geneid | 165055 |
---|---|
ensemblid | ENSG00000163006.12 |
hgncid | 26531 |
symbol | CCDC138 |
name | coiled-coil domain containing 138 |
refseq_nuc | NM_144978.3 |
refseq_prot | NP_659415.1 |
ensembl_nuc | ENST00000295124.9 |
ensembl_prot | ENSP00000295124.4 |
mane_status | MANE Select |
chr | chr2 |
start | 108786771 |
end | 108876578 |
strand | + |
ver | v1.2 |
region | chr2:108786771-108876578 |
region5000 | chr2:108781771-108881578 |
regionname0 | CCDC138_chr2_108786771_108876578 |
regionname5000 | CCDC138_chr2_108781771_108881578 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 665 | 140 | 59 | 23 | 39 | 7 | 10 | 36 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0002 | 0/0 | 665 | 36 | 20 | 5 | 5 | 1 | 5 | 4 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0003 | 0/0 | 665 | 35 | 3 | 8 | 17 | 2 | 5 | 16 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0004 | 0/0 | 665 | 5 | 5 | 0 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0005 | 0/0 | 665 | 1 | 0 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0006 | 0/0 | 665 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0007 | 0/0 | 665 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0008 | 0/0 | 665 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 0/1 | 1998 | 86 | 19 | 17 | 32 | 7 | 10 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
c0002 | 0/0 | 1998 | 36 | 20 | 5 | 5 | 1 | 5 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
c0003 | 0/0 | 1998 | 35 | 3 | 8 | 17 | 2 | 5 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
c0004 | 1/0 | 1998 | 23 | 21 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
c0005 | 0/0 | 1998 | 20 | 18 | 2 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
c0006 | 0/0 | 1998 | 7 | 0 | 1 | 6 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
c0007 | 0/0 | 1998 | 5 | 5 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
c0008 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
c0009 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
c0010 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
c0011 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
c0012 | 0/0 | 1998 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
c0013 | 0/0 | 1998 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
c0014 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
c0015 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 378 | 114 | 60 | 13 | 30 | 2 | 9 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
t0002 | 0/1 | 378 | 99 | 28 | 21 | 32 | 8 | 9 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
t0003 | 1/0 | 378 | 6 | 2 | 1 | 0 | 0 | 2 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
t0004 | 0/0 | 378 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 0/1 | 1998 | 86 | 19 | 17 | 32 | 7 | 10 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0001c0004 | 1/0 | 1998 | 23 | 21 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0001c0005 | 0/0 | 1998 | 20 | 18 | 2 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0001c0006 | 0/0 | 1998 | 7 | 0 | 1 | 6 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0001c0010 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0001c0011 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0001c0012 | 0/0 | 1998 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0001c0013 | 0/0 | 1998 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0002c0002 | 0/0 | 1998 | 36 | 20 | 5 | 5 | 1 | 5 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0003c0003 | 0/0 | 1998 | 35 | 3 | 8 | 17 | 2 | 5 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0004c0007 | 0/0 | 1998 | 5 | 5 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0005c0009 | 0/0 | 1998 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0006c0008 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0007c0014 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0008c0015 | 0/0 | 1998 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 2375 | 4 | 2 | 0 | 1 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0001c0001t0002 | 0/1 | 2375 | 82 | 17 | 17 | 31 | 7 | 9 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0001c0004t0001 | 0/0 | 2375 | 18 | 17 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0001c0004t0002 | 0/0 | 2375 | 4 | 4 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0001c0004t0003 | 1/0 | 2375 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0001c0005t0001 | 0/0 | 2375 | 19 | 18 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0001c0005t0002 | 0/0 | 2375 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0001c0006t0001 | 0/0 | 2375 | 7 | 0 | 1 | 6 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0001c0010t0002 | 0/0 | 2375 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0001c0011t0002 | 0/0 | 2375 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0001c0012t0001 | 0/0 | 2375 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0001c0013t0002 | 0/0 | 2375 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0002c0002t0001 | 0/0 | 2375 | 26 | 17 | 1 | 5 | 0 | 3 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0002c0002t0002 | 0/0 | 2375 | 4 | 1 | 2 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0002c0002t0003 | 0/0 | 2375 | 5 | 2 | 1 | 0 | 0 | 2 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0002c0002t0004 | 0/0 | 2375 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0003c0003t0001 | 0/0 | 2375 | 35 | 3 | 8 | 17 | 2 | 5 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0004c0007t0002 | 0/0 | 2375 | 5 | 5 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0005c0009t0001 | 0/0 | 2375 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0006c0008t0001 | 0/0 | 2375 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0007c0014t0001 | 0/0 | 2375 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
a0008c0015t0001 | 0/0 | 2375 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | copy fasta | chr2 | 108781771 | 108881578 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0001g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0001g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0003 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0006 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0007 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0017 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0022 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0023 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0024 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0025 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0028 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0031 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0032 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0034 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0035 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0036 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0038 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0039 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0040 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0041 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0042 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0046 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0049 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0054 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0058 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0059 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0060 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0062 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0063 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0069 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0084 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0086 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0087 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0088 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0089 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0092 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0094 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0096 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0001t0002g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0001g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0001g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0001g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0001g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0001g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0001g0015 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0001g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0001g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0001g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0001g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0001g0106 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0001g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0001g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0001g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0001g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0001g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0001g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0002g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0002g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0002g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0002g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0004t0003g0090 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0120 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0211 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0212 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0213 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0214 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0216 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0001g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0005t0002g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0006t0001g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0006t0001g0200 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0006t0001g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0006t0001g0202 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0006t0001g0203 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0006t0001g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0006t0001g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0010t0002g0068 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0011t0002g0030 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0012t0001g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0001c0013t0002g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0167 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0173 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0192 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0001g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0002g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0002g0185 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0002g0186 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0002g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0003g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0003g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0003g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0003g0193 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0003g0196 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0002c0002t0004g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0137 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0150 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0151 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0153 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0157 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0159 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0160 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0180 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0181 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0003c0003t0001g0184 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0004c0007t0002g0122 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0004c0007t0002g0123 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0004c0007t0002g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0004c0007t0002g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0004c0007t0002g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0005c0009t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0006c0008t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0007c0014t0001g0136 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
a0008c0015t0001g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0002 | g0067 | EUR | GBR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG00099 | hp2 | a0003 | c0003 | t0001 | g0150 | EUR | GBR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG00408 | hp1 | a0001 | c0001 | t0002 | g0040 | EAS | CHS | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG00408 | hp2 | a0003 | c0003 | t0001 | g0138 | EAS | CHS | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG00738 | hp1 | a0003 | c0003 | t0001 | g0154 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG00738 | hp2 | a0003 | c0003 | t0001 | g0142 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG00741 | hp1 | a0003 | c0003 | t0001 | g0181 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG00741 | hp2 | a0001 | c0001 | t0002 | g0087 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01074 | hp1 | a0001 | c0001 | t0002 | g0018 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01074 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01081 | hp1 | a0001 | c0001 | t0002 | g0021 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01081 | hp2 | a0001 | c0004 | t0001 | g0106 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01099 | hp1 | a0002 | c0002 | t0003 | g0187 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01099 | hp2 | a0001 | c0001 | t0002 | g0001 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01109 | hp1 | a0001 | c0013 | t0002 | g0076 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01109 | hp2 | a0003 | c0003 | t0001 | g0137 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01167 | hp1 | a0001 | c0001 | t0002 | g0007 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01167 | hp2 | a0003 | c0003 | t0001 | g0164 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01168 | hp1 | a0001 | c0001 | t0002 | g0045 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01168 | hp2 | a0003 | c0003 | t0001 | g0146 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01169 | hp1 | a0001 | c0001 | t0002 | g0006 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01169 | hp2 | a0003 | c0003 | t0001 | g0155 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01175 | hp1 | a0001 | c0005 | t0002 | g0215 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01175 | hp2 | a0002 | c0002 | t0002 | g0190 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01243 | hp1 | a0001 | c0012 | t0001 | g0010 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01243 | hp2 | a0001 | c0005 | t0001 | g0113 | AMR | PUR | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01257 | hp1 | a0002 | c0002 | t0002 | g0186 | AMR | CLM | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01257 | hp2 | a0001 | c0001 | t0002 | g0064 | AMR | CLM | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01261 | hp1 | a0001 | c0006 | t0001 | g0205 | AMR | CLM | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01261 | hp2 | a0002 | c0002 | t0001 | g0192 | AMR | CLM | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01358 | hp1 | a0003 | c0003 | t0001 | g0151 | AMR | CLM | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01358 | hp2 | a0001 | c0001 | t0002 | g0019 | AMR | CLM | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01361 | hp1 | a0001 | c0001 | t0002 | g0047 | AMR | CLM | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01361 | hp2 | a0001 | c0001 | t0002 | g0071 | AMR | CLM | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01515 | hp1 | a0001 | c0001 | t0002 | g0055 | EUR | IBS | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01515 | hp2 | a0001 | c0001 | t0002 | g0086 | EUR | IBS | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01516 | hp1 | a0002 | c0002 | t0002 | g0185 | EUR | IBS | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01516 | hp2 | a0001 | c0001 | t0002 | g0081 | EUR | IBS | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01884 | hp1 | a0002 | c0002 | t0001 | g0131 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0052 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01891 | hp1 | a0007 | c0014 | t0001 | g0136 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01891 | hp2 | a0002 | c0002 | t0001 | g0178 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01978 | hp1 | a0001 | c0001 | t0002 | g0043 | AMR | PEL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01978 | hp2 | a0001 | c0001 | t0002 | g0044 | AMR | PEL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01981 | hp1 | a0001 | c0001 | t0002 | g0050 | AMR | PEL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01981 | hp2 | a0001 | c0001 | t0002 | g0066 | AMR | PEL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01993 | hp1 | a0001 | c0001 | t0002 | g0046 | AMR | PEL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG01993 | hp2 | a0002 | c0002 | t0004 | g0188 | AMR | PEL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02040 | hp1 | a0001 | c0001 | t0002 | g0034 | EAS | KHV | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02040 | hp2 | a0002 | c0002 | t0001 | g0172 | EAS | KHV | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02055 | hp1 | a0006 | c0008 | t0001 | g0166 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02055 | hp2 | a0002 | c0002 | t0001 | g0132 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02145 | hp1 | a0001 | c0005 | t0001 | g0211 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02145 | hp2 | a0001 | c0001 | t0002 | g0075 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02257 | hp1 | a0001 | c0005 | t0001 | g0217 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02257 | hp2 | a0002 | c0002 | t0001 | g0174 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02258 | hp1 | a0001 | c0001 | t0002 | g0056 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02258 | hp2 | a0001 | c0004 | t0001 | g0107 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02280 | hp1 | a0001 | c0005 | t0001 | g0218 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0133 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0008 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02451 | hp2 | a0002 | c0002 | t0001 | g0175 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02523 | hp1 | a0005 | c0009 | t0001 | g0165 | EAS | KHV | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02523 | hp2 | a0001 | c0001 | t0002 | g0032 | EAS | KHV | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02572 | hp1 | a0001 | c0004 | t0001 | g0014 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02572 | hp2 | a0001 | c0001 | t0002 | g0206 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02602 | hp1 | a0002 | c0002 | t0001 | g0134 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02602 | hp2 | a0001 | c0001 | t0002 | g0054 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02615 | hp1 | a0001 | c0005 | t0001 | g0120 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02615 | hp2 | a0001 | c0001 | t0002 | g0085 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02622 | hp1 | a0001 | c0001 | t0002 | g0096 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02622 | hp2 | a0002 | c0002 | t0001 | g0167 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02647 | hp1 | a0001 | c0005 | t0001 | g0208 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02647 | hp2 | a0001 | c0004 | t0002 | g0097 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02698 | hp1 | a0001 | c0001 | t0002 | g0088 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02698 | hp2 | a0002 | c0002 | t0001 | g0197 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02717 | hp1 | a0001 | c0001 | t0002 | g0060 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02717 | hp2 | a0002 | c0002 | t0001 | g0195 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02723 | hp1 | a0002 | c0002 | t0001 | g0179 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02723 | hp2 | a0003 | c0003 | t0001 | g0160 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02735 | hp1 | a0001 | c0001 | t0002 | g0082 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02735 | hp2 | a0003 | c0003 | t0001 | g0180 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02738 | hp1 | a0001 | c0001 | t0002 | g0078 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02738 | hp2 | a0002 | c0002 | t0003 | g0193 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02818 | hp1 | a0001 | c0005 | t0001 | g0116 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02818 | hp2 | a0001 | c0001 | t0002 | g0092 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02886 | hp1 | a0001 | c0004 | t0001 | g0105 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02886 | hp2 | a0001 | c0004 | t0001 | g0015 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0130 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02895 | hp2 | a0001 | c0004 | t0001 | g0101 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02896 | hp1 | a0001 | c0004 | t0001 | g0104 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02896 | hp2 | a0001 | c0005 | t0001 | g0119 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02897 | hp1 | a0001 | c0004 | t0001 | g0102 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02897 | hp2 | a0001 | c0005 | t0001 | g0118 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02922 | hp1 | a0001 | c0004 | t0001 | g0108 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02922 | hp2 | a0002 | c0002 | t0001 | g0173 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02965 | hp1 | a0001 | c0001 | t0001 | g0005 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02965 | hp2 | a0001 | c0005 | t0001 | g0216 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02970 | hp1 | a0001 | c0004 | t0001 | g0012 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0080 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02976 | hp1 | a0001 | c0001 | t0002 | g0051 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02976 | hp2 | a0001 | c0001 | t0002 | g0091 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03041 | hp1 | a0001 | c0004 | t0001 | g0011 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03041 | hp2 | a0001 | c0005 | t0001 | g0112 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0128 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03098 | hp2 | a0003 | c0003 | t0001 | g0159 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03130 | hp1 | a0002 | c0002 | t0001 | g0127 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03130 | hp2 | a0002 | c0002 | t0001 | g0176 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03195 | hp1 | a0001 | c0004 | t0001 | g0111 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03195 | hp2 | a0001 | c0004 | t0002 | g0100 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03209 | hp1 | a0001 | c0004 | t0001 | g0013 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0079 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03225 | hp1 | a0001 | c0005 | t0001 | g0212 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03225 | hp2 | a0001 | c0004 | t0001 | g0109 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03453 | hp1 | a0001 | c0004 | t0001 | g0110 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03453 | hp2 | a0002 | c0002 | t0002 | g0183 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03486 | hp1 | a0001 | c0005 | t0001 | g0209 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03486 | hp2 | a0004 | c0007 | t0002 | g0123 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03516 | hp1 | a0001 | c0004 | t0001 | g0009 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03516 | hp2 | a0001 | c0005 | t0001 | g0210 | AFR | ESN | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03540 | hp1 | a0001 | c0005 | t0001 | g0213 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03540 | hp2 | a0001 | c0001 | t0002 | g0069 | AFR | GWD | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03579 | hp1 | a0001 | c0001 | t0002 | g0095 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03579 | hp2 | a0004 | c0007 | t0002 | g0126 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03654 | hp1 | a0003 | c0003 | t0001 | g0147 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0171 | SAS | PJL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03688 | hp1 | a0002 | c0002 | t0003 | g0196 | SAS | STU | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03688 | hp2 | a0001 | c0001 | t0002 | g0083 | SAS | STU | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03927 | hp1 | a0001 | c0001 | t0002 | g0077 | SAS | BEB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03927 | hp2 | a0003 | c0003 | t0001 | g0184 | SAS | BEB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG04115 | hp1 | a0003 | c0003 | t0001 | g0135 | SAS | STU | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG04115 | hp2 | a0001 | c0001 | t0002 | g0059 | SAS | STU | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG04199 | hp1 | a0001 | c0001 | t0002 | g0062 | SAS | STU | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG04199 | hp2 | a0003 | c0003 | t0001 | g0157 | SAS | STU | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0057 | SAS | STU | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG04204 | hp2 | a0001 | c0001 | t0002 | g0058 | SAS | STU | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18522 | hp1 | a0001 | c0005 | t0001 | g0214 | AFR | YRI | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18522 | hp2 | a0001 | c0001 | t0002 | g0093 | AFR | YRI | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18941 | hp1 | a0001 | c0006 | t0001 | g0199 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18941 | hp2 | a0001 | c0001 | t0002 | g0017 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0027 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18942 | hp2 | a0001 | c0001 | t0002 | g0061 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18945 | hp1 | a0003 | c0003 | t0001 | g0163 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0041 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18946 | hp1 | a0001 | c0001 | t0002 | g0037 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18946 | hp2 | a0001 | c0006 | t0001 | g0200 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18954 | hp1 | a0001 | c0001 | t0002 | g0073 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18954 | hp2 | a0001 | c0006 | t0001 | g0203 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18959 | hp1 | a0001 | c0006 | t0001 | g0204 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18959 | hp2 | a0001 | c0001 | t0002 | g0049 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18968 | hp1 | a0001 | c0001 | t0002 | g0036 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18968 | hp2 | a0003 | c0003 | t0001 | g0161 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18969 | hp1 | a0001 | c0001 | t0002 | g0035 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18969 | hp2 | a0001 | c0001 | t0002 | g0020 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18970 | hp1 | a0001 | c0006 | t0001 | g0201 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18970 | hp2 | a0003 | c0003 | t0001 | g0149 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18971 | hp1 | a0001 | c0001 | t0001 | g0029 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18971 | hp2 | a0001 | c0001 | t0002 | g0070 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18974 | hp1 | a0002 | c0002 | t0001 | g0168 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18974 | hp2 | a0003 | c0003 | t0001 | g0121 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18977 | hp1 | a0001 | c0001 | t0002 | g0072 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18977 | hp2 | a0003 | c0003 | t0001 | g0141 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18984 | hp1 | a0001 | c0001 | t0002 | g0022 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18984 | hp2 | a0003 | c0003 | t0001 | g0153 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18985 | hp1 | a0001 | c0001 | t0002 | g0048 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18985 | hp2 | a0001 | c0001 | t0002 | g0039 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0031 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18988 | hp2 | a0002 | c0002 | t0001 | g0207 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18993 | hp1 | a0001 | c0001 | t0002 | g0004 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18993 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18994 | hp1 | a0003 | c0003 | t0001 | g0143 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18994 | hp2 | a0001 | c0011 | t0002 | g0030 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18998 | hp1 | a0003 | c0003 | t0001 | g0158 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18998 | hp2 | a0001 | c0001 | t0002 | g0053 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18999 | hp1 | a0003 | c0003 | t0001 | g0152 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18999 | hp2 | a0001 | c0001 | t0002 | g0028 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19011 | hp1 | a0003 | c0003 | t0001 | g0156 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0065 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19030 | hp1 | a0003 | c0003 | t0001 | g0140 | AFR | LWK | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19030 | hp2 | a0001 | c0005 | t0001 | g0115 | AFR | LWK | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19043 | hp1 | a0004 | c0007 | t0002 | g0125 | AFR | LWK | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19043 | hp2 | a0001 | c0004 | t0001 | g0198 | AFR | LWK | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0024 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19056 | hp2 | a0003 | c0003 | t0001 | g0144 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19058 | hp1 | a0002 | c0002 | t0001 | g0170 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0042 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19070 | hp1 | a0001 | c0001 | t0002 | g0023 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19070 | hp2 | a0003 | c0003 | t0001 | g0148 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0033 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19081 | hp2 | a0003 | c0003 | t0001 | g0145 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19082 | hp1 | a0001 | c0001 | t0002 | g0016 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19082 | hp2 | a0003 | c0003 | t0001 | g0002 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19087 | hp1 | a0001 | c0001 | t0002 | g0025 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19087 | hp2 | a0003 | c0003 | t0001 | g0162 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0026 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19088 | hp2 | a0001 | c0006 | t0001 | g0202 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19240 | hp1 | a0001 | c0005 | t0001 | g0117 | AFR | YRI | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA19240 | hp2 | a0001 | c0001 | t0002 | g0074 | AFR | YRI | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA20129 | hp1 | a0004 | c0007 | t0002 | g0124 | AFR | ASW | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA20129 | hp2 | a0001 | c0004 | t0001 | g0103 | AFR | ASW | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA20752 | hp1 | a0003 | c0003 | t0001 | g0139 | EUR | TSI | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA20752 | hp2 | a0001 | c0001 | t0002 | g0084 | EUR | TSI | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA20805 | hp1 | a0001 | c0001 | t0002 | g0063 | EUR | TSI | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA20805 | hp2 | a0001 | c0001 | t0002 | g0003 | EUR | TSI | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02486 | hp1 | a0001 | c0004 | t0002 | g0099 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02486 | hp2 | a0001 | c0010 | t0002 | g0068 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02559 | hp1 | a0002 | c0002 | t0003 | g0191 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG02559 | hp2 | a0001 | c0005 | t0001 | g0114 | AFR | ACB | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03471 | hp1 | a0004 | c0007 | t0002 | g0122 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG03471 | hp2 | a0001 | c0001 | t0002 | g0094 | AFR | MSL | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG06807 | hp1 | a0001 | c0004 | t0002 | g0098 | AFR | USA | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
