geneid | 51164 |
---|---|
ensemblid | ENSG00000132912.13 |
hgncid | 15518 |
symbol | DCTN4 |
name | dynactin subunit 4 |
refseq_nuc | NM_016221.4 |
refseq_prot | NP_057305.1 |
ensembl_nuc | ENST00000447998.7 |
ensembl_prot | ENSP00000416968.2 |
mane_status | MANE Select |
chr | chr5 |
start | 150708440 |
end | 150759017 |
strand | - |
ver | v1.2 |
region | chr5:150708440-150759017 |
region5000 | chr5:150703440-150764017 |
regionname0 | DCTN4_chr5_150708440_150759017 |
regionname5000 | DCTN4_chr5_150703440_150764017 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 460 | 155 | 35 | 31 | 61 | 0 | 26 | 49 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0002 | 0/0 | 460 | 112 | 61 | 13 | 32 | 0 | 6 | 26 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0003 | 0/0 | 460 | 14 | 0 | 0 | 14 | 0 | 0 | 10 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0004 | 0/0 | 460 | 3 | 0 | 0 | 3 | 0 | 0 | 3 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0005 | 0/0 | 460 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0006 | 0/0 | 460 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
chapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 1383 | 147 | 28 | 31 | 60 | 0 | 26 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
c0002 | 0/0 | 1383 | 104 | 55 | 11 | 32 | 0 | 6 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
c0003 | 0/0 | 1383 | 14 | 0 | 0 | 14 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
c0004 | 0/0 | 1383 | 7 | 5 | 2 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
c0005 | 0/0 | 1383 | 7 | 7 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
c0006 | 0/0 | 1383 | 3 | 0 | 0 | 3 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
c0007 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
c0008 | 0/0 | 1383 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
c0009 | 0/0 | 1383 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
c0010 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 1/0 | 2734 | 152 | 35 | 31 | 62 | 0 | 23 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0002 | 0/0 | 2734 | 31 | 1 | 6 | 21 | 0 | 3 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0003 | 0/0 | 2733 | 20 | 18 | 2 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0004 | 0/0 | 2733 | 17 | 0 | 0 | 17 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0005 | 0/0 | 2734 | 17 | 16 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0006 | 0/0 | 2734 | 7 | 7 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0007 | 0/0 | 2734 | 6 | 0 | 1 | 0 | 0 | 5 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0008 | 0/0 | 2734 | 4 | 4 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0009 | 0/0 | 2732 | 4 | 4 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0010 | 0/0 | 2734 | 3 | 2 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0011 | 0/0 | 2734 | 3 | 3 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0012 | 0/0 | 2734 | 3 | 0 | 0 | 3 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0013 | 0/0 | 2734 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0014 | 0/0 | 2734 | 2 | 2 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0015 | 0/1 | 2734 | 2 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0016 | 0/0 | 2734 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0017 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0018 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0019 | 0/0 | 2734 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0020 | 0/0 | 2734 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0021 | 0/0 | 2734 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0022 | 0/0 | 2734 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0023 | 0/0 | 2734 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0024 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0025 | 0/0 | 2734 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0026 | 0/0 | 2734 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
t0027 | 0/0 | 2734 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0002 | 0/0 | 6 | 1 | 2 | 3 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0009 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0014 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0173 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 1383 | 147 | 28 | 31 | 60 | 0 | 26 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0005 | 0/0 | 1383 | 7 | 7 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0010 | 0/0 | 1383 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0002c0002 | 0/0 | 1383 | 104 | 55 | 11 | 32 | 0 | 6 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0002c0004 | 0/0 | 1383 | 7 | 5 | 2 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0002c0007 | 0/0 | 1383 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0003c0003 | 0/0 | 1383 | 14 | 0 | 0 | 14 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0004c0006 | 0/0 | 1383 | 3 | 0 | 0 | 3 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0005c0009 | 0/0 | 1383 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0006c0008 | 0/0 | 1383 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 1/0 | 4116 | 123 | 22 | 26 | 55 | 0 | 19 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0001t0002 | 0/0 | 4116 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0001t0003 | 0/0 | 4115 | 2 | 2 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0001t0007 | 0/0 | 4116 | 6 | 0 | 1 | 0 | 0 | 5 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0001t0010 | 0/0 | 4116 | 2 | 2 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0001t0013 | 0/0 | 4116 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0001t0015 | 0/1 | 4116 | 2 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0001t0019 | 0/0 | 4116 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0001t0020 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0001t0021 | 0/0 | 4116 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0001t0022 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0001t0023 | 0/0 | 4116 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0001t0024 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0001t0025 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0001t0026 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0001t0027 | 0/0 | 4116 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0005t0006 | 0/0 | 4116 | 7 | 7 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0001c0010t0001 | 0/0 | 4116 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0002c0002t0001 | 0/0 | 4116 | 24 | 12 | 2 | 6 | 0 | 4 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0002c0002t0002 | 0/0 | 4116 | 30 | 1 | 6 | 21 | 0 | 2 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0002c0002t0003 | 0/0 | 4115 | 18 | 16 | 2 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0002c0002t0005 | 0/0 | 4116 | 17 | 16 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0002c0002t0009 | 0/0 | 4114 | 4 | 4 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0002c0002t0011 | 0/0 | 4116 | 3 | 3 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0002c0002t0012 | 0/0 | 4116 | 3 | 0 | 0 | 3 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0002c0002t0014 | 0/0 | 4116 | 2 | 2 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0002c0002t0016 | 0/0 | 4116 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0002c0002t0017 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0002c0004t0001 | 0/0 | 4116 | 3 | 1 | 2 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0002c0004t0008 | 0/0 | 4116 | 4 | 4 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0002c0007t0018 | 0/0 | 4116 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0003c0003t0004 | 0/0 | 4115 | 14 | 0 | 0 | 14 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0004c0006t0004 | 0/0 | 4115 | 3 | 0 | 0 | 3 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0005c0009t0001 | 0/0 | 4116 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
a0006c0008t0010 | 0/0 | 4116 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | copy fasta | chr5 | 150703440 | 150764017 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0001 | 0/0 | 7 | 0 | 1 | 5 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0002 | 0/0 | 6 | 1 | 2 | 3 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0003 | 0/0 | 3 | 0 | 3 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0007 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0008 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0009 | 0/0 | 2 | 1 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0010 | 0/0 | 2 | 0 | 0 | 1 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0011 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0012 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0013 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0015 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0016 | 0/0 | 2 | 0 | 1 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0064 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0065 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0067 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0069 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0072 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0073 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0075 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0082 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0083 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0087 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0088 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0093 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0098 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0099 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0100 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0103 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0104 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0106 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0107 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0112 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0113 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0114 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0115 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0116 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0117 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0118 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0124 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0125 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0127 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0130 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0134 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0135 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0139 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0146 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0147 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0153 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0154 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0158 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0164 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0166 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0167 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0170 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0173 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0001g0174 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0002g0137 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0003g0078 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0003g0248 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0007g0070 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0007g0071 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0007g0079 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0007g0080 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0007g0133 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0007g0172 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0010g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0010g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0013g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0013g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0015g0014 | 0/1 | 2 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0019g0046 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0020g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0021g0162 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0022g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0023g0076 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0024g0085 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0025g0081 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0026g0171 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0001t0027g0109 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0005t0006g0179 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0005t0006g0180 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0005t0006g0181 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0005t0006g0182 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0005t0006g0183 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0005t0006g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0005t0006g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0001c0010t0001g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0006 | 0/0 | 2 | 2 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0033 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0043 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0058 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0059 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0184 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0192 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0201 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0202 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0210 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0001g0245 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0018 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0019 | 0/0 | 2 | 0 | 1 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0020 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0187 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0212 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0217 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0222 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0223 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0239 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0003g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0003g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0003g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0003g0026 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0003g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0003g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0003g0032 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0003g0035 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0003g0036 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0003g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0003g0038 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0003g0039 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0003g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0003g0041 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0003g0042 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0003g0044 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0003g0045 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0005g0047 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0005g0048 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0005g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0005g0050 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0005g0051 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0005g0052 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0005g0053 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0005g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0005g0055 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0005g0056 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0005g0057 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0005g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0005g0061 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0005g0062 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0005g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0005g0178 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0005g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0009g0188 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0009g0189 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0009g0190 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0009g0191 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0011g0027 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0011g0194 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0011g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0012g0017 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0012g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0014g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0014g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0016g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0016g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0002t0017g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0004t0001g0022 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0004t0001g0251 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0004t0008g0249 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0004t0008g0250 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0004t0008g0252 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0004t0008g0253 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0002c0007t0018g0025 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0003c0003t0004g0021 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0003c0003t0004g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0003c0003t0004g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0003c0003t0004g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0003c0003t0004g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0003c0003t0004g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0003c0003t0004g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0003c0003t0004g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0003c0003t0004g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0003c0003t0004g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0003c0003t0004g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0003c0003t0004g0241 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0003c0003t0004g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0004c0006t0004g0004 | 0/0 | 3 | 0 | 0 | 3 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0005c0009t0001g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
a0006c0008t0010g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00408 | hp1 | a0003 | c0003 | t0004 | g0021 | EAS | CHS | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG00408 | hp2 | a0002 | c0002 | t0001 | g0195 | EAS | CHS | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0067 | EAS | CHS | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG00558 | hp2 | a0002 | c0002 | t0001 | g0197 | EAS | CHS | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG00597 | hp1 | a0001 | c0001 | t0001 | g0100 | EAS | CHS | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG00597 | hp2 | a0002 | c0002 | t0002 | g0231 | EAS | CHS | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG00639 | hp1 | a0002 | c0002 | t0002 | g0019 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG00639 | hp2 | a0001 | c0001 | t0023 | g0076 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG00642 | hp1 | a0001 | c0001 | t0001 | g0110 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG00642 | hp2 | a0005 | c0009 | t0001 | g0092 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG00735 | hp1 | a0001 | c0001 | t0001 | g0146 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG00735 | hp2 | a0002 | c0002 | t0003 | g0005 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG00738 | hp1 | a0001 | c0001 | t0001 | g0012 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG00738 | hp2 | a0002 | c0002 | t0002 | g0237 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01069 | hp1 | a0002 | c0004 | t0001 | g0022 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01069 | hp2 | a0001 | c0001 | t0001 | g0001 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01071 | hp1 | a0002 | c0004 | t0001 | g0022 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01071 | hp2 | a0001 | c0001 | t0001 | g0115 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01081 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01081 | hp2 | a0001 | c0001 | t0001 | g0174 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01109 | hp1 | a0001 | c0001 | t0001 | g0113 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01109 | hp2 | a0001 | c0001 | t0001 | g0121 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01167 | hp1 | a0002 | c0002 | t0002 | g0018 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01167 | hp2 | a0001 | c0001 | t0015 | g0014 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01175 | hp1 | a0001 | c0001 | t0001 | g0088 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01175 | hp2 | a0001 | c0001 | t0001 | g0125 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01243 | hp1 | a0002 | c0002 | t0001 | g0034 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01243 | hp2 | a0002 | c0002 | t0001 | g0185 | AMR | PUR | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01255 | hp1 | a0001 | c0001 | t0001 | g0068 | AMR | CLM | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01255 | hp2 | a0001 | c0001 | t0001 | g0136 | AMR | CLM | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01261 | hp1 | a0001 | c0001 | t0001 | g0112 | AMR | CLM | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01261 | hp2 | a0001 | c0001 | t0001 | g0011 | AMR | CLM | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01433 | hp1 | a0001 | c0001 | t0001 | g0016 | AMR | CLM | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01433 | hp2 | a0006 | c0008 | t0010 | g0101 | AMR | CLM | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01496 | hp1 | a0002 | c0002 | t0003 | g0005 | AMR | CLM | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01496 | hp2 | a0002 | c0002 | t0002 | g0236 | AMR | CLM | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01884 | hp1 | a0002 | c0002 | t0003 | g0039 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01884 | hp2 | a0001 | c0001 | t0001 | g0090 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01891 | hp1 | a0002 | c0002 | t0005 | g0051 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01891 | hp2 | a0001 | c0001 | t0010 | g0111 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01928 | hp1 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01928 | hp2 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01934 | hp1 | a0001 | c0001 | t0001 | g0002 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01934 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01943 | hp1 | a0002 | c0002 | t0002 | g0223 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01943 | hp2 | a0001 | c0001 | t0027 | g0109 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01952 | hp1 | a0001 | c0001 | t0001 | g0167 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01952 | hp2 | a0001 | c0001 | t0001 | g0126 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0164 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01975 | hp2 | a0001 | c0001 | t0001 | g0069 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01978 | hp1 | a0001 | c0001 | t0007 | g0071 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01978 | hp2 | a0001 | c0001 | t0001 | g0003 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01981 | hp1 | a0002 | c0002 | t0005 | g0060 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG01981 | hp2 | a0001 | c0001 | t0001 | g0163 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0097 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02015 | hp2 | a0003 | c0003 | t0004 | g0021 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02040 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02040 | hp2 | a0001 | c0001 | t0020 | g0108 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02055 | hp1 | a0002 | c0002 | t0005 | g0048 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02055 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02071 | hp1 | a0001 | c0001 | t0001 | g0158 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02071 | hp2 | a0003 | c0003 | t0004 | g0238 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02080 | hp1 | a0002 | c0002 | t0001 | g0228 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02080 | hp2 | a0003 | c0003 | t0004 | g0196 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0159 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02129 | hp2 | a0002 | c0002 | t0001 | g0193 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02135 | hp1 | a0001 | c0001 | t0025 | g0081 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02135 | hp2 | a0001 | c0001 | t0001 | g0119 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02145 | hp1 | a0002 | c0002 | t0005 | g0057 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02145 | hp2 | a0002 | c0002 | t0001 | g0033 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02257 | hp1 | a0002 | c0004 | t0001 | g0251 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02257 | hp2 | a0001 | c0001 | t0010 | g0102 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02258 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02258 | hp2 | a0002 | c0002 | t0003 | g0040 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02280 | hp1 | a0002 | c0002 | t0011 | g0194 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02280 | hp2 | a0002 | c0002 | t0001 | g0031 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02300 | hp1 | a0001 | c0001 | t0021 | g0162 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02300 | hp2 | a0001 | c0001 | t0001 | g0168 | AMR | PEL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02451 | hp1 | a0002 | c0002 | t0005 | g0050 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02451 | hp2 | a0002 | c0002 | t0005 | g0176 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02523 | hp1 | a0001 | c0001 | t0001 | g0149 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02523 | hp2 | a0002 | c0002 | t0002 | g0234 | EAS | KHV | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02572 | hp1 | a0001 | c0001 | t0001 | g0083 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02572 | hp2 | a0002 | c0002 | t0003 | g0032 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02602 | hp1 | a0001 | c0001 | t0007 | g0133 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0082 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02615 | hp1 | a0002 | c0002 | t0001 | g0059 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02615 | hp2 | a0002 | c0002 | t0005 | g0052 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02622 | hp1 | a0002 | c0002 | t0005 | g0055 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02622 | hp2 | a0002 | c0002 | t0014 | g0177 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02630 | hp1 | a0002 | c0002 | t0001 | g0210 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02630 | hp2 | a0002 | c0002 | t0005 | g0054 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02647 | hp1 | a0002 | c0002 | t0003 | g0035 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02647 | hp2 | a0002 | c0002 | t0001 | g0192 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0073 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02683 | hp2 | a0001 | c0001 | t0001 | g0116 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02717 | hp1 | a0002 | c0002 | t0003 | g0037 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02717 | hp2 | a0002 | c0002 | t0005 | g0186 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02723 | hp1 | a0002 | c0002 | t0003 | g0026 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02723 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02735 | hp1 | a0001 | c0001 | t0007 | g0080 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02735 | hp2 | a0001 | c0001 | t0001 | g0117 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02738 | hp1 | a0001 | c0001 | t0019 | g0046 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02738 | hp2 | a0001 | c0001 | t0002 | g0137 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02809 | hp1 | a0002 | c0002 | t0009 | g0190 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02809 | hp2 | a0002 | c0002 | t0003 | g0041 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02818 | hp1 | a0001 | c0001 | t0001 | g0128 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02818 | hp2 | a0001 | c0001 | t0001 | g0091 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02886 | hp1 | a0002 | c0002 | t0003 | g0045 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02886 | hp2 | a0002 | c0002 | t0003 | g0023 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02895 | hp1 | a0002 | c0002 | t0001 | g0006 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02895 | hp2 | a0001 | c0001 | t0001 | g0084 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02896 | hp1 | a0002 | c0004 | t0008 | g0249 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02896 | hp2 | a0001 | c0005 | t0006 | g0203 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02897 | hp1 | a0001 | c0005 | t0006 | g0204 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02897 | hp2 | a0001 | c0001 | t0001 | g0077 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02922 | hp1 | a0002 | c0002 | t0001 | g0184 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02922 | hp2 | a0001 | c0001 | t0001 | g0089 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02965 | hp1 | a0002 | c0002 | t0005 | g0062 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02965 | hp2 | a0001 | c0001 | t0003 | g0078 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02970 | hp1 | a0001 | c0001 | t0003 | g0248 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02970 | hp2 | a0002 | c0002 | t0001 | g0209 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03017 | hp1 | a0002 | c0002 | t0001 | g0202 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03017 | hp2 | a0001 | c0001 | t0001 | g0135 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03041 | hp1 | a0002 | c0004 | t0008 | g0252 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03041 | hp2 | a0001 | c0001 | t0001 | g0131 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03098 | hp1 | a0002 | c0002 | t0001 | g0208 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03098 | hp2 | a0002 | c0002 | t0002 | g0239 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03130 | hp1 | a0002 | c0002 | t0017 | g0030 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03130 | hp2 | a0002 | c0002 | t0003 | g0029 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03139 | hp1 | a0001 | c0005 | t0006 | g0182 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03139 | hp2 | a0002 | c0002 | t0005 | g0047 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03195 | hp1 | a0002 | c0004 | t0008 | g0253 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03195 | hp2 | a0001 | c0001 | t0001 | g0086 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03209 | hp1 | a0002 | c0002 | t0011 | g0207 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03209 | hp2 | a0002 | c0002 | t0009 | g0191 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03225 | hp1 | a0001 | c0005 | t0006 | g0183 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03225 | hp2 | a0001 | c0001 | t0001 | g0008 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03239 | hp1 | a0001 | c0001 | t0001 | g0153 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03239 | hp2 | a0001 | c0001 | t0001 | g0072 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03453 | hp1 | a0002 | c0002 | t0001 | g0043 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03453 | hp2 | a0001 | c0005 | t0006 | g0180 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03486 | hp1 | a0001 | c0005 | t0006 | g0181 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03486 | hp2 | a0002 | c0007 | t0018 | g0025 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03492 | hp1 | a0001 | c0001 | t0007 | g0172 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03492 | hp2 | a0001 | c0001 | t0001 | g0075 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03516 | hp1 | a0002 | c0002 | t0009 | g0189 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03516 | hp2 | a0001 | c0001 | t0001 | g0170 | AFR | ESN | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03540 | hp1 | a0002 | c0002 | t0005 | g0178 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03540 | hp2 | a0002 | c0002 | t0003 | g0038 | AFR | GWD | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03579 | hp1 | a0001 | c0005 | t0006 | g0179 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03579 | hp2 | a0002 | c0002 | t0005 | g0056 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0106 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03654 | hp2 | a0002 | c0002 | t0001 | g0201 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03688 | hp1 | a0001 | c0001 | t0001 | g0147 | SAS | STU | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03688 | hp2 | a0002 | c0002 | t0001 | g0200 | SAS | STU | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0098 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03704 | hp2 | a0001 | c0001 | t0001 | g0139 | SAS | PJL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03831 | hp1 | a0001 | c0001 | t0001 | g0099 | SAS | BEB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03831 | hp2 | a0001 | c0001 | t0007 | g0079 | SAS | BEB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03834 | hp1 | a0002 | c0002 | t0002 | g0019 | SAS | BEB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03834 | hp2 | a0001 | c0001 | t0001 | g0009 | SAS | BEB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG04115 | hp1 | a0001 | c0001 | t0001 | g0134 | SAS | STU | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0107 | SAS | STU | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG04204 | hp1 | a0001 | c0001 | t0001 | g0001 | SAS | STU | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG04204 | hp2 | a0001 | c0001 | t0007 | g0070 | SAS | STU | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG04228 | hp1 | a0002 | c0002 | t0002 | g0222 | SAS | STU | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0010 | SAS | STU | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18522 | hp1 | a0002 | c0002 | t0003 | g0028 | AFR | YRI | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18522 | hp2 | a0001 | c0001 | t0001 | g0130 | AFR | YRI | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18612 | hp1 | a0001 | c0001 | t0001 | g0155 | EAS | CHB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18612 | hp2 | a0001 | c0001 | t0001 | g0074 | EAS | CHB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18906 | hp1 | a0002 | c0002 | t0003 | g0042 | AFR | YRI | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18906 | hp2 | a0001 | c0001 | t0024 | g0085 | AFR | YRI | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18939 | hp1 | a0003 | c0003 | t0004 | g0225 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18939 | hp2 | a0001 | c0001 | t0001 | g0151 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18944 | hp1 | a0001 | c0001 | t0001 | g0141 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18944 | hp2 | a0002 | c0002 | t0016 | g0247 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18945 | hp1 | a0002 | c0002 | t0012 | g0017 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18945 | hp2 | a0001 | c0001 | t0001 | g0093 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18946 | hp1 | a0002 | c0002 | t0002 | g0214 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18946 | hp2 | a0001 | c0001 | t0001 | g0150 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18947 | hp1 | a0001 | c0001 | t0001 | g0012 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18947 | hp2 | a0002 | c0002 | t0012 | g0017 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18950 | hp1 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18950 | hp2 | a0002 | c0002 | t0002 | g0244 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18951 | hp1 | a0003 | c0003 | t0004 | g0229 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18951 | hp2 | a0001 | c0001 | t0001 | g0138 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18959 | hp1 | a0001 | c0001 | t0001 | g0010 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18959 | hp2 | a0002 | c0002 | t0002 | g0205 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18960 | hp1 | a0001 | c0001 | t0013 | g0152 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18960 | hp2 | a0002 | c0002 | t0002 | g0233 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18964 | hp1 | a0001 | c0001 | t0001 | g0165 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18964 | hp2 | a0001 | c0001 | t0001 | g0156 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18965 | hp1 | a0001 | c0001 | t0001 | g0132 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18965 | hp2 | a0003 | c0003 | t0004 | g0213 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18966 | hp1 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18966 | hp2 | a0001 | c0001 | t0001 | g0142 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18968 | hp1 | a0002 | c0002 | t0002 | g0221 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18968 | hp2 | a0001 | c0001 | t0001 | g0104 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18969 | hp1 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18969 | hp2 | a0002 | c0002 | t0002 | g0217 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18974 | hp1 | a0001 | c0001 | t0001 | g0094 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18974 | hp2 | a0003 | c0003 | t0004 | g0241 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18975 | hp1 | a0002 | c0002 | t0002 | g0212 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18975 | hp2 | a0001 | c0001 | t0001 | g0148 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18977 | hp1 | a0001 | c0001 | t0022 | g0144 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18977 | hp2 | a0001 | c0010 | t0001 | g0123 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18979 | hp1 | a0001 | c0001 | t0001 | g0064 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18979 | hp2 | a0003 | c0003 | t0004 | g0240 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18982 | hp1 | a0002 | c0002 | t0002 | g0211 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18982 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18983 | hp1 | a0002 | c0002 | t0002 | g0243 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18983 | hp2 | a0004 | c0006 | t0004 | g0004 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18984 | hp1 | a0001 | c0001 | t0001 | g0016 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18984 | hp2 | a0002 | c0002 | t0002 | g0220 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18988 | hp1 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18989 | hp1 | a0001 | c0001 | t0001 | g0103 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18989 | hp2 | a0004 | c0006 | t0004 | g0004 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18990 | hp1 | a0002 | c0002 | t0012 | g0199 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18990 | hp2 | a0001 | c0001 | t0001 | g0160 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18992 | hp1 | a0001 | c0001 | t0001 | g0169 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18992 | hp2 | a0002 | c0002 | t0002 | g0235 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19003 | hp1 | a0002 | c0002 | t0002 | g0218 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19003 | hp2 | a0001 | c0001 | t0001 | g0013 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19004 | hp1 | a0001 | c0001 | t0001 | g0096 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19004 | hp2 | a0002 | c0002 | t0002 | g0216 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19009 | hp1 | a0001 | c0001 | t0001 | g0105 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19009 | hp2 | a0002 | c0002 | t0002 | g0232 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19012 | hp1 | a0001 | c0001 | t0001 | g0161 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19012 | hp2 | a0002 | c0002 | t0001 | g0198 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19030 | hp1 | a0001 | c0001 | t0001 | g0063 | AFR | LWK | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19030 | hp2 | a0002 | c0002 | t0005 | g0061 | AFR | LWK | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19043 | hp1 | a0001 | c0001 | t0026 | g0171 | AFR | LWK | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19043 | hp2 | a0002 | c0002 | t0005 | g0049 | AFR | LWK | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19062 | hp1 | a0003 | c0003 | t0004 | g0230 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19062 | hp2 | a0001 | c0001 | t0001 | g0001 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19066 | hp1 | a0001 | c0001 | t0001 | g0065 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19066 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19067 | hp1 | a0003 | c0003 | t0004 | g0224 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19067 | hp2 | a0001 | c0001 | t0001 | g0127 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19070 | hp1 | a0003 | c0003 | t0004 | g0227 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19070 | hp2 | a0001 | c0001 | t0001 | g0095 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19075 | hp1 | a0001 | c0001 | t0001 | g0122 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19075 | hp2 | a0002 | c0002 | t0002 | g0187 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19080 | hp1 | a0002 | c0002 | t0002 | g0206 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19080 | hp2 | a0001 | c0001 | t0001 | g0124 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19083 | hp1 | a0001 | c0001 | t0001 | g0118 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19083 | hp2 | a0003 | c0003 | t0004 | g0242 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19084 | hp1 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19084 | hp2 | a0001 | c0001 | t0001 | g0015 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19086 | hp1 | a0001 | c0001 | t0013 | g0143 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19086 | hp2 | a0003 | c0003 | t0004 | g0226 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19087 | hp1 | a0002 | c0002 | t0002 | g0219 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19087 | hp2 | a0001 | c0001 | t0001 | g0066 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19088 | hp1 | a0001 | c0001 | t0001 | g0157 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19088 | hp2 | a0002 | c0002 | t0002 | g0020 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19089 | hp1 | a0002 | c0002 | t0001 | g0215 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19089 | hp2 | a0001 | c0001 | t0001 | g0002 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19090 | hp1 | a0001 | c0001 | t0001 | g0120 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19090 | hp2 | a0001 | c0001 | t0001 | g0145 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19091 | hp1 | a0004 | c0006 | t0004 | g0004 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19091 | hp2 | a0001 | c0001 | t0001 | g0140 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19240 | hp1 | a0002 | c0002 | t0003 | g0044 | AFR | YRI | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA19240 | hp2 | a0001 | c0001 | t0001 | g0007 | AFR | YRI | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA20129 | hp1 | a0002 | c0002 | t0005 | g0053 | AFR | ASW | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA20129 | hp2 | a0002 | c0002 | t0014 | g0175 | AFR | ASW | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0011 | SAS | GIH | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA20905 | hp2 | a0002 | c0002 | t0001 | g0245 | SAS | GIH | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02109 | hp1 | a0002 | c0002 | t0003 | g0036 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02109 | hp2 | a0001 | c0001 | t0001 | g0129 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02486 | hp1 | a0001 | c0001 | t0001 | g0154 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02486 | hp2 | a0002 | c0004 | t0008 | g0250 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02559 | hp1 | a0001 | c0001 | t0001 | g0002 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG02559 | hp2 | a0002 | c0002 | t0003 | g0024 | AFR | ACB | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03471 | hp1 | a0002 | c0002 | t0001 | g0058 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG03471 | hp2 | a0001 | c0001 | t0001 | g0087 | AFR | MSL | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG06807 | hp1 | a0002 | c0002 | t0011 | g0027 | AFR | USA | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
HG06807 | hp2 | a0001 | c0001 | t0001 | g0166 | AFR | USA | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18955 | hp1 | a0002 | c0002 | t0016 | g0246 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0114 | EAS | JPT | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA20300 | hp1 | a0001 | c0001 | t0001 | g0009 | AFR | USA | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
NA20300 | hp2 | a0002 | c0002 | t0009 | g0188 | AFR | USA | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0015 | g0014 | REF | REF | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0001 | g0173 | REF | REF | DCTN4_chr5_150703440_150764017 | DCTN4 | chr5 | 150703440 | 150764017 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:150711219
|
C | T | 2 | a0003a0004 | 17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
missense_variant | MODERATE | c.1313G>A | p.Ser438Asn | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1337/4116 | 1313/1383 | 438/460 | chr5 | 150711219 | ||
chr5:150718321
|
G | C | 3 | a0002a0003a0004 | 129 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(126): Show |
missense_variant | MODERATE | c.1026C>G | p.Phe342Leu | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/13 | 1050/4116 | 1026/1383 | 342/460 | chr5 | 150718321 | ||
chr5:150719768
|
T | C | 1 | a0006 | 1 | HG01433.hp2 | missense_variant&splice_region_variant | MODERATE | c.911A>G | p.Asn304Ser | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/13 | 935/4116 | 911/1383 | 304/460 | chr5 | 150719768 | ||
