | a0001 | c0001 | t0001 | g0189 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02896 | hp2 | a0001 | c0001 | t0013 | g0034 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02897 | hp1 | a0001 | c0001 | t0031 | g0149 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02897 | hp2 | a0001 | c0001 | t0013 | g0034 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02922 | hp1 | a0001 | c0001 | t0001 | g0188 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02922 | hp2 | a0001 | c0001 | t0009 | g0137 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0218 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02965 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02970 | hp1 | a0001 | c0002 | t0027 | g0110 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02970 | hp2 | a0001 | c0001 | t0003 | g0259 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03017 | hp1 | a0002 | c0003 | t0001 | g0181 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03017 | hp2 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03041 | hp1 | a0001 | c0001 | t0001 | g0048 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03041 | hp2 | a0001 | c0001 | t0010 | g0090 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03098 | hp1 | a0001 | c0001 | t0003 | g0258 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03098 | hp2 | a0001 | c0001 | t0010 | g0035 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03139 | hp1 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03139 | hp2 | a0001 | c0001 | t0018 | g0133 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03195 | hp1 | a0001 | c0001 | t0009 | g0138 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0219 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03209 | hp1 | a0001 | c0001 | t0008 | g0150 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03209 | hp2 | a0001 | c0001 | t0017 | g0253 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0075 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03225 | hp2 | a0001 | c0002 | t0005 | g0227 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03239 | hp1 | a0001 | c0001 | t0006 | g0022 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03239 | hp2 | a0002 | c0003 | t0001 | g0178 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03453 | hp1 | a0001 | c0001 | t0001 | g0140 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03453 | hp2 | a0001 | c0001 | t0010 | g0020 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03486 | hp1 | a0001 | c0001 | t0018 | g0131 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03486 | hp2 | a0001 | c0001 | t0013 | g0093 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03490 | hp1 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03490 | hp2 | a0001 | c0001 | t0002 | g0070 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03492 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0050 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03516 | hp1 | a0001 | c0001 | t0013 | g0087 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03516 | hp2 | a0001 | c0001 | t0009 | g0134 | AFR | ESN | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03540 | hp1 | a0001 | c0001 | t0010 | g0111 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03540 | hp2 | a0001 | c0001 | t0001 | g0141 | AFR | GWD | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03579 | hp1 | a0001 | c0001 | t0001 | g0003 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03579 | hp2 | a0001 | c0002 | t0016 | g0057 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03654 | hp2 | a0002 | c0003 | t0001 | g0051 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03669 | hp1 | a0001 | c0001 | t0006 | g0040 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03669 | hp2 | a0001 | c0001 | t0007 | g0015 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03688 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03688 | hp2 | a0001 | c0001 | t0007 | g0015 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03704 | hp1 | a0001 | c0001 | t0006 | g0022 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0002 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03710 | hp1 | a0002 | c0003 | t0001 | g0018 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03710 | hp2 | a0004 | c0005 | t0001 | g0160 | SAS | PJL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0085 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03831 | hp2 | a0001 | c0001 | t0008 | g0168 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03834 | hp1 | a0001 | c0001 | t0003 | g0031 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03834 | hp2 | a0002 | c0003 | t0001 | g0018 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03927 | hp1 | a0001 | c0001 | t0008 | g0196 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03927 | hp2 | a0001 | c0001 | t0002 | g0069 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03942 | hp1 | a0002 | c0003 | t0008 | g0179 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03942 | hp2 | a0001 | c0001 | t0026 | g0066 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG04115 | hp2 | a0001 | c0001 | t0012 | g0096 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG04184 | hp1 | a0001 | c0002 | t0005 | g0004 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG04184 | hp2 | a0001 | c0001 | t0009 | g0129 | SAS | BEB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0001 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG04199 | hp2 | a0001 | c0001 | t0009 | g0044 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG04204 | hp1 | a0001 | c0001 | t0009 | g0128 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG04204 | hp2 | a0001 | c0001 | t0006 | g0022 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0002 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG04228 | hp2 | a0001 | c0001 | t0021 | g0073 | SAS | STU | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18522 | hp1 | a0001 | c0002 | t0014 | g0056 | AFR | YRI | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18522 | hp2 | a0001 | c0001 | t0003 | g0245 | AFR | YRI | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18612 | hp1 | a0002 | c0003 | t0001 | g0026 | EAS | CHB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18612 | hp2 | a0001 | c0001 | t0003 | g0237 | EAS | CHB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18747 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | CHB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | CHB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18906 | hp1 | a0001 | c0002 | t0005 | g0059 | AFR | YRI | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18906 | hp2 | a0001 | c0001 | t0001 | g0145 | AFR | YRI | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18939 | hp1 | a0003 | c0004 | t0011 | g0143 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18939 | hp2 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18940 | hp1 | a0001 | c0002 | t0005 | g0233 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18940 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18941 | hp1 | a0001 | c0002 | t0005 | g0232 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18941 | hp2 | a0002 | c0003 | t0001 | g0026 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18942 | hp1 | a0001 | c0001 | t0025 | g0072 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18942 | hp2 | a0001 | c0002 | t0005 | g0027 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18944 | hp1 | a0003 | c0004 | t0011 | g0006 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18944 | hp2 | a0001 | c0001 | t0003 | g0249 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18945 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18945 | hp2 | a0001 | c0001 | t0007 | g0097 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18947 | hp1 | a0003 | c0004 | t0011 | g0006 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18947 | hp2 | a0005 | c0007 | t0002 | g0068 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18948 | hp1 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18948 | hp2 | a0001 | c0001 | t0001 | g0209 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0211 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18952 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18952 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18953 | hp1 | a0001 | c0002 | t0005 | g0004 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18953 | hp2 | a0001 | c0001 | t0006 | g0123 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18954 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18954 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18956 | hp1 | a0001 | c0001 | t0008 | g0207 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18956 | hp2 | a0001 | c0001 | t0004 | g0037 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18957 | hp1 | a0002 | c0003 | t0001 | g0234 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18957 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18959 | hp2 | a0001 | c0001 | t0003 | g0240 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18960 | hp1 | a0001 | c0002 | t0005 | g0027 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18960 | hp2 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18961 | hp1 | a0001 | c0001 | t0015 | g0054 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18961 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18962 | hp1 | a0003 | c0004 | t0011 | g0006 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0200 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18964 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18964 | hp2 | a0001 | c0001 | t0002 | g0082 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18965 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18965 | hp2 | a0001 | c0001 | t0001 | g0212 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18966 | hp1 | a0003 | c0004 | t0011 | g0142 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18966 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18967 | hp1 | a0001 | c0001 | t0008 | g0049 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18967 | hp2 | a0001 | c0001 | t0001 | g0197 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18968 | hp1 | a0001 | c0001 | t0001 | g0216 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18968 | hp2 | a0001 | c0001 | t0003 | g0244 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18969 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18969 | hp2 | a0003 | c0004 | t0011 | g0006 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18971 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18971 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18972 | hp1 | a0001 | c0001 | t0017 | g0246 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18972 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18973 | hp1 | a0001 | c0001 | t0001 | g0008 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18973 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18974 | hp1 | a0003 | c0004 | t0011 | g0006 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18974 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18975 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18977 | hp1 | a0001 | c0001 | t0007 | g0094 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18977 | hp2 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18978 | hp1 | a0001 | c0001 | t0024 | g0042 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18978 | hp2 | a0001 | c0001 | t0017 | g0250 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18979 | hp1 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18979 | hp2 | a0001 | c0001 | t0006 | g0041 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18980 | hp1 | a0001 | c0001 | t0001 | g0198 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18980 | hp2 | a0001 | c0001 | t0007 | g0102 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18982 | hp1 | a0001 | c0001 | t0001 | g0208 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18982 | hp2 | a0001 | c0001 | t0012 | g0098 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18983 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18983 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0205 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18984 | hp2 | a0001 | c0001 | t0015 | g0054 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18985 | hp2 | a0001 | c0001 | t0019 | g0095 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18986 | hp1 | a0001 | c0001 | t0013 | g0086 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18986 | hp2 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18987 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18987 | hp2 | a0001 | c0001 | t0020 | g0084 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18988 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18988 | hp2 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18989 | hp1 | a0001 | c0001 | t0006 | g0041 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18989 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18990 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18991 | hp1 | a0001 | c0001 | t0004 | g0117 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18991 | hp2 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18992 | hp1 | a0001 | c0002 | t0005 | g0004 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18992 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18993 | hp1 | a0001 | c0001 | t0004 | g0195 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18993 | hp2 | a0001 | c0001 | t0001 | g0164 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18994 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18994 | hp2 | a0001 | c0001 | t0004 | g0118 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18995 | hp1 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18995 | hp2 | a0001 | c0001 | t0006 | g0126 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18998 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18999 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19000 | hp1 | a0001 | c0001 | t0022 | g0192 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19000 | hp2 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19001 | hp1 | a0001 | c0002 | t0033 | g0231 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19001 | hp2 | a0001 | c0001 | t0004 | g0016 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19002 | hp1 | a0001 | c0001 | t0001 | g0024 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19002 | hp2 | a0001 | c0001 | t0003 | g0030 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19003 | hp1 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19003 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19004 | hp1 | a0001 | c0001 | t0002 | g0014 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19004 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19005 | hp1 | a0001 | c0001 | t0004 | g0039 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19005 | hp2 | a0002 | c0003 | t0001 | g0121 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19006 | hp1 | a0003 | c0004 | t0023 | g0047 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19006 | hp2 | a0001 | c0002 | t0005 | g0004 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19007 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19007 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19009 | hp1 | a0001 | c0001 | t0006 | g0011 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19010 | hp1 | a0001 | c0001 | t0012 | g0036 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19010 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19011 | hp1 | a0001 | c0002 | t0005 | g0004 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19012 | hp1 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19012 | hp2 | a0001 | c0001 | t0007 | g0015 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19030 | hp1 | a0001 | c0001 | t0009 | g0135 | AFR | LWK | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19030 | hp2 | a0001 | c0001 | t0008 | g0187 | AFR | LWK | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19054 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19054 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19056 | hp1 | a0001 | c0001 | t0022 | g0120 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19056 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19057 | hp1 | a0001 | c0001 | t0003 | g0257 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19057 | hp2 | a0002 | c0003 | t0001 | g0018 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19058 | hp1 | a0001 | c0001 | t0006 | g0124 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19058 | hp2 | a0001 | c0001 | t0004 | g0191 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19059 | hp1 | a0001 | c0002 | t0034 | g0222 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19059 | hp2 | a0001 | c0001 | t0006 | g0122 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0166 