geneid | 22832 |
---|---|
ensemblid | ENSG00000135315.12 |
hgncid | 21107 |
symbol | CEP162 |
name | centrosomal protein 162 |
refseq_nuc | NM_014895.4 |
refseq_prot | NP_055710.2 |
ensembl_nuc | ENST00000403245.8 |
ensembl_prot | ENSP00000385215.3 |
mane_status | MANE Select |
chr | chr6 |
start | 84124250 |
end | 84227643 |
strand | - |
ver | v1.2 |
region | chr6:84124250-84227643 |
region5000 | chr6:84119250-84232643 |
regionname0 | CEP162_chr6_84124250_84227643 |
regionname5000 | CEP162_chr6_84119250_84232643 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 1403 | 172 | 60 | 40 | 41 | 5 | 24 | 31 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0002 | 0/0 | 1403 | 17 | 12 | 3 | 0 | 1 | 1 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0003 | 0/0 | 1417 | 13 | 1 | 8 | 0 | 0 | 4 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0004 | 0/0 | 1403 | 3 | 2 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0005 | 0/0 | 1403 | 2 | 2 | 0 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0006 | 0/0 | 1403 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0007 | 0/0 | 1403 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0008 | 0/0 | 1403 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0009 | 0/0 | 1403 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0010 | 0/0 | 1403 | 1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0011 | 0/0 | 1417 | 1 | 0 | 0 | 0 | 0 | 1 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0012 | 0/0 | 1403 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 4212 | 135 | 30 | 38 | 39 | 5 | 21 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0002 | 0/0 | 4212 | 14 | 9 | 3 | 0 | 1 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0003 | 0/0 | 4254 | 12 | 1 | 7 | 0 | 0 | 4 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0004 | 0/0 | 4212 | 11 | 9 | 2 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0005 | 0/0 | 4212 | 9 | 9 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0006 | 0/0 | 4212 | 6 | 1 | 0 | 2 | 0 | 3 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0007 | 0/0 | 4212 | 5 | 5 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0008 | 0/0 | 4212 | 4 | 4 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0009 | 0/0 | 4212 | 3 | 2 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0010 | 0/0 | 4212 | 2 | 2 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0011 | 0/0 | 4212 | 2 | 2 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0012 | 0/0 | 4212 | 2 | 2 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0013 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0014 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0015 | 0/0 | 4212 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0016 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0017 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0018 | 0/0 | 4254 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0019 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0020 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
c0021 | 0/0 | 4254 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/1 | 944 | 119 | 13 | 36 | 40 | 4 | 24 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
t0002 | 0/0 | 944 | 57 | 51 | 4 | 0 | 1 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
t0003 | 0/0 | 944 | 15 | 1 | 9 | 0 | 0 | 5 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
t0004 | 0/0 | 944 | 10 | 10 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
t0005 | 0/0 | 944 | 5 | 5 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
t0006 | 0/0 | 944 | 2 | 0 | 1 | 0 | 1 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
t0007 | 0/0 | 944 | 2 | 1 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
t0008 | 0/0 | 944 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
t0009 | 0/0 | 944 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
t0010 | 0/0 | 944 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
t0011 | 0/0 | 944 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0094 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 4212 | 135 | 30 | 38 | 39 | 5 | 21 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0004 | 0/0 | 4212 | 11 | 9 | 2 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0005 | 0/0 | 4212 | 9 | 9 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0006 | 0/0 | 4212 | 6 | 1 | 0 | 2 | 0 | 3 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0007 | 0/0 | 4212 | 5 | 5 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0008 | 0/0 | 4212 | 4 | 4 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0011 | 0/0 | 4212 | 2 | 2 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0002c0002 | 0/0 | 4212 | 14 | 9 | 3 | 0 | 1 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0002c0012 | 0/0 | 4212 | 2 | 2 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0002c0016 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0003c0003 | 0/0 | 4254 | 12 | 1 | 7 | 0 | 0 | 4 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0003c0021 | 0/0 | 4254 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0004c0009 | 0/0 | 4212 | 3 | 2 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0005c0010 | 0/0 | 4212 | 2 | 2 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0006c0013 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0007c0017 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0008c0014 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0009c0019 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0010c0020 | 0/0 | 4212 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0011c0018 | 0/0 | 4254 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0012c0015 | 0/0 | 4212 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/1 | 5155 | 108 | 10 | 34 | 37 | 4 | 21 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0001t0002 | 0/0 | 5155 | 20 | 20 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0001t0003 | 0/0 | 5155 | 2 | 0 | 2 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0001t0006 | 0/0 | 5155 | 2 | 0 | 1 | 0 | 1 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0001t0008 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0001t0009 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0001t0011 | 0/0 | 5155 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0004t0002 | 0/0 | 5155 | 9 | 8 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0004t0007 | 0/0 | 5155 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0004t0010 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0005t0004 | 0/0 | 5155 | 8 | 8 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0005t0005 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0006t0001 | 0/0 | 5155 | 5 | 0 | 0 | 2 | 0 | 3 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0006t0002 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0007t0002 | 0/0 | 5155 | 5 | 5 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0008t0005 | 0/0 | 5155 | 4 | 4 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0001c0011t0002 | 0/0 | 5155 | 2 | 2 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0002c0002t0002 | 0/0 | 5155 | 13 | 8 | 3 | 0 | 1 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0002c0002t0007 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0002c0012t0002 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0002c0012t0004 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0002c0016t0002 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0003c0003t0001 | 0/0 | 5197 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0003c0003t0003 | 0/0 | 5197 | 11 | 1 | 6 | 0 | 0 | 4 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0003c0021t0003 | 0/0 | 5197 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0004c0009t0001 | 0/0 | 5155 | 3 | 2 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0005c0010t0002 | 0/0 | 5155 | 2 | 2 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0006c0013t0002 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0007c0017t0001 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0008c0014t0004 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0009c0019t0002 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0010c0020t0002 | 0/0 | 5155 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0011c0018t0003 | 0/0 | 5197 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
a0012c0015t0001 | 0/0 | 5155 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | copy fasta | chr6 | 84119250 | 84232643 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0008 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0009 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0010 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0016 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0021 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0022 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0025 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0026 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0027 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0044 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0050 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0053 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0054 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0055 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0056 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0057 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0058 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0061 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0073 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0077 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0078 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0079 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0081 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0084 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0094 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0097 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0108 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0109 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0123 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0127 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0128 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0152 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0154 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0170 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0171 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0177 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0178 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0179 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0186 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0188 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0002g0001 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0002g0002 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0002g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0002g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0002g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0002g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0002g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0002g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0002g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0002g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0002g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0002g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0002g0110 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0002g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0002g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0002g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0002g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0002g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0003g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0006g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0006g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0008g0175 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0009g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0001t0011g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0004t0002g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0004t0002g0095 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0004t0002g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0004t0002g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0004t0002g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0004t0002g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0004t0002g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0004t0002g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0004t0002g0211 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0004t0007g0207 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0004t0010g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0005t0004g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0005t0004g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0005t0004g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0005t0004g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0005t0004g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0005t0004g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0005t0004g0195 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0005t0004g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0005t0005g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0006t0001g0007 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0006t0001g0011 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0006t0001g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0006t0001g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0006t0001g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0006t0002g0156 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0007t0002g0017 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0007t0002g0018 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0007t0002g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0007t0002g0117 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0007t0002g0118 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0008t0005g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0008t0005g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0008t0005g0205 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0008t0005g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0011t0002g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0001c0011t0002g0020 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0002c0002t0002g0003 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0002c0002t0002g0006 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0002c0002t0002g0013 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0002c0002t0002g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0002c0002t0002g0119 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0002c0002t0002g0141 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0002c0002t0002g0144 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0002c0002t0002g0145 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0002c0002t0002g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0002c0002t0002g0147 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0002c0002t0002g0155 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0002c0002t0002g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0002c0002t0007g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0002c0012t0002g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0002c0012t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0002c0016t0002g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0003c0003t0001g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0003c0003t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0003c0003t0003g0041 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0003c0003t0003g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0003c0003t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0003c0003t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0003c0003t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0003c0003t0003g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0003c0003t0003g0090 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0003c0003t0003g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0003c0003t0003g0165 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0003c0003t0003g0166 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0003c0021t0003g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0004c0009t0001g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0004c0009t0001g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0004c0009t0001g0135 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0005c0010t0002g0163 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0005c0010t0002g0164 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0006c0013t0002g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0007c0017t0001g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0008c0014t0004g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0009c0019t0002g0143 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0010c0020t0002g0142 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0011c0018t0003g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
a0012c0015t0001g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00280 | hp1 | a0001 | c0001 | t0001 | g0055 | EUR | FIN | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG00280 | hp2 | a0001 | c0001 | t0001 | g0125 | EUR | FIN | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG00408 | hp1 | a0001 | c0001 | t0001 | g0160 | EAS | CHS | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG00408 | hp2 | a0001 | c0001 | t0001 | g0170 | EAS | CHS | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0044 | EAS | CHS | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG00558 | hp2 | a0001 | c0001 | t0001 | g0158 | EAS | CHS | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG00639 | hp1 | a0001 | c0001 | t0001 | g0136 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG00639 | hp2 | a0001 | c0001 | t0001 | g0064 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG00673 | hp1 | a0001 | c0001 | t0001 | g0062 | EAS | CHS | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG00673 | hp2 | a0001 | c0001 | t0001 | g0184 | EAS | CHS | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0027 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG00738 | hp2 | a0001 | c0001 | t0001 | g0025 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG00741 | hp1 | a0001 | c0001 | t0001 | g0082 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG00741 | hp2 | a0001 | c0004 | t0002 | g0211 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01074 | hp1 | a0001 | c0001 | t0001 | g0071 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01074 | hp2 | a0003 | c0003 | t0003 | g0041 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01081 | hp1 | a0001 | c0001 | t0011 | g0111 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0026 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01106 | hp1 | a0001 | c0001 | t0001 | g0185 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01106 | hp2 | a0001 | c0001 | t0001 | g0157 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01109 | hp1 | a0001 | c0004 | t0007 | g0207 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01109 | hp2 | a0002 | c0002 | t0002 | g0141 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01169 | hp1 | a0001 | c0001 | t0001 | g0024 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01169 | hp2 | a0001 | c0001 | t0001 | g0188 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01192 | hp1 | a0001 | c0001 | t0001 | g0063 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0050 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0009 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01243 | hp2 | a0003 | c0003 | t0003 | g0042 | AMR | PUR | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01256 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01256 | hp2 | a0001 | c0001 | t0001 | g0075 | AMR | CLM | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01257 | hp1 | a0001 | c0001 | t0001 | g0128 | AMR | CLM | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01257 | hp2 | a0003 | c0021 | t0003 | g0049 | AMR | CLM | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01258 | hp1 | a0002 | c0002 | t0002 | g0003 | AMR | CLM | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01258 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | CLM | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0053 | AMR | CLM | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0153 | AMR | CLM | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01346 | hp1 | a0004 | c0009 | t0001 | g0135 | AMR | CLM | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01346 | hp2 | a0001 | c0001 | t0003 | g0112 | AMR | CLM | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01358 | hp1 | a0001 | c0001 | t0003 | g0065 | AMR | CLM | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01358 | hp2 | a0001 | c0001 | t0001 | g0138 | AMR | CLM | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01496 | hp1 | a0001 | c0001 | t0001 | g0070 | AMR | CLM | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01496 | hp2 | a0001 | c0001 | t0001 | g0178 | AMR | CLM | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01515 | hp1 | a0001 | c0001 | t0001 | g0123 | EUR | IBS | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01515 | hp2 | a0001 | c0001 | t0001 | g0081 | EUR | IBS | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01884 | hp1 | a0001 | c0001 | t0002 | g0110 | AFR | ACB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01884 | hp2 | a0001 | c0001 | t0002 | g0031 | AFR | ACB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0177 | AMR | PEL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01928 | hp2 | a0003 | c0003 | t0003 | g0048 | AMR | PEL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01943 | hp1 | a0001 | c0001 | t0006 | g0060 | AMR | PEL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0148 | AMR | PEL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0066 | AMR | PEL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0176 | AMR | PEL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01981 | hp1 | a0001 | c0001 | t0001 | g0162 | AMR | PEL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG01981 | hp2 | a0003 | c0003 | t0001 | g0043 | AMR | PEL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02004 | hp1 | a0001 | c0001 | t0001 | g0083 | AMR | PEL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02004 | hp2 | a0001 | c0001 | t0001 | g0021 | AMR | PEL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02055 | hp1 | a0001 | c0001 | t0002 | g0029 | AFR | ACB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02055 | hp2 | a0004 | c0009 | t0001 | g0134 | AFR | ACB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0151 | EAS | KHV | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02056 | hp2 | a0001 | c0001 | t0001 | g0186 | EAS | KHV | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02080 | hp1 | a0001 | c0001 | t0001 | g0078 | EAS | KHV | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02080 | hp2 | a0001 | c0001 | t0001 | g0004 | EAS | KHV | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02148 | hp1 | a0003 | c0003 | t0003 | g0166 | AMR | PEL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02148 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02257 | hp1 | a0002 | c0012 | t0002 | g0193 | AFR | ACB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02257 | hp2 | a0001 | c0007 | t0002 | g0017 | AFR | ACB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02258 | hp1 | a0008 | c0014 | t0004 | g0115 | AFR | ACB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02258 | hp2 | a0001 | c0005 | t0004 | g0105 | AFR | ACB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02273 | hp1 | a0001 | c0001 | t0001 | g0022 | AMR | PEL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02273 | hp2 | a0001 | c0001 | t0001 | g0152 | AMR | PEL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02280 | hp1 | a0001 | c0001 | t0002 | g0140 | AFR | ACB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02280 | hp2 | a0006 | c0013 | t0002 | g0113 | AFR | ACB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02293 | hp1 | a0001 | c0001 | t0001 | g0169 | AMR | PEL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02293 | hp2 | a0003 | c0003 | t0003 | g0045 | AMR | PEL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0054 | AMR | PEL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02300 | hp2 | a0003 | c0003 | t0003 | g0047 | AMR | PEL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02451 | hp1 | a0001 | c0001 | t0002 | g0002 | AFR | ACB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02451 | hp2 | a0004 | c0009 | t0001 | g0124 | AFR | ACB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02602 | hp1 | a0001 | c0001 | t0001 | g0137 | SAS | PJL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0057 | SAS | PJL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02615 | hp1 | a0001 | c0001 | t0001 | g0074 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02615 | hp2 | a0002 | c0002 | t0002 | g0119 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02622 | hp1 | a0001 | c0001 | t0001 | g0098 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02622 | hp2 | a0001 | c0001 | t0002 | g0028 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02630 | hp1 | a0001 | c0001 | t0001 | g0073 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02630 | hp2 | a0001 | c0001 | t0002 | g0035 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02647 | hp1 | a0001 | c0011 | t0002 | g0020 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02647 | hp2 | a0001 | c0001 | t0002 | g0200 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0077 | SAS | PJL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02683 | hp2 | a0001 | c0006 | t0001 | g0133 | SAS | PJL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02717 | hp1 | a0001 | c0008 | t0005 | g0203 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02717 | hp2 | a0001 | c0004 | t0002 | g0102 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02723 | hp1 | a0002 | c0002 | t0002 | g0146 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02723 | hp2 | a0001 | c0007 | t0002 | g0117 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02735 | hp1 | a0003 | c0003 | t0003 | g0046 | SAS | PJL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0109 | SAS | PJL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02809 | hp1 | a0001 | c0001 | t0002 | g0201 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02809 | hp2 | a0001 | c0007 | t0002 | g0118 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0099 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02818 | hp2 | a0005 | c0010 | t0002 | g0163 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02886 | hp1 | a0003 | c0003 | t0003 | g0091 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02886 | hp2 | a0001 | c0005 | t0004 | g0086 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02897 | hp1 | a0001 | c0001 | t0001 | g0209 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02897 | hp2 | a0002 | c0002 | t0002 | g0147 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02922 | hp1 | a0001 | c0004 | t0002 | g0210 | AFR | ESN | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02922 | hp2 | a0001 | c0001 | t0002 | g0038 | AFR | ESN | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02965 | hp1 | a0005 | c0010 | t0002 | g0164 | AFR | ESN | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02965 | hp2 | a0001 | c0004 | t0002 | g0103 | AFR | ESN | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02970 | hp1 | a0001 | c0005 | t0004 | g0198 | AFR | ESN | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02970 | hp2 | a0001 | c0001 | t0002 | g0199 | AFR | ESN | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02976 | hp1 | a0001 | c0005 | t0004 | g0106 | AFR | ESN | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02976 | hp2 | a0001 | c0004 | t0010 | g0104 | AFR | ESN | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03017 | hp1 | a0001 | c0006 | t0001 | g0011 | SAS | PJL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03041 | hp1 | a0001 | c0004 | t0002 | g0114 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0023 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03098 | hp1 | a0002 | c0002 | t0002 | g0145 | AFR | MSL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03098 | hp2 | a0001 | c0001 | t0002 | g0001 | AFR | MSL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03130 | hp1 | a0001 | c0001 | t0002 | g0197 | AFR | ESN | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03130 | hp2 | a0001 | c0005 | t0004 | g0005 | AFR | ESN | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03139 | hp1 | a0001 | c0008 | t0005 | g0206 | AFR | ESN | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03139 | hp2 | a0001 | c0004 | t0002 | g0190 | AFR | ESN | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03195 | hp1 | a0002 | c0016 | t0002 | g0196 | AFR | ESN | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03195 | hp2 | a0001 | c0001 | t0002 | g0002 | AFR | ESN | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03209 | hp1 | a0001 | c0011 | t0002 | g0019 | AFR | MSL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03209 | hp2 | a0001 | c0001 | t0001 | g0097 | AFR | MSL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03225 | hp1 | a0001 | c0001 | t0002 | g0032 | AFR | MSL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03225 | hp2 | a0001 | c0006 | t0002 | g0156 | AFR | MSL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0108 | SAS | PJL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0084 | SAS | PJL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03453 | hp1 | a0001 | c0001 | t0002 | g0033 | AFR | MSL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03453 | hp2 | a0001 | c0008 | t0005 | g0204 | AFR | MSL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03486 | hp1 | a0001 | c0005 | t0004 | g0107 | AFR | MSL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03486 | hp2 | a0001 | c0004 | t0002 | g0012 | AFR | MSL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03492 | hp1 | a0003 | c0003 | t0003 | g0040 | SAS | PJL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0174 | SAS | PJL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03516 | hp1 | a0001 | c0005 | t0004 | g0085 | AFR | ESN | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03516 | hp2 | a0002 | c0002 | t0002 | g0144 | AFR | ESN | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03540 | hp1 | a0001 | c0001 | t0002 | g0037 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03540 | hp2 | a0002 | c0002 | t0007 | g0202 | AFR | GWD | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03579 | hp1 | a0001 | c0008 | t0005 | g0205 | AFR | MSL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03579 | hp2 | a0001 | c0004 | t0002 | g0095 | AFR | MSL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0061 | SAS | PJL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03654 | hp2 | a0001 | c0001 | t0001 | g0056 | SAS | PJL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03669 | hp1 | a0003 | c0003 | t0003 | g0090 | SAS | PJL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03669 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | PJL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0179 | SAS | PJL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0154 | SAS | PJL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0096 | SAS | BEB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03831 | hp2 | a0001 | c0001 | t0001 | g0080 | SAS | BEB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03834 | hp1 | a0001 | c0001 | t0001 | g0171 | SAS | BEB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03834 | hp2 | a0011 | c0018 | t0003 | g0039 | SAS | BEB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03942 | hp1 | a0003 | c0003 | t0003 | g0165 | SAS | BEB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03942 | hp2 | a0001 | c0006 | t0001 | g0007 | SAS | BEB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0072 | SAS | STU | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0121 | SAS | STU | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG04228 | hp1 | a0001 | c0001 | t0001 | g0068 | SAS | STU | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0120 | SAS | STU | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18522 | hp1 | a0010 | c0020 | t0002 | g0142 | AFR | YRI | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18522 | hp2 | a0002 | c0002 | t0002 | g0155 | AFR | YRI | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18906 | hp1 | a0007 | c0017 | t0001 | g0149 | AFR | YRI | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18906 | hp2 | a0001 | c0005 | t0004 | g0195 | AFR | YRI | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18940 | hp1 | a0001 | c0001 | t0001 | g0058 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18940 | hp2 | a0001 | c0001 | t0001 | g0168 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18942 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18942 | hp2 | a0001 | c0001 | t0001 | g0167 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18945 | hp1 | a0001 | c0001 | t0009 | g0122 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0183 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0059 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18950 | hp2 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18957 | hp1 | a0001 | c0001 | t0001 | g0187 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18957 | hp2 | a0001 | c0001 | t0001 | g0088 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18962 | hp1 | a0012 | c0015 | t0001 | g0052 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18962 | hp2 | a0001 | c0001 | t0001 | g0181 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18971 | hp1 | a0001 | c0006 | t0001 | g0015 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18971 | hp2 | a0001 | c0001 | t0001 | g0129 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18981 | hp1 | a0001 | c0001 | t0001 | g0092 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18981 | hp2 | a0001 | c0001 | t0001 | g0051 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18986 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18986 | hp2 | a0001 | c0001 | t0001 | g0173 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0180 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0087 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18999 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA18999 | hp2 | a0001 | c0001 | t0001 | g0172 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0076 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0191 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0036 | AFR | LWK | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA19030 | hp2 | a0002 | c0002 | t0002 | g0194 | AFR | LWK | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA19056 | hp1 | a0001 | c0001 | t0001 | g0192 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA19056 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0182 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA19085 | hp2 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA19087 | hp1 | a0001 | c0001 | t0001 | g0130 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0079 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA19091 | hp1 | a0001 | c0006 | t0001 | g0131 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA19091 | hp2 | a0001 | c0001 | t0008 | g0175 | EAS | JPT | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA20129 | hp1 | a0001 | c0001 | t0002 | g0001 | AFR | ASW | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA20129 | hp2 | a0001 | c0007 | t0002 | g0116 | AFR | ASW | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA20805 | hp1 | a0002 | c0002 | t0002 | g0013 | EUR | TSI | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA20805 | hp2 | a0001 | c0001 | t0006 | g0093 | EUR | TSI | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0008 | SAS | GIH | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA20905 | hp2 | a0002 | c0002 | t0002 | g0006 | SAS | GIH | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02109 | hp1 | a0001 | c0005 | t0005 | g0208 | AFR | ACB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0101 | AFR | ACB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02486 | hp1 | a0001 | c0004 | t0002 | g0189 | AFR | ACB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02486 | hp2 | a0001 | c0001 | t0002 | g0034 | AFR | ACB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0100 | AFR | ACB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG02559 | hp2 | a0001 | c0001 | t0002 | g0030 | AFR | ACB | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03471 | hp1 | a0009 | c0019 | t0002 | g0143 | AFR | MSL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