chr5:150722908
|
C | T | 1 | a0004 | 3 | NA18983.hp2 NA18989.hp2 NA19091.hp1 |
missense_variant&splice_region_variant | MODERATE | c.907G>A | p.Val303Ile | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/13 | 931/4116 | 907/1383 | 303/460 | chr5 | 150722908 | ||
chr5:150730677
|
T | C | 1 | a0005 | 1 | HG00642.hp2 | missense_variant | MODERATE | c.788A>G | p.Tyr263Cys | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/13 | 812/4116 | 788/1383 | 263/460 | chr5 | 150730677 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:150711239
|
G | T | 1 | a0002c0007 | 1 | HG03486.hp2 | synonymous_variant | LOW | c.1293C>A | p.Pro431Pro | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1317/4116 | 1293/1383 | 431/460 | chr5 | 150711239 | ||
chr5:150715603
|
A | G | 1 | a0001c0005 | 7 | HG02896.hp2 HG02897.hp1 HG03139.hp1 others(4): Show |
synonymous_variant | LOW | c.1131T>C | p.Asp377Asp | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/13 | 1155/4116 | 1131/1383 | 377/460 | chr5 | 150715603 | ||
chr5:150719764
|
A | G | 1 | a0002c0004 | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
synonymous_variant | LOW | c.915T>C | p.Tyr305Tyr | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/13 | 939/4116 | 915/1383 | 305/460 | chr5 | 150719764 | ||
chr5:150731436
|
G | A | 1 | a0001c0010 | 1 | NA18977.hp2 | synonymous_variant | LOW | c.591C>T | p.Ile197Ile | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 6/13 | 615/4116 | 591/1383 | 197/460 | chr5 | 150731436 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:150708519
|
A | G | 8 | a0001c0005t0006a0002c0002t0005a0002c0002t0014others(5): Show | 49 | HG00408.hp1 HG01891.hp1 HG01981.hp1 others(46): Show |
3_prime_UTR_variant | MODIFIER | c.*2630T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 2630 | chr5 | 150708519 | |||||
chr5:150708557
|
A | C | 2 | a0001c0001t0010a0006c0008t0010 | 3 | HG01433.hp2 HG01891.hp2 HG02257.hp2 |
3_prime_UTR_variant | MODIFIER | c.*2592T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 2592 | chr5 | 150708557 | |||||
chr5:150708578
|
A | G | 1 | a0002c0002t0017 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2571T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 2571 | chr5 | 150708578 | |||||
chr5:150708647
|
C | T | 2 | a0003c0003t0004a0004c0006t0004 | 17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2502G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 2502 | chr5 | 150708647 | |||||
chr5:150708983
|
G | A | 3 | a0002c0004t0008a0003c0003t0004a0004c0006t0004 | 21 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*2166C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 2166 | chr5 | 150708983 | |||||
chr5:150709012
|
A | T | 1 | a0001c0001t0021 | 1 | HG02300.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2137T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 2137 | chr5 | 150709012 | |||||
chr5:150709052
|
T | C | 1 | a0001c0005t0006 | 7 | HG02896.hp2 HG02897.hp1 HG03139.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*2097A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 2097 | chr5 | 150709052 | |||||
chr5:150709065
|
A | G | 2 | a0003c0003t0004a0004c0006t0004 | 17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*2084T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 2084 | chr5 | 150709065 | |||||
chr5:150709208
|
G | A | 7 | a0001c0005t0006a0002c0002t0005a0002c0002t0014others(4): Show | 48 | HG00408.hp1 HG01891.hp1 HG01981.hp1 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*1941C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1941 | chr5 | 150709208 | |||||
chr5:150709234
|
T | C | 3 | a0002c0004t0008a0003c0003t0004a0004c0006t0004 | 21 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1915A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1915 | chr5 | 150709234 | |||||
chr5:150709259
|
G | A | 2 | a0003c0003t0004a0004c0006t0004 | 17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1890C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1890 | chr5 | 150709259 | |||||
chr5:150709271
|
T | A | 1 | a0002c0002t0011 | 3 | HG02280.hp1 HG03209.hp1 HG06807.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1878A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1878 | chr5 | 150709271 | |||||
chr5:150709437
|
G | A | 1 | a0002c0004t0008 | 4 | HG02486.hp2 HG02896.hp1 HG03041.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1712C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1712 | chr5 | 150709437 | |||||
chr5:150709463
|
T | C | 1 | a0001c0001t0025 | 1 | HG02135.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1686A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1686 | chr5 | 150709463 | |||||
chr5:150709522
|
T | C | 1 | a0001c0001t0013 | 2 | NA18960.hp1 NA19086.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1627A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1627 | chr5 | 150709522 | |||||
chr5:150709560
|
G | A | 2 | a0003c0003t0004a0004c0006t0004 | 17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1589C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1589 | chr5 | 150709560 | |||||
chr5:150709581
|
AT | A | 2 | a0001c0001t0003a0002c0002t0003 | 20 | HG00735.hp2 HG01496.hp1 HG01884.hp1 others(17): Show |
3_prime_UTR_variant | MODIFIER | c.*1567delA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1567 | chr5 | 150709581 | |||||
chr5:150709583
|
G | A | 3 | a0001c0001t0022a0003c0003t0004a0004c0006t0004 | 18 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1566C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1566 | chr5 | 150709583 | |||||
chr5:150709743
|
G | A | 2 | a0003c0003t0004a0004c0006t0004 | 17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*1406C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1406 | chr5 | 150709743 | |||||
chr5:150709890
|
C | T | 2 | a0001c0001t0015a0001c0001t0020 | 3 | HG01167.hp2 HG02040.hp2 homoSapiens_chm13v2.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1259G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 1259 | chr5 | 150709890 | |||||
chr5:150710204
|
G | A | 2 | a0003c0003t0004a0004c0006t0004 | 17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*945C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 945 | chr5 | 150710204 | |||||
chr5:150710265
|
C | A | 1 | a0002c0002t0012 | 3 | NA18945.hp1 NA18947.hp2 NA18990.hp1 |
3_prime_UTR_variant | MODIFIER | c.*884G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 884 | chr5 | 150710265 | |||||
chr5:150710265
|
C | T | 1 | a0001c0001t0019 | 1 | HG02738.hp1 | 3_prime_UTR_variant | MODIFIER | c.*884G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 884 | chr5 | 150710265 | |||||
chr5:150710318
|
G | A | 1 | a0001c0001t0023 | 1 | HG00639.hp2 | 3_prime_UTR_variant | MODIFIER | c.*831C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 831 | chr5 | 150710318 | |||||
chr5:150710327
|
G | A | 1 | a0002c0002t0014 | 2 | HG02622.hp2 NA20129.hp2 |
3_prime_UTR_variant | MODIFIER | c.*822C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 822 | chr5 | 150710327 | |||||
chr5:150710398
|
C | T | 1 | a0002c0007t0018 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*751G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 751 | chr5 | 150710398 | |||||
chr5:150710464
|
A | T | 3 | a0001c0001t0007a0001c0001t0015a0001c0001t0025 | 9 | HG01167.hp2 HG01978.hp1 HG02135.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*685T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 685 | chr5 | 150710464 | |||||
chr5:150710545
|
G | A | 1 | a0001c0001t0024 | 1 | NA18906.hp2 | 3_prime_UTR_variant | MODIFIER | c.*604C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 604 | chr5 | 150710545 | |||||
chr5:150710580
|
G | A | 3 | a0002c0004t0008a0003c0003t0004a0004c0006t0004 | 21 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*569C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 569 | chr5 | 150710580 | |||||
chr5:150710602
|
T | G | 4 | a0001c0001t0007a0001c0001t0015a0001c0001t0025others(1): Show | 10 | HG01167.hp2 HG01978.hp1 HG02135.hp1 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*547A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 547 | chr5 | 150710602 | |||||
chr5:150710606
|
G | A | 2 | a0003c0003t0004a0004c0006t0004 | 17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*543C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 543 | chr5 | 150710606 | |||||
chr5:150710669
|
T | G | 1 | a0001c0001t0027 | 1 | HG01943.hp2 | 3_prime_UTR_variant | MODIFIER | c.*480A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 480 | chr5 | 150710669 | |||||
chr5:150710683
|
TG | T | 2 | a0003c0003t0004a0004c0006t0004 | 17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*465delC | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 465 | chr5 | 150710683 | |||||
chr5:150710726
|
A | G | 1 | a0002c0002t0016 | 2 | NA18944.hp2 NA18955.hp1 |
3_prime_UTR_variant | MODIFIER | c.*423T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 423 | chr5 | 150710726 | |||||
chr5:150710782
|
T | C | 3 | a0001c0001t0002a0002c0002t0002a0002c0002t0016 | 33 | HG00597.hp2 HG00639.hp1 HG00738.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*367A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 367 | chr5 | 150710782 | |||||
chr5:150710786
|
A | G | 1 | a0002c0002t0017 | 1 | HG03130.hp1 | 3_prime_UTR_variant | MODIFIER | c.*363T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 363 | chr5 | 150710786 | |||||
chr5:150710818
|
C | T | 2 | a0003c0003t0004a0004c0006t0004 | 17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*331G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 331 | chr5 | 150710818 | |||||
chr5:150710914
|
AG | A | 1 | a0002c0002t0009 | 4 | HG02809.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*234delC | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 234 | chr5 | 150710914 | |||||
chr5:150710922
|
GT | G | 1 | a0002c0002t0009 | 4 | HG02809.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*226delA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 13/13 | 226 | chr5 | 150710922 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr5:150711395
|
G | T | 2 | a0002c0002t0001g0034a0002c0002t0001g0043 | 2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.1170-33C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150711395 | ||||||
chr5:150711599
|
G | A | 14 | a0003c0003t0004g0021a0003c0003t0004g0196a0003c0003t0004g0213others(11): Show | 17 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(14): Show |
intron_variant | MODIFIER | c.1170-237C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150711599 | ||||||
chr5:150711673
|
C | T | 1 | a0001c0001t0001g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.1170-311G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150711673 | ||||||
chr5:150711688
|
C | T | 2 | a0002c0002t0009g0190a0002c0002t0009g0191 | 2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.1170-326G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150711688 | ||||||
chr5:150711917
|
A | C | 11 | a0002c0002t0005g0047a0002c0002t0005g0048a0002c0002t0005g0049others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.1170-555T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150711917 | ||||||
chr5:150712341
|
A | G | 18 | a0002c0004t0008g0249a0002c0004t0008g0250a0002c0004t0008g0252others(15): Show | 21 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1170-979T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150712341 | ||||||
chr5:150712446
|
G | A | 1 | a0002c0002t0003g0041 | 1 | HG02809.hp2 | intron_variant | MODIFIER | c.1170-1084C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150712446 | ||||||
chr5:150712490
|
C | T | 1 | a0002c0002t0003g0037 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.1170-1128G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150712490 | ||||||
chr5:150712530
|
T | C | 18 | a0002c0004t0008g0249a0002c0004t0008g0250a0002c0004t0008g0252others(15): Show | 21 | HG00408.hp1 HG02015.hp2 HG02071.hp2 others(18): Show |
intron_variant | MODIFIER | c.1170-1168A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150712530 | ||||||
chr5:150712970
|
T | C | 1 | a0001c0001t0001g0147 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.1170-1608A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150712970 | ||||||
chr5:150713120
|
A | T | 19 | a0001c0001t0001g0007a0001c0001t0001g0088a0001c0001t0001g0089others(16): Show | 20 | HG01175.hp1 HG01884.hp2 HG01891.hp1 others(17): Show |
intron_variant | MODIFIER | c.1170-1758T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713120 | ||||||
chr5:150713235
|
C | A | 1 | a0001c0001t0001g0122 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.1170-1873G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713235 | ||||||
chr5:150713313
|
G | C | 10 | a0001c0001t0001g0007a0001c0001t0001g0063a0002c0002t0001g0058others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(9): Show |
intron_variant | MODIFIER | c.1170-1951C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713313 | ||||||
chr5:150713339
|
C | A | 2 | a0002c0002t0011g0194a0002c0002t0011g0207 | 2 | HG02280.hp1 HG03209.hp1 |
intron_variant | MODIFIER | c.1170-1977G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713339 | ||||||
chr5:150713394
|
T | TA | 10 | a0002c0002t0001g0006a0002c0002t0001g0184a0002c0002t0001g0185others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1170-2033dupT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713394 | ||||||
chr5:150713416
|
T | A | 1 | a0001c0001t0003g0248 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1170-2054A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713416 | ||||||
chr5:150713445
|
C | CT | 6 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0005g0062others(3): Show | 6 | HG02615.hp1 HG02809.hp1 HG02965.hp1 others(3): Show |
intron_variant | MODIFIER | c.1170-2084dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713445 | ||||||
chr5:150713445
|
CTT | C | 7 | a0002c0002t0001g0006a0002c0004t0001g0022a0002c0004t0001g0251others(4): Show | 9 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170-2085_1170-208 others(6): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713445 | ||||||
chr5:150713450
|
T | C | 7 | a0002c0002t0001g0006a0002c0004t0001g0022a0002c0004t0001g0251others(4): Show | 9 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170-2088A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713450 | ||||||
chr5:150713462
|
G | GA | 9 | a0001c0005t0006g0179a0001c0005t0006g0180a0001c0005t0006g0181others(6): Show | 9 | HG02451.hp2 HG02896.hp2 HG02897.hp1 others(6): Show |
intron_variant | MODIFIER | c.1170-2101dupT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713462 | ||||||
chr5:150713529
|
C | G | 1 | a0001c0001t0001g0159 | 1 | HG02129.hp1 | intron_variant | MODIFIER | c.1169+2036G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713529 | ||||||
chr5:150713627
|
A | G | 1 | a0002c0002t0002g0222 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1169+1938T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713627 | ||||||
chr5:150713628
|
G | C | 15 | a0001c0001t0003g0248a0001c0005t0006g0179a0001c0005t0006g0180others(12): Show | 15 | HG02717.hp1 HG02723.hp1 HG02886.hp1 others(12): Show |
intron_variant | MODIFIER | c.1169+1937C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713628 | ||||||
chr5:150713726
|
C | G | 10 | a0002c0002t0001g0006a0002c0002t0001g0184a0002c0002t0001g0185others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1169+1839G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713726 | ||||||
chr5:150713732
|
C | T | 1 | a0001c0001t0001g0008 | 2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.1169+1833G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713732 | ||||||
chr5:150713830
|
A | C | 7 | a0002c0002t0001g0006a0002c0004t0001g0022a0002c0004t0001g0251others(4): Show | 9 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1169+1735T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150713830 | ||||||
chr5:150714224
|
T | C | 1 | a0001c0001t0001g0116 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.1169+1341A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714224 | ||||||
chr5:150714225
|
G | A | 1 | a0002c0002t0002g0223 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1169+1340C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714225 | ||||||
chr5:150714271
|
C | T | 10 | a0002c0002t0001g0006a0002c0002t0001g0184a0002c0002t0001g0185others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1169+1294G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714271 | ||||||
chr5:150714425
|
C | A | 1 | a0001c0001t0026g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.1169+1140G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714425 | ||||||
chr5:150714431
|
TAC | T | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1169+1132_1169+113 others(6): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714431 | ||||||
chr5:150714467
|
A | G | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1169+1098T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714467 | ||||||
chr5:150714470
|
G | A | 1 | a0001c0001t0010g0111 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.1169+1095C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714470 | ||||||
chr5:150714574
|
TA | T | 127 | a0001c0001t0003g0248a0001c0005t0006g0179a0001c0005t0006g0180others(124): Show | 137 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.1169+990delT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714574 | ||||||
chr5:150714640
|
G | A | 1 | a0002c0002t0002g0223 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.1169+925C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714640 | ||||||
chr5:150714716
|
T | C | 4 | a0001c0001t0001g0145a0002c0002t0003g0005a0002c0002t0003g0023others(1): Show | 5 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.1169+849A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714716 | ||||||
chr5:150714757
|
T | C | 1 | a0002c0002t0002g0222 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.1169+808A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714757 | ||||||
chr5:150714809
|
T | A | 7 | a0002c0002t0001g0006a0002c0004t0001g0022a0002c0004t0001g0251others(4): Show | 9 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1169+756A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714809 | ||||||
chr5:150714829
|
A | G | 5 | a0001c0005t0006g0179a0001c0005t0006g0180a0001c0005t0006g0181others(2): Show | 5 | HG03139.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.1169+736T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714829 | ||||||
chr5:150714923
|
A | G | 7 | a0002c0002t0001g0006a0002c0004t0001g0022a0002c0004t0001g0251others(4): Show | 9 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1169+642T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150714923 | ||||||
chr5:150715048
|
A | T | 10 | a0002c0002t0001g0006a0002c0002t0001g0184a0002c0002t0001g0185others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1169+517T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715048 | ||||||
chr5:150715094
|
T | G | 3 | a0002c0002t0005g0054a0002c0002t0005g0056a0002c0002t0005g0057 | 3 | HG02145.hp1 HG02630.hp2 HG03579.hp2 |
intron_variant | MODIFIER | c.1169+471A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715094 | ||||||
chr5:150715117
|
A | T | 1 | a0002c0002t0002g0231 | 1 | HG00597.hp2 | intron_variant | MODIFIER | c.1169+448T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715117 | ||||||
chr5:150715188
|
A | G | 7 | a0002c0002t0001g0006a0002c0004t0001g0022a0002c0004t0001g0251others(4): Show | 9 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.1169+377T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715188 | ||||||
chr5:150715270
|
A | G | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1169+295T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715270 | ||||||
chr5:150715472
|
T | A | 8 | a0001c0001t0003g0248a0001c0005t0006g0179a0001c0005t0006g0180others(5): Show | 8 | HG02896.hp2 HG02897.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.1169+93A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715472 | ||||||
chr5:150715488
|
A | G | 6 | a0002c0004t0001g0022a0002c0004t0001g0251a0002c0004t0008g0249others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.1169+77T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715488 | ||||||
chr5:150715489
|
G | T | 4 | a0002c0002t0005g0176a0002c0002t0005g0178a0002c0002t0014g0175others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.1169+76C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715489 | ||||||
chr5:150715524
|
T | A | 2 | a0002c0002t0014g0175a0002c0002t0014g0177 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.1169+41A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715524 | ||||||
chr5:150715540
|
T | C | 3 | a0002c0002t0003g0005a0002c0002t0003g0023a0002c0002t0003g0024 | 4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1169+25A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 12/12 | chr5 | 150715540 | ||||||
chr5:150715726
|
C | T | 2 | a0001c0001t0001g0007a0001c0001t0001g0063 | 3 | HG02723.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1072-64G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150715726 | ||||||
chr5:150715896
|
T | TAA | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1072-235_1072-234i others(4): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150715896 | ||||||
chr5:150715916
|
T | G | 18 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.1072-254A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150715916 | ||||||
chr5:150715999
|
G | T | 2 | a0001c0005t0006g0203a0001c0005t0006g0204 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.1072-337C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150715999 | ||||||
chr5:150716196
|
G | A | 1 | a0001c0001t0001g0150 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.1072-534C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716196 | ||||||
chr5:150716207
|
A | T | 1 | a0001c0001t0023g0076 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1072-545T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716207 | ||||||
chr5:150716218
|
C | G | 3 | a0002c0002t0003g0005a0002c0002t0003g0023a0002c0002t0003g0024 | 4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.1072-556G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716218 | ||||||
chr5:150716245
|
T | C | 1 | a0001c0001t0023g0076 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.1072-583A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716245 | ||||||
chr5:150716259
|
C | T | 10 | a0002c0002t0001g0006a0002c0002t0001g0184a0002c0002t0001g0185others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1072-597G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716259 | ||||||
chr5:150716272
|
G | T | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02135.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.1072-610C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716272 | ||||||
chr5:150716337
|
T | C | 1 | a0001c0001t0003g0248 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.1072-675A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716337 | ||||||
chr5:150716415
|
A | G | 10 | a0002c0002t0001g0006a0002c0002t0001g0184a0002c0002t0001g0185others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1072-753T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716415 | ||||||
chr5:150716683
|
C | G | 10 | a0002c0002t0001g0006a0002c0002t0001g0184a0002c0002t0001g0185others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1072-1021G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716683 | ||||||