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19060 | hp2 | a0001 | c0001 | t0007 | g0103 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19064 | hp1 | a0003 | c0004 | t0011 | g0006 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19064 | hp2 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19065 | hp1 | a0001 | c0001 | t0004 | g0038 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19065 | hp2 | a0001 | c0002 | t0005 | g0004 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19066 | hp1 | a0001 | c0001 | t0002 | g0019 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19066 | hp2 | a0002 | c0003 | t0001 | g0012 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19067 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19067 | hp2 | a0003 | c0004 | t0023 | g0047 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19068 | hp1 | a0001 | c0001 | t0001 | g0215 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19068 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19070 | hp1 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19070 | hp2 | a0001 | c0001 | t0032 | g0206 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19072 | hp1 | a0001 | c0002 | t0005 | g0225 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19072 | hp2 | a0001 | c0001 | t0004 | g0017 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19074 | hp1 | a0002 | c0003 | t0001 | g0172 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19074 | hp2 | a0001 | c0001 | t0003 | g0028 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19075 | hp1 | a0001 | c0001 | t0003 | g0243 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19075 | hp2 | a0001 | c0001 | t0019 | g0105 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19076 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19076 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19077 | hp1 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19077 | hp2 | a0001 | c0001 | t0002 | g0077 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19079 | hp1 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19079 | hp2 | a0002 | c0003 | t0036 | g0175 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19080 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19080 | hp2 | a0001 | c0001 | t0003 | g0013 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0001 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19081 | hp2 | a0001 | c0001 | t0003 | g0062 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19082 | hp1 | a0001 | c0001 | t0003 | g0236 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19082 | hp2 | a0001 | c0001 | t0024 | g0042 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19083 | hp1 | a0001 | c0001 | t0015 | g0194 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19083 | hp2 | a0001 | c0001 | t0003 | g0029 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19084 | hp1 | a0001 | c0001 | t0003 | g0248 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19084 | hp2 | a0001 | c0001 | t0007 | g0005 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19085 | hp1 | a0003 | c0004 | t0011 | g0006 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0025 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19086 | hp1 | a0001 | c0001 | t0008 | g0049 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19086 | hp2 | a0001 | c0001 | t0002 | g0081 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19088 | hp1 | a0001 | c0002 | t0005 | g0027 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19088 | hp2 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19090 | hp1 | a0001 | c0001 | t0003 | g0031 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19090 | hp2 | a0002 | c0003 | t0001 | g0182 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19091 | hp1 | a0001 | c0001 | t0003 | g0063 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19091 | hp2 | a0001 | c0002 | t0005 | g0226 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19240 | hp1 | a0001 | c0002 | t0014 | g0056 | AFR | YRI | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA19240 | hp2 | a0001 | c0001 | t0009 | g0132 | AFR | YRI | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0185 | AFR | ASW | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA20129 | hp2 | a0001 | c0001 | t0001 | g0002 | AFR | ASW | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA20805 | hp1 | a0004 | c0005 | t0001 | g0007 | EUR | TSI | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA20805 | hp2 | a0001 | c0001 | t0009 | g0044 | EUR | TSI | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA20905 | hp1 | a0001 | c0001 | t0006 | g0125 | SAS | GIH | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA20905 | hp2 | a0002 | c0003 | t0001 | g0051 | SAS | GIH | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01123 | hp1 | a0001 | c0001 | t0003 | g0009 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG01123 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | CLM | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02109 | hp1 | a0001 | c0002 | t0005 | g0230 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02109 | hp2 | a0001 | c0001 | t0008 | g0147 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0167 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02486 | hp2 | a0001 | c0001 | t0008 | g0201 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02559 | hp1 | a0001 | c0001 | t0009 | g0136 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG02559 | hp2 | a0001 | c0001 | t0008 | g0154 | AFR | ACB | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03471 | hp1 | a0001 | c0001 | t0003 | g0064 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | MSL | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG06807 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | USA | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
HG06807 | hp2 | a0001 | c0001 | t0008 | g0146 | AFR | USA | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18955 | hp1 | a0001 | c0001 | t0001 | g0003 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA18955 | hp2 | a0001 | c0001 | t0006 | g0010 | EAS | JPT | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA20300 | hp1 | a0002 | c0003 | t0001 | g0173 | AFR | USA | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
NA20300 | hp2 | a0001 | c0001 | t0002 | g0083 | AFR | USA | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0158 | REF | REF | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0003 | g0064 | REF | REF | CCDC122_chr13_43831352_43884740 | CCDC122 | chr13 | 43831352 | 43884740 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:43837285
|
C | T | 1 | a0004 | 7 | HG00323.hp2 HG00735.hp2 HG01346.hp1 others(4): Show |
missense_variant | MODERATE | c.817G>A | p.Glu273Lys | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 1126/2059 | 817/822 | 273/273 | chr13 | 43837285 | ||
chr13:43837296
|
A | G | 1 | a0002 | 30 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(27): Show |
missense_variant | MODERATE | c.806T>C | p.Ile269Thr | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 1115/2059 | 806/822 | 269/273 | chr13 | 43837296 | ||
chr13:43837350
|
C | T | 1 | a0006 | 1 | HG02809.hp2 | stop_gained | HIGH | c.752G>A | p.Trp251* | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 1061/2059 | 752/822 | 251/273 | chr13 | 43837350 | ||
chr13:43858837
|
T | C | 1 | a0005 | 1 | NA18947.hp2 | missense_variant | MODERATE | c.616A>G | p.Thr206Ala | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/7 | 925/2059 | 616/822 | 206/273 | chr13 | 43858837 | ||
chr13:43859905
|
T | G | 1 | a0007 | 1 | HG02056.hp2 | missense_variant | MODERATE | c.322A>C | p.Lys108Gln | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 5/7 | 631/2059 | 322/822 | 108/273 | chr13 | 43859905 | ||
chr13:43868738
|
C | T | 1 | a0003 | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
missense_variant | MODERATE | c.112G>A | p.Ala38Thr | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/7 | 421/2059 | 112/822 | 38/273 | chr13 | 43868738 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:43837427
|
T | C | 1 | a0001c0002 | 38 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(35): Show |
splice_region_variant&synonymous_variant | LOW | c.675A>G | p.Val225Val | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 984/2059 | 675/822 | 225/273 | chr13 | 43837427 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:43836417
|
G | A | 9 | a0001c0001t0002a0001c0001t0006a0001c0001t0020others(6): Show | 82 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(79): Show |
3_prime_UTR_variant | MODIFIER | c.*863C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 863 | chr13 | 43836417 | |||||
chr13:43836472
|
C | A | 1 | a0001c0001t0026 | 1 | HG03942.hp2 | 3_prime_UTR_variant | MODIFIER | c.*808G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 808 | chr13 | 43836472 | |||||
chr13:43836476
|
G | T | 1 | a0001c0001t0032 | 1 | NA19070.hp2 | 3_prime_UTR_variant | MODIFIER | c.*804C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 804 | chr13 | 43836476 | |||||
chr13:43836533
|
T | C | 18 | a0001c0001t0002a0001c0001t0006a0001c0001t0009others(15): Show | 141 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(138): Show |
3_prime_UTR_variant | MODIFIER | c.*747A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 747 | chr13 | 43836533 | |||||
chr13:43836622
|
G | A | 3 | a0001c0001t0004a0001c0001t0015a0001c0001t0022 | 33 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*658C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 658 | chr13 | 43836622 | |||||
chr13:43836712
|
C | T | 4 | a0001c0002t0005a0001c0002t0027a0001c0002t0033others(1): Show | 28 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*568G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 568 | chr13 | 43836712 | |||||
chr13:43836774
|
C | T | 1 | a0001c0001t0025 | 1 | NA18942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*506G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 506 | chr13 | 43836774 | |||||
chr13:43836775
|
A | G | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(35): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
3_prime_UTR_variant | MODIFIER | c.*505T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 505 | chr13 | 43836775 | |||||
chr13:43836826
|
C | T | 18 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(15): Show | 219 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(216): Show |
3_prime_UTR_variant | MODIFIER | c.*454G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 454 | chr13 | 43836826 | |||||
chr13:43836856
|
C | CA | 20 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(17): Show | 278 | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(275): Show |
3_prime_UTR_variant | MODIFIER | c.*423dupT | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 423 | chr13 | 43836856 | |||||
chr13:43836856
|
C | CAA | 12 | a0001c0001t0008a0001c0001t0012a0001c0001t0015others(9): Show | 70 | HG00280.hp1 HG00438.hp2 HG00673.hp2 others(67): Show |
3_prime_UTR_variant | MODIFIER | c.*422_*423dupTT | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 423 | chr13 | 43836856 | |||||
chr13:43836923
|
G | T | 38 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(35): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
3_prime_UTR_variant | MODIFIER | c.*357C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 357 | chr13 | 43836923 | |||||
chr13:43837009
|
C | T | 1 | a0001c0001t0030 | 1 | HG02300.hp2 | 3_prime_UTR_variant | MODIFIER | c.*271G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 271 | chr13 | 43837009 | |||||
chr13:43837011
|
T | C | 2 | a0001c0002t0016a0001c0002t0035 | 5 | HG02258.hp1 HG02572.hp1 HG02717.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*269A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 269 | chr13 | 43837011 | |||||
chr13:43837013
|
T | G | 7 | a0001c0002t0005a0001c0002t0014a0001c0002t0016others(4): Show | 38 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*267A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 267 | chr13 | 43837013 | |||||
chr13:43837121
|
G | C | 1 | a0002c0003t0036 | 1 | NA19079.hp2 | 3_prime_UTR_variant | MODIFIER | c.*159C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 159 | chr13 | 43837121 | |||||
chr13:43837164
|
T | TAAGACAG others(324): Show |
1 | a0001c0001t0028 | 1 | HG01496.hp2 | 3_prime_UTR_variant | MODIFIER | c.*115_*116insTTTTTT others(325): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 115 | chr13 | 43837164 | |||||
chr13:43837274
|
G | A | 2 | a0001c0001t0009a0001c0001t0018 | 21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*6C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 7/7 | 6 | chr13 | 43837274 | |||||
chr13:43869426
|
C | A | 1 | a0001c0001t0010 | 9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
5_prime_UTR_variant | MODIFIER | c.-50G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 3/7 | 50 | chr13 | 43869426 | |||||
chr13:43869475
|
T | C | 1 | a0001c0001t0029 | 1 | HG00642.hp1 | 5_prime_UTR_variant | MODIFIER | c.-99A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 3/7 | 99 | chr13 | 43869475 | |||||
chr13:43879647
|
G | A | 26 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(23): Show | 283 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(280): Show |
5_prime_UTR_premature_start_codon_gain_variant | LOW | c.-216C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/7 | chr13 | 43879647 | ||||||
chr13:43879737
|
A | G | 40 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(37): Show | 387 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(384): Show |
5_prime_UTR_variant | MODIFIER | c.-306T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/7 | 10361 | chr13 | 43879737 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr13:43837548
|
ATAAT | A | 2 | a0001c0001t0010g0020a0001c0001t0010g0111 | 4 | HG01243.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-123_673-120del others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43837548 | ||||||
chr13:43837637
|
T | TAATTAAA others(327): Show |
1 | a0001c0001t0009g0135 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.673-209_673-208ins others(334): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43837637 | ||||||
chr13:43837637
|
T | TAATTAAA others(328): Show |
1 | a0001c0001t0009g0134 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.673-209_673-208ins others(335): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43837637 | ||||||
chr13:43837637
|
T | TAATTAAA others(329): Show |
4 | a0001c0001t0009g0045a0001c0001t0009g0046a0001c0001t0009g0132others(1): Show | 6 | HG01361.hp1 HG02257.hp1 HG02615.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-209_673-208ins others(336): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43837637 | ||||||
chr13:43837637
|
T | TAATTAAA others(334): Show |
4 | a0001c0001t0009g0136a0001c0001t0009g0137a0001c0001t0009g0138others(1): Show | 4 | HG02559.hp1 HG02922.hp2 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-209_673-208ins others(341): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43837637 | ||||||
chr13:43837652
|
AAC | A | 78 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0019others(75): Show | 141 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.673-225_673-224del others(2): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43837652 | ||||||
chr13:43837760
|
T | C | 2 | a0001c0001t0007g0094a0001c0001t0007g0097 | 2 | NA18945.hp2 NA18977.hp1 |
intron_variant | MODIFIER | c.673-331A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43837760 | ||||||
chr13:43837834
|
A | G | 24 | a0001c0002t0005g0004a0001c0002t0005g0027a0001c0002t0005g0058others(21): Show | 38 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.673-405T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43837834 | ||||||
chr13:43837855
|
T | G | 1 | a0001c0002t0005g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.673-426A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43837855 | ||||||
chr13:43838330
|
T | A | 37 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0019others(34): Show | 82 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.673-901A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43838330 | ||||||
chr13:43838552
|
G | A | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-1123C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43838552 | ||||||
chr13:43838853
|
T | C | 2 | a0001c0001t0004g0191a0001c0001t0004g0193 | 2 | HG02027.hp2 NA19058.hp2 |
intron_variant | MODIFIER | c.673-1424A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43838853 | ||||||
chr13:43839069
|
G | A | 4 | a0001c0001t0001g0023a0001c0001t0001g0148a0001c0001t0008g0150others(1): Show | 6 | HG01884.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-1640C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839069 | ||||||
chr13:43839119
|
T | C | 1 | a0001c0001t0012g0106 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.673-1690A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839119 | ||||||