HG03471 | hp2 | a0001 | c0007 | t0002 | g0018 | AFR | MSL | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA21309 | hp1 | a0002 | c0012 | t0004 | g0014 | AFR | LWK | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
NA21309 | hp2 | a0002 | c0002 | t0002 | g0089 | AFR | LWK | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0001 | g0127 | REF | REF | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0094 | REF | REF | CEP162_chr6_84119250_84232643 | CEP162 | chr6 | 84119250 | 84232643 |
chr:pos | ref | alt | # # of ahapid:amino-acid(protein) level |
ahapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:84152827
|
C | T | 1 | a0006 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.3347G>A | p.Arg1116Lys | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/27 | 3470/5155 | 3347/4212 | 1116/1403 | chr6 | 84152827 | ||
chr6:84152981
|
C | T | 1 | a0009 | 1 | HG03471.hp1 | missense_variant | MODERATE | c.3193G>A | p.Asp1065Asn | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/27 | 3316/5155 | 3193/4212 | 1065/1403 | chr6 | 84152981 | ||
chr6:84153087
|
C | A | 1 | a0008 | 1 | HG02258.hp1 | missense_variant | MODERATE | c.3087G>T | p.Lys1029Asn | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/27 | 3210/5155 | 3087/4212 | 1029/1403 | chr6 | 84153087 | ||
chr6:84155380
|
T | C | 1 | a0010 | 1 | NA18522.hp1 | missense_variant | MODERATE | c.2912A>G | p.Lys971Arg | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/27 | 3035/5155 | 2912/4212 | 971/1403 | chr6 | 84155380 | ||
chr6:84171619
|
C | T | 1 | a0007 | 1 | NA18906.hp1 | missense_variant | MODERATE | c.2266G>A | p.Val756Ile | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/27 | 2389/5155 | 2266/4212 | 756/1403 | chr6 | 84171619 | ||
chr6:84174139
|
C | T | 1 | a0005 | 2 | HG02818.hp2 HG02965.hp1 |
missense_variant | MODERATE | c.2075G>A | p.Gly692Glu | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/27 | 2198/5155 | 2075/4212 | 692/1403 | chr6 | 84174139 | ||
chr6:84174775
|
T | TTCCTGTT others(38): Show |
2 | a0003a0011 | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
disruptive_inframe_insertion | MODERATE | c.1932_1976dupGAAAGA others(39): Show |
p.Glu659_Lys660insLy others(43): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 15/27 | 2099/5155 | 1976/4212 | 659/1403 | chr6 | 84174775 | ||
chr6:84186595
|
TTTC | T | 2 | a0003a0011 | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
conservative_inframe_deletion | MODERATE | c.1135_1137delGAA | p.Glu379del | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 12/27 | 1260/5155 | 1135/4212 | 379/1403 | chr6 | 84186595 | ||
chr6:84193676
|
C | G | 3 | a0002a0009a0010 | 19 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
missense_variant | MODERATE | c.1042G>C | p.Glu348Gln | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/27 | 1165/5155 | 1042/4212 | 348/1403 | chr6 | 84193676 | ||
chr6:84194886
|
G | C | 1 | a0004 | 3 | HG01346.hp1 HG02055.hp2 HG02451.hp2 |
missense_variant&splice_region_variant | MODERATE | c.1025C>G | p.Ser342Cys | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/27 | 1148/5155 | 1025/4212 | 342/1403 | chr6 | 84194886 | ||
chr6:84200854
|
T | C | 1 | a0011 | 1 | HG03834.hp2 | missense_variant | MODERATE | c.770A>G | p.Gln257Arg | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/27 | 893/5155 | 770/4212 | 257/1403 | chr6 | 84200854 | ||
chr6:84215403
|
G | T | 1 | a0006 | 1 | HG02280.hp2 | missense_variant | MODERATE | c.382C>A | p.Gln128Lys | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/27 | 505/5155 | 382/4212 | 128/1403 | chr6 | 84215403 | ||
chr6:84215865
|
A | G | 1 | a0012 | 1 | NA18962.hp1 | missense_variant | MODERATE | c.230T>C | p.Met77Thr | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 4/27 | 353/5155 | 230/4212 | 77/1403 | chr6 | 84215865 |
chr:pos | ref | alt | # # of chapid |
chapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:84125115
|
A | C | 1 | a0005c0010 | 2 | HG02818.hp2 HG02965.hp1 |
synonymous_variant | LOW | c.4167T>G | p.Val1389Val | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 27/27 | 4290/5155 | 4167/4212 | 1389/1403 | chr6 | 84125115 | ||
chr6:84146690
|
T | C | 6 | a0001c0004a0001c0007a0002c0002others(3): Show | 33 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(30): Show |
synonymous_variant | LOW | c.3867A>G | p.Lys1289Lys | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/27 | 3990/5155 | 3867/4212 | 1289/1403 | chr6 | 84146690 | ||
chr6:84146726
|
G | A | 1 | a0001c0008 | 4 | HG02717.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
synonymous_variant | LOW | c.3831C>T | p.Leu1277Leu | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/27 | 3954/5155 | 3831/4212 | 1277/1403 | chr6 | 84146726 | ||
chr6:84153021
|
A | C | 1 | a0001c0011 | 2 | HG02647.hp1 HG03209.hp1 |
synonymous_variant | LOW | c.3153T>G | p.Val1051Val | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/27 | 3276/5155 | 3153/4212 | 1051/1403 | chr6 | 84153021 | ||
chr6:84171710
|
T | C | 2 | a0001c0006a0004c0009 | 9 | HG01346.hp1 HG02055.hp2 HG02451.hp2 others(6): Show |
synonymous_variant | LOW | c.2175A>G | p.Glu725Glu | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/27 | 2298/5155 | 2175/4212 | 725/1403 | chr6 | 84171710 | ||
chr6:84185218
|
C | A | 1 | a0005c0010 | 2 | HG02818.hp2 HG02965.hp1 |
synonymous_variant | LOW | c.1632G>T | p.Ser544Ser | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/27 | 1755/5155 | 1632/4212 | 544/1403 | chr6 | 84185218 | ||
chr6:84212963
|
G | A | 4 | a0002c0002a0002c0012a0009c0019others(1): Show | 18 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(15): Show |
synonymous_variant | LOW | c.565C>T | p.Leu189Leu | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/27 | 688/5155 | 565/4212 | 189/1403 | chr6 | 84212963 | ||
chr6:84215431
|
G | A | 1 | a0003c0021 | 1 | HG01257.hp2 | synonymous_variant | LOW | c.354C>T | p.Leu118Leu | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/27 | 477/5155 | 354/4212 | 118/1403 | chr6 | 84215431 | ||
chr6:84215918
|
A | C | 6 | a0001c0005a0001c0007a0001c0008others(3): Show | 22 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(19): Show |
synonymous_variant | LOW | c.177T>G | p.Leu59Leu | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 4/27 | 300/5155 | 177/4212 | 59/1403 | chr6 | 84215918 |
chr:pos | ref | alt | # # of thapid:transcript level |
thapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:84124321
|
C | G | 5 | a0001c0005t0004a0001c0005t0005a0001c0008t0005others(2): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*749G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 27/27 | 749 | chr6 | 84124321 | |||||
chr6:84124359
|
A | G | 1 | a0001c0004t0010 | 1 | HG02976.hp2 | 3_prime_UTR_variant | MODIFIER | c.*711T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 27/27 | 711 | chr6 | 84124359 | |||||
chr6:84124360
|
G | T | 5 | a0001c0005t0004a0001c0005t0005a0001c0008t0005others(2): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*710C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 27/27 | 710 | chr6 | 84124360 | |||||
chr6:84124366
|
G | T | 1 | a0001c0001t0009 | 1 | NA18945.hp1 | 3_prime_UTR_variant | MODIFIER | c.*704C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 27/27 | 704 | chr6 | 84124366 | |||||
chr6:84124382
|
A | G | 1 | a0001c0001t0008 | 1 | NA19091.hp2 | 3_prime_UTR_variant | MODIFIER | c.*688T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 27/27 | 688 | chr6 | 84124382 | |||||
chr6:84124535
|
G | C | 24 | a0001c0001t0002a0001c0001t0003a0001c0004t0002others(21): Show | 90 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*535C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 27/27 | 535 | chr6 | 84124535 | |||||
chr6:84124563
|
T | C | 1 | a0001c0001t0006 | 2 | HG01943.hp1 NA20805.hp2 |
3_prime_UTR_variant | MODIFIER | c.*507A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 27/27 | 507 | chr6 | 84124563 | |||||
chr6:84124705
|
C | T | 4 | a0001c0001t0003a0003c0003t0003a0003c0021t0003others(1): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*365G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 27/27 | 365 | chr6 | 84124705 | |||||
chr6:84226406
|
T | C | 4 | a0001c0004t0007a0001c0005t0005a0001c0008t0005others(1): Show | 7 | HG01109.hp1 HG02109.hp1 HG02717.hp1 others(4): Show |
5_prime_UTR_variant | MODIFIER | c.-13A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/27 | 13 | chr6 | 84226406 | |||||
chr6:84226444
|
T | C | 1 | a0001c0001t0011 | 1 | HG01081.hp1 | 5_prime_UTR_variant | MODIFIER | c.-51A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/27 | 51 | chr6 | 84226444 |
chr:pos | ref | alt | # # of ghapid:genebody level |
ghapids | # # of haplotypeids |
haplotypeids | annotation | impact | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | genebody_biotype | rank | cdna cdna pos length |
cds cds pos length |
aa aa pos length |
distance | status | chr | pos |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr6:84125316
|
A | G | 1 | a0001c0001t0002g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.4006-40T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 26/26 | chr6 | 84125316 | ||||||
chr6:84125376
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.4006-100T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 26/26 | chr6 | 84125376 | ||||||
chr6:84125402
|
G | A | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.4006-126C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 26/26 | chr6 | 84125402 | ||||||
chr6:84125426
|
AAGG | A | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.4006-153_4006-151d others(5): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 26/26 | chr6 | 84125426 | ||||||
chr6:84125463
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.4006-187A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 26/26 | chr6 | 84125463 | ||||||
chr6:84125529
|
A | C | 1 | a0001c0001t0001g0151 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.4006-253T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 26/26 | chr6 | 84125529 | ||||||
chr6:84125687
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.4006-411C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 26/26 | chr6 | 84125687 | ||||||
chr6:84125697
|
G | A | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.4006-421C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 26/26 | chr6 | 84125697 | ||||||
chr6:84125812
|
A | C | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.4006-536T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 26/26 | chr6 | 84125812 | ||||||
chr6:84125887
|
C | T | 1 | a0011c0018t0003g0039 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.4005+491G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 26/26 | chr6 | 84125887 | ||||||
chr6:84125930
|
A | G | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.4005+448T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 26/26 | chr6 | 84125930 | ||||||
chr6:84125955
|
C | T | 4 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0081others(1): Show | 4 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.4005+423G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 26/26 | chr6 | 84125955 | ||||||
chr6:84126012
|
A | G | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.4005+366T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 26/26 | chr6 | 84126012 | ||||||
chr6:84126082
|
C | T | 1 | a0004c0009t0001g0124 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.4005+296G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 26/26 | chr6 | 84126082 | ||||||
chr6:84126211
|
G | C | 17 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(14): Show | 17 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.4005+167C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 26/26 | chr6 | 84126211 | ||||||
chr6:84126289
|
A | T | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.4005+89T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 26/26 | chr6 | 84126289 | ||||||
chr6:84126680
|
C | A | 16 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(13): Show | 16 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.3871-168G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84126680 | ||||||
chr6:84126791
|
T | G | 4 | a0001c0004t0002g0102a0001c0004t0002g0103a0001c0004t0002g0114others(1): Show | 4 | HG02717.hp2 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.3871-279A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84126791 | ||||||
chr6:84127019
|
C | T | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3871-507G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84127019 | ||||||
chr6:84127087
|
C | A | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3871-575G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84127087 | ||||||
chr6:84127274
|
C | T | 35 | a0001c0001t0003g0065a0001c0001t0003g0112a0001c0005t0004g0005others(32): Show | 35 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(32): Show |
intron_variant | MODIFIER | c.3871-762G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84127274 | ||||||
chr6:84127324
|
C | CTAATAA | 34 | a0001c0001t0003g0065a0001c0001t0003g0112a0001c0005t0004g0005others(31): Show | 34 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.3871-813_3871-812i others(8): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84127324 | ||||||
chr6:84127353
|
T | C | 1 | a0003c0003t0003g0046 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.3871-841A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84127353 | ||||||
chr6:84127458
|
A | G | 16 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(13): Show | 16 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.3871-946T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84127458 | ||||||
chr6:84127458
|
A | T | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3871-946T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84127458 | ||||||
chr6:84127552
|
T | C | 32 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0026others(29): Show | 32 | HG00280.hp2 HG00673.hp1 HG00738.hp1 others(29): Show |
intron_variant | MODIFIER | c.3871-1040A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84127552 | ||||||
chr6:84127588
|
A | G | 3 | a0001c0001t0001g0059a0001c0001t0001g0062a0001c0001t0001g0168 | 3 | HG00673.hp1 NA18940.hp2 NA18950.hp1 |
intron_variant | MODIFIER | c.3871-1076T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84127588 | ||||||
chr6:84127758
|
C | T | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3871-1246G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84127758 | ||||||
chr6:84127793
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0187 | 2 | NA18957.hp1 NA18988.hp2 |
intron_variant | MODIFIER | c.3871-1281C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84127793 | ||||||
chr6:84127823
|
G | C | 2 | a0001c0001t0002g0110a0001c0001t0002g0140 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.3871-1311C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84127823 | ||||||
chr6:84128007
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3871-1495G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84128007 | ||||||
chr6:84128104
|
C | T | 3 | a0002c0012t0004g0014a0005c0010t0002g0163a0005c0010t0002g0164 | 3 | HG02818.hp2 HG02965.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3871-1592G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84128104 | ||||||
chr6:84128172
|
A | G | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3871-1660T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84128172 | ||||||
chr6:84128296
|
G | A | 1 | a0001c0001t0001g0064 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.3871-1784C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84128296 | ||||||
chr6:84128369
|
CAT | C | 33 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(30): Show | 34 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.3871-1859_3871-185 others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84128369 | ||||||
chr6:84128452
|
G | T | 1 | a0001c0001t0001g0181 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.3871-1940C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84128452 | ||||||
chr6:84128508
|
G | C | 1 | a0001c0001t0001g0170 | 1 | HG00408.hp2 | intron_variant | MODIFIER | c.3871-1996C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84128508 | ||||||
chr6:84128767
|
C | T | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3871-2255G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84128767 | ||||||
chr6:84128866
|
C | T | 4 | a0001c0001t0001g0021a0001c0001t0001g0053a0001c0001t0001g0066others(1): Show | 4 | HG01261.hp1 HG01952.hp1 HG02004.hp2 others(1): Show |
intron_variant | MODIFIER | c.3871-2354G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84128866 | ||||||
chr6:84129034
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3871-2522A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84129034 | ||||||
chr6:84129135
|
A | G | 32 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(29): Show | 33 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.3871-2623T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84129135 | ||||||
chr6:84129200
|
T | C | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3871-2688A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84129200 | ||||||
chr6:84129381
|
C | T | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3871-2869G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84129381 | ||||||
chr6:84129430
|
T | C | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3871-2918A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84129430 | ||||||
chr6:84129452
|
T | C | 32 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(29): Show | 33 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.3871-2940A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84129452 | ||||||
chr6:84129531
|
A | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3871-3019T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84129531 | ||||||
chr6:84129867
|
T | C | 1 | a0001c0001t0001g0056 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.3871-3355A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84129867 | ||||||
chr6:84130071
|
C | T | 2 | a0003c0003t0003g0046a0011c0018t0003g0039 | 2 | HG02735.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.3871-3559G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84130071 | ||||||
chr6:84130092
|
G | A | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3871-3580C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84130092 | ||||||
chr6:84130216
|
C | A | 1 | a0001c0001t0001g0138 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.3871-3704G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84130216 | ||||||
chr6:84130567
|
C | T | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(46): Show | 52 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.3871-4055G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84130567 | ||||||
chr6:84130726
|
C | T | 1 | a0001c0001t0002g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3871-4214G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84130726 | ||||||
chr6:84130727
|
G | A | 1 | a0001c0001t0002g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3871-4215C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84130727 | ||||||
chr6:84130737
|
T | C | 1 | a0002c0012t0004g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3871-4225A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84130737 | ||||||
chr6:84130894
|
C | T | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3871-4382G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84130894 | ||||||
chr6:84130938
|
T | C | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3871-4426A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84130938 | ||||||
chr6:84131032
|
T | C | 1 | a0001c0001t0001g0044 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.3871-4520A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131032 | ||||||
chr6:84131047
|
T | G | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3871-4535A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131047 | ||||||
chr6:84131049
|
C | T | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3871-4537G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131049 | ||||||
chr6:84131050
|
G | A | 1 | a0002c0002t0002g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3871-4538C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131050 | ||||||
chr6:84131126
|
T | C | 5 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.3871-4614A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131126 | ||||||
chr6:84131161
|
A | G | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3871-4649T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131161 | ||||||
chr6:84131264
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3871-4752A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131264 | ||||||
chr6:84131457
|
T | C | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(82): Show | 88 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.3871-4945A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131457 | ||||||
chr6:84131530
|
C | G | 30 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0026others(27): Show | 30 | HG00280.hp2 HG00673.hp1 HG00738.hp1 others(27): Show |
intron_variant | MODIFIER | c.3871-5018G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131530 | ||||||
chr6:84131665
|
CT | C | 37 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(34): Show | 38 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(35): Show |
intron_variant | MODIFIER | c.3871-5154delA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131665 | ||||||
chr6:84131673
|
TTG | T | 25 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(22): Show | 27 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.3871-5163_3871-516 others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131673 | ||||||
chr6:84131674
|
TG | T | 4 | a0001c0001t0002g0197a0002c0012t0002g0193a0005c0010t0002g0163others(1): Show | 4 | HG02257.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.3871-5163delC | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131674 | ||||||
chr6:84131675
|
G | T | 17 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(14): Show | 17 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(14): Show |
intron_variant | MODIFIER | c.3871-5163C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131675 | ||||||
chr6:84131680
|
G | T | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3871-5168C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131680 | ||||||
chr6:84131720
|
C | G | 1 | a0001c0001t0001g0075 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.3871-5208G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131720 | ||||||
chr6:84131760
|
A | G | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3871-5248T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131760 | ||||||
chr6:84131771
|
C | G | 8 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(5): Show | 8 | HG02109.hp1 HG02258.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.3871-5259G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131771 | ||||||
chr6:84131780
|
T | C | 1 | a0001c0004t0002g0114 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3871-5268A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131780 | ||||||
chr6:84131796
|
G | A | 1 | a0001c0004t0002g0114 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3871-5284C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131796 | ||||||
chr6:84131822
|
GAGCATTT | G | 3 | a0001c0007t0002g0116a0001c0007t0002g0117a0001c0007t0002g0118 | 3 | HG02723.hp2 HG02809.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.3871-5317_3871-531 others(11): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84131822 | ||||||
chr6:84132025
|
A | G | 1 | a0001c0007t0002g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.3871-5513T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84132025 | ||||||
chr6:84132031
|
T | G | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3871-5519A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84132031 | ||||||
chr6:84132463
|
G | A | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3871-5951C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84132463 | ||||||
chr6:84132490
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3871-5978A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84132490 | ||||||
chr6:84132537
|
C | T | 2 | a0001c0004t0002g0210a0001c0004t0002g0211 | 2 | HG00741.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.3871-6025G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84132537 | ||||||
chr6:84132555
|
T | C | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3871-6043A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84132555 | ||||||
chr6:84132658
|
A | G | 87 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(84): Show | 90 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(87): Show |
intron_variant | MODIFIER | c.3871-6146T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84132658 | ||||||
chr6:84132672
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.3871-6160C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84132672 | ||||||
chr6:84132963
|
GCT | G | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3871-6453_3871-645 others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84132963 | ||||||
chr6:84133148
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3871-6636A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84133148 | ||||||
chr6:84133217
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3871-6705A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84133217 | ||||||
chr6:84133243
|
C | T | 1 | a0004c0009t0001g0124 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.3871-6731G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84133243 | ||||||
chr6:84133259
|
C | T | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3871-6747G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84133259 | ||||||
chr6:84133324
|
A | G | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3871-6812T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84133324 | ||||||
chr6:84133360
|
C | CT | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3871-6849dupA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84133360 | ||||||
chr6:84133566
|
G | A | 1 | a0001c0001t0001g0108 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.3871-7054C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84133566 | ||||||
chr6:84133610
|
C | T | 1 | a0001c0001t0009g0122 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.3871-7098G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84133610 | ||||||
chr6:84133756
|
C | T | 2 | a0001c0006t0001g0007a0001c0006t0001g0011 | 2 | HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.3871-7244G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84133756 | ||||||
chr6:84133757
|
G | A | 11 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(8): Show | 13 | HG01884.hp2 HG02055.hp1 HG02257.hp1 others(10): Show |
intron_variant | MODIFIER | c.3871-7245C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84133757 | ||||||
chr6:84133840
|
C | T | 16 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(13): Show | 17 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.3871-7328G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84133840 | ||||||
chr6:84133861
|
T | C | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(82): Show | 88 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.3871-7349A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84133861 | ||||||
chr6:84134066
|
G | A | 1 | a0004c0009t0001g0135 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.3871-7554C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134066 | ||||||
chr6:84134129
|
G | A | 1 | a0001c0007t0002g0018 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.3871-7617C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134129 | ||||||
chr6:84134218
|
T | G | 1 | a0001c0001t0001g0174 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3871-7706A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134218 | ||||||
chr6:84134223
|
A | G | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3871-7711T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134223 | ||||||
chr6:84134298
|
G | C | 1 | a0001c0001t0002g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3871-7786C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134298 | ||||||
chr6:84134531
|
T | C | 1 | a0001c0001t0001g0092 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.3871-8019A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134531 | ||||||
chr6:84134577
|
C | T | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3871-8065G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134577 | ||||||
chr6:84134609
|
G | A | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3871-8097C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134609 | ||||||
chr6:84134693
|
C | T | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3871-8181G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134693 | ||||||
chr6:84134737
|
C | G | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3871-8225G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134737 | ||||||
chr6:84134837
|
AATTAT | A | 7 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(4): Show | 7 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.3871-8330_3871-832 others(9): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134837 | ||||||
chr6:84134877
|
A | G | 16 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(13): Show | 16 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.3871-8365T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134877 | ||||||
chr6:84134913
|
C | CAT | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG02055.hp1 HG02451.hp1 HG02486.hp2 others(9): Show |
intron_variant | MODIFIER | c.3871-8403_3871-840 others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134913 | ||||||
chr6:84134919
|
T | C | 4 | a0001c0001t0002g0199a0001c0001t0002g0200a0001c0001t0002g0201others(1): Show | 4 | HG02647.hp2 HG02809.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.3871-8407A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134919 | ||||||
chr6:84134919
|
T | TAC | 2 | a0002c0012t0004g0014a0012c0015t0001g0052 | 2 | NA18962.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.3871-8409_3871-840 others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134919 | ||||||
chr6:84134919
|
T | TATAC | 2 | a0001c0001t0002g0031a0005c0010t0002g0163 | 2 | HG01884.hp2 HG02818.hp2 |
intron_variant | MODIFIER | c.3871-8408_3871-840 others(8): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134919 | ||||||
chr6:84134919
|
TAC | T | 37 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(34): Show | 38 | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(35): Show |
intron_variant | MODIFIER | c.3871-8409_3871-840 others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134919 | ||||||
chr6:84134919
|
TACAC | T | 114 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(111): Show | 114 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(111): Show |
intron_variant | MODIFIER | c.3871-8411_3871-840 others(8): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134919 | ||||||
chr6:84134919
|
TACACAC | T | 8 | a0001c0001t0001g0022a0001c0001t0001g0139a0001c0004t0002g0012others(5): Show | 8 | HG02257.hp2 HG02273.hp1 HG02723.hp2 others(5): Show |
intron_variant | MODIFIER | c.3871-8413_3871-840 others(10): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134919 | ||||||
chr6:84134919
|
TACACACA others(3): Show |
T | 1 | a0008c0014t0004g0115 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.3871-8417_3871-840 others(14): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134919 | ||||||
chr6:84134919
|
TACACACA others(11): Show |
T | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3871-8425_3871-840 others(22): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134919 | ||||||
chr6:84134921
|
C | T | 3 | a0001c0006t0002g0156a0003c0003t0003g0090a0003c0003t0003g0091 | 3 | HG02886.hp1 HG03225.hp2 HG03669.hp1 |
intron_variant | MODIFIER | c.3871-8409G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134921 | ||||||
chr6:84134923
|
C | T | 16 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0003g0065others(13): Show | 17 | HG01074.hp2 HG01243.hp2 HG01256.hp1 others(14): Show |
intron_variant | MODIFIER | c.3871-8411G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134923 | ||||||
chr6:84134925
|
C | T | 23 | a0001c0001t0002g0037a0001c0001t0002g0197a0001c0004t0002g0102others(20): Show | 23 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.3871-8413G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134925 | ||||||
chr6:84134927
|
C | T | 6 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0007t0002g0017others(3): Show | 6 | HG02257.hp2 HG02723.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.3871-8415G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134927 | ||||||
chr6:84134929
|
C | A | 1 | a0001c0006t0002g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3871-8417G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134929 | ||||||
chr6:84134939
|
C | T | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3871-8427G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134939 | ||||||
chr6:84134949
|
C | T | 1 | a0001c0006t0002g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3871-8437G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134949 | ||||||
chr6:84134957
|
T | C | 1 | a0001c0001t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.3871-8445A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84134957 | ||||||
chr6:84135106
|
T | C | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3871-8594A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84135106 | ||||||
chr6:84135323
|
T | G | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3871-8811A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84135323 | ||||||
chr6:84135386
|
C | T | 1 | a0001c0001t0001g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.3871-8874G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84135386 | ||||||
chr6:84135451
|
C | CAGACTGC others(10): Show |
5 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.3871-8956_3871-894 others(21): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84135451 | ||||||
chr6:84135601
|
G | A | 1 | a0001c0001t0001g0130 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.3871-9089C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84135601 | ||||||
chr6:84135620
|