HG06807 | hp2 | a0002 | c0002 | t0001 | g0177 | AFR | USA | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18955 | hp1 | a0001 | c0001 | t0002 | g0038 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA18955 | hp2 | a0002 | c0002 | t0001 | g0169 | EAS | JPT | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA20300 | hp1 | a0002 | c0002 | t0001 | g0129 | AFR | USA | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA20300 | hp2 | a0002 | c0002 | t0001 | g0182 | AFR | USA | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA21309 | hp1 | a0002 | c0002 | t0003 | g0189 | AFR | LWK | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
NA21309 | hp2 | a0008 | c0015 | t0001 | g0194 | AFR | LWK | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0002 | g0089 | REF | REF | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
homoSapiens_grch38 | hp1 | a0001 | c0004 | t0003 | g0090 | REF | REF | CCDC138_chr2_108781771_108881578 | CCDC138 | chr2 | 108781771 | 108881578 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:108788965
|
T | C | 1 | a0004 | 5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
missense_variant&splice_region_variant | MODERATE | c.265T>C | p.Cys89Arg | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/15 | 317/2375 | 265/1998 | 89/665 | chr2 | 108788965 | ||
chr2:108791703
|
G | T | 3 | a0003a0007a0008 | 37 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(34): Show |
missense_variant | MODERATE | c.295G>T | p.Asp99Tyr | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/15 | 347/2375 | 295/1998 | 99/665 | chr2 | 108791703 | ||
chr2:108791752
|
G | A | 7 | a0002a0003a0004others(4): Show | 80 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(77): Show |
missense_variant | MODERATE | c.344G>A | p.Arg115Lys | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/15 | 396/2375 | 344/1998 | 115/665 | chr2 | 108791752 | ||
chr2:108812821
|
G | C | 1 | a0006 | 1 | HG02055.hp1 | missense_variant&splice_region_variant | MODERATE | c.935G>C | p.Arg312Thr | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/15 | 987/2375 | 935/1998 | 312/665 | chr2 | 108812821 | ||
chr2:108815996
|
C | T | 1 | a0005 | 1 | HG02523.hp1 | missense_variant | MODERATE | c.1097C>T | p.Ser366Leu | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/15 | 1149/2375 | 1097/1998 | 366/665 | chr2 | 108815996 | ||
chr2:108846814
|
A | G | 1 | a0008 | 1 | NA21309.hp2 | missense_variant | MODERATE | c.1400A>G | p.Asp467Gly | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/15 | 1452/2375 | 1400/1998 | 467/665 | chr2 | 108846814 | ||
chr2:108876166
|
T | G | 1 | a0007 | 1 | HG01891.hp1 | missense_variant | MODERATE | c.1911T>G | p.His637Gln | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 15/15 | 1963/2375 | 1911/1998 | 637/665 | chr2 | 108876166 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:108788928
|
A | G | 1 | a0001c0006 | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
synonymous_variant | LOW | c.228A>G | p.Thr76Thr | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/15 | 280/2375 | 228/1998 | 76/665 | chr2 | 108788928 | ||
chr2:108794691
|
C | T | 2 | a0001c0005a0001c0013 | 21 | HG01109.hp1 HG01175.hp1 HG01243.hp2 others(18): Show |
synonymous_variant | LOW | c.546C>T | p.Asp182Asp | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/15 | 598/2375 | 546/1998 | 182/665 | chr2 | 108794691 | ||
chr2:108812645
|
T | C | 1 | a0001c0010 | 1 | HG02486.hp2 | synonymous_variant | LOW | c.870T>C | p.Ser290Ser | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 8/15 | 922/2375 | 870/1998 | 290/665 | chr2 | 108812645 | ||
chr2:108812690
|
T | A | 4 | a0001c0001a0001c0010a0001c0011others(1): Show | 89 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(86): Show |
synonymous_variant | LOW | c.915T>A | p.Ala305Ala | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 8/15 | 967/2375 | 915/1998 | 305/665 | chr2 | 108812690 | ||
chr2:108816096
|
G | A | 1 | a0001c0012 | 1 | HG01243.hp1 | synonymous_variant | LOW | c.1197G>A | p.Lys399Lys | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/15 | 1249/2375 | 1197/1998 | 399/665 | chr2 | 108816096 | ||
chr2:108846839
|
G | A | 1 | a0001c0011 | 1 | NA18994.hp2 | synonymous_variant | LOW | c.1425G>A | p.Glu475Glu | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/15 | 1477/2375 | 1425/1998 | 475/665 | chr2 | 108846839 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:108876275
|
G | A | 1 | a0002c0002t0004 | 1 | HG01993.hp2 | 3_prime_UTR_variant | MODIFIER | c.*22G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 15/15 | 22 | chr2 | 108876275 | |||||
chr2:108876451
|
A | G | 19 | a0001c0001t0001a0001c0001t0002a0001c0004t0001others(16): Show | 213 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(210): Show |
3_prime_UTR_variant | MODIFIER | c.*198A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 15/15 | 198 | chr2 | 108876451 | |||||
chr2:108876546
|
T | A | 8 | a0001c0001t0002a0001c0004t0002a0001c0005t0002others(5): Show | 99 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*293T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 15/15 | 293 | chr2 | 108876546 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr2:108786919
|
A | C | 11 | a0001c0005t0001g0208a0001c0005t0001g0209a0001c0005t0001g0210others(8): Show | 11 | HG01175.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
splice_region_variant&intron_variant | LOW | c.93+4A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108786919 | ||||||
chr2:108786941
|
G | C | 2 | a0001c0005t0001g0208a0001c0005t0001g0209 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.93+26G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108786941 | ||||||
chr2:108786999
|
G | A | 11 | a0001c0005t0001g0208a0001c0005t0001g0209a0001c0005t0001g0210others(8): Show | 11 | HG01175.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.93+84G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108786999 | ||||||
chr2:108787034
|
C | G | 1 | a0002c0002t0001g0207 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.93+119C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108787034 | ||||||
chr2:108787461
|
A | G | 1 | a0001c0001t0002g0206 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.93+546A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108787461 | ||||||
chr2:108787482
|
G | T | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-550G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108787482 | ||||||
chr2:108787500
|
C | T | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.94-532C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108787500 | ||||||
chr2:108787608
|
C | T | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.94-424C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108787608 | ||||||
chr2:108787610
|
A | ATAAAATT others(12): Show |
1 | a0002c0002t0001g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.94-422_94-421insTA others(17): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108787610 | ||||||
chr2:108787611
|
G | C | 1 | a0002c0002t0001g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.94-421G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108787611 | ||||||
chr2:108787651
|
T | C | 1 | a0001c0001t0002g0003 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.94-381T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108787651 | ||||||
chr2:108787757
|
C | T | 1 | a0002c0002t0003g0196 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.94-275C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | chr2 | 108787757 | ||||||
chr2:108788018
|
C | CT | 78 | a0002c0002t0001g0127a0002c0002t0001g0128a0002c0002t0001g0129others(75): Show | 79 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(76): Show |
splice_acceptor_variant&intron_variant | HIGH | c.94-3dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr2 | 108788018 | |||||
chr2:108788295
|
C | A | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.151+206C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 2/14 | chr2 | 108788295 | ||||||
chr2:108788443
|
G | A | 5 | a0004c0007t0002g0122a0004c0007t0002g0123a0004c0007t0002g0124others(2): Show | 5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.151+354G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 2/14 | chr2 | 108788443 | ||||||
chr2:108788447
|
G | A | 1 | a0001c0001t0002g0004 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.151+358G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 2/14 | chr2 | 108788447 | ||||||
chr2:108788461
|
G | A | 11 | a0001c0005t0001g0208a0001c0005t0001g0209a0001c0005t0001g0210others(8): Show | 11 | HG01175.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.151+372G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 2/14 | chr2 | 108788461 | ||||||
chr2:108788578
|
G | C | 7 | a0002c0002t0001g0127a0002c0002t0001g0128a0002c0002t0001g0129others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.152-274G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 2/14 | chr2 | 108788578 | ||||||
chr2:108788719
|
CAAAGAAA others(3): Show |
C | 5 | a0004c0007t0002g0122a0004c0007t0002g0123a0004c0007t0002g0124others(2): Show | 5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.152-119_152-110del others(10): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 2/14 | INFO_REALIGN_3_PRIME | chr2 | 108788719 | |||||
chr2:108789026
|
G | A | 1 | a0002c0002t0001g0134 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.266+60G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108789026 | ||||||
chr2:108789083
|
T | C | 1 | a0001c0001t0001g0005 | 1 | HG02965.hp1 | intron_variant | MODIFIER | c.266+117T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108789083 | ||||||
chr2:108789248
|
C | G | 5 | a0004c0007t0002g0122a0004c0007t0002g0123a0004c0007t0002g0124others(2): Show | 5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.266+282C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108789248 | ||||||
chr2:108789330
|
C | T | 79 | a0002c0002t0001g0127a0002c0002t0001g0128a0002c0002t0001g0129others(76): Show | 80 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.266+364C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108789330 | ||||||
chr2:108789408
|
C | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.266+442C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108789408 | ||||||
chr2:108789585
|
T | G | 2 | a0001c0001t0002g0006a0001c0001t0002g0007 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.266+619T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108789585 | ||||||
chr2:108789630
|
A | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.266+664A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108789630 | ||||||
chr2:108790021
|
C | T | 1 | a0002c0002t0001g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.266+1055C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108790021 | ||||||
chr2:108790022
|
A | G | 1 | a0008c0015t0001g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.266+1056A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108790022 | ||||||
chr2:108790097
|
A | G | 2 | a0001c0005t0001g0208a0001c0005t0001g0209 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.266+1131A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108790097 | ||||||
chr2:108790109
|
C | T | 20 | a0001c0005t0001g0112a0001c0005t0001g0113a0001c0005t0001g0114others(17): Show | 20 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.266+1143C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108790109 | ||||||
chr2:108790575
|
GC | G | 5 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(2): Show | 5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.267-1098delC | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr2 | 108790575 | |||||
chr2:108790595
|
G | A | 1 | a0001c0001t0002g0008 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.267-1080G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108790595 | ||||||
chr2:108790627
|
G | A | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.267-1048G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108790627 | ||||||
chr2:108790913
|
A | G | 129 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(126): Show | 130 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(127): Show |
intron_variant | MODIFIER | c.267-762A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108790913 | ||||||
chr2:108791042
|
G | A | 211 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(208): Show | 213 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(210): Show |
intron_variant | MODIFIER | c.267-633G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108791042 | ||||||
chr2:108791054
|
G | A | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.267-621G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108791054 | ||||||
chr2:108791113
|
ATATAT | A | 3 | a0001c0005t0001g0112a0001c0005t0001g0210a0001c0005t0001g0211 | 3 | HG02145.hp1 HG03041.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.267-554_267-550del others(5): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr2 | 108791113 | |||||
chr2:108791198
|
T | C | 6 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0004t0001g0103others(3): Show | 6 | HG01081.hp2 HG02886.hp1 HG02895.hp2 others(3): Show |
intron_variant | MODIFIER | c.267-477T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108791198 | ||||||
chr2:108791438
|
A | G | 9 | a0001c0001t0002g0081a0001c0001t0002g0082a0001c0001t0002g0083others(6): Show | 9 | HG00741.hp2 HG01515.hp2 HG01516.hp2 others(6): Show |
intron_variant | MODIFIER | c.267-237A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 3/14 | chr2 | 108791438 | ||||||
chr2:108791865
|
C | T | 1 | a0001c0005t0001g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.394+63C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108791865 | ||||||
chr2:108792078
|
A | T | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.394+276A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108792078 | ||||||
chr2:108792233
|
A | C | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394+431A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108792233 | ||||||
chr2:108792282
|
C | T | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.394+480C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108792282 | ||||||
chr2:108792312
|
C | G | 1 | a0001c0001t0002g0080 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.394+510C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108792312 | ||||||
chr2:108792320
|
T | C | 122 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(119): Show | 123 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(120): Show |
intron_variant | MODIFIER | c.394+518T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108792320 | ||||||
chr2:108792502
|
C | T | 2 | a0001c0001t0001g0005a0001c0001t0001g0079 | 2 | HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.394+700C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108792502 | ||||||
chr2:108792503
|
T | A | 1 | a0003c0003t0001g0135 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.394+701T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108792503 | ||||||
chr2:108792538
|
G | A | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.394+736G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108792538 | ||||||
chr2:108792995
|
C | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.394+1193C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108792995 | ||||||
chr2:108793017
|
CTG | C | 5 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(2): Show | 5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.394+1218_394+1219d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 108793017 | |||||
chr2:108793061
|
C | CAAAAAAA others(5): Show |
1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.394+1269_394+1270i others(14): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 108793061 | |||||
chr2:108793175
|
G | A | 1 | a0002c0002t0001g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.395-1365G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108793175 | ||||||
chr2:108793193
|
TA | T | 79 | a0002c0002t0001g0127a0002c0002t0001g0128a0002c0002t0001g0129others(76): Show | 80 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.395-1336delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 108793193 | |||||
chr2:108793576
|
C | T | 7 | a0002c0002t0001g0127a0002c0002t0001g0128a0002c0002t0001g0129others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.395-964C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108793576 | ||||||
chr2:108793589
|
T | G | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.395-951T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108793589 | ||||||
chr2:108793621
|
G | A | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.395-919G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108793621 | ||||||
chr2:108793631
|
C | G | 1 | a0001c0005t0001g0218 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.395-909C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108793631 | ||||||
chr2:108793777
|
T | C | 20 | a0001c0005t0001g0112a0001c0005t0001g0113a0001c0005t0001g0114others(17): Show | 20 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.395-763T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108793777 | ||||||
chr2:108793796
|
A | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.395-744A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108793796 | ||||||
chr2:108793854
|
G | A | 22 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0005t0001g0112others(19): Show | 22 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.395-686G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108793854 | ||||||
chr2:108794092
|
CATATAAA | C | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.395-439_395-433del others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 108794092 | |||||
chr2:108794175
|
A | G | 5 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.395-365A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108794175 | ||||||
chr2:108794182
|
C | T | 80 | a0001c0004t0001g0198a0002c0002t0001g0127a0002c0002t0001g0128others(77): Show | 81 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(78): Show |
intron_variant | MODIFIER | c.395-358C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108794182 | ||||||
chr2:108794361
|
CT | C | 27 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0004t0001g0107others(24): Show | 27 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.395-177delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | INFO_REALIGN_3_PRIME | chr2 | 108794361 | |||||
chr2:108794393
|
C | T | 10 | a0002c0002t0001g0192a0002c0002t0002g0185a0002c0002t0002g0186others(7): Show | 10 | HG01099.hp1 HG01175.hp2 HG01257.hp1 others(7): Show |
intron_variant | MODIFIER | c.395-147C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108794393 | ||||||
chr2:108794403
|
A | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.395-137A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108794403 | ||||||
chr2:108794458
|
A | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.395-82A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108794458 | ||||||
chr2:108794471
|
G | A | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.395-69G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 4/14 | chr2 | 108794471 | ||||||
chr2:108794724
|
A | G | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
splice_region_variant&intron_variant | LOW | c.576+3A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108794724 | ||||||
chr2:108794792
|
GAATAT | G | 137 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(134): Show | 138 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(135): Show |
intron_variant | MODIFIER | c.576+78_576+82delAT others(3): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 108794792 | |||||
chr2:108795051
|
G | A | 1 | a0008c0015t0001g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.576+330G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108795051 | ||||||
chr2:108795057
|
A | AT | 92 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(89): Show | 93 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(90): Show |
intron_variant | MODIFIER | c.576+337dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 108795057 | |||||
chr2:108795061
|
A | G | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+340A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108795061 | ||||||
chr2:108795150
|
A | AT | 38 | a0001c0001t0002g0017a0001c0001t0002g0206a0001c0004t0001g0009others(35): Show | 38 | HG00741.hp1 HG01175.hp1 HG01243.hp1 others(35): Show |
intron_variant | MODIFIER | c.576+451dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 108795150 | |||||
chr2:108795150
|
A | ATT | 92 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(89): Show | 93 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(90): Show |
intron_variant | MODIFIER | c.576+450_576+451dup others(2): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 108795150 | |||||
chr2:108795150
|
A | ATTT | 17 | a0001c0001t0002g0071a0001c0001t0002g0072a0001c0001t0002g0073others(14): Show | 17 | HG01109.hp1 HG01261.hp1 HG01361.hp2 others(14): Show |
intron_variant | MODIFIER | c.576+449_576+451dup others(3): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 108795150 | |||||
chr2:108795174
|
C | T | 20 | a0001c0005t0001g0112a0001c0005t0001g0113a0001c0005t0001g0114others(17): Show | 20 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.576+453C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108795174 | ||||||
chr2:108795792
|
G | A | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.576+1071G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108795792 | ||||||
chr2:108795876
|
A | G | 4 | a0001c0004t0001g0103a0001c0004t0001g0104a0001c0004t0001g0105others(1): Show | 4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.576+1155A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108795876 | ||||||
chr2:108795934
|
G | T | 5 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(2): Show | 5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.576+1213G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108795934 | ||||||
chr2:108796090
|
C | T | 2 | a0001c0005t0001g0210a0001c0005t0001g0211 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.576+1369C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796090 | ||||||
chr2:108796173
|
C | G | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.576+1452C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796173 | ||||||
chr2:108796203
|
C | T | 1 | a0001c0001t0002g0070 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.576+1482C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796203 | ||||||
chr2:108796209
|
C | T | 4 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0087others(1): Show | 4 | HG00741.hp2 HG01515.hp2 HG02615.hp2 others(1): Show |
intron_variant | MODIFIER | c.576+1488C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796209 | ||||||
chr2:108796277
|
A | C | 1 | a0003c0003t0001g0184 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.576+1556A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796277 | ||||||
chr2:108796388
|
T | C | 1 | a0007c0014t0001g0136 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.576+1667T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796388 | ||||||
chr2:108796503
|
G | A | 138 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(135): Show | 139 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(136): Show |
intron_variant | MODIFIER | c.576+1782G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796503 | ||||||
chr2:108796674
|
A | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.577-1754A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796674 | ||||||
chr2:108796874
|
TTAGA | T | 3 | a0001c0005t0001g0118a0001c0005t0001g0119a0001c0005t0001g0120 | 3 | HG02615.hp1 HG02896.hp2 HG02897.hp2 |
intron_variant | MODIFIER | c.577-1550_577-1547d others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 108796874 | |||||
chr2:108796956
|
C | G | 5 | a0004c0007t0002g0122a0004c0007t0002g0123a0004c0007t0002g0124others(2): Show | 5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.577-1472C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796956 | ||||||
chr2:108796970
|
T | C | 1 | a0002c0002t0002g0185 | 1 | HG01516.hp1 | intron_variant | MODIFIER | c.577-1458T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108796970 | ||||||
chr2:108797136
|
A | G | 1 | a0003c0003t0001g0180 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.577-1292A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108797136 | ||||||
chr2:108797354
|
G | A | 44 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(41): Show | 45 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.577-1074G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108797354 | ||||||
chr2:108797390
|
A | G | 7 | a0001c0001t0002g0069a0001c0001t0002g0091a0001c0001t0002g0092others(4): Show | 7 | HG02622.hp1 HG02818.hp2 HG02976.hp2 others(4): Show |
intron_variant | MODIFIER | c.577-1038A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108797390 | ||||||
chr2:108797402
|
G | A | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.577-1026G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108797402 | ||||||
chr2:108797647
|
T | C | 92 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(89): Show | 93 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(90): Show |
intron_variant | MODIFIER | c.577-781T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108797647 | ||||||
chr2:108797825
|
G | A | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.577-603G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108797825 | ||||||
chr2:108797933
|
C | T | 174 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.577-495C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108797933 | ||||||
chr2:108797962
|
AT | A | 176 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(173): Show | 178 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(175): Show |
intron_variant | MODIFIER | c.577-450delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr2 | 108797962 | |||||
chr2:108797974
|
T | A | 4 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0071others(1): Show | 4 | HG01074.hp1 HG01358.hp2 HG01361.hp2 others(1): Show |
intron_variant | MODIFIER | c.577-454T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108797974 | ||||||
chr2:108798010
|
C | T | 1 | a0003c0003t0001g0164 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.577-418C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108798010 | ||||||
chr2:108798099
|
A | G | 37 | a0002c0002t0001g0195a0003c0003t0001g0002a0003c0003t0001g0121others(34): Show | 38 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.577-329A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108798099 | ||||||
chr2:108798168
|
T | C | 35 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0004t0001g0103others(32): Show | 35 | HG01081.hp2 HG01175.hp1 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.577-260T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108798168 | ||||||
chr2:108798266
|
G | A | 1 | a0005c0009t0001g0165 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.577-162G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 5/14 | chr2 | 108798266 | ||||||
chr2:108798610
|
A | C | 1 | a0001c0004t0002g0100 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.735+24A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108798610 | ||||||
chr2:108798643
|
C | G | 1 | a0001c0010t0002g0068 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.735+57C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108798643 | ||||||
chr2:108798708
|
T | TAC | 21 | a0001c0004t0001g0104a0001c0004t0001g0105a0001c0004t0001g0106others(18): Show | 21 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(18): Show |
intron_variant | MODIFIER | c.735+153_735+154dup others(2): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798708 | |||||
chr2:108798708
|
T | TACAC | 11 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0004t0001g0103others(8): Show | 11 | HG02895.hp2 HG02897.hp1 NA18941.hp1 others(8): Show |
intron_variant | MODIFIER | c.735+151_735+154dup others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798708 | |||||
chr2:108798708
|
TAC | T | 54 | a0001c0001t0001g0029a0001c0001t0002g0004a0001c0001t0002g0006others(51): Show | 54 | HG00408.hp1 HG01081.hp1 HG01167.hp1 others(51): Show |
intron_variant | MODIFIER | c.735+153_735+154del others(2): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798708 | |||||
chr2:108798708
|
TACAC | T | 45 | a0001c0001t0001g0057a0001c0001t0001g0079a0001c0001t0002g0001others(42): Show | 46 | HG00099.hp1 HG00741.hp2 HG01074.hp1 others(43): Show |
intron_variant | MODIFIER | c.735+151_735+154del others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798708 | |||||
chr2:108798708
|
TACACACA others(3): Show |
T | 37 | a0002c0002t0001g0195a0003c0003t0001g0002a0003c0003t0001g0121others(34): Show | 38 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.735+145_735+154del others(10): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798708 | |||||
chr2:108798740
|
C | T | 1 | a0001c0001t0002g0020 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.735+154C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108798740 | ||||||
chr2:108798816
|
T | TAC | 33 | a0001c0001t0002g0067a0001c0001t0002g0070a0001c0001t0002g0072others(30): Show | 33 | HG00099.hp1 HG00408.hp2 HG00741.hp2 others(30): Show |
intron_variant | MODIFIER | c.735+266_735+267dup others(2): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798816 | |||||
chr2:108798816
|
T | TACAC | 31 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0002g0001others(28): Show | 32 | HG01074.hp1 HG01074.hp2 HG01099.hp2 others(29): Show |
intron_variant | MODIFIER | c.735+264_735+267dup others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798816 | |||||
chr2:108798816
|
T | TACACAC | 48 | a0001c0001t0001g0029a0001c0001t0002g0003a0001c0001t0002g0004others(45): Show | 48 | HG00408.hp1 HG01167.hp1 HG01168.hp1 others(45): Show |
intron_variant | MODIFIER | c.735+262_735+267dup others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798816 | |||||
chr2:108798816
|
T | TACACACA others(1): Show |
16 | a0001c0001t0001g0057a0001c0001t0002g0021a0001c0001t0002g0022others(13): Show | 16 | HG01081.hp1 HG01109.hp2 HG01515.hp1 others(13): Show |
intron_variant | MODIFIER | c.735+260_735+267dup others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798816 | |||||
chr2:108798816
|
T | TACACACA others(5): Show |
1 | a0001c0001t0002g0080 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.735+256_735+267dup others(12): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798816 | |||||
chr2:108798816
|
TAC | T | 2 | a0001c0006t0001g0204a0007c0014t0001g0136 | 2 | HG01891.hp1 NA18959.hp1 |
intron_variant | MODIFIER | c.735+266_735+267del others(2): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798816 | |||||
chr2:108798816
|
TACAC | T | 9 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0004t0001g0198others(6): Show | 9 | HG01175.hp2 HG01257.hp1 HG02723.hp1 others(6): Show |
intron_variant | MODIFIER | c.735+264_735+267del others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798816 | |||||
chr2:108798816
|