chr13:43839240
|
C | T | 6 | a0001c0001t0010g0020a0001c0001t0010g0035a0001c0001t0010g0090others(3): Show | 9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.673-1811G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839240 | ||||||
chr13:43839285
|
A | G | 19 | a0001c0001t0007g0005a0001c0001t0007g0015a0001c0001t0007g0094others(16): Show | 29 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.673-1856T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839285 | ||||||
chr13:43839331
|
T | C | 15 | a0001c0001t0001g0002a0001c0001t0001g0024a0001c0001t0001g0050others(12): Show | 42 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(39): Show |
intron_variant | MODIFIER | c.673-1902A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839331 | ||||||
chr13:43839349
|
G | A | 1 | a0001c0001t0001g0189 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.673-1920C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839349 | ||||||
chr13:43839360
|
A | T | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(131): Show | 229 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.673-1931T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839360 | ||||||
chr13:43839387
|
C | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(173): Show | 289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.673-1958G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839387 | ||||||
chr13:43839463
|
T | C | 17 | a0001c0001t0009g0043a0001c0001t0009g0044a0001c0001t0009g0045others(14): Show | 21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.673-2034A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839463 | ||||||
chr13:43839496
|
G | T | 1 | a0001c0002t0014g0223 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.673-2067C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839496 | ||||||
chr13:43839558
|
T | A | 1 | a0001c0001t0007g0101 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.673-2129A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839558 | ||||||
chr13:43839576
|
AAT | A | 19 | a0001c0001t0007g0005a0001c0001t0007g0015a0001c0001t0007g0094others(16): Show | 29 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.673-2149_673-2148d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839576 | ||||||
chr13:43839827
|
T | A | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-2398A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839827 | ||||||
chr13:43839857
|
G | A | 1 | a0001c0001t0003g0257 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.673-2428C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839857 | ||||||
chr13:43839911
|
C | T | 1 | a0001c0001t0003g0062 | 2 | NA19056.hp2 NA19081.hp2 |
intron_variant | MODIFIER | c.673-2482G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839911 | ||||||
chr13:43839934
|
C | T | 1 | a0004c0005t0001g0160 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.673-2505G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43839934 | ||||||
chr13:43840054
|
T | G | 1 | a0001c0001t0003g0243 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.673-2625A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840054 | ||||||
chr13:43840065
|
C | T | 1 | a0001c0001t0001g0205 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.673-2636G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840065 | ||||||
chr13:43840165
|
T | C | 2 | a0001c0001t0004g0017a0001c0001t0022g0120 | 5 | NA18952.hp2 NA18979.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.673-2736A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840165 | ||||||
chr13:43840214
|
C | T | 2 | a0001c0001t0002g0079a0001c0001t0021g0080 | 2 | HG01074.hp1 HG02055.hp2 |
intron_variant | MODIFIER | c.673-2785G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840214 | ||||||
chr13:43840267
|
C | T | 2 | a0001c0001t0002g0070a0001c0001t0002g0085 | 2 | HG03490.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.673-2838G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840267 | ||||||
chr13:43840565
|
T | C | 17 | a0001c0001t0009g0043a0001c0001t0009g0044a0001c0001t0009g0045others(14): Show | 21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.673-3136A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840565 | ||||||
chr13:43840587
|
A | C | 21 | a0001c0001t0001g0184a0002c0003t0001g0012a0002c0003t0001g0018others(18): Show | 31 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.673-3158T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840587 | ||||||
chr13:43840606
|
T | G | 1 | a0001c0001t0001g0162 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.673-3177A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840606 | ||||||
chr13:43840626
|
C | T | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(210): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.673-3197G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840626 | ||||||
chr13:43840630
|
C | T | 38 | a0001c0001t0001g0185a0001c0001t0002g0001a0001c0001t0002g0014others(35): Show | 83 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(80): Show |
intron_variant | MODIFIER | c.673-3201G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840630 | ||||||
chr13:43840633
|
T | C | 1 | a0001c0001t0010g0035 | 2 | HG02257.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.673-3204A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840633 | ||||||
chr13:43840639
|
G | C | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(210): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.673-3210C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840639 | ||||||
chr13:43840777
|
T | C | 79 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0014others(76): Show | 142 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.673-3348A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840777 | ||||||
chr13:43840780
|
C | T | 78 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0019others(75): Show | 141 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.673-3351G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840780 | ||||||
chr13:43840781
|
A | C | 78 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0019others(75): Show | 141 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(138): Show |
intron_variant | MODIFIER | c.673-3352T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840781 | ||||||
chr13:43840800
|
G | T | 42 | a0001c0001t0001g0219a0001c0001t0009g0043a0001c0001t0009g0044others(39): Show | 60 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.673-3371C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840800 | ||||||
chr13:43840862
|
A | G | 17 | a0001c0001t0009g0043a0001c0001t0009g0044a0001c0001t0009g0045others(14): Show | 21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.673-3433T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840862 | ||||||
chr13:43840960
|
A | G | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-3531T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840960 | ||||||
chr13:43840976
|
T | A | 7 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0145others(4): Show | 7 | HG01884.hp1 HG01981.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-3547A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43840976 | ||||||
chr13:43841004
|
T | A | 1 | a0001c0001t0012g0098 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.673-3575A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841004 | ||||||
chr13:43841067
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.673-3638C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841067 | ||||||
chr13:43841102
|
C | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(210): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.673-3673G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841102 | ||||||
chr13:43841233
|
A | G | 70 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0055others(67): Show | 97 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.673-3804T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841233 | ||||||
chr13:43841260
|
A | G | 1 | a0001c0001t0006g0041 | 2 | NA18979.hp2 NA18989.hp1 |
intron_variant | MODIFIER | c.673-3831T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841260 | ||||||
chr13:43841356
|
T | C | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(210): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.673-3927A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841356 | ||||||
chr13:43841462
|
T | C | 6 | a0001c0001t0010g0020a0001c0001t0010g0035a0001c0001t0010g0090others(3): Show | 9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.673-4033A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841462 | ||||||
chr13:43841503
|
T | C | 20 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0021others(17): Show | 33 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.673-4074A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841503 | ||||||
chr13:43841567
|
T | C | 1 | a0001c0001t0003g0237 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.673-4138A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841567 | ||||||
chr13:43841642
|
A | G | 20 | a0002c0003t0001g0012a0002c0003t0001g0018a0002c0003t0001g0026others(17): Show | 30 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(27): Show |
intron_variant | MODIFIER | c.673-4213T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841642 | ||||||
chr13:43841664
|
T | C | 1 | a0001c0001t0004g0037 | 2 | NA18948.hp1 NA18956.hp2 |
intron_variant | MODIFIER | c.673-4235A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841664 | ||||||
chr13:43841692
|
T | C | 1 | a0001c0001t0001g0215 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.673-4263A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841692 | ||||||
chr13:43841783
|
T | A | 37 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0019others(34): Show | 82 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.673-4354A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841783 | ||||||
chr13:43841829
|
G | A | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-4400C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841829 | ||||||
chr13:43841847
|
A | C | 1 | a0001c0001t0001g0215 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.673-4418T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841847 | ||||||
chr13:43841859
|
C | T | 14 | a0001c0001t0003g0241a0001c0001t0004g0016a0001c0001t0004g0017others(11): Show | 25 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(22): Show |
intron_variant | MODIFIER | c.673-4430G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841859 | ||||||
chr13:43841864
|
T | G | 1 | a0001c0001t0002g0065 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.673-4435A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43841864 | ||||||
chr13:43842083
|
C | CT | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(220): Show | 385 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.673-4655dupA | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842083 | ||||||
chr13:43842141
|
A | C | 4 | a0001c0001t0013g0034a0001c0001t0013g0087a0001c0001t0013g0088others(1): Show | 5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.673-4712T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842141 | ||||||
chr13:43842199
|
G | C | 40 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(37): Show | 88 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.673-4770C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842199 | ||||||
chr13:43842265
|
G | A | 1 | a0001c0001t0006g0040 | 2 | HG02738.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.673-4836C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842265 | ||||||
chr13:43842528
|
C | G | 1 | a0001c0001t0001g0208 | 1 | NA18982.hp1 | intron_variant | MODIFIER | c.673-5099G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842528 | ||||||
chr13:43842591
|
A | T | 1 | a0001c0001t0003g0245 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.673-5162T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842591 | ||||||
chr13:43842669
|
T | G | 77 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0055others(74): Show | 106 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.673-5240A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842669 | ||||||
chr13:43842809
|
C | T | 1 | a0001c0001t0001g0159 | 1 | HG01257.hp1 | intron_variant | MODIFIER | c.673-5380G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842809 | ||||||
chr13:43842880
|
A | G | 1 | a0001c0001t0013g0093 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.673-5451T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842880 | ||||||
chr13:43842883
|
AG | A | 6 | a0001c0001t0001g0208a0001c0001t0001g0209a0001c0001t0001g0211others(3): Show | 6 | HG00438.hp2 NA18948.hp2 NA18950.hp1 others(3): Show |
intron_variant | MODIFIER | c.673-5455delC | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842883 | ||||||
chr13:43842958
|
T | A | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-5529A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43842958 | ||||||
chr13:43843254
|
T | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(210): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.673-5825A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43843254 | ||||||
chr13:43843283
|
C | G | 4 | a0001c0001t0001g0023a0001c0001t0001g0148a0001c0001t0008g0150others(1): Show | 6 | HG01884.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.673-5854G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43843283 | ||||||
chr13:43843305
|
G | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(173): Show | 289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.673-5876C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43843305 | ||||||
chr13:43843321
|
T | A | 1 | a0001c0001t0009g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.673-5892A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43843321 | ||||||
chr13:43843633
|
G | A | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-6204C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43843633 | ||||||
chr13:43843824
|
AT | A | 202 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(199): Show | 347 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(344): Show |
intron_variant | MODIFIER | c.673-6396delA | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43843824 | ||||||
chr13:43843951
|
A | G | 3 | a0001c0001t0002g0075a0001c0001t0002g0079a0001c0001t0021g0080 | 3 | HG01074.hp1 HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.673-6522T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43843951 | ||||||
chr13:43844028
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(173): Show | 289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.673-6599C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844028 | ||||||
chr13:43844069
|
CTTCT | C | 24 | a0001c0001t0001g0219a0001c0002t0005g0004a0001c0002t0005g0027others(21): Show | 38 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.673-6644_673-6641d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844069 | ||||||
chr13:43844112
|
G | A | 6 | a0001c0001t0010g0020a0001c0001t0010g0035a0001c0001t0010g0090others(3): Show | 9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.673-6683C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844112 | ||||||
chr13:43844126
|
T | C | 1 | a0001c0001t0009g0132 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.673-6697A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844126 | ||||||
chr13:43844224
|
G | A | 1 | a0001c0002t0014g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.673-6795C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844224 | ||||||
chr13:43844303
|
G | C | 1 | a0006c0006t0001g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.673-6874C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844303 | ||||||
chr13:43844308
|
A | G | 1 | a0001c0001t0022g0120 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.673-6879T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844308 | ||||||
chr13:43844639
|
T | G | 4 | a0001c0001t0006g0010a0001c0001t0006g0122a0001c0001t0006g0123others(1): Show | 8 | NA18953.hp2 NA18955.hp2 NA18965.hp1 others(5): Show |
intron_variant | MODIFIER | c.673-7210A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844639 | ||||||
chr13:43844841
|
C | G | 3 | a0001c0001t0004g0037a0001c0001t0004g0039a0001c0001t0004g0117 | 5 | NA18945.hp1 NA18948.hp1 NA18956.hp2 others(2): Show |
intron_variant | MODIFIER | c.673-7412G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844841 | ||||||
chr13:43844979
|
A | G | 19 | a0001c0001t0007g0005a0001c0001t0007g0015a0001c0001t0007g0094others(16): Show | 29 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.673-7550T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43844979 | ||||||
chr13:43845087
|
T | C | 1 | a0002c0003t0001g0176 | 1 | HG02132.hp2 | intron_variant | MODIFIER | c.673-7658A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845087 | ||||||
chr13:43845185
|
