geneid | 83544 |
---|---|
ensemblid | ENSG00000119661.15 |
hgncid | 23247 |
symbol | DNAL1 |
name | dynein axonemal light chain 1 |
refseq_nuc | NM_031427.4 |
refseq_prot | NP_113615.2 |
ensembl_nuc | ENST00000553645.7 |
ensembl_prot | ENSP00000452037.1 |
mane_status | MANE Select |
chr | chr14 |
start | 73644986 |
end | 73703732 |
strand | + |
ver | v1.2 |
region | chr14:73644986-73703732 |
region5000 | chr14:73639986-73708732 |
regionname0 | DNAL1_chr14_73644986_73703732 |
regionname5000 | DNAL1_chr14_73639986_73708732 |
ahapid | grch38/chm13v2 | alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 190 | 339 | 90 | 67 | 128 | 14 | 38 | 88 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0002 | 0/0 | 190 | 1 | 0 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
thapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 7851 | 39 | 1 | 6 | 24 | 0 | 8 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0002 | 0/0 | 7842 | 31 | 4 | 0 | 25 | 1 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0003 | 0/0 | 7839 | 23 | 1 | 13 | 1 | 3 | 5 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0004 | 1/1 | 7845 | 18 | 1 | 7 | 3 | 1 | 4 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0005 | 0/0 | 7844 | 17 | 0 | 2 | 15 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0006 | 0/0 | 7851 | 15 | 0 | 0 | 15 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0007 | 0/0 | 7844 | 11 | 0 | 0 | 9 | 0 | 2 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0008 | 0/0 | 7843 | 10 | 5 | 2 | 0 | 2 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0009 | 0/0 | 7843 | 10 | 8 | 2 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0010 | 0/0 | 7851 | 9 | 0 | 4 | 4 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0011 | 0/0 | 7853 | 7 | 1 | 2 | 3 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0012 | 0/0 | 7845 | 5 | 5 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0013 | 0/0 | 7839 | 5 | 0 | 3 | 1 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0014 | 0/0 | 7849 | 5 | 2 | 0 | 0 | 1 | 2 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0015 | 0/0 | 7845 | 5 | 1 | 0 | 3 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0016 | 0/0 | 7848 | 5 | 5 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0017 | 0/0 | 7843 | 4 | 3 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0018 | 0/0 | 7844 | 4 | 0 | 4 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0019 | 0/0 | 7852 | 4 | 0 | 0 | 2 | 1 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0020 | 0/0 | 7852 | 4 | 4 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0021 | 0/0 | 7848 | 4 | 3 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0022 | 0/0 | 7839 | 3 | 0 | 3 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0023 | 0/0 | 7845 | 3 | 0 | 3 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0024 | 0/0 | 7842 | 3 | 1 | 2 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0025 | 0/0 | 7844 | 3 | 0 | 2 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0026 | 0/0 | 7845 | 3 | 0 | 0 | 3 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0027 | 0/0 | 7844 | 3 | 0 | 0 | 3 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0028 | 0/0 | 7844 | 3 | 3 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0029 | 0/0 | 7837 | 2 | 2 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0030 | 0/0 | 7845 | 2 | 0 | 0 | 2 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0031 | 0/0 | 7844 | 2 | 0 | 0 | 1 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0032 | 0/0 | 7853 | 2 | 2 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0033 | 0/0 | 7845 | 2 | 2 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0034 | 0/0 | 7843 | 2 | 0 | 1 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0035 | 0/0 | 7844 | 2 | 0 | 2 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0036 | 0/0 | 7844 | 2 | 0 | 0 | 2 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0037 | 0/0 | 7837 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0038 | 0/0 | 7845 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0039 | 0/0 | 7845 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0040 | 0/0 | 7845 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0041 | 0/0 | 7845 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0042 | 0/0 | 7845 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0043 | 0/0 | 7842 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0044 | 0/0 | 7838 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0045 | 0/0 | 7841 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0046 | 0/0 | 7838 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0047 | 0/0 | 7839 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0048 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0049 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0050 | 0/0 | 7840 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0051 | 0/0 | 7846 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0052 | 0/0 | 7841 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0053 | 0/0 | 7845 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0054 | 0/0 | 7845 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0055 | 0/0 | 7845 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0056 | 0/0 | 7850 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0057 | 0/0 | 7845 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0058 | 0/0 | 7844 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0059 | 0/0 | 7843 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0060 | 0/0 | 7837 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0061 | 0/0 | 7845 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0062 | 0/0 | 7845 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0063 | 0/0 | 7844 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0064 | 0/0 | 7843 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0065 | 0/0 | 7844 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0066 | 0/0 | 7840 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0067 | 0/0 | 7844 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0068 | 0/0 | 7849 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0069 | 0/0 | 7851 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0070 | 0/0 | 7852 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0071 | 0/0 | 7853 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0072 | 0/0 | 7853 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0073 | 0/0 | 7847 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0074 | 0/0 | 7851 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0075 | 0/0 | 7851 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0076 | 0/0 | 7852 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0077 | 0/0 | 7850 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0078 | 0/0 | 7852 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0079 | 0/0 | 7850 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0080 | 0/0 | 7843 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0081 | 0/0 | 7842 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0082 | 0/0 | 7844 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0083 | 0/0 | 7847 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0084 | 0/0 | 7843 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0085 | 0/0 | 7843 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0086 | 0/0 | 7841 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0087 | 0/0 | 7843 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0088 | 0/0 | 7845 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0089 | 0/0 | 7843 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0090 | 0/0 | 7845 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0091 | 0/0 | 7844 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0092 | 0/0 | 7846 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0093 | 0/0 | 7846 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0094 | 0/0 | 7844 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0095 | 0/0 | 7844 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0096 | 0/0 | 7844 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0097 | 0/0 | 7840 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0098 | 0/0 | 7842 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0099 | 0/0 | 7844 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0100 | 0/0 | 7843 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0101 | 0/0 | 7842 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0102 | 0/0 | 7852 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0103 | 0/0 | 7844 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
t0104 | 0/0 | 7847 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
ghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0004 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0031 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
achapid | grch38/chm13v2 | clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 573 | 339 | 90 | 67 | 128 | 14 | 38 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0002c0002 | 0/0 | 573 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 8423 | 39 | 1 | 6 | 24 | 0 | 8 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0002 | 0/0 | 8414 | 31 | 4 | 0 | 25 | 1 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0003 | 0/0 | 8411 | 22 | 1 | 12 | 1 | 3 | 5 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0004 | 1/1 | 8417 | 18 | 1 | 7 | 3 | 1 | 4 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0005 | 0/0 | 8416 | 17 | 0 | 2 | 15 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0006 | 0/0 | 8423 | 15 | 0 | 0 | 15 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0007 | 0/0 | 8416 | 11 | 0 | 0 | 9 | 0 | 2 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0008 | 0/0 | 8415 | 10 | 5 | 2 | 0 | 2 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0009 | 0/0 | 8415 | 10 | 8 | 2 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0010 | 0/0 | 8423 | 9 | 0 | 4 | 4 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0011 | 0/0 | 8425 | 7 | 1 | 2 | 3 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0012 | 0/0 | 8417 | 5 | 5 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0013 | 0/0 | 8411 | 5 | 0 | 3 | 1 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0014 | 0/0 | 8421 | 5 | 2 | 0 | 0 | 1 | 2 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0015 | 0/0 | 8417 | 5 | 1 | 0 | 3 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0016 | 0/0 | 8420 | 5 | 5 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0017 | 0/0 | 8415 | 4 | 3 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0018 | 0/0 | 8416 | 4 | 0 | 4 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0019 | 0/0 | 8424 | 4 | 0 | 0 | 2 | 1 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0020 | 0/0 | 8424 | 4 | 4 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0021 | 0/0 | 8420 | 4 | 3 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0022 | 0/0 | 8411 | 3 | 0 | 3 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0023 | 0/0 | 8417 | 3 | 0 | 3 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0024 | 0/0 | 8414 | 3 | 1 | 2 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0025 | 0/0 | 8416 | 3 | 0 | 2 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0026 | 0/0 | 8417 | 3 | 0 | 0 | 3 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0027 | 0/0 | 8416 | 3 | 0 | 0 | 3 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0028 | 0/0 | 8416 | 3 | 3 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0029 | 0/0 | 8409 | 2 | 2 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0030 | 0/0 | 8417 | 2 | 0 | 0 | 2 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0031 | 0/0 | 8416 | 2 | 0 | 0 | 1 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0032 | 0/0 | 8425 | 2 | 2 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0033 | 0/0 | 8417 | 2 | 2 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0034 | 0/0 | 8415 | 2 | 0 | 1 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0035 | 0/0 | 8416 | 2 | 0 | 2 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0036 | 0/0 | 8416 | 2 | 0 | 0 | 2 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0037 | 0/0 | 8409 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0038 | 0/0 | 8417 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0039 | 0/0 | 8417 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0040 | 0/0 | 8417 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0041 | 0/0 | 8417 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0042 | 0/0 | 8417 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0043 | 0/0 | 8414 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0044 | 0/0 | 