T | TG | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3871-9109dupC | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84135620 | ||||||
chr6:84135720
|
G | A | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3871-9208C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84135720 | ||||||
chr6:84136078
|
C | A | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3871-9566G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84136078 | ||||||
chr6:84136111
|
T | G | 2 | a0003c0003t0003g0046a0011c0018t0003g0039 | 2 | HG02735.hp1 HG03834.hp2 |
intron_variant | MODIFIER | c.3871-9599A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84136111 | ||||||
chr6:84136200
|
T | C | 1 | a0001c0005t0005g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.3871-9688A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84136200 | ||||||
chr6:84136215
|
C | T | 4 | a0001c0008t0005g0203a0001c0008t0005g0204a0001c0008t0005g0205others(1): Show | 4 | HG02717.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3871-9703G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84136215 | ||||||
chr6:84136221
|
T | C | 2 | a0001c0005t0004g0005a0001c0005t0004g0195 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3871-9709A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84136221 | ||||||
chr6:84136243
|
T | C | 11 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(8): Show | 13 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.3871-9731A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84136243 | ||||||
chr6:84136246
|
T | TAA | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3871-9735_3871-973 others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84136246 | ||||||
chr6:84136368
|
A | G | 1 | a0001c0001t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.3871-9856T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84136368 | ||||||
chr6:84136520
|
C | T | 1 | a0001c0001t0002g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.3871-10008G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84136520 | ||||||
chr6:84136903
|
C | T | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3870+9784G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84136903 | ||||||
chr6:84136924
|
G | A | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3870+9763C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84136924 | ||||||
chr6:84136998
|
C | T | 4 | a0001c0008t0005g0203a0001c0008t0005g0204a0001c0008t0005g0205others(1): Show | 4 | HG02717.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.3870+9689G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84136998 | ||||||
chr6:84137025
|
T | C | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3870+9662A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84137025 | ||||||
chr6:84137069
|
G | A | 2 | a0001c0001t0002g0199a0001c0001t0002g0201 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3870+9618C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84137069 | ||||||
chr6:84137294
|
C | T | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(83): Show | 89 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(86): Show |
intron_variant | MODIFIER | c.3870+9393G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84137294 | ||||||
chr6:84137372
|
TTCCACTA | T | 3 | a0001c0004t0002g0189a0001c0004t0002g0190a0001c0004t0007g0207 | 3 | HG01109.hp1 HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.3870+9308_3870+931 others(11): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84137372 | ||||||
chr6:84137537
|
A | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3870+9150T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84137537 | ||||||
chr6:84137549
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3870+9138G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84137549 | ||||||
chr6:84137646
|
A | G | 25 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(22): Show | 25 | HG01884.hp1 HG02109.hp1 HG02258.hp1 others(22): Show |
intron_variant | MODIFIER | c.3870+9041T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84137646 | ||||||
chr6:84138035
|
C | A | 1 | a0001c0001t0002g0033 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3870+8652G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84138035 | ||||||
chr6:84138125
|
T | C | 87 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(84): Show | 90 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(87): Show |
intron_variant | MODIFIER | c.3870+8562A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84138125 | ||||||
chr6:84138300
|
G | C | 11 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(8): Show | 11 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.3870+8387C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84138300 | ||||||
chr6:84138431
|
C | G | 35 | a0001c0001t0003g0065a0001c0001t0003g0112a0001c0005t0004g0005others(32): Show | 35 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(32): Show |
intron_variant | MODIFIER | c.3870+8256G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84138431 | ||||||
chr6:84138439
|
G | A | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3870+8248C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84138439 | ||||||
chr6:84138458
|
C | T | 1 | a0002c0002t0002g0003 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.3870+8229G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84138458 | ||||||
chr6:84138502
|
A | T | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3870+8185T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84138502 | ||||||
chr6:84138604
|
G | C | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3870+8083C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84138604 | ||||||
chr6:84138758
|
A | T | 2 | a0001c0001t0001g0076a0001c0001t0001g0150 | 2 | NA19009.hp1 NA19056.hp2 |
intron_variant | MODIFIER | c.3870+7929T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84138758 | ||||||
chr6:84138853
|
G | A | 1 | a0001c0005t0004g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.3870+7834C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84138853 | ||||||
chr6:84138879
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3870+7808G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84138879 | ||||||
chr6:84139203
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3870+7484G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84139203 | ||||||
chr6:84139574
|
TGGAACCT others(3): Show |
T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3870+7103_3870+711 others(14): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84139574 | ||||||
chr6:84139692
|
A | C | 32 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(29): Show | 33 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.3870+6995T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84139692 | ||||||
chr6:84139933
|
G | GCTGGTGT others(19): Show |
10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3870+6753_3870+675 others(30): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84139933 | ||||||
chr6:84139933
|
G | GCTGGTGT others(19): Show |
73 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0197others(70): Show | 74 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(71): Show |
intron_variant | MODIFIER | c.3870+6728_3870+675 others(30): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84139933 | ||||||
chr6:84139998
|
G | A | 117 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0026others(114): Show | 120 | HG00280.hp2 HG00408.hp2 HG00673.hp1 others(117): Show |
intron_variant | MODIFIER | c.3870+6689C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84139998 | ||||||
chr6:84140115
|
A | G | 18 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(15): Show | 18 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(15): Show |
intron_variant | MODIFIER | c.3870+6572T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84140115 | ||||||
chr6:84140250
|
G | A | 1 | a0001c0001t0002g0028 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.3870+6437C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84140250 | ||||||
chr6:84140280
|
G | C | 1 | a0001c0001t0001g0024 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.3870+6407C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84140280 | ||||||
chr6:84140528
|
TTTTG | T | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3870+6155_3870+615 others(8): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84140528 | ||||||
chr6:84140915
|
A | G | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3870+5772T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84140915 | ||||||
chr6:84140941
|
G | A | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3870+5746C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84140941 | ||||||
chr6:84141102
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3870+5585A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84141102 | ||||||
chr6:84141107
|
C | T | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3870+5580G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84141107 | ||||||
chr6:84141108
|
G | GC | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.3870+5578dupG | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84141108 | ||||||
chr6:84141153
|
A | G | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3870+5534T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84141153 | ||||||
chr6:84141253
|
AT | A | 86 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(83): Show | 89 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(86): Show |
intron_variant | MODIFIER | c.3870+5433delA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84141253 | ||||||
chr6:84141582
|
C | A | 1 | a0001c0001t0001g0129 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.3870+5105G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84141582 | ||||||
chr6:84141678
|
G | T | 31 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0026others(28): Show | 31 | HG00280.hp2 HG00408.hp2 HG00673.hp1 others(28): Show |
intron_variant | MODIFIER | c.3870+5009C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84141678 | ||||||
chr6:84141754
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3870+4933G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84141754 | ||||||
chr6:84141965
|
G | A | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3870+4722C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84141965 | ||||||
chr6:84142044
|
C | T | 1 | a0001c0001t0001g0153 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3870+4643G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84142044 | ||||||
chr6:84142071
|
A | G | 1 | a0001c0001t0001g0162 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.3870+4616T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84142071 | ||||||
chr6:84142598
|
T | G | 3 | a0001c0001t0002g0199a0001c0001t0002g0200a0001c0001t0002g0201 | 3 | HG02647.hp2 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3870+4089A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84142598 | ||||||
chr6:84142774
|
C | T | 4 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0029others(1): Show | 6 | HG02055.hp1 HG02451.hp1 HG02559.hp2 others(3): Show |
intron_variant | MODIFIER | c.3870+3913G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84142774 | ||||||
chr6:84142870
|
GCCTA | G | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3870+3813_3870+381 others(8): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84142870 | ||||||
chr6:84142875
|
A | T | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3870+3812T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84142875 | ||||||
chr6:84142876
|
C | G | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3870+3811G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84142876 | ||||||
chr6:84143047
|
T | G | 1 | a0001c0001t0001g0174 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.3870+3640A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84143047 | ||||||
chr6:84143059
|
T | A | 2 | a0001c0001t0001g0123a0001c0001t0001g0136 | 2 | HG00639.hp1 HG01515.hp1 |
intron_variant | MODIFIER | c.3870+3628A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84143059 | ||||||
chr6:84143540
|
G | A | 1 | a0001c0001t0001g0077 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.3870+3147C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84143540 | ||||||
chr6:84143719
|
C | G | 1 | a0001c0001t0002g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3870+2968G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84143719 | ||||||
chr6:84143904
|
T | C | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(82): Show | 88 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.3870+2783A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84143904 | ||||||
chr6:84143922
|
T | C | 1 | a0002c0002t0002g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.3870+2765A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84143922 | ||||||
chr6:84144019
|
A | T | 16 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(13): Show | 17 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.3870+2668T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84144019 | ||||||
chr6:84144086
|
A | G | 1 | a0001c0001t0002g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3870+2601T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84144086 | ||||||
chr6:84144212
|
C | T | 1 | a0002c0012t0004g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3870+2475G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84144212 | ||||||
chr6:84144227
|
A | G | 80 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(77): Show | 83 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(80): Show |
intron_variant | MODIFIER | c.3870+2460T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84144227 | ||||||
chr6:84144235
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3870+2452A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84144235 | ||||||
chr6:84144287
|
C | T | 2 | a0001c0001t0001g0066a0001c0001t0001g0069 | 2 | HG01952.hp1 HG02148.hp2 |
intron_variant | MODIFIER | c.3870+2400G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84144287 | ||||||
chr6:84144457
|
T | C | 87 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(84): Show | 90 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(87): Show |
intron_variant | MODIFIER | c.3870+2230A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84144457 | ||||||
chr6:84144628
|
C | T | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3870+2059G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84144628 | ||||||
chr6:84144694
|
C | T | 1 | a0001c0001t0001g0073 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.3870+1993G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84144694 | ||||||
chr6:84145352
|
A | G | 1 | a0001c0001t0001g0057 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.3870+1335T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84145352 | ||||||
chr6:84145371
|
T | A | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3870+1316A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84145371 | ||||||
chr6:84145666
|
C | G | 1 | a0001c0001t0001g0169 | 1 | HG02293.hp1 | intron_variant | MODIFIER | c.3870+1021G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84145666 | ||||||
chr6:84145955
|
G | A | 83 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(80): Show | 86 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(83): Show |
intron_variant | MODIFIER | c.3870+732C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84145955 | ||||||
chr6:84146115
|
A | G | 1 | a0001c0001t0002g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3870+572T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84146115 | ||||||
chr6:84146224
|
T | C | 1 | a0001c0001t0001g0176 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.3870+463A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84146224 | ||||||
chr6:84146238
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3870+449G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84146238 | ||||||
chr6:84146252
|
C | T | 1 | a0002c0012t0004g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3870+435G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84146252 | ||||||
chr6:84146385
|
C | T | 2 | a0001c0001t0003g0065a0001c0001t0003g0112 | 2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.3870+302G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84146385 | ||||||
chr6:84146471
|
T | G | 1 | a0001c0008t0005g0204 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.3870+216A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84146471 | ||||||
chr6:84146590
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.3870+97A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 25/26 | chr6 | 84146590 | ||||||
chr6:84146961
|
T | A | 1 | a0002c0012t0004g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3772-176A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84146961 | ||||||
chr6:84146965
|
C | T | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3772-180G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84146965 | ||||||
chr6:84147099
|
C | T | 2 | a0001c0001t0001g0130a0001c0001t0001g0182 | 2 | NA19085.hp1 NA19087.hp1 |
intron_variant | MODIFIER | c.3772-314G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84147099 | ||||||
chr6:84147255
|
TCTCA | T | 5 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.3772-474_3772-471d others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84147255 | ||||||
chr6:84147323
|
A | G | 32 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(29): Show | 33 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.3772-538T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84147323 | ||||||
chr6:84147458
|
G | A | 1 | a0001c0001t0001g0079 | 1 | NA19087.hp2 | intron_variant | MODIFIER | c.3772-673C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84147458 | ||||||
chr6:84147548
|
T | A | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3772-763A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84147548 | ||||||
chr6:84147629
|
A | G | 11 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(8): Show | 13 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.3772-844T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84147629 | ||||||
chr6:84147739
|
T | C | 1 | a0001c0006t0002g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3772-954A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84147739 | ||||||
chr6:84147839
|
T | C | 1 | a0001c0006t0002g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.3772-1054A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84147839 | ||||||
chr6:84147845
|
A | T | 1 | a0001c0001t0002g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3772-1060T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84147845 | ||||||
chr6:84147986
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.3772-1201G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84147986 | ||||||
chr6:84148025
|
T | C | 5 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.3772-1240A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84148025 | ||||||
chr6:84148134
|
G | C | 11 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(8): Show | 13 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.3772-1349C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84148134 | ||||||
chr6:84148283
|
C | T | 1 | a0001c0001t0001g0025 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3771+1279G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84148283 | ||||||
chr6:84148385
|
C | T | 7 | a0001c0001t0001g0016a0001c0001t0001g0171a0001c0001t0001g0173others(4): Show | 7 | HG00673.hp2 HG02056.hp2 HG03834.hp1 others(4): Show |
intron_variant | MODIFIER | c.3771+1177G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84148385 | ||||||
chr6:84148434
|
C | T | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3771+1128G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84148434 | ||||||
chr6:84148472
|
T | C | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3771+1090A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84148472 | ||||||
chr6:84148699
|
T | G | 2 | a0001c0001t0001g0158a0001c0001t0001g0161 | 2 | HG00558.hp2 NA18950.hp2 |
intron_variant | MODIFIER | c.3771+863A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84148699 | ||||||
chr6:84148734
|
G | A | 1 | a0001c0001t0002g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3771+828C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84148734 | ||||||
chr6:84148735
|
A | C | 1 | a0001c0001t0002g0032 | 1 | HG03225.hp1 | intron_variant | MODIFIER | c.3771+827T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84148735 | ||||||
chr6:84149112
|
G | C | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3771+450C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84149112 | ||||||
chr6:84149160
|
C | A | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3771+402G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84149160 | ||||||
chr6:84149350
|
AAAATT | A | 3 | a0002c0002t0002g0119a0002c0002t0002g0146a0002c0002t0002g0155 | 3 | HG02615.hp2 HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.3771+207_3771+211d others(7): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84149350 | ||||||
chr6:84149421
|
T | C | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.3771+141A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 24/26 | chr6 | 84149421 | ||||||
chr6:84149760
|
A | G | 1 | a0002c0012t0004g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3630-57T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84149760 | ||||||
chr6:84149952
|
A | AT | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(82): Show | 88 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.3630-250_3630-249i others(3): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84149952 | ||||||
chr6:84149984
|
T | C | 3 | a0001c0001t0001g0171a0001c0001t0001g0184a0001c0001t0001g0186 | 3 | HG00673.hp2 HG02056.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.3630-281A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84149984 | ||||||
chr6:84150151
|
T | C | 40 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(37): Show | 41 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(38): Show |
intron_variant | MODIFIER | c.3630-448A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84150151 | ||||||
chr6:84150175
|
T | A | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3630-472A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84150175 | ||||||
chr6:84150226
|
A | AT | 34 | a0001c0001t0003g0065a0001c0001t0003g0112a0001c0005t0004g0005others(31): Show | 34 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.3630-524dupA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84150226 | ||||||
chr6:84150585
|
G | A | 14 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(11): Show | 14 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.3630-882C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84150585 | ||||||
chr6:84151020
|
G | A | 1 | a0001c0001t0002g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3630-1317C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84151020 | ||||||
chr6:84151048
|
G | A | 1 | a0003c0003t0001g0043 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.3630-1345C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84151048 | ||||||
chr6:84151093
|
G | A | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3630-1390C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84151093 | ||||||
chr6:84151272
|
G | A | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.3629+1273C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84151272 | ||||||
chr6:84151454
|
T | C | 16 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(13): Show | 16 | HG00741.hp2 HG01109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.3629+1091A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84151454 | ||||||
chr6:84151503
|
C | T | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3629+1042G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84151503 | ||||||
chr6:84151596
|
G | A | 14 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(11): Show | 14 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.3629+949C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84151596 | ||||||
chr6:84151772
|
G | A | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(82): Show | 88 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.3629+773C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84151772 | ||||||
chr6:84151808
|
T | C | 2 | a0001c0001t0001g0126a0001c0001t0001g0128 | 2 | HG01257.hp1 HG01258.hp2 |
intron_variant | MODIFIER | c.3629+737A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84151808 | ||||||
chr6:84151933
|
T | G | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(82): Show | 88 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.3629+612A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84151933 | ||||||
chr6:84152075
|
T | G | 17 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(14): Show | 17 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(14): Show |
intron_variant | MODIFIER | c.3629+470A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84152075 | ||||||
chr6:84152077
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3629+468A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84152077 | ||||||
chr6:84152164
|
C | T | 2 | a0001c0001t0002g0199a0001c0001t0002g0201 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3629+381G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84152164 | ||||||
chr6:84152306
|
C | T | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.3629+239G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84152306 | ||||||
chr6:84152336
|
G | A | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.3629+209C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84152336 | ||||||
chr6:84152341
|
G | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.3629+204C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84152341 | ||||||
chr6:84152394
|
C | T | 1 | a0001c0001t0002g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.3629+151G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84152394 | ||||||
chr6:84152447
|
C | T | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.3629+98G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84152447 | ||||||
chr6:84152448
|
G | A | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.3629+97C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 23/26 | chr6 | 84152448 | ||||||
chr6:84153421
|
A | G | 1 | a0001c0005t0005g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.2995-242T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84153421 | ||||||
chr6:84153546
|
T | G | 3 | a0001c0004t0002g0189a0001c0004t0002g0190a0001c0004t0007g0207 | 3 | HG01109.hp1 HG02486.hp1 HG03139.hp2 |
intron_variant | MODIFIER | c.2995-367A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84153546 | ||||||
chr6:84153564
|
C | T | 16 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(13): Show | 17 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.2995-385G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84153564 | ||||||
chr6:84153630
|
G | T | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2995-451C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84153630 | ||||||
chr6:84153800
|
A | C | 1 | a0007c0017t0001g0149 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.2995-621T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84153800 | ||||||
chr6:84153823
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.2995-644G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84153823 | ||||||
chr6:84153853
|
G | A | 1 | a0001c0001t0001g0157 | 1 | HG01106.hp2 | intron_variant | MODIFIER | c.2995-674C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84153853 | ||||||
chr6:84153867
|
C | G | 1 | a0001c0001t0001g0050 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.2995-688G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84153867 | ||||||
chr6:84153925
|
C | T | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2995-746G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84153925 | ||||||
chr6:84153932
|
G | A | 48 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(45): Show | 51 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(48): Show |
intron_variant | MODIFIER | c.2995-753C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84153932 | ||||||
chr6:84154056
|
T | C | 19 | a0001c0001t0001g0072a0001c0001t0001g0120a0001c0001t0001g0139others(16): Show | 19 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2995-877A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154056 | ||||||
chr6:84154244
|
A | G | 197 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(194): Show | 200 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(197): Show |
intron_variant | MODIFIER | c.2994+1054T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154244 | ||||||
chr6:84154312
|
A | ATATC | 8 | a0001c0001t0001g0072a0001c0001t0002g0110a0001c0001t0002g0140others(5): Show | 8 | HG01884.hp1 HG02280.hp1 HG02647.hp2 others(5): Show |
intron_variant | MODIFIER | c.2994+982_2994+985d others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154312 | ||||||
chr6:84154312
|
A | ATATCTAT others(1): Show |
2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2994+978_2994+985d others(10): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154312 | ||||||
chr6:84154312
|
ATATC | A | 34 | a0001c0001t0002g0197a0001c0004t0002g0012a0001c0004t0002g0095others(31): Show | 34 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(31): Show |
intron_variant | MODIFIER | c.2994+982_2994+985d others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154312 | ||||||
chr6:84154312
|
ATATCTAT others(5): Show |
A | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2994+974_2994+985d others(14): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154312 | ||||||
chr6:84154312
|
ATATCTAT others(9): Show |
A | 16 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(13): Show | 16 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(13): Show |
intron_variant | MODIFIER | c.2994+970_2994+985d others(18): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154312 | ||||||
chr6:84154330
|
A | ATCTG | 20 | a0001c0001t0001g0109a0001c0001t0002g0037a0001c0001t0002g0038others(17): Show | 20 | HG01074.hp2 HG01109.hp2 HG02109.hp1 others(17): Show |
intron_variant | MODIFIER | c.2994+964_2994+967d others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154330 | ||||||
chr6:84154330
|
A | ATCTGTCT others(1): Show |
14 | a0001c0005t0004g0005a0001c0005t0004g0106a0001c0005t0004g0195others(11): Show | 14 | HG02258.hp1 HG02615.hp2 HG02723.hp1 others(11): Show |
intron_variant | MODIFIER | c.2994+960_2994+967d others(10): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154330 | ||||||
chr6:84154330
|
A | ATCTGTCT others(5): Show |
17 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(14): Show | 18 | HG01109.hp1 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2994+956_2994+967d others(14): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154330 | ||||||
chr6:84154330
|
A | ATCTGTCT others(9): Show |
1 | a0002c0002t0002g0006 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.2994+952_2994+967d others(18): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154330 | ||||||
chr6:84154330
|
A | G | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2994+968T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154330 | ||||||
chr6:84154330
|
ATCTG | A | 3 | a0001c0001t0001g0063a0001c0001t0001g0096a0001c0001t0001g0154 | 3 | HG01192.hp1 HG03704.hp2 HG03831.hp1 |
intron_variant | MODIFIER | c.2994+964_2994+967d others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154330 | ||||||
chr6:84154350
|
G | GTCTA | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2994+947_2994+948i others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154350 | ||||||
chr6:84154354
|
G | A | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2994+944C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154354 | ||||||
chr6:84154358
|
G | A | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2994+940C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154358 | ||||||
chr6:84154358
|
G | GTCTA | 2 | a0001c0006t0001g0133a0004c0009t0001g0124 | 2 | HG02451.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.2994+936_2994+939d others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154358 | ||||||
chr6:84154358
|
G | GTCTGTCT others(5): Show |
1 | a0005c0010t0002g0163 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.2994+939_2994+940i others(14): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154358 | ||||||
chr6:84154358
|
G | GTCTGTCT others(21): Show |
1 | a0001c0005t0004g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2994+939_2994+940i others(30): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154358 | ||||||
chr6:84154358
|
G | GTCTGTCT others(9): Show |
2 | a0001c0004t0002g0211a0005c0010t0002g0164 | 2 | HG00741.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2994+939_2994+940i others(18): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154358 | ||||||
chr6:84154362
|
A | G | 25 | a0001c0001t0002g0197a0001c0001t0002g0199a0001c0001t0002g0201others(22): Show | 25 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(22): Show |
intron_variant | MODIFIER | c.2994+936T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154362 | ||||||
chr6:84154366
|
A | G | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2994+932T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154366 | ||||||
chr6:84154367
|
TCTATCTA others(5): Show |
T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2994+919_2994+930d others(14): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154367 | ||||||
chr6:84154370
|
A | G | 14 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.2994+928T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154370 | ||||||
chr6:84154375
|
T | C | 2 | a0001c0001t0002g0197a0001c0006t0002g0156 | 2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2994+923A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154375 | ||||||
chr6:84154379
|
C | T | 34 | a0001c0001t0002g0199a0001c0001t0002g0201a0001c0001t0003g0065others(31): Show | 34 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.2994+919G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154379 | ||||||
chr6:84154383
|
T | C | 2 | a0001c0001t0002g0199a0001c0001t0002g0201 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.2994+915A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154383 | ||||||
chr6:84154416
|
C | G | 87 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(84): Show | 90 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(87): Show |
intron_variant | MODIFIER | c.2994+882G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154416 | ||||||
chr6:84154421
|
T | C | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2994+877A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154421 | ||||||
chr6:84154491
|
C | A | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2994+807G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154491 | ||||||
chr6:84154564
|
A | G | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2994+734T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154564 | ||||||
chr6:84154637
|
T | C | 1 | a0001c0001t0003g0112 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.2994+661A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154637 | ||||||
chr6:84154668
|
T | C | 5 | a0001c0001t0001g0097a0001c0001t0001g0098a0001c0001t0001g0099others(2): Show | 5 | HG02109.hp2 HG02559.hp1 HG02622.hp1 others(2): Show |
intron_variant | MODIFIER | c.2994+630A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154668 | ||||||
chr6:84154837
|
C | A | 1 | a0001c0001t0002g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2994+461G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84154837 | ||||||
chr6:84155131
|