T | C | 1 | a0002c0003t0001g0174 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.673-7756A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845185 | ||||||
chr13:43845351
|
C | T | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-7922G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845351 | ||||||
chr13:43845396
|
A | G | 79 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0014others(76): Show | 142 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.673-7967T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845396 | ||||||
chr13:43845554
|
T | A | 5 | a0001c0001t0009g0043a0001c0001t0009g0044a0001c0001t0009g0127others(2): Show | 7 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-8125A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845554 | ||||||
chr13:43845581
|
G | A | 2 | a0001c0001t0007g0107a0001c0001t0012g0108 | 2 | HG00408.hp1 HG02056.hp1 |
intron_variant | MODIFIER | c.673-8152C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845581 | ||||||
chr13:43845588
|
T | TATAGTCC others(25): Show |
1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-8160_673-8159i others(34): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845588 | ||||||
chr13:43845637
|
G | A | 13 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0021others(10): Show | 24 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.673-8208C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845637 | ||||||
chr13:43845711
|
A | AAAAAC | 212 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(209): Show | 370 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(367): Show |
intron_variant | MODIFIER | c.673-8287_673-8283d others(7): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845711 | ||||||
chr13:43845711
|
A | AAAAACAA others(3): Show |
1 | a0001c0001t0001g0186 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.673-8292_673-8283d others(12): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845711 | ||||||
chr13:43845769
|
T | C | 1 | a0001c0002t0016g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.673-8340A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845769 | ||||||
chr13:43845794
|
T | C | 2 | a0001c0001t0003g0242a0001c0001t0003g0244 | 2 | HG02165.hp1 NA18968.hp2 |
intron_variant | MODIFIER | c.673-8365A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845794 | ||||||
chr13:43845967
|
C | T | 1 | a0001c0002t0016g0224 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.673-8538G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845967 | ||||||
chr13:43845985
|
T | C | 1 | a0001c0001t0018g0131 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.673-8556A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43845985 | ||||||
chr13:43846081
|
C | CT | 17 | a0001c0001t0009g0043a0001c0001t0009g0044a0001c0001t0009g0045others(14): Show | 21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.673-8653dupA | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846081 | ||||||
chr13:43846094
|
G | A | 2 | a0001c0001t0010g0020a0001c0001t0010g0111 | 4 | HG01243.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.673-8665C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846094 | ||||||
chr13:43846114
|
G | A | 3 | a0001c0001t0010g0090a0001c0001t0010g0091a0001c0001t0010g0092 | 3 | HG01109.hp1 HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.673-8685C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846114 | ||||||
chr13:43846124
|
G | C | 5 | a0001c0001t0009g0043a0001c0001t0009g0044a0001c0001t0009g0127others(2): Show | 7 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-8695C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846124 | ||||||
chr13:43846149
|
A | G | 3 | a0001c0001t0004g0016a0001c0001t0004g0038a0001c0001t0004g0114 | 7 | HG01167.hp2 NA18954.hp2 NA18972.hp2 others(4): Show |
intron_variant | MODIFIER | c.673-8720T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846149 | ||||||
chr13:43846175
|
A | G | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-8746T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846175 | ||||||
chr13:43846176
|
G | A | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-8747C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846176 | ||||||
chr13:43846193
|
G | C | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-8764C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846193 | ||||||
chr13:43846194
|
C | G | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-8765G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846194 | ||||||
chr13:43846271
|
A | C | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-8842T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846271 | ||||||
chr13:43846337
|
G | A | 26 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0019others(23): Show | 58 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.673-8908C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846337 | ||||||
chr13:43846369
|
C | G | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-8940G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846369 | ||||||
chr13:43846371
|
G | C | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-8942C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846371 | ||||||
chr13:43846372
|
C | G | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-8943G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846372 | ||||||
chr13:43846669
|
C | T | 16 | a0001c0002t0005g0004a0001c0002t0005g0027a0001c0002t0005g0058others(13): Show | 28 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.673-9240G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846669 | ||||||
chr13:43846875
|
AAG | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(131): Show | 229 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.673-9448_673-9447d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43846875 | ||||||
chr13:43847009
|
A | G | 1 | a0001c0001t0002g0079 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.673-9580T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847009 | ||||||
chr13:43847173
|
C | T | 1 | a0002c0003t0001g0182 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.673-9744G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847173 | ||||||
chr13:43847352
|
T | C | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.673-9923A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847352 | ||||||
chr13:43847416
|
T | A | 2 | a0001c0001t0001g0202a0001c0001t0008g0203 | 2 | HG00642.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.673-9987A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847416 | ||||||
chr13:43847528
|
C | A | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(210): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.673-10099G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847528 | ||||||
chr13:43847610
|
A | G | 30 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(27): Show | 78 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.673-10181T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847610 | ||||||
chr13:43847749
|
G | C | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-10320C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847749 | ||||||
chr13:43847750
|
C | G | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-10321G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847750 | ||||||
chr13:43847797
|
C | G | 2 | a0001c0001t0003g0063a0001c0001t0017g0246 | 3 | NA18969.hp1 NA18972.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.673-10368G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847797 | ||||||
chr13:43847850
|
T | C | 1 | a0001c0001t0001g0204 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.673-10421A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847850 | ||||||
chr13:43847851
|
T | C | 23 | a0001c0001t0001g0219a0001c0002t0005g0004a0001c0002t0005g0027others(20): Show | 37 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.673-10422A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847851 | ||||||
chr13:43847927
|
A | C | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-10498T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847927 | ||||||
chr13:43847963
|
C | T | 1 | a0001c0001t0001g0200 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.673-10534G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847963 | ||||||
chr13:43847990
|
G | T | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(107): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.673-10561C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43847990 | ||||||
chr13:43848059
|
G | C | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-10630C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848059 | ||||||
chr13:43848060
|
C | G | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.673-10631G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848060 | ||||||
chr13:43848196
|
C | T | 1 | a0001c0001t0007g0104 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.672+10585G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848196 | ||||||
chr13:43848235
|
A | G | 79 | a0001c0001t0001g0219a0001c0001t0002g0001a0001c0001t0002g0014others(76): Show | 142 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(139): Show |
intron_variant | MODIFIER | c.672+10546T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848235 | ||||||
chr13:43848392
|
G | A | 5 | a0002c0003t0001g0026a0002c0003t0001g0176a0002c0003t0001g0190others(2): Show | 7 | HG02071.hp1 HG02074.hp2 HG02080.hp1 others(4): Show |
intron_variant | MODIFIER | c.672+10389C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848392 | ||||||
chr13:43848516
|
G | A | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(210): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.672+10265C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848516 | ||||||
chr13:43848587
|
A | T | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(220): Show | 385 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.672+10194T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848587 | ||||||
chr13:43848828
|
C | A | 17 | a0001c0001t0009g0043a0001c0001t0009g0044a0001c0001t0009g0045others(14): Show | 21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.672+9953G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848828 | ||||||
chr13:43848946
|
C | T | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(220): Show | 385 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.672+9835G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848946 | ||||||
chr13:43848952
|
A | G | 26 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0019others(23): Show | 58 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.672+9829T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43848952 | ||||||
chr13:43849032
|
T | A | 1 | a0001c0001t0030g0213 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.672+9749A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849032 | ||||||
chr13:43849066
|
C | T | 25 | a0001c0001t0001g0219a0001c0002t0005g0004a0001c0002t0005g0027others(22): Show | 39 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.672+9715G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849066 | ||||||
chr13:43849134
|
G | A | 1 | a0001c0001t0009g0137 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.672+9647C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849134 | ||||||
chr13:43849162
|
T | C | 3 | a0001c0001t0001g0055a0001c0001t0015g0194a0001c0001t0030g0213 | 4 | HG00099.hp2 HG01433.hp2 HG02300.hp2 others(1): Show |
intron_variant | MODIFIER | c.672+9619A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849162 | ||||||
chr13:43849204
|
G | A | 2 | a0001c0001t0004g0016a0001c0001t0004g0038 | 6 | NA18954.hp2 NA18972.hp2 NA18983.hp2 others(3): Show |
intron_variant | MODIFIER | c.672+9577C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849204 | ||||||
chr13:43849289
|
T | C | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(220): Show | 385 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.672+9492A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849289 | ||||||
chr13:43849376
|
G | C | 4 | a0001c0002t0005g0027a0001c0002t0005g0226a0001c0002t0005g0232others(1): Show | 6 | NA18941.hp1 NA18942.hp2 NA18960.hp1 others(3): Show |
intron_variant | MODIFIER | c.672+9405C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849376 | ||||||
chr13:43849447
|
A | C | 31 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0144others(28): Show | 39 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.672+9334T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849447 | ||||||
chr13:43849484
|
C | T | 1 | a0002c0003t0001g0177 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.672+9297G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849484 | ||||||
chr13:43849485
|
T | G | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(131): Show | 229 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.672+9296A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849485 | ||||||
chr13:43849531
|
T | G | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.672+9250A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849531 | ||||||
chr13:43849674
|
A | G | 1 | a0001c0001t0004g0119 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.672+9107T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849674 | ||||||
chr13:43849737
|
T | C | 1 | a0001c0002t0005g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.672+9044A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849737 | ||||||
chr13:43849927
|
T | C | 40 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(37): Show | 88 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.672+8854A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849927 | ||||||
chr13:43849948
|
G | A | 1 | a0001c0001t0004g0119 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.672+8833C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43849948 | ||||||
chr13:43850010
|
G | C | 1 | a0001c0001t0007g0101 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.672+8771C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850010 | ||||||
chr13:43850074
|
T | C | 125 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(122): Show | 211 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(208): Show |
intron_variant | MODIFIER | c.672+8707A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850074 | ||||||
chr13:43850208
|
A | G | 10 | a0001c0001t0010g0020a0001c0001t0010g0035a0001c0001t0010g0090others(7): Show | 14 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.672+8573T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850208 | ||||||
chr13:43850236
|
G | T | 4 | a0001c0001t0006g0011a0001c0001t0006g0041a0001c0001t0006g0126others(1): Show | 10 | NA18939.hp2 NA18964.hp1 NA18978.hp1 others(7): Show |
intron_variant | MODIFIER | c.672+8545C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850236 | ||||||
chr13:43850269
|
T | A | 4 | a0001c0001t0013g0034a0001c0001t0013g0087a0001c0001t0013g0088others(1): Show | 5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.672+8512A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850269 | ||||||
chr13:43850578
|
A | T | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.672+8203T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850578 | ||||||
chr13:43850602
|
A | G | 1 | a0001c0001t0007g0094 | 1 | NA18977.hp1 | intron_variant | MODIFIER | c.672+8179T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850602 | ||||||
chr13:43850630
|
A | G | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(127): Show | 218 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.672+8151T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850630 | ||||||
chr13:43850872
|
T | C | 1 | a0001c0001t0004g0038 | 2 | NA19054.hp1 NA19065.hp1 |
intron_variant | MODIFIER | c.672+7909A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850872 | ||||||
chr13:43850921
|
G | A | 3 | a0002c0003t0001g0051a0002c0003t0001g0178a0002c0003t0008g0179 | 4 | HG03239.hp2 HG03654.hp2 HG03942.hp1 others(1): Show |
intron_variant | MODIFIER | c.672+7860C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43850921 | ||||||
chr13:43851014
|
T | C | 1 | a0001c0001t0018g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.672+7767A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851014 | ||||||
chr13:43851091
|
T | A | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.672+7690A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851091 | ||||||
chr13:43851092
|
C | T | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.672+7689G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851092 | ||||||
chr13:43851094
|
A | C | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.672+7687T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851094 | ||||||
chr13:43851285
|
T | C | 3 | a0001c0001t0002g0075a0001c0001t0002g0079a0001c0001t0021g0080 | 3 | HG01074.hp1 HG02055.hp2 HG03225.hp1 |
intron_variant | MODIFIER | c.672+7496A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851285 | ||||||
chr13:43851324
|