TACACACA others(1): Show |
T | 20 | a0001c0005t0001g0112a0001c0005t0001g0113a0001c0005t0001g0114others(17): Show | 20 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.735+260_735+267del others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798816 | |||||
chr2:108798816
|
TACACACA others(3): Show |
T | 5 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(2): Show | 5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.735+258_735+267del others(10): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108798816 | |||||
chr2:108798891
|
A | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.735+305A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108798891 | ||||||
chr2:108799084
|
G | T | 5 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(2): Show | 5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.735+498G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108799084 | ||||||
chr2:108799264
|
T | C | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.735+678T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108799264 | ||||||
chr2:108799293
|
T | C | 175 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.735+707T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108799293 | ||||||
chr2:108799300
|
T | C | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.735+714T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108799300 | ||||||
chr2:108799303
|
T | A | 175 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.735+717T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108799303 | ||||||
chr2:108799779
|
A | C | 175 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.735+1193A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108799779 | ||||||
chr2:108799879
|
C | T | 2 | a0001c0005t0001g0208a0001c0005t0001g0209 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.735+1293C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108799879 | ||||||
chr2:108799964
|
ATTT | A | 5 | a0004c0007t0002g0122a0004c0007t0002g0123a0004c0007t0002g0124others(2): Show | 5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.735+1381_735+1383d others(5): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108799964 | |||||
chr2:108800161
|
A | C | 7 | a0002c0002t0001g0173a0002c0002t0001g0174a0002c0002t0001g0175others(4): Show | 7 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+1575A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800161 | ||||||
chr2:108800222
|
G | C | 7 | a0001c0005t0001g0210a0001c0005t0001g0211a0001c0005t0001g0213others(4): Show | 7 | HG01175.hp1 HG02145.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.735+1636G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800222 | ||||||
chr2:108800368
|
G | A | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+1782G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800368 | ||||||
chr2:108800384
|
T | C | 217 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(214): Show | 219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.735+1798T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800384 | ||||||
chr2:108800421
|
T | C | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.735+1835T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800421 | ||||||
chr2:108800425
|
C | T | 1 | a0002c0002t0001g0168 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.735+1839C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800425 | ||||||
chr2:108800466
|
T | C | 4 | a0001c0004t0001g0103a0001c0004t0001g0104a0001c0004t0001g0105others(1): Show | 4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.735+1880T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800466 | ||||||
chr2:108800471
|
G | C | 7 | a0002c0002t0001g0127a0002c0002t0001g0128a0002c0002t0001g0129others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+1885G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800471 | ||||||
chr2:108800516
|
C | T | 1 | a0001c0001t0002g0078 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.735+1930C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800516 | ||||||
chr2:108800574
|
C | T | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.735+1988C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800574 | ||||||
chr2:108800592
|
T | A | 3 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0204 | 3 | NA18941.hp1 NA18946.hp2 NA18959.hp1 |
intron_variant | MODIFIER | c.735+2006T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800592 | ||||||
chr2:108800608
|
CT | C | 101 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(98): Show | 102 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(99): Show |
intron_variant | MODIFIER | c.735+2052delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108800608 | |||||
chr2:108800608
|
CTT | C | 19 | a0001c0001t0002g0021a0001c0001t0002g0027a0001c0001t0002g0051others(16): Show | 19 | HG00738.hp2 HG00741.hp1 HG01081.hp1 others(16): Show |
intron_variant | MODIFIER | c.735+2051_735+2052d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108800608 | |||||
chr2:108800608
|
CTTTTTTT others(10): Show |
C | 1 | a0001c0006t0001g0201 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.735+2036_735+2052d others(19): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108800608 | |||||
chr2:108800610
|
T | C | 1 | a0005c0009t0001g0165 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.735+2024T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800610 | ||||||
chr2:108800637
|
T | A | 1 | a0001c0005t0001g0212 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.735+2051T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800637 | ||||||
chr2:108800638
|
T | A | 135 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(132): Show | 137 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(134): Show |
intron_variant | MODIFIER | c.735+2052T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800638 | ||||||
chr2:108800638
|
T | TA | 20 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0004t0002g0099others(17): Show | 20 | HG01243.hp2 HG01261.hp1 HG02486.hp1 others(17): Show |
intron_variant | MODIFIER | c.735+2054dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108800638 | |||||
chr2:108800638
|
T | TTA | 14 | a0001c0004t0001g0103a0001c0004t0001g0104a0001c0004t0001g0105others(11): Show | 14 | HG01081.hp2 HG01175.hp1 HG02145.hp1 others(11): Show |
intron_variant | MODIFIER | c.735+2052_735+2053i others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800638 | ||||||
chr2:108800734
|
A | G | 187 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(184): Show | 189 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.735+2148A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800734 | ||||||
chr2:108800896
|
C | G | 1 | a0001c0001t0002g0077 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.735+2310C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800896 | ||||||
chr2:108800992
|
A | G | 175 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.735+2406A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108800992 | ||||||
chr2:108801072
|
A | G | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+2486A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801072 | ||||||
chr2:108801077
|
A | G | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+2491A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801077 | ||||||
chr2:108801247
|
G | T | 174 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.735+2661G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801247 | ||||||
chr2:108801337
|
G | A | 174 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.735+2751G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801337 | ||||||
chr2:108801346
|
A | T | 5 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(2): Show | 5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.735+2760A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801346 | ||||||
chr2:108801374
|
G | A | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.735+2788G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801374 | ||||||
chr2:108801402
|
G | A | 1 | a0001c0001t0002g0028 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.735+2816G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801402 | ||||||
chr2:108801405
|
T | G | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+2819T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801405 | ||||||
chr2:108801454
|
C | T | 2 | a0001c0001t0002g0026a0001c0001t0002g0048 | 2 | NA18985.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.735+2868C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801454 | ||||||
chr2:108801668
|
A | G | 1 | a0003c0003t0001g0141 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.735+3082A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801668 | ||||||
chr2:108801705
|
C | T | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.735+3119C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801705 | ||||||
chr2:108801861
|
T | C | 99 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(96): Show | 100 | HG00099.hp1 HG00408.hp1 HG00738.hp2 others(97): Show |
intron_variant | MODIFIER | c.736-3028T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801861 | ||||||
chr2:108801944
|
T | A | 2 | a0001c0001t0001g0029a0001c0001t0002g0016 | 2 | NA18971.hp1 NA19082.hp1 |
intron_variant | MODIFIER | c.736-2945T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801944 | ||||||
chr2:108801946
|
C | T | 1 | a0007c0014t0001g0136 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.736-2943C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108801946 | ||||||
chr2:108802067
|
G | C | 1 | a0006c0008t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.736-2822G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802067 | ||||||
chr2:108802105
|
G | A | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.736-2784G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802105 | ||||||
chr2:108802107
|
T | C | 5 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(2): Show | 5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.736-2782T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802107 | ||||||
chr2:108802240
|
A | G | 63 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0003others(60): Show | 63 | HG00099.hp1 HG00408.hp1 HG00738.hp2 others(60): Show |
intron_variant | MODIFIER | c.736-2649A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802240 | ||||||
chr2:108802358
|
T | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.736-2531T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802358 | ||||||
chr2:108802417
|
G | T | 27 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0004t0001g0107others(24): Show | 27 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.736-2472G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802417 | ||||||
chr2:108802436
|
T | C | 7 | a0002c0002t0001g0127a0002c0002t0001g0128a0002c0002t0001g0129others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.736-2453T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802436 | ||||||
chr2:108802468
|
T | C | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.736-2421T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802468 | ||||||
chr2:108802526
|
T | G | 1 | a0001c0005t0001g0217 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.736-2363T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802526 | ||||||
chr2:108802567
|
G | A | 5 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(2): Show | 5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.736-2322G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802567 | ||||||
chr2:108802602
|
C | T | 1 | a0001c0005t0001g0114 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.736-2287C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802602 | ||||||
chr2:108802606
|
C | T | 217 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(214): Show | 219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.736-2283C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802606 | ||||||
chr2:108802626
|
TCTC | T | 2 | a0001c0004t0001g0101a0001c0004t0001g0102 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.736-2260_736-2258d others(5): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108802626 | |||||
chr2:108802688
|
A | G | 175 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.736-2201A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802688 | ||||||
chr2:108802755
|
C | T | 2 | a0001c0001t0002g0084a0001c0001t0002g0089 | 2 | NA20752.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.736-2134C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802755 | ||||||
chr2:108802831
|
C | G | 1 | a0003c0003t0001g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.736-2058C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108802831 | ||||||
chr2:108803061
|
G | C | 1 | a0001c0005t0001g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.736-1828G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108803061 | ||||||
chr2:108803125
|
G | T | 1 | a0001c0005t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.736-1764G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108803125 | ||||||
chr2:108803144
|
A | G | 180 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(177): Show | 182 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.736-1745A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108803144 | ||||||
chr2:108803232
|
C | T | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.736-1657C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108803232 | ||||||
chr2:108803393
|
AT | A | 175 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.736-1493delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108803393 | |||||
chr2:108803441
|
A | T | 3 | a0002c0002t0003g0187a0002c0002t0003g0193a0002c0002t0004g0188 | 3 | HG01099.hp1 HG01993.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.736-1448A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108803441 | ||||||
chr2:108803442
|
T | A | 3 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0011t0002g0030 | 3 | HG02895.hp2 HG02897.hp1 NA18994.hp2 |
intron_variant | MODIFIER | c.736-1447T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108803442 | ||||||
chr2:108803514
|
C | T | 2 | a0004c0007t0002g0122a0004c0007t0002g0123 | 2 | HG03471.hp1 HG03486.hp2 |
intron_variant | MODIFIER | c.736-1375C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108803514 | ||||||
chr2:108803518
|
A | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.736-1371A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108803518 | ||||||
chr2:108803624
|
C | T | 6 | a0001c0001t0002g0091a0001c0001t0002g0092a0001c0001t0002g0093others(3): Show | 6 | HG02622.hp1 HG02818.hp2 HG02976.hp2 others(3): Show |
intron_variant | MODIFIER | c.736-1265C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108803624 | ||||||
chr2:108804169
|
A | G | 1 | a0002c0002t0001g0172 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.736-720A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108804169 | ||||||
chr2:108804567
|
A | G | 1 | a0002c0002t0001g0207 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.736-322A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108804567 | ||||||
chr2:108804777
|
A | G | 1 | a0001c0004t0001g0108 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.736-112A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108804777 | ||||||
chr2:108804841
|
T | C | 1 | a0003c0003t0001g0184 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.736-48T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | chr2 | 108804841 | ||||||
chr2:108804878
|
TCTC | T | 35 | a0002c0002t0001g0195a0003c0003t0001g0002a0003c0003t0001g0121others(32): Show | 36 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(33): Show |
splice_region_variant&intron_variant | LOW | c.736-5_736-3delCCT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr2 | 108804878 | |||||
chr2:108805074
|
A | T | 1 | a0002c0002t0001g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.855+66A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805074 | ||||||
chr2:108805165
|
G | A | 175 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.855+157G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805165 | ||||||
chr2:108805376
|
A | G | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.855+368A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805376 | ||||||
chr2:108805396
|
T | C | 1 | a0002c0002t0001g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.855+388T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805396 | ||||||
chr2:108805454
|
G | A | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.855+446G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805454 | ||||||
chr2:108805463
|
C | T | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.855+455C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805463 | ||||||
chr2:108805496
|
T | C | 94 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(91): Show | 95 | HG00099.hp1 HG00408.hp1 HG00738.hp2 others(92): Show |
intron_variant | MODIFIER | c.855+488T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805496 | ||||||
chr2:108805569
|
C | CA | 171 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(168): Show | 173 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.855+570dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108805569 | |||||
chr2:108805775
|
A | G | 5 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(2): Show | 5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.855+767A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805775 | ||||||
chr2:108805809
|
T | C | 5 | a0004c0007t0002g0122a0004c0007t0002g0123a0004c0007t0002g0124others(2): Show | 5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.855+801T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805809 | ||||||
chr2:108805968
|
G | T | 1 | a0001c0001t0002g0081 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.855+960G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108805968 | ||||||
chr2:108806016
|
AGT | A | 105 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(102): Show | 106 | HG00099.hp1 HG00408.hp1 HG00738.hp2 others(103): Show |
intron_variant | MODIFIER | c.855+1009_855+1010d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108806016 | ||||||
chr2:108806077
|
T | A | 1 | a0001c0006t0001g0201 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.855+1069T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108806077 | ||||||
chr2:108806655
|
G | A | 2 | a0001c0004t0001g0101a0001c0004t0001g0102 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.855+1647G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108806655 | ||||||
chr2:108806806
|
A | G | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.855+1798A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108806806 | ||||||
chr2:108807357
|
C | A | 1 | a0001c0001t0002g0028 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.855+2349C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108807357 | ||||||
chr2:108807659
|
C | T | 174 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.855+2651C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108807659 | ||||||
chr2:108807743
|
G | A | 5 | a0004c0007t0002g0122a0004c0007t0002g0123a0004c0007t0002g0124others(2): Show | 5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.855+2735G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108807743 | ||||||
chr2:108808299
|
C | T | 2 | a0002c0002t0002g0186a0002c0002t0002g0190 | 2 | HG01175.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.855+3291C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108808299 | ||||||
chr2:108808448
|
G | A | 1 | a0002c0002t0001g0129 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.855+3440G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108808448 | ||||||
chr2:108808496
|
C | T | 1 | a0001c0004t0001g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.855+3488C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108808496 | ||||||
chr2:108808619
|
A | G | 1 | a0006c0008t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.855+3611A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108808619 | ||||||
chr2:108808925
|
T | C | 1 | a0002c0002t0003g0191 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.856-3706T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108808925 | ||||||
chr2:108809225
|
A | G | 1 | a0002c0002t0001g0132 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.856-3406A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809225 | ||||||
chr2:108809274
|
G | A | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.856-3357G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809274 | ||||||
chr2:108809350
|
A | C | 1 | a0001c0001t0002g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.856-3281A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809350 | ||||||
chr2:108809410
|
T | A | 7 | a0002c0002t0001g0173a0002c0002t0001g0174a0002c0002t0001g0175others(4): Show | 7 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.856-3221T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809410 | ||||||
chr2:108809448
|
T | TTG | 12 | a0001c0001t0002g0026a0002c0002t0001g0173a0002c0002t0001g0174others(9): Show | 12 | HG01175.hp2 HG01261.hp2 HG01891.hp2 others(9): Show |
intron_variant | MODIFIER | c.856-3144_856-3143d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809448 | |||||
chr2:108809448
|
T | TTGTG | 3 | a0001c0004t0002g0099a0002c0002t0001g0172a0002c0002t0001g0179 | 3 | HG02040.hp2 HG02486.hp1 HG02723.hp1 |
intron_variant | MODIFIER | c.856-3146_856-3143d others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809448 | |||||
chr2:108809448
|
T | TTGTGTGT others(1): Show |
6 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0202others(3): Show | 6 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.856-3150_856-3143d others(10): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809448 | |||||
chr2:108809448
|
TTG | T | 116 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0001others(113): Show | 118 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(115): Show |
intron_variant | MODIFIER | c.856-3144_856-3143d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809448 | |||||
chr2:108809448
|
TTGTG | T | 15 | a0001c0001t0002g0031a0001c0001t0002g0062a0001c0005t0001g0112others(12): Show | 15 | HG02055.hp1 HG02257.hp1 HG02523.hp1 others(12): Show |
intron_variant | MODIFIER | c.856-3146_856-3143d others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809448 | |||||
chr2:108809448
|
TTGTGTG | T | 11 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0005t0001g0113others(8): Show | 11 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.856-3148_856-3143d others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809448 | |||||
chr2:108809448
|
TTGTGTGT others(1): Show |
T | 9 | a0001c0004t0001g0198a0001c0005t0001g0116a0001c0005t0001g0117others(6): Show | 9 | HG02615.hp1 HG02647.hp1 HG02818.hp1 others(6): Show |
intron_variant | MODIFIER | c.856-3150_856-3143d others(10): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809448 | |||||
chr2:108809448
|
TTGTGTGT others(3): Show |
T | 7 | a0002c0002t0001g0127a0002c0002t0001g0128a0002c0002t0001g0129others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.856-3152_856-3143d others(12): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809448 | |||||
chr2:108809448
|
TTGTGTGT others(5): Show |
T | 1 | a0003c0003t0001g0164 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.856-3154_856-3143d others(14): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809448 | |||||
chr2:108809450
|
G | T | 9 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(6): Show | 9 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(6): Show |
intron_variant | MODIFIER | c.856-3181G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809450 | ||||||
chr2:108809452
|
G | T | 34 | a0002c0002t0001g0195a0003c0003t0001g0002a0003c0003t0001g0121others(31): Show | 35 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.856-3179G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809452 | ||||||
chr2:108809462
|
G | T | 1 | a0003c0003t0001g0164 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.856-3169G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809462 | ||||||
chr2:108809480
|
G | T | 4 | a0001c0004t0001g0103a0001c0004t0001g0104a0001c0004t0001g0105others(1): Show | 4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-3151G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809480 | ||||||
chr2:108809487
|
T | A | 1 | a0006c0008t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.856-3144T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809487 | ||||||
chr2:108809796
|
T | TTTTG | 4 | a0001c0004t0001g0198a0003c0003t0001g0159a0003c0003t0001g0160others(1): Show | 4 | HG02723.hp2 HG03098.hp2 NA19043.hp2 others(1): Show |
intron_variant | MODIFIER | c.856-2809_856-2806d others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809796 | |||||
chr2:108809796
|
TTTTG | T | 115 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(112): Show | 116 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(113): Show |
intron_variant | MODIFIER | c.856-2809_856-2806d others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108809796 | |||||
chr2:108809868
|
C | T | 4 | a0001c0004t0001g0103a0001c0004t0001g0104a0001c0004t0001g0105others(1): Show | 4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-2763C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809868 | ||||||
chr2:108809881
|
C | T | 1 | a0001c0001t0002g0081 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.856-2750C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108809881 | ||||||
chr2:108810195
|
G | A | 5 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(2): Show | 5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.856-2436G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108810195 | ||||||
chr2:108810258
|
A | G | 1 | a0002c0002t0001g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.856-2373A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108810258 | ||||||
chr2:108810263
|
G | T | 1 | a0001c0001t0002g0087 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.856-2368G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108810263 | ||||||
chr2:108810328
|
A | T | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.856-2303A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108810328 | ||||||
chr2:108810364
|
G | T | 1 | a0002c0002t0002g0183 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856-2267G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108810364 | ||||||
chr2:108810474
|
T | A | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.856-2157T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108810474 | ||||||
chr2:108810771
|
G | T | 175 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.856-1860G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108810771 | ||||||
chr2:108810776
|
A | T | 1 | a0003c0003t0001g0139 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.856-1855A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108810776 | ||||||
chr2:108810815
|
G | A | 2 | a0001c0010t0002g0068a0003c0003t0001g0140 | 2 | HG02486.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.856-1816G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108810815 | ||||||
chr2:108811021
|
G | C | 1 | a0002c0002t0002g0183 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.856-1610G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108811021 | ||||||
chr2:108811087
|
CCTTTTTT others(17): Show |
C | 1 | a0001c0004t0001g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.856-1532_856-1509d others(26): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811087 | |||||
chr2:108811100
|
C | CT | 10 | a0002c0002t0001g0134a0002c0002t0001g0167a0002c0002t0001g0168others(7): Show | 10 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.856-1520dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811100 | |||||
chr2:108811100
|
CTTTTTTT | C | 173 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(170): Show | 175 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(172): Show |
intron_variant | MODIFIER | c.856-1526_856-1520d others(9): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811100 | |||||
chr2:108811241
|
C | G | 11 | a0001c0005t0001g0208a0001c0005t0001g0209a0001c0005t0001g0210others(8): Show | 11 | HG01175.hp1 HG02145.hp1 HG02257.hp1 others(8): Show |
intron_variant | MODIFIER | c.856-1390C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108811241 | ||||||
chr2:108811245
|
C | CTTTT | 85 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(82): Show | 86 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(83): Show |
intron_variant | MODIFIER | c.856-1385_856-1384i others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811245 | |||||
chr2:108811245
|
C | CTTTTT | 10 | a0001c0001t0002g0008a0001c0001t0002g0025a0001c0001t0002g0047others(7): Show | 10 | HG01361.hp1 HG01361.hp2 HG01884.hp2 others(7): Show |
intron_variant | MODIFIER | c.856-1385_856-1384i others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811245 | |||||
chr2:108811245
|
C | CTTTTTT | 7 | a0001c0001t0002g0078a0001c0004t0001g0101a0001c0004t0001g0102others(4): Show | 7 | HG01243.hp2 HG02738.hp1 HG02895.hp2 others(4): Show |
intron_variant | MODIFIER | c.856-1385_856-1384i others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811245 | |||||
chr2:108811245
|
C | CTTTTTTT | 20 | a0001c0005t0001g0115a0001c0005t0001g0116a0001c0005t0001g0117others(17): Show | 20 | HG01175.hp1 HG01261.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.856-1385_856-1384i others(9): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811245 | |||||
chr2:108811245
|
C | CTTTTTTT others(2): Show |
8 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(5): Show | 8 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(5): Show |
intron_variant | MODIFIER | c.856-1385_856-1384i others(11): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811245 | |||||
chr2:108811245
|
C | CTTTTTTT others(3): Show |
1 | a0004c0007t0002g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.856-1385_856-1384i others(12): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811245 | |||||
chr2:108811247
|
C | CTCTTTTT others(4): Show |
1 | a0003c0003t0001g0147 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.856-1383_856-1382i others(13): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | |||||
chr2:108811247
|
C | CTCTTTTT others(9): Show |
3 | a0003c0003t0001g0137a0003c0003t0001g0139a0003c0003t0001g0148 | 3 | HG01109.hp2 NA19070.hp2 NA20752.hp1 |
intron_variant | MODIFIER | c.856-1383_856-1382i others(18): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | |||||
chr2:108811247
|
C | CTCTTTTT others(15): Show |
2 | a0001c0004t0001g0011a0001c0012t0001g0010 | 2 | HG01243.hp1 HG03041.hp1 |
intron_variant | MODIFIER | c.856-1383_856-1382i others(24): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | |||||
chr2:108811247
|
C | CTCTTTTT others(16): Show |
5 | a0001c0004t0001g0009a0001c0004t0001g0012a0001c0004t0001g0013others(2): Show | 5 | HG02572.hp1 HG02970.hp1 HG03209.hp1 others(2): Show |
intron_variant | MODIFIER | c.856-1383_856-1382i others(25): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | |||||
chr2:108811247
|
C | CTCTTTTT others(18): Show |
1 | a0001c0004t0001g0015 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.856-1383_856-1382i others(27): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | |||||
chr2:108811247
|
C | CTCTTTTT others(19): Show |
1 | a0003c0003t0001g0180 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.856-1383_856-1382i others(28): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | |||||
chr2:108811247
|
C | CTCTTTTT others(20): Show |
1 | a0008c0015t0001g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.856-1383_856-1382i others(29): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | |||||
chr2:108811247
|
C | CTCTTTTT others(21): Show |
8 | a0003c0003t0001g0135a0003c0003t0001g0138a0003c0003t0001g0143others(5): Show | 8 | HG00099.hp2 HG00408.hp2 HG01358.hp1 others(5): Show |
intron_variant | MODIFIER | c.856-1383_856-1382i others(30): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | |||||