C | T | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2994+167G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 22/26 | chr6 | 84155131 | ||||||
chr6:84155668
|
T | C | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(82): Show | 88 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.2782-158A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84155668 | ||||||
chr6:84155894
|
C | T | 34 | a0001c0001t0003g0065a0001c0001t0003g0112a0001c0005t0004g0005others(31): Show | 34 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.2782-384G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84155894 | ||||||
chr6:84155984
|
T | C | 1 | a0002c0012t0004g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2782-474A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84155984 | ||||||
chr6:84156031
|
A | ACAT | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2782-524_2782-522d others(5): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156031 | ||||||
chr6:84156067
|
T | A | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2782-557A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156067 | ||||||
chr6:84156080
|
CT | C | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2782-571delA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156080 | ||||||
chr6:84156236
|
C | T | 2 | a0001c0001t0002g0197a0001c0006t0002g0156 | 2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2782-726G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156236 | ||||||
chr6:84156313
|
G | A | 2 | a0001c0001t0002g0197a0001c0006t0002g0156 | 2 | HG03130.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.2782-803C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156313 | ||||||
chr6:84156358
|
C | A | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2782-848G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156358 | ||||||
chr6:84156374
|
G | A | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2782-864C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156374 | ||||||
chr6:84156389
|
A | G | 16 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(13): Show | 16 | HG00741.hp2 HG01109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.2782-879T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156389 | ||||||
chr6:84156416
|
C | T | 5 | a0001c0007t0002g0017a0001c0007t0002g0018a0001c0007t0002g0116others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2782-906G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156416 | ||||||
chr6:84156514
|
G | A | 1 | a0001c0006t0002g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2782-1004C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156514 | ||||||
chr6:84156611
|
T | C | 1 | a0001c0001t0001g0192 | 1 | NA19056.hp1 | intron_variant | MODIFIER | c.2782-1101A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156611 | ||||||
chr6:84156743
|
G | GAC | 14 | a0001c0001t0001g0023a0001c0001t0001g0073a0001c0001t0001g0074others(11): Show | 14 | HG00408.hp1 HG00408.hp2 HG00673.hp2 others(11): Show |
intron_variant | MODIFIER | c.2782-1235_2782-123 others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156743 | ||||||
chr6:84156743
|
G | GACAC | 5 | a0001c0001t0001g0167a0001c0001t0002g0197a0001c0006t0002g0156others(2): Show | 6 | HG01256.hp1 HG01258.hp1 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.2782-1237_2782-123 others(8): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156743 | ||||||
chr6:84156743
|
G | GACACAC | 16 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(13): Show | 18 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(15): Show |
intron_variant | MODIFIER | c.2782-1239_2782-123 others(10): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156743 | ||||||
chr6:84156743
|
G | GACACACA others(1): Show |
7 | a0001c0001t0002g0140a0001c0004t0002g0103a0001c0004t0002g0114others(4): Show | 7 | HG02280.hp1 HG02717.hp1 HG02965.hp2 others(4): Show |
intron_variant | MODIFIER | c.2782-1241_2782-123 others(12): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156743 | ||||||
chr6:84156743
|
G | GACACACA others(3): Show |
14 | a0001c0001t0002g0199a0001c0001t0002g0201a0001c0004t0002g0012others(11): Show | 14 | HG01074.hp2 HG02109.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2782-1243_2782-123 others(14): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156743 | ||||||
chr6:84156743
|
G | GACACACA others(5): Show |
15 | a0001c0004t0002g0189a0001c0004t0002g0190a0001c0004t0007g0207others(12): Show | 15 | HG01109.hp1 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2782-1245_2782-123 others(16): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156743 | ||||||
chr6:84156743
|
G | GACACACA others(7): Show |
6 | a0001c0001t0003g0065a0001c0001t0003g0112a0001c0004t0002g0210others(3): Show | 6 | HG01346.hp2 HG01358.hp1 HG02647.hp1 others(3): Show |
intron_variant | MODIFIER | c.2782-1247_2782-123 others(18): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156743 | ||||||
chr6:84156743
|
G | GACACACA others(9): Show |
1 | a0001c0004t0002g0211 | 1 | HG00741.hp2 | intron_variant | MODIFIER | c.2782-1249_2782-123 others(20): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156743 | ||||||
chr6:84156743
|
G | GACACACA others(11): Show |
2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2782-1251_2782-123 others(22): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156743 | ||||||
chr6:84156743
|
GACACAC | G | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2782-1239_2782-123 others(10): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156743 | ||||||
chr6:84156773
|
A | C | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(46): Show | 52 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.2782-1263T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84156773 | ||||||
chr6:84157118
|
A | G | 1 | a0001c0001t0001g0025 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2782-1608T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84157118 | ||||||
chr6:84157181
|
T | C | 1 | a0002c0012t0004g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2782-1671A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84157181 | ||||||
chr6:84157203
|
C | T | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2782-1693G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84157203 | ||||||
chr6:84157219
|
G | A | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(82): Show | 88 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.2782-1709C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84157219 | ||||||
chr6:84157257
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.2782-1747G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84157257 | ||||||
chr6:84157264
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.2782-1754C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84157264 | ||||||
chr6:84157524
|
A | G | 1 | a0001c0001t0001g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.2782-2014T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84157524 | ||||||
chr6:84157595
|
G | C | 5 | a0001c0007t0002g0017a0001c0007t0002g0018a0001c0007t0002g0116others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2782-2085C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84157595 | ||||||
chr6:84157865
|
C | T | 1 | a0001c0001t0001g0066 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.2782-2355G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84157865 | ||||||
chr6:84157866
|
G | T | 34 | a0001c0001t0003g0065a0001c0001t0003g0112a0001c0005t0004g0005others(31): Show | 34 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(31): Show |
intron_variant | MODIFIER | c.2782-2356C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84157866 | ||||||
chr6:84157968
|
T | A | 1 | a0001c0006t0002g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2782-2458A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84157968 | ||||||
chr6:84158006
|
A | C | 35 | a0001c0001t0003g0065a0001c0001t0003g0112a0001c0005t0004g0005others(32): Show | 35 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(32): Show |
intron_variant | MODIFIER | c.2782-2496T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84158006 | ||||||
chr6:84158032
|
T | C | 16 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(13): Show | 16 | HG00741.hp2 HG01109.hp1 HG02257.hp2 others(13): Show |
intron_variant | MODIFIER | c.2782-2522A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84158032 | ||||||
chr6:84158284
|
G | A | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(12): Show |
intron_variant | MODIFIER | c.2781+2528C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84158284 | ||||||
chr6:84159091
|
A | G | 1 | a0002c0012t0004g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2781+1721T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159091 | ||||||
chr6:84159208
|
T | C | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2781+1604A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159208 | ||||||
chr6:84159323
|
C | T | 2 | a0001c0001t0001g0059a0001c0001t0001g0062 | 2 | HG00673.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.2781+1489G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159323 | ||||||
chr6:84159355
|
A | G | 1 | a0001c0001t0001g0044 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.2781+1457T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159355 | ||||||
chr6:84159391
|
T | G | 49 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(46): Show | 52 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(49): Show |
intron_variant | MODIFIER | c.2781+1421A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159391 | ||||||
chr6:84159519
|
T | TTA | 3 | a0003c0003t0003g0047a0003c0003t0003g0048a0003c0021t0003g0049 | 3 | HG01257.hp2 HG01928.hp2 HG02300.hp2 |
intron_variant | MODIFIER | c.2781+1291_2781+129 others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159519 | ||||||
chr6:84159519
|
T | TTATATAT others(3): Show |
1 | a0011c0018t0003g0039 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.2781+1292_2781+129 others(14): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159519 | ||||||
chr6:84159523
|
T | A | 22 | a0001c0001t0001g0009a0001c0001t0001g0050a0001c0001t0001g0063others(19): Show | 22 | HG01074.hp2 HG01192.hp1 HG01192.hp2 others(19): Show |
intron_variant | MODIFIER | c.2781+1289A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159523 | ||||||
chr6:84159523
|
T | TTA | 13 | a0001c0001t0001g0053a0001c0001t0001g0077a0001c0001t0001g0100others(10): Show | 13 | HG00408.hp1 HG00408.hp2 HG01261.hp1 others(10): Show |
intron_variant | MODIFIER | c.2781+1287_2781+128 others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159523 | ||||||
chr6:84159525
|
A | T | 3 | a0001c0001t0001g0025a0001c0001t0002g0197a0001c0004t0002g0210 | 3 | HG00738.hp2 HG02922.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.2781+1287T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159525 | ||||||
chr6:84159539
|
ATATATAT others(5): Show |
A | 1 | a0001c0001t0001g0075 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.2781+1261_2781+127 others(16): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159539 | ||||||
chr6:84159541
|
ATATATAT others(6): Show |
A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2781+1258_2781+127 others(17): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159541 | ||||||
chr6:84159542
|
T | C | 1 | a0001c0001t0001g0051 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.2781+1270A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159542 | ||||||
chr6:84159545
|
ATATTTTT others(3): Show |
A | 1 | a0001c0001t0002g0029 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.2781+1257_2781+126 others(14): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159545 | ||||||
chr6:84159545
|
ATATTTTT others(4): Show |
A | 7 | a0001c0001t0002g0001a0001c0001t0002g0028a0001c0001t0002g0031others(4): Show | 8 | HG01884.hp2 HG02486.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.2781+1256_2781+126 others(15): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159545 | ||||||
chr6:84159545
|
ATATTTTT others(5): Show |
A | 1 | a0001c0001t0002g0002 | 2 | HG02451.hp1 HG03195.hp2 |
intron_variant | MODIFIER | c.2781+1255_2781+126 others(16): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159545 | ||||||
chr6:84159545
|
ATATTTTT others(7): Show |
A | 1 | a0001c0007t0002g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.2781+1253_2781+126 others(18): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159545 | ||||||
chr6:84159545
|
ATATTTTT others(8): Show |
A | 5 | a0001c0004t0007g0207a0001c0007t0002g0018a0001c0007t0002g0116others(2): Show | 5 | HG01109.hp1 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.2781+1252_2781+126 others(19): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159545 | ||||||
chr6:84159547
|
A | ATATATAT others(22): Show |
1 | a0001c0005t0004g0085 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.2781+1264_2781+126 others(33): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159547 | ||||||
chr6:84159547
|
A | ATATATAT others(21): Show |
1 | a0001c0005t0004g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.2781+1264_2781+126 others(32): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159547 | ||||||
chr6:84159547
|
A | ATATATAT others(18): Show |
2 | a0001c0005t0004g0105a0001c0005t0004g0106 | 2 | HG02258.hp2 HG02976.hp1 |
intron_variant | MODIFIER | c.2781+1264_2781+126 others(29): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159547 | ||||||
chr6:84159547
|
A | ATATATAT others(18): Show |
1 | a0001c0005t0004g0086 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.2781+1264_2781+126 others(29): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159547 | ||||||
chr6:84159547
|
A | ATATATAT others(9): Show |
1 | a0001c0008t0005g0204 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.2781+1264_2781+126 others(20): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159547 | ||||||
chr6:84159547
|
A | ATATATAT others(14): Show |
2 | a0001c0005t0004g0005a0001c0005t0004g0195 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2781+1264_2781+126 others(25): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159547 | ||||||
chr6:84159547
|
A | ATATATAT others(4): Show |
1 | a0001c0008t0005g0205 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.2781+1264_2781+126 others(15): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159547 | ||||||
chr6:84159547
|
A | ATATATAT others(3): Show |
1 | a0001c0008t0005g0206 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.2781+1264_2781+126 others(14): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159547 | ||||||
chr6:84159547
|
AT | A | 33 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0025others(30): Show | 33 | HG00280.hp1 HG00738.hp2 HG01081.hp1 others(30): Show |
intron_variant | MODIFIER | c.2781+1264delA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159547 | ||||||
chr6:84159547
|
ATT | A | 10 | a0001c0001t0001g0057a0001c0001t0001g0071a0001c0001t0001g0087others(7): Show | 10 | HG01074.hp1 HG01169.hp2 HG01981.hp2 others(7): Show |
intron_variant | MODIFIER | c.2781+1263_2781+126 others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159547 | ||||||
chr6:84159547
|
ATTTTTTT others(3): Show |
A | 3 | a0001c0001t0001g0072a0001c0001t0001g0120a0001c0001t0001g0154 | 3 | HG03704.hp2 HG04204.hp1 HG04228.hp2 |
intron_variant | MODIFIER | c.2781+1255_2781+126 others(14): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159547 | ||||||
chr6:84159547
|
ATTTTTTT others(4): Show |
A | 2 | a0001c0001t0002g0030a0001c0004t0002g0190 | 2 | HG02559.hp2 HG03139.hp2 |
intron_variant | MODIFIER | c.2781+1254_2781+126 others(15): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159547 | ||||||
chr6:84159547
|
ATTTTTTT others(5): Show |
A | 3 | a0001c0001t0001g0125a0001c0001t0001g0130a0001c0001t0001g0153 | 3 | HG00280.hp2 HG01261.hp2 NA19087.hp1 |
intron_variant | MODIFIER | c.2781+1253_2781+126 others(16): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159547 | ||||||
chr6:84159547
|
ATTTTTTT others(7): Show |
A | 4 | a0001c0004t0002g0103a0002c0002t0002g0119a0002c0002t0002g0146others(1): Show | 4 | HG02615.hp2 HG02723.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.2781+1251_2781+126 others(18): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159547 | ||||||
chr6:84159547
|
ATTTTTTT others(8): Show |
A | 7 | a0001c0001t0001g0026a0001c0004t0002g0012a0001c0004t0002g0095others(4): Show | 7 | HG01081.hp2 HG02486.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.2781+1250_2781+126 others(19): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159547 | ||||||
chr6:84159547
|
ATTTTTTT others(9): Show |
A | 24 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0027others(21): Show | 24 | HG00738.hp1 HG00741.hp1 HG00741.hp2 others(21): Show |
intron_variant | MODIFIER | c.2781+1249_2781+126 others(20): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159547 | ||||||
chr6:84159547
|
ATTTTTTT others(10): Show |
A | 1 | a0001c0001t0001g0062 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.2781+1248_2781+126 others(21): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159547 | ||||||
chr6:84159548
|
T | TA | 15 | a0001c0001t0001g0051a0001c0001t0001g0069a0001c0001t0001g0074others(12): Show | 15 | HG00673.hp2 HG01346.hp1 HG02055.hp2 others(12): Show |
intron_variant | MODIFIER | c.2781+1263_2781+126 others(5): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159548 | ||||||
chr6:84159548
|
T | TATA | 6 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0123others(3): Show | 6 | HG01515.hp1 HG02148.hp1 HG02293.hp2 others(3): Show |
intron_variant | MODIFIER | c.2781+1263_2781+126 others(7): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159548 | ||||||
chr6:84159548
|
T | TATATA | 6 | a0001c0001t0001g0044a0001c0001t0003g0112a0003c0003t0003g0040others(3): Show | 6 | HG00558.hp1 HG01074.hp2 HG01346.hp2 others(3): Show |
intron_variant | MODIFIER | c.2781+1263_2781+126 others(9): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159548 | ||||||
chr6:84159548
|
T | TATATATA others(2): Show |
4 | a0001c0001t0002g0140a0001c0001t0002g0199a0001c0001t0002g0201others(1): Show | 4 | HG02257.hp1 HG02280.hp1 HG02809.hp1 others(1): Show |
intron_variant | MODIFIER | c.2781+1263_2781+126 others(13): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159548 | ||||||
chr6:84159548
|
T | TATATATA others(6): Show |
1 | a0003c0003t0003g0165 | 1 | HG03942.hp1 | intron_variant | MODIFIER | c.2781+1263_2781+126 others(17): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159548 | ||||||
chr6:84159548
|
T | TATATATA others(8): Show |
1 | a0001c0001t0002g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.2781+1263_2781+126 others(19): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159548 | ||||||
chr6:84159548
|
T | TATATATA others(12): Show |
1 | a0003c0003t0003g0090 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.2781+1263_2781+126 others(23): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159548 | ||||||
chr6:84159548
|
T | TATATATA others(18): Show |
1 | a0001c0001t0002g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.2781+1263_2781+126 others(29): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159548 | ||||||
chr6:84159549
|
T | A | 38 | a0001c0001t0001g0009a0001c0001t0001g0021a0001c0001t0001g0058others(35): Show | 38 | HG00408.hp1 HG00558.hp2 HG00639.hp2 others(35): Show |
intron_variant | MODIFIER | c.2781+1263A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159549 | ||||||
chr6:84159550
|
T | A | 52 | a0001c0001t0001g0010a0001c0001t0001g0022a0001c0001t0001g0023others(49): Show | 52 | HG00280.hp1 HG00558.hp1 HG01074.hp2 others(49): Show |
intron_variant | MODIFIER | c.2781+1262A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159550 | ||||||
chr6:84159551
|
T | A | 33 | a0001c0001t0001g0057a0001c0001t0001g0071a0001c0001t0001g0150others(30): Show | 33 | HG01074.hp1 HG01106.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.2781+1261A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159551 | ||||||
chr6:84159552
|
T | A | 23 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0067others(20): Show | 23 | HG00558.hp1 HG01074.hp2 HG01346.hp2 others(20): Show |
intron_variant | MODIFIER | c.2781+1260A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159552 | ||||||
chr6:84159553
|
T | A | 18 | a0001c0001t0001g0139a0001c0005t0004g0198a0001c0006t0001g0007others(15): Show | 18 | HG01109.hp2 HG02965.hp1 HG02970.hp1 others(15): Show |
intron_variant | MODIFIER | c.2781+1259A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159553 | ||||||
chr6:84159554
|
T | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0074a0001c0001t0003g0065others(4): Show | 7 | HG00558.hp1 HG01346.hp2 HG01358.hp1 others(4): Show |
intron_variant | MODIFIER | c.2781+1258A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159554 | ||||||
chr6:84159555
|
T | A | 14 | a0001c0001t0001g0139a0001c0005t0004g0198a0002c0002t0002g0013others(11): Show | 14 | HG01109.hp2 HG02965.hp1 HG02970.hp1 others(11): Show |
intron_variant | MODIFIER | c.2781+1257A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159555 | ||||||
chr6:84159556
|
T | A | 4 | a0001c0001t0001g0044a0002c0002t0002g0006a0002c0002t0002g0147others(1): Show | 4 | HG00558.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2781+1256A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159556 | ||||||
chr6:84159557
|
T | A | 15 | a0001c0001t0001g0139a0001c0005t0004g0198a0002c0002t0002g0003others(12): Show | 16 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(13): Show |
intron_variant | MODIFIER | c.2781+1255A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159557 | ||||||
chr6:84159558
|
T | A | 4 | a0001c0001t0001g0098a0002c0002t0002g0006a0002c0002t0002g0147others(1): Show | 4 | HG02622.hp1 HG02818.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.2781+1254A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159558 | ||||||
chr6:84159559
|
T | A | 16 | a0001c0001t0001g0072a0001c0001t0001g0120a0001c0001t0001g0139others(13): Show | 17 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.2781+1253A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159559 | ||||||
chr6:84159560
|
T | A | 3 | a0001c0004t0002g0190a0002c0002t0002g0006a0002c0002t0002g0147 | 3 | HG02897.hp2 HG03139.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2781+1252A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159560 | ||||||
chr6:84159561
|
T | A | 16 | a0001c0001t0001g0072a0001c0001t0001g0120a0001c0001t0001g0125others(13): Show | 16 | HG00280.hp2 HG01109.hp2 HG01261.hp2 others(13): Show |
intron_variant | MODIFIER | c.2781+1251A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159561 | ||||||
chr6:84159562
|
T | A | 3 | a0001c0004t0002g0190a0002c0002t0002g0006a0002c0002t0002g0147 | 3 | HG02897.hp2 HG03139.hp2 NA20905.hp2 |
intron_variant | MODIFIER | c.2781+1250A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159562 | ||||||
chr6:84159563
|
T | A | 9 | a0001c0001t0001g0072a0001c0001t0001g0120a0001c0001t0001g0125others(6): Show | 9 | HG00280.hp2 HG01261.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.2781+1249A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159563 | ||||||
chr6:84159564
|
T | A | 1 | a0001c0001t0001g0026 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.2781+1248A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159564 | ||||||
chr6:84159565
|
T | A | 26 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0027others(23): Show | 26 | HG00738.hp1 HG00741.hp1 HG01169.hp1 others(23): Show |
intron_variant | MODIFIER | c.2781+1247A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159565 | ||||||
chr6:84159567
|
T | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0162a0001c0001t0001g0192 | 3 | HG01943.hp2 HG01981.hp1 NA19056.hp1 |
intron_variant | MODIFIER | c.2781+1245A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159567 | ||||||
chr6:84159601
|
A | T | 19 | a0001c0001t0003g0065a0001c0001t0003g0112a0001c0011t0002g0019others(16): Show | 19 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2781+1211T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159601 | ||||||
chr6:84159624
|
G | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2781+1188C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159624 | ||||||
chr6:84159642
|
C | G | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(81): Show | 87 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(84): Show |
intron_variant | MODIFIER | c.2781+1170G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159642 | ||||||
chr6:84159873
|
C | T | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2781+939G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159873 | ||||||
chr6:84159975
|
T | G | 19 | a0001c0001t0003g0065a0001c0001t0003g0112a0001c0011t0002g0019others(16): Show | 19 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2781+837A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84159975 | ||||||
chr6:84160003
|
C | T | 1 | a0001c0004t0002g0210 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.2781+809G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84160003 | ||||||
chr6:84160093
|
T | A | 1 | a0001c0001t0002g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.2781+719A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84160093 | ||||||
chr6:84160207
|
T | C | 1 | a0002c0012t0004g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2781+605A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84160207 | ||||||
chr6:84160321
|
C | T | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2781+491G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84160321 | ||||||
chr6:84160412
|
T | G | 19 | a0001c0001t0003g0065a0001c0001t0003g0112a0001c0011t0002g0019others(16): Show | 19 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2781+400A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 21/26 | chr6 | 84160412 | ||||||
chr6:84161061
|
C | T | 2 | a0001c0001t0001g0084a0001c0001t0001g0138 | 2 | HG01358.hp2 HG03239.hp2 |
intron_variant | MODIFIER | c.2677-145G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 20/26 | chr6 | 84161061 | ||||||
chr6:84161093
|
C | A | 16 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(13): Show | 17 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.2677-177G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 20/26 | chr6 | 84161093 | ||||||
chr6:84161164
|
G | C | 7 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(4): Show | 7 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.2677-248C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 20/26 | chr6 | 84161164 | ||||||
chr6:84161396
|
A | G | 14 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(11): Show | 14 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2676+350T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 20/26 | chr6 | 84161396 | ||||||
chr6:84161546
|
T | A | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2676+200A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 20/26 | chr6 | 84161546 | ||||||
chr6:84161552
|
G | T | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2676+194C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 20/26 | chr6 | 84161552 | ||||||
chr6:84161695
|
C | T | 14 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(11): Show | 14 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2676+51G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 20/26 | chr6 | 84161695 | ||||||
chr6:84161711
|
T | G | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2676+35A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 20/26 | chr6 | 84161711 | ||||||
chr6:84161714
|
AGAG | A | 15 | a0001c0001t0003g0065a0001c0001t0003g0112a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.2676+29_2676+31del others(3): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 20/26 | chr6 | 84161714 | ||||||
chr6:84162014
|
C | CA | 32 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(29): Show | 33 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(30): Show |
intron_variant | MODIFIER | c.2513-106dupT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 19/26 | chr6 | 84162014 | ||||||
chr6:84162131
|
T | C | 1 | a0001c0001t0001g0067 | 1 | NA18986.hp1 | intron_variant | MODIFIER | c.2513-222A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 19/26 | chr6 | 84162131 | ||||||
chr6:84162146
|
T | C | 1 | a0001c0001t0002g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2513-237A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 19/26 | chr6 | 84162146 | ||||||
chr6:84162285
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2513-376G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 19/26 | chr6 | 84162285 | ||||||
chr6:84162385
|
C | T | 14 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(11): Show | 14 | HG02109.hp1 HG02258.hp1 HG02258.hp2 others(11): Show |
intron_variant | MODIFIER | c.2513-476G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 19/26 | chr6 | 84162385 | ||||||
chr6:84162544
|
C | T | 16 | a0001c0001t0003g0065a0001c0001t0003g0112a0002c0012t0004g0014others(13): Show | 16 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(13): Show |
intron_variant | MODIFIER | c.2512+600G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 19/26 | chr6 | 84162544 | ||||||
chr6:84162683
|
A | AT | 5 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2512+460dupA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 19/26 | chr6 | 84162683 | ||||||
chr6:84162741
|
C | G | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2512+403G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 19/26 | chr6 | 84162741 | ||||||
chr6:84162923
|
A | G | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2512+221T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 19/26 | chr6 | 84162923 | ||||||
chr6:84163042
|
A | G | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2512+102T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 19/26 | chr6 | 84163042 | ||||||
chr6:84163300
|
G | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2386-30C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84163300 | ||||||
chr6:84163361
|
G | T | 68 | a0001c0001t0001g0129a0001c0001t0001g0172a0001c0001t0002g0001others(65): Show | 71 | HG01074.hp2 HG01243.hp2 HG01256.hp1 others(68): Show |
intron_variant | MODIFIER | c.2386-91C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84163361 | ||||||
chr6:84163732
|
A | G | 133 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0026others(130): Show | 136 | HG00280.hp2 HG00408.hp2 HG00673.hp1 others(133): Show |
intron_variant | MODIFIER | c.2386-462T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84163732 | ||||||
chr6:84164005
|
CA | C | 38 | a0001c0001t0001g0076a0001c0001t0002g0197a0001c0001t0002g0199others(35): Show | 39 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(36): Show |
intron_variant | MODIFIER | c.2386-736delT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84164005 | ||||||
chr6:84164078
|
C | T | 1 | a0002c0012t0004g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.2386-808G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84164078 | ||||||
chr6:84164081
|
T | C | 83 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(80): Show | 86 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(83): Show |
intron_variant | MODIFIER | c.2386-811A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84164081 | ||||||
chr6:84164085
|
C | A | 19 | a0001c0011t0002g0019a0001c0011t0002g0020a0002c0012t0004g0014others(16): Show | 19 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2386-815G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84164085 | ||||||
chr6:84164356
|
C | T | 1 | a0001c0001t0001g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.2386-1086G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84164356 | ||||||
chr6:84164411
|
G | C | 4 | a0001c0011t0002g0019a0001c0011t0002g0020a0005c0010t0002g0163others(1): Show | 4 | HG02647.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2386-1141C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84164411 | ||||||
chr6:84164535
|
T | C | 17 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(14): Show | 18 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2386-1265A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84164535 | ||||||
chr6:84164626
|
C | T | 4 | a0001c0011t0002g0019a0001c0011t0002g0020a0005c0010t0002g0163others(1): Show | 4 | HG02647.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2386-1356G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84164626 | ||||||
chr6:84164694
|
C | T | 5 | a0001c0011t0002g0019a0001c0011t0002g0020a0002c0012t0004g0014others(2): Show | 5 | HG02647.hp1 HG02818.hp2 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.2386-1424G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84164694 | ||||||
chr6:84164697
|
G | C | 4 | a0001c0011t0002g0019a0001c0011t0002g0020a0005c0010t0002g0163others(1): Show | 4 | HG02647.hp1 HG02818.hp2 HG02965.hp1 others(1): Show |
intron_variant | MODIFIER | c.2386-1427C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84164697 | ||||||
chr6:84164720
|
A | G | 1 | a0001c0001t0002g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2386-1450T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84164720 | ||||||
chr6:84164728
|
G | A | 3 | a0001c0001t0001g0075a0001c0001t0003g0065a0001c0001t0003g0112 | 3 | HG01256.hp2 HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.2386-1458C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84164728 | ||||||
chr6:84164763
|
C | G | 20 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(17): Show | 20 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.2386-1493G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84164763 | ||||||
chr6:84164834
|
T | G | 1 | a0001c0001t0001g0008 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.2386-1564A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84164834 | ||||||
chr6:84164894
|
A | C | 1 | a0001c0001t0001g0025 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2386-1624T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84164894 | ||||||
chr6:84164898
|
C | T | 207 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(204): Show | 210 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.2386-1628G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84164898 | ||||||
chr6:84165010
|
T | C | 2 | a0001c0001t0002g0110a0001c0001t0002g0140 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2386-1740A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84165010 | ||||||
chr6:84165050
|
A | G | 2 | a0001c0001t0002g0110a0001c0001t0002g0140 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.2386-1780T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84165050 | ||||||
chr6:84165086
|
T | C | 1 | a0001c0001t0001g0076 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.2386-1816A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84165086 | ||||||
chr6:84165102
|
T | G | 2 | a0001c0005t0004g0005a0001c0005t0004g0195 | 2 | HG03130.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.2386-1832A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84165102 | ||||||
chr6:84165121
|
C | T | 21 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(18): Show | 21 | HG02109.hp1 HG02257.hp1 HG02257.hp2 others(18): Show |
intron_variant | MODIFIER | c.2386-1851G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84165121 | ||||||
chr6:84165253
|
T | G | 1 | a0001c0005t0004g0106 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2386-1983A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84165253 | ||||||
chr6:84165524
|
A | T | 1 | a0001c0001t0001g0078 | 1 | HG02080.hp1 | intron_variant | MODIFIER | c.2386-2254T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84165524 | ||||||
chr6:84165556
|
T | A | 19 | a0001c0011t0002g0019a0001c0011t0002g0020a0002c0012t0004g0014others(16): Show | 19 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(16): Show |
intron_variant | MODIFIER | c.2386-2286A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84165556 | ||||||