C | T | 1 | a0006c0006t0001g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.672+7457G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851324 | ||||||
chr13:43851386
|
A | G | 1 | a0001c0001t0003g0242 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.672+7395T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851386 | ||||||
chr13:43851615
|
C | T | 1 | a0001c0001t0003g0241 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.672+7166G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851615 | ||||||
chr13:43851685
|
C | G | 1 | a0001c0001t0008g0199 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.672+7096G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851685 | ||||||
chr13:43851776
|
C | T | 1 | a0001c0001t0009g0129 | 1 | HG04184.hp2 | intron_variant | MODIFIER | c.672+7005G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851776 | ||||||
chr13:43851850
|
G | A | 24 | a0001c0001t0001g0219a0001c0002t0005g0004a0001c0002t0005g0027others(21): Show | 38 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(35): Show |
intron_variant | MODIFIER | c.672+6931C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851850 | ||||||
chr13:43851860
|
G | T | 4 | a0001c0001t0010g0035a0001c0001t0010g0090a0001c0001t0010g0091others(1): Show | 5 | HG01109.hp1 HG02145.hp1 HG02257.hp2 others(2): Show |
intron_variant | MODIFIER | c.672+6921C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851860 | ||||||
chr13:43851952
|
G | GA | 9 | a0001c0002t0005g0004a0001c0002t0005g0027a0001c0002t0005g0058others(6): Show | 19 | HG00673.hp2 HG01069.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.672+6828dupT | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851952 | ||||||
chr13:43851952
|
GA | G | 42 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(39): Show | 91 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(88): Show |
intron_variant | MODIFIER | c.672+6828delT | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851952 | ||||||
chr13:43851958
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.672+6823T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851958 | ||||||
chr13:43851968
|
A | G | 1 | a0001c0001t0001g0148 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.672+6813T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43851968 | ||||||
chr13:43852133
|
C | T | 117 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(114): Show | 194 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(191): Show |
intron_variant | MODIFIER | c.672+6648G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852133 | ||||||
chr13:43852178
|
G | A | 1 | a0001c0001t0003g0030 | 3 | HG00621.hp2 HG02027.hp1 NA19002.hp2 |
intron_variant | MODIFIER | c.672+6603C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852178 | ||||||
chr13:43852268
|
A | T | 1 | a0001c0001t0003g0251 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.672+6513T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852268 | ||||||
chr13:43852392
|
G | A | 17 | a0001c0001t0009g0043a0001c0001t0009g0044a0001c0001t0009g0045others(14): Show | 21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.672+6389C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852392 | ||||||
chr13:43852668
|
C | A | 40 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(37): Show | 88 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.672+6113G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852668 | ||||||
chr13:43852732
|
TAGAG | T | 40 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(37): Show | 88 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.672+6045_672+6048d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852732 | ||||||
chr13:43852738
|
G | T | 1 | a0001c0002t0005g0058 | 2 | HG01069.hp1 HG01192.hp1 |
intron_variant | MODIFIER | c.672+6043C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852738 | ||||||
chr13:43852921
|
T | A | 1 | a0001c0002t0005g0060 | 2 | HG01515.hp1 HG02055.hp1 |
intron_variant | MODIFIER | c.672+5860A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852921 | ||||||
chr13:43852928
|
A | C | 3 | a0001c0001t0002g0014a0001c0001t0002g0081a0001c0001t0002g0082 | 6 | NA18961.hp2 NA18964.hp2 NA18973.hp2 others(3): Show |
intron_variant | MODIFIER | c.672+5853T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852928 | ||||||
chr13:43852968
|
A | G | 10 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0145others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.672+5813T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852968 | ||||||
chr13:43852971
|
A | C | 1 | a0001c0001t0001g0185 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.672+5810T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852971 | ||||||
chr13:43852987
|
G | A | 17 | a0001c0001t0009g0043a0001c0001t0009g0044a0001c0001t0009g0045others(14): Show | 21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.672+5794C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43852987 | ||||||
chr13:43853111
|
T | G | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.672+5670A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853111 | ||||||
chr13:43853121
|
A | T | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.672+5660T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853121 | ||||||
chr13:43853122
|
A | G | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.672+5659T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853122 | ||||||
chr13:43853126
|
T | C | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.672+5655A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853126 | ||||||
chr13:43853146
|
T | C | 4 | a0001c0001t0013g0034a0001c0001t0013g0087a0001c0001t0013g0088others(1): Show | 5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.672+5635A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853146 | ||||||
chr13:43853299
|
CA | C | 7 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0145others(4): Show | 7 | HG01884.hp1 HG01981.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.672+5481delT | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853299 | ||||||
chr13:43853388
|
A | C | 25 | a0001c0001t0001g0219a0001c0002t0005g0004a0001c0002t0005g0027others(22): Show | 39 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.672+5393T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853388 | ||||||
chr13:43853409
|
G | A | 1 | a0001c0001t0002g0076 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.672+5372C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853409 | ||||||
chr13:43853436
|
C | T | 17 | a0001c0001t0009g0043a0001c0001t0009g0044a0001c0001t0009g0045others(14): Show | 21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.672+5345G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853436 | ||||||
chr13:43853599
|
A | G | 7 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0145others(4): Show | 7 | HG01884.hp1 HG01981.hp1 HG02559.hp2 others(4): Show |
intron_variant | MODIFIER | c.672+5182T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853599 | ||||||
chr13:43853852
|
T | A | 1 | a0001c0001t0003g0257 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.672+4929A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853852 | ||||||
chr13:43853862
|
T | C | 1 | a0001c0001t0001g0156 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.672+4919A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853862 | ||||||
chr13:43853983
|
A | C | 6 | a0001c0001t0010g0020a0001c0001t0010g0035a0001c0001t0010g0090others(3): Show | 9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.672+4798T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43853983 | ||||||
chr13:43854067
|
C | T | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.672+4714G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854067 | ||||||
chr13:43854085
|
A | G | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.672+4696T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854085 | ||||||
chr13:43854156
|
CA | C | 218 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(215): Show | 379 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(376): Show |
intron_variant | MODIFIER | c.672+4624delT | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854156 | ||||||
chr13:43854169
|
C | T | 26 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0019others(23): Show | 58 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.672+4612G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854169 | ||||||
chr13:43854291
|
G | A | 1 | a0002c0003t0001g0012 | 5 | NA18971.hp1 NA18988.hp1 NA18991.hp2 others(2): Show |
intron_variant | MODIFIER | c.672+4490C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854291 | ||||||
chr13:43854592
|
T | C | 1 | a0001c0002t0005g0228 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.672+4189A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854592 | ||||||
chr13:43854601
|
A | G | 25 | a0001c0001t0001g0219a0001c0002t0005g0004a0001c0002t0005g0027others(22): Show | 39 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.672+4180T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854601 | ||||||
chr13:43854611
|
C | T | 1 | a0001c0001t0001g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.672+4170G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854611 | ||||||
chr13:43854657
|
G | A | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(127): Show | 218 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.672+4124C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854657 | ||||||
chr13:43854697
|
T | C | 3 | a0001c0001t0007g0099a0001c0001t0007g0101a0001c0001t0012g0100 | 3 | HG01928.hp2 HG01993.hp1 HG02015.hp1 |
intron_variant | MODIFIER | c.672+4084A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854697 | ||||||
chr13:43854911
|
G | T | 1 | a0001c0001t0002g0033 | 2 | HG01168.hp2 HG01169.hp1 |
intron_variant | MODIFIER | c.672+3870C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43854911 | ||||||
chr13:43855036
|
A | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(173): Show | 289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.672+3745T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855036 | ||||||
chr13:43855040
|
G | A | 1 | a0001c0001t0003g0249 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.672+3741C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855040 | ||||||
chr13:43855067
|
A | T | 1 | a0001c0001t0006g0122 | 1 | NA19059.hp2 | intron_variant | MODIFIER | c.672+3714T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855067 | ||||||
chr13:43855213
|
A | C | 1 | a0001c0001t0003g0255 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.672+3568T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855213 | ||||||
chr13:43855237
|
G | A | 1 | a0001c0001t0001g0211 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.672+3544C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855237 | ||||||
chr13:43855256
|
C | G | 1 | a0001c0002t0005g0233 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.672+3525G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855256 | ||||||
chr13:43855331
|
A | T | 1 | a0001c0001t0001g0185 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.672+3450T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855331 | ||||||
chr13:43855362
|
G | GACACACA others(1): Show |
4 | a0001c0001t0010g0020a0001c0001t0010g0035a0001c0001t0010g0091others(1): Show | 7 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.672+3418_672+3419i others(10): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855362 | ||||||
chr13:43855363
|
C | A | 6 | a0001c0001t0010g0020a0001c0001t0010g0035a0001c0001t0010g0090others(3): Show | 9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.672+3418G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855363 | ||||||
chr13:43855363
|
C | CCA | 57 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0141others(54): Show | 77 | HG00423.hp2 HG00438.hp1 HG00438.hp2 others(74): Show |
intron_variant | MODIFIER | c.672+3416_672+3417d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855363 | ||||||
chr13:43855363
|
C | CCACA | 22 | a0001c0001t0001g0184a0001c0001t0001g0188a0001c0001t0001g0217others(19): Show | 27 | HG01167.hp1 HG01169.hp2 HG01361.hp1 others(24): Show |
intron_variant | MODIFIER | c.672+3414_672+3417d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855363 | ||||||
chr13:43855363
|
CCA | C | 80 | a0001c0001t0001g0197a0001c0001t0001g0219a0001c0001t0002g0001others(77): Show | 150 | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(147): Show |
intron_variant | MODIFIER | c.672+3416_672+3417d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855363 | ||||||
chr13:43855363
|
CCACA | C | 9 | a0001c0001t0001g0164a0001c0001t0001g0167a0001c0001t0003g0028others(6): Show | 13 | HG01891.hp1 HG02486.hp1 NA18969.hp1 others(10): Show |
intron_variant | MODIFIER | c.672+3414_672+3417d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855363 | ||||||
chr13:43855363
|
CCACACA | C | 16 | a0001c0002t0005g0004a0001c0002t0005g0027a0001c0002t0005g0058others(13): Show | 28 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.672+3412_672+3417d others(8): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855363 | ||||||
chr13:43855363
|
CCACACAC others(7): Show |
C | 1 | a0001c0001t0006g0123 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.672+3404_672+3417d others(16): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855363 | ||||||
chr13:43855393
|
A | C | 18 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0021others(15): Show | 31 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(28): Show |
intron_variant | MODIFIER | c.672+3388T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855393 | ||||||
chr13:43855395
|
C | A | 1 | a0001c0001t0007g0102 | 1 | NA18980.hp2 | intron_variant | MODIFIER | c.672+3386G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855395 | ||||||
chr13:43855417
|
G | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(173): Show | 289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.672+3364C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855417 | ||||||
chr13:43855418
|
A | G | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(173): Show | 289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.672+3363T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855418 | ||||||
chr13:43855537
|
G | T | 1 | a0001c0002t0034g0222 | 1 | NA19059.hp1 | intron_variant | MODIFIER | c.672+3244C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855537 | ||||||
chr13:43855580
|
T | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(173): Show | 289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.672+3201A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855580 | ||||||
chr13:43855681
|
AT | A | 113 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(110): Show | 195 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(192): Show |
intron_variant | MODIFIER | c.672+3099delA | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855681 | ||||||
chr13:43855682
|
T | A | 21 | a0001c0001t0001g0212a0001c0001t0004g0016a0001c0001t0004g0017others(18): Show | 34 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(31): Show |
intron_variant | MODIFIER | c.672+3099A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855682 | ||||||
chr13:43855688
|
AAAAC | A | 44 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0144others(41): Show | 65 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(62): Show |
intron_variant | MODIFIER | c.672+3089_672+3092d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43855688 | ||||||
chr13:43856178
|
G | A | 1 | a0001c0002t0016g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.672+2603C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856178 | ||||||
chr13:43856358
|
C | T | 1 | a0001c0001t0001g0217 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.672+2423G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856358 | ||||||
chr13:43856397
|
G | A | 10 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0022others(7): Show | 23 | HG02738.hp2 HG03239.hp1 HG03669.hp1 others(20): Show |
intron_variant | MODIFIER | c.672+2384C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856397 | ||||||
chr13:43856528
|
G | A | 20 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0021others(17): Show | 33 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.672+2253C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856528 | ||||||
chr13:43856570
|
C | T | 1 | a0001c0001t0004g0191 | 1 | NA19058.hp2 | intron_variant | MODIFIER | c.672+2211G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856570 | ||||||
chr13:43856579
|
G | A | 10 | a0001c0001t0002g0078a0001c0001t0007g0005a0001c0001t0007g0103others(7): Show | 17 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(14): Show |
intron_variant | MODIFIER | c.672+2202C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856579 | ||||||
chr13:43856642
|
A | G | 20 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0021others(17): Show | 33 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.672+2139T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856642 | ||||||