chr5:150716746
|
C | T | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.1072-1084G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716746 | ||||||
chr5:150716747
|
G | A | 13 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(10): Show | 17 | HG01255.hp1 HG01433.hp1 HG01928.hp1 others(14): Show |
intron_variant | MODIFIER | c.1072-1085C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716747 | ||||||
chr5:150716750
|
T | G | 1 | a0001c0001t0001g0153 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.1072-1088A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716750 | ||||||
chr5:150716782
|
G | A | 2 | a0001c0001t0001g0098a0001c0001t0001g0115 | 2 | HG01071.hp2 HG03704.hp1 |
intron_variant | MODIFIER | c.1072-1120C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716782 | ||||||
chr5:150716833
|
C | T | 1 | a0002c0002t0005g0060 | 1 | HG01981.hp1 | intron_variant | MODIFIER | c.1072-1171G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716833 | ||||||
chr5:150716850
|
C | T | 3 | a0002c0002t0001g0208a0002c0002t0001g0209a0002c0002t0001g0245 | 3 | HG02970.hp2 HG03098.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.1072-1188G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716850 | ||||||
chr5:150716881
|
T | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0063 | 3 | HG02723.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.1072-1219A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716881 | ||||||
chr5:150716917
|
C | CA | 88 | a0001c0001t0001g0127a0001c0001t0001g0154a0001c0001t0002g0137others(85): Show | 95 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(92): Show |
intron_variant | MODIFIER | c.1072-1256dupT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716917 | ||||||
chr5:150716917
|
CA | C | 10 | a0002c0002t0001g0006a0002c0002t0001g0184a0002c0002t0001g0185others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1072-1256delT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716917 | ||||||
chr5:150716929
|
A | G | 1 | a0001c0005t0006g0180 | 1 | HG03453.hp2 | intron_variant | MODIFIER | c.1072-1267T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150716929 | ||||||
chr5:150717240
|
CTTTAACA others(6): Show |
C | 1 | a0002c0002t0001g0185 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.1071+1023_1071+103 others(17): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717240 | ||||||
chr5:150717352
|
T | C | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(249): Show | 285 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(282): Show |
intron_variant | MODIFIER | c.1071+924A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717352 | ||||||
chr5:150717431
|
T | G | 4 | a0002c0002t0005g0060a0002c0002t0005g0061a0002c0002t0005g0062others(1): Show | 4 | HG01981.hp1 HG02965.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.1071+845A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717431 | ||||||
chr5:150717499
|
T | C | 129 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0003g0248others(126): Show | 140 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.1071+777A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717499 | ||||||
chr5:150717566
|
G | A | 2 | a0002c0002t0002g0243a0002c0002t0002g0244 | 2 | NA18950.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.1071+710C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717566 | ||||||
chr5:150717583
|
T | C | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.1071+693A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717583 | ||||||
chr5:150717644
|
G | C | 1 | a0002c0002t0017g0030 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.1071+632C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717644 | ||||||
chr5:150717911
|
T | G | 1 | a0001c0001t0001g0146 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.1071+365A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717911 | ||||||
chr5:150717985
|
T | C | 1 | a0002c0002t0002g0237 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.1071+291A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717985 | ||||||
chr5:150717995
|
A | G | 10 | a0002c0002t0001g0006a0002c0002t0001g0184a0002c0002t0001g0185others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.1071+281T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150717995 | ||||||
chr5:150718005
|
C | T | 19 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(16): Show | 19 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.1071+271G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 11/12 | chr5 | 150718005 | ||||||
chr5:150718466
|
G | A | 4 | a0001c0001t0001g0011a0001c0001t0001g0110a0001c0001t0001g0113others(1): Show | 5 | HG00642.hp1 HG00642.hp2 HG01109.hp1 others(2): Show |
intron_variant | MODIFIER | c.964-83C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150718466 | ||||||
chr5:150718477
|
T | G | 1 | a0001c0001t0001g0087 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.964-94A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150718477 | ||||||
chr5:150718544
|
T | C | 1 | a0002c0002t0002g0239 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.964-161A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150718544 | ||||||
chr5:150718555
|
T | C | 1 | a0002c0002t0003g0029 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.964-172A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150718555 | ||||||
chr5:150718651
|
A | G | 1 | a0001c0001t0001g0151 | 1 | NA18939.hp2 | intron_variant | MODIFIER | c.964-268T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150718651 | ||||||
chr5:150718711
|
G | A | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.964-328C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150718711 | ||||||
chr5:150718816
|
ATTAT | A | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.964-437_964-434del others(4): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150718816 | ||||||
chr5:150718994
|
A | AT | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.964-612dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150718994 | ||||||
chr5:150719005
|
A | C | 69 | a0001c0001t0001g0003a0001c0001t0001g0016a0001c0001t0001g0065others(66): Show | 79 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.964-622T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150719005 | ||||||
chr5:150719008
|
T | C | 4 | a0002c0002t0005g0176a0002c0002t0005g0178a0002c0002t0014g0175others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.964-625A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150719008 | ||||||
chr5:150719182
|
A | G | 1 | a0001c0001t0001g0158 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.963+534T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150719182 | ||||||
chr5:150719222
|
T | C | 1 | a0001c0001t0010g0102 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.963+494A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150719222 | ||||||
chr5:150719294
|
CTGGGTGT others(1): Show |
C | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.963+414_963+421del others(8): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150719294 | ||||||
chr5:150719406
|
C | G | 2 | a0002c0002t0001g0184a0002c0002t0001g0185 | 2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.963+310G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 10/12 | chr5 | 150719406 | ||||||
chr5:150719782
|
TAAA | T | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.909-15_909-13delTT others(1): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150719782 | ||||||
chr5:150719804
|
T | C | 2 | a0001c0001t0001g0083a0001c0001t0003g0078 | 2 | HG02572.hp1 HG02965.hp2 |
intron_variant | MODIFIER | c.909-34A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150719804 | ||||||
chr5:150719937
|
CAT | C | 3 | a0001c0001t0010g0102a0001c0001t0010g0111a0006c0008t0010g0101 | 3 | HG01433.hp2 HG01891.hp2 HG02257.hp2 |
intron_variant | MODIFIER | c.909-169_909-168del others(2): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150719937 | ||||||
chr5:150719938
|
A | G | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.909-168T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150719938 | ||||||
chr5:150720006
|
CCA | C | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.909-238_909-237del others(2): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150720006 | ||||||
chr5:150720228
|
A | G | 7 | a0002c0002t0001g0006a0002c0004t0001g0022a0002c0004t0001g0251others(4): Show | 9 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.909-458T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150720228 | ||||||
chr5:150720481
|
AT | A | 15 | a0001c0001t0001g0067a0001c0001t0001g0090a0001c0005t0006g0204others(12): Show | 17 | HG00558.hp1 HG01069.hp1 HG01071.hp1 others(14): Show |
intron_variant | MODIFIER | c.909-712delA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150720481 | ||||||
chr5:150720754
|
C | T | 2 | a0002c0002t0002g0232a0002c0002t0002g0233 | 2 | NA18960.hp2 NA19009.hp2 |
intron_variant | MODIFIER | c.909-984G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150720754 | ||||||
chr5:150720764
|
C | A | 1 | a0002c0002t0001g0184 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.909-994G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150720764 | ||||||
chr5:150720962
|
T | C | 20 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0005g0047others(17): Show | 20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.909-1192A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150720962 | ||||||
chr5:150721049
|
T | C | 1 | a0002c0002t0002g0019 | 2 | HG00639.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.909-1279A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150721049 | ||||||
chr5:150721077
|
T | G | 10 | a0002c0002t0001g0006a0002c0002t0001g0184a0002c0002t0001g0185others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.909-1307A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150721077 | ||||||
chr5:150721099
|
C | T | 1 | a0002c0004t0008g0252 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.909-1329G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150721099 | ||||||
chr5:150721124
|
T | C | 10 | a0002c0002t0001g0006a0002c0002t0001g0184a0002c0002t0001g0185others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.909-1354A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150721124 | ||||||
chr5:150721405
|
A | G | 1 | a0001c0001t0001g0008 | 2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.908+1502T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150721405 | ||||||
chr5:150721406
|
T | C | 2 | a0002c0002t0016g0246a0002c0002t0016g0247 | 2 | NA18944.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.908+1501A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150721406 | ||||||
chr5:150721429
|
G | A | 1 | a0001c0001t0001g0154 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.908+1478C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150721429 | ||||||
chr5:150721840
|
T | G | 1 | a0002c0002t0017g0030 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.908+1067A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150721840 | ||||||
chr5:150721893
|
T | C | 5 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0005g0060others(2): Show | 5 | HG01981.hp1 HG02615.hp1 HG02965.hp1 others(2): Show |
intron_variant | MODIFIER | c.908+1014A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150721893 | ||||||
chr5:150722085
|
C | T | 19 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(16): Show | 19 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.908+822G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150722085 | ||||||
chr5:150722152
|
T | A | 1 | a0002c0002t0005g0055 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.908+755A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150722152 | ||||||
chr5:150722275
|
T | G | 6 | a0002c0004t0001g0022a0002c0004t0001g0251a0002c0004t0008g0249others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.908+632A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150722275 | ||||||
chr5:150722500
|
G | A | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.908+407C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150722500 | ||||||
chr5:150722601
|
C | A | 1 | a0001c0001t0010g0111 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.908+306G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150722601 | ||||||
chr5:150722682
|
T | C | 86 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(83): Show | 93 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(90): Show |
intron_variant | MODIFIER | c.908+225A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 9/12 | chr5 | 150722682 | ||||||
chr5:150723116
|
T | C | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.835-136A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723116 | ||||||
chr5:150723122
|
A | G | 10 | a0002c0002t0001g0006a0002c0002t0001g0184a0002c0002t0001g0185others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.835-142T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723122 | ||||||
chr5:150723167
|
A | G | 1 | a0003c0003t0004g0240 | 1 | NA18979.hp2 | intron_variant | MODIFIER | c.835-187T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723167 | ||||||
chr5:150723243
|
A | G | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.835-263T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723243 | ||||||
chr5:150723314
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.835-334C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723314 | ||||||
chr5:150723336
|
T | A | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.835-356A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723336 | ||||||
chr5:150723465
|
T | A | 3 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130 | 3 | HG02109.hp2 HG02818.hp1 NA18522.hp2 |
intron_variant | MODIFIER | c.835-485A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723465 | ||||||
chr5:150723556
|
A | G | 7 | a0002c0002t0001g0006a0002c0004t0001g0022a0002c0004t0001g0251others(4): Show | 9 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(6): Show |
intron_variant | MODIFIER | c.835-576T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723556 | ||||||
chr5:150723578
|
C | T | 1 | a0001c0001t0019g0046 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.835-598G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723578 | ||||||
chr5:150723830
|
C | T | 4 | a0001c0001t0001g0077a0001c0001t0001g0083a0001c0001t0001g0084others(1): Show | 4 | HG02572.hp1 HG02895.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.835-850G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723830 | ||||||
chr5:150723895
|
A | G | 3 | a0002c0002t0005g0060a0002c0002t0005g0061a0002c0002t0005g0062 | 3 | HG01981.hp1 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.835-915T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150723895 | ||||||
chr5:150724136
|
C | T | 132 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0072others(129): Show | 143 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(140): Show |
intron_variant | MODIFIER | c.835-1156G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150724136 | ||||||
chr5:150724238
|
A | G | 1 | a0001c0001t0001g0107 | 1 | HG04115.hp2 | intron_variant | MODIFIER | c.835-1258T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150724238 | ||||||
chr5:150724320
|
C | T | 10 | a0002c0002t0001g0006a0002c0002t0001g0184a0002c0002t0001g0185others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.835-1340G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150724320 | ||||||
chr5:150724475
|
T | C | 1 | a0001c0001t0001g0008 | 2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.835-1495A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150724475 | ||||||
chr5:150724615
|
G | A | 2 | a0002c0002t0001g0184a0002c0002t0001g0185 | 2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.835-1635C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150724615 | ||||||
chr5:150724641
|
T | C | 1 | a0002c0002t0014g0175 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.835-1661A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150724641 | ||||||
chr5:150724674
|
A | C | 2 | a0001c0001t0001g0087a0001c0001t0001g0170 | 2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.835-1694T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150724674 | ||||||
chr5:150724928
|
C | T | 4 | a0001c0001t0003g0248a0002c0002t0001g0184a0002c0002t0001g0185others(1): Show | 4 | HG01243.hp2 HG02717.hp2 HG02922.hp1 others(1): Show |
intron_variant | MODIFIER | c.835-1948G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150724928 | ||||||
chr5:150724973
|
C | T | 20 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0005g0047others(17): Show | 20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.835-1993G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150724973 | ||||||
chr5:150725048
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 5 | HG02129.hp1 NA18988.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.835-2068G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725048 | ||||||
chr5:150725071
|
T | C | 6 | a0002c0004t0001g0022a0002c0004t0001g0251a0002c0004t0008g0249others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.835-2091A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725071 | ||||||
chr5:150725076
|
T | C | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.835-2096A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725076 | ||||||
chr5:150725157
|
C | CA | 34 | a0001c0001t0001g0063a0001c0001t0001g0088a0001c0001t0001g0103others(31): Show | 34 | HG00738.hp2 HG01071.hp2 HG01175.hp1 others(31): Show |
intron_variant | MODIFIER | c.835-2178dupT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725157 | ||||||
chr5:150725157
|
CA | C | 26 | a0001c0001t0001g0106a0001c0001t0001g0142a0001c0001t0001g0149others(23): Show | 27 | HG01069.hp1 HG01071.hp1 HG01243.hp1 others(24): Show |
intron_variant | MODIFIER | c.835-2178delT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725157 | ||||||
chr5:150725181
|
G | T | 6 | a0003c0003t0004g0213a0003c0003t0004g0225a0003c0003t0004g0226others(3): Show | 6 | HG02071.hp2 NA18939.hp1 NA18965.hp2 others(3): Show |
intron_variant | MODIFIER | c.835-2201C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725181 | ||||||
chr5:150725230
|
G | A | 65 | a0002c0002t0001g0192a0002c0002t0001g0193a0002c0002t0001g0195others(62): Show | 72 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.835-2250C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725230 | ||||||
chr5:150725304
|
A | T | 10 | a0002c0002t0001g0006a0002c0002t0001g0184a0002c0002t0001g0185others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.835-2324T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725304 | ||||||
chr5:150725365
|
C | A | 84 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(81): Show | 91 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(88): Show |
intron_variant | MODIFIER | c.835-2385G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725365 | ||||||
chr5:150725569
|
T | C | 1 | a0001c0001t0001g0113 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.835-2589A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725569 | ||||||
chr5:150725784
|
C | T | 7 | a0001c0005t0006g0179a0001c0005t0006g0180a0001c0005t0006g0181others(4): Show | 7 | HG02896.hp2 HG02897.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.835-2804G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725784 | ||||||
chr5:150725794
|
A | T | 1 | a0001c0001t0001g0105 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.835-2814T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725794 | ||||||
chr5:150725796
|
C | G | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.835-2816G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725796 | ||||||
chr5:150725944
|
C | T | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.835-2964G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725944 | ||||||
chr5:150725950
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.835-2970G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725950 | ||||||
chr5:150725964
|
G | A | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.835-2984C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150725964 | ||||||
chr5:150726054
|
A | T | 4 | a0001c0001t0003g0248a0002c0002t0003g0005a0002c0002t0003g0023others(1): Show | 5 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(2): Show |
intron_variant | MODIFIER | c.835-3074T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726054 | ||||||
chr5:150726307
|
C | T | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.835-3327G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726307 | ||||||
chr5:150726365
|
C | CT | 6 | a0002c0004t0001g0022a0002c0004t0001g0251a0002c0004t0008g0249others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.835-3386dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726365 | ||||||
chr5:150726401
|
A | G | 1 | a0001c0001t0001g0073 | 1 | HG02683.hp1 | intron_variant | MODIFIER | c.835-3421T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726401 | ||||||
chr5:150726421
|
T | C | 10 | a0002c0002t0001g0006a0002c0002t0001g0184a0002c0002t0001g0185others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.835-3441A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726421 | ||||||
chr5:150726527
|
T | C | 10 | a0002c0002t0001g0006a0002c0002t0001g0184a0002c0002t0001g0185others(7): Show | 12 | HG01069.hp1 HG01071.hp1 HG01243.hp2 others(9): Show |
intron_variant | MODIFIER | c.835-3547A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726527 | ||||||
chr5:150726562
|
T | C | 1 | a0001c0001t0002g0137 | 1 | HG02738.hp2 | intron_variant | MODIFIER | c.835-3582A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726562 | ||||||
chr5:150726657
|
G | C | 1 | a0002c0002t0001g0185 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.835-3677C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726657 | ||||||
chr5:150726774
|
A | C | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.835-3794T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726774 | ||||||
chr5:150726815
|
A | G | 1 | a0003c0003t0004g0021 | 2 | HG00408.hp1 HG02015.hp2 |
intron_variant | MODIFIER | c.834+3816T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726815 | ||||||
chr5:150726846
|
G | A | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.834+3785C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150726846 | ||||||
chr5:150727011
|
G | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0063 | 3 | HG02723.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.834+3620C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727011 | ||||||
chr5:150727098
|
T | A | 2 | a0002c0002t0014g0175a0002c0002t0014g0177 | 2 | HG02622.hp2 NA20129.hp2 |
intron_variant | MODIFIER | c.834+3533A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727098 | ||||||
chr5:150727134
|
T | C | 20 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0005g0047others(17): Show | 20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.834+3497A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727134 | ||||||
chr5:150727162
|
T | G | 19 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(16): Show | 19 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.834+3469A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727162 | ||||||
chr5:150727198
|
G | A | 2 | a0001c0005t0006g0203a0001c0005t0006g0204 | 2 | HG02896.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.834+3433C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727198 | ||||||
chr5:150727293
|