chr6:84165664
|
C | T | 1 | a0004c0009t0001g0135 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.2386-2394G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84165664 | ||||||
chr6:84165707
|
A | G | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2386-2437T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84165707 | ||||||
chr6:84165842
|
G | A | 7 | a0001c0001t0001g0044a0001c0001t0001g0055a0001c0001t0001g0067others(4): Show | 7 | HG00280.hp1 HG00558.hp1 HG01257.hp1 others(4): Show |
intron_variant | MODIFIER | c.2386-2572C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84165842 | ||||||
chr6:84165845
|
G | T | 1 | a0001c0006t0002g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.2386-2575C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84165845 | ||||||
chr6:84165856
|
A | G | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2386-2586T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84165856 | ||||||
chr6:84165856
|
A | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2386-2586T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84165856 | ||||||
chr6:84165931
|
G | A | 1 | a0001c0001t0001g0191 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.2386-2661C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84165931 | ||||||
chr6:84166213
|
G | C | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2386-2943C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84166213 | ||||||
chr6:84166271
|
G | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2386-3001C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84166271 | ||||||
chr6:84166592
|
A | C | 1 | a0001c0001t0001g0024 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.2385+2736T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84166592 | ||||||
chr6:84166619
|
C | G | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2385+2709G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84166619 | ||||||
chr6:84166799
|
A | G | 5 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2385+2529T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84166799 | ||||||
chr6:84166803
|
A | G | 2 | a0001c0001t0002g0197a0002c0016t0002g0196 | 2 | HG03130.hp1 HG03195.hp1 |
intron_variant | MODIFIER | c.2385+2525T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84166803 | ||||||
chr6:84166817
|
T | C | 1 | a0002c0016t0002g0196 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2385+2511A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84166817 | ||||||
chr6:84166924
|
T | C | 5 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.2385+2404A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84166924 | ||||||
chr6:84166997
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2385+2331A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84166997 | ||||||
chr6:84167359
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2385+1969A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84167359 | ||||||
chr6:84167364
|
G | T | 18 | a0001c0011t0002g0019a0001c0011t0002g0020a0003c0003t0001g0043others(15): Show | 18 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(15): Show |
intron_variant | MODIFIER | c.2385+1964C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84167364 | ||||||
chr6:84167418
|
A | AT | 4 | a0001c0004t0002g0102a0001c0004t0002g0103a0001c0004t0002g0114others(1): Show | 4 | HG02717.hp2 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.2385+1909dupA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84167418 | ||||||
chr6:84167568
|
G | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2385+1760C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84167568 | ||||||
chr6:84167648
|
G | T | 16 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(13): Show | 16 | HG00741.hp2 HG01109.hp1 HG01884.hp1 others(13): Show |
intron_variant | MODIFIER | c.2385+1680C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84167648 | ||||||
chr6:84167780
|
G | A | 1 | a0001c0005t0004g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.2385+1548C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84167780 | ||||||
chr6:84167793
|
C | T | 6 | a0001c0001t0001g0056a0001c0001t0001g0068a0001c0001t0001g0080others(3): Show | 6 | HG01943.hp1 HG02897.hp1 HG03654.hp2 others(3): Show |
intron_variant | MODIFIER | c.2385+1535G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84167793 | ||||||
chr6:84167908
|
C | A | 43 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(40): Show | 46 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(43): Show |
intron_variant | MODIFIER | c.2385+1420G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84167908 | ||||||
chr6:84168097
|
C | T | 83 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(80): Show | 86 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(83): Show |
intron_variant | MODIFIER | c.2385+1231G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84168097 | ||||||
chr6:84168294
|
T | C | 1 | a0001c0001t0002g0201 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.2385+1034A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84168294 | ||||||
chr6:84168385
|
C | T | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2385+943G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84168385 | ||||||
chr6:84168429
|
C | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2385+899G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84168429 | ||||||
chr6:84168498
|
T | C | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2385+830A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84168498 | ||||||
chr6:84169122
|
A | G | 1 | a0001c0001t0001g0137 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.2385+206T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 18/26 | chr6 | 84169122 | ||||||
chr6:84169667
|
G | T | 3 | a0001c0007t0002g0116a0001c0007t0002g0117a0001c0007t0002g0118 | 3 | HG02723.hp2 HG02809.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.2280-234C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84169667 | ||||||
chr6:84169736
|
C | T | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.2280-303G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84169736 | ||||||
chr6:84169767
|
G | C | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(82): Show | 88 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.2280-334C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84169767 | ||||||
chr6:84169924
|
G | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2280-491C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84169924 | ||||||
chr6:84170016
|
T | C | 1 | a0001c0007t0002g0118 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.2280-583A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84170016 | ||||||
chr6:84170242
|
C | T | 1 | a0001c0001t0002g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.2280-809G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84170242 | ||||||
chr6:84170322
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2280-889G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84170322 | ||||||
chr6:84170330
|
C | T | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2280-897G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84170330 | ||||||
chr6:84170373
|
C | CA | 35 | a0001c0001t0001g0004a0001c0001t0001g0009a0001c0001t0001g0010others(32): Show | 35 | HG00558.hp2 HG00738.hp1 HG00741.hp1 others(32): Show |
intron_variant | MODIFIER | c.2280-941dupT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84170373 | ||||||
chr6:84170373
|
C | CAAAAAAA others(7): Show |
1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2280-954_2280-941d others(16): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84170373 | ||||||
chr6:84170373
|
CA | C | 5 | a0001c0001t0001g0016a0001c0001t0001g0056a0001c0001t0001g0150others(2): Show | 5 | HG02056.hp2 HG03654.hp2 NA18999.hp1 others(2): Show |
intron_variant | MODIFIER | c.2280-941delT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84170373 | ||||||
chr6:84170373
|
CAAA | C | 17 | a0001c0001t0002g0200a0001c0004t0002g0211a0002c0012t0004g0014others(14): Show | 17 | HG00741.hp2 HG01074.hp2 HG01243.hp2 others(14): Show |
intron_variant | MODIFIER | c.2280-943_2280-941d others(5): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84170373 | ||||||
chr6:84170373
|
CAAAA | C | 9 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(6): Show | 9 | HG01109.hp1 HG02486.hp1 HG02717.hp2 others(6): Show |
intron_variant | MODIFIER | c.2280-944_2280-941d others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84170373 | ||||||
chr6:84170373
|
CAAAAA | C | 7 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(4): Show | 7 | HG01884.hp1 HG02280.hp1 HG02809.hp1 others(4): Show |
intron_variant | MODIFIER | c.2280-945_2280-941d others(7): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84170373 | ||||||
chr6:84170373
|
CAAAAAAA | C | 26 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(23): Show | 28 | HG01109.hp2 HG01884.hp2 HG02055.hp1 others(25): Show |
intron_variant | MODIFIER | c.2280-947_2280-941d others(9): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84170373 | ||||||
chr6:84170373
|
CAAAAAAA others(1): Show |
C | 15 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(12): Show | 16 | HG01256.hp1 HG01258.hp1 HG02615.hp2 others(13): Show |
intron_variant | MODIFIER | c.2280-948_2280-941d others(10): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84170373 | ||||||
chr6:84170415
|
G | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2280-982C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84170415 | ||||||
chr6:84170491
|
GAT | G | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2280-1060_2280-105 others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84170491 | ||||||
chr6:84170665
|
C | T | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.2279+941G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84170665 | ||||||
chr6:84170891
|
G | A | 5 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(2): Show | 5 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.2279+715C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84170891 | ||||||
chr6:84170978
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2279+628G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84170978 | ||||||
chr6:84171094
|
G | A | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2279+512C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84171094 | ||||||
chr6:84171392
|
A | T | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2279+214T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84171392 | ||||||
chr6:84171404
|
C | T | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2279+202G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84171404 | ||||||
chr6:84171429
|
G | A | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(82): Show | 88 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.2279+177C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 17/26 | chr6 | 84171429 | ||||||
chr6:84171853
|
T | A | 1 | a0001c0001t0001g0025 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.2167-135A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84171853 | ||||||
chr6:84171915
|
A | G | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(82): Show | 88 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.2167-197T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84171915 | ||||||
chr6:84172050
|
G | A | 13 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(10): Show | 13 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2167-332C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84172050 | ||||||
chr6:84172114
|
GA | G | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2167-397delT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84172114 | ||||||
chr6:84172213
|
T | C | 1 | a0008c0014t0004g0115 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.2167-495A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84172213 | ||||||
chr6:84172239
|
G | A | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2167-521C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84172239 | ||||||
chr6:84172539
|
C | T | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2167-821G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84172539 | ||||||
chr6:84172840
|
G | A | 1 | a0002c0016t0002g0196 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.2167-1122C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84172840 | ||||||
chr6:84172874
|
G | C | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2167-1156C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84172874 | ||||||
chr6:84172909
|
T | A | 83 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(80): Show | 86 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(83): Show |
intron_variant | MODIFIER | c.2166+1139A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84172909 | ||||||
chr6:84173007
|
C | T | 3 | a0002c0002t0002g0013a0002c0002t0002g0089a0002c0002t0007g0202 | 3 | HG03540.hp2 NA20805.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.2166+1041G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84173007 | ||||||
chr6:84173096
|
A | G | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.2166+952T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84173096 | ||||||
chr6:84173489
|
T | G | 18 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(15): Show | 19 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.2166+559A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84173489 | ||||||
chr6:84173686
|
C | CT | 59 | a0001c0001t0001g0154a0001c0001t0001g0169a0001c0001t0001g0179others(56): Show | 62 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(59): Show |
intron_variant | MODIFIER | c.2166+361dupA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84173686 | ||||||
chr6:84173686
|
C | CTT | 6 | a0001c0001t0002g0197a0001c0004t0002g0012a0001c0004t0002g0095others(3): Show | 6 | HG02818.hp2 HG02965.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.2166+360_2166+361d others(4): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84173686 | ||||||
chr6:84173686
|
C | CTTTT | 18 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(15): Show | 18 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.2166+358_2166+361d others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84173686 | ||||||
chr6:84173716
|
C | A | 11 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(8): Show | 13 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.2166+332G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84173716 | ||||||
chr6:84173847
|
C | A | 4 | a0001c0001t0001g0056a0001c0001t0001g0068a0001c0001t0001g0080others(1): Show | 4 | HG02897.hp1 HG03654.hp2 HG03831.hp2 others(1): Show |
intron_variant | MODIFIER | c.2166+201G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84173847 | ||||||
chr6:84173909
|
T | C | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.2166+139A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 16/26 | chr6 | 84173909 | ||||||
chr6:84174241
|
G | A | 1 | a0001c0005t0004g0106 | 1 | HG02976.hp1 | intron_variant | MODIFIER | c.2026-53C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 15/26 | chr6 | 84174241 | ||||||
chr6:84174354
|
G | A | 2 | a0001c0004t0002g0012a0001c0004t0002g0095 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.2026-166C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 15/26 | chr6 | 84174354 | ||||||
chr6:84174546
|
A | T | 3 | a0001c0001t0001g0157a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG00408.hp2 HG01106.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.2025+181T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 15/26 | chr6 | 84174546 | ||||||
chr6:84174549
|
G | T | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.2025+178C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 15/26 | chr6 | 84174549 | ||||||
chr6:84174570
|
G | A | 1 | a0001c0001t0001g0158 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.2025+157C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 15/26 | chr6 | 84174570 | ||||||
chr6:84174674
|
CT | C | 40 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(37): Show | 40 | HG00741.hp2 HG01109.hp1 HG01884.hp1 others(37): Show |
intron_variant | MODIFIER | c.2025+52delA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 15/26 | chr6 | 84174674 | ||||||
chr6:84174687
|
T | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.2025+40A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 15/26 | chr6 | 84174687 | ||||||
chr6:84174718
|
A | G | 13 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(10): Show | 13 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.2025+9T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 15/26 | chr6 | 84174718 | ||||||
chr6:84175012
|
G | A | 1 | a0001c0001t0001g0109 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1798-58C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 14/26 | chr6 | 84175012 | ||||||
chr6:84175148
|
A | G | 23 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(20): Show | 24 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.1797+66T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 14/26 | chr6 | 84175148 | ||||||
chr6:84175399
|
A | G | 36 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(33): Show | 36 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(33): Show |
intron_variant | MODIFIER | c.1664-52T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84175399 | ||||||
chr6:84175435
|
T | C | 1 | a0001c0006t0001g0015 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1664-88A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84175435 | ||||||
chr6:84175472
|
G | A | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1664-125C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84175472 | ||||||
chr6:84175512
|
C | T | 11 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(8): Show | 13 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1664-165G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84175512 | ||||||
chr6:84175571
|
A | G | 18 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(15): Show | 19 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1664-224T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84175571 | ||||||
chr6:84175738
|
A | G | 5 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1664-391T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84175738 | ||||||
chr6:84175902
|
A | G | 1 | a0001c0001t0001g0130 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.1664-555T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84175902 | ||||||
chr6:84176007
|
A | T | 1 | a0001c0001t0002g0031 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.1664-660T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84176007 | ||||||
chr6:84176054
|
T | C | 12 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(9): Show | 12 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(9): Show |
intron_variant | MODIFIER | c.1664-707A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84176054 | ||||||
chr6:84176077
|
C | T | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1664-730G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84176077 | ||||||
chr6:84176166
|
A | AAT | 21 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(18): Show | 21 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1664-820_1664-819i others(4): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84176166 | ||||||
chr6:84176182
|
C | T | 1 | a0001c0001t0003g0065 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1664-835G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84176182 | ||||||
chr6:84176614
|
C | T | 13 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(10): Show | 13 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1664-1267G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84176614 | ||||||
chr6:84176671
|
T | A | 1 | a0002c0002t0002g0003 | 2 | HG01256.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.1664-1324A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84176671 | ||||||
chr6:84176731
|
C | G | 17 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(14): Show | 18 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1664-1384G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84176731 | ||||||
chr6:84176892
|
TA | T | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1664-1546delT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84176892 | ||||||
chr6:84176894
|
A | T | 11 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(8): Show | 11 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1664-1547T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84176894 | ||||||
chr6:84176916
|
C | G | 21 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(18): Show | 21 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1664-1569G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84176916 | ||||||
chr6:84176922
|
C | T | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1664-1575G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84176922 | ||||||
chr6:84177059
|
C | T | 1 | a0002c0012t0004g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1664-1712G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84177059 | ||||||
chr6:84177378
|
G | A | 1 | a0004c0009t0001g0134 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.1664-2031C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84177378 | ||||||
chr6:84177387
|
A | G | 1 | a0001c0006t0001g0133 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1664-2040T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84177387 | ||||||
chr6:84177394
|
CAA | C | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1664-2049_1664-204 others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84177394 | ||||||
chr6:84177599
|
G | A | 1 | a0010c0020t0002g0142 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.1664-2252C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84177599 | ||||||
chr6:84177621
|
C | T | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1664-2274G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84177621 | ||||||
chr6:84177680
|
C | T | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1664-2333G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84177680 | ||||||
chr6:84177756
|
C | T | 1 | a0001c0006t0001g0131 | 1 | NA19091.hp1 | intron_variant | MODIFIER | c.1664-2409G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84177756 | ||||||
chr6:84177767
|
C | T | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1664-2420G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84177767 | ||||||
chr6:84177828
|
T | C | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1664-2481A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84177828 | ||||||
chr6:84177963
|
A | G | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1664-2616T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84177963 | ||||||
chr6:84178150
|
CAAAT | C | 35 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(32): Show | 35 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(32): Show |
intron_variant | MODIFIER | c.1664-2807_1664-280 others(8): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84178150 | ||||||
chr6:84178237
|
C | T | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1664-2890G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84178237 | ||||||
chr6:84178261
|
T | C | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1664-2914A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84178261 | ||||||
chr6:84178298
|
T | A | 2 | a0001c0001t0001g0150a0001c0001t0001g0191 | 2 | NA19009.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1664-2951A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84178298 | ||||||
chr6:84178384
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.1664-3037C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84178384 | ||||||
chr6:84178403
|
A | C | 21 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(18): Show | 21 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.1664-3056T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84178403 | ||||||
chr6:84178474
|
T | C | 7 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(4): Show | 7 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1664-3127A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84178474 | ||||||
chr6:84178678
|
T | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0159 | 2 | HG02080.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.1664-3331A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84178678 | ||||||
chr6:84178824
|
C | T | 11 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(8): Show | 13 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1664-3477G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84178824 | ||||||
chr6:84178832
|
C | T | 10 | a0001c0001t0001g0151a0001c0006t0001g0007a0001c0006t0001g0011others(7): Show | 10 | HG01346.hp1 HG02055.hp2 HG02056.hp1 others(7): Show |
intron_variant | MODIFIER | c.1664-3485G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84178832 | ||||||
chr6:84179153
|
T | C | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1664-3806A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84179153 | ||||||
chr6:84179210
|
G | A | 13 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(10): Show | 13 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1664-3863C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84179210 | ||||||
chr6:84179274
|
C | T | 1 | a0002c0002t0002g0089 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1664-3927G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84179274 | ||||||
chr6:84179278
|
CA | C | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1664-3932delT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84179278 | ||||||
chr6:84179346
|
C | T | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1664-3999G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84179346 | ||||||
chr6:84179419
|
A | G | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1664-4072T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84179419 | ||||||
chr6:84179515
|
G | C | 11 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(8): Show | 13 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1664-4168C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84179515 | ||||||
chr6:84179518
|
TG | T | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1664-4172delC | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84179518 | ||||||
chr6:84179524
|
T | C | 2 | a0001c0006t0001g0007a0001c0006t0001g0011 | 2 | HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.1664-4177A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84179524 | ||||||
chr6:84179537
|
T | G | 1 | a0001c0001t0002g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1664-4190A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84179537 | ||||||
chr6:84179670
|
T | C | 1 | a0002c0012t0004g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1664-4323A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84179670 | ||||||
chr6:84179683
|
T | A | 5 | a0001c0001t0001g0024a0001c0001t0001g0026a0001c0001t0001g0027others(2): Show | 5 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(2): Show |
intron_variant | MODIFIER | c.1664-4336A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84179683 | ||||||
chr6:84179813
|
T | G | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1664-4466A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84179813 | ||||||
chr6:84179818
|
C | G | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1664-4471G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84179818 | ||||||
chr6:84179979
|
C | T | 1 | a0008c0014t0004g0115 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1664-4632G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84179979 | ||||||
chr6:84180077
|
T | C | 4 | a0001c0001t0001g0055a0001c0001t0001g0126a0001c0001t0001g0127others(1): Show | 4 | HG00280.hp1 HG01257.hp1 HG01258.hp2 others(1): Show |
intron_variant | MODIFIER | c.1664-4730A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180077 | ||||||
chr6:84180194
|
G | A | 1 | a0008c0014t0004g0115 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1664-4847C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180194 | ||||||
chr6:84180246
|
C | T | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1664-4899G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180246 | ||||||
chr6:84180339
|
G | A | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1663+4848C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180339 | ||||||
chr6:84180404
|
A | T | 5 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1663+4783T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180404 | ||||||
chr6:84180429
|
T | C | 6 | a0002c0002t0002g0141a0002c0002t0002g0144a0002c0002t0002g0145others(3): Show | 6 | HG01109.hp2 HG02897.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1663+4758A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180429 | ||||||
chr6:84180459
|
A | G | 2 | a0001c0001t0001g0150a0001c0001t0001g0191 | 2 | NA19009.hp2 NA19056.hp2 |
intron_variant | MODIFIER | c.1663+4728T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180459 | ||||||
chr6:84180471
|
C | A | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1663+4716G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180471 | ||||||
chr6:84180513
|
A | G | 9 | a0001c0006t0001g0007a0001c0006t0001g0011a0001c0006t0001g0015others(6): Show | 9 | HG01346.hp1 HG02055.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1663+4674T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180513 | ||||||
chr6:84180557
|
T | C | 9 | a0001c0006t0001g0007a0001c0006t0001g0011a0001c0006t0001g0015others(6): Show | 9 | HG01346.hp1 HG02055.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1663+4630A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180557 | ||||||
chr6:84180561
|
G | C | 9 | a0001c0006t0001g0007a0001c0006t0001g0011a0001c0006t0001g0015others(6): Show | 9 | HG01346.hp1 HG02055.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1663+4626C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180561 | ||||||
chr6:84180582
|
G | A | 92 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(89): Show | 95 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(92): Show |
intron_variant | MODIFIER | c.1663+4605C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180582 | ||||||
chr6:84180592
|
T | A | 9 | a0001c0006t0001g0007a0001c0006t0001g0011a0001c0006t0001g0015others(6): Show | 9 | HG01346.hp1 HG02055.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1663+4595A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180592 | ||||||
chr6:84180600
|
T | C | 9 | a0001c0006t0001g0007a0001c0006t0001g0011a0001c0006t0001g0015others(6): Show | 9 | HG01346.hp1 HG02055.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1663+4587A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180600 | ||||||
chr6:84180601
|
G | A | 9 | a0001c0006t0001g0007a0001c0006t0001g0011a0001c0006t0001g0015others(6): Show | 9 | HG01346.hp1 HG02055.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1663+4586C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180601 | ||||||
chr6:84180672
|
A | G | 1 | a0001c0004t0002g0095 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.1663+4515T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180672 | ||||||
chr6:84180674
|
A | T | 8 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(5): Show | 8 | HG02109.hp1 HG02258.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.1663+4513T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180674 | ||||||
chr6:84180858
|
AT | A | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1663+4328delA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180858 | ||||||
chr6:84180860
|
G | A | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1663+4327C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180860 | ||||||
chr6:84180861
|
G | A | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1663+4326C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180861 | ||||||
chr6:84180874
|
T | C | 1 | a0002c0012t0004g0014 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.1663+4313A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84180874 | ||||||
chr6:84181012
|
A | G | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1663+4175T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84181012 | ||||||
chr6:84181156
|
T | C | 3 | a0001c0001t0002g0199a0001c0001t0002g0200a0001c0001t0002g0201 | 3 | HG02647.hp2 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1663+4031A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84181156 | ||||||
chr6:84181180
|
A | G | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1663+4007T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84181180 | ||||||
chr6:84181320
|
T | G | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02004.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.1663+3867A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84181320 | ||||||
chr6:84181487
|
T | C | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1663+3700A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84181487 | ||||||
chr6:84181736
|
G | A | 1 | a0001c0001t0001g0209 | 1 | HG02897.hp1 | intron_variant | MODIFIER | c.1663+3451C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84181736 | ||||||
chr6:84181866
|
T | G | 16 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(13): Show | 17 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1663+3321A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84181866 | ||||||
chr6:84181905
|
A | T | 1 | a0001c0001t0001g0066 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.1663+3282T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84181905 | ||||||
chr6:84182156
|
G | A | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1663+3031C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84182156 | ||||||
chr6:84182204
|
G | C | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1663+2983C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84182204 | ||||||
chr6:84182289
|
G | C | 17 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(14): Show | 18 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.1663+2898C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84182289 | ||||||
chr6:84182338
|
G | A | 83 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(80): Show | 86 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(83): Show |
intron_variant | MODIFIER | c.1663+2849C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84182338 | ||||||
chr6:84182353
|
T | A | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1663+2834A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84182353 | ||||||
chr6:84182372
|
C | CA | 16 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(13): Show | 17 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.1663+2814dupT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84182372 | ||||||
chr6:84182396
|
T | C | 1 | a0001c0001t0001g0109 | 1 | HG02735.hp2 | intron_variant | MODIFIER | c.1663+2791A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84182396 | ||||||
chr6:84182458
|
T | C | 4 | a0001c0011t0002g0019a0001c0011t0002g0020a0002c0012t0004g0014others(1): Show | 4 | HG02280.hp2 HG02647.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663+2729A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84182458 | ||||||
chr6:84182502
|
A | C | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1663+2685T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84182502 | ||||||
chr6:84182624
|
G | A | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1663+2563C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84182624 | ||||||
chr6:84182693
|
T | C | 1 | a0001c0001t0001g0181 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.1663+2494A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84182693 | ||||||
chr6:84182705
|