8410 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0045 | 0/0 | 8413 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0046 | 0/0 | 8410 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0047 | 0/0 | 8411 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0048 | 0/0 | 8413 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0049 | 0/0 | 8413 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0050 | 0/0 | 8412 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0051 | 0/0 | 8418 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0052 | 0/0 | 8413 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0053 | 0/0 | 8417 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0054 | 0/0 | 8417 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0055 | 0/0 | 8417 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0056 | 0/0 | 8422 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0057 | 0/0 | 8417 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0058 | 0/0 | 8416 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0059 | 0/0 | 8415 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0060 | 0/0 | 8409 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0061 | 0/0 | 8417 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0062 | 0/0 | 8417 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0063 | 0/0 | 8416 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0064 | 0/0 | 8415 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0065 | 0/0 | 8416 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0066 | 0/0 | 8412 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0067 | 0/0 | 8416 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0068 | 0/0 | 8421 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0069 | 0/0 | 8423 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0070 | 0/0 | 8424 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0071 | 0/0 | 8425 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0072 | 0/0 | 8425 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0073 | 0/0 | 8419 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0074 | 0/0 | 8423 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0075 | 0/0 | 8423 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0076 | 0/0 | 8424 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0077 | 0/0 | 8422 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0078 | 0/0 | 8424 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0079 | 0/0 | 8422 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0080 | 0/0 | 8415 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0081 | 0/0 | 8414 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0082 | 0/0 | 8416 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0083 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0084 | 0/0 | 8415 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0085 | 0/0 | 8415 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0086 | 0/0 | 8413 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0087 | 0/0 | 8415 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0088 | 0/0 | 8417 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0089 | 0/0 | 8415 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0090 | 0/0 | 8417 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0091 | 0/0 | 8416 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0092 | 0/0 | 8418 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0093 | 0/0 | 8418 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0094 | 0/0 | 8416 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0095 | 0/0 | 8416 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0096 | 0/0 | 8416 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0097 | 0/0 | 8412 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0098 | 0/0 | 8414 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0099 | 0/0 | 8416 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0100 | 0/0 | 8415 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0101 | 0/0 | 8414 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0102 | 0/0 | 8424 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0103 | 0/0 | 8416 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0001c0001t0104 | 0/0 | 8419 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
a0002c0002t0003 | 0/0 | 8411 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | copy fasta | chr14 | 73639986 | 73708732 |
actghapid | grch38/chm13v2 | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0237 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0240 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0241 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0242 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0245 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0246 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0247 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0248 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0256 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0262 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0267 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0269 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0271 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0272 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0276 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0277 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0279 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0283 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0284 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0286 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0287 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0288 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0290 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0291 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0292 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0294 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0298 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0299 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0003 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0154 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0155 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0157 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0159 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0174 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0185 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0186 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0187 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0188 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0193 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0002g0194 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0010 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0040 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0041 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0042 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0046 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0047 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0053 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0054 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0055 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0056 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0060 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0061 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0062 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0063 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0064 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0065 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0066 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0068 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0069 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0003g0308 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0004g0011 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0004g0013 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0004g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0004g0015 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0004g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0004g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0004g0019 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0004g0022 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0004g0023 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0004g0026 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0004g0031 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0004g0032 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0004g0034 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0004g0035 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0004g0038 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0004g0039 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0004g0177 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0004g0243 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0005g0085 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0005g0091 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0005g0092 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0005g0097 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0005g0098 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0005g0105 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0005g0106 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0005g0107 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0005g0108 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0005g0113 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0005g0116 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0005g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0005g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0005g0136 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0005g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0005g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0005g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0006g0004 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0006g0006 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0006g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0006g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0006g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0006g0263 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0006g0268 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0006g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0006g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0006g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0006g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0006g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0006g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0006g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0007g0210 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0007g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0007g0212 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0007g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0007g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0007g0216 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0007g0219 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0007g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0007g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0007g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0007g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0008g0090 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0008g0126 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0008g0127 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0008g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0008g0130 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0008g0139 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0008g0144 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0008g0145 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0008g0146 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0009g0086 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0009g0093 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0009g0101 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0009g0102 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0009g0111 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0009g0149 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0009g0150 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0009g0151 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0009g0153 