chr13:43856659
|
CT | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(127): Show | 218 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.672+2121delA | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856659 | ||||||
chr13:43856808
|
C | A | 4 | a0001c0001t0001g0024a0001c0001t0001g0164a0001c0001t0001g0166others(1): Show | 6 | HG00408.hp2 NA18952.hp1 NA18968.hp1 others(3): Show |
intron_variant | MODIFIER | c.672+1973G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856808 | ||||||
chr13:43856887
|
C | G | 1 | a0001c0001t0002g0069 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.672+1894G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856887 | ||||||
chr13:43856943
|
AAT | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(131): Show | 229 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.672+1836_672+1837d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43856943 | ||||||
chr13:43857059
|
T | C | 2 | a0001c0001t0001g0055a0001c0001t0030g0213 | 3 | HG00099.hp2 HG01433.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.672+1722A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857059 | ||||||
chr13:43857174
|
C | T | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.672+1607G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857174 | ||||||
chr13:43857449
|
A | AGT | 6 | a0001c0001t0003g0239a0001c0001t0003g0240a0001c0001t0010g0035others(3): Show | 7 | HG01109.hp1 HG02135.hp2 HG02145.hp1 others(4): Show |
intron_variant | MODIFIER | c.672+1330_672+1331d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857449 | ||||||
chr13:43857449
|
A | AGTGT | 3 | a0001c0001t0003g0061a0001c0001t0003g0238a0001c0001t0013g0088 | 4 | HG01496.hp1 HG02451.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.672+1328_672+1331d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857449 | ||||||
chr13:43857449
|
A | AGTGTGT | 3 | a0001c0001t0013g0034a0001c0001t0013g0087a0001c0001t0013g0089 | 4 | HG02280.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.672+1326_672+1331d others(8): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857449 | ||||||
chr13:43857449
|
AGT | A | 13 | a0001c0001t0003g0031a0001c0001t0003g0245a0001c0001t0003g0251others(10): Show | 18 | HG00558.hp2 HG00738.hp2 HG01167.hp1 others(15): Show |
intron_variant | MODIFIER | c.672+1330_672+1331d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857449 | ||||||
chr13:43857449
|
AGTGT | A | 8 | a0001c0001t0006g0022a0001c0001t0006g0040a0001c0001t0006g0125others(5): Show | 12 | HG02257.hp1 HG02559.hp1 HG02630.hp1 others(9): Show |
intron_variant | MODIFIER | c.672+1328_672+1331d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857449 | ||||||
chr13:43857449
|
AGTGTGT | A | 33 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0001g0165others(30): Show | 57 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.672+1326_672+1331d others(8): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857449 | ||||||
chr13:43857449
|
AGTGTGTG others(1): Show |
A | 109 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(106): Show | 209 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(206): Show |
intron_variant | MODIFIER | c.672+1324_672+1331d others(10): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857449 | ||||||
chr13:43857449
|
AGTGTGTG others(3): Show |
A | 26 | a0001c0001t0001g0152a0001c0001t0001g0184a0001c0001t0002g0014others(23): Show | 39 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(36): Show |
intron_variant | MODIFIER | c.672+1322_672+1331d others(12): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857449 | ||||||
chr13:43857449
|
AGTGTGTG others(5): Show |
A | 26 | a0001c0001t0001g0219a0001c0001t0006g0122a0001c0002t0005g0004others(23): Show | 40 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.672+1320_672+1331d others(14): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857449 | ||||||
chr13:43857524
|
A | G | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(174): Show | 290 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.672+1257T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857524 | ||||||
chr13:43857602
|
T | C | 110 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(107): Show | 185 | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(182): Show |
intron_variant | MODIFIER | c.672+1179A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857602 | ||||||
chr13:43857605
|
T | G | 17 | a0001c0001t0009g0043a0001c0001t0009g0044a0001c0001t0009g0045others(14): Show | 21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.672+1176A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857605 | ||||||
chr13:43857765
|
T | C | 1 | a0001c0001t0001g0165 | 1 | HG02135.hp1 | intron_variant | MODIFIER | c.672+1016A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857765 | ||||||
chr13:43857774
|
G | A | 17 | a0001c0001t0009g0043a0001c0001t0009g0044a0001c0001t0009g0045others(14): Show | 21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.672+1007C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857774 | ||||||
chr13:43857808
|
T | A | 1 | a0006c0006t0001g0155 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.672+973A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857808 | ||||||
chr13:43857828
|
G | A | 1 | a0001c0001t0001g0166 | 1 | NA19060.hp1 | intron_variant | MODIFIER | c.672+953C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857828 | ||||||
chr13:43857895
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(174): Show | 290 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.672+886A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857895 | ||||||
chr13:43857932
|
A | T | 1 | a0001c0001t0006g0125 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.672+849T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43857932 | ||||||
chr13:43858047
|
A | C | 4 | a0001c0001t0013g0034a0001c0001t0013g0087a0001c0001t0013g0088others(1): Show | 5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.672+734T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43858047 | ||||||
chr13:43858089
|
G | T | 1 | a0001c0001t0008g0196 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.672+692C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43858089 | ||||||
chr13:43858261
|
G | T | 1 | a0001c0001t0009g0127 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.672+520C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43858261 | ||||||
chr13:43858504
|
T | G | 1 | a0001c0001t0001g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.672+277A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43858504 | ||||||
chr13:43858662
|
GTTCT | G | 2 | a0001c0001t0003g0063a0001c0001t0017g0246 | 3 | NA18969.hp1 NA18972.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.672+115_672+118del others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43858662 | ||||||
chr13:43858747
|
A | G | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.672+34T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 6/6 | chr13 | 43858747 | ||||||
chr13:43859227
|
G | A | 36 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0019others(33): Show | 81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.556-330C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 5/6 | chr13 | 43859227 | ||||||
chr13:43859429
|
A | G | 36 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0019others(33): Show | 81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.555+243T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 5/6 | chr13 | 43859429 | ||||||
chr13:43859431
|
G | A | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(220): Show | 385 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.555+241C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 5/6 | chr13 | 43859431 | ||||||
chr13:43859494
|
C | A | 70 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0055others(67): Show | 97 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(94): Show |
intron_variant | MODIFIER | c.555+178G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 5/6 | chr13 | 43859494 | ||||||
chr13:43859564
|
G | A | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(210): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.555+108C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 5/6 | chr13 | 43859564 | ||||||
chr13:43859598
|
A | T | 1 | a0005c0007t0002g0068 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.555+74T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 5/6 | chr13 | 43859598 | ||||||
chr13:43859644
|
A | T | 1 | a0001c0002t0005g0225 | 1 | NA19072.hp1 | intron_variant | MODIFIER | c.555+28T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 5/6 | chr13 | 43859644 | ||||||
chr13:43860145
|
TAATG | T | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(127): Show | 218 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.157-79_157-76delCA others(2): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860145 | ||||||
chr13:43860159
|
A | T | 2 | a0002c0003t0001g0173a0002c0003t0001g0174 | 2 | HG01993.hp2 NA20300.hp1 |
intron_variant | MODIFIER | c.157-89T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860159 | ||||||
chr13:43860224
|
T | C | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.157-154A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860224 | ||||||
chr13:43860231
|
AATT | A | 26 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0019others(23): Show | 58 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.157-164_157-162del others(3): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860231 | ||||||
chr13:43860279
|
T | C | 4 | a0001c0001t0013g0034a0001c0001t0013g0087a0001c0001t0013g0088others(1): Show | 5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.157-209A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860279 | ||||||
chr13:43860527
|
T | C | 43 | a0001c0001t0001g0219a0001c0001t0006g0122a0001c0001t0009g0043others(40): Show | 61 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.157-457A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860527 | ||||||
chr13:43860552
|
G | GATATTTA others(3): Show |
26 | a0001c0001t0001g0219a0001c0001t0006g0122a0001c0002t0005g0004others(23): Show | 40 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.157-492_157-483dup others(10): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860552 | ||||||
chr13:43860599
|
C | T | 17 | a0001c0001t0009g0043a0001c0001t0009g0044a0001c0001t0009g0045others(14): Show | 21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.157-529G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860599 | ||||||
chr13:43860612
|
C | T | 43 | a0001c0001t0001g0219a0001c0001t0006g0122a0001c0001t0009g0043others(40): Show | 61 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.157-542G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860612 | ||||||
chr13:43860632
|
T | C | 1 | a0001c0001t0002g0081 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.157-562A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860632 | ||||||
chr13:43860700
|
C | G | 40 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(37): Show | 88 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.157-630G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43860700 | ||||||
chr13:43861204
|
T | C | 4 | a0001c0001t0001g0023a0001c0001t0001g0148a0001c0001t0008g0150others(1): Show | 6 | HG01884.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.157-1134A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861204 | ||||||
chr13:43861259
|
T | C | 3 | a0001c0001t0001g0048a0001c0001t0001g0167a0001c0001t0008g0147 | 4 | HG02109.hp2 HG02486.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-1189A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861259 | ||||||
chr13:43861267
|
T | C | 10 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0145others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.157-1197A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861267 | ||||||
chr13:43861374
|
C | T | 1 | a0001c0001t0022g0120 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.157-1304G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861374 | ||||||
chr13:43861396
|
G | A | 4 | a0002c0003t0001g0112a0002c0003t0001g0121a0002c0003t0001g0172others(1): Show | 4 | HG00438.hp1 HG00673.hp1 NA19005.hp2 others(1): Show |
intron_variant | MODIFIER | c.157-1326C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861396 | ||||||
chr13:43861406
|
C | T | 252 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(249): Show | 434 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(431): Show |
intron_variant | MODIFIER | c.157-1336G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861406 | ||||||
chr13:43861453
|
G | C | 1 | a0001c0001t0008g0168 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.157-1383C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861453 | ||||||
chr13:43861672
|
A | T | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.157-1602T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861672 | ||||||
chr13:43861826
|
CAT | C | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.157-1758_157-1757d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861826 | ||||||
chr13:43861852
|
T | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(131): Show | 229 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.157-1782A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861852 | ||||||
chr13:43861933
|
C | A | 1 | a0001c0001t0003g0248 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.157-1863G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43861933 | ||||||
chr13:43862250
|
C | T | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.157-2180G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43862250 | ||||||
chr13:43862300
|
C | T | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.157-2230G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43862300 | ||||||
chr13:43862308
|
C | T | 13 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0021others(10): Show | 24 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.157-2238G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43862308 | ||||||
chr13:43862350
|
C | T | 1 | a0001c0001t0017g0253 | 1 | HG03209.hp2 | intron_variant | MODIFIER | c.157-2280G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43862350 | ||||||
chr13:43862817
|
C | T | 1 | a0001c0001t0002g0067 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.157-2747G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43862817 | ||||||
chr13:43862876
|
C | A | 1 | a0001c0001t0003g0251 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.157-2806G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43862876 | ||||||
chr13:43862916
|
C | T | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(210): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.157-2846G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43862916 | ||||||
chr13:43862936
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(174): Show | 290 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.157-2866A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43862936 | ||||||
chr13:43862968
|
C | T | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(131): Show | 229 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.157-2898G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43862968 | ||||||
chr13:43863029
|
G | A | 1 | a0001c0001t0003g0252 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.157-2959C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863029 | ||||||
chr13:43863035
|
AAATT | A | 17 | a0001c0001t0006g0122a0001c0002t0005g0004a0001c0002t0005g0027others(14): Show | 29 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(26): Show |
intron_variant | MODIFIER | c.157-2969_157-2966d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863035 | ||||||
chr13:43863488
|
A | G | 2 | a0002c0003t0001g0121a0002c0003t0001g0172 | 2 | NA19005.hp2 NA19074.hp1 |
intron_variant | MODIFIER | c.157-3418T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863488 | ||||||
chr13:43863596
|
G | A | 1 | a0001c0001t0001g0169 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.157-3526C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863596 | ||||||
chr13:43863675
|
T | TTG | 7 | a0001c0001t0003g0013a0001c0001t0003g0061a0001c0001t0003g0249others(4): Show | 12 | HG00423.hp2 HG00558.hp2 HG00621.hp1 others(9): Show |
intron_variant | MODIFIER | c.157-3607_157-3606d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863675 | ||||||
chr13:43863675
|
T | TTGTGTG | 3 | a0001c0001t0010g0090a0001c0001t0010g0091a0001c0001t0010g0092 | 3 | HG01109.hp1 HG02145.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.157-3611_157-3606d others(8): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863675 | ||||||
chr13:43863675
|
TTG | T | 64 | a0001c0001t0001g0170a0001c0001t0001g0171a0001c0001t0002g0001others(61): Show | 129 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(126): Show |