G | T | 1 | a0003c0003t0004g0226 | 1 | NA19086.hp2 | intron_variant | MODIFIER | c.834+3338C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727293 | ||||||
chr5:150727339
|
T | C | 1 | a0001c0001t0001g0093 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.834+3292A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727339 | ||||||
chr5:150727422
|
A | T | 8 | a0001c0001t0003g0248a0001c0005t0006g0179a0001c0005t0006g0180others(5): Show | 8 | HG02896.hp2 HG02897.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.834+3209T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727422 | ||||||
chr5:150727447
|
T | G | 60 | a0002c0002t0001g0193a0002c0002t0001g0195a0002c0002t0001g0197others(57): Show | 67 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.834+3184A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727447 | ||||||
chr5:150727499
|
G | A | 1 | a0001c0005t0006g0182 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.834+3132C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727499 | ||||||
chr5:150727503
|
G | A | 2 | a0001c0001t0001g0093a0001c0001t0001g0114 | 2 | NA18945.hp2 NA18955.hp2 |
intron_variant | MODIFIER | c.834+3128C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727503 | ||||||
chr5:150727531
|
T | C | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.834+3100A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727531 | ||||||
chr5:150727590
|
A | C | 3 | a0002c0002t0001g0208a0002c0002t0001g0209a0002c0002t0001g0245 | 3 | HG02970.hp2 HG03098.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.834+3041T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727590 | ||||||
chr5:150727636
|
C | T | 1 | a0001c0001t0001g0141 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.834+2995G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727636 | ||||||
chr5:150727644
|
C | T | 1 | a0002c0002t0001g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.834+2987G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727644 | ||||||
chr5:150727645
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.834+2986C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727645 | ||||||
chr5:150727648
|
C | T | 1 | a0001c0001t0003g0248 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.834+2983G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727648 | ||||||
chr5:150727652
|
T | C | 91 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(88): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.834+2979A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727652 | ||||||
chr5:150727669
|
G | A | 6 | a0002c0004t0001g0022a0002c0004t0001g0251a0002c0004t0008g0249others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.834+2962C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727669 | ||||||
chr5:150727692
|
C | T | 1 | a0001c0001t0023g0076 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.834+2939G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727692 | ||||||
chr5:150727701
|
G | A | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.834+2930C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727701 | ||||||
chr5:150727712
|
C | G | 19 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(16): Show | 19 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.834+2919G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727712 | ||||||
chr5:150727762
|
C | T | 3 | a0002c0002t0003g0005a0002c0002t0003g0023a0002c0002t0003g0024 | 4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.834+2869G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727762 | ||||||
chr5:150727771
|
G | A | 92 | a0001c0005t0006g0182a0002c0002t0001g0031a0002c0002t0001g0033others(89): Show | 100 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(97): Show |
intron_variant | MODIFIER | c.834+2860C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727771 | ||||||
chr5:150727775
|
CA | C | 119 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(116): Show | 141 | HG00558.hp1 HG00597.hp1 HG00639.hp2 others(138): Show |
intron_variant | MODIFIER | c.834+2855delT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727775 | ||||||
chr5:150727792
|
AAAAAAC | A | 8 | a0002c0002t0003g0026a0002c0002t0003g0028a0002c0002t0003g0037others(5): Show | 8 | HG02280.hp1 HG02717.hp1 HG02723.hp1 others(5): Show |
intron_variant | MODIFIER | c.834+2833_834+2838d others(8): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727792 | ||||||
chr5:150727793
|
AAAAAC | A | 26 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0043others(23): Show | 28 | HG00408.hp2 HG00558.hp2 HG01069.hp1 others(25): Show |
intron_variant | MODIFIER | c.834+2833_834+2837d others(7): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727793 | ||||||
chr5:150727794
|
AAAAC | A | 42 | a0002c0002t0001g0034a0002c0002t0001g0184a0002c0002t0001g0185others(39): Show | 47 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(44): Show |
intron_variant | MODIFIER | c.834+2833_834+2836d others(6): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727794 | ||||||
chr5:150727795
|
AAAC | A | 18 | a0002c0002t0001g0210a0002c0002t0001g0215a0002c0002t0002g0020others(15): Show | 19 | HG00738.hp2 HG01496.hp2 HG02071.hp2 others(16): Show |
intron_variant | MODIFIER | c.834+2833_834+2835d others(5): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150727795 | ||||||
chr5:150728053
|
C | A | 127 | a0001c0001t0003g0248a0001c0005t0006g0179a0001c0005t0006g0180others(124): Show | 137 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.834+2578G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728053 | ||||||
chr5:150728073
|
T | C | 91 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(88): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.834+2558A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728073 | ||||||
chr5:150728314
|
T | C | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.834+2317A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728314 | ||||||
chr5:150728393
|
T | C | 7 | a0001c0005t0006g0179a0001c0005t0006g0180a0001c0005t0006g0181others(4): Show | 7 | HG02896.hp2 HG02897.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.834+2238A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728393 | ||||||
chr5:150728491
|
G | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0063 | 3 | HG02723.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.834+2140C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728491 | ||||||
chr5:150728534
|
T | C | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.834+2097A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728534 | ||||||
chr5:150728651
|
T | A | 1 | a0002c0002t0002g0222 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.834+1980A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728651 | ||||||
chr5:150728789
|
T | C | 19 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(16): Show | 19 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.834+1842A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728789 | ||||||
chr5:150728817
|
T | C | 91 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(88): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.834+1814A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728817 | ||||||
chr5:150728847
|
G | C | 1 | a0001c0001t0001g0156 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.834+1784C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728847 | ||||||
chr5:150728873
|
C | T | 94 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(91): Show | 102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.834+1758G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728873 | ||||||
chr5:150728874
|
A | G | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.834+1757T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728874 | ||||||
chr5:150728879
|
C | CT | 22 | a0001c0001t0001g0067a0001c0001t0001g0086a0001c0001t0001g0087others(19): Show | 24 | HG00558.hp1 HG00597.hp1 HG01069.hp1 others(21): Show |
intron_variant | MODIFIER | c.834+1751dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728879 | ||||||
chr5:150728956
|
C | T | 1 | a0002c0002t0017g0030 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.834+1675G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150728956 | ||||||
chr5:150729025
|
G | A | 1 | a0002c0002t0017g0030 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.834+1606C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729025 | ||||||
chr5:150729042
|
C | CCTT | 4 | a0002c0002t0001g0193a0002c0002t0001g0201a0002c0002t0011g0194others(1): Show | 4 | HG02129.hp2 HG02280.hp1 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.834+1588_834+1589i others(5): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
C | CCTTT | 5 | a0002c0002t0001g0195a0002c0002t0001g0197a0002c0002t0001g0198others(2): Show | 7 | HG00408.hp2 HG00558.hp2 NA18983.hp2 others(4): Show |
intron_variant | MODIFIER | c.834+1588_834+1589i others(6): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
C | CCTTTT | 18 | a0002c0002t0001g0200a0002c0002t0001g0215a0002c0002t0001g0228others(15): Show | 21 | HG00408.hp1 HG00639.hp1 HG02015.hp2 others(18): Show |
intron_variant | MODIFIER | c.834+1588_834+1589i others(7): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
C | CCTTTTT | 18 | a0002c0002t0001g0210a0002c0002t0002g0020a0002c0002t0002g0187others(15): Show | 19 | HG02071.hp2 HG02630.hp1 HG02809.hp1 others(16): Show |
intron_variant | MODIFIER | c.834+1588_834+1589i others(8): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
C | CCTTTTTT | 12 | a0002c0002t0001g0192a0002c0002t0001g0202a0002c0002t0002g0018others(9): Show | 13 | HG00597.hp2 HG00738.hp2 HG01081.hp1 others(10): Show |
intron_variant | MODIFIER | c.834+1588_834+1589i others(9): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
C | CCTTTTTT others(1): Show |
4 | a0002c0002t0001g0006a0002c0002t0002g0222a0002c0002t0002g0236others(1): Show | 5 | HG01496.hp2 HG02258.hp1 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.834+1588_834+1589i others(10): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
C | CCTTTTTT others(2): Show |
3 | a0002c0002t0001g0208a0002c0002t0001g0209a0002c0002t0002g0239 | 3 | HG02970.hp2 HG03098.hp1 HG03098.hp2 |
intron_variant | MODIFIER | c.834+1588_834+1589i others(11): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
C | CCTTTTTT others(3): Show |
1 | a0002c0002t0009g0189 | 1 | HG03516.hp1 | intron_variant | MODIFIER | c.834+1588_834+1589i others(12): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
C | CT | 43 | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0009others(40): Show | 52 | HG00597.hp1 HG00642.hp2 HG00735.hp1 others(49): Show |
intron_variant | MODIFIER | c.834+1588dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
C | CTT | 12 | a0001c0001t0001g0016a0001c0001t0001g0066a0001c0001t0001g0091others(9): Show | 13 | HG01433.hp1 HG02300.hp1 HG02300.hp2 others(10): Show |
intron_variant | MODIFIER | c.834+1587_834+1588d others(4): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
C | CTTTTTTT others(7): Show |
1 | a0002c0002t0005g0052 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.834+1575_834+1588d others(16): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
C | CTTTTTTT others(10): Show |
1 | a0002c0002t0005g0050 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.834+1572_834+1588d others(19): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
C | CTTTTTTT others(12): Show |
1 | a0002c0002t0005g0049 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.834+1570_834+1588d others(21): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
C | CTTTTTTT others(13): Show |
2 | a0002c0002t0005g0051a0002c0002t0005g0053 | 2 | HG01891.hp1 NA20129.hp1 |
intron_variant | MODIFIER | c.834+1569_834+1588d others(22): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
C | CTTTTTTT others(14): Show |
2 | a0002c0002t0005g0048a0002c0002t0005g0057 | 2 | HG02055.hp1 HG02145.hp1 |
intron_variant | MODIFIER | c.834+1568_834+1588d others(23): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
C | CTTTTTTT others(16): Show |
1 | a0002c0002t0005g0056 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.834+1566_834+1588d others(25): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
C | CTTTTTTT others(18): Show |
1 | a0002c0002t0005g0047 | 1 | HG03139.hp2 | intron_variant | MODIFIER | c.834+1564_834+1588d others(27): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
C | CTTTTTTT others(21): Show |
2 | a0002c0002t0005g0054a0002c0002t0005g0055 | 2 | HG02622.hp1 HG02630.hp2 |
intron_variant | MODIFIER | c.834+1561_834+1588d others(30): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
CT | C | 23 | a0001c0001t0001g0084a0001c0001t0001g0119a0001c0001t0001g0155others(20): Show | 24 | HG00735.hp2 HG01243.hp1 HG01496.hp1 others(21): Show |
intron_variant | MODIFIER | c.834+1588delA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
CTT | C | 6 | a0002c0002t0001g0184a0002c0002t0005g0186a0002c0004t0001g0022others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.834+1587_834+1588d others(4): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
CTTTTTTT others(4): Show |
C | 2 | a0002c0002t0005g0060a0002c0002t0005g0062 | 2 | HG01981.hp1 HG02965.hp1 |
intron_variant | MODIFIER | c.834+1578_834+1588d others(13): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
CTTTTTTT others(5): Show |
C | 2 | a0001c0001t0001g0074a0002c0007t0018g0025 | 2 | HG03486.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.834+1577_834+1588d others(14): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
CTTTTTTT others(7): Show |
C | 1 | a0002c0002t0002g0205 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.834+1575_834+1588d others(16): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0001g0007a0001c0001t0001g0063 | 3 | HG02723.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.834+1574_834+1588d others(17): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729042
|
CTTTTTTT others(11): Show |
C | 1 | a0001c0001t0001g0093 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.834+1571_834+1588d others(20): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729042 | ||||||
chr5:150729043
|
T | C | 5 | a0002c0002t0001g0033a0002c0002t0003g0029a0002c0002t0003g0035others(2): Show | 5 | HG02109.hp1 HG02145.hp2 HG02647.hp1 others(2): Show |
intron_variant | MODIFIER | c.834+1588A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729043 | ||||||
chr5:150729044
|
T | C | 16 | a0002c0002t0001g0031a0002c0002t0001g0034a0002c0002t0001g0043others(13): Show | 16 | HG01243.hp1 HG01884.hp1 HG02257.hp1 others(13): Show |
intron_variant | MODIFIER | c.834+1587A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729044 | ||||||
chr5:150729045
|
T | C | 6 | a0002c0002t0001g0184a0002c0002t0005g0186a0002c0004t0001g0022others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02717.hp2 others(4): Show |
intron_variant | MODIFIER | c.834+1586A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729045 | ||||||
chr5:150729046
|
T | C | 1 | a0002c0002t0001g0185 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.834+1585A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729046 | ||||||
chr5:150729047
|
T | C | 1 | a0002c0002t0017g0030 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.834+1584A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729047 | ||||||
chr5:150729057
|
T | C | 1 | a0002c0002t0002g0205 | 1 | NA18959.hp2 | intron_variant | MODIFIER | c.834+1574A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729057 | ||||||
chr5:150729210
|
A | G | 1 | a0002c0002t0016g0246 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.834+1421T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729210 | ||||||
chr5:150729249
|
GT | G | 25 | a0002c0002t0002g0019a0002c0002t0002g0020a0002c0002t0002g0187others(22): Show | 27 | HG00597.hp2 HG00639.hp1 HG00738.hp2 others(24): Show |
intron_variant | MODIFIER | c.834+1381delA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729249 | ||||||
chr5:150729292
|
A | G | 1 | a0001c0001t0007g0079 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.834+1339T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729292 | ||||||
chr5:150729333
|
C | T | 1 | a0001c0001t0001g0139 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.834+1298G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729333 | ||||||
chr5:150729374
|
T | C | 11 | a0002c0002t0005g0047a0002c0002t0005g0048a0002c0002t0005g0049others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.834+1257A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729374 | ||||||
chr5:150729610
|
C | CT | 35 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0003g0248others(32): Show | 38 | HG00735.hp2 HG01496.hp1 HG01891.hp1 others(35): Show |
intron_variant | MODIFIER | c.834+1020dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729610 | ||||||
chr5:150729610
|
C | CTT | 89 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(86): Show | 97 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(94): Show |
intron_variant | MODIFIER | c.834+1019_834+1020d others(4): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729610 | ||||||
chr5:150729632
|
C | CTTTTTTT others(3): Show |
1 | a0001c0001t0001g0074 | 1 | NA18612.hp2 | intron_variant | MODIFIER | c.834+998_834+999ins others(10): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729632 | ||||||
chr5:150729652
|
T | C | 3 | a0002c0002t0001g0208a0002c0002t0001g0209a0002c0002t0001g0245 | 3 | HG02970.hp2 HG03098.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.834+979A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729652 | ||||||
chr5:150729664
|
C | T | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.834+967G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729664 | ||||||
chr5:150729695
|
A | G | 1 | a0002c0002t0003g0032 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.834+936T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729695 | ||||||
chr5:150729940
|
C | G | 91 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(88): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.834+691G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150729940 | ||||||
chr5:150730078
|
T | C | 1 | a0001c0001t0001g0130 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.834+553A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150730078 | ||||||
chr5:150730084
|
C | A | 1 | a0002c0002t0005g0053 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.834+547G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150730084 | ||||||
chr5:150730115
|
C | T | 94 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(91): Show | 102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.834+516G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150730115 | ||||||
chr5:150730334
|
C | G | 6 | a0002c0004t0001g0022a0002c0004t0001g0251a0002c0004t0008g0249others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.834+297G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150730334 | ||||||
chr5:150730342
|
T | C | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.834+289A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150730342 | ||||||
chr5:150730370
|
G | GT | 2 | a0001c0001t0001g0007a0001c0001t0001g0063 | 3 | HG02723.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.834+260dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150730370 | ||||||
chr5:150730376
|
C | T | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.834+255G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150730376 | ||||||
chr5:150730514
|
A | G | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.834+117T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150730514 | ||||||
chr5:150730542
|
C | T | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.834+89G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 8/12 | chr5 | 150730542 | ||||||
chr5:150730853
|
A | C | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.725-113T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 7/12 | chr5 | 150730853 | ||||||
chr5:150731325
|
C | CTG | 44 | a0002c0002t0001g0215a0002c0002t0001g0228a0002c0002t0002g0018others(41): Show | 50 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(47): Show |
intron_variant | MODIFIER | c.611+89_611+90dupCA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 6/12 | chr5 | 150731325 | ||||||
chr5:150731770
|
G | A | 1 | a0001c0001t0007g0070 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.538-281C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150731770 | ||||||
chr5:150731776
|
G | C | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG01884.hp2 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.538-287C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150731776 | ||||||
chr5:150731974
|
C | T | 1 | a0002c0002t0014g0175 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.538-485G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150731974 | ||||||
chr5:150731982
|
G | A | 1 | a0001c0001t0001g0095 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.538-493C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150731982 | ||||||
chr5:150732051
|
C | T | 94 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(91): Show | 102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.538-562G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732051 | ||||||
chr5:150732235
|
C | T | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.538-746G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732235 | ||||||
chr5:150732269
|
C | A | 1 | a0001c0001t0001g0116 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.538-780G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732269 | ||||||
chr5:150732282
|
T | C | 91 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(88): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.538-793A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732282 | ||||||
chr5:150732308
|
C | T | 1 | a0001c0001t0003g0078 | 1 | HG02965.hp2 | intron_variant | MODIFIER | c.538-819G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732308 | ||||||
chr5:150732335
|
G | C | 1 | a0002c0002t0002g0237 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.538-846C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732335 | ||||||
chr5:150732551
|
C | T | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.537+817G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732551 | ||||||
chr5:150732571
|
T | C | 1 | a0001c0001t0001g0013 | 2 | NA18950.hp1 NA19003.hp2 |
intron_variant | MODIFIER | c.537+797A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732571 | ||||||
chr5:150732691
|
T | C | 4 | a0002c0002t0005g0176a0002c0002t0005g0178a0002c0002t0014g0175others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.537+677A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732691 | ||||||
chr5:150732810
|
C | T | 3 | a0001c0001t0001g0089a0001c0001t0001g0090a0001c0001t0001g0091 | 3 | HG01884.hp2 HG02818.hp2 HG02922.hp2 |
intron_variant | MODIFIER | c.537+558G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732810 | ||||||
chr5:150732847
|
T | C | 1 | a0001c0001t0003g0248 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.537+521A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150732847 | ||||||
chr5:150733000
|
C | T | 1 | a0001c0005t0006g0179 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.537+368G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150733000 | ||||||
chr5:150733082
|
G | A | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.537+286C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 5/12 | chr5 | 150733082 | ||||||
chr5:150733523
|