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0009g0327 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0010g0072 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0010g0073 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0010g0075 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0010g0076 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0010g0077 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0010g0078 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0010g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0010g0254 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0010g0255 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0011g0005 | 0/0 | 2 | 0 | 2 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0011g0236 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0011g0238 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0011g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0011g0275 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0011g0285 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0012g0198 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0012g0199 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0012g0200 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0012g0201 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0012g0202 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0013g0001 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0013g0043 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0013g0049 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0013g0051 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0013g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0014g0328 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0014g0329 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0014g0330 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0014g0331 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0014g0333 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0015g0109 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0015g0121 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0015g0122 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0015g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0015g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0016g0320 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0016g0321 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0016g0322 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0016g0323 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0016g0324 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0017g0205 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0017g0207 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0017g0208 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0017g0209 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0018g0215 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0018g0228 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0018g0229 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0018g0230 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0019g0239 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0019g0259 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0019g0278 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0019g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0020g0310 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0020g0311 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0020g0313 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0020g0315 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0021g0317 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0021g0318 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0021g0319 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0021g0325 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0022g0057 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0022g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0022g0059 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0023g0024 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0023g0028 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0023g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0024g0172 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0024g0173 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0024g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0025g0156 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0025g0163 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0025g0169 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0026g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0026g0096 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0026g0120 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0027g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0027g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0028g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0028g0134 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0028g0135 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0029g0079 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0029g0081 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0030g0029 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0030g0033 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0031g0221 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0031g0227 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0032g0088 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0032g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0033g0226 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0033g0232 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0034g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0034g0190 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0035g0168 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0035g0170 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0036g0095 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0036g0119 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0037g0080 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0038g0084 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0039g0197 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0040g0206 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0041g0203 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0042g0196 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0043g0204 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0044g0050 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0045g0044 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0046g0048 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0047g0067 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0048g0082 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0049g0071 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0050g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0051g0020 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0052g0235 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0053g0037 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0054g0030 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0055g0016 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0056g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0057g0234 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0058g0220 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0059g0176 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0060g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0061g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0062g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0063g0021 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0064g0233 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0065g0218 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0066g0141 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0067g0217 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0068g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0069g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0070g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0071g0273 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0072g0027 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0073g0083 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0074g0252 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0075g0289 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0076g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0077g0266 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0078g0074 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0079g0244 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0080g0225 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0081g0129 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0082g0140 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0083g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0084g0110 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0085g0125 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0086g0094 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0087g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0088g0112 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0089g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0090g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0091g0133 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0092g0131 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0093g0142 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0094g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0095g0148 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0096g0123 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0097g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0098g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0099g0195 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0100g0132 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0101g0314 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0102g0316 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0103g0309 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0001c0001t0104g0312 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
a0002c0002t0003g0070 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0003 | g0040 | EUR | GBR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00099 | hp2 | a0001 | c0001 | t0002 | g0188 | EUR | GBR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00140 | hp1 | a0001 | c0001 | t0047 | g0067 | EUR | GBR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00140 | hp2 | a0001 | c0001 | t0011 | g0275 | EUR | GBR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00323 | hp1 | a0001 | c0001 | t0003 | g0046 | EUR | FIN | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00323 | hp2 | a0001 | c0001 | t0013 | g0051 | EUR | FIN | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00423 | hp1 | a0001 | c0001 | t0053 | g0037 | EAS | CHS | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00423 | hp2 | a0001 | c0001 | t0001 | g0293 | EAS | CHS | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00438 | hp1 | a0001 | c0001 | t0005 | g0085 | EAS | CHS | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00438 | hp2 | a0001 | c0001 | t0006 | g0304 | EAS | CHS | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00544 | hp1 | a0001 | c0001 | t0006 | g0249 | EAS | CHS | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00544 | hp2 | a0001 | c0001 | t0005 | g0117 | EAS | CHS | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00558 | hp1 | a0001 | c0001 | t0005 | g0106 | EAS | CHS | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00558 | hp2 | a0001 | c0001 | t0002 | g0184 | EAS | CHS | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0004 | EAS | CHS | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00621 | hp2 | a0001 | c0001 | t0096 | g0123 | EAS | CHS | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00639 | hp1 | a0001 | c0001 | t0023 | g0036 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00639 | hp2 | a0001 | c0001 | t0022 | g0058 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00642 | hp1 | a0001 | c0001 | t0034 | g0190 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00642 | hp2 | a0001 | c0001 | t0011 | g0005 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00733 | hp1 | a0001 | c0001 | t0003 | g0063 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00733 | hp2 | a0001 | c0001 | t0025 | g0163 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00735 | hp1 | a0001 | c0001 | t0011 | g0005 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00735 | hp2 | a0001 | c0001 | t0004 | g0032 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00738 | hp1 | a0001 | c0001 | t0035 | g0168 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG00738 | hp2 | a0001 | c0001 | t0008 | g0090 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01069 | hp1 | a0001 | c0001 | t0003 | g0061 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01069 | hp2 | a0001 | c0001 | t0018 | g0229 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0276 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01070 | hp2 | a0001 | c0001 | t0022 | g0059 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01071 | hp1 | a0001 | c0001 | t0018 | g0228 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01071 | hp2 | a0001 | c0001 | t0022 | g0057 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01074 | hp1 | a0001 | c0001 | t0024 | g0172 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01074 | hp2 | a0001 | c0001 | t0009 | g0102 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01081 | hp1 | a0001 | c0001 | t0008 | g0130 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01081 | hp2 | a0001 | c0001 | t0005 | g0136 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01099 | hp1 | a0001 | c0001 | t0046 | g0048 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01099 | hp2 | a0001 | c0001 | t0024 | g0173 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01109 | hp1 | a0001 | c0001 | t0084 | g0110 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01109 | hp2 | a0001 | c0001 | t0021 | g0319 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01167 | hp1 | a0001 | c0001 | t0079 | g0244 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01167 | hp2 | a0001 | c0001 | t0023 | g0024 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01168 | hp1 | a0001 | c0001 | t0056 | g0332 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01168 | hp2 | a0001 | c0001 | t0003 | g0068 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01169 | hp1 | a0001 | c0001 | t0003 | g0060 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01169 | hp2 | a0001 | c0001 | t0010 | g0254 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01175 | hp1 | a0001 | c0001 | t0013 | g0043 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01175 | hp2 | a0001 | c0001 | t0059 | g0176 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01192 | hp1 | a0001 | c0001 | t0018 | g0230 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01192 | hp2 | a0001 | c0001 | t0001 | g0277 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01243 | hp1 | a0001 | c0001 | t0009 | g0101 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01243 | hp2 | a0001 | c0001 | t0017 | g0205 | AMR | PUR | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01255 | hp1 | a0001 | c0001 | t0004 | g0019 | AMR | CLM | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01255 | hp2 | a0002 | c0002 | t0003 | g0070 | AMR | CLM | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01256 | hp1 | a0001 | c0001 | t0003 | g0047 | AMR | CLM | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01256 | hp2 | a0001 | c0001 | t0005 | g0118 | AMR | CLM | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01261 | hp1 | a0001 | c0001 | t0004 | g0013 | AMR | CLM | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01261 | hp2 | a0001 | c0001 | t0023 | g0028 | AMR | CLM | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01358 | hp1 | a0001 | c0001 | t0025 | g0169 | AMR | CLM | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01358 | hp2 | a0001 | c0001 | t0010 | g0073 | AMR | CLM | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01433 | hp1 | a0001 | c0001 | t0004 | g0011 | AMR | CLM | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01433 | hp2 | a0001 | c0001 | t0003 | g0062 | AMR | CLM | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01496 | hp1 | a0001 | c0001 | t0003 | g0045 | AMR | CLM | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01496 | hp2 | a0001 | c0001 | t0093 | g0142 | AMR | CLM | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01515 | hp1 | a0001 | c0001 | t0008 | g0144 | EUR | IBS | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01515 | hp2 | a0001 | c0001 | t0014 | g0330 | EUR | IBS | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01517 | hp1 | a0001 | c0001 | t0071 | g0273 | EUR | IBS | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01517 | hp2 | a0001 | c0001 | t0008 | g0145 | EUR | IBS | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01884 | hp1 | a0001 | c0001 | t0100 | g0132 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01884 | hp2 | a0001 | c0001 | t0101 | g0314 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01891 | hp1 | a0001 | c0001 | t0040 | g0206 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01891 | hp2 | a0001 | c0001 | t0020 | g0315 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01928 | hp1 | a0001 | c0001 | t0003 | g0056 | AMR | PEL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01928 | hp2 | a0001 | c0001 | t0076 | g0265 | AMR | PEL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01934 | hp1 | a0001 | c0001 | t0018 | g0215 | AMR | PEL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01934 | hp2 | a0001 | c0001 | t0013 | g0049 | AMR | PEL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01943 | hp1 | a0001 | c0001 | t0003 | g0010 | AMR | PEL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01943 | hp2 | a0001 | c0001 | t0001 | g0256 | AMR | PEL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01952 | hp1 | a0001 | c0001 | t0004 | g0018 | AMR | PEL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01952 | hp2 | a0001 | c0001 | t0010 | g0255 | AMR | PEL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0248 | AMR | PEL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01975 | hp2 | a0001 | c0001 | t0003 | g0001 | AMR | PEL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01978 | hp1 | a0001 | c0001 | t0010 | g0072 | AMR | PEL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01978 | hp2 | a0001 | c0001 | t0003 | g0064 | AMR | PEL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01993 | hp1 | a0001 | c0001 | t0004 | g0034 | AMR | PEL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01993 | hp2 | a0001 | c0001 | t0001 | g0245 | AMR | PEL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02015 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02015 | hp2 | a0001 | c0001 | t0002 | g0161 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02027 | hp1 | a0001 | c0001 | t0015 | g0109 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02027 | hp2 | a0001 | c0001 | t0011 | g0285 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02040 | hp1 | a0001 | c0001 | t0030 | g0033 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02040 | hp2 | a0001 | c0001 | t0013 | g0052 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02055 | hp1 | a0001 | c0001 | t0016 | g0320 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02055 | hp2 | a0001 | c0001 | t0004 | g0014 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02056 | hp1 | a0001 | c0001 | t0001 | g0242 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02056 | hp2 | a0001 | c0001 | t0002 | g0193 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02071 | hp1 | a0001 | c0001 | t0006 | g0250 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02071 | hp2 | a0001 | c0001 | t0030 | g0029 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02074 | hp1 | a0001 | c0001 | t0051 | g0020 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02074 | hp2 | a0001 | c0001 | t0006 | g0305 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02080 | hp1 | a0001 | c0001 | t0019 | g0278 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02080 | hp2 | a0001 | c0001 | t0007 | g0213 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02083 | hp1 | a0001 | c0001 | t0007 | g0214 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02083 | hp2 | a0001 | c0001 | t0001 | g0297 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02129 | hp1 | a0001 | c0001 | t0001 | g0261 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02129 | hp2 | a0001 | c0001 | t0003 | g0066 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02135 | hp1 | a0001 | c0001 | t0007 | g0222 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02135 | hp2 | a0001 | c0001 | t0006 | g0260 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02145 | hp1 | a0001 | c0001 | t0008 | g0146 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02145 | hp2 | a0001 | c0001 | t0083 | g0104 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02148 | hp1 | a0001 | c0001 | t0013 | g0001 | AMR | PEL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02148 | hp2 | a0001 | c0001 | t0055 | g0016 | AMR | PEL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02155 | hp1 | a0001 | c0001 | t0002 | g0164 | EAS | CDX | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02155 | hp2 | a0001 | c0001 | t0006 | g0006 | EAS | CDX | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02165 | hp1 | a0001 | c0001 | t0010 | g0253 | EAS | CDX | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02165 | hp2 | a0001 | c0001 | t0002 | g0154 | EAS | CDX | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02257 | hp1 | a0001 | c0001 | t0002 | g0157 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02257 | hp2 | a0001 | c0001 | t0016 | g0324 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02258 | hp1 | a0001 | c0001 | t0061 | g0008 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02258 | hp2 | a0001 | c0001 | t0009 | g0151 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02293 | hp1 | a0001 | c0001 | t0003 | g0055 | AMR | PEL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02293 | hp2 | a0001 | c0001 | t0001 | g0247 | AMR | PEL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02451 | hp1 | a0001 | c0001 | t0016 | g0323 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02451 | hp2 | a0001 | c0001 | t0021 | g0325 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02523 | hp1 | a0001 | c0001 | t0006 | g0263 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02523 | hp2 | a0001 | c0001 | t0004 | g0015 | EAS | KHV | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02602 | hp1 | a0001 | c0001 | t0003 | g0053 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02602 | hp2 | a0001 | c0001 | t0001 | g0279 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02615 | hp1 | a0001 | c0001 | t0016 | g0322 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02615 | hp2 | a0001 | c0001 | t0065 | g0218 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02622 | hp1 | a0001 | c0001 | t0009 | g0327 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02622 | hp2 | a0001 | c0001 | t0014 | g0331 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02630 | hp1 | a0001 | c0001 | t0041 | g0203 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02630 | hp2 | a0001 | c0001 | t0008 | g0099 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02647 | hp1 | a0001 | c0001 | t0024 | g0175 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02647 | hp2 | a0001 | c0001 | t0008 | g0128 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02683 | hp1 | a0001 | c0001 | t0001 | g0294 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02683 | hp2 | a0001 | c0001 | t0008 | g0127 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02698 | hp1 | a0001 | c0001 | t0004 | g0038 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02698 | hp2 | a0001 | c0001 | t0073 | g0083 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02717 | hp1 | a0001 | c0001 | t0039 | g0197 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02717 | hp2 | a0001 | c0001 | t0089 | g0124 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02723 | hp1 | a0001 | c0001 | t0033 | g0232 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02723 | hp2 | a0001 | c0001 | t0012 | g0200 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02735 | hp1 | a0001 | c0001 | t0058 | g0220 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02735 | hp2 | a0001 | c0001 | t0003 | g0065 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02738 | hp1 | a0001 | c0001 | t0003 | g0308 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02738 | hp2 | a0001 | c0001 | t0019 | g0239 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02818 | hp1 | a0001 | c0001 | t0087 | g0103 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02818 | hp2 | a0001 | c0001 | t0042 | g0196 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02886 | hp1 | a0001 | c0001 | t0048 | g0082 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02886 | hp2 | a0001 | c0001 | t0052 | g0235 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02895 | hp1 | a0001 | c0001 | t0043 | g0204 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02895 | hp2 | a0001 | c0001 | t0002 | g0186 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02897 | hp1 | a0001 | c0001 | t0002 | g0187 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02897 | hp2 | a0001 | c0001 | t0009 | g0149 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02922 | hp1 | a0001 | c0001 | t0015 | g0334 | AFR | ESN | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02922 | hp2 | a0001 | c0001 | t0080 | g0225 | AFR | ESN | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02970 | hp1 | a0001 | c0001 | t0009 | g0093 | AFR | ESN | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02970 | hp2 | a0001 | c0001 | t0060 | g0009 | AFR | ESN | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02976 | hp1 | a0001 | c0001 | t0091 | g0133 | AFR | ESN | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02976 | hp2 | a0001 | c0001 | t0012 | g0199 | AFR | ESN | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03017 | hp1 | a0001 | c0001 | t0095 | g0148 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03017 | hp2 | a0001 | c0001 | t0010 | g0078 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03041 | hp1 | a0001 | c0001 | t0037 | g0080 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03041 | hp2 | a0001 | c0001 | t0094 | g0100 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0086 | AFR | MSL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03098 | hp2 | a0001 | c0001 | t0090 | g0114 | AFR | MSL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03130 | hp1 | a0001 | c0001 | t0029 | g0079 | AFR | ESN | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03130 | hp2 | a0001 | c0001 | t0008 | g0126 | AFR | ESN | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03139 | hp1 | a0001 | c0001 | t0038 | g0084 | AFR | ESN | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03139 | hp2 | a0001 | c0001 | t0020 | g0310 | AFR | ESN | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03195 | hp1 | a0001 | c0001 | t0088 | g0112 | AFR | ESN | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03195 | hp2 | a0001 | c0001 | t0085 | g0125 | AFR | ESN | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03209 | hp1 | a0001 | c0001 | t0021 | g0318 | AFR | MSL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03209 | hp2 | a0001 | c0001 | t0092 | g0131 | AFR | MSL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03225 | hp1 | a0001 | c0001 | t0098 | g0326 | AFR | MSL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03225 | hp2 | a0001 | c0001 | t0021 | g0317 | AFR | MSL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03239 | hp1 | a0001 | c0001 | t0044 | g0050 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03239 | hp2 | a0001 | c0001 | t0004 | g0017 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03453 | hp1 | a0001 | c0001 | t0049 | g0071 | AFR | MSL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03453 | hp2 | a0001 | c0001 | t0002 | g0174 | AFR | MSL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03486 | hp1 | a0001 | c0001 | t0028 | g0135 | AFR | MSL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03486 | hp2 | a0001 | c0001 | t0017 | g0208 | AFR | MSL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03491 | hp1 | a0001 | c0001 | t0077 | g0266 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03491 | hp2 | a0001 | c0001 | t0003 | g0069 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03492 | hp1 | a0001 | c0001 | t0001 | g0267 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03492 | hp2 | a0001 | c0001 | t0014 | g0333 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03516 | hp1 | a0001 | c0001 | t0012 | g0201 | AFR | ESN | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03516 | hp2 | a0001 | c0001 | t0009 | g0150 | AFR | ESN | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03540 | hp1 | a0001 | c0001 | t0050 | g0012 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03540 | hp2 | a0001 | c0001 | t0017 | g0207 | AFR | GWD | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03579 | hp1 | a0001 | c0001 | t0066 | g0141 | AFR | MSL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03579 | hp2 | a0001 | c0001 | t0104 | g0312 | AFR | MSL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03654 | hp1 | a0001 | c0001 | t0001 | g0246 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03654 | hp2 | a0001 | c0001 | t0062 | g0025 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03688 | hp1 | a0001 | c0001 | t0074 | g0252 | SAS | STU | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03688 | hp2 | a0001 | c0001 | t0034 | g0158 | SAS | STU | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03704 | hp1 | a0001 | c0001 | t0001 | g0237 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03704 | hp2 | a0001 | c0001 | t0014 | g0329 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03710 | hp1 | a0001 | c0001 | t0007 | g0212 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03710 | hp2 | a0001 | c0001 | t0015 | g0122 | SAS | PJL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03927 | hp1 | a0001 | c0001 | t0004 | g0023 | SAS | BEB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03927 | hp2 | a0001 | c0001 | t0003 | g0042 | SAS | BEB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03942 | hp1 | a0001 | c0001 | t0054 | g0030 | SAS | BEB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03942 | hp2 | a0001 | c0001 | t0031 | g0227 | SAS | BEB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG04115 | hp1 | a0001 | c0001 | t0007 | g0219 | SAS | STU | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG04115 | hp2 | a0001 | c0001 | t0001 | g0241 | SAS | STU | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG04184 | hp1 | a0001 | c0001 | t0045 | g0044 | SAS | BEB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG04184 | hp2 | a0001 | c0001 | t0002 | g0159 | SAS | BEB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG04204 | hp1 | a0001 | c0001 | t0067 | g0217 | SAS | STU | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG04204 | hp2 | a0001 | c0001 | t0001 | g0257 | SAS | STU | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG04228 | hp1 | a0001 | c0001 | t0004 | g0022 | SAS | STU | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0298 | SAS | STU | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18522 | hp1 | a0001 | c0001 | t0028 | g0115 | AFR | YRI | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18522 | hp2 | a0001 | c0001 | t0033 | g0226 | AFR | YRI | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18612 | hp1 | a0001 | c0001 | t0027 | g0002 | EAS | CHB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18612 | hp2 | a0001 | c0001 | t0002 | g0165 | EAS | CHB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18747 | hp1 | a0001 | c0001 | t0027 | g0002 | EAS | CHB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18747 | hp2 | a0001 | c0001 | t0001 | g0287 | EAS | CHB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18906 | hp1 | a0001 | c0001 | t0017 | g0209 | AFR | YRI | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18906 | hp2 | a0001 | c0001 | t0032 | g0088 | AFR | YRI | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18942 | hp1 | a0001 | c0001 | t0070 | g0306 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18942 | hp2 | a0001 | c0001 | t0005 | g0138 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18944 | hp1 | a0001 | c0001 | t0007 | g0210 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18944 | hp2 | a0001 | c0001 | t0001 | g0296 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18945 | hp1 | a0001 | c0001 | t0001 | g0291 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18945 | hp2 | a0001 | c0001 | t0002 | g0155 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0288 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18946 | hp2 | a0001 | c0001 | t0099 | g0195 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18947 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18947 | hp2 | a0001 | c0001 | t0010 | g0075 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18950 | hp1 | a0001 | c0001 | t0011 | g0236 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18950 | hp2 | a0001 | c0001 | t0002 | g0167 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18952 | hp1 | a0001 | c0001 | t0002 | g0166 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18952 | hp2 | a0001 | c0001 | t0005 | g0116 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18954 | hp1 | a0001 | c0001 | t0005 | g0113 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18954 | hp2 | a0001 | c0001 | t0006 | g0301 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18956 | hp1 | a0001 | c0001 | t0001 | g0264 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18956 | hp2 | a0001 | c0001 | t0026 | g0087 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18957 | hp1 | a0001 | c0001 | t0002 | g0194 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18957 | hp2 | a0001 | c0001 | t0015 | g0121 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18961 | hp1 | a0001 | c0001 | t0002 | g0003 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18961 | hp2 | a0001 | c0001 | t0036 | g0095 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18962 | hp1 | a0001 | c0001 | t0002 | g0182 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18962 | hp2 | a0001 | c0001 | t0011 | g0238 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18964 | hp1 | a0001 | c0001 | t0006 | g0302 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18964 | hp2 | a0001 | c0001 | t0007 | g0223 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18971 | hp1 | a0001 | c0001 | t0005 | g0108 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18971 | hp2 | a0001 | c0001 | t0010 | g0076 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18972 | hp1 | a0001 | c0001 | t0015 | g0143 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18972 | hp2 | a0001 | c0001 | t0002 | g0183 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18973 | hp1 | a0001 | c0001 | t0078 | g0074 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18973 | hp2 | a0001 | c0001 | t0086 | g0094 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18978 | hp1 | a0001 | c0001 | t0004 | g0243 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18978 | hp2 | a0001 | c0001 | t0072 | g0027 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18979 | hp1 | a0001 | c0001 | t0006 | g0280 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18979 | hp2 | a0001 | c0001 | t0026 | g0096 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18980 | hp1 | a0001 | c0001 | t0004 | g0026 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18980 | hp2 | a0001 | c0001 | t0007 | g0216 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18981 | hp1 | a0001 | c0001 | t0027 | g0152 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18981 | hp2 | a0001 | c0001 | t0068 | g0251 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18984 | hp1 | a0001 | c0001 | t0063 | g0021 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18984 | hp2 | a0001 | c0001 | t0006 | g0281 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18986 | hp1 | a0001 | c0001 | t0006 | g0006 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18986 | hp2 | a0001 | c0001 | t0007 | g0224 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18988 | hp1 | a0001 | c0001 | t0002 | g0179 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18988 | hp2 | a0001 | c0001 | t0001 | g0270 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18991 | hp1 | a0001 | c0001 | t0005 | g0098 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18991 | hp2 | a0001 | c0001 | t0001 | g0292 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0162 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18994 | hp2 | a0001 | c0001 | t0026 | g0120 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18998 | hp1 | a0001 | c0001 | t0002 | g0191 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18998 | hp2 | a0001 | c0001 | t0001 | g0271 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18999 | hp1 | a0001 | c0001 | t0069 | g0282 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA18999 | hp2 | a0001 | c0001 | t0005 | g0097 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19000 | hp1 | a0001 | c0001 | t0002 | g0189 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19000 | hp2 | a0001 | c0001 | t0001 | g0272 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19007 | hp1 | a0001 | c0001 | t0010 | g0077 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19007 | hp2 | a0001 | c0001 | t0002 | g0181 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19009 | hp1 | a0001 | c0001 | t0007 | g0231 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0269 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0286 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19010 | hp2 | a0001 | c0001 | t0002 | g0171 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19011 | hp1 | a0001 | c0001 | t0005 | g0137 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19011 | hp2 | a0001 | c0001 | t0001 | g0283 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19012 | hp1 | a0001 | c0001 | t0036 | g0119 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19012 | hp2 | a0001 | c0001 | t0001 | g0258 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19030 | hp1 | a0001 | c0001 | t0020 | g0311 | AFR | LWK | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19030 | hp2 | a0001 | c0001 | t0009 | g0111 | AFR | LWK | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19043 | hp1 | a0001 | c0001 | t0028 | g0134 | AFR | LWK | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19043 | hp2 | a0001 | c0001 | t0057 | g0234 | AFR | LWK | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19055 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19055 | hp2 | a0001 | c0001 | t0002 | g0192 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19056 | hp1 | a0001 | c0001 | t0002 | g0178 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19056 | hp2 | a0001 | c0001 | t0005 | g0091 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19057 | hp1 | a0001 | c0001 | t0002 | g0185 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19057 | hp2 | a0001 | c0001 | t0001 | g0290 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19058 | hp1 | a0001 | c0001 | t0006 | g0268 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19058 | hp2 | a0001 | c0001 | t0002 | g0160 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19060 | hp1 | a0001 | c0001 | t0001 | g0284 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19060 | hp2 | a0001 | c0001 | t0006 | g0303 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19064 | hp1 | a0001 | c0001 | t0005 | g0092 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0262 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19066 | hp1 | a0001 | c0001 | t0075 | g0289 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19066 | hp2 | a0001 | c0001 | t0005 | g0147 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19078 | hp1 | a0001 | c0001 | t0031 | g0221 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19078 | hp2 | a0001 | c0001 | t0006 | g0004 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19079 | hp1 | a0001 | c0001 | t0002 | g0180 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19079 | hp2 | a0001 | c0001 | t0007 | g0211 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19085 | hp1 | a0001 | c0001 | t0001 | g0240 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19085 | hp2 | a0001 | c0001 | t0005 | g0107 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19090 | hp1 | a0001 | c0001 | t0019 | g0307 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19090 | hp2 | a0001 | c0001 | t0005 | g0105 | EAS | JPT | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19240 | hp1 | a0001 | c0001 | t0097 | g0007 | AFR | YRI | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA19240 | hp2 | a0001 | c0001 | t0102 | g0316 | AFR | YRI | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA20129 | hp1 | a0001 | c0001 | t0001 | g0299 | AFR | ASW | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA20129 | hp2 | a0001 | c0001 | t0016 | g0321 | AFR | ASW | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA20752 | hp1 | a0001 | c0001 | t0025 | g0156 | EUR | TSI | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA20752 | hp2 | a0001 | c0001 | t0004 | g0039 | EUR | TSI | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA20805 | hp1 | a0001 | c0001 | t0003 | g0041 | EUR | TSI | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA20805 | hp2 | a0001 | c0001 | t0019 | g0259 | EUR | TSI | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0035 | AMR | CLM | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG01123 | hp2 | a0001 | c0001 | t0035 | g0170 | AMR | CLM | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02109 | hp1 | a0001 | c0001 | t0012 | g0202 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02109 | hp2 | a0001 | c0001 | t0014 | g0328 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02486 | hp1 | a0001 | c0001 | t0081 | g0129 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02486 | hp2 | a0001 | c0001 | t0032 | g0089 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02559 | hp1 | a0001 | c0001 | t0064 | g0233 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG02559 | hp2 | a0001 | c0001 | t0012 | g0198 | AFR | ACB | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03471 | hp1 | a0001 | c0001 | t0029 | g0081 | AFR | MSL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG03471 | hp2 | a0001 | c0001 | t0020 | g0313 | AFR | MSL | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG06807 | hp1 | a0001 | c0001 | t0009 | g0153 | AFR | USA | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
HG06807 | hp2 | a0001 | c0001 | t0082 | g0140 | AFR | USA | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA20300 | hp1 | a0001 | c0001 | t0003 | g0054 | AFR | USA | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA20300 | hp2 | a0001 | c0001 | t0008 | g0139 | AFR | USA | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA21309 | hp1 | a0001 | c0001 | t0103 | g0309 | AFR | LWK | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
NA21309 | hp2 | a0001 | c0001 | t0011 | g0274 | AFR | LWK | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0004 | g0031 | REF | REF | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0004 | g0177 | REF | REF | DNAL1_chr14_73639986_73708732 | DNAL1 | chr14 | 73639986 | 73708732 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73689398
|
C | G | 1 | a0002 | 1 | HG01255.hp2 | missense_variant | MODERATE | c.415C>G | p.Leu139Val | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/8 | 469/8417 | 415/573 | 139/190 | chr14 | 73689398 |
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 |
---|
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73696077
|
C | CT | 7 | a0001c0001t0016a0001c0001t0020a0001c0001t0021others(4): Show | 17 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*144dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 145 | INFO_REALIGN_3_PRIME | chr14 | 73696077 | ||||
chr14:73696142
|
C | G | 28 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(25): Show | 73 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
3_prime_UTR_variant | MODIFIER | c.*200C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 200 | chr14 | 73696142 | |||||
chr14:73696144
|
A | G | 1 | a0001c0001t0080 | 1 | HG02922.hp2 | 3_prime_UTR_variant | MODIFIER | c.*202A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 202 | chr14 | 73696144 | |||||
chr14:73696147
|
T | C | 27 | a0001c0001t0003a0001c0001t0012a0001c0001t0013others(24): Show | 72 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*205T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 205 | chr14 | 73696147 | |||||
chr14:73696198
|
G | A | 1 | a0001c0001t0016 | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*256G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 256 | chr14 | 73696198 | |||||
chr14:73696287
|
A | AT | 17 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(14): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*353dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 354 | INFO_REALIGN_3_PRIME | chr14 | 73696287 | ||||
chr14:73696366
|
A | G | 1 | a0001c0001t0067 | 1 | HG04204.hp1 | 3_prime_UTR_variant | MODIFIER | c.*424A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 424 | chr14 | 73696366 | |||||
chr14:73696442
|
G | A | 2 | a0001c0001t0029a0001c0001t0037 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*500G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 500 | chr14 | 73696442 | |||||
chr14:73696922
|
G | A | 17 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(14): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*980G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 980 | chr14 | 73696922 | |||||
chr14:73697156
|
G | A | 2 | a0001c0001t0029a0001c0001t0037 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1214G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 1214 | chr14 | 73697156 | |||||
chr14:73697268
|
C | T | 1 | a0001c0001t0016 | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*1326C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 1326 | chr14 | 73697268 | |||||
chr14:73697347
|
C | A | 6 | a0001c0001t0016a0001c0001t0020a0001c0001t0101others(3): Show | 13 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*1405C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 1405 | chr14 | 73697347 | |||||
chr14:73697463
|
C | A | 1 | a0001c0001t0081 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1521C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 1521 | chr14 | 73697463 | |||||
chr14:73697515
|
G | T | 2 | a0001c0001t0048a0001c0001t0049 | 2 | HG02886.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1573G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 1573 | chr14 | 73697515 | |||||
chr14:73697632
|
A | G | 2 | a0001c0001t0029a0001c0001t0037 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1690A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 1690 | chr14 | 73697632 | |||||
chr14:73697675
|
G | A | 1 | a0001c0001t0038 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1733G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 1733 | chr14 | 73697675 | |||||
chr14:73697695
|
A | G | 1 | a0001c0001t0047 | 1 | HG00140.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1753A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 1753 | chr14 | 73697695 | |||||
chr14:73697701
|
C | G | 3 | a0001c0001t0010a0001c0001t0078a0001c0001t0079 | 11 | HG01167.hp1 HG01169.hp2 HG01358.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1759C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 1759 | chr14 | 73697701 | |||||
chr14:73697743
|
T | TA | 14 | a0001c0001t0012a0001c0001t0017a0001c0001t0019others(11): Show | 26 | HG01243.hp2 HG01891.hp1 HG02074.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*1823dupA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 1824 | INFO_REALIGN_3_PRIME | chr14 | 73697743 | ||||
chr14:73697743
|
T | TAA | 4 | a0001c0001t0016a0001c0001t0020a0001c0001t0101others(1): Show | 11 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1822_*1823dupAA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 1824 | INFO_REALIGN_3_PRIME | chr14 | 73697743 | ||||
chr14:73697743
|
TA | T | 20 | a0001c0001t0002a0001c0001t0024a0001c0001t0025others(17): Show | 57 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(54): Show |
3_prime_UTR_variant | MODIFIER | c.*1823delA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 1823 | INFO_REALIGN_3_PRIME | chr14 | 73697743 | ||||
chr14:73697744
|
A | T | 7 | a0001c0001t0003a0001c0001t0021a0001c0001t0022others(4): Show | 33 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*1802A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 1802 | chr14 | 73697744 | |||||
chr14:73697745
|
A | T | 1 | a0001c0001t0046 | 1 | HG01099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1803A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 1803 | chr14 | 73697745 | |||||
chr14:73697788
|
C | G | 17 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(14): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*1846C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 1846 | chr14 | 73697788 | |||||
chr14:73697793
|
A | C | 1 | a0001c0001t0062 | 1 | HG03654.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1851A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 1851 | chr14 | 73697793 | |||||
chr14:73697842
|
T | C | 4 | a0001c0001t0006a0001c0001t0068a0001c0001t0069others(1): Show | 18 | HG00438.hp2 HG00544.hp1 HG02071.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1900T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 1900 | chr14 | 73697842 | |||||
chr14:73698015
|
A | G | 10 | a0001c0001t0003a0001c0001t0013a0001c0001t0022others(7): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*2073A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 2073 | chr14 | 73698015 | |||||