chr2:108811247
|
C | CTCTTTTT others(22): Show |
11 | a0002c0002t0001g0195a0003c0003t0001g0140a0003c0003t0001g0145others(8): Show | 11 | HG00738.hp1 HG01168.hp2 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.856-1383_856-1382i others(31): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | |||||
chr2:108811247
|
C | CTCTTTTT others(23): Show |
3 | a0003c0003t0001g0002a0003c0003t0001g0141a0003c0003t0001g0158 | 4 | NA18977.hp2 NA18993.hp2 NA18998.hp1 others(1): Show |
intron_variant | MODIFIER | c.856-1383_856-1382i others(32): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | |||||
chr2:108811247
|
C | CTCTTTTT others(24): Show |
2 | a0003c0003t0001g0162a0003c0003t0001g0163 | 2 | NA18945.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.856-1383_856-1382i others(33): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | |||||
chr2:108811247
|
C | CTCTTTTT others(27): Show |
1 | a0003c0003t0001g0121 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.856-1383_856-1382i others(36): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | |||||
chr2:108811247
|
C | CTCTTTTT others(47): Show |
2 | a0003c0003t0001g0142a0003c0003t0001g0181 | 2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.856-1383_856-1382i others(56): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | |||||
chr2:108811247
|
C | CTTTTTTT others(5): Show |
1 | a0002c0002t0001g0130 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.856-1380_856-1369d others(14): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | |||||
chr2:108811247
|
C | CTTTTTTT others(6): Show |
6 | a0002c0002t0001g0127a0002c0002t0001g0128a0002c0002t0001g0129others(3): Show | 6 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(3): Show |
intron_variant | MODIFIER | c.856-1381_856-1369d others(15): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | INFO_REALIGN_3_PRIME | chr2 | 108811247 | |||||
chr2:108811247
|
C | T | 135 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(132): Show | 136 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(133): Show |
intron_variant | MODIFIER | c.856-1384C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108811247 | ||||||
chr2:108811287
|
T | C | 178 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(175): Show | 180 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(177): Show |
intron_variant | MODIFIER | c.856-1344T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108811287 | ||||||
chr2:108811320
|
A | G | 1 | a0001c0001t0002g0044 | 1 | HG01978.hp2 | intron_variant | MODIFIER | c.856-1311A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108811320 | ||||||
chr2:108811395
|
C | T | 2 | a0001c0001t0002g0001a0001c0005t0001g0112 | 3 | HG01074.hp2 HG01099.hp2 HG03041.hp2 |
intron_variant | MODIFIER | c.856-1236C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108811395 | ||||||
chr2:108812045
|
A | G | 1 | a0001c0005t0001g0117 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.856-586A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108812045 | ||||||
chr2:108812085
|
A | G | 1 | a0001c0004t0001g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.856-546A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108812085 | ||||||
chr2:108812150
|
T | C | 1 | a0001c0010t0002g0068 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.856-481T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108812150 | ||||||
chr2:108812219
|
T | C | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.856-412T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108812219 | ||||||
chr2:108812387
|
A | G | 27 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0004t0001g0107others(24): Show | 27 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.856-244A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108812387 | ||||||
chr2:108812472
|
C | T | 7 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0004t0001g0107others(4): Show | 7 | HG02258.hp2 HG02895.hp2 HG02897.hp1 others(4): Show |
intron_variant | MODIFIER | c.856-159C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 7/14 | chr2 | 108812472 | ||||||
chr2:108812806
|
A | G | 31 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0004t0001g0103others(28): Show | 31 | HG01081.hp2 HG01175.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.934-14A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 8/14 | chr2 | 108812806 | ||||||
chr2:108812968
|
G | A | 5 | a0004c0007t0002g0122a0004c0007t0002g0123a0004c0007t0002g0124others(2): Show | 5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1041+41G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108812968 | ||||||
chr2:108812983
|
C | T | 1 | a0003c0003t0001g0158 | 1 | NA18998.hp1 | intron_variant | MODIFIER | c.1041+56C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108812983 | ||||||
chr2:108813076
|
C | T | 5 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(2): Show | 5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1041+149C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813076 | ||||||
chr2:108813121
|
C | T | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041+194C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813121 | ||||||
chr2:108813141
|
C | T | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1041+214C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813141 | ||||||
chr2:108813188
|
G | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(85): Show | 89 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.1041+261G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813188 | ||||||
chr2:108813248
|
C | CA | 12 | a0001c0004t0001g0198a0001c0004t0002g0100a0001c0005t0001g0117others(9): Show | 12 | HG01099.hp1 HG01109.hp2 HG01167.hp2 others(9): Show |
intron_variant | MODIFIER | c.1041+345dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108813248 | |||||
chr2:108813248
|
C | CAA | 57 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(54): Show | 58 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1041+344_1041+345d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108813248 | |||||
chr2:108813248
|
C | CAAA | 84 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(81): Show | 85 | HG00099.hp1 HG00408.hp1 HG00741.hp1 others(82): Show |
intron_variant | MODIFIER | c.1041+343_1041+345d others(5): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108813248 | |||||
chr2:108813248
|
C | CAAAA | 16 | a0001c0001t0002g0004a0001c0001t0002g0032a0001c0001t0002g0033others(13): Show | 16 | HG00741.hp2 HG01361.hp2 HG01978.hp2 others(13): Show |
intron_variant | MODIFIER | c.1041+342_1041+345d others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108813248 | |||||
chr2:108813269
|
A | G | 2 | a0001c0004t0001g0101a0001c0004t0001g0102 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1041+342A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813269 | ||||||
chr2:108813365
|
A | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1041+438A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813365 | ||||||
chr2:108813484
|
T | C | 7 | a0002c0002t0001g0127a0002c0002t0001g0128a0002c0002t0001g0129others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041+557T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813484 | ||||||
chr2:108813760
|
A | C | 2 | a0003c0003t0001g0142a0003c0003t0001g0181 | 2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1041+833A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813760 | ||||||
chr2:108813782
|
C | T | 22 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0005t0001g0112others(19): Show | 22 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1041+855C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813782 | ||||||
chr2:108813848
|
G | T | 1 | a0002c0002t0001g0130 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1041+921G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813848 | ||||||
chr2:108813934
|
A | G | 2 | a0002c0002t0002g0186a0002c0002t0002g0190 | 2 | HG01175.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1041+1007A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108813934 | ||||||
chr2:108814249
|
G | C | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1041+1322G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108814249 | ||||||
chr2:108814353
|
A | G | 1 | a0003c0003t0001g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1041+1426A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108814353 | ||||||
chr2:108814419
|
C | T | 175 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1041+1492C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108814419 | ||||||
chr2:108814450
|
T | A | 1 | a0001c0001t0002g0082 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1042-1491T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108814450 | ||||||
chr2:108814549
|
C | T | 1 | a0003c0003t0001g0147 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1042-1392C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108814549 | ||||||
chr2:108814632
|
AT | A | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1042-1302delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108814632 | |||||
chr2:108814761
|
G | A | 5 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(2): Show | 5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-1180G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108814761 | ||||||
chr2:108814881
|
C | G | 1 | a0001c0001t0002g0055 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1042-1060C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108814881 | ||||||
chr2:108814947
|
A | T | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1042-994A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108814947 | ||||||
chr2:108815109
|
CAG | C | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1042-829_1042-828d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108815109 | |||||
chr2:108815205
|
G | A | 5 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(2): Show | 5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1042-736G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815205 | ||||||
chr2:108815284
|
A | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1042-657A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815284 | ||||||
chr2:108815369
|
A | G | 2 | a0001c0004t0002g0099a0001c0004t0002g0100 | 2 | HG02486.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.1042-572A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815369 | ||||||
chr2:108815393
|
T | C | 5 | a0004c0007t0002g0122a0004c0007t0002g0123a0004c0007t0002g0124others(2): Show | 5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1042-548T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815393 | ||||||
chr2:108815448
|
G | A | 175 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1042-493G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815448 | ||||||
chr2:108815461
|
G | GT | 106 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(103): Show | 107 | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(104): Show |
intron_variant | MODIFIER | c.1042-457dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108815461 | |||||
chr2:108815461
|
G | GTT | 17 | a0001c0001t0001g0079a0001c0001t0002g0043a0001c0001t0002g0062others(14): Show | 17 | HG01175.hp1 HG01516.hp2 HG01978.hp1 others(14): Show |
intron_variant | MODIFIER | c.1042-458_1042-457d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108815461 | |||||
chr2:108815461
|
G | GTTT | 5 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0202others(2): Show | 5 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(2): Show |
intron_variant | MODIFIER | c.1042-459_1042-457d others(5): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108815461 | |||||
chr2:108815461
|
GT | G | 13 | a0002c0002t0001g0129a0002c0002t0001g0130a0002c0002t0001g0131others(10): Show | 13 | HG01167.hp2 HG01884.hp1 HG02280.hp2 others(10): Show |
intron_variant | MODIFIER | c.1042-457delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108815461 | |||||
chr2:108815464
|
T | TG | 2 | a0001c0004t0001g0101a0001c0004t0001g0102 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1042-477_1042-476i others(3): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815464 | ||||||
chr2:108815466
|
T | G | 1 | a0002c0002t0001g0207 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1042-475T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815466 | ||||||
chr2:108815473
|
T | TTG | 9 | a0001c0004t0001g0103a0001c0004t0001g0104a0001c0004t0001g0105others(6): Show | 9 | HG01081.hp2 HG02258.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.1042-467_1042-466i others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | INFO_REALIGN_3_PRIME | chr2 | 108815473 | |||||
chr2:108815479
|
T | G | 4 | a0001c0004t0001g0103a0001c0004t0001g0104a0001c0004t0001g0105others(1): Show | 4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1042-462T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815479 | ||||||
chr2:108815516
|
G | C | 44 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(41): Show | 45 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1042-425G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815516 | ||||||
chr2:108815530
|
G | A | 5 | a0004c0007t0002g0122a0004c0007t0002g0123a0004c0007t0002g0124others(2): Show | 5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1042-411G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 9/14 | chr2 | 108815530 | ||||||
chr2:108816366
|
G | A | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+261G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108816366 | ||||||
chr2:108816552
|
T | TA | 180 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(177): Show | 182 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(179): Show |
intron_variant | MODIFIER | c.1206+447_1206+448i others(3): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108816552 | ||||||
chr2:108816696
|
T | A | 31 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0004t0001g0103others(28): Show | 31 | HG01081.hp2 HG01175.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1206+591T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108816696 | ||||||
chr2:108816814
|
A | G | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+709A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108816814 | ||||||
chr2:108816873
|
T | A | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1206+768T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108816873 | ||||||
chr2:108817079
|
G | A | 1 | a0002c0002t0001g0168 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1206+974G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108817079 | ||||||
chr2:108817299
|
C | CT | 5 | a0001c0001t0002g0025a0001c0004t0001g0109a0001c0004t0001g0110others(2): Show | 5 | HG03195.hp1 HG03225.hp2 HG03453.hp1 others(2): Show |
intron_variant | MODIFIER | c.1206+1206dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108817299 | |||||
chr2:108817316
|
C | T | 2 | a0003c0003t0001g0159a0003c0003t0001g0160 | 2 | HG02723.hp2 HG03098.hp2 |
intron_variant | MODIFIER | c.1206+1211C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108817316 | ||||||
chr2:108817481
|
C | T | 1 | a0003c0003t0001g0164 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1206+1376C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108817481 | ||||||
chr2:108817520
|
C | T | 174 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1206+1415C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108817520 | ||||||
chr2:108817542
|
C | T | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+1437C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108817542 | ||||||
chr2:108817641
|
G | A | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+1536G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108817641 | ||||||
chr2:108817859
|
C | T | 187 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(184): Show | 189 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.1206+1754C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108817859 | ||||||
chr2:108818056
|
T | C | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+1951T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108818056 | ||||||
chr2:108818325
|
G | A | 1 | a0001c0004t0002g0098 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1206+2220G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108818325 | ||||||
chr2:108818820
|
C | CT | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+2727dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108818820 | |||||
chr2:108818820
|
CT | C | 36 | a0002c0002t0001g0195a0003c0003t0001g0002a0003c0003t0001g0121others(33): Show | 37 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(34): Show |
intron_variant | MODIFIER | c.1206+2727delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108818820 | |||||
chr2:108819176
|
T | C | 5 | a0001c0001t0002g0047a0001c0004t0002g0097a0001c0004t0002g0098others(2): Show | 5 | HG01361.hp1 HG02486.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1206+3071T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108819176 | ||||||
chr2:108819257
|
T | C | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1206+3152T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108819257 | ||||||
chr2:108819296
|
G | A | 1 | a0002c0002t0001g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1206+3191G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108819296 | ||||||
chr2:108819331
|
C | G | 1 | a0001c0013t0002g0076 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1206+3226C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108819331 | ||||||
chr2:108819447
|
A | C | 1 | a0003c0003t0001g0141 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.1206+3342A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108819447 | ||||||
chr2:108819523
|
G | A | 174 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1206+3418G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108819523 | ||||||
chr2:108819547
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0079 | 2 | HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1206+3442A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108819547 | ||||||
chr2:108819868
|
GA | G | 95 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(92): Show | 96 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(93): Show |
intron_variant | MODIFIER | c.1206+3765delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108819868 | |||||
chr2:108820052
|
A | G | 1 | a0001c0004t0001g0111 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1206+3947A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820052 | ||||||
chr2:108820061
|
AGCAGACT others(7): Show |
A | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1206+3962_1206+397 others(18): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108820061 | |||||
chr2:108820236
|
C | T | 3 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0071 | 3 | HG01074.hp1 HG01358.hp2 HG01361.hp2 |
intron_variant | MODIFIER | c.1206+4131C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820236 | ||||||
chr2:108820273
|
T | C | 1 | a0001c0001t0002g0080 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1206+4168T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820273 | ||||||
chr2:108820329
|
A | C | 2 | a0001c0004t0001g0101a0001c0004t0001g0102 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1206+4224A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820329 | ||||||
chr2:108820384
|
G | T | 9 | a0002c0002t0001g0173a0002c0002t0001g0174a0002c0002t0001g0175others(6): Show | 9 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1206+4279G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820384 | ||||||
chr2:108820503
|
G | A | 1 | a0002c0002t0003g0189 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1206+4398G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820503 | ||||||
chr2:108820681
|
G | T | 7 | a0002c0002t0001g0127a0002c0002t0001g0128a0002c0002t0001g0129others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+4576G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820681 | ||||||
chr2:108820690
|
T | G | 2 | a0003c0003t0001g0121a0003c0003t0001g0153 | 2 | NA18974.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1206+4585T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820690 | ||||||
chr2:108820712
|
A | AAAAAC | 34 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0002g0001others(31): Show | 35 | HG00408.hp2 HG01074.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.1206+4610_1206+461 others(9): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108820712 | |||||
chr2:108820712
|
A | AAAC | 9 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0006t0001g0199others(6): Show | 9 | HG01261.hp1 HG02895.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1206+4609_1206+461 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108820712 | |||||
chr2:108820712
|
A | C | 1 | a0001c0001t0002g0055 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1206+4607A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820712 | ||||||
chr2:108820713
|
A | T | 1 | a0001c0001t0002g0055 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1206+4608A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820713 | ||||||
chr2:108820720
|
C | A | 45 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0002g0001others(42): Show | 46 | HG00408.hp2 HG01074.hp2 HG01099.hp2 others(43): Show |
intron_variant | MODIFIER | c.1206+4615C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820720 | ||||||
chr2:108820720
|
C | CAAAA | 162 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0003others(159): Show | 163 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.1206+4617_1206+461 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108820720 | |||||
chr2:108820971
|
G | A | 175 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1206+4866G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108820971 | ||||||
chr2:108821018
|
T | TA | 171 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(168): Show | 173 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(170): Show |
intron_variant | MODIFIER | c.1206+4921dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108821018 | |||||
chr2:108821100
|
G | A | 1 | a0003c0003t0001g0154 | 1 | HG00738.hp1 | intron_variant | MODIFIER | c.1206+4995G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108821100 | ||||||
chr2:108821119
|
AGGCTAAG others(6): Show |
A | 1 | a0003c0003t0001g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1206+5017_1206+502 others(17): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108821119 | |||||
chr2:108821129
|
A | G | 1 | a0002c0002t0001g0177 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.1206+5024A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108821129 | ||||||
chr2:108821352
|
C | T | 1 | a0001c0001t0002g0075 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.1206+5247C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108821352 | ||||||
chr2:108821357
|
C | CA | 31 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0004t0001g0103others(28): Show | 31 | HG01081.hp2 HG01175.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1206+5260dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108821357 | |||||
chr2:108821415
|
A | G | 187 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(184): Show | 189 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.1206+5310A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108821415 | ||||||
chr2:108821622
|
A | G | 1 | a0001c0001t0002g0055 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1206+5517A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108821622 | ||||||
chr2:108821711
|
G | GA | 2 | a0003c0003t0001g0137a0003c0003t0001g0164 | 2 | HG01109.hp2 HG01167.hp2 |
intron_variant | MODIFIER | c.1206+5607dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108821711 | |||||
chr2:108821826
|
T | A | 1 | a0001c0001t0002g0003 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1206+5721T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108821826 | ||||||
chr2:108821892
|
C | T | 2 | a0001c0004t0001g0101a0001c0004t0001g0102 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1206+5787C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108821892 | ||||||
chr2:108821928
|
C | CA | 125 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(122): Show | 126 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(123): Show |
intron_variant | MODIFIER | c.1206+5840dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108821928 | |||||
chr2:108821928
|
C | CAA | 9 | a0001c0005t0001g0115a0001c0005t0002g0215a0001c0006t0001g0199others(6): Show | 9 | HG01175.hp1 HG01261.hp1 NA18941.hp1 others(6): Show |
intron_variant | MODIFIER | c.1206+5839_1206+584 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108821928 | |||||
chr2:108822248
|
C | G | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+6143C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108822248 | ||||||
chr2:108822268
|
A | G | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+6163A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108822268 | ||||||
chr2:108822449
|
C | T | 1 | a0002c0002t0001g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1206+6344C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108822449 | ||||||
chr2:108822644
|
A | G | 2 | a0001c0001t0001g0057a0001c0001t0002g0058 | 2 | HG04204.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.1206+6539A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108822644 | ||||||
chr2:108822699
|
A | G | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+6594A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108822699 | ||||||
chr2:108822837
|
T | G | 31 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0004t0001g0103others(28): Show | 31 | HG01081.hp2 HG01175.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1206+6732T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108822837 | ||||||
chr2:108822996
|
T | A | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1206+6891T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108822996 | ||||||
chr2:108823358
|
G | A | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+7253G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108823358 | ||||||
chr2:108823485
|
A | G | 31 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0004t0001g0103others(28): Show | 31 | HG01081.hp2 HG01175.hp1 HG01243.hp2 others(28): Show |
intron_variant | MODIFIER | c.1206+7380A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108823485 | ||||||
chr2:108823586
|
T | C | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1206+7481T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108823586 | ||||||
chr2:108823777
|
C | T | 88 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(85): Show | 89 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.1206+7672C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108823777 | ||||||
chr2:108823945
|
C | T | 143 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(140): Show | 145 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(142): Show |
intron_variant | MODIFIER | c.1206+7840C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108823945 | ||||||
chr2:108823996
|
TG | T | 37 | a0002c0002t0001g0195a0003c0003t0001g0002a0003c0003t0001g0121others(34): Show | 38 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1206+7897delG | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108823996 | |||||
chr2:108824170
|
AT | A | 174 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1206+8071delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108824170 | |||||
chr2:108824504
|
A | G | 1 | a0001c0001t0002g0031 | 1 | NA18988.hp1 | intron_variant | MODIFIER | c.1206+8399A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108824504 | ||||||
chr2:108824604
|
T | A | 2 | a0001c0005t0001g0208a0003c0003t0001g0152 | 2 | HG02647.hp1 NA18999.hp1 |
intron_variant | MODIFIER | c.1206+8499T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108824604 | ||||||
chr2:108824744
|
A | G | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+8639A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108824744 | ||||||
chr2:108824848
|
G | T | 19 | a0001c0005t0001g0113a0001c0005t0001g0114a0001c0005t0001g0115others(16): Show | 19 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1206+8743G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108824848 | ||||||
chr2:108824994
|
A | G | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+8889A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108824994 | ||||||
chr2:108825044
|
A | G | 4 | a0001c0004t0001g0103a0001c0004t0001g0104a0001c0004t0001g0105others(1): Show | 4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1206+8939A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108825044 | ||||||
chr2:108825058
|
A | G | 1 | a0001c0001t0002g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1206+8953A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108825058 | ||||||
chr2:108825231
|
A | G | 1 | a0002c0002t0001g0131 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1206+9126A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108825231 | ||||||
chr2:108825274
|
TTTTG | T | 99 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(96): Show | 100 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(97): Show |
intron_variant | MODIFIER | c.1206+9186_1206+918 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108825274 | |||||
chr2:108825394
|
G | A | 2 | a0002c0002t0001g0176a0002c0002t0001g0177 | 2 | HG03130.hp2 HG06807.hp2 |
intron_variant | MODIFIER | c.1206+9289G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108825394 | ||||||
chr2:108825440
|
A | C | 1 | a0001c0011t0002g0030 | 1 | NA18994.hp2 | intron_variant | MODIFIER | c.1206+9335A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108825440 | ||||||
chr2:108825558
|
G | A | 187 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(184): Show | 189 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(186): Show |
intron_variant | MODIFIER | c.1206+9453G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108825558 | ||||||
chr2:108825588
|
A | G | 5 | a0004c0007t0002g0122a0004c0007t0002g0123a0004c0007t0002g0124others(2): Show | 5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1206+9483A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108825588 | ||||||
chr2:108825737
|
T | C | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1206+9632T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108825737 | ||||||
chr2:108825787
|
A | G | 174 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(171): Show | 176 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(173): Show |
intron_variant | MODIFIER | c.1206+9682A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108825787 | ||||||
chr2:108826128
|
G | A | 1 | a0001c0001t0002g0036 | 1 | NA18968.hp1 | intron_variant | MODIFIER | c.1206+10023G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108826128 | ||||||
chr2:108826170
|
C | A | 1 | a0004c0007t0002g0122 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.1206+10065C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108826170 | ||||||
chr2:108826203
|
G | A | 1 | a0001c0001t0002g0081 | 1 | HG01516.hp2 | intron_variant | MODIFIER | c.1206+10098G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108826203 | ||||||
chr2:108826264
|
A | G | 1 | a0001c0005t0001g0120 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.1206+10159A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108826264 | ||||||
chr2:108826296
|
A | G | 2 | a0001c0001t0002g0082a0001c0001t0002g0083 | 2 | HG02735.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.1206+10191A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108826296 | ||||||
chr2:108826348
|
T | G | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+10243T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108826348 | ||||||
chr2:108826474
|
A | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1206+10369A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108826474 | ||||||
chr2:108826687
|
A | G | 175 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1206+10582A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108826687 | ||||||