A | G | 1 | a0001c0007t0002g0018 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.1663+2482T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84182705 | ||||||
chr6:84182755
|
T | G | 1 | a0002c0016t0002g0196 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1663+2432A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84182755 | ||||||
chr6:84182847
|
G | A | 1 | a0001c0001t0001g0070 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.1663+2340C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84182847 | ||||||
chr6:84182890
|
T | C | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1663+2297A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84182890 | ||||||
chr6:84183046
|
A | G | 2 | a0001c0001t0003g0065a0001c0001t0003g0112 | 2 | HG01346.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.1663+2141T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84183046 | ||||||
chr6:84183056
|
A | G | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1663+2131T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84183056 | ||||||
chr6:84183117
|
T | C | 1 | a0001c0001t0003g0065 | 1 | HG01358.hp1 | intron_variant | MODIFIER | c.1663+2070A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84183117 | ||||||
chr6:84183283
|
A | G | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1663+1904T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84183283 | ||||||
chr6:84183337
|
G | A | 83 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(80): Show | 86 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(83): Show |
intron_variant | MODIFIER | c.1663+1850C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84183337 | ||||||
chr6:84183347
|
A | T | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1663+1840T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84183347 | ||||||
chr6:84183419
|
C | CA | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1663+1767dupT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84183419 | ||||||
chr6:84183498
|
T | C | 4 | a0001c0001t0001g0053a0001c0001t0001g0066a0001c0001t0001g0069others(1): Show | 4 | HG01261.hp1 HG01952.hp1 HG02004.hp1 others(1): Show |
intron_variant | MODIFIER | c.1663+1689A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84183498 | ||||||
chr6:84183646
|
G | A | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1663+1541C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84183646 | ||||||
chr6:84183949
|
G | C | 2 | a0001c0004t0002g0012a0001c0004t0002g0095 | 2 | HG03486.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1663+1238C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84183949 | ||||||
chr6:84184045
|
C | T | 13 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(10): Show | 13 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1663+1142G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84184045 | ||||||
chr6:84184089
|
T | A | 6 | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0180others(3): Show | 6 | HG00673.hp2 HG02056.hp2 NA18962.hp2 others(3): Show |
intron_variant | MODIFIER | c.1663+1098A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84184089 | ||||||
chr6:84184131
|
C | A | 1 | a0001c0001t0002g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1663+1056G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84184131 | ||||||
chr6:84184140
|
G | A | 3 | a0001c0001t0001g0096a0002c0012t0004g0014a0006c0013t0002g0113 | 3 | HG02280.hp2 HG03831.hp1 NA21309.hp1 |
intron_variant | MODIFIER | c.1663+1047C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84184140 | ||||||
chr6:84184578
|
A | G | 1 | a0002c0016t0002g0196 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.1663+609T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84184578 | ||||||
chr6:84184598
|
G | C | 1 | a0001c0001t0001g0167 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.1663+589C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84184598 | ||||||
chr6:84184906
|
CTCAG | C | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1663+277_1663+280d others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84184906 | ||||||
chr6:84184976
|
A | T | 9 | a0001c0006t0001g0007a0001c0006t0001g0011a0001c0006t0001g0015others(6): Show | 9 | HG01346.hp1 HG02055.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.1663+211T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84184976 | ||||||
chr6:84185067
|
TG | T | 3 | a0002c0002t0002g0013a0002c0002t0002g0089a0002c0002t0007g0202 | 3 | HG03540.hp2 NA20805.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1663+119delC | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84185067 | ||||||
chr6:84185072
|
C | T | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1663+115G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 13/26 | chr6 | 84185072 | ||||||
chr6:84185519
|
T | C | 1 | a0001c0001t0002g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1402-71A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 12/26 | chr6 | 84185519 | ||||||
chr6:84185685
|
GC | G | 5 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.1402-238delG | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 12/26 | chr6 | 84185685 | ||||||
chr6:84185697
|
G | T | 4 | a0001c0008t0005g0203a0001c0008t0005g0204a0001c0008t0005g0205others(1): Show | 4 | HG02717.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.1402-249C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 12/26 | chr6 | 84185697 | ||||||
chr6:84185803
|
A | G | 1 | a0001c0001t0001g0125 | 1 | HG00280.hp2 | intron_variant | MODIFIER | c.1402-355T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 12/26 | chr6 | 84185803 | ||||||
chr6:84185881
|
T | G | 2 | a0002c0012t0004g0014a0006c0013t0002g0113 | 2 | HG02280.hp2 NA21309.hp1 |
intron_variant | MODIFIER | c.1402-433A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 12/26 | chr6 | 84185881 | ||||||
chr6:84185894
|
C | A | 11 | a0001c0001t0001g0051a0001c0001t0001g0076a0001c0001t0001g0078others(8): Show | 11 | HG00673.hp2 HG02056.hp2 HG02080.hp1 others(8): Show |
intron_variant | MODIFIER | c.1401+438G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 12/26 | chr6 | 84185894 | ||||||
chr6:84186145
|
A | G | 11 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(8): Show | 11 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1401+187T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 12/26 | chr6 | 84186145 | ||||||
chr6:84186179
|
A | G | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1401+153T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 12/26 | chr6 | 84186179 | ||||||
chr6:84186228
|
T | A | 1 | a0001c0001t0001g0025 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1401+104A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 12/26 | chr6 | 84186228 | ||||||
chr6:84186729
|
T | C | 6 | a0002c0002t0002g0141a0002c0002t0002g0144a0002c0002t0002g0145others(3): Show | 6 | HG01109.hp2 HG02897.hp2 HG03098.hp1 others(3): Show |
intron_variant | MODIFIER | c.1110-106A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84186729 | ||||||
chr6:84186753
|
A | C | 36 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(33): Show | 36 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(33): Show |
intron_variant | MODIFIER | c.1110-130T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84186753 | ||||||
chr6:84186784
|
C | CAG | 83 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(80): Show | 86 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(83): Show |
intron_variant | MODIFIER | c.1110-163_1110-162d others(4): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84186784 | ||||||
chr6:84187170
|
A | C | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.1110-547T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84187170 | ||||||
chr6:84187263
|
G | A | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1110-640C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84187263 | ||||||
chr6:84187289
|
C | T | 1 | a0001c0001t0009g0122 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.1110-666G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84187289 | ||||||
chr6:84187292
|
C | T | 2 | a0002c0002t0002g0119a0002c0002t0002g0146 | 2 | HG02615.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.1110-669G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84187292 | ||||||
chr6:84187488
|
G | A | 16 | a0001c0001t0001g0010a0001c0001t0001g0025a0001c0001t0001g0053others(13): Show | 16 | HG00639.hp2 HG00738.hp2 HG01256.hp2 others(13): Show |
intron_variant | MODIFIER | c.1110-865C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84187488 | ||||||
chr6:84187702
|
G | A | 33 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(30): Show | 36 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(33): Show |
intron_variant | MODIFIER | c.1110-1079C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84187702 | ||||||
chr6:84187778
|
G | C | 1 | a0001c0001t0001g0062 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1110-1155C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84187778 | ||||||
chr6:84187780
|
C | G | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1110-1157G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84187780 | ||||||
chr6:84187828
|
T | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1110-1205A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84187828 | ||||||
chr6:84187859
|
T | C | 6 | a0001c0005t0004g0198a0001c0008t0005g0203a0001c0008t0005g0204others(3): Show | 6 | HG02258.hp1 HG02717.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.1110-1236A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84187859 | ||||||
chr6:84187885
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1110-1262G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84187885 | ||||||
chr6:84188027
|
T | A | 1 | a0001c0001t0001g0062 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.1110-1404A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188027 | ||||||
chr6:84188103
|
C | CA | 27 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0051others(24): Show | 27 | HG00408.hp1 HG00639.hp1 HG00673.hp2 others(24): Show |
intron_variant | MODIFIER | c.1110-1481dupT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188103 | ||||||
chr6:84188103
|
C | CAA | 11 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(8): Show | 13 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1110-1482_1110-148 others(6): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188103 | ||||||
chr6:84188103
|
CA | C | 7 | a0001c0001t0001g0057a0001c0001t0002g0110a0001c0001t0002g0140others(4): Show | 7 | HG01884.hp1 HG02280.hp1 HG02602.hp2 others(4): Show |
intron_variant | MODIFIER | c.1110-1481delT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188103 | ||||||
chr6:84188120
|
AG | A | 3 | a0001c0001t0002g0038a0001c0011t0002g0019a0001c0011t0002g0020 | 3 | HG02647.hp1 HG02922.hp2 HG03209.hp1 |
intron_variant | MODIFIER | c.1110-1498delC | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188120 | ||||||
chr6:84188129
|
T | A | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1110-1506A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188129 | ||||||
chr6:84188146
|
T | C | 1 | a0003c0003t0001g0043 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.1110-1523A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188146 | ||||||
chr6:84188156
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.1110-1533T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188156 | ||||||
chr6:84188180
|
C | T | 5 | a0002c0002t0002g0141a0002c0002t0002g0144a0002c0002t0002g0145others(2): Show | 5 | HG01109.hp2 HG03098.hp1 HG03471.hp1 others(2): Show |
intron_variant | MODIFIER | c.1110-1557G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188180 | ||||||
chr6:84188215
|
T | G | 36 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(33): Show | 36 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(33): Show |
intron_variant | MODIFIER | c.1110-1592A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188215 | ||||||
chr6:84188290
|
C | T | 25 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(22): Show | 26 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(23): Show |
intron_variant | MODIFIER | c.1110-1667G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188290 | ||||||
chr6:84188295
|
A | G | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1110-1672T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188295 | ||||||
chr6:84188373
|
C | T | 1 | a0002c0002t0002g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.1110-1750G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188373 | ||||||
chr6:84188405
|
C | T | 2 | a0002c0002t0002g0003a0002c0002t0002g0006 | 3 | HG01256.hp1 HG01258.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1110-1782G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188405 | ||||||
chr6:84188448
|
G | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1110-1825C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188448 | ||||||
chr6:84188502
|
A | G | 3 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0139 | 3 | HG03017.hp2 HG04204.hp2 HG04228.hp2 |
intron_variant | MODIFIER | c.1110-1879T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188502 | ||||||
chr6:84188514
|
A | C | 11 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(8): Show | 13 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.1110-1891T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188514 | ||||||
chr6:84188553
|
A | G | 83 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(80): Show | 86 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(83): Show |
intron_variant | MODIFIER | c.1110-1930T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188553 | ||||||
chr6:84188798
|
G | C | 1 | a0003c0003t0003g0090 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.1110-2175C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188798 | ||||||
chr6:84188803
|
C | T | 2 | a0001c0001t0001g0056a0001c0001t0001g0068 | 2 | HG03654.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.1110-2180G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188803 | ||||||
chr6:84188985
|
A | G | 1 | a0001c0006t0001g0015 | 1 | NA18971.hp1 | intron_variant | MODIFIER | c.1110-2362T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84188985 | ||||||
chr6:84189115
|
G | A | 1 | a0002c0002t0002g0147 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.1110-2492C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189115 | ||||||
chr6:84189123
|
C | T | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1110-2500G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189123 | ||||||
chr6:84189215
|
C | CA | 34 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(31): Show | 37 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.1110-2593dupT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189215 | ||||||
chr6:84189358
|
G | C | 2 | a0001c0006t0001g0015a0001c0006t0001g0131 | 2 | NA18971.hp1 NA19091.hp1 |
intron_variant | MODIFIER | c.1110-2735C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189358 | ||||||
chr6:84189394
|
C | T | 34 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(31): Show | 37 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.1110-2771G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189394 | ||||||
chr6:84189396
|
G | A | 1 | a0001c0001t0001g0177 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.1110-2773C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189396 | ||||||
chr6:84189510
|
C | T | 11 | a0001c0001t0001g0154a0001c0001t0002g0110a0001c0001t0002g0140others(8): Show | 11 | HG01884.hp1 HG02258.hp1 HG02280.hp1 others(8): Show |
intron_variant | MODIFIER | c.1110-2887G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189510 | ||||||
chr6:84189511
|
G | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1110-2888C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189511 | ||||||
chr6:84189538
|
A | G | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.1110-2915T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189538 | ||||||
chr6:84189557
|
C | T | 12 | a0001c0001t0001g0098a0001c0001t0002g0001a0001c0001t0002g0002others(9): Show | 14 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(11): Show |
intron_variant | MODIFIER | c.1110-2934G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189557 | ||||||
chr6:84189566
|
G | A | 3 | a0002c0002t0002g0013a0002c0002t0002g0089a0002c0002t0007g0202 | 3 | HG03540.hp2 NA20805.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.1110-2943C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189566 | ||||||
chr6:84189570
|
C | A | 1 | a0008c0014t0004g0115 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.1110-2947G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189570 | ||||||
chr6:84189621
|
G | C | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.1110-2998C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189621 | ||||||
chr6:84189632
|
C | T | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1110-3009G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189632 | ||||||
chr6:84189633
|
G | A | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG00408.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.1110-3010C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189633 | ||||||
chr6:84189635
|
C | G | 13 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(10): Show | 13 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1110-3012G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189635 | ||||||
chr6:84189676
|
C | T | 1 | a0001c0001t0002g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.1110-3053G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189676 | ||||||
chr6:84189688
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1110-3065G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189688 | ||||||
chr6:84189716
|
G | A | 3 | a0001c0001t0001g0148a0001c0001t0001g0152a0001c0001t0001g0162 | 3 | HG01943.hp2 HG01981.hp1 HG02273.hp2 |
intron_variant | MODIFIER | c.1110-3093C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189716 | ||||||
chr6:84189717
|
C | A | 207 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(204): Show | 210 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(207): Show |
intron_variant | MODIFIER | c.1110-3094G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189717 | ||||||
chr6:84189752
|
C | T | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1110-3129G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189752 | ||||||
chr6:84189774
|
C | G | 1 | a0001c0001t0001g0026 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.1110-3151G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189774 | ||||||
chr6:84189790
|
C | T | 14 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0158others(11): Show | 14 | HG00408.hp1 HG00558.hp2 HG01106.hp1 others(11): Show |
intron_variant | MODIFIER | c.1110-3167G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189790 | ||||||
chr6:84189802
|
G | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1110-3179C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189802 | ||||||
chr6:84189928
|
T | C | 1 | a0001c0001t0001g0178 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1110-3305A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189928 | ||||||
chr6:84189936
|
G | A | 1 | a0001c0001t0001g0178 | 1 | HG01496.hp2 | intron_variant | MODIFIER | c.1110-3313C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189936 | ||||||
chr6:84189936
|
GACACTCT others(112): Show |
G | 1 | a0001c0001t0002g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1110-3432_1110-331 others(4): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189936 | ||||||
chr6:84189984
|
T | C | 1 | a0001c0006t0001g0133 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1110-3361A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84189984 | ||||||
chr6:84190011
|
A | ATCAGCAC others(112): Show |
1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1110-3389_1110-338 others(123): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84190011 | ||||||
chr6:84190055
|
A | G | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1110-3432T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84190055 | ||||||
chr6:84190232
|
G | A | 2 | a0001c0001t0001g0067a0001c0001t0001g0132 | 2 | NA18986.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.1109+3377C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84190232 | ||||||
chr6:84190292
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1109+3317G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84190292 | ||||||
chr6:84190409
|
C | T | 11 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(8): Show | 11 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1109+3200G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84190409 | ||||||
chr6:84190445
|
C | T | 3 | a0001c0001t0002g0197a0005c0010t0002g0163a0005c0010t0002g0164 | 3 | HG02818.hp2 HG02965.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.1109+3164G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84190445 | ||||||
chr6:84190591
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.1109+3018G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84190591 | ||||||
chr6:84190740
|
G | A | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1109+2869C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84190740 | ||||||
chr6:84190808
|
A | G | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1109+2801T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84190808 | ||||||
chr6:84190839
|
C | T | 1 | a0001c0001t0001g0168 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.1109+2770G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84190839 | ||||||
chr6:84190971
|
G | A | 2 | a0001c0008t0005g0205a0001c0008t0005g0206 | 2 | HG03139.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.1109+2638C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84190971 | ||||||
chr6:84190998
|
G | T | 7 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(4): Show | 7 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1109+2611C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84190998 | ||||||
chr6:84191343
|
G | A | 13 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(10): Show | 13 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.1109+2266C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84191343 | ||||||
chr6:84191394
|
C | T | 1 | a0001c0001t0001g0186 | 1 | HG02056.hp2 | intron_variant | MODIFIER | c.1109+2215G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84191394 | ||||||
chr6:84191563
|
T | C | 3 | a0001c0001t0002g0199a0001c0001t0002g0200a0001c0001t0002g0201 | 3 | HG02647.hp2 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1109+2046A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84191563 | ||||||
chr6:84191673
|
C | T | 34 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(31): Show | 37 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.1109+1936G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84191673 | ||||||
chr6:84191710
|
T | C | 1 | a0011c0018t0003g0039 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.1109+1899A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84191710 | ||||||
chr6:84191933
|
T | C | 11 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(8): Show | 11 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.1109+1676A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84191933 | ||||||
chr6:84192011
|
T | C | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1109+1598A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192011 | ||||||
chr6:84192062
|
A | G | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1109+1547T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192062 | ||||||
chr6:84192121
|
G | A | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1109+1488C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192121 | ||||||
chr6:84192201
|
T | C | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1109+1408A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192201 | ||||||
chr6:84192213
|
A | G | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1109+1396T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192213 | ||||||
chr6:84192217
|
T | A | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1109+1392A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192217 | ||||||
chr6:84192262
|
C | T | 1 | a0001c0001t0001g0132 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.1109+1347G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192262 | ||||||
chr6:84192263
|
G | C | 1 | a0001c0001t0002g0200 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.1109+1346C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192263 | ||||||
chr6:84192296
|
T | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1109+1313A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192296 | ||||||
chr6:84192339
|
C | A | 1 | a0001c0001t0002g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.1109+1270G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192339 | ||||||
chr6:84192363
|
T | A | 34 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(31): Show | 37 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(34): Show |
intron_variant | MODIFIER | c.1109+1246A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192363 | ||||||
chr6:84192375
|
T | C | 1 | a0002c0002t0002g0089 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.1109+1234A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192375 | ||||||
chr6:84192418
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1109+1191A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192418 | ||||||
chr6:84192532
|
G | A | 2 | a0001c0001t0001g0072a0001c0001t0001g0179 | 2 | HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.1109+1077C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192532 | ||||||
chr6:84192579
|
G | A | 2 | a0001c0001t0001g0125a0001c0001t0001g0153 | 2 | HG00280.hp2 HG01261.hp2 |
intron_variant | MODIFIER | c.1109+1030C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192579 | ||||||
chr6:84192583
|
G | A | 1 | a0001c0001t0001g0185 | 1 | HG01106.hp1 | intron_variant | MODIFIER | c.1109+1026C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192583 | ||||||
chr6:84192643
|
A | G | 1 | a0001c0001t0001g0061 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.1109+966T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192643 | ||||||
chr6:84192876
|
G | A | 1 | a0001c0001t0001g0092 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.1109+733C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192876 | ||||||
chr6:84192897
|
T | G | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1109+712A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84192897 | ||||||
chr6:84193315
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1109+294G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84193315 | ||||||
chr6:84193337
|
C | T | 1 | a0002c0002t0002g0006 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.1109+272G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84193337 | ||||||
chr6:84193507
|
G | C | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(82): Show | 88 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.1109+102C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84193507 | ||||||
chr6:84193552
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1109+57A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84193552 | ||||||
chr6:84193579
|
A | G | 1 | a0001c0001t0001g0071 | 1 | HG01074.hp1 | intron_variant | MODIFIER | c.1109+30T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 11/26 | chr6 | 84193579 | ||||||
chr6:84193717
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1028-27G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84193717 | ||||||
chr6:84193823
|
G | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1028-133C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84193823 | ||||||
chr6:84193926
|
T | C | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(82): Show | 88 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.1028-236A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84193926 | ||||||
chr6:84193946
|
A | C | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1028-256T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84193946 | ||||||
chr6:84194284
|
G | A | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1028-594C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84194284 | ||||||
chr6:84194291
|
G | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1027+593C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84194291 | ||||||
chr6:84194354
|
C | CA | 31 | a0001c0001t0001g0070a0001c0001t0001g0108a0001c0001t0001g0109others(28): Show | 31 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(28): Show |
intron_variant | MODIFIER | c.1027+529dupT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84194354 | ||||||
chr6:84194367
|
AG | A | 2 | a0001c0001t0002g0199a0001c0001t0002g0201 | 2 | HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.1027+516delC | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84194367 | ||||||
chr6:84194368
|
G | A | 70 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(67): Show | 73 | HG01074.hp2 HG01109.hp2 HG01243.hp2 others(70): Show |
intron_variant | MODIFIER | c.1027+516C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84194368 | ||||||
chr6:84194400
|
T | TTTGGCTC others(23): Show |
14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.1027+454_1027+483d others(32): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84194400 | ||||||
chr6:84194455
|
C | CT | 5 | a0001c0001t0001g0080a0001c0001t0001g0096a0001c0001t0002g0037others(2): Show | 5 | HG02055.hp2 HG02922.hp2 HG03540.hp1 others(2): Show |
intron_variant | MODIFIER | c.1027+428dupA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84194455 | ||||||
chr6:84194455
|
CT | C | 76 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(73): Show | 79 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(76): Show |
intron_variant | MODIFIER | c.1027+428delA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84194455 | ||||||
chr6:84194455
|
CTT | C | 5 | a0001c0007t0002g0017a0001c0007t0002g0018a0001c0007t0002g0116others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.1027+427_1027+428d others(4): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84194455 | ||||||
chr6:84194563
|
C | G | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1027+321G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84194563 | ||||||
chr6:84194568
|
C | T | 1 | a0001c0001t0001g0076 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.1027+316G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84194568 | ||||||
chr6:84194642
|
T | C | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1027+242A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84194642 | ||||||
chr6:84194649
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1027+235A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84194649 | ||||||
chr6:84194674
|
A | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1027+210T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84194674 | ||||||
chr6:84194703
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.1027+181G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84194703 | ||||||
chr6:84194747
|
T | C | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.1027+137A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84194747 | ||||||
chr6:84194757
|
A | G | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.1027+127T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84194757 | ||||||
chr6:84194802
|
A | G | 7 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(4): Show | 7 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.1027+82T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 10/26 | chr6 | 84194802 | ||||||
chr6:84195123
|
T | C | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.836-48A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84195123 | ||||||
chr6:84195129
|
C | T | 15 | a0001c0007t0002g0018a0003c0003t0001g0043a0003c0003t0003g0040others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.836-54G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84195129 | ||||||
chr6:84195218
|
A | C | 21 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(18): Show | 21 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.836-143T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84195218 | ||||||
chr6:84195303
|
G | A | 1 | a0001c0001t0001g0050 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.836-228C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84195303 | ||||||
chr6:84195605
|
A | G | 1 | a0001c0005t0005g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.836-530T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84195605 | ||||||
chr6:84195664
|
C | T | 2 | a0001c0001t0001g0170a0001c0001t0001g0171 | 2 | HG00408.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.836-589G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84195664 | ||||||
chr6:84195815
|
G | C | 1 | a0001c0005t0004g0107 | 1 | HG03486.hp1 | intron_variant | MODIFIER | c.836-740C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84195815 | ||||||
chr6:84195995
|
C | T | 1 | a0001c0001t0001g0136 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.836-920G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84195995 | ||||||
chr6:84196144
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.836-1069A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84196144 | ||||||
chr6:84196226
|
C | T | 2 | a0001c0004t0002g0210a0001c0004t0002g0211 | 2 | HG00741.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.836-1151G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84196226 | ||||||
chr6:84196277
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.836-1202G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84196277 | ||||||
chr6:84196292
|
G | A | 20 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(17): Show | 20 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(17): Show |
intron_variant | MODIFIER | c.836-1217C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84196292 | ||||||
chr6:84196519
|
G | A | 1 | a0001c0001t0001g0062 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.836-1444C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84196519 | ||||||
chr6:84196580
|
C | T | 13 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(10): Show | 13 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.836-1505G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84196580 | ||||||
chr6:84196585
|
T | A | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.836-1510A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84196585 | ||||||
chr6:84196607
|
G | A | 7 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(4): Show | 7 | HG01884.hp1 HG02280.hp1 HG02647.hp2 others(4): Show |
intron_variant | MODIFIER | c.836-1532C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84196607 | ||||||
chr6:84196777
|
G | C | 36 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(33): Show | 36 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(33): Show |
intron_variant | MODIFIER | c.836-1702C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84196777 | ||||||
chr6:84196811
|
G | A | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.836-1736C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84196811 | ||||||
chr6:84196860
|
T | C | 1 | a0001c0001t0001g0188 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.836-1785A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84196860 | ||||||
chr6:84196924
|
G | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.836-1849C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84196924 | ||||||
chr6:84196984
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.836-1909G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84196984 | ||||||
chr6:84196990
|
T | A | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.836-1915A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84196990 | ||||||
chr6:84197031