intron_variant | MODIFIER | c.157-3607_157-3606d others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863675 | ||||||
chr13:43863675
|
TTGTG | T | 148 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(145): Show | 241 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(238): Show |
intron_variant | MODIFIER | c.157-3609_157-3606d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863675 | ||||||
chr13:43863768
|
C | T | 1 | a0001c0001t0003g0255 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.157-3698G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863768 | ||||||
chr13:43863854
|
A | G | 26 | a0001c0001t0001g0219a0001c0001t0006g0122a0001c0002t0005g0004others(23): Show | 40 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(37): Show |
intron_variant | MODIFIER | c.157-3784T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863854 | ||||||
chr13:43863957
|
G | C | 1 | a0001c0001t0002g0019 | 3 | NA18988.hp2 NA19007.hp1 NA19066.hp1 |
intron_variant | MODIFIER | c.157-3887C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43863957 | ||||||
chr13:43864046
|
A | G | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.157-3976T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43864046 | ||||||
chr13:43864130
|
C | T | 1 | a0001c0001t0001g0157 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.157-4060G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43864130 | ||||||
chr13:43864142
|
T | C | 2 | a0001c0001t0003g0254a0001c0001t0017g0253 | 2 | HG00639.hp2 HG03209.hp2 |
intron_variant | MODIFIER | c.157-4072A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43864142 | ||||||
chr13:43864391
|
G | A | 9 | a0001c0001t0009g0045a0001c0001t0009g0046a0001c0001t0009g0132others(6): Show | 11 | HG01361.hp1 HG02257.hp1 HG02559.hp1 others(8): Show |
intron_variant | MODIFIER | c.156+4303C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43864391 | ||||||
chr13:43864420
|
G | C | 17 | a0001c0001t0009g0043a0001c0001t0009g0044a0001c0001t0009g0045others(14): Show | 21 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(18): Show |
intron_variant | MODIFIER | c.156+4274C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43864420 | ||||||
chr13:43864821
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(174): Show | 290 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.156+3873A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43864821 | ||||||
chr13:43864867
|
T | G | 1 | a0001c0001t0001g0215 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.156+3827A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43864867 | ||||||
chr13:43865014
|
T | C | 40 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(37): Show | 88 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.156+3680A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865014 | ||||||
chr13:43865033
|
T | C | 35 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0019others(32): Show | 80 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(77): Show |
intron_variant | MODIFIER | c.156+3661A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865033 | ||||||
chr13:43865083
|
A | G | 20 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0021others(17): Show | 33 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.156+3611T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865083 | ||||||
chr13:43865129
|
T | G | 30 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(27): Show | 78 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.156+3565A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865129 | ||||||
chr13:43865211
|
C | T | 11 | a0001c0001t0001g0156a0001c0001t0006g0010a0001c0001t0006g0011others(8): Show | 24 | HG01981.hp1 HG02738.hp2 HG03239.hp1 others(21): Show |
intron_variant | MODIFIER | c.156+3483G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865211 | ||||||
chr13:43865321
|
T | C | 4 | a0001c0001t0013g0034a0001c0001t0013g0087a0001c0001t0013g0088others(1): Show | 5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+3373A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865321 | ||||||
chr13:43865452
|
T | C | 1 | a0001c0001t0002g0082 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.156+3242A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865452 | ||||||
chr13:43865462
|
G | GT | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.156+3231dupA | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865462 | ||||||
chr13:43865475
|
A | G | 19 | a0001c0001t0007g0005a0001c0001t0007g0015a0001c0001t0007g0094others(16): Show | 29 | HG00408.hp1 HG00423.hp1 HG00642.hp1 others(26): Show |
intron_variant | MODIFIER | c.156+3219T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865475 | ||||||
chr13:43865484
|
T | C | 10 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0022others(7): Show | 23 | HG02738.hp2 HG03239.hp1 HG03669.hp1 others(20): Show |
intron_variant | MODIFIER | c.156+3210A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865484 | ||||||
chr13:43865524
|
G | C | 43 | a0001c0001t0001g0219a0001c0001t0006g0122a0001c0001t0009g0043others(40): Show | 61 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(58): Show |
intron_variant | MODIFIER | c.156+3170C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865524 | ||||||
chr13:43865742
|
C | T | 6 | a0001c0001t0010g0020a0001c0001t0010g0035a0001c0001t0010g0090others(3): Show | 9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.156+2952G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865742 | ||||||
chr13:43865821
|
A | G | 2 | a0001c0001t0006g0122a0001c0002t0034g0222 | 2 | NA19059.hp1 NA19059.hp2 |
intron_variant | MODIFIER | c.156+2873T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865821 | ||||||
chr13:43865912
|
G | T | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(174): Show | 290 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.156+2782C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43865912 | ||||||
chr13:43866012
|
A | T | 1 | a0001c0001t0003g0239 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.156+2682T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866012 | ||||||
chr13:43866085
|
A | G | 4 | a0001c0001t0013g0034a0001c0001t0013g0087a0001c0001t0013g0088others(1): Show | 5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+2609T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866085 | ||||||
chr13:43866305
|
C | G | 36 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0019others(33): Show | 81 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(78): Show |
intron_variant | MODIFIER | c.156+2389G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866305 | ||||||
chr13:43866380
|
A | C | 1 | a0001c0001t0010g0091 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.156+2314T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866380 | ||||||
chr13:43866391
|
T | C | 177 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(174): Show | 290 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(287): Show |
intron_variant | MODIFIER | c.156+2303A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866391 | ||||||
chr13:43866435
|
A | G | 1 | a0001c0001t0002g0065 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.156+2259T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866435 | ||||||
chr13:43866457
|
G | A | 1 | a0001c0001t0001g0171 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.156+2237C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866457 | ||||||
chr13:43866605
|
C | T | 3 | a0001c0001t0006g0010a0001c0001t0006g0123a0001c0001t0006g0124 | 7 | NA18953.hp2 NA18955.hp2 NA18965.hp1 others(4): Show |
intron_variant | MODIFIER | c.156+2089G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866605 | ||||||
chr13:43866684
|
C | T | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.156+2010G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866684 | ||||||
chr13:43866879
|
C | T | 1 | a0001c0001t0018g0133 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.156+1815G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866879 | ||||||
chr13:43866888
|
T | G | 1 | a0001c0002t0005g0230 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.156+1806A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866888 | ||||||
chr13:43866956
|
G | A | 1 | a0002c0003t0001g0181 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.156+1738C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43866956 | ||||||
chr13:43867072
|
T | G | 10 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0022others(7): Show | 23 | HG02738.hp2 HG03239.hp1 HG03669.hp1 others(20): Show |
intron_variant | MODIFIER | c.156+1622A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43867072 | ||||||
chr13:43867085
|
C | T | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(210): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.156+1609G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43867085 | ||||||
chr13:43867238
|
A | G | 20 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0021others(17): Show | 33 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(30): Show |
intron_variant | MODIFIER | c.156+1456T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43867238 | ||||||
chr13:43867327
|
G | C | 1 | a0001c0001t0004g0119 | 1 | HG02132.hp1 | intron_variant | MODIFIER | c.156+1367C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43867327 | ||||||
chr13:43867510
|
T | C | 3 | a0001c0001t0003g0009a0001c0001t0003g0255a0001c0001t0017g0256 | 8 | HG01123.hp1 HG01257.hp2 HG01258.hp2 others(5): Show |
intron_variant | MODIFIER | c.156+1184A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43867510 | ||||||
chr13:43867698
|
G | C | 30 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(27): Show | 78 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(75): Show |
intron_variant | MODIFIER | c.156+996C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43867698 | ||||||
chr13:43867897
|
A | G | 225 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(222): Show | 388 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(385): Show |
intron_variant | MODIFIER | c.156+797T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43867897 | ||||||
chr13:43867901
|
G | A | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(210): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.156+793C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43867901 | ||||||
chr13:43867982
|
A | C | 1 | a0001c0001t0001g0152 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.156+712T>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43867982 | ||||||
chr13:43868057
|
T | TTCAA | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(210): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.156+636_156+637ins others(4): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868057 | ||||||
chr13:43868102
|
T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(173): Show | 289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.156+592A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868102 | ||||||
chr13:43868154
|
G | A | 4 | a0001c0001t0013g0034a0001c0001t0013g0087a0001c0001t0013g0088others(1): Show | 5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.156+540C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868154 | ||||||
chr13:43868199
|
T | G | 1 | a0001c0001t0006g0126 | 1 | NA18995.hp2 | intron_variant | MODIFIER | c.156+495A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868199 | ||||||
chr13:43868220
|
T | G | 1 | a0001c0001t0001g0156 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.156+474A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868220 | ||||||
chr13:43868238
|
G | A | 2 | a0001c0001t0002g0032a0001c0001t0002g0083 | 3 | HG01952.hp1 HG02004.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.156+456C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868238 | ||||||
chr13:43868271
|
T | G | 1 | a0001c0001t0013g0089 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.156+423A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868271 | ||||||
chr13:43868459
|
A | T | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.156+235T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868459 | ||||||
chr13:43868508
|
T | C | 2 | a0001c0002t0005g0232a0001c0002t0033g0231 | 2 | NA18941.hp1 NA19001.hp1 |
intron_variant | MODIFIER | c.156+186A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868508 | ||||||
chr13:43868619
|
G | A | 1 | a0001c0001t0020g0084 | 1 | NA18987.hp2 | intron_variant | MODIFIER | c.156+75C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 4/6 | chr13 | 43868619 | ||||||
chr13:43868903
|
C | T | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(131): Show | 229 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.47-100G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 3/6 | chr13 | 43868903 | ||||||
chr13:43869087
|
T | C | 1 | a0002c0003t0001g0182 | 1 | NA19090.hp2 | intron_variant | MODIFIER | c.46+244A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 3/6 | chr13 | 43869087 | ||||||
chr13:43869201
|
T | C | 2 | a0001c0001t0004g0017a0001c0001t0022g0120 | 5 | NA18952.hp2 NA18979.hp1 NA19003.hp2 others(2): Show |
intron_variant | MODIFIER | c.46+130A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 3/6 | chr13 | 43869201 | ||||||
chr13:43869587
|
A | T | 40 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0023others(37): Show | 88 | HG00323.hp2 HG00408.hp2 HG00597.hp1 others(85): Show |
intron_variant | MODIFIER | c.-113-98T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43869587 | ||||||
chr13:43869717
|
A | AAAGT | 10 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0001g0145others(7): Show | 10 | HG01884.hp1 HG01891.hp2 HG01981.hp1 others(7): Show |
intron_variant | MODIFIER | c.-113-232_-113-229d others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43869717 | ||||||
chr13:43869841
|
T | C | 37 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0019others(34): Show | 82 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(79): Show |
intron_variant | MODIFIER | c.-113-352A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43869841 | ||||||
chr13:43870153
|
G | A | 1 | a0002c0003t0008g0183 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.-113-664C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870153 | ||||||
chr13:43870233
|
T | G | 1 | a0001c0002t0016g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-113-744A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870233 | ||||||
chr13:43870272
|
C | T | 1 | a0001c0001t0001g0151 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.-113-783G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870272 | ||||||
chr13:43870344
|
T | G | 1 | a0001c0001t0001g0184 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.-113-855A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870344 | ||||||
chr13:43870438
|
T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(173): Show | 289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.-113-949A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870438 | ||||||
chr13:43870570
|
C | T | 25 | a0001c0001t0001g0219a0001c0002t0005g0004a0001c0002t0005g0027others(22): Show | 39 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.-113-1081G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870570 | ||||||
chr13:43870680
|
A | G | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(131): Show | 229 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.-113-1191T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870680 | ||||||
chr13:43870682
|
G | A | 1 | a0002c0003t0001g0051 | 2 | HG03654.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.-113-1193C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870682 | ||||||
chr13:43870766
|
C | T | 4 | a0001c0001t0001g0023a0001c0001t0001g0148a0001c0001t0008g0150others(1): Show | 6 | HG01884.hp2 HG02647.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.-113-1277G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870766 | ||||||
chr13:43870854
|
T | C | 42 | a0001c0001t0001g0219a0001c0001t0009g0043a0001c0001t0009g0044others(39): Show | 60 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-113-1365A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870854 | ||||||
chr13:43870934
|
G | C | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-113-1445C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870934 | ||||||
chr13:43870965
|
T | C | 1 | a0001c0001t0003g0257 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.-113-1476A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43870965 | ||||||
chr13:43871017
|
G | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(173): Show | 289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.-113-1528C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871017 | ||||||
chr13:43871048
|
G | A | 1 | a0001c0002t0005g0233 | 1 | NA18940.hp1 | intron_variant | MODIFIER | c.-113-1559C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871048 | ||||||
chr13:43871062
|