chr2:108826691
|
TC | T | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1206+10588delC | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108826691 | |||||
chr2:108826930
|
C | T | 5 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(2): Show | 5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1206+10825C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108826930 | ||||||
chr2:108827051
|
T | C | 5 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1206+10946T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827051 | ||||||
chr2:108827334
|
C | T | 20 | a0001c0005t0001g0112a0001c0005t0001g0113a0001c0005t0001g0114others(17): Show | 20 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.1206+11229C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827334 | ||||||
chr2:108827473
|
A | C | 22 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0005t0001g0112others(19): Show | 22 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1206+11368A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827473 | ||||||
chr2:108827483
|
A | G | 92 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(89): Show | 93 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(90): Show |
intron_variant | MODIFIER | c.1206+11378A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827483 | ||||||
chr2:108827542
|
C | T | 1 | a0002c0002t0001g0134 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1206+11437C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827542 | ||||||
chr2:108827591
|
C | CA | 37 | a0002c0002t0001g0195a0003c0003t0001g0002a0003c0003t0001g0121others(34): Show | 38 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1206+11486_1206+11 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827591 | ||||||
chr2:108827594
|
ATC | A | 37 | a0002c0002t0001g0195a0003c0003t0001g0002a0003c0003t0001g0121others(34): Show | 38 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(35): Show |
intron_variant | MODIFIER | c.1206+11490_1206+11 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827594 | ||||||
chr2:108827611
|
C | T | 1 | a0001c0006t0001g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1206+11506C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827611 | ||||||
chr2:108827612
|
G | C | 1 | a0001c0006t0001g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1206+11507G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827612 | ||||||
chr2:108827614
|
A | G | 1 | a0001c0006t0001g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1206+11509A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827614 | ||||||
chr2:108827617
|
C | G | 1 | a0001c0006t0001g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1206+11512C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827617 | ||||||
chr2:108827618
|
T | C | 1 | a0001c0006t0001g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1206+11513T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827618 | ||||||
chr2:108827673
|
A | G | 1 | a0001c0013t0002g0076 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1207-11512A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827673 | ||||||
chr2:108827676
|
C | T | 44 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(41): Show | 45 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1207-11509C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827676 | ||||||
chr2:108827748
|
G | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0108 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1207-11437G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827748 | ||||||
chr2:108827814
|
T | TA | 11 | a0001c0004t0001g0012a0001c0006t0001g0205a0002c0002t0001g0172others(8): Show | 11 | HG01109.hp2 HG01167.hp2 HG01261.hp1 others(8): Show |
intron_variant | MODIFIER | c.1207-11353dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108827814 | |||||
chr2:108827814
|
TA | T | 113 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(110): Show | 114 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(111): Show |
intron_variant | MODIFIER | c.1207-11353delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108827814 | |||||
chr2:108827814
|
TAA | T | 5 | a0001c0001t0002g0007a0001c0004t0002g0097a0001c0004t0002g0098others(2): Show | 5 | HG01167.hp1 HG02486.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-11354_1207-11 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108827814 | |||||
chr2:108827817
|
A | T | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207-11368A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827817 | ||||||
chr2:108827902
|
C | T | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1207-11283C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108827902 | ||||||
chr2:108828027
|
A | G | 5 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(2): Show | 5 | HG02258.hp2 HG02922.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207-11158A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828027 | ||||||
chr2:108828040
|
A | G | 12 | a0001c0001t0001g0029a0001c0001t0002g0004a0001c0001t0002g0016others(9): Show | 12 | HG00408.hp1 HG01978.hp1 HG02040.hp1 others(9): Show |
intron_variant | MODIFIER | c.1207-11145A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828040 | ||||||
chr2:108828176
|
A | G | 1 | a0001c0001t0002g0080 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.1207-11009A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828176 | ||||||
chr2:108828244
|
G | A | 7 | a0002c0002t0001g0173a0002c0002t0001g0174a0002c0002t0001g0175others(4): Show | 7 | HG01891.hp2 HG02257.hp2 HG02451.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-10941G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828244 | ||||||
chr2:108828370
|
A | G | 1 | a0001c0005t0001g0217 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1207-10815A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828370 | ||||||
chr2:108828408
|
T | C | 1 | a0001c0004t0001g0013 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.1207-10777T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828408 | ||||||
chr2:108828662
|
G | A | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-10523G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828662 | ||||||
chr2:108828760
|
C | G | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207-10425C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828760 | ||||||
chr2:108828864
|
G | C | 2 | a0001c0004t0001g0101a0001c0004t0001g0102 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1207-10321G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828864 | ||||||
chr2:108828927
|
G | A | 88 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(85): Show | 89 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(86): Show |
intron_variant | MODIFIER | c.1207-10258G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828927 | ||||||
chr2:108828958
|
A | G | 7 | a0002c0002t0001g0127a0002c0002t0001g0128a0002c0002t0001g0129others(4): Show | 7 | HG01884.hp1 HG02055.hp2 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-10227A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108828958 | ||||||
chr2:108829246
|
T | C | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-9939T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829246 | ||||||
chr2:108829348
|
A | G | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-9837A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829348 | ||||||
chr2:108829413
|
A | G | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-9772A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829413 | ||||||
chr2:108829469
|
A | AACAGGGC others(3): Show |
1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1207-9713_1207-971 others(14): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108829469 | |||||
chr2:108829472
|
A | G | 1 | a0001c0006t0001g0202 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.1207-9713A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829472 | ||||||
chr2:108829490
|
A | G | 103 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(100): Show | 104 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(101): Show |
intron_variant | MODIFIER | c.1207-9695A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829490 | ||||||
chr2:108829533
|
G | A | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1207-9652G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829533 | ||||||
chr2:108829555
|
G | C | 1 | a0001c0001t0002g0003 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1207-9630G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829555 | ||||||
chr2:108829565
|
G | C | 1 | a0001c0001t0002g0037 | 1 | NA18946.hp1 | intron_variant | MODIFIER | c.1207-9620G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829565 | ||||||
chr2:108829626
|
G | A | 22 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0005t0001g0112others(19): Show | 22 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(19): Show |
intron_variant | MODIFIER | c.1207-9559G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829626 | ||||||
chr2:108829657
|
A | C | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1207-9528A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108829657 | ||||||
chr2:108830000
|
AAAG | A | 27 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0004t0001g0107others(24): Show | 27 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.1207-9181_1207-917 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108830000 | |||||
chr2:108830187
|
G | A | 1 | a0003c0003t0001g0137 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.1207-8998G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108830187 | ||||||
chr2:108830498
|
CT | C | 5 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-8684delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108830498 | |||||
chr2:108830585
|
TC | T | 19 | a0001c0005t0001g0112a0001c0005t0001g0113a0001c0005t0001g0114others(16): Show | 19 | HG01175.hp1 HG01243.hp2 HG02145.hp1 others(16): Show |
intron_variant | MODIFIER | c.1207-8599delC | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108830585 | ||||||
chr2:108830607
|
G | C | 1 | a0001c0004t0001g0104 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.1207-8578G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108830607 | ||||||
chr2:108830608
|
T | A | 175 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(172): Show | 177 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(174): Show |
intron_variant | MODIFIER | c.1207-8577T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108830608 | ||||||
chr2:108830693
|
A | T | 2 | a0001c0001t0002g0056a0001c0001t0002g0074 | 2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1207-8492A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108830693 | ||||||
chr2:108830722
|
C | T | 101 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0003others(98): Show | 101 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(98): Show |
intron_variant | MODIFIER | c.1207-8463C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108830722 | ||||||
chr2:108830736
|
A | C | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1207-8449A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108830736 | ||||||
chr2:108830874
|
A | C | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1207-8311A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108830874 | ||||||
chr2:108830880
|
G | A | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-8305G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108830880 | ||||||
chr2:108831059
|
C | T | 27 | a0001c0005t0001g0112a0001c0005t0001g0113a0001c0005t0001g0114others(24): Show | 27 | HG01243.hp2 HG02055.hp1 HG02145.hp1 others(24): Show |
intron_variant | MODIFIER | c.1207-8126C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831059 | ||||||
chr2:108831100
|
C | T | 1 | a0001c0001t0002g0054 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1207-8085C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831100 | ||||||
chr2:108831151
|
C | G | 5 | a0004c0007t0002g0122a0004c0007t0002g0123a0004c0007t0002g0124others(2): Show | 5 | HG03471.hp1 HG03486.hp2 HG03579.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-8034C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831151 | ||||||
chr2:108831178
|
CA | C | 28 | a0001c0001t0001g0029a0001c0001t0002g0083a0001c0005t0001g0112others(25): Show | 28 | HG01243.hp2 HG02055.hp1 HG02145.hp1 others(25): Show |
intron_variant | MODIFIER | c.1207-7998delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108831178 | |||||
chr2:108831210
|
G | A | 186 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(183): Show | 188 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(185): Show |
intron_variant | MODIFIER | c.1207-7975G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831210 | ||||||
chr2:108831331
|
T | G | 17 | a0001c0001t0001g0079a0001c0001t0002g0018a0001c0001t0002g0075others(14): Show | 17 | HG01074.hp1 HG01167.hp2 HG01175.hp1 others(14): Show |
intron_variant | MODIFIER | c.1207-7854T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831331 | ||||||
chr2:108831420
|
A | G | 1 | a0002c0002t0003g0191 | 1 | HG02559.hp1 | intron_variant | MODIFIER | c.1207-7765A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831420 | ||||||
chr2:108831700
|
T | TCTTC | 28 | a0001c0001t0002g0003a0001c0001t0002g0019a0001c0001t0002g0071others(25): Show | 28 | HG01261.hp2 HG01358.hp2 HG01361.hp2 others(25): Show |
intron_variant | MODIFIER | c.1207-7451_1207-744 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108831700 | |||||
chr2:108831700
|
T | TCTTCCTT others(1): Show |
29 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0079others(26): Show | 29 | HG00099.hp1 HG00741.hp2 HG01074.hp1 others(26): Show |
intron_variant | MODIFIER | c.1207-7455_1207-744 others(12): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108831700 | |||||
chr2:108831700
|
T | TCTTCCTT others(5): Show |
65 | a0001c0001t0002g0001a0001c0001t0002g0004a0001c0001t0002g0006others(62): Show | 66 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(63): Show |
intron_variant | MODIFIER | c.1207-7459_1207-744 others(16): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108831700 | |||||
chr2:108831700
|
T | TCTTCCTT others(9): Show |
35 | a0001c0001t0002g0016a0001c0001t0002g0023a0001c0001t0002g0027others(32): Show | 36 | HG01081.hp2 HG01109.hp2 HG01175.hp1 others(33): Show |
intron_variant | MODIFIER | c.1207-7463_1207-744 others(20): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108831700 | |||||
chr2:108831700
|
T | TCTTCCTT others(13): Show |
10 | a0001c0001t0001g0029a0001c0001t0002g0008a0001c0001t0002g0070others(7): Show | 10 | HG01167.hp2 HG02451.hp1 HG02717.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207-7467_1207-744 others(24): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108831700 | |||||
chr2:108831700
|
T | TCTTCCTT others(17): Show |
26 | a0001c0004t0001g0012a0001c0004t0001g0013a0001c0004t0001g0014others(23): Show | 26 | HG01243.hp1 HG01261.hp1 HG02523.hp1 others(23): Show |
intron_variant | MODIFIER | c.1207-7471_1207-744 others(28): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108831700 | |||||
chr2:108831700
|
T | TCTTCCTT others(21): Show |
7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0107others(4): Show | 7 | HG02055.hp1 HG02258.hp2 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.1207-7475_1207-744 others(32): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108831700 | |||||
chr2:108831700
|
TCTTC | T | 4 | a0001c0001t0002g0092a0001c0001t0002g0093a0001c0001t0002g0094others(1): Show | 4 | HG02818.hp2 HG03471.hp2 HG03579.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207-7451_1207-744 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108831700 | |||||
chr2:108831785
|
C | T | 9 | a0001c0001t0001g0029a0002c0002t0001g0134a0002c0002t0001g0168others(6): Show | 9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207-7400C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831785 | ||||||
chr2:108831809
|
T | G | 1 | a0003c0003t0001g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1207-7376T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831809 | ||||||
chr2:108831857
|
C | T | 4 | a0002c0002t0001g0167a0003c0003t0001g0159a0003c0003t0001g0160others(1): Show | 4 | HG02622.hp2 HG02723.hp2 HG03098.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207-7328C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831857 | ||||||
chr2:108831985
|
G | A | 7 | a0003c0003t0001g0146a0003c0003t0001g0147a0003c0003t0001g0150others(4): Show | 7 | HG00099.hp2 HG00738.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-7200G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831985 | ||||||
chr2:108831992
|
C | T | 1 | a0003c0003t0001g0148 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.1207-7193C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108831992 | ||||||
chr2:108832024
|
C | T | 1 | a0002c0002t0001g0134 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1207-7161C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832024 | ||||||
chr2:108832107
|
T | G | 204 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1207-7078T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832107 | ||||||
chr2:108832170
|
C | T | 4 | a0002c0002t0001g0175a0002c0002t0001g0176a0002c0002t0001g0177others(1): Show | 4 | HG02451.hp2 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207-7015C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832170 | ||||||
chr2:108832173
|
G | T | 4 | a0001c0004t0001g0103a0001c0004t0001g0104a0001c0004t0001g0105others(1): Show | 4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1207-7012G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832173 | ||||||
chr2:108832216
|
G | A | 2 | a0001c0004t0001g0009a0001c0004t0001g0011 | 2 | HG03041.hp1 HG03516.hp1 |
intron_variant | MODIFIER | c.1207-6969G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832216 | ||||||
chr2:108832336
|
ATTTC | A | 5 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-6841_1207-683 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108832336 | |||||
chr2:108832344
|
C | CT | 12 | a0001c0001t0001g0029a0001c0004t0001g0014a0002c0002t0001g0134others(9): Show | 12 | HG01099.hp1 HG01993.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.1207-6821dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108832344 | |||||
chr2:108832344
|
CT | C | 79 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0002g0033others(76): Show | 80 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(77): Show |
intron_variant | MODIFIER | c.1207-6821delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108832344 | |||||
chr2:108832348
|
T | C | 2 | a0001c0001t0002g0031a0002c0002t0001g0182 | 2 | NA18988.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.1207-6837T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832348 | ||||||
chr2:108832349
|
T | C | 14 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(11): Show | 14 | HG01261.hp1 HG02055.hp2 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.1207-6836T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832349 | ||||||
chr2:108832425
|
G | A | 9 | a0001c0001t0001g0029a0002c0002t0001g0134a0002c0002t0001g0168others(6): Show | 9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207-6760G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832425 | ||||||
chr2:108832479
|
C | G | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-6706C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832479 | ||||||
chr2:108832530
|
A | G | 8 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1207-6655A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832530 | ||||||
chr2:108832766
|
A | C | 1 | a0001c0005t0001g0218 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1207-6419A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832766 | ||||||
chr2:108832796
|
T | C | 9 | a0001c0001t0001g0029a0002c0002t0001g0134a0002c0002t0001g0168others(6): Show | 9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207-6389T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832796 | ||||||
chr2:108832814
|
A | G | 1 | a0001c0001t0002g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1207-6371A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832814 | ||||||
chr2:108832935
|
A | C | 5 | a0001c0004t0001g0109a0001c0004t0001g0110a0001c0004t0001g0111others(2): Show | 5 | HG02055.hp2 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1207-6250A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832935 | ||||||
chr2:108832998
|
C | A | 185 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0001others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1207-6187C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108832998 | ||||||
chr2:108833317
|
G | A | 1 | a0003c0003t0001g0146 | 1 | HG01168.hp2 | intron_variant | MODIFIER | c.1207-5868G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108833317 | ||||||
chr2:108833418
|
T | A | 7 | a0003c0003t0001g0146a0003c0003t0001g0147a0003c0003t0001g0150others(4): Show | 7 | HG00099.hp2 HG00738.hp1 HG01168.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-5767T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108833418 | ||||||
chr2:108833546
|
A | G | 1 | a0002c0002t0001g0176 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1207-5639A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108833546 | ||||||
chr2:108833726
|
CT | C | 188 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0001t0002g0001others(185): Show | 190 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(187): Show |
intron_variant | MODIFIER | c.1207-5440delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108833726 | |||||
chr2:108833726
|
CTT | C | 11 | a0001c0001t0002g0024a0001c0001t0002g0073a0001c0005t0001g0114others(8): Show | 11 | HG02145.hp1 HG02280.hp1 HG02559.hp2 others(8): Show |
intron_variant | MODIFIER | c.1207-5441_1207-544 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108833726 | |||||
chr2:108833770
|
C | G | 7 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1207-5415C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108833770 | ||||||
chr2:108833889
|
G | A | 9 | a0001c0001t0001g0029a0002c0002t0001g0134a0002c0002t0001g0168others(6): Show | 9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207-5296G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108833889 | ||||||
chr2:108833894
|
A | AT | 134 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0003others(131): Show | 136 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(133): Show |
intron_variant | MODIFIER | c.1207-5267dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108833894 | |||||
chr2:108833894
|
A | ATT | 36 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0079others(33): Show | 36 | HG00741.hp2 HG01175.hp1 HG01257.hp1 others(33): Show |
intron_variant | MODIFIER | c.1207-5268_1207-526 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108833894 | |||||
chr2:108833894
|
A | ATTT | 13 | a0001c0001t0002g0025a0001c0001t0002g0060a0001c0004t0001g0107others(10): Show | 13 | HG01175.hp2 HG01884.hp1 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.1207-5269_1207-526 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108833894 | |||||
chr2:108833894
|
A | ATTTT | 5 | a0001c0004t0001g0109a0001c0004t0001g0110a0001c0004t0001g0111others(2): Show | 5 | HG02055.hp2 HG03195.hp1 HG03225.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-5270_1207-526 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108833894 | |||||
chr2:108833894
|
AT | A | 5 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02897.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-5267delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108833894 | |||||
chr2:108833894
|
ATTTTTTT | A | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-5273_1207-526 others(11): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108833894 | |||||
chr2:108834048
|
T | C | 104 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0003others(101): Show | 105 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(102): Show |
intron_variant | MODIFIER | c.1207-5137T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108834048 | ||||||
chr2:108834214
|
A | AT | 43 | a0001c0001t0002g0072a0001c0004t0001g0107a0001c0004t0001g0108others(40): Show | 44 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(41): Show |
intron_variant | MODIFIER | c.1207-4955dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108834214 | |||||
chr2:108834215
|
T | A | 1 | a0002c0002t0001g0168 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1207-4970T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108834215 | ||||||
chr2:108834215
|
T | TTTTTTTT others(5997): Show |
6 | a0001c0004t0001g0011a0001c0004t0001g0012a0001c0004t0001g0013others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207-4959_1207-495 others(6008): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108834215 | |||||
chr2:108834215
|
T | TTTTTTTT others(5998): Show |
1 | a0001c0004t0001g0009 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.1207-4959_1207-495 others(6009): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108834215 | |||||
chr2:108834274
|
G | A | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-4911G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108834274 | ||||||
chr2:108834460
|
A | G | 204 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1207-4725A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108834460 | ||||||
chr2:108834461
|
C | T | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-4724C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108834461 | ||||||
chr2:108834662
|
A | G | 38 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(35): Show | 38 | HG00408.hp1 HG01081.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1207-4523A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108834662 | ||||||
chr2:108834758
|
C | T | 1 | a0002c0002t0001g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1207-4427C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108834758 | ||||||
chr2:108834801
|
A | G | 51 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(48): Show | 52 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1207-4384A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108834801 | ||||||
chr2:108834982
|
T | C | 1 | a0001c0005t0001g0212 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1207-4203T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108834982 | ||||||
chr2:108835089
|
A | G | 51 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(48): Show | 52 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(49): Show |
intron_variant | MODIFIER | c.1207-4096A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108835089 | ||||||
chr2:108835094
|
G | T | 170 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0003others(167): Show | 172 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(169): Show |
intron_variant | MODIFIER | c.1207-4091G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108835094 | ||||||
chr2:108835174
|
CATT | C | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1207-4009_1207-400 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108835174 | |||||
chr2:108835264
|
T | G | 1 | a0001c0001t0002g0064 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1207-3921T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108835264 | ||||||
chr2:108835301
|
T | A | 6 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(3): Show | 6 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207-3884T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108835301 | ||||||
chr2:108835651
|
C | T | 1 | a0002c0002t0001g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1207-3534C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108835651 | ||||||
chr2:108835754
|
A | G | 6 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(3): Show | 6 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1207-3431A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108835754 | ||||||
chr2:108835862
|
T | C | 1 | a0002c0002t0001g0192 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1207-3323T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108835862 | ||||||
chr2:108835972
|
G | A | 9 | a0001c0001t0001g0029a0002c0002t0001g0134a0002c0002t0001g0168others(6): Show | 9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207-3213G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108835972 | ||||||
chr2:108836045
|
G | A | 1 | a0001c0005t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1207-3140G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836045 | ||||||
chr2:108836082
|
G | A | 1 | a0003c0003t0001g0164 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1207-3103G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836082 | ||||||
chr2:108836110
|
A | G | 104 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0003others(101): Show | 105 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(102): Show |
intron_variant | MODIFIER | c.1207-3075A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836110 | ||||||
chr2:108836357
|
A | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1207-2828A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836357 | ||||||
chr2:108836417
|
G | C | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-2768G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836417 | ||||||
chr2:108836481
|
T | C | 1 | a0001c0004t0001g0014 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.1207-2704T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836481 | ||||||
chr2:108836487
|
G | A | 1 | a0001c0006t0001g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1207-2698G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836487 | ||||||
chr2:108836629
|
T | C | 17 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0005t0001g0112others(14): Show | 17 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1207-2556T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836629 | ||||||
chr2:108836936
|
A | G | 1 | a0002c0002t0001g0171 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.1207-2249A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836936 | ||||||
chr2:108836978
|
C | T | 1 | a0002c0002t0001g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1207-2207C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836978 | ||||||
chr2:108836985
|
T | A | 1 | a0001c0001t0002g0082 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.1207-2200T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108836985 | ||||||
chr2:108837084
|
G | A | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1207-2101G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837084 | ||||||
chr2:108837099
|
G | A | 2 | a0001c0004t0001g0101a0001c0004t0001g0102 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1207-2086G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837099 | ||||||
chr2:108837102
|
T | C | 185 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0001others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1207-2083T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837102 | ||||||
chr2:108837248
|
G | C | 39 | a0002c0002t0001g0167a0002c0002t0001g0173a0002c0002t0001g0174others(36): Show | 40 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1207-1937G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837248 | ||||||
chr2:108837268
|
C | T | 1 | a0001c0006t0001g0205 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.1207-1917C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837268 | ||||||
chr2:108837296
|
G | A | 45 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(42): Show | 46 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(43): Show |
intron_variant | MODIFIER | c.1207-1889G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837296 | ||||||
chr2:108837419
|
C | T | 1 | a0003c0003t0001g0139 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.1207-1766C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837419 | ||||||
chr2:108837653
|
A | G | 217 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(214): Show | 219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.1207-1532A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837653 | ||||||