|
C | T | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.836-1956G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84197031 | ||||||
chr6:84197051
|
T | C | 1 | a0001c0004t0002g0103 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.836-1976A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84197051 | ||||||
chr6:84197088
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.836-2013G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84197088 | ||||||
chr6:84197251
|
G | GA | 7 | a0001c0001t0001g0072a0001c0001t0001g0074a0003c0003t0003g0045others(4): Show | 7 | HG01257.hp2 HG01928.hp2 HG02148.hp1 others(4): Show |
intron_variant | MODIFIER | c.836-2177dupT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84197251 | ||||||
chr6:84197340
|
A | G | 8 | a0001c0006t0001g0007a0001c0006t0001g0011a0001c0006t0001g0015others(5): Show | 8 | HG01346.hp1 HG02055.hp2 HG02451.hp2 others(5): Show |
intron_variant | MODIFIER | c.836-2265T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84197340 | ||||||
chr6:84197447
|
T | C | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.836-2372A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84197447 | ||||||
chr6:84197632
|
G | A | 3 | a0001c0001t0001g0056a0001c0001t0001g0068a0001c0001t0001g0080 | 3 | HG03654.hp2 HG03831.hp2 HG04228.hp1 |
intron_variant | MODIFIER | c.836-2557C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84197632 | ||||||
chr6:84197672
|
C | A | 8 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(5): Show | 8 | HG02109.hp1 HG02258.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.836-2597G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84197672 | ||||||
chr6:84197764
|
C | T | 5 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.836-2689G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84197764 | ||||||
chr6:84197779
|
T | G | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.836-2704A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84197779 | ||||||
chr6:84197825
|
C | CA | 38 | a0001c0001t0001g0009a0001c0001t0001g0080a0001c0001t0001g0157others(35): Show | 38 | HG00741.hp2 HG01074.hp2 HG01106.hp2 others(35): Show |
intron_variant | MODIFIER | c.836-2751dupT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84197825 | ||||||
chr6:84197827
|
A | AAAC | 8 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(5): Show | 8 | HG02109.hp1 HG02258.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.836-2753_836-2752i others(5): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84197827 | ||||||
chr6:84197828
|
A | AAC | 12 | a0001c0005t0004g0198a0001c0007t0002g0017a0001c0007t0002g0018others(9): Show | 12 | HG02257.hp2 HG02258.hp1 HG02280.hp2 others(9): Show |
intron_variant | MODIFIER | c.836-2754_836-2753i others(4): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84197828 | ||||||
chr6:84197842
|
A | AG | 18 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(15): Show | 19 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.836-2768_836-2767i others(3): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84197842 | ||||||
chr6:84197842
|
A | G | 1 | a0001c0001t0001g0138 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.836-2767T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84197842 | ||||||
chr6:84197945
|
T | C | 1 | a0001c0007t0002g0017 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.835+2844A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84197945 | ||||||
chr6:84198085
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.835+2704G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84198085 | ||||||
chr6:84198335
|
T | C | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.835+2454A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84198335 | ||||||
chr6:84198351
|
C | A | 1 | a0001c0005t0004g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.835+2438G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84198351 | ||||||
chr6:84198370
|
C | T | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.835+2419G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84198370 | ||||||
chr6:84198409
|
C | G | 1 | a0001c0001t0002g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.835+2380G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84198409 | ||||||
chr6:84198608
|
T | A | 1 | a0001c0001t0002g0110 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.835+2181A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84198608 | ||||||
chr6:84198699
|
A | G | 2 | a0001c0001t0001g0004a0001c0001t0001g0159 | 2 | HG02080.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.835+2090T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84198699 | ||||||
chr6:84198763
|
A | G | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.835+2026T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84198763 | ||||||
chr6:84198921
|
T | C | 1 | a0001c0001t0002g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.835+1868A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84198921 | ||||||
chr6:84199052
|
T | C | 1 | a0001c0001t0001g0132 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.835+1737A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84199052 | ||||||
chr6:84199150
|
C | T | 1 | a0003c0003t0001g0043 | 1 | HG01981.hp2 | intron_variant | MODIFIER | c.835+1639G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84199150 | ||||||
chr6:84199208
|
A | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.835+1581T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84199208 | ||||||
chr6:84199225
|
C | G | 1 | a0001c0001t0001g0098 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.835+1564G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84199225 | ||||||
chr6:84199235
|
G | A | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.835+1554C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84199235 | ||||||
chr6:84199249
|
A | G | 82 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(79): Show | 85 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(82): Show |
intron_variant | MODIFIER | c.835+1540T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84199249 | ||||||
chr6:84199539
|
T | C | 1 | a0001c0005t0004g0198 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.835+1250A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84199539 | ||||||
chr6:84199558
|
CA | C | 119 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(116): Show | 120 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(117): Show |
intron_variant | MODIFIER | c.835+1230delT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84199558 | ||||||
chr6:84199558
|
CAA | C | 69 | a0001c0001t0001g0097a0001c0001t0002g0001a0001c0001t0002g0002others(66): Show | 71 | HG00741.hp2 HG01109.hp1 HG01109.hp2 others(68): Show |
intron_variant | MODIFIER | c.835+1229_835+1230d others(4): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84199558 | ||||||
chr6:84199558
|
CAAA | C | 15 | a0001c0004t0010g0104a0003c0003t0003g0040a0003c0003t0003g0041others(12): Show | 15 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(12): Show |
intron_variant | MODIFIER | c.835+1228_835+1230d others(5): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84199558 | ||||||
chr6:84199729
|
G | A | 17 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(14): Show | 18 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.835+1060C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84199729 | ||||||
chr6:84200021
|
C | T | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.835+768G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84200021 | ||||||
chr6:84200026
|
G | A | 3 | a0001c0001t0001g0157a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG00408.hp2 HG01106.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.835+763C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84200026 | ||||||
chr6:84200084
|
A | G | 6 | a0001c0005t0004g0198a0001c0008t0005g0203a0001c0008t0005g0204others(3): Show | 6 | HG02258.hp1 HG02717.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.835+705T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84200084 | ||||||
chr6:84200157
|
A | G | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.835+632T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84200157 | ||||||
chr6:84200164
|
T | G | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(81): Show | 87 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(84): Show |
intron_variant | MODIFIER | c.835+625A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84200164 | ||||||
chr6:84200167
|
A | G | 1 | a0001c0001t0001g0072 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.835+622T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84200167 | ||||||
chr6:84200202
|
G | A | 82 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(79): Show | 85 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(82): Show |
intron_variant | MODIFIER | c.835+587C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84200202 | ||||||
chr6:84200207
|
G | A | 4 | a0001c0008t0005g0203a0001c0008t0005g0204a0001c0008t0005g0205others(1): Show | 4 | HG02717.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.835+582C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84200207 | ||||||
chr6:84200295
|
G | C | 1 | a0001c0004t0010g0104 | 1 | HG02976.hp2 | intron_variant | MODIFIER | c.835+494C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84200295 | ||||||
chr6:84200402
|
G | T | 19 | a0001c0001t0001g0150a0002c0002t0002g0003a0002c0002t0002g0006others(16): Show | 20 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(17): Show |
intron_variant | MODIFIER | c.835+387C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84200402 | ||||||
chr6:84200443
|
T | C | 1 | a0001c0001t0001g0101 | 1 | HG02109.hp2 | intron_variant | MODIFIER | c.835+346A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84200443 | ||||||
chr6:84200764
|
C | T | 1 | a0001c0001t0001g0096 | 1 | HG03831.hp1 | intron_variant | MODIFIER | c.835+25G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 9/26 | chr6 | 84200764 | ||||||
chr6:84200929
|
A | G | 11 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(8): Show | 13 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.719-24T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 8/26 | chr6 | 84200929 | ||||||
chr6:84201017
|
G | A | 17 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(14): Show | 18 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.719-112C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 8/26 | chr6 | 84201017 | ||||||
chr6:84201066
|
C | G | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.719-161G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 8/26 | chr6 | 84201066 | ||||||
chr6:84201072
|
A | T | 11 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(8): Show | 11 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.719-167T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 8/26 | chr6 | 84201072 | ||||||
chr6:84201109
|
T | A | 22 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(19): Show | 24 | HG00741.hp2 HG01109.hp1 HG01884.hp2 others(21): Show |
intron_variant | MODIFIER | c.719-204A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 8/26 | chr6 | 84201109 | ||||||
chr6:84201283
|
C | CAACA | 15 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(12): Show | 17 | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(14): Show |
intron_variant | MODIFIER | c.719-382_719-379dup others(4): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 8/26 | chr6 | 84201283 | ||||||
chr6:84201283
|
C | CAACAAAC others(1): Show |
3 | a0001c0001t0002g0199a0001c0001t0002g0200a0001c0001t0002g0201 | 3 | HG02647.hp2 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.719-386_719-379dup others(8): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 8/26 | chr6 | 84201283 | ||||||
chr6:84201283
|
CAACA | C | 41 | a0001c0001t0001g0179a0001c0005t0004g0005a0001c0005t0004g0085others(38): Show | 42 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(39): Show |
intron_variant | MODIFIER | c.719-382_719-379del others(4): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 8/26 | chr6 | 84201283 | ||||||
chr6:84201393
|
A | G | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.718+344T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 8/26 | chr6 | 84201393 | ||||||
chr6:84201460
|
AG | A | 2 | a0001c0001t0001g0054a0001c0001t0001g0169 | 2 | HG02293.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.718+276delC | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 8/26 | chr6 | 84201460 | ||||||
chr6:84201618
|
C | T | 132 | a0001c0001t0001g0004a0001c0001t0001g0016a0001c0001t0001g0023others(129): Show | 135 | HG00280.hp2 HG00408.hp2 HG00673.hp1 others(132): Show |
intron_variant | MODIFIER | c.718+119G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 8/26 | chr6 | 84201618 | ||||||
chr6:84201646
|
C | A | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.718+91G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 8/26 | chr6 | 84201646 | ||||||
chr6:84201841
|
G | C | 1 | a0002c0002t0002g0006 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.688-74C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 7/26 | chr6 | 84201841 | ||||||
chr6:84201916
|
A | G | 11 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(8): Show | 13 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.688-149T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 7/26 | chr6 | 84201916 | ||||||
chr6:84202040
|
A | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.688-273T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 7/26 | chr6 | 84202040 | ||||||
chr6:84202284
|
T | C | 6 | a0001c0005t0004g0198a0001c0008t0005g0203a0001c0008t0005g0204others(3): Show | 6 | HG02258.hp1 HG02717.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.688-517A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 7/26 | chr6 | 84202284 | ||||||
chr6:84202518
|
C | CT | 16 | a0001c0001t0001g0004a0001c0001t0001g0024a0001c0001t0001g0026others(13): Show | 16 | HG00741.hp1 HG01081.hp2 HG01169.hp1 others(13): Show |
intron_variant | MODIFIER | c.688-752dupA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 7/26 | chr6 | 84202518 | ||||||
chr6:84202518
|
CT | C | 58 | a0001c0001t0001g0053a0001c0001t0001g0054a0001c0001t0001g0088others(55): Show | 60 | HG00741.hp2 HG01074.hp2 HG01109.hp2 others(57): Show |
intron_variant | MODIFIER | c.688-752delA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 7/26 | chr6 | 84202518 | ||||||
chr6:84202518
|
CTT | C | 11 | a0001c0001t0002g0037a0001c0001t0002g0038a0001c0005t0004g0195others(8): Show | 11 | HG02109.hp1 HG02257.hp2 HG02647.hp1 others(8): Show |
intron_variant | MODIFIER | c.688-753_688-752del others(2): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 7/26 | chr6 | 84202518 | ||||||
chr6:84202518
|
CTTT | C | 6 | a0001c0005t0004g0198a0001c0008t0005g0203a0001c0008t0005g0204others(3): Show | 6 | HG02258.hp1 HG02717.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.688-754_688-752del others(3): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 7/26 | chr6 | 84202518 | ||||||
chr6:84202518
|
CTTTTTTT others(5): Show |
C | 3 | a0001c0001t0001g0072a0001c0001t0001g0179a0006c0013t0002g0113 | 3 | HG02280.hp2 HG03704.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.688-763_688-752del others(12): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 7/26 | chr6 | 84202518 | ||||||
chr6:84202518
|
CTTTTTTT others(15): Show |
C | 3 | a0001c0001t0001g0023a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG02615.hp1 HG02630.hp1 HG03041.hp2 |
intron_variant | MODIFIER | c.688-773_688-752del others(22): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 7/26 | chr6 | 84202518 | ||||||
chr6:84202528
|
T | C | 11 | a0001c0001t0001g0009a0001c0001t0001g0050a0001c0001t0001g0071others(8): Show | 11 | HG01074.hp1 HG01081.hp1 HG01169.hp2 others(8): Show |
intron_variant | MODIFIER | c.688-761A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 7/26 | chr6 | 84202528 | ||||||
chr6:84202633
|
T | G | 1 | a0001c0001t0001g0075 | 1 | HG01256.hp2 | intron_variant | MODIFIER | c.688-866A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 7/26 | chr6 | 84202633 | ||||||
chr6:84202785
|
A | G | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.688-1018T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 7/26 | chr6 | 84202785 | ||||||
chr6:84203097
|
C | A | 1 | a0012c0015t0001g0052 | 1 | NA18962.hp1 | intron_variant | MODIFIER | c.687+884G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 7/26 | chr6 | 84203097 | ||||||
chr6:84203248
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.687+733A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 7/26 | chr6 | 84203248 | ||||||
chr6:84203564
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.687+417A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 7/26 | chr6 | 84203564 | ||||||
chr6:84203586
|
A | G | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(82): Show | 88 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.687+395T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 7/26 | chr6 | 84203586 | ||||||
chr6:84203712
|
A | G | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.687+269T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 7/26 | chr6 | 84203712 | ||||||
chr6:84204133
|
T | A | 1 | a0001c0001t0002g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.572-37A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84204133 | ||||||
chr6:84204334
|
C | T | 1 | a0003c0003t0003g0091 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.572-238G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84204334 | ||||||
chr6:84204738
|
T | C | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.572-642A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84204738 | ||||||
chr6:84204763
|
C | T | 4 | a0001c0008t0005g0203a0001c0008t0005g0204a0001c0008t0005g0205others(1): Show | 4 | HG02717.hp1 HG03139.hp1 HG03453.hp2 others(1): Show |
intron_variant | MODIFIER | c.572-667G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84204763 | ||||||
chr6:84204816
|
A | G | 1 | a0002c0002t0002g0155 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.572-720T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84204816 | ||||||
chr6:84204863
|
C | T | 22 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(19): Show | 22 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(19): Show |
intron_variant | MODIFIER | c.572-767G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84204863 | ||||||
chr6:84204944
|
AC | A | 80 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(77): Show | 83 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(80): Show |
intron_variant | MODIFIER | c.572-849delG | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84204944 | ||||||
chr6:84204988
|
A | AT | 80 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(77): Show | 83 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(80): Show |
intron_variant | MODIFIER | c.572-893dupA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84204988 | ||||||
chr6:84205116
|
C | T | 2 | a0001c0001t0006g0060a0001c0001t0006g0093 | 2 | HG01943.hp1 NA20805.hp2 |
intron_variant | MODIFIER | c.572-1020G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205116 | ||||||
chr6:84205160
|
T | A | 1 | a0001c0001t0001g0138 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.572-1064A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205160 | ||||||
chr6:84205202
|
G | A | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.572-1106C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205202 | ||||||
chr6:84205372
|
C | T | 13 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(10): Show | 13 | HG02109.hp1 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.572-1276G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205372 | ||||||
chr6:84205460
|
A | G | 80 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(77): Show | 83 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(80): Show |
intron_variant | MODIFIER | c.572-1364T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205460 | ||||||
chr6:84205485
|
T | A | 2 | a0001c0006t0001g0007a0001c0006t0001g0011 | 2 | HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.572-1389A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205485 | ||||||
chr6:84205523
|
T | G | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.572-1427A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205523 | ||||||
chr6:84205531
|
A | G | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.572-1435T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205531 | ||||||
chr6:84205535
|
A | C | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.572-1439T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205535 | ||||||
chr6:84205571
|
A | T | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.572-1475T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205571 | ||||||
chr6:84205658
|
A | C | 4 | a0001c0004t0002g0102a0001c0004t0002g0103a0001c0004t0002g0114others(1): Show | 4 | HG02717.hp2 HG02965.hp2 HG02976.hp2 others(1): Show |
intron_variant | MODIFIER | c.572-1562T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205658 | ||||||
chr6:84205782
|
C | T | 8 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(5): Show | 8 | HG02109.hp1 HG02258.hp2 HG02886.hp2 others(5): Show |
intron_variant | MODIFIER | c.572-1686G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205782 | ||||||
chr6:84205824
|
C | T | 62 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(59): Show | 64 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(61): Show |
intron_variant | MODIFIER | c.572-1728G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205824 | ||||||
chr6:84205882
|
C | T | 6 | a0001c0005t0004g0198a0001c0008t0005g0203a0001c0008t0005g0204others(3): Show | 6 | HG02258.hp1 HG02717.hp1 HG02970.hp1 others(3): Show |
intron_variant | MODIFIER | c.572-1786G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205882 | ||||||
chr6:84205907
|
A | G | 21 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(18): Show | 21 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.572-1811T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205907 | ||||||
chr6:84205913
|
C | T | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.572-1817G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205913 | ||||||
chr6:84205927
|
C | G | 1 | a0001c0001t0006g0060 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.572-1831G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205927 | ||||||
chr6:84205946
|
A | AT | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.572-1851_572-1850i others(3): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205946 | ||||||
chr6:84205958
|
T | C | 2 | a0001c0001t0002g0110a0001c0001t0002g0140 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.572-1862A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84205958 | ||||||
chr6:84206011
|
A | G | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.572-1915T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206011 | ||||||
chr6:84206047
|
C | A | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.572-1951G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206047 | ||||||
chr6:84206049
|
C | A | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.572-1953G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206049 | ||||||
chr6:84206157
|
C | T | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.572-2061G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206157 | ||||||
chr6:84206162
|
A | T | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.572-2066T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206162 | ||||||
chr6:84206186
|
C | G | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.572-2090G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206186 | ||||||
chr6:84206235
|
G | GAACCAAA others(1): Show |
19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.572-2147_572-2140d others(10): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206235 | ||||||
chr6:84206251
|
T | C | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.572-2155A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206251 | ||||||
chr6:84206252
|
G | A | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.572-2156C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206252 | ||||||
chr6:84206253
|
C | T | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.572-2157G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206253 | ||||||
chr6:84206256
|
T | A | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.572-2160A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206256 | ||||||
chr6:84206257
|
A | G | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.572-2161T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206257 | ||||||
chr6:84206276
|
G | A | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.572-2180C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206276 | ||||||
chr6:84206284
|
A | C | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.572-2188T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206284 | ||||||
chr6:84206287
|
G | C | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.572-2191C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206287 | ||||||
chr6:84206320
|
C | T | 62 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(59): Show | 64 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(61): Show |
intron_variant | MODIFIER | c.572-2224G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206320 | ||||||
chr6:84206339
|
G | C | 51 | a0001c0001t0002g0037a0001c0001t0002g0038a0001c0004t0002g0012others(48): Show | 51 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.572-2243C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206339 | ||||||
chr6:84206374
|
G | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.572-2278C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206374 | ||||||
chr6:84206508
|
C | G | 1 | a0001c0001t0001g0154 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.572-2412G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206508 | ||||||
chr6:84206651
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.572-2555A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206651 | ||||||
chr6:84206658
|
G | A | 2 | a0001c0001t0001g0004a0001c0001t0001g0159 | 2 | HG02080.hp2 NA18942.hp1 |
intron_variant | MODIFIER | c.572-2562C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206658 | ||||||
chr6:84206820
|
C | A | 51 | a0001c0001t0002g0037a0001c0001t0002g0038a0001c0004t0002g0012others(48): Show | 51 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(48): Show |
intron_variant | MODIFIER | c.572-2724G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84206820 | ||||||
chr6:84207048
|
A | G | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.572-2952T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84207048 | ||||||
chr6:84207118
|
T | C | 13 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(10): Show | 13 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(10): Show |
intron_variant | MODIFIER | c.572-3022A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84207118 | ||||||
chr6:84207203
|
C | T | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.572-3107G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84207203 | ||||||
chr6:84207278
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.572-3182A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84207278 | ||||||
chr6:84207305
|
C | G | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.572-3209G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84207305 | ||||||
chr6:84207364
|
T | C | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.572-3268A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84207364 | ||||||
chr6:84207415
|
T | C | 11 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(8): Show | 11 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.572-3319A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84207415 | ||||||
chr6:84207440
|
C | G | 1 | a0001c0001t0001g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.572-3344G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84207440 | ||||||
chr6:84207483
|
C | T | 3 | a0001c0001t0001g0058a0001c0001t0001g0059a0003c0003t0003g0090 | 3 | HG03669.hp1 NA18940.hp1 NA18950.hp1 |
intron_variant | MODIFIER | c.572-3387G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84207483 | ||||||
chr6:84207504
|
G | A | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.572-3408C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84207504 | ||||||
chr6:84207536
|
G | A | 29 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0051others(26): Show | 29 | HG00408.hp1 HG00558.hp2 HG00639.hp1 others(26): Show |
intron_variant | MODIFIER | c.572-3440C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84207536 | ||||||
chr6:84207619
|
T | C | 1 | a0001c0001t0002g0035 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.572-3523A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84207619 | ||||||
chr6:84207713
|
T | TA | 84 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(81): Show | 87 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(84): Show |
intron_variant | MODIFIER | c.572-3618dupT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84207713 | ||||||
chr6:84207754
|
A | C | 11 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(8): Show | 13 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(10): Show |
intron_variant | MODIFIER | c.572-3658T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84207754 | ||||||
chr6:84207786
|
T | C | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.572-3690A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84207786 | ||||||
chr6:84207792
|
T | C | 80 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(77): Show | 83 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(80): Show |
intron_variant | MODIFIER | c.572-3696A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84207792 | ||||||
chr6:84207877
|
A | G | 80 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(77): Show | 83 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(80): Show |
intron_variant | MODIFIER | c.572-3781T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84207877 | ||||||
chr6:84208016
|
T | C | 4 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0139others(1): Show | 4 | HG03017.hp2 HG03704.hp2 HG04204.hp2 others(1): Show |
intron_variant | MODIFIER | c.572-3920A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84208016 | ||||||
chr6:84208019
|
A | AT | 23 | a0001c0001t0001g0036a0001c0001t0001g0057a0001c0001t0002g0037others(20): Show | 24 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(21): Show |
intron_variant | MODIFIER | c.572-3924dupA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84208019 | ||||||
chr6:84208019
|
A | ATT | 32 | a0001c0001t0002g0197a0001c0004t0002g0012a0001c0004t0002g0095others(29): Show | 32 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(29): Show |
intron_variant | MODIFIER | c.572-3925_572-3924d others(4): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84208019 | ||||||
chr6:84208090
|
C | T | 3 | a0001c0001t0001g0051a0001c0001t0001g0078a0001c0001t0001g0079 | 3 | HG02080.hp1 NA18981.hp2 NA19087.hp2 |
intron_variant | MODIFIER | c.572-3994G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84208090 | ||||||
chr6:84208242
|
T | C | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.572-4146A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84208242 | ||||||
chr6:84208249
|
G | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.572-4153C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84208249 | ||||||
chr6:84208290
|
A | AT | 3 | a0001c0001t0002g0199a0001c0001t0002g0200a0001c0001t0002g0201 | 3 | HG02647.hp2 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.572-4195dupA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84208290 | ||||||
chr6:84208518
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.572-4422G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84208518 | ||||||
chr6:84208723
|
T | G | 3 | a0001c0001t0002g0199a0001c0001t0002g0200a0001c0001t0002g0201 | 3 | HG02647.hp2 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.571+4234A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84208723 | ||||||
chr6:84208955
|
G | C | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.571+4002C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84208955 | ||||||
chr6:84208985
|
A | G | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.571+3972T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84208985 | ||||||
chr6:84209048
|
G | T | 21 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(18): Show | 21 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.571+3909C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84209048 | ||||||
chr6:84209085
|
G | T | 7 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(4): Show | 7 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.571+3872C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84209085 | ||||||
chr6:84209117
|
T | A | 3 | a0002c0002t0002g0119a0002c0002t0002g0146a0002c0002t0002g0155 | 3 | HG02615.hp2 HG02723.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.571+3840A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84209117 | ||||||
chr6:84209150
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.571+3807G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84209150 | ||||||
chr6:84209373
|
CT | C | 35 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(32): Show | 37 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(34): Show |
intron_variant | MODIFIER | c.571+3583delA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84209373 | ||||||
chr6:84209405
|
G | T | 11 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(8): Show | 11 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.571+3552C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84209405 | ||||||
chr6:84209591
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.571+3366A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84209591 | ||||||
chr6:84209605
|
T | C | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.571+3352A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84209605 | ||||||
chr6:84209697
|
A | T | 1 | a0001c0001t0001g0130 | 1 | NA19087.hp1 | intron_variant | MODIFIER | c.571+3260T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84209697 | ||||||
chr6:84209774
|
A | G | 18 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(15): Show | 19 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(16): Show |
intron_variant | MODIFIER | c.571+3183T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84209774 | ||||||
chr6:84209988
|
T | A | 1 | a0001c0006t0002g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.571+2969A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84209988 | ||||||
chr6:84209990
|
A | G | 1 | a0001c0001t0001g0056 | 1 | HG03654.hp2 | intron_variant | MODIFIER | c.571+2967T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84209990 | ||||||
chr6:84210374
|
A | G | 1 | a0001c0001t0002g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.571+2583T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84210374 | ||||||
chr6:84210536
|
G | T | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.571+2421C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84210536 | ||||||
chr6:84210556
|
G | A | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.571+2401C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84210556 | ||||||
chr6:84210828
|
G | A | 1 | a0001c0001t0001g0172 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.571+2129C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84210828 | ||||||
chr6:84210983
|
C | T | 1 | a0001c0001t0001g0055 | 1 | HG00280.hp1 | intron_variant | MODIFIER | c.571+1974G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84210983 | ||||||
chr6:84211163
|