A | G | 7 | a0002c0002t0005g0047a0002c0002t0005g0048a0002c0002t0005g0049others(4): Show | 7 | HG01891.hp1 HG02055.hp1 HG02451.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-48T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150733523 | ||||||
chr5:150733556
|
A | G | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0170others(1): Show | 4 | HG03195.hp2 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-81T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150733556 | ||||||
chr5:150733568
|
G | A | 90 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(87): Show | 98 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.430-93C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150733568 | ||||||
chr5:150733646
|
G | A | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.430-171C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150733646 | ||||||
chr5:150733802
|
A | G | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.430-327T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150733802 | ||||||
chr5:150733912
|
T | C | 127 | a0001c0001t0003g0248a0001c0005t0006g0179a0001c0005t0006g0180others(124): Show | 137 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.430-437A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150733912 | ||||||
chr5:150734024
|
C | G | 4 | a0002c0002t0005g0054a0002c0002t0005g0055a0002c0002t0005g0056others(1): Show | 4 | HG02145.hp1 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-549G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150734024 | ||||||
chr5:150734181
|
C | T | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.430-706G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150734181 | ||||||
chr5:150734418
|
T | G | 2 | a0001c0001t0001g0007a0001c0001t0001g0063 | 3 | HG02723.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.430-943A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150734418 | ||||||
chr5:150734483
|
G | A | 2 | a0001c0001t0001g0129a0001c0001t0001g0130 | 2 | HG02109.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.430-1008C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150734483 | ||||||
chr5:150734536
|
C | T | 3 | a0002c0002t0003g0005a0002c0002t0003g0023a0002c0002t0003g0024 | 4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-1061G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150734536 | ||||||
chr5:150734617
|
G | A | 1 | a0001c0001t0001g0156 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.430-1142C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150734617 | ||||||
chr5:150734930
|
A | G | 2 | a0002c0002t0001g0034a0002c0002t0001g0043 | 2 | HG01243.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.430-1455T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150734930 | ||||||
chr5:150734943
|
C | T | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.430-1468G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150734943 | ||||||
chr5:150735038
|
C | A | 5 | a0002c0002t0001g0192a0002c0002t0009g0188a0002c0002t0009g0189others(2): Show | 5 | HG02647.hp2 HG02809.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.430-1563G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735038 | ||||||
chr5:150735219
|
C | CTCAAG | 129 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0003g0248others(126): Show | 140 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.430-1745_430-1744i others(7): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735219 | ||||||
chr5:150735226
|
T | C | 2 | a0002c0002t0002g0236a0002c0002t0002g0237 | 2 | HG00738.hp2 HG01496.hp2 |
intron_variant | MODIFIER | c.430-1751A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735226 | ||||||
chr5:150735247
|
C | A | 1 | a0001c0001t0003g0248 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.430-1772G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735247 | ||||||
chr5:150735328
|
C | T | 90 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(87): Show | 98 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.430-1853G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735328 | ||||||
chr5:150735329
|
G | A | 20 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0005g0047others(17): Show | 20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.430-1854C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735329 | ||||||
chr5:150735377
|
G | A | 1 | a0001c0001t0026g0171 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.430-1902C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735377 | ||||||
chr5:150735559
|
G | A | 3 | a0002c0002t0005g0060a0002c0002t0005g0061a0002c0002t0005g0062 | 3 | HG01981.hp1 HG02965.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.430-2084C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735559 | ||||||
chr5:150735605
|
G | C | 2 | a0001c0001t0001g0117a0001c0001t0001g0125 | 2 | HG01175.hp2 HG02735.hp2 |
intron_variant | MODIFIER | c.430-2130C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735605 | ||||||
chr5:150735749
|
T | C | 6 | a0002c0004t0001g0022a0002c0004t0001g0251a0002c0004t0008g0249others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-2274A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735749 | ||||||
chr5:150735914
|
TA | T | 24 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0073others(21): Show | 25 | HG00408.hp2 HG01175.hp1 HG01243.hp2 others(22): Show |
intron_variant | MODIFIER | c.430-2440delT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735914 | ||||||
chr5:150735914
|
TAA | T | 80 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(77): Show | 88 | HG00408.hp1 HG00558.hp2 HG00597.hp2 others(85): Show |
intron_variant | MODIFIER | c.430-2441_430-2440d others(4): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735914 | ||||||
chr5:150735914
|
TAAA | T | 7 | a0002c0002t0002g0187a0002c0004t0001g0022a0002c0004t0001g0251others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.430-2442_430-2440d others(5): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735914 | ||||||
chr5:150735965
|
A | G | 1 | a0002c0002t0002g0243 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.430-2490T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150735965 | ||||||
chr5:150736084
|
A | T | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.430-2609T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736084 | ||||||
chr5:150736302
|
C | CAG | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.430-2829_430-2828d others(4): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736302 | ||||||
chr5:150736373
|
A | C | 1 | a0002c0004t0008g0249 | 1 | HG02896.hp1 | intron_variant | MODIFIER | c.430-2898T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736373 | ||||||
chr5:150736416
|
C | T | 7 | a0001c0001t0002g0137a0002c0004t0001g0022a0002c0004t0001g0251others(4): Show | 8 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(5): Show |
intron_variant | MODIFIER | c.430-2941G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736416 | ||||||
chr5:150736417
|
G | A | 1 | a0001c0001t0001g0121 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.430-2942C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736417 | ||||||
chr5:150736421
|
C | T | 1 | a0001c0001t0001g0120 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.430-2946G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736421 | ||||||
chr5:150736609
|
G | A | 2 | a0001c0001t0001g0118a0001c0001t0001g0119 | 2 | HG02135.hp2 NA19083.hp1 |
intron_variant | MODIFIER | c.430-3134C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736609 | ||||||
chr5:150736711
|
A | C | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.430-3236T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736711 | ||||||
chr5:150736858
|
G | A | 2 | a0001c0001t0001g0087a0001c0001t0001g0170 | 2 | HG03471.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.430-3383C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736858 | ||||||
chr5:150736949
|
G | A | 6 | a0002c0004t0001g0022a0002c0004t0001g0251a0002c0004t0008g0249others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.430-3474C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736949 | ||||||
chr5:150736972
|
T | C | 1 | a0002c0002t0009g0188 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.430-3497A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736972 | ||||||
chr5:150736975
|
C | G | 94 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(91): Show | 102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.430-3500G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150736975 | ||||||
chr5:150737160
|
A | T | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.430-3685T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150737160 | ||||||
chr5:150737359
|
G | A | 2 | a0002c0002t0009g0190a0002c0002t0009g0191 | 2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.430-3884C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150737359 | ||||||
chr5:150737418
|
G | T | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.430-3943C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150737418 | ||||||
chr5:150737529
|
A | C | 3 | a0002c0002t0003g0005a0002c0002t0003g0023a0002c0002t0003g0024 | 4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-4054T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150737529 | ||||||
chr5:150737532
|
G | GAAATCAG others(12): Show |
3 | a0002c0002t0003g0005a0002c0002t0003g0023a0002c0002t0003g0024 | 4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.430-4076_430-4058d others(21): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150737532 | ||||||
chr5:150737738
|
A | C | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.430-4263T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150737738 | ||||||
chr5:150737825
|
C | T | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.429+4289G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150737825 | ||||||
chr5:150737848
|
A | T | 91 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(88): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.429+4266T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150737848 | ||||||
chr5:150738392
|
C | T | 4 | a0002c0002t0005g0047a0002c0002t0005g0048a0002c0002t0005g0049others(1): Show | 4 | HG02055.hp1 HG02451.hp1 HG03139.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+3722G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738392 | ||||||
chr5:150738441
|
G | C | 65 | a0002c0002t0001g0192a0002c0002t0001g0193a0002c0002t0001g0195others(62): Show | 72 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.429+3673C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738441 | ||||||
chr5:150738458
|
G | A | 127 | a0001c0001t0003g0248a0001c0005t0006g0179a0001c0005t0006g0180others(124): Show | 137 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(134): Show |
intron_variant | MODIFIER | c.429+3656C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738458 | ||||||
chr5:150738554
|
A | G | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.429+3560T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738554 | ||||||
chr5:150738662
|
C | T | 65 | a0002c0002t0001g0192a0002c0002t0001g0193a0002c0002t0001g0195others(62): Show | 72 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.429+3452G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738662 | ||||||
chr5:150738672
|
T | C | 1 | a0002c0002t0001g0192 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.429+3442A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738672 | ||||||
chr5:150738783
|
T | G | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG02683.hp1 HG03239.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.429+3331A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738783 | ||||||
chr5:150738853
|
A | G | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.429+3261T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738853 | ||||||
chr5:150738866
|
G | T | 1 | a0001c0001t0001g0136 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.429+3248C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738866 | ||||||
chr5:150738959
|
C | T | 1 | a0002c0002t0003g0029 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.429+3155G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738959 | ||||||
chr5:150738986
|
G | A | 4 | a0002c0002t0005g0176a0002c0002t0005g0178a0002c0002t0014g0175others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+3128C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150738986 | ||||||
chr5:150739023
|
A | G | 140 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(137): Show | 154 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(151): Show |
intron_variant | MODIFIER | c.429+3091T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739023 | ||||||
chr5:150739100
|
G | C | 1 | a0001c0001t0001g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.429+3014C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739100 | ||||||
chr5:150739162
|
CAG | C | 4 | a0001c0001t0001g0086a0001c0001t0001g0087a0001c0001t0001g0170others(1): Show | 4 | HG03195.hp2 HG03471.hp2 HG03516.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+2950_429+2951d others(4): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739162 | ||||||
chr5:150739180
|
CA | C | 9 | a0001c0001t0023g0076a0002c0002t0001g0184a0002c0002t0001g0185others(6): Show | 9 | HG00639.hp2 HG01243.hp2 HG02451.hp2 others(6): Show |
intron_variant | MODIFIER | c.429+2933delT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739180 | ||||||
chr5:150739222
|
A | G | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.429+2892T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739222 | ||||||
chr5:150739237
|
A | C | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.429+2877T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739237 | ||||||
chr5:150739365
|
C | T | 1 | a0002c0002t0005g0186 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.429+2749G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739365 | ||||||
chr5:150739376
|
A | C | 1 | a0001c0001t0001g0125 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.429+2738T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739376 | ||||||
chr5:150739459
|
T | C | 1 | a0002c0002t0011g0207 | 1 | HG03209.hp1 | intron_variant | MODIFIER | c.429+2655A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739459 | ||||||
chr5:150739709
|
T | C | 1 | a0002c0002t0001g0193 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.429+2405A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739709 | ||||||
chr5:150739710
|
A | G | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.429+2404T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739710 | ||||||
chr5:150739754
|
G | A | 1 | a0003c0003t0004g0196 | 1 | HG02080.hp2 | intron_variant | MODIFIER | c.429+2360C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739754 | ||||||
chr5:150739830
|
G | A | 1 | a0002c0002t0003g0042 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.429+2284C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150739830 | ||||||
chr5:150740191
|
T | C | 252 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(249): Show | 285 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(282): Show |
intron_variant | MODIFIER | c.429+1923A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740191 | ||||||
chr5:150740194
|
A | G | 4 | a0002c0002t0005g0176a0002c0002t0005g0178a0002c0002t0014g0175others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.429+1920T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740194 | ||||||
chr5:150740246
|
T | C | 129 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0003g0248others(126): Show | 140 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.429+1868A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740246 | ||||||
chr5:150740266
|
T | G | 1 | a0002c0002t0001g0192 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.429+1848A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740266 | ||||||
chr5:150740287
|
T | C | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.429+1827A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740287 | ||||||
chr5:150740600
|
G | A | 1 | a0001c0001t0007g0071 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.429+1514C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740600 | ||||||
chr5:150740626
|
G | A | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.429+1488C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740626 | ||||||
chr5:150740628
|
C | T | 19 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(16): Show | 19 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.429+1486G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740628 | ||||||
chr5:150740719
|
A | AT | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.429+1394dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740719 | ||||||
chr5:150740811
|
A | T | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.429+1303T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740811 | ||||||
chr5:150740888
|
C | A | 6 | a0002c0004t0001g0022a0002c0004t0001g0251a0002c0004t0008g0249others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.429+1226G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150740888 | ||||||
chr5:150741031
|
C | G | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.429+1083G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741031 | ||||||
chr5:150741164
|
C | CAAAAA | 63 | a0002c0002t0001g0034a0002c0002t0001g0193a0002c0002t0001g0195others(60): Show | 71 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(68): Show |
intron_variant | MODIFIER | c.429+945_429+949dup others(5): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741164 | ||||||
chr5:150741164
|
C | CAAAAAA | 24 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0043others(21): Show | 24 | HG01884.hp1 HG02071.hp2 HG02109.hp1 others(21): Show |
intron_variant | MODIFIER | c.429+944_429+949dup others(6): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741164 | ||||||
chr5:150741164
|
C | CAAAAAAA others(3): Show |
1 | a0002c0002t0001g0184 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.429+940_429+949dup others(10): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741164 | ||||||
chr5:150741164
|
C | CAAAAAAA others(4): Show |
1 | a0002c0002t0001g0185 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.429+939_429+949dup others(11): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741164 | ||||||
chr5:150741164
|
C | CAAAAAAA others(5): Show |
1 | a0002c0002t0005g0186 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.429+938_429+949dup others(12): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741164 | ||||||
chr5:150741164
|
CA | C | 12 | a0001c0001t0001g0067a0001c0001t0001g0077a0001c0001t0001g0122others(9): Show | 12 | HG00558.hp1 HG02896.hp2 HG02897.hp1 others(9): Show |
intron_variant | MODIFIER | c.429+949delT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741164 | ||||||
chr5:150741193
|
C | A | 2 | a0002c0002t0001g0184a0002c0002t0001g0185 | 2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.429+921G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741193 | ||||||
chr5:150741221
|
A | C | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.429+893T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741221 | ||||||
chr5:150741352
|
T | C | 91 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(88): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.429+762A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741352 | ||||||
chr5:150741518
|
T | C | 1 | a0001c0001t0003g0248 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.429+596A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741518 | ||||||
chr5:150741530
|
G | A | 1 | a0002c0002t0017g0030 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.429+584C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741530 | ||||||
chr5:150741533
|
C | T | 1 | a0002c0002t0003g0029 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.429+581G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741533 | ||||||
chr5:150741621
|
T | C | 4 | a0002c0002t0005g0054a0002c0002t0005g0055a0002c0002t0005g0056others(1): Show | 4 | HG02145.hp1 HG02622.hp1 HG02630.hp2 others(1): Show |
intron_variant | MODIFIER | c.429+493A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741621 | ||||||
chr5:150741660
|
T | C | 1 | a0001c0001t0001g0157 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.429+454A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741660 | ||||||
chr5:150741896
|
G | C | 1 | a0005c0009t0001g0092 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.429+218C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150741896 | ||||||
chr5:150742007
|
A | T | 1 | a0002c0002t0003g0029 | 1 | HG03130.hp2 | intron_variant | MODIFIER | c.429+107T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 4/12 | chr5 | 150742007 | ||||||
chr5:150742161
|
C | T | 2 | a0001c0001t0001g0134a0001c0001t0007g0133 | 2 | HG02602.hp1 HG04115.hp1 |
splice_region_variant&intron_variant | LOW | c.386-4G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742161 | ||||||
chr5:150742502
|
C | T | 3 | a0001c0001t0001g0090a0001c0001t0001g0127a0001c0001t0001g0132 | 3 | HG01884.hp2 NA18965.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.386-345G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742502 | ||||||
chr5:150742513
|
T | C | 1 | a0001c0001t0001g0090 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.386-356A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742513 | ||||||
chr5:150742717
|
G | C | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.386-560C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742717 | ||||||
chr5:150742829
|
C | A | 4 | a0001c0001t0001g0088a0001c0001t0001g0089a0001c0001t0001g0090others(1): Show | 4 | HG01175.hp1 HG01884.hp2 HG02818.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-672G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742829 | ||||||
chr5:150742919
|
C | T | 7 | a0001c0005t0006g0179a0001c0005t0006g0180a0001c0005t0006g0181others(4): Show | 7 | HG02896.hp2 HG02897.hp1 HG03139.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-762G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742919 | ||||||
chr5:150742960
|
C | T | 1 | a0002c0002t0001g0210 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.386-803G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742960 | ||||||
chr5:150742965
|
C | A | 1 | a0001c0001t0001g0120 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.386-808G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742965 | ||||||
chr5:150742965
|
C | G | 6 | a0002c0004t0001g0022a0002c0004t0001g0251a0002c0004t0008g0249others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-808G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742965 | ||||||
chr5:150742997
|
G | A | 1 | a0002c0002t0001g0043 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.386-840C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150742997 | ||||||
chr5:150743000
|
C | T | 1 | a0001c0001t0001g0131 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.386-843G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743000 | ||||||
chr5:150743002
|
C | T | 1 | a0002c0002t0009g0190 | 1 | HG02809.hp1 | intron_variant | MODIFIER | c.386-845G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743002 | ||||||
chr5:150743042
|
G | A | 60 | a0002c0002t0001g0193a0002c0002t0001g0195a0002c0002t0001g0197others(57): Show | 67 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.386-885C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743042 | ||||||
chr5:150743082
|