chr2:108837922
|
C | T | 8 | a0001c0001t0002g0062a0001c0004t0001g0009a0001c0004t0001g0011others(5): Show | 8 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1207-1263C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837922 | ||||||
chr2:108837924
|
AT | A | 10 | a0001c0001t0002g0064a0001c0004t0001g0107a0001c0004t0001g0108others(7): Show | 10 | HG01257.hp1 HG01257.hp2 HG02055.hp2 others(7): Show |
intron_variant | MODIFIER | c.1207-1247delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr2 | 108837924 | |||||
chr2:108837978
|
C | T | 1 | a0002c0002t0001g0207 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1207-1207C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108837978 | ||||||
chr2:108838219
|
C | T | 3 | a0002c0002t0001g0173a0002c0002t0001g0174a0002c0002t0001g0178 | 3 | HG01891.hp2 HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1207-966C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108838219 | ||||||
chr2:108838269
|
C | G | 5 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1207-916C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108838269 | ||||||
chr2:108838377
|
C | T | 8 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(5): Show | 8 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1207-808C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108838377 | ||||||
chr2:108838583
|
C | T | 9 | a0001c0001t0001g0029a0002c0002t0001g0134a0002c0002t0001g0168others(6): Show | 9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1207-602C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108838583 | ||||||
chr2:108838705
|
A | T | 1 | a0003c0003t0001g0184 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1207-480A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108838705 | ||||||
chr2:108838900
|
T | C | 1 | a0001c0001t0002g0034 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1207-285T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 10/14 | chr2 | 108838900 | ||||||
chr2:108839360
|
T | A | 5 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1323+59T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108839360 | ||||||
chr2:108839723
|
A | T | 9 | a0001c0001t0001g0029a0002c0002t0001g0134a0002c0002t0001g0168others(6): Show | 9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1323+422A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108839723 | ||||||
chr2:108839907
|
G | A | 9 | a0001c0001t0001g0029a0002c0002t0001g0134a0002c0002t0001g0168others(6): Show | 9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1323+606G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108839907 | ||||||
chr2:108840313
|
CTT | C | 5 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1323+1014_1323+101 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108840313 | |||||
chr2:108840507
|
GT | G | 2 | a0001c0001t0002g0048a0001c0001t0002g0053 | 2 | NA18985.hp1 NA18998.hp2 |
intron_variant | MODIFIER | c.1323+1208delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108840507 | |||||
chr2:108840540
|
C | G | 136 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0003others(133): Show | 137 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(134): Show |
intron_variant | MODIFIER | c.1323+1239C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108840540 | ||||||
chr2:108840607
|
G | A | 1 | a0003c0003t0001g0184 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1323+1306G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108840607 | ||||||
chr2:108840693
|
T | A | 5 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0087others(2): Show | 5 | HG00741.hp2 HG01515.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1323+1392T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108840693 | ||||||
chr2:108840782
|
T | C | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1323+1481T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108840782 | ||||||
chr2:108840784
|
A | ATTTCTTT others(1): Show |
42 | a0001c0001t0002g0001a0001c0001t0002g0008a0001c0001t0002g0035others(39): Show | 43 | HG00738.hp2 HG00741.hp1 HG01074.hp2 others(40): Show |
intron_variant | MODIFIER | c.1323+1509_1323+151 others(12): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108840784 | |||||
chr2:108840784
|
ATTTCTTT others(1): Show |
A | 21 | a0001c0001t0002g0060a0001c0004t0001g0107a0001c0004t0001g0108others(18): Show | 21 | HG01261.hp1 HG01884.hp1 HG02055.hp2 others(18): Show |
intron_variant | MODIFIER | c.1323+1509_1323+151 others(12): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108840784 | |||||
chr2:108840964
|
A | G | 1 | a0002c0002t0001g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1323+1663A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108840964 | ||||||
chr2:108840993
|
G | T | 15 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(12): Show | 15 | HG01261.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1323+1692G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108840993 | ||||||
chr2:108841003
|
T | G | 1 | a0001c0001t0002g0073 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.1323+1702T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841003 | ||||||
chr2:108841004
|
T | TTTTG | 10 | a0001c0004t0002g0097a0001c0004t0002g0099a0001c0004t0002g0100others(7): Show | 10 | HG01243.hp2 HG02486.hp1 HG02559.hp2 others(7): Show |
intron_variant | MODIFIER | c.1323+1731_1323+173 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108841004 | |||||
chr2:108841004
|
TTTTGTTT others(1): Show |
T | 6 | a0001c0001t0002g0023a0001c0005t0001g0116a0001c0005t0001g0117others(3): Show | 6 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(3): Show |
intron_variant | MODIFIER | c.1323+1727_1323+173 others(12): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108841004 | |||||
chr2:108841108
|
T | C | 1 | a0001c0005t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1323+1807T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841108 | ||||||
chr2:108841237
|
G | T | 1 | a0001c0005t0001g0116 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1323+1936G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841237 | ||||||
chr2:108841306
|
A | G | 5 | a0001c0004t0001g0109a0001c0004t0001g0110a0001c0004t0001g0111others(2): Show | 5 | HG02055.hp2 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1323+2005A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841306 | ||||||
chr2:108841318
|
A | G | 39 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(36): Show | 40 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1323+2017A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841318 | ||||||
chr2:108841376
|
A | G | 17 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0005t0001g0112others(14): Show | 17 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1323+2075A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841376 | ||||||
chr2:108841513
|
A | C | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1323+2212A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841513 | ||||||
chr2:108841540
|
T | C | 1 | a0001c0005t0001g0116 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1323+2239T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841540 | ||||||
chr2:108841642
|
T | A | 2 | a0001c0005t0001g0112a0003c0003t0001g0140 | 2 | HG03041.hp2 NA19030.hp1 |
intron_variant | MODIFIER | c.1323+2341T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841642 | ||||||
chr2:108841662
|
C | T | 185 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0001others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1323+2361C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841662 | ||||||
chr2:108841784
|
C | T | 40 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(37): Show | 41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1323+2483C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108841784 | ||||||
chr2:108842016
|
G | C | 8 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1323+2715G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842016 | ||||||
chr2:108842072
|
C | T | 2 | a0003c0003t0001g0142a0003c0003t0001g0181 | 2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1323+2771C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842072 | ||||||
chr2:108842075
|
G | A | 34 | a0002c0002t0001g0167a0003c0003t0001g0002a0003c0003t0001g0121others(31): Show | 35 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1323+2774G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842075 | ||||||
chr2:108842117
|
T | C | 9 | a0001c0001t0001g0029a0002c0002t0001g0134a0002c0002t0001g0168others(6): Show | 9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1323+2816T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842117 | ||||||
chr2:108842132
|
A | G | 1 | a0001c0001t0002g0024 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1323+2831A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842132 | ||||||
chr2:108842185
|
A | G | 1 | a0002c0002t0001g0192 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.1323+2884A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842185 | ||||||
chr2:108842202
|
GT | G | 134 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0003others(131): Show | 135 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(132): Show |
intron_variant | MODIFIER | c.1323+2917delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108842202 | |||||
chr2:108842428
|
A | G | 2 | a0003c0003t0001g0121a0003c0003t0001g0153 | 2 | NA18974.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1323+3127A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842428 | ||||||
chr2:108842525
|
G | C | 4 | a0001c0004t0001g0103a0001c0004t0001g0104a0001c0004t0001g0105others(1): Show | 4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1323+3224G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842525 | ||||||
chr2:108842545
|
A | T | 40 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(37): Show | 41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1323+3244A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842545 | ||||||
chr2:108842901
|
G | A | 4 | a0001c0004t0001g0103a0001c0004t0001g0104a0001c0004t0001g0105others(1): Show | 4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1323+3600G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842901 | ||||||
chr2:108842955
|
AACC | A | 5 | a0002c0002t0001g0173a0002c0002t0001g0174a0002c0002t0001g0178others(2): Show | 5 | HG01109.hp2 HG01167.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1323+3657_1323+365 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108842955 | |||||
chr2:108842992
|
G | A | 204 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1323+3691G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108842992 | ||||||
chr2:108843118
|
A | G | 40 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(37): Show | 41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1324-3620A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843118 | ||||||
chr2:108843124
|
T | TTAGAGGA others(6042): Show |
1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1324-3600_1324-359 others(6053): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843124 | |||||
chr2:108843186
|
C | T | 5 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1324-3552C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843186 | ||||||
chr2:108843408
|
G | A | 1 | a0001c0010t0002g0068 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1324-3330G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843408 | ||||||
chr2:108843542
|
T | C | 204 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1324-3196T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843542 | ||||||
chr2:108843564
|
C | T | 8 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1324-3174C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843564 | ||||||
chr2:108843777
|
C | A | 4 | a0001c0001t0002g0031a0001c0001t0002g0049a0001c0001t0002g0072others(1): Show | 4 | NA18954.hp1 NA18959.hp2 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324-2961C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843777 | ||||||
chr2:108843844
|
T | TTGTG | 16 | a0001c0001t0001g0005a0001c0004t0001g0101a0001c0004t0001g0102others(13): Show | 16 | HG01243.hp2 HG01261.hp2 HG02040.hp2 others(13): Show |
intron_variant | MODIFIER | c.1324-2862_1324-285 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843844 | |||||
chr2:108843844
|
T | TTGTGTGT others(3): Show |
2 | a0001c0005t0001g0208a0001c0005t0001g0209 | 2 | HG02647.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.1324-2868_1324-285 others(14): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843844 | |||||
chr2:108843844
|
T | TTGTGTGT others(9): Show |
1 | a0003c0003t0001g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1324-2874_1324-285 others(20): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843844 | |||||
chr2:108843844
|
TTG | T | 15 | a0001c0001t0002g0001a0001c0001t0002g0016a0001c0001t0002g0025others(12): Show | 16 | HG00099.hp1 HG01074.hp2 HG01099.hp2 others(13): Show |
intron_variant | MODIFIER | c.1324-2860_1324-285 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843844 | |||||
chr2:108843844
|
TTGTGTG | T | 126 | a0001c0001t0001g0057a0001c0001t0002g0003a0001c0001t0002g0004others(123): Show | 127 | HG00099.hp2 HG00408.hp1 HG00408.hp2 others(124): Show |
intron_variant | MODIFIER | c.1324-2864_1324-285 others(10): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843844 | |||||
chr2:108843872
|
G | T | 6 | a0001c0001t0002g0016a0001c0001t0002g0025a0001c0001t0002g0037others(3): Show | 6 | HG01978.hp2 HG02615.hp2 HG03688.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324-2866G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843872 | ||||||
chr2:108843876
|
G | GTGTGTGT others(13): Show |
2 | a0001c0004t0001g0107a0001c0004t0001g0108 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1324-2859_1324-285 others(24): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843876 | |||||
chr2:108843876
|
G | GTGTGTGT others(11): Show |
4 | a0001c0004t0001g0111a0001c0006t0001g0201a0002c0002t0001g0127others(1): Show | 4 | HG02055.hp2 HG03130.hp1 HG03195.hp1 others(1): Show |
intron_variant | MODIFIER | c.1324-2859_1324-285 others(22): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843876 | |||||
chr2:108843876
|
G | GTGTGTGT others(9): Show |
8 | a0001c0004t0001g0109a0001c0004t0001g0110a0001c0006t0001g0199others(5): Show | 8 | HG01261.hp1 HG03225.hp2 HG03453.hp1 others(5): Show |
intron_variant | MODIFIER | c.1324-2859_1324-285 others(20): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843876 | |||||
chr2:108843876
|
G | GTGTGTGT others(7): Show |
2 | a0001c0004t0001g0105a0002c0002t0001g0195 | 2 | HG02717.hp2 HG02886.hp1 |
intron_variant | MODIFIER | c.1324-2859_1324-285 others(18): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843876 | |||||
chr2:108843876
|
G | GTGTGTGT others(5): Show |
11 | a0001c0001t0001g0029a0001c0004t0001g0103a0001c0004t0001g0104others(8): Show | 11 | HG01081.hp2 HG02523.hp1 HG02602.hp1 others(8): Show |
intron_variant | MODIFIER | c.1324-2859_1324-285 others(16): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843876 | |||||
chr2:108843876
|
G | GTGTGTGT others(1): Show |
10 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(7): Show | 10 | HG01109.hp2 HG01167.hp2 HG01891.hp2 others(7): Show |
intron_variant | MODIFIER | c.1324-2859_1324-285 others(12): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843876 | |||||
chr2:108843876
|
G | T | 146 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0003others(143): Show | 148 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(145): Show |
intron_variant | MODIFIER | c.1324-2862G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843876 | ||||||
chr2:108843878
|
G | C | 7 | a0001c0001t0002g0016a0001c0001t0002g0025a0001c0001t0002g0037others(4): Show | 7 | HG00099.hp1 HG01978.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324-2860G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843878 | ||||||
chr2:108843880
|
T | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1324-2858T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843880 | ||||||
chr2:108843882
|
C | G | 8 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1324-2856C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843882 | ||||||
chr2:108843884
|
T | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1324-2854T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843884 | ||||||
chr2:108843884
|
TTC | T | 5 | a0001c0001t0002g0016a0001c0001t0002g0025a0001c0001t0002g0067others(2): Show | 5 | HG00099.hp1 HG02615.hp2 HG03688.hp2 others(2): Show |
intron_variant | MODIFIER | c.1324-2852_1324-285 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843884 | |||||
chr2:108843886
|
C | CT | 57 | a0001c0001t0001g0057a0001c0001t0002g0003a0001c0001t0002g0004others(54): Show | 57 | HG00741.hp2 HG01081.hp2 HG01109.hp1 others(54): Show |
intron_variant | MODIFIER | c.1324-2830dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843886 | |||||
chr2:108843886
|
C | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1324-2852C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843886 | ||||||
chr2:108843886
|
CTT | C | 38 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(35): Show | 39 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(36): Show |
intron_variant | MODIFIER | c.1324-2831_1324-283 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108843886 | |||||
chr2:108843893
|
T | C | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1324-2845T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843893 | ||||||
chr2:108843915
|
G | A | 11 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(8): Show | 11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1324-2823G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843915 | ||||||
chr2:108843959
|
C | T | 1 | a0003c0003t0001g0184 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.1324-2779C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843959 | ||||||
chr2:108843990
|
A | T | 1 | a0002c0002t0001g0130 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.1324-2748A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108843990 | ||||||
chr2:108844062
|
A | C | 99 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0003others(96): Show | 100 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(97): Show |
intron_variant | MODIFIER | c.1324-2676A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108844062 | ||||||
chr2:108844132
|
A | T | 5 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1324-2606A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108844132 | ||||||
chr2:108844167
|
A | G | 2 | a0001c0004t0001g0107a0001c0004t0001g0108 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1324-2571A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108844167 | ||||||
chr2:108844177
|
C | T | 1 | a0001c0004t0001g0108 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1324-2561C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108844177 | ||||||
chr2:108844419
|
TG | T | 69 | a0001c0001t0001g0057a0001c0001t0002g0003a0001c0001t0002g0004others(66): Show | 69 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(66): Show |
intron_variant | MODIFIER | c.1324-2317delG | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108844419 | |||||
chr2:108844433
|
G | A | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324-2305G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108844433 | ||||||
chr2:108844748
|
A | AT | 6 | a0001c0001t0002g0016a0001c0001t0002g0032a0001c0001t0002g0043others(3): Show | 6 | HG01978.hp1 HG01978.hp2 HG02055.hp2 others(3): Show |
intron_variant | MODIFIER | c.1324-1973dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108844748 | |||||
chr2:108844748
|
A | ATT | 10 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(7): Show | 10 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(7): Show |
intron_variant | MODIFIER | c.1324-1974_1324-197 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108844748 | |||||
chr2:108844748
|
AT | A | 46 | a0001c0001t0002g0001a0001c0001t0002g0051a0001c0001t0002g0052others(43): Show | 48 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1324-1973delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108844748 | |||||
chr2:108844772
|
G | C | 3 | a0003c0003t0001g0142a0003c0003t0001g0181a0003c0003t0001g0184 | 3 | HG00738.hp2 HG00741.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1324-1966G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108844772 | ||||||
chr2:108844971
|
A | C | 185 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0001others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1324-1767A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108844971 | ||||||
chr2:108844975
|
T | C | 1 | a0001c0001t0002g0020 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1324-1763T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108844975 | ||||||
chr2:108845158
|
T | C | 1 | a0003c0003t0001g0121 | 1 | NA18974.hp2 | intron_variant | MODIFIER | c.1324-1580T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108845158 | ||||||
chr2:108845218
|
T | A | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324-1520T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108845218 | ||||||
chr2:108845367
|
C | T | 1 | a0001c0005t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1324-1371C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108845367 | ||||||
chr2:108845571
|
AT | A | 182 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0079others(179): Show | 184 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(181): Show |
intron_variant | MODIFIER | c.1324-1149delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108845571 | |||||
chr2:108845664
|
C | T | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324-1074C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108845664 | ||||||
chr2:108845665
|
G | A | 1 | a0006c0008t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1324-1073G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108845665 | ||||||
chr2:108845712
|
T | C | 185 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0001others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1324-1026T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108845712 | ||||||
chr2:108845817
|
T | C | 204 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1324-921T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108845817 | ||||||
chr2:108846060
|
A | T | 204 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1324-678A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108846060 | ||||||
chr2:108846195
|
T | C | 1 | a0002c0002t0001g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1324-543T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108846195 | ||||||
chr2:108846205
|
A | G | 2 | a0001c0001t0002g0056a0001c0001t0002g0074 | 2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1324-533A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108846205 | ||||||
chr2:108846221
|
A | C | 103 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0003others(100): Show | 104 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(101): Show |
intron_variant | MODIFIER | c.1324-517A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108846221 | ||||||
chr2:108846281
|
TTTAAGTT others(44): Show |
T | 1 | a0003c0003t0001g0140 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.1324-453_1324-403d others(53): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108846281 | |||||
chr2:108846336
|
G | A | 1 | a0002c0002t0003g0193 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.1324-402G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108846336 | ||||||
chr2:108846339
|
A | G | 1 | a0005c0009t0001g0165 | 1 | HG02523.hp1 | intron_variant | MODIFIER | c.1324-399A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108846339 | ||||||
chr2:108846442
|
G | T | 1 | a0008c0015t0001g0194 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1324-296G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108846442 | ||||||
chr2:108846516
|
G | GA | 10 | a0001c0001t0002g0067a0001c0001t0002g0078a0001c0004t0002g0097others(7): Show | 10 | HG00099.hp1 HG00738.hp2 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.1324-208dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | INFO_REALIGN_3_PRIME | chr2 | 108846516 | |||||
chr2:108846521
|
A | T | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324-217A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108846521 | ||||||
chr2:108846633
|
C | T | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1324-105C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 11/14 | chr2 | 108846633 | ||||||
chr2:108847148
|
G | A | 3 | a0003c0003t0001g0142a0003c0003t0001g0181a0003c0003t0001g0184 | 3 | HG00738.hp2 HG00741.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1516+218G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108847148 | ||||||
chr2:108847160
|
A | G | 15 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(12): Show | 15 | HG01261.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1516+230A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108847160 | ||||||
chr2:108847318
|
A | T | 118 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0003others(115): Show | 119 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(116): Show |
intron_variant | MODIFIER | c.1516+388A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108847318 | ||||||
chr2:108847351
|
T | C | 10 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0005t0001g0210others(7): Show | 10 | HG02145.hp1 HG02257.hp1 HG02280.hp1 others(7): Show |
intron_variant | MODIFIER | c.1516+421T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108847351 | ||||||
chr2:108847419
|
G | A | 40 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(37): Show | 41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1516+489G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108847419 | ||||||
chr2:108847484
|
A | C | 6 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0045others(3): Show | 6 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1516+554A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108847484 | ||||||
chr2:108848058
|
A | G | 7 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1516+1128A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108848058 | ||||||
chr2:108848096
|
C | T | 1 | a0001c0001t0002g0064 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.1516+1166C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108848096 | ||||||
chr2:108848247
|
A | G | 1 | a0002c0002t0001g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1516+1317A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108848247 | ||||||
chr2:108848488
|
A | T | 8 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1516+1558A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108848488 | ||||||
chr2:108848553
|
C | T | 2 | a0002c0002t0001g0172a0002c0002t0001g0192 | 2 | HG01261.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.1516+1623C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108848553 | ||||||
chr2:108848615
|
A | C | 11 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(8): Show | 11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1516+1685A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108848615 | ||||||
chr2:108848678
|
C | T | 5 | a0002c0002t0001g0173a0002c0002t0001g0174a0002c0002t0001g0178others(2): Show | 5 | HG01109.hp2 HG01167.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1516+1748C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108848678 | ||||||
chr2:108848747
|
A | G | 1 | a0001c0001t0001g0029 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1516+1817A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108848747 | ||||||
chr2:108848782
|
T | C | 59 | a0001c0001t0001g0057a0001c0001t0002g0003a0001c0001t0002g0004others(56): Show | 59 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(56): Show |
intron_variant | MODIFIER | c.1516+1852T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108848782 | ||||||
chr2:108849152
|
A | G | 2 | a0001c0001t0001g0005a0001c0001t0001g0079 | 2 | HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1516+2222A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108849152 | ||||||
chr2:108849544
|
G | A | 18 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(15): Show | 18 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(15): Show |
intron_variant | MODIFIER | c.1516+2614G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108849544 | ||||||
chr2:108849564
|
T | C | 1 | a0001c0001t0002g0055 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.1516+2634T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108849564 | ||||||
chr2:108849625
|
C | A | 11 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(8): Show | 11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1516+2695C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108849625 | ||||||
chr2:108849715
|
G | C | 34 | a0002c0002t0001g0167a0003c0003t0001g0002a0003c0003t0001g0121others(31): Show | 35 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1516+2785G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108849715 | ||||||
chr2:108849735
|
C | G | 1 | a0001c0005t0001g0212 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.1516+2805C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108849735 | ||||||
chr2:108849744
|
C | T | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1516+2814C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108849744 | ||||||
chr2:108849985
|
G | A | 17 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0005t0001g0112others(14): Show | 17 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1516+3055G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108849985 | ||||||
chr2:108850030
|
C | T | 1 | a0001c0006t0001g0204 | 1 | NA18959.hp1 | intron_variant | MODIFIER | c.1516+3100C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108850030 | ||||||
chr2:108850589
|
T | C | 17 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0005t0001g0112others(14): Show | 17 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1516+3659T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108850589 | ||||||
chr2:108850672
|
C | T | 2 | a0001c0001t0002g0056a0001c0001t0002g0074 | 2 | HG02258.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1516+3742C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108850672 | ||||||
chr2:108850742
|
C | T | 1 | a0003c0003t0001g0162 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1516+3812C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108850742 | ||||||
chr2:108850841
|
CAGA | C | 5 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1516+3918_1516+392 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108850841 | |||||
chr2:108850893
|
G | A | 1 | a0001c0001t0002g0059 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.1516+3963G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108850893 | ||||||
chr2:108850955
|
C | G | 1 | a0001c0004t0001g0106 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1516+4025C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108850955 | ||||||
chr2:108851595
|
G | GC | 11 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(8): Show | 11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1516+4668dupC | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108851595 | |||||
chr2:108851598
|
C | T | 1 | a0001c0004t0001g0103 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.1516+4668C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108851598 | ||||||
chr2:108851600
|
G | A | 1 | a0001c0001t0002g0066 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1516+4670G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108851600 | ||||||
chr2:108851611
|
G | T | 3 | a0004c0007t0002g0124a0004c0007t0002g0125a0004c0007t0002g0126 | 3 | HG03579.hp2 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1516+4681G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108851611 | ||||||
chr2:108851612
|
G | C | 3 | a0004c0007t0002g0124a0004c0007t0002g0125a0004c0007t0002g0126 | 3 | HG03579.hp2 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1516+4682G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108851612 | ||||||