A | C | 2 | a0001c0006t0001g0007a0001c0006t0001g0011 | 2 | HG03017.hp1 HG03942.hp2 |
intron_variant | MODIFIER | c.571+1794T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84211163 | ||||||
chr6:84211211
|
T | G | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.571+1746A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84211211 | ||||||
chr6:84211218
|
G | A | 2 | a0001c0001t0002g0110a0001c0001t0002g0140 | 2 | HG01884.hp1 HG02280.hp1 |
intron_variant | MODIFIER | c.571+1739C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84211218 | ||||||
chr6:84211522
|
A | G | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.571+1435T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84211522 | ||||||
chr6:84211526
|
C | CA | 11 | a0001c0001t0001g0036a0001c0001t0001g0051a0001c0001t0001g0054others(8): Show | 11 | HG02080.hp1 HG02280.hp2 HG02300.hp1 others(8): Show |
intron_variant | MODIFIER | c.571+1430dupT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84211526 | ||||||
chr6:84211526
|
C | CAA | 17 | a0001c0005t0004g0005a0001c0005t0004g0086a0001c0005t0004g0105others(14): Show | 17 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(14): Show |
intron_variant | MODIFIER | c.571+1429_571+1430d others(4): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84211526 | ||||||
chr6:84211526
|
CA | C | 15 | a0001c0001t0001g0148a0001c0001t0001g0173a0001c0001t0002g0001others(12): Show | 17 | HG01257.hp2 HG01884.hp2 HG01943.hp2 others(14): Show |
intron_variant | MODIFIER | c.571+1430delT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84211526 | ||||||
chr6:84211526
|
CAA | C | 17 | a0001c0001t0002g0028a0001c0001t0002g0199a0001c0001t0002g0200others(14): Show | 17 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(14): Show |
intron_variant | MODIFIER | c.571+1429_571+1430d others(4): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84211526 | ||||||
chr6:84211707
|
T | A | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.571+1250A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84211707 | ||||||
chr6:84211824
|
A | T | 1 | a0001c0001t0001g0172 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.571+1133T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84211824 | ||||||
chr6:84211873
|
T | A | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.571+1084A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84211873 | ||||||
chr6:84211968
|
G | A | 1 | a0001c0001t0001g0008 | 1 | NA20905.hp1 | intron_variant | MODIFIER | c.571+989C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84211968 | ||||||
chr6:84212039
|
G | GA | 15 | a0001c0001t0001g0009a0001c0004t0002g0012a0001c0004t0002g0095others(12): Show | 15 | HG00741.hp2 HG01109.hp1 HG01243.hp1 others(12): Show |
intron_variant | MODIFIER | c.571+917dupT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84212039 | ||||||
chr6:84212399
|
A | G | 7 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(4): Show | 7 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(4): Show |
intron_variant | MODIFIER | c.571+558T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84212399 | ||||||
chr6:84212696
|
A | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.571+261T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84212696 | ||||||
chr6:84212831
|
A | C | 14 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(11): Show | 14 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.571+126T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 6/26 | chr6 | 84212831 | ||||||
chr6:84213095
|
C | G | 3 | a0001c0001t0001g0157a0001c0001t0001g0170a0001c0001t0001g0171 | 3 | HG00408.hp2 HG01106.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.504-71G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84213095 | ||||||
chr6:84213102
|
A | T | 2 | a0001c0001t0002g0197a0006c0013t0002g0113 | 2 | HG02280.hp2 HG03130.hp1 |
intron_variant | MODIFIER | c.504-78T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84213102 | ||||||
chr6:84213170
|
G | A | 17 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(14): Show | 18 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.504-146C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84213170 | ||||||
chr6:84213413
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02004.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.504-389G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84213413 | ||||||
chr6:84213525
|
T | C | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.504-501A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84213525 | ||||||
chr6:84213531
|
T | C | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.504-507A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84213531 | ||||||
chr6:84213617
|
T | C | 1 | a0001c0001t0001g0009 | 1 | HG01243.hp1 | intron_variant | MODIFIER | c.504-593A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84213617 | ||||||
chr6:84213808
|
C | T | 3 | a0001c0001t0001g0054a0001c0001t0001g0169a0006c0013t0002g0113 | 3 | HG02280.hp2 HG02293.hp1 HG02300.hp1 |
intron_variant | MODIFIER | c.504-784G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84213808 | ||||||
chr6:84214038
|
G | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.504-1014C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84214038 | ||||||
chr6:84214103
|
C | G | 1 | a0001c0006t0002g0156 | 1 | HG03225.hp2 | intron_variant | MODIFIER | c.504-1079G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84214103 | ||||||
chr6:84214247
|
C | T | 1 | a0001c0001t0001g0053 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.503+1035G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84214247 | ||||||
chr6:84214265
|
C | A | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.503+1017G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84214265 | ||||||
chr6:84214394
|
T | TGGGGAAC others(3): Show |
1 | a0001c0001t0001g0088 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.503+878_503+887dup others(10): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84214394 | ||||||
chr6:84214479
|
C | T | 21 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(18): Show | 21 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.503+803G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84214479 | ||||||
chr6:84214573
|
C | T | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.503+709G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84214573 | ||||||
chr6:84214662
|
T | A | 1 | a0001c0001t0001g0121 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.503+620A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84214662 | ||||||
chr6:84214880
|
G | A | 1 | a0002c0002t0002g0147 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.503+402C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84214880 | ||||||
chr6:84214900
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.503+382A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84214900 | ||||||
chr6:84214964
|
A | G | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.503+318T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84214964 | ||||||
chr6:84214987
|
G | A | 1 | a0010c0020t0002g0142 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.503+295C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84214987 | ||||||
chr6:84215180
|
G | T | 85 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(82): Show | 88 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(85): Show |
intron_variant | MODIFIER | c.503+102C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84215180 | ||||||
chr6:84215273
|
G | A | 1 | a0001c0001t0001g0188 | 1 | HG01169.hp2 | intron_variant | MODIFIER | c.503+9C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 5/26 | chr6 | 84215273 | ||||||
chr6:84215481
|
A | G | 1 | a0001c0001t0001g0123 | 1 | HG01515.hp1 | intron_variant | MODIFIER | c.320-16T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 4/26 | chr6 | 84215481 | ||||||
chr6:84215743
|
A | G | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.319+33T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 4/26 | chr6 | 84215743 | ||||||
chr6:84216179
|
G | A | 1 | a0001c0001t0001g0025 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.173-257C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84216179 | ||||||
chr6:84216288
|
A | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.173-366T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84216288 | ||||||
chr6:84216317
|
T | C | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.173-395A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84216317 | ||||||
chr6:84216342
|
T | G | 63 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(60): Show | 65 | HG00741.hp2 HG01074.hp2 HG01109.hp1 others(62): Show |
intron_variant | MODIFIER | c.173-420A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84216342 | ||||||
chr6:84216399
|
A | G | 1 | a0001c0001t0001g0168 | 1 | NA18940.hp2 | intron_variant | MODIFIER | c.173-477T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84216399 | ||||||
chr6:84216474
|
T | C | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.173-552A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84216474 | ||||||
chr6:84216637
|
T | C | 3 | a0001c0001t0002g0199a0001c0001t0002g0200a0001c0001t0002g0201 | 3 | HG02647.hp2 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.173-715A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84216637 | ||||||
chr6:84216755
|
G | C | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.173-833C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84216755 | ||||||
chr6:84217177
|
A | T | 1 | a0001c0001t0001g0051 | 1 | NA18981.hp2 | intron_variant | MODIFIER | c.173-1255T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84217177 | ||||||
chr6:84217269
|
A | C | 13 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(10): Show | 13 | HG02109.hp1 HG02257.hp2 HG02258.hp2 others(10): Show |
intron_variant | MODIFIER | c.173-1347T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84217269 | ||||||
chr6:84217387
|
C | T | 2 | a0001c0001t0001g0191a0001c0001t0001g0192 | 2 | NA19009.hp2 NA19056.hp1 |
intron_variant | MODIFIER | c.173-1465G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84217387 | ||||||
chr6:84217483
|
C | G | 1 | a0001c0001t0001g0132 | 1 | NA19085.hp2 | intron_variant | MODIFIER | c.173-1561G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84217483 | ||||||
chr6:84217581
|
G | A | 14 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(11): Show | 14 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(11): Show |
intron_variant | MODIFIER | c.173-1659C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84217581 | ||||||
chr6:84217639
|
T | C | 1 | a0002c0002t0002g0147 | 1 | HG02897.hp2 | intron_variant | MODIFIER | c.173-1717A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84217639 | ||||||
chr6:84217867
|
C | T | 1 | a0002c0016t0002g0196 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.173-1945G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84217867 | ||||||
chr6:84217877
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.173-1955G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84217877 | ||||||
chr6:84217913
|
A | C | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.173-1991T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84217913 | ||||||
chr6:84217979
|
C | A | 1 | a0001c0001t0002g0197 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.173-2057G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84217979 | ||||||
chr6:84218085
|
A | G | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.173-2163T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84218085 | ||||||
chr6:84218108
|
T | C | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.173-2186A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84218108 | ||||||
chr6:84218390
|
A | G | 1 | a0001c0001t0001g0023 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.173-2468T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84218390 | ||||||
chr6:84218391
|
G | A | 1 | a0001c0001t0001g0080 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.173-2469C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84218391 | ||||||
chr6:84218523
|
T | C | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(16): Show |
intron_variant | MODIFIER | c.172+2534A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84218523 | ||||||
chr6:84218655
|
T | C | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.172+2402A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84218655 | ||||||
chr6:84218839
|
G | C | 2 | a0001c0005t0004g0198a0008c0014t0004g0115 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.172+2218C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84218839 | ||||||
chr6:84218893
|
G | A | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.172+2164C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84218893 | ||||||
chr6:84218923
|
T | C | 11 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(8): Show | 11 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.172+2134A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84218923 | ||||||
chr6:84219023
|
G | A | 4 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0081others(1): Show | 4 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.172+2034C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84219023 | ||||||
chr6:84219035
|
C | T | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.172+2022G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84219035 | ||||||
chr6:84219090
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.172+1967A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84219090 | ||||||
chr6:84219122
|
G | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.172+1935C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84219122 | ||||||
chr6:84219123
|
C | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.172+1934G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84219123 | ||||||
chr6:84219200
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.172+1857A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84219200 | ||||||
chr6:84219298
|
C | T | 2 | a0002c0002t0002g0141a0010c0020t0002g0142 | 2 | HG01109.hp2 NA18522.hp1 |
intron_variant | MODIFIER | c.172+1759G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84219298 | ||||||
chr6:84219327
|
G | C | 4 | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0001g0081others(1): Show | 4 | HG00738.hp1 HG00741.hp1 HG01081.hp2 others(1): Show |
intron_variant | MODIFIER | c.172+1730C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84219327 | ||||||
chr6:84219418
|
T | C | 4 | a0001c0001t0002g0197a0001c0001t0002g0199a0001c0001t0002g0200others(1): Show | 4 | HG02647.hp2 HG02809.hp1 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.172+1639A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84219418 | ||||||
chr6:84219690
|
A | G | 1 | a0011c0018t0003g0039 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.172+1367T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84219690 | ||||||
chr6:84219749
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.172+1308A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84219749 | ||||||
chr6:84219820
|
A | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.172+1237T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84219820 | ||||||
chr6:84219822
|
C | T | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.172+1235G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84219822 | ||||||
chr6:84219912
|
G | C | 1 | a0003c0003t0003g0091 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.172+1145C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84219912 | ||||||
chr6:84220164
|
T | C | 1 | a0001c0001t0002g0140 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.172+893A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84220164 | ||||||
chr6:84220363
|
G | A | 6 | a0001c0008t0005g0203a0001c0008t0005g0204a0001c0008t0005g0205others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.172+694C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84220363 | ||||||
chr6:84220379
|
G | A | 1 | a0001c0001t0001g0083 | 1 | HG02004.hp1 | intron_variant | MODIFIER | c.172+678C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84220379 | ||||||
chr6:84220470
|
A | G | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.172+587T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84220470 | ||||||
chr6:84220586
|
C | G | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.172+471G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84220586 | ||||||
chr6:84220619
|
A | G | 1 | a0002c0016t0002g0196 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.172+438T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84220619 | ||||||
chr6:84220635
|
T | C | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.172+422A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84220635 | ||||||
chr6:84220728
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.172+329T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84220728 | ||||||
chr6:84220873
|
G | A | 1 | a0001c0005t0005g0208 | 1 | HG02109.hp1 | intron_variant | MODIFIER | c.172+184C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84220873 | ||||||
chr6:84220945
|
A | G | 1 | a0001c0001t0001g0010 | 1 | HG03669.hp2 | intron_variant | MODIFIER | c.172+112T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84220945 | ||||||
chr6:84221043
|
T | G | 1 | a0002c0016t0002g0196 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.172+14A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 3/26 | chr6 | 84221043 | ||||||
chr6:84221417
|
C | T | 1 | a0001c0001t0001g0050 | 1 | HG01192.hp2 | intron_variant | MODIFIER | c.58-246G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84221417 | ||||||
chr6:84222005
|
T | C | 5 | a0001c0001t0002g0110a0001c0001t0002g0140a0001c0001t0002g0199others(2): Show | 5 | HG01884.hp1 HG02280.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-834A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84222005 | ||||||
chr6:84222009
|
A | G | 18 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(15): Show | 18 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(15): Show |
intron_variant | MODIFIER | c.58-838T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84222009 | ||||||
chr6:84222020
|
C | T | 17 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(14): Show | 18 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.58-849G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84222020 | ||||||
chr6:84222053
|
G | GA | 8 | a0001c0001t0001g0036a0001c0005t0004g0005a0001c0005t0004g0085others(5): Show | 8 | HG02258.hp2 HG02886.hp2 HG02976.hp1 others(5): Show |
intron_variant | MODIFIER | c.58-883dupT | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84222053 | ||||||
chr6:84222160
|
T | G | 14 | a0003c0003t0001g0043a0003c0003t0003g0040a0003c0003t0003g0041others(11): Show | 14 | HG01074.hp2 HG01243.hp2 HG01257.hp2 others(11): Show |
intron_variant | MODIFIER | c.58-989A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84222160 | ||||||
chr6:84222223
|
T | C | 5 | a0001c0007t0002g0017a0001c0007t0002g0018a0001c0007t0002g0116others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.58-1052A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84222223 | ||||||
chr6:84222403
|
G | A | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.58-1232C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84222403 | ||||||
chr6:84222455
|
T | A | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.58-1284A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84222455 | ||||||
chr6:84222692
|
T | C | 17 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(14): Show | 18 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(15): Show |
intron_variant | MODIFIER | c.58-1521A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84222692 | ||||||
chr6:84222694
|
C | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.58-1523G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84222694 | ||||||
chr6:84222766
|
G | A | 3 | a0001c0001t0002g0199a0001c0001t0002g0200a0001c0001t0002g0201 | 3 | HG02647.hp2 HG02809.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.58-1595C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84222766 | ||||||
chr6:84222772
|
G | GCA | 19 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(16): Show | 19 | HG02109.hp1 HG02257.hp2 HG02258.hp2 others(16): Show |
intron_variant | MODIFIER | c.58-1603_58-1602dup others(2): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84222772 | ||||||
chr6:84222772
|
G | GCACA | 2 | a0001c0005t0004g0198a0008c0014t0004g0115 | 2 | HG02258.hp1 HG02970.hp1 |
intron_variant | MODIFIER | c.58-1605_58-1602dup others(4): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84222772 | ||||||
chr6:84222772
|
GCA | G | 2 | a0001c0001t0001g0129a0001c0006t0001g0131 | 2 | NA18971.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.58-1603_58-1602del others(2): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84222772 | ||||||
chr6:84222772
|
GCACA | G | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.58-1605_58-1602del others(4): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84222772 | ||||||
chr6:84222825
|
C | T | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.58-1654G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84222825 | ||||||
chr6:84222833
|
T | C | 6 | a0001c0008t0005g0203a0001c0008t0005g0204a0001c0008t0005g0205others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.58-1662A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84222833 | ||||||
chr6:84223223
|
G | A | 1 | a0002c0012t0002g0193 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.58-2052C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223223 | ||||||
chr6:84223226
|
C | T | 1 | a0001c0006t0001g0007 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.58-2055G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223226 | ||||||
chr6:84223266
|
C | T | 1 | a0001c0001t0001g0167 | 1 | NA18942.hp2 | intron_variant | MODIFIER | c.58-2095G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223266 | ||||||
chr6:84223276
|
G | A | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.58-2105C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223276 | ||||||
chr6:84223282
|
C | T | 1 | a0008c0014t0004g0115 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.58-2111G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223282 | ||||||
chr6:84223307
|
T | G | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.58-2136A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223307 | ||||||
chr6:84223327
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.58-2156A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223327 | ||||||
chr6:84223446
|
C | A | 16 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(13): Show | 17 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.58-2275G>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223446 | ||||||
chr6:84223452
|
T | C | 1 | a0001c0001t0001g0084 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.58-2281A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223452 | ||||||
chr6:84223455
|
C | T | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.58-2284G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223455 | ||||||
chr6:84223500
|
A | AAAAT | 19 | a0001c0001t0001g0044a0001c0001t0001g0130a0001c0001t0002g0197others(16): Show | 19 | HG00558.hp1 HG01074.hp2 HG01243.hp2 others(16): Show |
intron_variant | MODIFIER | c.58-2333_58-2330dup others(4): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223500 | ||||||
chr6:84223500
|
A | AAAATAAA others(5): Show |
2 | a0001c0001t0002g0199a0001c0001t0002g0200 | 2 | HG02647.hp2 HG02970.hp2 |
intron_variant | MODIFIER | c.58-2341_58-2330dup others(12): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223500 | ||||||
chr6:84223500
|
AAAATAAA others(1): Show |
A | 3 | a0005c0010t0002g0163a0005c0010t0002g0164a0006c0013t0002g0113 | 3 | HG02280.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.58-2337_58-2330del others(8): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223500 | ||||||
chr6:84223545
|
T | C | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.58-2374A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223545 | ||||||
chr6:84223569
|
G | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.58-2398C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223569 | ||||||
chr6:84223622
|
C | G | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.58-2451G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223622 | ||||||
chr6:84223659
|
C | T | 2 | a0001c0001t0001g0021a0001c0001t0001g0022 | 2 | HG02004.hp2 HG02273.hp1 |
intron_variant | MODIFIER | c.58-2488G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223659 | ||||||
chr6:84223740
|
C | T | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.58-2569G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223740 | ||||||
chr6:84223820
|
T | G | 1 | a0001c0001t0001g0036 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.57+2517A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223820 | ||||||
chr6:84223908
|
G | GAA | 6 | a0001c0008t0005g0203a0001c0008t0005g0204a0001c0008t0005g0205others(3): Show | 6 | HG02647.hp1 HG02717.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.57+2427_57+2428dup others(2): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84223908 | ||||||
chr6:84224038
|
A | G | 1 | a0001c0001t0001g0129 | 1 | NA18971.hp2 | intron_variant | MODIFIER | c.57+2299T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84224038 | ||||||
chr6:84224078
|
T | C | 5 | a0001c0007t0002g0017a0001c0007t0002g0018a0001c0007t0002g0116others(2): Show | 5 | HG02257.hp2 HG02723.hp2 HG02809.hp2 others(2): Show |
intron_variant | MODIFIER | c.57+2259A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84224078 | ||||||
chr6:84224201
|
T | G | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.57+2136A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84224201 | ||||||
chr6:84224285
|
C | T | 16 | a0002c0002t0002g0003a0002c0002t0002g0006a0002c0002t0002g0013others(13): Show | 17 | HG01109.hp2 HG01256.hp1 HG01258.hp1 others(14): Show |
intron_variant | MODIFIER | c.57+2052G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84224285 | ||||||
chr6:84224355
|
G | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.57+1982C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84224355 | ||||||
chr6:84224421
|
A | G | 1 | a0002c0016t0002g0196 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.57+1916T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84224421 | ||||||
chr6:84224559
|
T | C | 2 | a0001c0001t0002g0037a0001c0001t0002g0038 | 2 | HG02922.hp2 HG03540.hp1 |
intron_variant | MODIFIER | c.57+1778A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84224559 | ||||||
chr6:84224773
|
G | A | 11 | a0001c0004t0002g0012a0001c0004t0002g0095a0001c0004t0002g0102others(8): Show | 11 | HG00741.hp2 HG01109.hp1 HG02486.hp1 others(8): Show |
intron_variant | MODIFIER | c.57+1564C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84224773 | ||||||
chr6:84224779
|
T | C | 15 | a0001c0005t0004g0005a0001c0005t0004g0085a0001c0005t0004g0086others(12): Show | 15 | HG02109.hp1 HG02257.hp2 HG02258.hp1 others(12): Show |
intron_variant | MODIFIER | c.57+1558A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84224779 | ||||||
chr6:84224807
|
G | A | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.57+1530C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84224807 | ||||||
chr6:84224888
|
A | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | NA18957.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.57+1449T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84224888 | ||||||
chr6:84224890
|
G | T | 2 | a0005c0010t0002g0163a0005c0010t0002g0164 | 2 | HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.57+1447C>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84224890 | ||||||
chr6:84224989
|
A | T | 3 | a0005c0010t0002g0163a0005c0010t0002g0164a0006c0013t0002g0113 | 3 | HG02280.hp2 HG02818.hp2 HG02965.hp1 |
intron_variant | MODIFIER | c.57+1348T>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84224989 | ||||||
chr6:84225036
|
C | T | 1 | a0001c0001t0001g0092 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.57+1301G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84225036 | ||||||
chr6:84225095
|
G | A | 1 | a0006c0013t0002g0113 | 1 | HG02280.hp2 | intron_variant | MODIFIER | c.57+1242C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84225095 | ||||||
chr6:84225366
|
T | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0088 | 2 | NA18957.hp2 NA18988.hp2 |
intron_variant | MODIFIER | c.57+971A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84225366 | ||||||
chr6:84225378
|
C | G | 15 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(12): Show | 17 | HG01884.hp2 HG02055.hp1 HG02280.hp2 others(14): Show |
intron_variant | MODIFIER | c.57+959G>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84225378 | ||||||
chr6:84225533
|
A | G | 10 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(7): Show | 12 | HG01884.hp2 HG02055.hp1 HG02451.hp1 others(9): Show |
intron_variant | MODIFIER | c.57+804T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84225533 | ||||||
chr6:84225576
|
GTATT | G | 12 | a0001c0001t0001g0120a0001c0001t0001g0121a0003c0003t0001g0043others(9): Show | 12 | HG01074.hp2 HG01243.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.57+757_57+760delAA others(2): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84225576 | ||||||
chr6:84225635
|
G | A | 40 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(37): Show | 42 | HG00741.hp2 HG01109.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.57+702C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84225635 | ||||||
chr6:84225636
|
T | C | 8 | a0001c0001t0002g0037a0001c0001t0002g0038a0001c0004t0002g0012others(5): Show | 8 | HG00741.hp2 HG02486.hp1 HG02922.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+701A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84225636 | ||||||
chr6:84225638
|
G | C | 40 | a0001c0001t0002g0001a0001c0001t0002g0002a0001c0001t0002g0028others(37): Show | 42 | HG00741.hp2 HG01109.hp1 HG01884.hp1 others(39): Show |
intron_variant | MODIFIER | c.57+699C>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84225638 | ||||||
chr6:84225692
|
CATACAAG others(39): Show |
C | 8 | a0001c0004t0007g0207a0001c0005t0005g0208a0001c0008t0005g0203others(5): Show | 8 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+599_57+644delTT others(44): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84225692 | ||||||
chr6:84225723
|
C | T | 12 | a0001c0001t0001g0120a0001c0001t0001g0121a0003c0003t0001g0043others(9): Show | 12 | HG01074.hp2 HG01243.hp2 HG01981.hp2 others(9): Show |
intron_variant | MODIFIER | c.57+614G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84225723 | ||||||
chr6:84225747
|
C | T | 25 | a0001c0001t0002g0037a0001c0001t0002g0038a0001c0001t0002g0110others(22): Show | 25 | HG00741.hp2 HG01109.hp1 HG01884.hp1 others(22): Show |
intron_variant | MODIFIER | c.57+590G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84225747 | ||||||
chr6:84225782
|
G | A | 8 | a0001c0004t0007g0207a0001c0005t0005g0208a0001c0008t0005g0203others(5): Show | 8 | HG01109.hp1 HG02109.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+555C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84225782 | ||||||
chr6:84225917
|
A | C | 161 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(158): Show | 163 | HG00280.hp1 HG00280.hp2 HG00408.hp1 others(160): Show |
intron_variant | MODIFIER | c.57+420T>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84225917 | ||||||
chr6:84225962
|
G | A | 10 | a0001c0001t0001g0157a0001c0005t0004g0198a0001c0006t0002g0156others(7): Show | 10 | HG01106.hp2 HG02258.hp1 HG02280.hp2 others(7): Show |
intron_variant | MODIFIER | c.57+375C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84225962 | ||||||
chr6:84225967
|
A | G | 4 | a0001c0005t0004g0198a0001c0011t0002g0019a0001c0011t0002g0020others(1): Show | 4 | HG02280.hp2 HG02647.hp1 HG02970.hp1 others(1): Show |
intron_variant | MODIFIER | c.57+370T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84225967 | ||||||
chr6:84225976
|
T | C | 75 | a0001c0001t0001g0016a0001c0001t0001g0036a0001c0001t0001g0096others(72): Show | 76 | HG00741.hp2 HG01106.hp2 HG01109.hp1 others(73): Show |
intron_variant | MODIFIER | c.57+361A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84225976 | ||||||
chr6:84226030
|
AAGG | A | 7 | a0001c0001t0002g0110a0001c0007t0002g0017a0001c0007t0002g0018others(4): Show | 7 | HG01884.hp1 HG02257.hp2 HG02615.hp2 others(4): Show |
intron_variant | MODIFIER | c.57+304_57+306delCC others(1): Show |
CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84226030 | ||||||
chr6:84226045
|
G | GT | 16 | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(13): Show | 18 | HG00738.hp1 HG00738.hp2 HG01081.hp2 others(15): Show |
intron_variant | MODIFIER | c.57+291dupA | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84226045 | ||||||
chr6:84226048
|
T | TG | 2 | a0001c0011t0002g0019a0001c0011t0002g0020 | 2 | HG02647.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.57+288_57+289insC | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84226048 | ||||||
chr6:84226049
|
T | G | 8 | a0001c0001t0001g0021a0001c0001t0001g0022a0001c0001t0001g0158others(5): Show | 8 | HG00408.hp1 HG00558.hp2 HG01981.hp1 others(5): Show |
intron_variant | MODIFIER | c.57+288A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84226049 | ||||||
chr6:84226148
|
A | G | 68 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(65): Show | 69 | HG00280.hp2 HG00408.hp1 HG00558.hp2 others(66): Show |
intron_variant | MODIFIER | c.57+189T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84226148 | ||||||
chr6:84226212
|
G | A | 1 | a0002c0016t0002g0196 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.57+125C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84226212 | ||||||
chr6:84226277
|
T | C | 12 | a0001c0001t0002g0197a0001c0001t0002g0199a0001c0001t0002g0200others(9): Show | 12 | HG01109.hp1 HG02109.hp1 HG02647.hp2 others(9): Show |
intron_variant | MODIFIER | c.57+60A>G | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 2/26 | chr6 | 84226277 | ||||||
chr6:84226524
|
C | T | 21 | a0001c0001t0002g0197a0001c0001t0002g0199a0001c0001t0002g0200others(18): Show | 21 | HG01109.hp1 HG02109.hp1 HG02258.hp1 others(18): Show |
intron_variant | MODIFIER | c.-59-72G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 1/26 | chr6 | 84226524 | ||||||
chr6:84226699
|
G | A | 1 | a0001c0001t0003g0112 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.-59-247C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 1/26 | chr6 | 84226699 | ||||||
chr6:84226705
|
T | A | 1 | a0002c0002t0002g0194 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.-59-253A>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 1/26 | chr6 | 84226705 | ||||||
chr6:84226931
|
G | A | 24 | a0001c0001t0001g0209a0001c0001t0002g0197a0001c0001t0002g0199others(21): Show | 24 | HG00741.hp2 HG01109.hp1 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.-59-479C>T | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 1/26 | chr6 | 84226931 | ||||||
chr6:84227260
|
A | G | 1 | a0001c0005t0004g0005 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.-60+320T>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 1/26 | chr6 | 84227260 | ||||||
chr6:84227460
|
T | G | 93 | a0001c0001t0001g0120a0001c0001t0001g0121a0001c0001t0001g0123others(90): Show | 94 | HG00280.hp2 HG00408.hp1 HG00408.hp2 others(91): Show |
intron_variant | MODIFIER | c.-60+120A>C | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 1/26 | chr6 | 84227460 | ||||||
chr6:84227527
|
C | T | 1 | a0001c0001t0001g0004 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.-60+53G>A | CEP162 | ENSG00000135315.12 | transcript | ENST00000403245.8 | protein_coding | 1/26 | chr6 | 84227527 |