chr14:73698036
|
C | G | 2 | a0001c0001t0029a0001c0001t0037 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2094C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 2094 | chr14 | 73698036 | |||||
chr14:73698178
|
T | G | 1 | a0001c0001t0027 | 3 | NA18612.hp1 NA18747.hp1 NA18981.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2236T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 2236 | chr14 | 73698178 | |||||
chr14:73698316
|
A | G | 1 | a0001c0001t0096 | 1 | HG00621.hp2 | 3_prime_UTR_variant | MODIFIER | c.*2374A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 2374 | chr14 | 73698316 | |||||
chr14:73698398
|
A | T | 95 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(92): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*2456A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 2456 | chr14 | 73698398 | |||||
chr14:73698526
|
T | TG | 2 | a0001c0001t0029a0001c0001t0037 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*2584_*2585insG | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 2585 | chr14 | 73698526 | |||||
chr14:73698813
|
A | G | 95 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(92): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*2871A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 2871 | chr14 | 73698813 | |||||
chr14:73699232
|
T | G | 1 | a0001c0001t0056 | 1 | HG01168.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3290T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 3290 | chr14 | 73699232 | |||||
chr14:73699237
|
T | C | 10 | a0001c0001t0003a0001c0001t0013a0001c0001t0022others(7): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
3_prime_UTR_variant | MODIFIER | c.*3295T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 3295 | chr14 | 73699237 | |||||
chr14:73699259
|
A | G | 1 | a0001c0001t0021 | 4 | HG01109.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*3317A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 3317 | chr14 | 73699259 | |||||
chr14:73699308
|
A | AT | 13 | a0001c0001t0016a0001c0001t0020a0001c0001t0029others(10): Show | 21 | HG01168.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3381dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 3382 | INFO_REALIGN_3_PRIME | chr14 | 73699308 | ||||
chr14:73699308
|
AT | A | 10 | a0001c0001t0007a0001c0001t0018a0001c0001t0031others(7): Show | 25 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*3381delT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 3381 | INFO_REALIGN_3_PRIME | chr14 | 73699308 | ||||
chr14:73699388
|
C | T | 1 | a0001c0001t0058 | 1 | HG02735.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3446C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 3446 | chr14 | 73699388 | |||||
chr14:73699453
|
G | A | 2 | a0001c0001t0048a0001c0001t0049 | 2 | HG02886.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3511G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 3511 | chr14 | 73699453 | |||||
chr14:73699469
|
C | T | 17 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(14): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*3527C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 3527 | chr14 | 73699469 | |||||
chr14:73699478
|
G | A | 1 | a0001c0001t0071 | 1 | HG01517.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3536G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 3536 | chr14 | 73699478 | |||||
chr14:73699497
|
C | CGTT | 28 | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(25): Show | 112 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(109): Show |
3_prime_UTR_variant | MODIFIER | c.*3556_*3558dupGTT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 3559 | INFO_REALIGN_3_PRIME | chr14 | 73699497 | ||||
chr14:73699595
|
C | T | 3 | a0001c0001t0012a0001c0001t0041a0001c0001t0042 | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3653C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 3653 | chr14 | 73699595 | |||||
chr14:73699740
|
CCT | C | 2 | a0001c0001t0029a0001c0001t0037 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*3803_*3804delCT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 3803 | INFO_REALIGN_3_PRIME | chr14 | 73699740 | ||||
chr14:73699847
|
G | A | 2 | a0001c0001t0084a0001c0001t0085 | 2 | HG01109.hp1 HG03195.hp2 |
3_prime_UTR_variant | MODIFIER | c.*3905G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 3905 | chr14 | 73699847 | |||||
chr14:73699887
|
A | C | 3 | a0001c0001t0025a0001c0001t0034a0001c0001t0035 | 7 | HG00642.hp1 HG00733.hp2 HG00738.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*3945A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 3945 | chr14 | 73699887 | |||||
chr14:73699974
|
A | G | 11 | a0001c0001t0007a0001c0001t0018a0001c0001t0031others(8): Show | 26 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(23): Show |
3_prime_UTR_variant | MODIFIER | c.*4032A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 4032 | chr14 | 73699974 | |||||
chr14:73700118
|
G | A | 35 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(32): Show | 116 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*4176G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 4176 | chr14 | 73700118 | |||||
chr14:73700150
|
G | A | 2 | a0001c0001t0048a0001c0001t0049 | 2 | HG02886.hp1 HG03453.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4208G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 4208 | chr14 | 73700150 | |||||
chr14:73700168
|
G | A | 2 | a0001c0001t0029a0001c0001t0037 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4226G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 4226 | chr14 | 73700168 | |||||
chr14:73700245
|
C | T | 7 | a0001c0001t0028a0001c0001t0083a0001c0001t0090others(4): Show | 9 | HG01496.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*4303C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 4303 | chr14 | 73700245 | |||||
chr14:73700279
|
G | A | 1 | a0001c0001t0030 | 2 | HG02040.hp1 HG02071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4337G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 4337 | chr14 | 73700279 | |||||
chr14:73700284
|
C | G | 2 | a0001c0001t0052a0001c0001t0057 | 2 | HG02886.hp2 NA19043.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4342C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 4342 | chr14 | 73700284 | |||||
chr14:73700347
|
C | T | 17 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(14): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*4405C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 4405 | chr14 | 73700347 | |||||
chr14:73700348
|
G | A | 1 | a0001c0001t0036 | 2 | NA18961.hp2 NA19012.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4406G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 4406 | chr14 | 73700348 | |||||
chr14:73700358
|
GA | G | 94 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(91): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
3_prime_UTR_variant | MODIFIER | c.*4427delA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 4427 | INFO_REALIGN_3_PRIME | chr14 | 73700358 | ||||
chr14:73700397
|
T | G | 1 | a0001c0001t0018 | 4 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4455T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 4455 | chr14 | 73700397 | |||||
chr14:73700398
|
G | T | 8 | a0001c0001t0012a0001c0001t0017a0001c0001t0038others(5): Show | 15 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(12): Show |
3_prime_UTR_variant | MODIFIER | c.*4456G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 4456 | chr14 | 73700398 | |||||
chr14:73700478
|
C | T | 1 | a0001c0001t0021 | 4 | HG01109.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*4536C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 4536 | chr14 | 73700478 | |||||
chr14:73700532
|
C | A | 1 | a0001c0001t0053 | 1 | HG00423.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4590C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 4590 | chr14 | 73700532 | |||||
chr14:73700668
|
C | T | 6 | a0001c0001t0002a0001c0001t0024a0001c0001t0025others(3): Show | 42 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(39): Show |
3_prime_UTR_variant | MODIFIER | c.*4726C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 4726 | chr14 | 73700668 | |||||
chr14:73700751
|
T | A | 1 | a0001c0001t0072 | 1 | NA18978.hp2 | 3_prime_UTR_variant | MODIFIER | c.*4809T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 4809 | chr14 | 73700751 | |||||
chr14:73700809
|
T | G | 2 | a0001c0001t0029a0001c0001t0037 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4867T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 4867 | chr14 | 73700809 | |||||
chr14:73701260
|
C | A | 1 | a0001c0001t0050 | 1 | HG03540.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5318C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 5318 | chr14 | 73701260 | |||||
chr14:73701381
|
TA | T | 27 | a0001c0001t0003a0001c0001t0012a0001c0001t0013others(24): Show | 72 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(69): Show |
3_prime_UTR_variant | MODIFIER | c.*5441delA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 5441 | INFO_REALIGN_3_PRIME | chr14 | 73701381 | ||||
chr14:73701384
|
C | G | 1 | a0001c0001t0089 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5442C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 5442 | chr14 | 73701384 | |||||
chr14:73701726
|
A | G | 2 | a0001c0001t0029a0001c0001t0037 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5784A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 5784 | chr14 | 73701726 | |||||
chr14:73701728
|
G | A | 8 | a0001c0001t0003a0001c0001t0013a0001c0001t0022others(5): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*5786G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 5786 | chr14 | 73701728 | |||||
chr14:73701803
|
G | C | 1 | a0001c0001t0104 | 1 | HG03579.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5861G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 5861 | chr14 | 73701803 | |||||
chr14:73701922
|
G | A | 95 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(92): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*5980G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 5980 | chr14 | 73701922 | |||||
chr14:73701944
|
TA | T | 59 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(56): Show | 204 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(201): Show |
3_prime_UTR_variant | MODIFIER | c.*6016delA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6016 | INFO_REALIGN_3_PRIME | chr14 | 73701944 | ||||
chr14:73701944
|
TAA | T | 31 | a0001c0001t0003a0001c0001t0005a0001c0001t0007others(28): Show | 99 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*6015_*6016delAA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6015 | INFO_REALIGN_3_PRIME | chr14 | 73701944 | ||||
chr14:73702078
|
G | GGT | 23 | a0001c0001t0005a0001c0001t0012a0001c0001t0015others(20): Show | 58 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(55): Show |
3_prime_UTR_variant | MODIFIER | c.*6162_*6163dupTG | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6164 | INFO_REALIGN_3_PRIME | chr14 | 73702078 | ||||
chr14:73702078
|
G | GGTGT | 18 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(15): Show | 87 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(84): Show |
3_prime_UTR_variant | MODIFIER | c.*6160_*6163dupTGTG | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6164 | INFO_REALIGN_3_PRIME | chr14 | 73702078 | ||||
chr14:73702078
|
G | GGTGTGT | 3 | a0001c0001t0011a0001c0001t0071a0001c0001t0072 | 9 | HG00140.hp2 HG00642.hp2 HG00735.hp1 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*6158_*6163dupTGTG others(2): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6164 | INFO_REALIGN_3_PRIME | chr14 | 73702078 | ||||
chr14:73702078
|
GGT | G | 12 | a0001c0001t0003a0001c0001t0013a0001c0001t0022others(9): Show | 39 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(36): Show |
3_prime_UTR_variant | MODIFIER | c.*6162_*6163delTG | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6162 | INFO_REALIGN_3_PRIME | chr14 | 73702078 | ||||
chr14:73702078
|
GGTGTGT | G | 6 | a0001c0001t0029a0001c0001t0037a0001c0001t0050others(3): Show | 7 | HG01884.hp2 HG02886.hp2 HG02970.hp2 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*6158_*6163delTGTG others(2): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6158 | INFO_REALIGN_3_PRIME | chr14 | 73702078 | ||||
chr14:73702086
|
T | G | 2 | a0001c0001t0029a0001c0001t0037 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6144T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6144 | chr14 | 73702086 | |||||
chr14:73702104
|