C | T | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-113-1573G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871062 | ||||||
chr13:43871184
|
C | T | 2 | a0001c0001t0001g0048a0001c0001t0008g0147 | 3 | HG02109.hp2 HG02717.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.-113-1695G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871184 | ||||||
chr13:43871285
|
T | C | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(173): Show | 289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.-113-1796A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871285 | ||||||
chr13:43871293
|
G | T | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-113-1804C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871293 | ||||||
chr13:43871373
|
A | T | 42 | a0001c0001t0001g0219a0001c0001t0009g0043a0001c0001t0009g0044others(39): Show | 60 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-113-1884T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871373 | ||||||
chr13:43871402
|
C | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(173): Show | 289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.-113-1913G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871402 | ||||||
chr13:43871731
|
A | G | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-113-2242T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871731 | ||||||
chr13:43871879
|
T | C | 1 | a0003c0004t0011g0143 | 1 | NA18939.hp1 | intron_variant | MODIFIER | c.-113-2390A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43871879 | ||||||
chr13:43872025
|
G | A | 26 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0019others(23): Show | 58 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.-113-2536C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43872025 | ||||||
chr13:43872031
|
T | A | 1 | a0001c0001t0001g0025 | 3 | NA18950.hp2 NA19070.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.-113-2542A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43872031 | ||||||
chr13:43872174
|
G | A | 1 | a0002c0003t0001g0190 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-114+2668C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43872174 | ||||||
chr13:43872337
|
G | T | 42 | a0001c0001t0001g0219a0001c0001t0009g0043a0001c0001t0009g0044others(39): Show | 60 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-114+2505C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43872337 | ||||||
chr13:43872476
|
T | C | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-114+2366A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43872476 | ||||||
chr13:43872681
|
A | G | 26 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0019others(23): Show | 58 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.-114+2161T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43872681 | ||||||
chr13:43872878
|
A | G | 1 | a0001c0001t0008g0146 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.-114+1964T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43872878 | ||||||
chr13:43873047
|
C | T | 21 | a0001c0001t0001g0184a0002c0003t0001g0012a0002c0003t0001g0018others(18): Show | 31 | HG00438.hp1 HG00609.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.-114+1795G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43873047 | ||||||
chr13:43873107
|
T | C | 178 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(175): Show | 291 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(288): Show |
intron_variant | MODIFIER | c.-114+1735A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43873107 | ||||||
chr13:43873144
|
C | T | 4 | a0001c0001t0013g0034a0001c0001t0013g0087a0001c0001t0013g0088others(1): Show | 5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-114+1698G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43873144 | ||||||
chr13:43873362
|
A | T | 1 | a0001c0001t0002g0032 | 2 | HG01952.hp1 HG02004.hp1 |
intron_variant | MODIFIER | c.-114+1480T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43873362 | ||||||
chr13:43873630
|
G | T | 1 | a0001c0001t0001g0145 | 1 | NA18906.hp2 | intron_variant | MODIFIER | c.-114+1212C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43873630 | ||||||
chr13:43873713
|
T | C | 1 | a0001c0002t0005g0027 | 3 | NA18942.hp2 NA18960.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.-114+1129A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43873713 | ||||||
chr13:43873726
|
A | G | 1 | a0001c0002t0005g0221 | 1 | HG00741.hp1 | intron_variant | MODIFIER | c.-114+1116T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43873726 | ||||||
chr13:43873749
|
T | C | 1 | a0001c0001t0018g0139 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.-114+1093A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43873749 | ||||||
chr13:43873996
|
C | A | 77 | a0001c0001t0001g0008a0001c0001t0001g0052a0001c0001t0001g0055others(74): Show | 106 | HG00099.hp2 HG00280.hp1 HG00408.hp1 others(103): Show |
intron_variant | MODIFIER | c.-114+846G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43873996 | ||||||
chr13:43874035
|
T | C | 1 | a0001c0001t0004g0039 | 2 | NA18945.hp1 NA19005.hp1 |
intron_variant | MODIFIER | c.-114+807A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43874035 | ||||||
chr13:43874386
|
T | C | 42 | a0001c0001t0001g0219a0001c0001t0009g0043a0001c0001t0009g0044others(39): Show | 60 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-114+456A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43874386 | ||||||
chr13:43874644
|
T | C | 3 | a0001c0001t0010g0035a0001c0001t0010g0091a0001c0001t0010g0092 | 4 | HG01109.hp1 HG02145.hp1 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.-114+198A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43874644 | ||||||
chr13:43874798
|
C | T | 42 | a0001c0001t0001g0219a0001c0001t0009g0043a0001c0001t0009g0044others(39): Show | 60 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-114+44G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43874798 | ||||||
chr13:43874825
|
A | G | 2 | a0001c0001t0009g0045a0001c0001t0009g0132 | 3 | HG02257.hp1 HG02630.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.-114+17T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 2/6 | chr13 | 43874825 | ||||||
chr13:43875136
|
G | A | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-199-209C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43875136 | ||||||
chr13:43875195
|
A | G | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-199-268T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43875195 | ||||||
chr13:43875232
|
G | C | 26 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0019others(23): Show | 58 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(55): Show |
intron_variant | MODIFIER | c.-199-305C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43875232 | ||||||
chr13:43875256
|
G | T | 1 | a0001c0001t0003g0237 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.-199-329C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43875256 | ||||||
chr13:43875369
|
C | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(173): Show | 289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.-199-442G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43875369 | ||||||
chr13:43875421
|
T | C | 1 | a0002c0003t0001g0190 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.-199-494A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43875421 | ||||||
chr13:43875425
|
G | T | 6 | a0001c0001t0004g0053a0001c0001t0004g0191a0001c0001t0004g0193others(3): Show | 8 | HG02027.hp2 HG02083.hp2 HG02523.hp2 others(5): Show |
intron_variant | MODIFIER | c.-199-498C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43875425 | ||||||
chr13:43875690
|
G | T | 2 | a0001c0001t0010g0020a0001c0001t0010g0111 | 4 | HG01243.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-199-763C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43875690 | ||||||
chr13:43875986
|
G | T | 7 | a0001c0001t0009g0043a0001c0001t0009g0044a0001c0001t0009g0127others(4): Show | 9 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(6): Show |
intron_variant | MODIFIER | c.-199-1059C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43875986 | ||||||
chr13:43876068
|
T | A | 1 | a0001c0001t0002g0085 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.-199-1141A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876068 | ||||||
chr13:43876086
|
G | C | 130 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(127): Show | 218 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(215): Show |
intron_variant | MODIFIER | c.-199-1159C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876086 | ||||||
chr13:43876110
|
T | G | 213 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(210): Show | 371 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(368): Show |
intron_variant | MODIFIER | c.-199-1183A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876110 | ||||||
chr13:43876153
|
C | T | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(131): Show | 229 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.-199-1226G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876153 | ||||||
chr13:43876210
|
G | A | 134 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(131): Show | 229 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(226): Show |
intron_variant | MODIFIER | c.-199-1283C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876210 | ||||||
chr13:43876355
|
T | C | 6 | a0001c0001t0010g0020a0001c0001t0010g0035a0001c0001t0010g0090others(3): Show | 9 | HG01109.hp1 HG01243.hp1 HG02145.hp1 others(6): Show |
intron_variant | MODIFIER | c.-199-1428A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876355 | ||||||
chr13:43876458
|
A | T | 42 | a0001c0001t0001g0219a0001c0001t0009g0043a0001c0001t0009g0044others(39): Show | 60 | HG00673.hp2 HG00738.hp2 HG00741.hp1 others(57): Show |
intron_variant | MODIFIER | c.-199-1531T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876458 | ||||||
chr13:43876485
|
G | A | 1 | a0001c0001t0001g0218 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-199-1558C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876485 | ||||||
chr13:43876591
|
C | G | 1 | a0001c0001t0003g0236 | 1 | NA19082.hp1 | intron_variant | MODIFIER | c.-199-1664G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876591 | ||||||
chr13:43876658
|
G | A | 31 | a0001c0001t0001g0008a0001c0001t0001g0055a0001c0001t0001g0144others(28): Show | 39 | HG00099.hp2 HG00280.hp1 HG00438.hp2 others(36): Show |
intron_variant | MODIFIER | c.-199-1731C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876658 | ||||||
chr13:43876833
|
T | TATAGCGG others(47): Show |
1 | a0001c0001t0001g0216 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.-199-1960_-199-190 others(58): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876833 | ||||||
chr13:43876853
|
G | A | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-199-1926C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876853 | ||||||
chr13:43876908
|
C | T | 13 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0021others(10): Show | 24 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.-199-1981G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876908 | ||||||
chr13:43876971
|
C | T | 1 | a0001c0001t0001g0144 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.-199-2044G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876971 | ||||||
chr13:43876983
|
C | T | 5 | a0001c0001t0001g0219a0001c0001t0010g0020a0001c0001t0010g0111others(2): Show | 8 | HG01243.hp1 HG02280.hp2 HG02818.hp1 others(5): Show |
intron_variant | MODIFIER | c.-199-2056G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876983 | ||||||
chr13:43876985
|
C | T | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-199-2058G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43876985 | ||||||
chr13:43877044
|
C | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(173): Show | 289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.-199-2117G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877044 | ||||||
chr13:43877097
|
C | A | 1 | a0001c0001t0001g0217 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.-199-2170G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877097 | ||||||
chr13:43877160
|
C | A | 1 | a0001c0001t0001g0218 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.-199-2233G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877160 | ||||||
chr13:43877276
|
A | G | 4 | a0001c0001t0013g0034a0001c0001t0013g0087a0001c0001t0013g0088others(1): Show | 5 | HG02280.hp1 HG02451.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.-199-2349T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877276 | ||||||
chr13:43877341
|
T | C | 25 | a0001c0001t0001g0219a0001c0002t0005g0004a0001c0002t0005g0027others(22): Show | 39 | HG00673.hp2 HG00741.hp1 HG01069.hp1 others(36): Show |
intron_variant | MODIFIER | c.-200+2290A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877341 | ||||||
chr13:43877403
|
A | T | 223 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(220): Show | 385 | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(382): Show |
intron_variant | MODIFIER | c.-200+2228T>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877403 | ||||||
chr13:43877440
|
C | A | 1 | a0002c0003t0001g0234 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.-200+2191G>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877440 | ||||||
chr13:43877684
|
C | T | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(173): Show | 289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.-200+1947G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877684 | ||||||
chr13:43877708
|
T | A | 176 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0008others(173): Show | 289 | HG00099.hp2 HG00280.hp1 HG00323.hp1 others(286): Show |
intron_variant | MODIFIER | c.-200+1923A>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877708 | ||||||
chr13:43877784
|
A | G | 4 | a0003c0004t0011g0006a0003c0004t0011g0142a0003c0004t0011g0143others(1): Show | 11 | NA18939.hp1 NA18944.hp1 NA18947.hp1 others(8): Show |
intron_variant | MODIFIER | c.-200+1847T>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43877784 | ||||||
chr13:43878091
|
TTC | T | 19 | a0001c0001t0001g0140a0001c0001t0001g0141a0001c0001t0009g0043others(16): Show | 23 | HG00738.hp2 HG01167.hp1 HG01169.hp2 others(20): Show |
intron_variant | MODIFIER | c.-200+1538_-200+153 others(6): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43878091 | ||||||
chr13:43878241
|
GTCTT | G | 11 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0022others(8): Show | 24 | HG02738.hp2 HG03239.hp1 HG03669.hp1 others(21): Show |
intron_variant | MODIFIER | c.-200+1386_-200+138 others(8): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43878241 | ||||||
chr13:43878456
|
T | G | 1 | a0001c0002t0016g0235 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.-200+1175A>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43878456 | ||||||
chr13:43878648
|
C | T | 11 | a0001c0001t0006g0010a0001c0001t0006g0011a0001c0001t0006g0022others(8): Show | 24 | HG02738.hp2 HG03239.hp1 HG03669.hp1 others(21): Show |
intron_variant | MODIFIER | c.-200+983G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43878648 | ||||||
chr13:43878959
|
G | A | 2 | a0001c0001t0010g0020a0001c0001t0010g0111 | 4 | HG01243.hp1 HG02818.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.-200+672C>T | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43878959 | ||||||
chr13:43878978
|
T | C | 1 | a0002c0003t0001g0121 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-200+653A>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43878978 | ||||||
chr13:43878979
|
G | C | 1 | a0002c0003t0001g0121 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-200+652C>G | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43878979 | ||||||
chr13:43879040
|
A | AAAAAAAG others(21): Show |
1 | a0002c0003t0001g0121 | 1 | NA19005.hp2 | intron_variant | MODIFIER | c.-200+590_-200+591i others(30): Show |
CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43879040 | ||||||
chr13:43879099
|
C | G | 13 | a0001c0001t0004g0016a0001c0001t0004g0017a0001c0001t0004g0021others(10): Show | 24 | HG00323.hp1 HG00597.hp2 HG00735.hp1 others(21): Show |
intron_variant | MODIFIER | c.-200+532G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43879099 | ||||||
chr13:43879324
|
C | G | 1 | a0001c0002t0014g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.-200+307G>C | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43879324 | ||||||
chr13:43879344
|
C | T | 27 | a0001c0001t0002g0001a0001c0001t0002g0014a0001c0001t0002g0019others(24): Show | 59 | HG00099.hp1 HG00280.hp2 HG00558.hp1 others(56): Show |
intron_variant | MODIFIER | c.-200+287G>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43879344 | ||||||
chr13:43879616
|
G | T | 1 | a0002c0003t0001g0112 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.-200+15C>A | CCDC122 | ENSG00000151773.13 | transcript | ENST00000444614.8 | protein_coding | 1/6 | chr13 | 43879616 |