G | A | 20 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0005g0047others(17): Show | 20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.386-925C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743082 | ||||||
chr5:150743120
|
C | T | 1 | a0002c0002t0001g0198 | 1 | NA19012.hp2 | intron_variant | MODIFIER | c.386-963G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743120 | ||||||
chr5:150743122
|
G | T | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-965C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743122 | ||||||
chr5:150743189
|
G | A | 1 | a0002c0002t0003g0044 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.386-1032C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743189 | ||||||
chr5:150743279
|
G | A | 1 | a0001c0001t0001g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.386-1122C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743279 | ||||||
chr5:150743306
|
T | TA | 16 | a0002c0002t0001g0193a0002c0002t0001g0195a0002c0002t0001g0197others(13): Show | 17 | HG00408.hp2 HG00558.hp2 HG02080.hp2 others(14): Show |
intron_variant | MODIFIER | c.386-1150dupT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743306 | ||||||
chr5:150743400
|
C | A | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-1243G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743400 | ||||||
chr5:150743445
|
A | G | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-1288T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743445 | ||||||
chr5:150743481
|
C | T | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-1324G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743481 | ||||||
chr5:150743587
|
C | T | 1 | a0001c0001t0001g0096 | 1 | NA19004.hp1 | intron_variant | MODIFIER | c.386-1430G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743587 | ||||||
chr5:150743689
|
G | A | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-1532C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743689 | ||||||
chr5:150743693
|
A | T | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-1536T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743693 | ||||||
chr5:150743797
|
C | T | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-1640G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743797 | ||||||
chr5:150743902
|
A | C | 4 | a0002c0002t0001g0006a0002c0002t0001g0184a0002c0002t0001g0185others(1): Show | 5 | HG01243.hp2 HG02258.hp1 HG02717.hp2 others(2): Show |
intron_variant | MODIFIER | c.386-1745T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743902 | ||||||
chr5:150743902
|
A | T | 91 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(88): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.386-1745T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743902 | ||||||
chr5:150743948
|
T | C | 91 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(88): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.386-1791A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743948 | ||||||
chr5:150743992
|
G | A | 1 | a0002c0002t0017g0030 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.386-1835C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150743992 | ||||||
chr5:150744044
|
A | C | 1 | a0002c0002t0016g0246 | 1 | NA18955.hp1 | intron_variant | MODIFIER | c.386-1887T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744044 | ||||||
chr5:150744099
|
G | C | 2 | a0001c0001t0001g0066a0001c0001t0001g0169 | 2 | NA18992.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.386-1942C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744099 | ||||||
chr5:150744191
|
T | C | 1 | a0001c0001t0001g0069 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.386-2034A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744191 | ||||||
chr5:150744192
|
G | A | 1 | a0001c0001t0001g0069 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.386-2035C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744192 | ||||||
chr5:150744194
|
C | T | 3 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0001g0069 | 4 | HG01975.hp2 HG02723.hp2 NA19030.hp1 others(1): Show |
intron_variant | MODIFIER | c.386-2037G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744194 | ||||||
chr5:150744195
|
G | A | 1 | a0001c0001t0001g0166 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.386-2038C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744195 | ||||||
chr5:150744202
|
G | C | 2 | a0001c0001t0001g0007a0001c0001t0001g0063 | 3 | HG02723.hp2 NA19030.hp1 NA19240.hp2 |
intron_variant | MODIFIER | c.386-2045C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744202 | ||||||
chr5:150744220
|
C | T | 20 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0005g0047others(17): Show | 20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.386-2063G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744220 | ||||||
chr5:150744238
|
G | GA | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-2082dupT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744238 | ||||||
chr5:150744258
|
C | T | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.386-2101G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744258 | ||||||
chr5:150744308
|
G | A | 2 | a0002c0002t0009g0190a0002c0002t0009g0191 | 2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.386-2151C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744308 | ||||||
chr5:150744315
|
T | C | 1 | a0002c0002t0005g0186 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.386-2158A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744315 | ||||||
chr5:150744440
|
T | C | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-2283A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744440 | ||||||
chr5:150744457
|
T | A | 20 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0005g0047others(17): Show | 20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.386-2300A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744457 | ||||||
chr5:150744534
|
C | T | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.386-2377G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744534 | ||||||
chr5:150744603
|
T | C | 91 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(88): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.386-2446A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744603 | ||||||
chr5:150744651
|
C | A | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-2494G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744651 | ||||||
chr5:150744754
|
G | A | 20 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0005g0047others(17): Show | 20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.386-2597C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744754 | ||||||
chr5:150744763
|
C | T | 1 | a0001c0001t0001g0063 | 1 | NA19030.hp1 | intron_variant | MODIFIER | c.386-2606G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744763 | ||||||
chr5:150744887
|
G | A | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.386-2730C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744887 | ||||||
chr5:150744912
|
C | A | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-2755G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744912 | ||||||
chr5:150744935
|
C | T | 1 | a0001c0001t0001g0072 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.386-2778G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744935 | ||||||
chr5:150744998
|
A | G | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-2841T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150744998 | ||||||
chr5:150745053
|
A | G | 65 | a0002c0002t0001g0192a0002c0002t0001g0193a0002c0002t0001g0195others(62): Show | 72 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.386-2896T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745053 | ||||||
chr5:150745107
|
A | C | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-2950T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745107 | ||||||
chr5:150745169
|
C | G | 1 | a0001c0001t0023g0076 | 1 | HG00639.hp2 | intron_variant | MODIFIER | c.386-3012G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745169 | ||||||
chr5:150745220
|
C | A | 8 | a0001c0001t0003g0248a0001c0005t0006g0179a0001c0005t0006g0180others(5): Show | 8 | HG02896.hp2 HG02897.hp1 HG02970.hp1 others(5): Show |
intron_variant | MODIFIER | c.386-3063G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745220 | ||||||
chr5:150745235
|
C | A | 93 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(90): Show | 101 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(98): Show |
intron_variant | MODIFIER | c.386-3078G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745235 | ||||||
chr5:150745305
|
C | T | 1 | a0002c0002t0001g0058 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.386-3148G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745305 | ||||||
chr5:150745435
|
C | G | 1 | a0001c0001t0001g0158 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.386-3278G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745435 | ||||||
chr5:150745436
|
C | T | 1 | a0001c0001t0001g0158 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.386-3279G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745436 | ||||||
chr5:150745437
|
A | G | 96 | a0001c0001t0001g0158a0002c0002t0001g0006a0002c0002t0001g0031others(93): Show | 105 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.386-3280T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745437 | ||||||
chr5:150745443
|
T | A | 1 | a0001c0001t0001g0158 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.386-3286A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745443 | ||||||
chr5:150745514
|
A | G | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.386-3357T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745514 | ||||||
chr5:150745607
|
C | A | 6 | a0002c0004t0001g0022a0002c0004t0001g0251a0002c0004t0008g0249others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.386-3450G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745607 | ||||||
chr5:150745746
|
G | C | 1 | a0002c0002t0017g0030 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.386-3589C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745746 | ||||||
chr5:150745788
|
A | C | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-3631T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745788 | ||||||
chr5:150745824
|
C | A | 3 | a0002c0002t0003g0005a0002c0002t0003g0023a0002c0002t0003g0024 | 4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-3667G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745824 | ||||||
chr5:150745825
|
C | T | 3 | a0002c0002t0003g0005a0002c0002t0003g0023a0002c0002t0003g0024 | 4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-3668G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745825 | ||||||
chr5:150745826
|
A | C | 9 | a0002c0002t0002g0020a0002c0002t0002g0211a0002c0002t0002g0212others(6): Show | 10 | NA18966.hp1 NA18968.hp1 NA18969.hp2 others(7): Show |
intron_variant | MODIFIER | c.386-3669T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745826 | ||||||
chr5:150745961
|
T | C | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-3804A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745961 | ||||||
chr5:150745995
|
A | G | 1 | a0002c0002t0002g0243 | 1 | NA18983.hp1 | intron_variant | MODIFIER | c.386-3838T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150745995 | ||||||
chr5:150746000
|
G | T | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.386-3843C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746000 | ||||||
chr5:150746147
|
G | C | 2 | a0002c0002t0001g0195a0003c0003t0004g0196 | 2 | HG00408.hp2 HG02080.hp2 |
intron_variant | MODIFIER | c.386-3990C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746147 | ||||||
chr5:150746169
|
T | C | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-4012A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746169 | ||||||
chr5:150746179
|
C | G | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.386-4022G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746179 | ||||||
chr5:150746211
|
C | T | 1 | a0001c0001t0001g0095 | 1 | NA19070.hp2 | intron_variant | MODIFIER | c.386-4054G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746211 | ||||||
chr5:150746242
|
C | G | 1 | a0001c0001t0001g0069 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.386-4085G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746242 | ||||||
chr5:150746266
|
C | T | 20 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0005g0047others(17): Show | 20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.386-4109G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746266 | ||||||
chr5:150746293
|
A | ATAAT | 129 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0003g0248others(126): Show | 140 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.386-4140_386-4137d others(6): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746293 | ||||||
chr5:150746359
|
A | G | 1 | a0001c0001t0001g0094 | 1 | NA18974.hp1 | intron_variant | MODIFIER | c.386-4202T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746359 | ||||||
chr5:150746443
|
C | T | 19 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(16): Show | 19 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.386-4286G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746443 | ||||||
chr5:150746467
|
T | C | 119 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(116): Show | 129 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(126): Show |
intron_variant | MODIFIER | c.386-4310A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746467 | ||||||
chr5:150746481
|
A | G | 1 | a0002c0002t0017g0030 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.386-4324T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746481 | ||||||
chr5:150746525
|
T | G | 1 | a0002c0002t0005g0186 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.386-4368A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746525 | ||||||
chr5:150746549
|
G | A | 1 | a0002c0002t0001g0202 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.386-4392C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746549 | ||||||
chr5:150746555
|
C | A | 1 | a0001c0001t0001g0121 | 1 | HG01109.hp2 | intron_variant | MODIFIER | c.386-4398G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746555 | ||||||
chr5:150746557
|
G | A | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-4400C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746557 | ||||||
chr5:150746561
|
G | C | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-4404C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746561 | ||||||
chr5:150746588
|
A | C | 1 | a0002c0002t0017g0030 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.386-4431T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746588 | ||||||
chr5:150746638
|
G | A | 91 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(88): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.386-4481C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746638 | ||||||
chr5:150746704
|
T | C | 1 | a0002c0002t0017g0030 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.386-4547A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746704 | ||||||
chr5:150746710
|
C | A | 2 | a0001c0001t0001g0122a0001c0010t0001g0123 | 2 | NA18977.hp2 NA19075.hp1 |
intron_variant | MODIFIER | c.386-4553G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746710 | ||||||
chr5:150746768
|
C | A | 11 | a0002c0002t0005g0047a0002c0002t0005g0048a0002c0002t0005g0049others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.386-4611G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746768 | ||||||
chr5:150746769
|
G | A | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-4612C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746769 | ||||||
chr5:150746903
|
A | G | 1 | a0001c0001t0001g0093 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.386-4746T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746903 | ||||||
chr5:150746917
|
T | C | 2 | a0002c0002t0002g0243a0002c0002t0002g0244 | 2 | NA18950.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.386-4760A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746917 | ||||||
chr5:150746926
|
G | A | 1 | a0001c0001t0001g0124 | 1 | NA19080.hp2 | intron_variant | MODIFIER | c.386-4769C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150746926 | ||||||
chr5:150747014
|
T | C | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-4857A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747014 | ||||||
chr5:150747083
|
C | T | 65 | a0002c0002t0001g0192a0002c0002t0001g0193a0002c0002t0001g0195others(62): Show | 72 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.386-4926G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747083 | ||||||
chr5:150747095
|
G | A | 1 | a0001c0001t0007g0172 | 1 | HG03492.hp1 | intron_variant | MODIFIER | c.386-4938C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747095 | ||||||
chr5:150747112
|
T | G | 65 | a0002c0002t0001g0192a0002c0002t0001g0193a0002c0002t0001g0195others(62): Show | 72 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(69): Show |
intron_variant | MODIFIER | c.386-4955A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747112 | ||||||
chr5:150747146
|
C | T | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.386-4989G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747146 | ||||||
chr5:150747236
|
C | T | 4 | a0001c0001t0001g0128a0001c0001t0001g0129a0001c0001t0001g0130others(1): Show | 4 | HG02109.hp2 HG02818.hp1 HG03486.hp2 others(1): Show |
intron_variant | MODIFIER | c.386-5079G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747236 | ||||||
chr5:150747471
|
C | T | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.386-5314G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747471 | ||||||
chr5:150747635
|
G | A | 94 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(91): Show | 102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.386-5478C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747635 | ||||||
chr5:150747640
|
T | C | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.386-5483A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747640 | ||||||
chr5:150747660
|
G | A | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-5503C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747660 | ||||||
chr5:150747661
|
A | G | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.386-5504T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747661 | ||||||
chr5:150747925
|
C | A | 20 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0005g0047others(17): Show | 20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.385+5554G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747925 | ||||||
chr5:150747975
|
A | G | 1 | a0001c0001t0001g0075 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.385+5504T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747975 | ||||||
chr5:150747988
|
T | A | 4 | a0002c0002t0009g0188a0002c0002t0009g0189a0002c0002t0009g0190others(1): Show | 4 | HG02809.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+5491A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150747988 | ||||||
chr5:150748024
|
T | C | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.385+5455A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748024 | ||||||
chr5:150748057
|
G | T | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.385+5422C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748057 | ||||||
chr5:150748299
|
G | A | 91 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(88): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.385+5180C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748299 | ||||||
chr5:150748359
|
C | T | 1 | a0002c0002t0001g0033 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.385+5120G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748359 | ||||||
chr5:150748385
|
C | T | 2 | a0002c0002t0001g0058a0002c0002t0001g0059 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.385+5094G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748385 | ||||||
chr5:150748443
|
A | G | 2 | a0002c0002t0001g0058a0002c0002t0001g0059 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.385+5036T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748443 | ||||||
chr5:150748488
|
A | G | 3 | a0002c0002t0003g0005a0002c0002t0003g0023a0002c0002t0003g0024 | 4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.385+4991T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748488 | ||||||
chr5:150748600
|
T | C | 5 | a0002c0002t0001g0215a0003c0003t0004g0021a0003c0003t0004g0240others(2): Show | 6 | HG00408.hp1 HG02015.hp2 NA18974.hp2 others(3): Show |
intron_variant | MODIFIER | c.385+4879A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748600 | ||||||
chr5:150748608
|
C | T | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.385+4871G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748608 | ||||||
chr5:150748639
|
G | A | 2 | a0002c0002t0009g0190a0002c0002t0009g0191 | 2 | HG02809.hp1 HG03209.hp2 |
intron_variant | MODIFIER | c.385+4840C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748639 | ||||||
chr5:150748704
|
G | A | 1 | a0001c0001t0001g0091 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.385+4775C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748704 | ||||||
chr5:150748800
|
G | T | 94 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(91): Show | 102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.385+4679C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748800 | ||||||
chr5:150748843
|
C | T | 1 | a0002c0002t0003g0032 | 1 | HG02572.hp2 | intron_variant | MODIFIER | c.385+4636G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748843 | ||||||
chr5:150748953
|
G | A | 1 | a0001c0001t0001g0127 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.385+4526C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748953 | ||||||
chr5:150748954
|
A | G | 1 | a0001c0001t0001g0127 | 1 | NA19067.hp2 | intron_variant | MODIFIER | c.385+4525T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150748954 | ||||||
chr5:150749162
|
G | A | 1 | a0002c0002t0016g0247 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.385+4317C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749162 | ||||||
chr5:150749245
|
A | G | 71 | a0002c0002t0001g0192a0002c0002t0001g0193a0002c0002t0001g0195others(68): Show | 79 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(76): Show |
intron_variant | MODIFIER | c.385+4234T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749245 | ||||||
chr5:150749332
|
C | T | 6 | a0002c0004t0001g0022a0002c0004t0001g0251a0002c0004t0008g0249others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.385+4147G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749332 | ||||||
chr5:150749390
|
G | C | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.385+4089C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749390 | ||||||
chr5:150749392
|
G | T | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.385+4087C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749392 | ||||||
chr5:150749475
|
C | T | 1 | a0001c0001t0001g0008 | 2 | HG02055.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.385+4004G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749475 | ||||||
chr5:150749586
|
C | T | 1 | a0005c0009t0001g0092 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.385+3893G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749586 | ||||||
chr5:150749602
|
G | T | 4 | a0002c0002t0005g0176a0002c0002t0005g0178a0002c0002t0014g0175others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+3877C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749602 | ||||||
chr5:150749658
|