chr2:108851680
|
G | A | 1 | a0002c0002t0003g0187 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.1516+4750G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108851680 | ||||||
chr2:108851994
|
C | T | 1 | a0001c0010t0002g0068 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1517-4800C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108851994 | ||||||
chr2:108852171
|
A | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1517-4623A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108852171 | ||||||
chr2:108852314
|
T | A | 6 | a0003c0003t0001g0002a0003c0003t0001g0141a0003c0003t0001g0148others(3): Show | 7 | NA18968.hp2 NA18977.hp2 NA18993.hp2 others(4): Show |
intron_variant | MODIFIER | c.1517-4480T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108852314 | ||||||
chr2:108852384
|
A | G | 1 | a0002c0002t0001g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1517-4410A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108852384 | ||||||
chr2:108852386
|
A | G | 39 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(36): Show | 40 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1517-4408A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108852386 | ||||||
chr2:108852550
|
A | G | 1 | a0002c0002t0001g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1517-4244A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108852550 | ||||||
chr2:108852807
|
C | G | 102 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(99): Show | 103 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(100): Show |
intron_variant | MODIFIER | c.1517-3987C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108852807 | ||||||
chr2:108852877
|
G | T | 199 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(196): Show | 201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.1517-3917G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108852877 | ||||||
chr2:108852939
|
A | T | 1 | a0002c0002t0001g0172 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1517-3855A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108852939 | ||||||
chr2:108853019
|
C | T | 3 | a0004c0007t0002g0124a0004c0007t0002g0125a0004c0007t0002g0126 | 3 | HG03579.hp2 NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1517-3775C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853019 | ||||||
chr2:108853093
|
G | A | 1 | a0001c0001t0002g0004 | 1 | NA18993.hp1 | intron_variant | MODIFIER | c.1517-3701G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853093 | ||||||
chr2:108853176
|
A | G | 1 | a0003c0003t0001g0138 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.1517-3618A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853176 | ||||||
chr2:108853295
|
G | A | 5 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1517-3499G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853295 | ||||||
chr2:108853528
|
C | CT | 22 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0060others(19): Show | 22 | HG01081.hp2 HG02055.hp1 HG02055.hp2 others(19): Show |
intron_variant | MODIFIER | c.1517-3252dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853528 | |||||
chr2:108853528
|
CT | C | 11 | a0001c0001t0002g0017a0001c0001t0002g0033a0001c0001t0002g0045others(8): Show | 11 | HG01168.hp1 HG01261.hp1 HG02040.hp2 others(8): Show |
intron_variant | MODIFIER | c.1517-3252delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853528 | |||||
chr2:108853563
|
A | G | 1 | a0001c0005t0001g0116 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1517-3231A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853563 | ||||||
chr2:108853592
|
G | C | 2 | a0003c0003t0001g0121a0003c0003t0001g0153 | 2 | NA18974.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1517-3202G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853592 | ||||||
chr2:108853641
|
C | T | 14 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0004t0001g0103others(11): Show | 14 | HG01081.hp2 HG02055.hp1 HG02523.hp1 others(11): Show |
intron_variant | MODIFIER | c.1517-3153C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853641 | ||||||
chr2:108853643
|
C | G | 98 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(95): Show | 99 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(96): Show |
intron_variant | MODIFIER | c.1517-3151C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853643 | ||||||
chr2:108853730
|
T | C | 8 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1517-3064T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853730 | ||||||
chr2:108853879
|
A | G | 1 | a0001c0005t0001g0216 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.1517-2915A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853879 | ||||||
chr2:108853882
|
T | G | 1 | a0002c0002t0001g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1517-2912T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853882 | ||||||
chr2:108853891
|
G | A | 1 | a0002c0002t0001g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1517-2903G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853891 | ||||||
chr2:108853893
|
ATATATAT | A | 6 | a0001c0005t0001g0210a0001c0005t0001g0211a0001c0005t0001g0213others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1517-2887_1517-288 others(11): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853893 | |||||
chr2:108853901
|
T | A | 1 | a0002c0002t0001g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1517-2893T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853901 | ||||||
chr2:108853908
|
T | C | 11 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0051others(8): Show | 11 | HG01074.hp1 HG01358.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.1517-2886T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853908 | ||||||
chr2:108853914
|
G | A | 1 | a0006c0008t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2880G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853914 | ||||||
chr2:108853923
|
TTA | T | 17 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0005t0001g0112others(14): Show | 17 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1517-2864_1517-286 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853923 | |||||
chr2:108853924
|
T | A | 1 | a0006c0008t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2870T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853924 | ||||||
chr2:108853932
|
A | T | 1 | a0006c0008t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2862A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853932 | ||||||
chr2:108853933
|
T | A | 1 | a0006c0008t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2861T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853933 | ||||||
chr2:108853935
|
T | A | 1 | a0006c0008t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2859T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853935 | ||||||
chr2:108853948
|
C | T | 1 | a0006c0008t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2846C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853948 | ||||||
chr2:108853956
|
A | T | 1 | a0006c0008t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2838A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853956 | ||||||
chr2:108853965
|
A | ATATAATA others(6): Show |
1 | a0006c0008t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2829_1517-282 others(17): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853965 | ||||||
chr2:108853966
|
AAATATAT others(19): Show |
A | 1 | a0001c0001t0002g0049 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1517-2825_1517-280 others(30): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853966 | |||||
chr2:108853970
|
A | ATATATAA others(20): Show |
1 | a0002c0002t0001g0134 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.1517-2818_1517-279 others(31): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853970 | |||||
chr2:108853970
|
A | T | 1 | a0006c0008t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2824A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853970 | ||||||
chr2:108853976
|
A | AATATATA others(47): Show |
8 | a0001c0001t0001g0029a0001c0001t0001g0057a0002c0002t0001g0168others(5): Show | 8 | HG02523.hp1 HG03654.hp2 HG04204.hp1 others(5): Show |
intron_variant | MODIFIER | c.1517-2792_1517-279 others(58): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853976 | |||||
chr2:108853976
|
A | AATATATA others(20): Show |
3 | a0001c0005t0001g0115a0002c0002t0001g0172a0003c0003t0001g0140 | 3 | HG02040.hp2 NA19030.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.1517-2756_1517-273 others(31): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853976 | |||||
chr2:108853976
|
A | AATATATA others(47): Show |
2 | a0001c0004t0001g0101a0001c0004t0001g0102 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1517-2783_1517-273 others(58): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853976 | |||||
chr2:108853976
|
A | T | 1 | a0006c0008t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1517-2818A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853976 | ||||||
chr2:108853976
|
AATATATA others(20): Show |
A | 123 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(120): Show | 124 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(121): Show |
intron_variant | MODIFIER | c.1517-2756_1517-273 others(31): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853976 | |||||
chr2:108853976
|
AATATATA others(47): Show |
A | 1 | a0001c0004t0001g0108 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.1517-2783_1517-273 others(58): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108853976 | |||||
chr2:108853981
|
ATAATATA others(21): Show |
A | 39 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(36): Show | 40 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1517-2812_1517-278 others(32): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853981 | ||||||
chr2:108853997
|
T | A | 1 | a0001c0001t0002g0049 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1517-2797T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108853997 | ||||||
chr2:108854003
|
T | A | 1 | a0001c0001t0002g0049 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1517-2791T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108854003 | ||||||
chr2:108854003
|
T | TATATATA others(27): Show |
1 | a0001c0005t0001g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1517-2780_1517-274 others(38): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108854003 | |||||
chr2:108854029
|
TTATATAT others(22): Show |
T | 12 | a0001c0004t0001g0110a0002c0002t0001g0128a0002c0002t0001g0129others(9): Show | 12 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(9): Show |
intron_variant | MODIFIER | c.1517-2757_1517-272 others(33): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108854029 | |||||
chr2:108854066
|
T | A | 2 | a0001c0005t0001g0210a0001c0005t0001g0211 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1517-2728T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108854066 | ||||||
chr2:108854074
|
TA | T | 5 | a0001c0004t0001g0109a0001c0004t0001g0110a0001c0004t0001g0111others(2): Show | 5 | HG02055.hp2 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1517-2718delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108854074 | |||||
chr2:108854106
|
AATAT | A | 3 | a0002c0002t0001g0173a0002c0002t0001g0174a0002c0002t0001g0178 | 3 | HG01891.hp2 HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1517-2682_1517-267 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108854106 | |||||
chr2:108854111
|
A | G | 5 | a0002c0002t0001g0167a0003c0003t0001g0159a0003c0003t0001g0160others(2): Show | 5 | HG01891.hp1 HG02622.hp2 HG02723.hp2 others(2): Show |
intron_variant | MODIFIER | c.1517-2683A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108854111 | ||||||
chr2:108854292
|
G | A | 4 | a0001c0004t0002g0097a0001c0004t0002g0098a0001c0004t0002g0099others(1): Show | 4 | HG02486.hp1 HG02647.hp2 HG03195.hp2 others(1): Show |
intron_variant | MODIFIER | c.1517-2502G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108854292 | ||||||
chr2:108854392
|
TTTTG | T | 39 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(36): Show | 40 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1517-2390_1517-238 others(8): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108854392 | |||||
chr2:108854652
|
CAATTCTT others(3): Show |
C | 1 | a0001c0001t0002g0049 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1517-2141_1517-213 others(14): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108854652 | ||||||
chr2:108854682
|
C | G | 40 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(37): Show | 41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1517-2112C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108854682 | ||||||
chr2:108854861
|
G | A | 9 | a0001c0001t0001g0029a0002c0002t0001g0134a0002c0002t0001g0168others(6): Show | 9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1517-1933G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108854861 | ||||||
chr2:108854962
|
A | G | 1 | a0001c0005t0001g0113 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1517-1832A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108854962 | ||||||
chr2:108855338
|
A | G | 1 | a0002c0002t0001g0176 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.1517-1456A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108855338 | ||||||
chr2:108855487
|
T | TA | 16 | a0001c0001t0001g0029a0001c0001t0002g0077a0001c0001t0002g0092others(13): Show | 16 | HG01081.hp2 HG01884.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.1517-1294dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108855487 | |||||
chr2:108855645
|
A | G | 99 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0003others(96): Show | 100 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(97): Show |
intron_variant | MODIFIER | c.1517-1149A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108855645 | ||||||
chr2:108855774
|
A | G | 13 | a0001c0001t0001g0029a0001c0004t0001g0103a0001c0004t0001g0104others(10): Show | 13 | HG01081.hp2 HG02055.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1517-1020A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108855774 | ||||||
chr2:108855782
|
T | C | 2 | a0001c0005t0001g0210a0001c0005t0001g0211 | 2 | HG02145.hp1 HG03516.hp2 |
intron_variant | MODIFIER | c.1517-1012T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108855782 | ||||||
chr2:108855944
|
C | T | 40 | a0001c0004t0001g0198a0001c0005t0001g0116a0001c0005t0001g0117others(37): Show | 41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1517-850C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108855944 | ||||||
chr2:108855946
|
G | GT | 4 | a0001c0001t0002g0025a0001c0001t0002g0033a0001c0001t0002g0077others(1): Show | 4 | HG03516.hp2 HG03927.hp1 NA19081.hp1 others(1): Show |
intron_variant | MODIFIER | c.1517-840dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108855946 | |||||
chr2:108856026
|
A | T | 3 | a0002c0002t0001g0173a0002c0002t0001g0174a0002c0002t0001g0178 | 3 | HG01891.hp2 HG02257.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.1517-768A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108856026 | ||||||
chr2:108856132
|
A | G | 1 | a0001c0006t0001g0203 | 1 | NA18954.hp2 | intron_variant | MODIFIER | c.1517-662A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108856132 | ||||||
chr2:108856163
|
T | TG | 5 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(2): Show | 5 | HG01884.hp1 HG02280.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.1517-628dupG | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108856163 | |||||
chr2:108856215
|
A | G | 202 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(199): Show | 204 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.1517-579A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108856215 | ||||||
chr2:108856221
|
C | T | 8 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1517-573C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108856221 | ||||||
chr2:108856306
|
C | CTT | 204 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1517-487_1517-486d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | INFO_REALIGN_3_PRIME | chr2 | 108856306 | |||||
chr2:108856700
|
T | G | 1 | a0003c0003t0001g0164 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1517-94T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108856700 | ||||||
chr2:108856765
|
G | A | 1 | a0001c0004t0002g0098 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.1517-29G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 12/14 | chr2 | 108856765 | ||||||
chr2:108856983
|
G | A | 6 | a0001c0005t0001g0210a0001c0005t0001g0211a0001c0005t0001g0213others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1693+13G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108856983 | ||||||
chr2:108857066
|
C | CT | 17 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0004t0001g0009others(14): Show | 17 | HG01109.hp2 HG01891.hp2 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1693+127dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108857066 | |||||
chr2:108857066
|
C | CTT | 6 | a0001c0001t0001g0079a0001c0001t0002g0052a0001c0005t0001g0211others(3): Show | 6 | HG01884.hp2 HG02145.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.1693+126_1693+127d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108857066 | |||||
chr2:108857066
|
CT | C | 65 | a0001c0001t0001g0029a0001c0001t0002g0020a0001c0001t0002g0035others(62): Show | 66 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(63): Show |
intron_variant | MODIFIER | c.1693+127delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108857066 | |||||
chr2:108857066
|
CTT | C | 87 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(84): Show | 88 | HG00099.hp1 HG00408.hp1 HG01074.hp1 others(85): Show |
intron_variant | MODIFIER | c.1693+126_1693+127d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108857066 | |||||
chr2:108857066
|
CTTTTTTT others(5): Show |
C | 1 | a0001c0001t0002g0062 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.1693+116_1693+127d others(14): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108857066 | |||||
chr2:108857066
|
CTTTTTTT others(7): Show |
C | 1 | a0001c0004t0001g0106 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1693+114_1693+127d others(16): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108857066 | |||||
chr2:108857204
|
G | A | 1 | a0001c0001t0002g0034 | 1 | HG02040.hp1 | intron_variant | MODIFIER | c.1693+234G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108857204 | ||||||
chr2:108857349
|
G | A | 4 | a0001c0004t0001g0103a0001c0004t0001g0104a0001c0004t0001g0105others(1): Show | 4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1693+379G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108857349 | ||||||
chr2:108857365
|
G | A | 99 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(96): Show | 100 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(97): Show |
intron_variant | MODIFIER | c.1693+395G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108857365 | ||||||
chr2:108857506
|
C | T | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693+536C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108857506 | ||||||
chr2:108857699
|
A | G | 3 | a0001c0004t0002g0097a0001c0004t0002g0099a0001c0004t0002g0100 | 3 | HG02486.hp1 HG02647.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.1693+729A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108857699 | ||||||
chr2:108857756
|
G | C | 98 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(95): Show | 99 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(96): Show |
intron_variant | MODIFIER | c.1693+786G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108857756 | ||||||
chr2:108857894
|
T | C | 2 | a0002c0002t0002g0186a0002c0002t0002g0190 | 2 | HG01175.hp2 HG01257.hp1 |
intron_variant | MODIFIER | c.1693+924T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108857894 | ||||||
chr2:108857962
|
A | T | 7 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1693+992A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108857962 | ||||||
chr2:108858058
|
A | G | 1 | a0001c0001t0002g0020 | 1 | NA18969.hp2 | intron_variant | MODIFIER | c.1693+1088A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108858058 | ||||||
chr2:108858061
|
C | T | 11 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(8): Show | 11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1693+1091C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108858061 | ||||||
chr2:108858114
|
C | T | 7 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1693+1144C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108858114 | ||||||
chr2:108858361
|
C | CA | 6 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(3): Show | 6 | HG01243.hp1 HG02572.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1693+1399dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108858361 | |||||
chr2:108858621
|
C | T | 98 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(95): Show | 99 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(96): Show |
intron_variant | MODIFIER | c.1693+1651C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108858621 | ||||||
chr2:108858695
|
T | C | 11 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(8): Show | 11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1693+1725T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108858695 | ||||||
chr2:108858710
|
T | A | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693+1740T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108858710 | ||||||
chr2:108858746
|
T | C | 103 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0003others(100): Show | 104 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(101): Show |
intron_variant | MODIFIER | c.1693+1776T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108858746 | ||||||
chr2:108858912
|
A | C | 136 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0003others(133): Show | 137 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(134): Show |
intron_variant | MODIFIER | c.1693+1942A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108858912 | ||||||
chr2:108859053
|
T | C | 1 | a0003c0003t0001g0164 | 1 | HG01167.hp2 | intron_variant | MODIFIER | c.1693+2083T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108859053 | ||||||
chr2:108859058
|
C | T | 57 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0005t0001g0112others(54): Show | 58 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(55): Show |
intron_variant | MODIFIER | c.1693+2088C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108859058 | ||||||
chr2:108859059
|
G | A | 2 | a0001c0004t0001g0107a0001c0004t0001g0108 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1693+2089G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108859059 | ||||||
chr2:108859244
|
G | A | 1 | a0003c0003t0001g0152 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.1693+2274G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108859244 | ||||||
chr2:108859812
|
AT | A | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693+2854delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108859812 | |||||
chr2:108860011
|
A | G | 13 | a0001c0001t0001g0029a0001c0004t0001g0103a0001c0004t0001g0104others(10): Show | 13 | HG01081.hp2 HG02055.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1693+3041A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108860011 | ||||||
chr2:108860049
|
G | T | 1 | a0002c0002t0001g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1693+3079G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108860049 | ||||||
chr2:108860513
|
G | GT | 6 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(3): Show | 6 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(3): Show |
intron_variant | MODIFIER | c.1693+3556dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860513 | |||||
chr2:108860513
|
GT | G | 7 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(4): Show | 7 | HG01516.hp1 HG01884.hp1 HG02280.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693+3556delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860513 | |||||
chr2:108860607
|
C | G | 5 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0087others(2): Show | 5 | HG00741.hp2 HG01515.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1693+3637C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108860607 | ||||||
chr2:108860823
|
G | A | 5 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(2): Show | 5 | HG02615.hp1 HG02818.hp1 HG02896.hp2 others(2): Show |
intron_variant | MODIFIER | c.1693+3853G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108860823 | ||||||
chr2:108860867
|
A | G | 13 | a0001c0001t0001g0029a0001c0004t0001g0103a0001c0004t0001g0104others(10): Show | 13 | HG01081.hp2 HG02055.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1693+3897A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108860867 | ||||||
chr2:108860904
|
G | A | 1 | a0002c0002t0001g0133 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1693+3934G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108860904 | ||||||
chr2:108860935
|
C | CT | 64 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0079others(61): Show | 65 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(62): Show |
intron_variant | MODIFIER | c.1693+3988dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860935 | |||||
chr2:108860935
|
C | CTT | 15 | a0001c0005t0001g0113a0001c0005t0001g0114a0002c0002t0001g0128others(12): Show | 15 | HG01109.hp2 HG01167.hp2 HG01243.hp2 others(12): Show |
intron_variant | MODIFIER | c.1693+3987_1693+398 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860935 | |||||
chr2:108860935
|
C | CTTT | 8 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(5): Show | 8 | HG01243.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1693+3986_1693+398 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860935 | |||||
chr2:108860935
|
C | CTTTTTTT | 5 | a0001c0001t0002g0022a0001c0001t0002g0027a0001c0001t0002g0031others(2): Show | 5 | HG01515.hp2 NA18942.hp1 NA18959.hp2 others(2): Show |
intron_variant | MODIFIER | c.1693+3982_1693+398 others(11): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860935 | |||||
chr2:108860935
|
C | CTTTTTTT others(1): Show |
64 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(61): Show | 65 | HG00408.hp1 HG00741.hp2 HG01074.hp2 others(62): Show |
intron_variant | MODIFIER | c.1693+3981_1693+398 others(12): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860935 | |||||
chr2:108860935
|
C | CTTTTTTT others(2): Show |
21 | a0001c0001t0001g0057a0001c0001t0002g0006a0001c0001t0002g0018others(18): Show | 21 | HG00099.hp1 HG01074.hp1 HG01169.hp1 others(18): Show |
intron_variant | MODIFIER | c.1693+3980_1693+398 others(13): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860935 | |||||
chr2:108860935
|
C | CTTTTTTT others(3): Show |
4 | a0001c0001t0002g0019a0001c0001t0002g0066a0001c0001t0002g0071others(1): Show | 4 | HG01358.hp2 HG01361.hp2 HG01981.hp2 others(1): Show |
intron_variant | MODIFIER | c.1693+3979_1693+398 others(14): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860935 | |||||
chr2:108860935
|
C | CTTTTTTT others(4): Show |
2 | a0004c0007t0002g0124a0004c0007t0002g0125 | 2 | NA19043.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.1693+3978_1693+398 others(15): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860935 | |||||
chr2:108860935
|
C | CTTTTTTT others(5): Show |
1 | a0004c0007t0002g0126 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1693+3977_1693+398 others(16): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108860935 | |||||
chr2:108861144
|
T | A | 15 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(12): Show | 15 | HG01261.hp1 HG02055.hp2 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.1693+4174T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108861144 | ||||||
chr2:108861472
|
C | CT | 54 | a0001c0004t0001g0101a0001c0004t0001g0102a0001c0004t0001g0107others(51): Show | 55 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1693+4528dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | |||||
chr2:108861472
|
C | CTT | 23 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0004t0001g0011others(20): Show | 23 | HG00741.hp1 HG01243.hp1 HG01261.hp1 others(20): Show |
intron_variant | MODIFIER | c.1693+4527_1693+452 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | |||||
chr2:108861472
|
C | CTTT | 10 | a0001c0004t0001g0009a0001c0004t0001g0014a0001c0004t0001g0015others(7): Show | 10 | HG01243.hp2 HG02145.hp1 HG02572.hp1 others(7): Show |
intron_variant | MODIFIER | c.1693+4526_1693+452 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | |||||
chr2:108861472
|
C | CTTTTTTT others(3): Show |
2 | a0002c0002t0001g0169a0002c0002t0001g0170 | 2 | NA18955.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.1693+4519_1693+452 others(14): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | |||||
chr2:108861472
|
C | CTTTTTTT others(4): Show |
3 | a0002c0002t0001g0168a0002c0002t0001g0171a0005c0009t0001g0165 | 3 | HG02523.hp1 HG03654.hp2 NA18974.hp1 |
intron_variant | MODIFIER | c.1693+4518_1693+452 others(15): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | |||||
chr2:108861472
|
C | CTTTTTTT others(5): Show |
2 | a0001c0001t0001g0057a0006c0008t0001g0166 | 2 | HG02055.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1693+4517_1693+452 others(16): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | |||||
chr2:108861472
|
C | CTTTTTTT others(6): Show |
1 | a0001c0001t0001g0029 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1693+4516_1693+452 others(17): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | |||||
chr2:108861472
|
CT | C | 6 | a0002c0002t0001g0175a0002c0002t0001g0176a0002c0002t0001g0177others(3): Show | 6 | HG01099.hp1 HG02451.hp2 HG02698.hp2 others(3): Show |
intron_variant | MODIFIER | c.1693+4528delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | |||||
chr2:108861472
|
CTTTTTTT others(5): Show |
C | 1 | a0002c0002t0001g0195 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.1693+4517_1693+452 others(16): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | |||||
chr2:108861472
|
CTTTTTTT others(6): Show |
C | 3 | a0001c0001t0002g0027a0001c0001t0002g0035a0001c0001t0002g0065 | 3 | NA18942.hp1 NA18969.hp1 NA19011.hp2 |
intron_variant | MODIFIER | c.1693+4516_1693+452 others(17): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | |||||
chr2:108861472
|
CTTTTTTT others(7): Show |
C | 98 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(95): Show | 99 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(96): Show |
intron_variant | MODIFIER | c.1693+4515_1693+452 others(18): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | |||||
chr2:108861472
|
CTTTTTTT others(8): Show |
C | 1 | a0001c0001t0002g0045 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.1693+4514_1693+452 others(19): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108861472 | |||||
chr2:108861724
|
G | A | 8 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(5): Show | 8 | HG01243.hp1 HG02572.hp1 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.1693+4754G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108861724 | ||||||
chr2:108861771
|
G | A | 1 | a0002c0002t0001g0172 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.1693+4801G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108861771 | ||||||
chr2:108861886
|
T | C | 1 | a0002c0002t0001g0197 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.1693+4916T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108861886 | ||||||
chr2:108862077
|
G | GT | 185 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0001others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1693+5121dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108862077 | |||||
chr2:108862139
|
C | A | 6 | a0001c0001t0002g0051a0001c0001t0002g0092a0001c0001t0002g0093others(3): Show | 6 | HG02622.hp1 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1693+5169C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108862139 | ||||||
chr2:108862195
|
T | TA | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693+5235dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108862195 | |||||
chr2:108862367
|
A | G | 185 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0001others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1693+5397A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108862367 | ||||||
chr2:108862398
|
A | G | 204 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1693+5428A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108862398 | ||||||
chr2:108862540
|
G | A | 1 | a0002c0002t0001g0207 | 1 | NA18988.hp2 | intron_variant | MODIFIER | c.1693+5570G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108862540 | ||||||
chr2:108862782
|
T | C | 2 | a0001c0001t0002g0052a0001c0001t0002g0091 | 2 | HG01884.hp2 HG02976.hp2 |
intron_variant | MODIFIER | c.1693+5812T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108862782 | ||||||
chr2:108862808
|
C | T | 3 | a0002c0002t0003g0187a0002c0002t0003g0193a0002c0002t0004g0188 | 3 | HG01099.hp1 HG01993.hp2 HG02738.hp2 |
intron_variant | MODIFIER | c.1693+5838C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108862808 | ||||||
chr2:108862848
|
G | A | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1693+5878G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108862848 | ||||||
chr2:108862936
|
T | C | 103 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0003others(100): Show | 104 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(101): Show |
intron_variant | MODIFIER | c.1693+5966T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108862936 | ||||||
chr2:108862948
|
TA | T | 204 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(201): Show | 206 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(203): Show |
intron_variant | MODIFIER | c.1693+5985delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108862948 | |||||
chr2:108863187
|
G | A | 2 | a0001c0001t0002g0006a0001c0001t0002g0007 | 2 | HG01167.hp1 HG01169.hp1 |
intron_variant | MODIFIER | c.1693+6217G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108863187 | ||||||
chr2:108863295
|
A | G | 34 | a0002c0002t0001g0167a0003c0003t0001g0002a0003c0003t0001g0121others(31): Show | 35 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1693+6325A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108863295 | ||||||
chr2:108863350
|
A | G | 40 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(37): Show | 41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1693+6380A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108863350 | ||||||
chr2:108863477
|
G | A | 11 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(8): Show | 11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1693+6507G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108863477 | ||||||
chr2:108863582
|
C | T | 4 | a0002c0002t0001g0175a0002c0002t0001g0176a0002c0002t0001g0177others(1): Show | 4 | HG02451.hp2 HG02723.hp1 HG03130.hp2 others(1): Show |
intron_variant | MODIFIER | c.1693+6612C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108863582 | ||||||
chr2:108863594
|
A | G | 1 | a0001c0001t0002g0003 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.1693+6624A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108863594 | ||||||
chr2:108863882
|
C | T | 2 | a0001c0001t0002g0089a0001c0001t0002g0206 | 2 | HG02572.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.1693+6912C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108863882 | ||||||
chr2:108864036
|
CAT | C | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693+7067_1693+706 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864036 | ||||||
chr2:108864123
|
TTA | T | 2 | a0001c0004t0001g0101a0001c0004t0001g0102 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1693+7158_1693+715 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108864123 | |||||
chr2:108864272
|
C | T | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1693+7302C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864272 | ||||||
chr2:108864405
|
G | A | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1693+7435G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864405 | ||||||
chr2:108864522
|
G | A | 1 | a0002c0002t0003g0189 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1693+7552G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864522 | ||||||
chr2:108864526
|
G | A | 5 | a0002c0002t0001g0173a0002c0002t0001g0174a0002c0002t0001g0178others(2): Show | 5 | HG01109.hp2 HG01167.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1693+7556G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864526 | ||||||
chr2:108864568
|
C | T | 26 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(23): Show | 26 | HG01109.hp2 HG01167.hp2 HG01243.hp1 others(23): Show |
intron_variant | MODIFIER | c.1693+7598C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864568 | ||||||
chr2:108864598
|
G | A | 6 | a0001c0005t0001g0210a0001c0005t0001g0211a0001c0005t0001g0213others(3): Show | 6 | HG02145.hp1 HG02280.hp1 HG02965.hp2 others(3): Show |
intron_variant | MODIFIER | c.1693+7628G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864598 | ||||||
chr2:108864598
|
G | C | 199 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(196): Show | 201 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(198): Show |
intron_variant | MODIFIER | c.1693+7628G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864598 | ||||||
chr2:108864639
|
A | T | 203 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(200): Show | 205 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(202): Show |
intron_variant | MODIFIER | c.1693+7669A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864639 | ||||||
chr2:108864649
|
C | A | 5 | a0001c0004t0001g0109a0001c0004t0001g0110a0001c0004t0001g0111others(2): Show | 5 | HG02055.hp2 HG03130.hp1 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.1693+7679C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864649 | ||||||
chr2:108864666
|
C | T | 40 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(37): Show | 41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1693+7696C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864666 | ||||||
chr2:108864676
|
C | T | 40 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(37): Show | 41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1693+7706C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864676 | ||||||
chr2:108864734
|
C | T | 8 | a0001c0004t0001g0198a0001c0006t0001g0199a0001c0006t0001g0200others(5): Show | 8 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1693+7764C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864734 | ||||||
chr2:108864791
|
C | G | 8 | a0001c0004t0001g0198a0001c0006t0001g0199a0001c0006t0001g0200others(5): Show | 8 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(5): Show |
intron_variant | MODIFIER | c.1693+7821C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864791 | ||||||
chr2:108864793
|
C | CA | 112 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0079others(109): Show | 113 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(110): Show |
intron_variant | MODIFIER | c.1693+7841dupA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108864793 | |||||
chr2:108864793
|
CA | C | 44 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(41): Show | 45 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(42): Show |
intron_variant | MODIFIER | c.1693+7841delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108864793 | |||||
chr2:108864828
|
G | T | 103 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0003others(100): Show | 104 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(101): Show |
intron_variant | MODIFIER | c.1693+7858G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108864828 | ||||||
chr2:108865005
|
A | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1693+8035A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108865005 | ||||||
chr2:108865027
|
G | A | 103 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0003others(100): Show | 104 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(101): Show |
intron_variant | MODIFIER | c.1693+8057G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108865027 | ||||||
chr2:108865201
|
A | T | 39 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(36): Show | 40 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1693+8231A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108865201 | ||||||
chr2:108865441
|
A | G | 2 | a0001c0004t0001g0107a0001c0004t0001g0108 | 2 | HG02258.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1694-8010A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108865441 | ||||||
chr2:108865442
|
T | C | 11 | a0001c0001t0002g0018a0001c0001t0002g0019a0001c0001t0002g0051others(8): Show | 11 | HG01074.hp1 HG01358.hp2 HG01361.hp2 others(8): Show |
intron_variant | MODIFIER | c.1694-8009T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108865442 | ||||||
chr2:108865915
|
C | G | 1 | a0002c0002t0001g0170 | 1 | NA19058.hp1 | intron_variant | MODIFIER | c.1694-7536C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108865915 | ||||||
chr2:108866233
|
A | T | 10 | a0001c0001t0001g0029a0001c0001t0001g0057a0002c0002t0001g0134others(7): Show | 10 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.1694-7218A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108866233 | ||||||
chr2:108866839
|
C | T | 38 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(35): Show | 38 | HG00408.hp1 HG01081.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1694-6612C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108866839 | ||||||
chr2:108866840
|
G | A | 2 | a0002c0002t0001g0172a0002c0002t0001g0192 | 2 | HG01261.hp2 HG02040.hp2 |
intron_variant | MODIFIER | c.1694-6611G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108866840 | ||||||
chr2:108866844
|
C | T | 1 | a0006c0008t0001g0166 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.1694-6607C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108866844 | ||||||
chr2:108866880
|
GA | G | 11 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(8): Show | 11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1694-6560delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108866880 | |||||
chr2:108866944
|
G | A | 4 | a0001c0005t0001g0117a0001c0005t0001g0118a0001c0005t0001g0119others(1): Show | 4 | HG02615.hp1 HG02896.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.1694-6507G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108866944 | ||||||
chr2:108867003
|
A | G | 3 | a0001c0004t0001g0103a0001c0004t0001g0104a0001c0004t0001g0105 | 3 | HG02886.hp1 HG02896.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.1694-6448A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867003 | ||||||
chr2:108867177
|
T | C | 1 | a0003c0003t0001g0162 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1694-6274T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867177 | ||||||
chr2:108867211
|
A | G | 39 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(36): Show | 40 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(37): Show |
intron_variant | MODIFIER | c.1694-6240A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867211 | ||||||
chr2:108867234
|
TAGA | T | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1694-6207_1694-620 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108867234 | |||||
chr2:108867273
|
C | T | 7 | a0001c0006t0001g0199a0001c0006t0001g0200a0001c0006t0001g0201others(4): Show | 7 | HG01261.hp1 NA18941.hp1 NA18946.hp2 others(4): Show |
intron_variant | MODIFIER | c.1694-6178C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867273 | ||||||
chr2:108867320
|
T | C | 7 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1694-6131T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867320 | ||||||
chr2:108867591
|
A | G | 1 | a0001c0001t0002g0027 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.1694-5860A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867591 | ||||||
chr2:108867627
|
G | A | 1 | a0001c0001t0001g0029 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1694-5824G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867627 | ||||||
chr2:108867712
|
T | G | 1 | a0001c0010t0002g0068 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.1694-5739T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867712 | ||||||
chr2:108867800
|
G | A | 1 | a0001c0001t0002g0024 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.1694-5651G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867800 | ||||||
chr2:108867979
|
G | T | 1 | a0001c0005t0001g0116 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.1694-5472G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108867979 | ||||||
chr2:108868222
|
AC | A | 9 | a0001c0001t0001g0029a0002c0002t0001g0134a0002c0002t0001g0168others(6): Show | 9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1694-5228delC | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108868222 | ||||||
chr2:108868225
|
C | T | 1 | a0003c0003t0001g0162 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1694-5226C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108868225 | ||||||
chr2:108868268
|
G | T | 1 | a0001c0005t0001g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1694-5183G>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108868268 | ||||||
chr2:108868649
|
T | A | 5 | a0001c0001t0002g0085a0001c0001t0002g0086a0001c0001t0002g0087others(2): Show | 5 | HG00741.hp2 HG01515.hp2 HG01516.hp1 others(2): Show |
intron_variant | MODIFIER | c.1694-4802T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108868649 | ||||||
chr2:108868786
|
A | G | 1 | a0001c0005t0001g0115 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1694-4665A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108868786 | ||||||
chr2:108868805
|
A | T | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1694-4646A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108868805 | ||||||
chr2:108869179
|
A | G | 1 | a0001c0004t0001g0109 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.1694-4272A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108869179 | ||||||
chr2:108869311
|
A | G | 1 | a0001c0001t0002g0043 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.1694-4140A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108869311 | ||||||
chr2:108869710
|
A | G | 1 | a0001c0001t0002g0023 | 1 | NA19070.hp1 | intron_variant | MODIFIER | c.1694-3741A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108869710 | ||||||
chr2:108869776
|
C | T | 8 | a0001c0001t0002g0043a0001c0006t0001g0199a0001c0006t0001g0200others(5): Show | 8 | HG01261.hp1 HG01978.hp1 NA18941.hp1 others(5): Show |
intron_variant | MODIFIER | c.1694-3675C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108869776 | ||||||
chr2:108869813
|
C | T | 202 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(199): Show | 204 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.1694-3638C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108869813 | ||||||
chr2:108869818
|
C | G | 2 | a0003c0003t0001g0142a0003c0003t0001g0181 | 2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1694-3633C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108869818 | ||||||
chr2:108870048
|
C | G | 40 | a0001c0005t0001g0116a0001c0005t0001g0117a0001c0005t0001g0118others(37): Show | 41 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(38): Show |
intron_variant | MODIFIER | c.1694-3403C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108870048 | ||||||
chr2:108870461
|
A | T | 1 | a0001c0001t0002g0049 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.1694-2990A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108870461 | ||||||
chr2:108870540
|
C | T | 2 | a0003c0003t0001g0121a0003c0003t0001g0153 | 2 | NA18974.hp2 NA18984.hp2 |
intron_variant | MODIFIER | c.1694-2911C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108870540 | ||||||
chr2:108870570
|
CAAAAGT | C | 6 | a0001c0001t0002g0051a0001c0001t0002g0092a0001c0001t0002g0093others(3): Show | 6 | HG02622.hp1 HG02818.hp2 HG02976.hp1 others(3): Show |
intron_variant | MODIFIER | c.1694-2875_1694-287 others(10): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108870570 | |||||
chr2:108870801
|
A | G | 2 | a0003c0003t0001g0142a0003c0003t0001g0181 | 2 | HG00738.hp2 HG00741.hp1 |
intron_variant | MODIFIER | c.1694-2650A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108870801 | ||||||
chr2:108870910
|
ATTTAC | A | 5 | a0002c0002t0001g0173a0002c0002t0001g0174a0002c0002t0001g0178others(2): Show | 5 | HG01109.hp2 HG01167.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1694-2538_1694-253 others(9): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108870910 | |||||
chr2:108871035
|
C | T | 11 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(8): Show | 11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1694-2416C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108871035 | ||||||
chr2:108871095
|
A | G | 13 | a0001c0001t0001g0029a0001c0004t0001g0103a0001c0004t0001g0104others(10): Show | 13 | HG01081.hp2 HG02055.hp1 HG02523.hp1 others(10): Show |
intron_variant | MODIFIER | c.1694-2356A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108871095 | ||||||
chr2:108871314
|
C | G | 5 | a0002c0002t0001g0173a0002c0002t0001g0174a0002c0002t0001g0178others(2): Show | 5 | HG01109.hp2 HG01167.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1694-2137C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108871314 | ||||||
chr2:108871365
|
T | C | 2 | a0001c0001t0001g0005a0001c0001t0001g0079 | 2 | HG02965.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1694-2086T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108871365 | ||||||
chr2:108871368
|
A | AC | 2 | a0001c0004t0001g0198a0001c0005t0001g0211 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1694-2083_1694-208 others(5): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108871368 | ||||||
chr2:108871369
|
T | C | 202 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(199): Show | 204 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(201): Show |
intron_variant | MODIFIER | c.1694-2082T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108871369 | ||||||
chr2:108871370
|
T | A | 2 | a0001c0004t0001g0198a0001c0005t0001g0211 | 2 | HG02145.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.1694-2081T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108871370 | ||||||
chr2:108871370
|
TA | T | 111 | a0001c0001t0001g0005a0001c0001t0001g0057a0001c0001t0001g0079others(108): Show | 112 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(109): Show |
intron_variant | MODIFIER | c.1694-2056delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108871370 | |||||
chr2:108871370
|
TAA | T | 55 | a0001c0001t0001g0029a0001c0001t0002g0006a0001c0001t0002g0021others(52): Show | 55 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(52): Show |
intron_variant | MODIFIER | c.1694-2057_1694-205 others(6): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108871370 | |||||
chr2:108871370
|
TAAA | T | 30 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(27): Show | 31 | HG01243.hp1 HG01261.hp1 HG02055.hp2 others(28): Show |
intron_variant | MODIFIER | c.1694-2058_1694-205 others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108871370 | |||||
chr2:108871659
|
T | C | 1 | a0003c0003t0001g0162 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.1694-1792T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108871659 | ||||||
chr2:108871834
|
C | A | 11 | a0002c0002t0001g0128a0002c0002t0001g0129a0002c0002t0001g0130others(8): Show | 11 | HG01109.hp2 HG01167.hp2 HG01884.hp1 others(8): Show |
intron_variant | MODIFIER | c.1694-1617C>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108871834 | ||||||
chr2:108872262
|
T | C | 185 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0001others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1694-1189T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872262 | ||||||
chr2:108872538
|
C | T | 4 | a0001c0004t0001g0103a0001c0004t0001g0104a0001c0004t0001g0105others(1): Show | 4 | HG01081.hp2 HG02886.hp1 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.1694-913C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872538 | ||||||
chr2:108872539
|
T | G | 112 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0001others(109): Show | 113 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(110): Show |
intron_variant | MODIFIER | c.1694-912T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872539 | ||||||
chr2:108872562
|
C | T | 112 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0001others(109): Show | 113 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(110): Show |
intron_variant | MODIFIER | c.1694-889C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872562 | ||||||
chr2:108872610
|
T | C | 112 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0001others(109): Show | 113 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(110): Show |
intron_variant | MODIFIER | c.1694-841T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872610 | ||||||
chr2:108872653
|
G | A | 112 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0001others(109): Show | 113 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(110): Show |
intron_variant | MODIFIER | c.1694-798G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872653 | ||||||
chr2:108872737
|
C | T | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1694-714C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872737 | ||||||
chr2:108872789
|
G | C | 17 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0005t0001g0112others(14): Show | 17 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(14): Show |
intron_variant | MODIFIER | c.1694-662G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872789 | ||||||
chr2:108872864
|
T | G | 1 | a0003c0003t0001g0180 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1694-587T>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872864 | ||||||
chr2:108872909
|
A | G | 112 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0001others(109): Show | 113 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(110): Show |
intron_variant | MODIFIER | c.1694-542A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872909 | ||||||
chr2:108872946
|
G | C | 112 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0001others(109): Show | 113 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(110): Show |
intron_variant | MODIFIER | c.1694-505G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872946 | ||||||
chr2:108872973
|
C | T | 73 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(70): Show | 74 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(71): Show |
intron_variant | MODIFIER | c.1694-478C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108872973 | ||||||
chr2:108873160
|
A | C | 47 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(44): Show | 48 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1694-291A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108873160 | ||||||
chr2:108873297
|
AATG | A | 98 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(95): Show | 99 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(96): Show |
intron_variant | MODIFIER | c.1694-148_1694-146d others(5): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | INFO_REALIGN_3_PRIME | chr2 | 108873297 | |||||
chr2:108873338
|
T | A | 1 | a0001c0001t0002g0054 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.1694-113T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108873338 | ||||||
chr2:108873370
|
A | G | 1 | a0001c0004t0001g0198 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.1694-81A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 13/14 | chr2 | 108873370 | ||||||
chr2:108873635
|
C | T | 1 | a0001c0005t0001g0112 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.1832+46C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108873635 | ||||||
chr2:108873648
|
A | G | 217 | a0001c0001t0001g0005a0001c0001t0001g0029a0001c0001t0001g0057others(214): Show | 219 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(216): Show |
intron_variant | MODIFIER | c.1832+59A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108873648 | ||||||
chr2:108873690
|
A | G | 102 | a0001c0001t0002g0001a0001c0001t0002g0003a0001c0001t0002g0004others(99): Show | 103 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(100): Show |
intron_variant | MODIFIER | c.1832+101A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108873690 | ||||||
chr2:108873700
|
A | G | 3 | a0003c0003t0001g0142a0003c0003t0001g0181a0003c0003t0001g0184 | 3 | HG00738.hp2 HG00741.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.1832+111A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108873700 | ||||||
chr2:108873737
|
C | T | 17 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0004t0001g0107others(14): Show | 17 | HG02055.hp1 HG02055.hp2 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.1832+148C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108873737 | ||||||
chr2:108873880
|
C | T | 1 | a0001c0001t0002g0048 | 1 | NA18985.hp1 | intron_variant | MODIFIER | c.1832+291C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108873880 | ||||||
chr2:108873920
|
A | T | 12 | a0003c0003t0001g0002a0003c0003t0001g0141a0003c0003t0001g0143others(9): Show | 13 | NA18968.hp2 NA18970.hp2 NA18977.hp2 others(10): Show |
intron_variant | MODIFIER | c.1832+331A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108873920 | ||||||
chr2:108874564
|
A | G | 47 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(44): Show | 48 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(45): Show |
intron_variant | MODIFIER | c.1832+975A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108874564 | ||||||
chr2:108874834
|
G | A | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1832+1245G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108874834 | ||||||
chr2:108874922
|
A | AT | 110 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0001others(107): Show | 111 | HG00099.hp1 HG00408.hp1 HG00741.hp2 others(108): Show |
intron_variant | MODIFIER | c.1833-1154dupT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 108874922 | |||||
chr2:108874988
|
A | G | 185 | a0001c0001t0001g0029a0001c0001t0001g0057a0001c0001t0002g0001others(182): Show | 187 | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(184): Show |
intron_variant | MODIFIER | c.1833-1100A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108874988 | ||||||
chr2:108875026
|
TA | T | 9 | a0001c0001t0001g0029a0002c0002t0001g0134a0002c0002t0001g0168others(6): Show | 9 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(6): Show |
intron_variant | MODIFIER | c.1833-1055delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 108875026 | |||||
chr2:108875146
|
T | C | 6 | a0001c0001t0002g0006a0001c0001t0002g0007a0001c0001t0002g0045others(3): Show | 6 | HG01167.hp1 HG01168.hp1 HG01169.hp1 others(3): Show |
intron_variant | MODIFIER | c.1833-942T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875146 | ||||||
chr2:108875159
|
A | G | 7 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(4): Show | 7 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(4): Show |
intron_variant | MODIFIER | c.1833-929A>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875159 | ||||||
chr2:108875316
|
TAA | T | 5 | a0002c0002t0001g0173a0002c0002t0001g0174a0002c0002t0001g0178others(2): Show | 5 | HG01109.hp2 HG01167.hp2 HG01891.hp2 others(2): Show |
intron_variant | MODIFIER | c.1833-771_1833-770d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875316 | ||||||
chr2:108875317
|
AAT | A | 25 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0004t0001g0009others(22): Show | 25 | HG01243.hp1 HG01243.hp2 HG02145.hp1 others(22): Show |
intron_variant | MODIFIER | c.1833-769_1833-768d others(4): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 108875317 | |||||
chr2:108875318
|
AT | A | 60 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(57): Show | 61 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(58): Show |
intron_variant | MODIFIER | c.1833-769delT | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875318 | ||||||
chr2:108875319
|
TA | T | 5 | a0001c0001t0002g0058a0001c0004t0001g0102a0002c0002t0001g0172others(2): Show | 5 | HG01261.hp2 HG02040.hp2 HG02451.hp2 others(2): Show |
intron_variant | MODIFIER | c.1833-752delA | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 108875319 | |||||
chr2:108875319
|
TAAA | T | 60 | a0001c0001t0001g0057a0001c0001t0002g0003a0001c0001t0002g0008others(57): Show | 60 | HG00099.hp1 HG00741.hp2 HG01081.hp2 others(57): Show |
intron_variant | MODIFIER | c.1833-754_1833-752d others(5): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 108875319 | |||||
chr2:108875328
|
AAAAAAAA others(2): Show |
A | 38 | a0001c0001t0002g0004a0001c0001t0002g0006a0001c0001t0002g0007others(35): Show | 38 | HG00408.hp1 HG01081.hp1 HG01167.hp1 others(35): Show |
intron_variant | MODIFIER | c.1833-756_1833-748d others(11): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 108875328 | |||||
chr2:108875332
|
AAAAAG | A | 7 | a0002c0002t0001g0134a0002c0002t0001g0168a0002c0002t0001g0169others(4): Show | 7 | HG02055.hp1 HG02602.hp1 HG03654.hp2 others(4): Show |
intron_variant | MODIFIER | c.1833-752_1833-748d others(7): Show |
CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | INFO_REALIGN_3_PRIME | chr2 | 108875332 | |||||
chr2:108875335
|
A | C | 1 | a0001c0001t0002g0060 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1833-753A>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875335 | ||||||
chr2:108875337
|
G | C | 65 | a0001c0001t0001g0057a0001c0001t0002g0001a0001c0001t0002g0003others(62): Show | 66 | HG00099.hp1 HG00741.hp2 HG01074.hp1 others(63): Show |
intron_variant | MODIFIER | c.1833-751G>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875337 | ||||||
chr2:108875352
|
T | C | 34 | a0002c0002t0001g0167a0003c0003t0001g0002a0003c0003t0001g0121others(31): Show | 35 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1833-736T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875352 | ||||||
chr2:108875587
|
G | A | 1 | a0002c0002t0001g0182 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.1833-501G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875587 | ||||||
chr2:108875690
|
T | C | 34 | a0002c0002t0001g0167a0003c0003t0001g0002a0003c0003t0001g0121others(31): Show | 35 | HG00099.hp2 HG00408.hp2 HG00738.hp1 others(32): Show |
intron_variant | MODIFIER | c.1833-398T>C | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875690 | ||||||
chr2:108875765
|
G | A | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1833-323G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875765 | ||||||
chr2:108875783
|
G | A | 7 | a0001c0004t0001g0009a0001c0004t0001g0011a0001c0004t0001g0012others(4): Show | 7 | HG01243.hp1 HG02572.hp1 HG02886.hp2 others(4): Show |
intron_variant | MODIFIER | c.1833-305G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875783 | ||||||
chr2:108875797
|
T | A | 1 | a0002c0002t0001g0168 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.1833-291T>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875797 | ||||||
chr2:108875820
|
C | T | 10 | a0001c0001t0001g0029a0001c0001t0001g0057a0002c0002t0001g0134others(7): Show | 10 | HG02055.hp1 HG02523.hp1 HG02602.hp1 others(7): Show |
intron_variant | MODIFIER | c.1833-268C>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875820 | ||||||
chr2:108875989
|
G | A | 8 | a0001c0004t0001g0107a0001c0004t0001g0108a0001c0004t0001g0109others(5): Show | 8 | HG02055.hp2 HG02258.hp2 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.1833-99G>A | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875989 | ||||||
chr2:108875999
|
C | G | 16 | a0001c0001t0001g0005a0001c0001t0001g0079a0001c0005t0001g0112others(13): Show | 16 | HG01243.hp2 HG02145.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.1833-89C>G | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108875999 | ||||||
chr2:108876075
|
A | T | 1 | a0003c0003t0001g0159 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.1833-13A>T | CCDC138 | ENSG00000163006.12 | transcript | ENST00000295124.9 | protein_coding | 14/14 | chr2 | 108876075 |