AAAAT | A | 19 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(16): Show | 19 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(16): Show |
intron_variant | MODIFIER | c.385+3817_385+3820d others(6): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749658 | ||||||
chr5:150749659
|
AAAT | A | 22 | a0002c0002t0001g0197a0002c0002t0001g0210a0002c0002t0001g0215others(19): Show | 23 | HG00558.hp2 HG01069.hp1 HG01071.hp1 others(20): Show |
intron_variant | MODIFIER | c.385+3817_385+3819d others(5): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749659 | ||||||
chr5:150749660
|
AAT | A | 50 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0001g0192others(47): Show | 57 | HG00408.hp1 HG00597.hp2 HG00639.hp1 others(54): Show |
intron_variant | MODIFIER | c.385+3817_385+3818d others(4): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749660 | ||||||
chr5:150749662
|
T | A | 1 | a0002c0002t0017g0030 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.385+3817A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749662 | ||||||
chr5:150749672
|
T | A | 94 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(91): Show | 102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.385+3807A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749672 | ||||||
chr5:150749965
|
AAGAC | A | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.385+3510_385+3513d others(6): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749965 | ||||||
chr5:150749989
|
G | A | 1 | a0001c0001t0001g0167 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.385+3490C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150749989 | ||||||
chr5:150750045
|
A | C | 1 | a0002c0002t0002g0019 | 2 | HG00639.hp1 HG03834.hp1 |
intron_variant | MODIFIER | c.385+3434T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750045 | ||||||
chr5:150750232
|
A | C | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.385+3247T>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750232 | ||||||
chr5:150750246
|
C | T | 1 | a0002c0002t0001g0208 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.385+3233G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750246 | ||||||
chr5:150750324
|
G | A | 4 | a0002c0002t0009g0188a0002c0002t0009g0189a0002c0002t0009g0190others(1): Show | 4 | HG02809.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.385+3155C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750324 | ||||||
chr5:150750344
|
A | T | 6 | a0002c0004t0001g0022a0002c0004t0001g0251a0002c0004t0008g0249others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.385+3135T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750344 | ||||||
chr5:150750414
|
G | A | 60 | a0002c0002t0001g0193a0002c0002t0001g0195a0002c0002t0001g0197others(57): Show | 67 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(64): Show |
intron_variant | MODIFIER | c.385+3065C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750414 | ||||||
chr5:150750479
|
T | G | 1 | a0001c0001t0001g0125 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.385+3000A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750479 | ||||||
chr5:150750522
|
A | G | 94 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(91): Show | 102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.385+2957T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750522 | ||||||
chr5:150750594
|
G | T | 20 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0005g0047others(17): Show | 20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.385+2885C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750594 | ||||||
chr5:150750721
|
C | T | 3 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0074 | 3 | HG02683.hp1 HG03239.hp2 NA18612.hp2 |
intron_variant | MODIFIER | c.385+2758G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750721 | ||||||
chr5:150750867
|
A | G | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.385+2612T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150750867 | ||||||
chr5:150751064
|
T | C | 1 | a0002c0002t0002g0206 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.385+2415A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150751064 | ||||||
chr5:150751146
|
T | C | 95 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(92): Show | 104 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(101): Show |
intron_variant | MODIFIER | c.385+2333A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150751146 | ||||||
chr5:150751172
|
C | T | 4 | a0001c0001t0001g0015a0001c0001t0001g0159a0001c0001t0001g0160others(1): Show | 5 | HG02129.hp1 NA18988.hp1 NA18990.hp2 others(2): Show |
intron_variant | MODIFIER | c.385+2307G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150751172 | ||||||
chr5:150751280
|
G | T | 129 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0003g0248others(126): Show | 140 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.385+2199C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150751280 | ||||||
chr5:150751322
|
CCTAGAGG others(10): Show |
C | 1 | a0002c0002t0017g0030 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.385+2140_385+2156d others(19): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150751322 | ||||||
chr5:150751509
|
A | G | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.385+1970T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150751509 | ||||||
chr5:150751531
|
G | A | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.385+1948C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150751531 | ||||||
chr5:150751754
|
G | GA | 20 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0005g0047others(17): Show | 20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.385+1724dupT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150751754 | ||||||
chr5:150751834
|
C | T | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.385+1645G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150751834 | ||||||
chr5:150752076
|
G | A | 1 | a0002c0002t0005g0186 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.385+1403C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752076 | ||||||
chr5:150752100
|
A | G | 1 | a0001c0001t0001g0126 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.385+1379T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752100 | ||||||
chr5:150752106
|
A | G | 2 | a0002c0002t0001g0058a0002c0002t0001g0059 | 2 | HG02615.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.385+1373T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752106 | ||||||
chr5:150752112
|
G | A | 39 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0067others(36): Show | 41 | HG00558.hp1 HG00597.hp1 HG00642.hp1 others(38): Show |
intron_variant | MODIFIER | c.385+1367C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752112 | ||||||
chr5:150752247
|
C | T | 1 | a0002c0002t0001g0210 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.385+1232G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752247 | ||||||
chr5:150752263
|
G | T | 2 | a0001c0001t0007g0070a0001c0001t0007g0071 | 2 | HG01978.hp1 HG04204.hp2 |
intron_variant | MODIFIER | c.385+1216C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752263 | ||||||
chr5:150752425
|
C | T | 194 | a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0009others(191): Show | 209 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(206): Show |
intron_variant | MODIFIER | c.385+1054G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752425 | ||||||
chr5:150752445
|
T | C | 1 | a0002c0002t0003g0024 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.385+1034A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752445 | ||||||
chr5:150752495
|
G | A | 94 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(91): Show | 102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.385+984C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752495 | ||||||
chr5:150752584
|
G | A | 94 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(91): Show | 102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.385+895C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752584 | ||||||
chr5:150752598
|
T | C | 1 | a0001c0001t0015g0014 | 2 | HG01167.hp2 homoSapiens_chm13v2.hp1 |
intron_variant | MODIFIER | c.385+881A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752598 | ||||||
chr5:150752662
|
C | T | 94 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(91): Show | 102 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(99): Show |
intron_variant | MODIFIER | c.385+817G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752662 | ||||||
chr5:150752727
|
T | C | 16 | a0001c0001t0001g0003a0001c0001t0001g0015a0001c0001t0001g0016others(13): Show | 20 | HG01255.hp1 HG01433.hp1 HG01928.hp1 others(17): Show |
intron_variant | MODIFIER | c.385+752A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752727 | ||||||
chr5:150752734
|
T | G | 2 | a0002c0002t0001g0208a0002c0002t0001g0209 | 2 | HG02970.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.385+745A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752734 | ||||||
chr5:150752786
|
C | T | 1 | a0001c0001t0001g0069 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.385+693G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752786 | ||||||
chr5:150752919
|
T | G | 1 | a0001c0001t0001g0168 | 1 | HG02300.hp2 | intron_variant | MODIFIER | c.385+560A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752919 | ||||||
chr5:150752944
|
G | A | 1 | a0002c0002t0003g0045 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.385+535C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150752944 | ||||||
chr5:150753092
|
C | A | 2 | a0002c0002t0002g0243a0002c0002t0002g0244 | 2 | NA18950.hp2 NA18983.hp1 |
intron_variant | MODIFIER | c.385+387G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150753092 | ||||||
chr5:150753161
|
G | A | 2 | a0001c0001t0001g0066a0001c0001t0001g0169 | 2 | NA18992.hp1 NA19087.hp2 |
intron_variant | MODIFIER | c.385+318C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 3/12 | chr5 | 150753161 | ||||||
chr5:150753772
|
T | A | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.207-115A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150753772 | ||||||
chr5:150753905
|
G | A | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.207-248C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150753905 | ||||||
chr5:150754159
|
C | T | 91 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(88): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.207-502G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150754159 | ||||||
chr5:150754422
|
A | G | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.207-765T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150754422 | ||||||
chr5:150754435
|
C | T | 3 | a0002c0002t0001g0208a0002c0002t0001g0209a0002c0002t0001g0245 | 3 | HG02970.hp2 HG03098.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.207-778G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150754435 | ||||||
chr5:150754839
|
C | T | 2 | a0002c0002t0009g0188a0002c0002t0009g0189 | 2 | HG03516.hp1 NA20300.hp2 |
intron_variant | MODIFIER | c.207-1182G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150754839 | ||||||
chr5:150754856
|
A | T | 11 | a0002c0002t0005g0047a0002c0002t0005g0048a0002c0002t0005g0049others(8): Show | 11 | HG01891.hp1 HG02055.hp1 HG02145.hp1 others(8): Show |
intron_variant | MODIFIER | c.207-1199T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150754856 | ||||||
chr5:150754877
|
T | C | 1 | a0001c0001t0001g0170 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.207-1220A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150754877 | ||||||
chr5:150754879
|
C | CT | 6 | a0002c0004t0001g0022a0002c0004t0001g0251a0002c0004t0008g0249others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.207-1223dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150754879 | ||||||
chr5:150754962
|
CA | C | 96 | a0001c0001t0001g0068a0002c0002t0001g0006a0002c0002t0001g0031others(93): Show | 105 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.207-1306delT | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150754962 | ||||||
chr5:150755128
|
C | T | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.206+1289G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150755128 | ||||||
chr5:150755345
|
T | C | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.206+1072A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150755345 | ||||||
chr5:150755406
|
C | T | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.206+1011G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150755406 | ||||||
chr5:150755614
|
A | G | 1 | a0001c0001t0001g0067 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.206+803T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150755614 | ||||||
chr5:150755622
|
C | T | 20 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0005g0047others(17): Show | 20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.206+795G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150755622 | ||||||
chr5:150755655
|
T | C | 20 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0005g0047others(17): Show | 20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.206+762A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150755655 | ||||||
chr5:150755665
|
G | A | 6 | a0002c0004t0001g0022a0002c0004t0001g0251a0002c0004t0008g0249others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.206+752C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150755665 | ||||||
chr5:150755862
|
G | A | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.206+555C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150755862 | ||||||
chr5:150755935
|
C | T | 16 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0005g0047others(13): Show | 16 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(13): Show |
intron_variant | MODIFIER | c.206+482G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150755935 | ||||||
chr5:150756039
|
C | CT | 7 | a0001c0001t0001g0064a0001c0001t0001g0065a0001c0001t0001g0066others(4): Show | 8 | HG01081.hp1 HG01167.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.206+377dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150756039 | ||||||
chr5:150756039
|
CT | C | 34 | a0001c0001t0003g0248a0001c0005t0006g0179a0001c0005t0006g0180others(31): Show | 35 | HG01243.hp2 HG01891.hp1 HG01981.hp1 others(32): Show |
intron_variant | MODIFIER | c.206+377delA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150756039 | ||||||
chr5:150756071
|
T | C | 2 | a0002c0002t0001g0184a0002c0002t0001g0185 | 2 | HG01243.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.206+346A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150756071 | ||||||
chr5:150756291
|
C | T | 2 | a0002c0002t0002g0205a0002c0002t0002g0206 | 2 | NA18959.hp2 NA19080.hp1 |
intron_variant | MODIFIER | c.206+126G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150756291 | ||||||
chr5:150756338
|
C | T | 90 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(87): Show | 98 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(95): Show |
intron_variant | MODIFIER | c.206+79G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150756338 | ||||||
chr5:150756366
|
GAGAACAG others(3): Show |
G | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.206+41_206+50delTG others(8): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150756366 | ||||||
chr5:150756368
|
G | GAAC | 18 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(15): Show | 18 | HG01243.hp1 HG01884.hp1 HG02109.hp1 others(15): Show |
intron_variant | MODIFIER | c.206+46_206+48dupGT others(1): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 2/12 | chr5 | 150756368 | ||||||
chr5:150756616
|
G | C | 1 | a0004c0006t0004g0004 | 3 | NA18983.hp2 NA18989.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.136-129C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150756616 | ||||||
chr5:150756617
|
G | T | 4 | a0002c0002t0009g0188a0002c0002t0009g0189a0002c0002t0009g0190others(1): Show | 4 | HG02809.hp1 HG03209.hp2 HG03516.hp1 others(1): Show |
intron_variant | MODIFIER | c.136-130C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150756617 | ||||||
chr5:150756639
|
G | GT | 224 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(221): Show | 255 | HG00408.hp1 HG00408.hp2 HG00558.hp1 others(252): Show |
intron_variant | MODIFIER | c.136-153dupA | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150756639 | ||||||
chr5:150756639
|
G | GTT | 22 | a0001c0001t0001g0064a0002c0002t0001g0006a0002c0002t0001g0058others(19): Show | 24 | HG00735.hp2 HG01496.hp1 HG01891.hp1 others(21): Show |
intron_variant | MODIFIER | c.136-154_136-153dup others(2): Show |
DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150756639 | ||||||
chr5:150756760
|
T | G | 91 | a0002c0002t0001g0031a0002c0002t0001g0033a0002c0002t0001g0034others(88): Show | 99 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(96): Show |
intron_variant | MODIFIER | c.136-273A>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150756760 | ||||||
chr5:150756762
|
G | C | 2 | a0002c0002t0016g0246a0002c0002t0016g0247 | 2 | NA18944.hp2 NA18955.hp1 |
intron_variant | MODIFIER | c.136-275C>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150756762 | ||||||
chr5:150756886
|
G | A | 96 | a0002c0002t0001g0006a0002c0002t0001g0031a0002c0002t0001g0033others(93): Show | 105 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(102): Show |
intron_variant | MODIFIER | c.136-399C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150756886 | ||||||
chr5:150757107
|
G | T | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.136-620C>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757107 | ||||||
chr5:150757290
|
C | G | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.136-803G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757290 | ||||||
chr5:150757298
|
C | T | 1 | a0001c0001t0001g0174 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.136-811G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757298 | ||||||
chr5:150757498
|
C | T | 20 | a0002c0002t0001g0058a0002c0002t0001g0059a0002c0002t0005g0047others(17): Show | 20 | HG01891.hp1 HG01981.hp1 HG02055.hp1 others(17): Show |
intron_variant | MODIFIER | c.136-1011G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757498 | ||||||
chr5:150757534
|
G | A | 1 | a0001c0001t0001g0174 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.136-1047C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757534 | ||||||
chr5:150757633
|
C | T | 1 | a0002c0002t0001g0006 | 2 | HG02258.hp1 HG02895.hp1 |
intron_variant | MODIFIER | c.136-1146G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757633 | ||||||
chr5:150757774
|
C | T | 1 | a0002c0002t0003g0023 | 1 | HG02886.hp2 | intron_variant | MODIFIER | c.135+1085G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757774 | ||||||
chr5:150757776
|
C | T | 10 | a0002c0002t0001g0193a0002c0002t0001g0195a0002c0002t0001g0197others(7): Show | 11 | HG00408.hp2 HG00558.hp2 HG02080.hp2 others(8): Show |
intron_variant | MODIFIER | c.135+1083G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757776 | ||||||
chr5:150757810
|
A | G | 3 | a0002c0002t0003g0026a0002c0002t0003g0028a0002c0002t0011g0027 | 3 | HG02723.hp1 HG06807.hp1 NA18522.hp1 |
intron_variant | MODIFIER | c.135+1049T>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757810 | ||||||
chr5:150757887
|
T | C | 129 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0003g0248others(126): Show | 140 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.135+972A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757887 | ||||||
chr5:150757937
|
C | T | 1 | a0002c0002t0011g0194 | 1 | HG02280.hp1 | intron_variant | MODIFIER | c.135+922G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757937 | ||||||
chr5:150757967
|
A | T | 129 | a0001c0001t0001g0007a0001c0001t0001g0063a0001c0001t0003g0248others(126): Show | 140 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(137): Show |
intron_variant | MODIFIER | c.135+892T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757967 | ||||||
chr5:150757968
|
A | T | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0001g0193 | 3 | HG01243.hp2 HG02129.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.135+891T>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150757968 | ||||||
chr5:150758152
|
T | C | 5 | a0001c0005t0006g0179a0001c0005t0006g0180a0001c0005t0006g0181others(2): Show | 5 | HG03139.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+707A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758152 | ||||||
chr5:150758159
|
C | G | 1 | a0001c0001t0019g0046 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.135+700G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758159 | ||||||
chr5:150758267
|
T | C | 4 | a0002c0002t0005g0176a0002c0002t0005g0178a0002c0002t0014g0175others(1): Show | 4 | HG02451.hp2 HG02622.hp2 HG03540.hp1 others(1): Show |
intron_variant | MODIFIER | c.135+592A>G | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758267 | ||||||
chr5:150758278
|
C | T | 5 | a0002c0002t0001g0192a0002c0002t0009g0188a0002c0002t0009g0189others(2): Show | 5 | HG02647.hp2 HG02809.hp1 HG03209.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+581G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758278 | ||||||
chr5:150758355
|
C | T | 1 | a0001c0001t0003g0248 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.135+504G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758355 | ||||||
chr5:150758371
|
G | A | 5 | a0001c0005t0006g0179a0001c0005t0006g0180a0001c0005t0006g0181others(2): Show | 5 | HG03139.hp1 HG03225.hp1 HG03453.hp2 others(2): Show |
intron_variant | MODIFIER | c.135+488C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758371 | ||||||
chr5:150758475
|
C | T | 98 | a0001c0005t0006g0203a0001c0005t0006g0204a0002c0002t0001g0006others(95): Show | 107 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(104): Show |
intron_variant | MODIFIER | c.135+384G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758475 | ||||||
chr5:150758481
|
C | T | 1 | a0002c0002t0002g0187 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.135+378G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758481 | ||||||
chr5:150758506
|
T | A | 3 | a0002c0002t0001g0184a0002c0002t0001g0185a0002c0002t0005g0186 | 3 | HG01243.hp2 HG02717.hp2 HG02922.hp1 |
intron_variant | MODIFIER | c.135+353A>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758506 | ||||||
chr5:150758528
|
C | T | 1 | a0002c0007t0018g0025 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.135+331G>A | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758528 | ||||||
chr5:150758634
|
C | A | 67 | a0001c0005t0006g0203a0001c0005t0006g0204a0002c0002t0001g0192others(64): Show | 74 | HG00408.hp1 HG00408.hp2 HG00558.hp2 others(71): Show |
intron_variant | MODIFIER | c.135+225G>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758634 | ||||||
chr5:150758685
|
C | G | 3 | a0002c0002t0003g0005a0002c0002t0003g0023a0002c0002t0003g0024 | 4 | HG00735.hp2 HG01496.hp1 HG02559.hp2 others(1): Show |
intron_variant | MODIFIER | c.135+174G>C | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758685 | ||||||
chr5:150758746
|
G | A | 1 | a0001c0001t0003g0248 | 1 | HG02970.hp1 | intron_variant | MODIFIER | c.135+113C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758746 | ||||||
chr5:150758768
|
G | A | 6 | a0002c0004t0001g0022a0002c0004t0001g0251a0002c0004t0008g0249others(3): Show | 7 | HG01069.hp1 HG01071.hp1 HG02257.hp1 others(4): Show |
intron_variant | MODIFIER | c.135+91C>T | DCTN4 | ENSG00000132912.13 | transcript | ENST00000447998.7 | protein_coding | 1/12 | chr5 | 150758768 |