T | TGTGCAC | 2 | a0001c0001t0014a0001c0001t0056 | 6 | HG01168.hp1 HG01515.hp2 HG02109.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*6163_*6164insTGCA others(2): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6164 | INFO_REALIGN_3_PRIME | chr14 | 73702104 | ||||
chr14:73702104
|
T | TGTGTGTG others(3): Show |
1 | a0001c0001t0032 | 2 | HG02486.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6163_*6164insTGTG others(6): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6164 | INFO_REALIGN_3_PRIME | chr14 | 73702104 | ||||
chr14:73702123
|
G | C | 1 | a0001c0001t0068 | 1 | NA18981.hp2 | 3_prime_UTR_variant | MODIFIER | c.*6181G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6181 | chr14 | 73702123 | |||||
chr14:73702214
|
T | C | 20 | a0001c0001t0007a0001c0001t0008a0001c0001t0012others(17): Show | 48 | HG00423.hp1 HG00639.hp1 HG00738.hp2 others(45): Show |
3_prime_UTR_variant | MODIFIER | c.*6272T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6272 | chr14 | 73702214 | |||||
chr14:73702243
|
C | T | 9 | a0001c0001t0003a0001c0001t0013a0001c0001t0022others(6): Show | 36 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(33): Show |
3_prime_UTR_variant | MODIFIER | c.*6301C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6301 | chr14 | 73702243 | |||||
chr14:73702266
|
G | A | 8 | a0001c0001t0003a0001c0001t0013a0001c0001t0022others(5): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*6324G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6324 | chr14 | 73702266 | |||||
chr14:73702285
|
G | A | 1 | a0001c0001t0022 | 3 | HG00639.hp2 HG01070.hp2 HG01071.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6343G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6343 | chr14 | 73702285 | |||||
chr14:73702287
|
A | C | 2 | a0001c0001t0041a0001c0001t0042 | 2 | HG02630.hp1 HG02818.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6345A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6345 | chr14 | 73702287 | |||||
chr14:73702429
|
C | T | 1 | a0001c0001t0032 | 2 | HG02486.hp2 NA18906.hp2 |
3_prime_UTR_variant | MODIFIER | c.*6487C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6487 | chr14 | 73702429 | |||||
chr14:73702440
|
A | C | 1 | a0001c0001t0103 | 1 | NA21309.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6498A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6498 | chr14 | 73702440 | |||||
chr14:73702471
|
T | C | 1 | a0001c0001t0091 | 1 | HG02976.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6529T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6529 | chr14 | 73702471 | |||||
chr14:73702634
|
A | G | 1 | a0001c0001t0037 | 1 | HG03041.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6692A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6692 | chr14 | 73702634 | |||||
chr14:73702636
|
A | G | 2 | a0001c0001t0029a0001c0001t0037 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6694A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6694 | chr14 | 73702636 | |||||
chr14:73702686
|
C | T | 2 | a0001c0001t0029a0001c0001t0037 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*6744C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6744 | chr14 | 73702686 | |||||
chr14:73702687
|
G | A | 1 | a0001c0001t0054 | 1 | HG03942.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6745G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6745 | chr14 | 73702687 | |||||
chr14:73702812
|
T | C | 2 | a0001c0001t0020a0001c0001t0102 | 5 | HG01891.hp2 HG03139.hp2 HG03471.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6870T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6870 | chr14 | 73702812 | |||||
chr14:73702929
|
G | A | 1 | a0001c0001t0038 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6987G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 6987 | chr14 | 73702929 | |||||
chr14:73702992
|
G | A | 28 | a0001c0001t0005a0001c0001t0008a0001c0001t0009others(25): Show | 75 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(72): Show |
3_prime_UTR_variant | MODIFIER | c.*7050G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 7050 | chr14 | 73702992 | |||||
chr14:73703252
|
T | C | 1 | a0001c0001t0035 | 2 | HG00738.hp1 HG01123.hp2 |
3_prime_UTR_variant | MODIFIER | c.*7310T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 7310 | chr14 | 73703252 | |||||
chr14:73703292
|
C | T | 95 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(92): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
3_prime_UTR_variant | MODIFIER | c.*7350C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 7350 | chr14 | 73703292 | |||||
chr14:73703435
|
G | A | 1 | a0001c0001t0081 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7493G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 7493 | chr14 | 73703435 | |||||
chr14:73703452
|
T | G | 1 | a0001c0001t0041 | 1 | HG02630.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7510T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 7510 | chr14 | 73703452 | |||||
chr14:73703465
|
C | T | 1 | a0001c0001t0081 | 1 | HG02486.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7523C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 7523 | chr14 | 73703465 | |||||
chr14:73703618
|
G | A | 35 | a0001c0001t0002a0001c0001t0005a0001c0001t0008others(32): Show | 116 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(113): Show |
3_prime_UTR_variant | MODIFIER | c.*7676G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 7676 | chr14 | 73703618 | |||||
chr14:73703632
|
C | T | 1 | a0001c0001t0039 | 1 | HG02717.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7690C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 7690 | chr14 | 73703632 | |||||
chr14:73703634
|
A | G | 8 | a0001c0001t0003a0001c0001t0013a0001c0001t0022others(5): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
3_prime_UTR_variant | MODIFIER | c.*7692A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 7692 | chr14 | 73703634 | |||||
chr14:73703643
|
G | A | 1 | a0001c0001t0075 | 1 | NA19066.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7701G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 7701 | chr14 | 73703643 | |||||
chr14:73703651
|
T | TCC | 8 | a0001c0001t0016a0001c0001t0020a0001c0001t0021others(5): Show | 18 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*7710_*7711dupCC | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 7712 | INFO_REALIGN_3_PRIME | chr14 | 73703651 | ||||
chr14:73703671
|
C | G | 5 | a0001c0001t0007a0001c0001t0018a0001c0001t0031others(2): Show | 19 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(16): Show |
3_prime_UTR_variant | MODIFIER | c.*7729C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 7729 | chr14 | 73703671 | |||||
chr14:73703690
|
G | A | 2 | a0001c0001t0029a0001c0001t0037 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7748G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 8/8 | 7748 | chr14 | 73703690 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr14:73645080
|
A | G | 1 | a0001c0001t0015g0334 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.3+38A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73645080 | ||||||
chr14:73645321
|
G | A | 1 | a0001c0001t0097g0007 | 1 | NA19240.hp1 | intron_variant | MODIFIER | c.3+279G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73645321 | ||||||
chr14:73645401
|
C | T | 8 | a0001c0001t0009g0327a0001c0001t0014g0328a0001c0001t0014g0329others(5): Show | 8 | HG01168.hp1 HG01515.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.3+359C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73645401 | ||||||
chr14:73645425
|
T | C | 2 | a0001c0001t0060g0009a0001c0001t0061g0008 | 2 | HG02258.hp1 HG02970.hp2 |
intron_variant | MODIFIER | c.3+383T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73645425 | ||||||
chr14:73645684
|
A | C | 17 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(14): Show | 17 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.3+642A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73645684 | ||||||
chr14:73645708
|
G | A | 1 | a0001c0001t0003g0010 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.3+666G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73645708 | ||||||
chr14:73646189
|
A | G | 6 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(3): Show | 6 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+1147A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73646189 | ||||||
chr14:73646291
|
T | G | 29 | a0001c0001t0004g0011a0001c0001t0004g0013a0001c0001t0004g0014others(26): Show | 29 | HG00423.hp1 HG00639.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.3+1249T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73646291 | ||||||
chr14:73646359
|
G | T | 29 | a0001c0001t0004g0011a0001c0001t0004g0013a0001c0001t0004g0014others(26): Show | 29 | HG00423.hp1 HG00639.hp1 HG00735.hp2 others(26): Show |
intron_variant | MODIFIER | c.3+1317G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73646359 | ||||||
chr14:73646368
|
A | G | 1 | a0001c0001t0003g0308 | 1 | HG02738.hp1 | intron_variant | MODIFIER | c.3+1326A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73646368 | ||||||
chr14:73646484
|
A | ACCTGTAA others(9): Show |
35 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.3+1456_3+1471dupAG others(14): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73646484 | |||||
chr14:73646661
|
C | A | 1 | a0001c0001t0049g0071 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.3+1619C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73646661 | ||||||
chr14:73646724
|
T | G | 7 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0010g0075others(4): Show | 7 | HG01358.hp2 HG01978.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.3+1682T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73646724 | ||||||
chr14:73646765
|
T | TAAAC | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3+1737_3+1740dupAA others(2): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73646765 | |||||
chr14:73646910
|
G | C | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.3+1868G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73646910 | ||||||
chr14:73647076
|
G | A | 1 | a0001c0001t0103g0309 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.3+2034G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73647076 | ||||||
chr14:73647084
|
C | T | 1 | a0001c0001t0004g0039 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3+2042C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73647084 | ||||||
chr14:73647125
|
G | A | 14 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3+2083G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73647125 | ||||||
chr14:73647135
|
G | C | 1 | a0001c0001t0004g0039 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3+2093G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73647135 | ||||||
chr14:73647136
|
A | T | 1 | a0001c0001t0004g0039 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.3+2094A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73647136 | ||||||
chr14:73647147
|
A | C | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3+2105A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73647147 | ||||||
chr14:73647165
|
T | C | 1 | a0001c0001t0073g0083 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.3+2123T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73647165 | ||||||
chr14:73647343
|
C | T | 1 | a0001c0001t0102g0316 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.3+2301C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73647343 | ||||||
chr14:73647364
|
C | CA | 65 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0053others(62): Show | 65 | HG00140.hp1 HG00323.hp2 HG00423.hp1 others(62): Show |
intron_variant | MODIFIER | c.3+2339dupA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73647364 | |||||
chr14:73647364
|
C | CAA | 9 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(6): Show | 9 | HG00099.hp1 HG00323.hp1 HG01175.hp1 others(6): Show |
intron_variant | MODIFIER | c.3+2338_3+2339dupAA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73647364 | |||||
chr14:73647367
|
AAAAAAAA others(8): Show |
A | 110 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(107): Show | 112 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.3+2331_3+2345delAA others(13): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73647367 | |||||
chr14:73647390
|
AAAAGAAA others(3): Show |
A | 14 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3+2352_3+2361delGA others(8): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73647390 | |||||
chr14:73647439
|
C | T | 2 | a0001c0001t0032g0088a0001c0001t0032g0089 | 2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.3+2397C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73647439 | ||||||
chr14:73647496
|
C | G | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.3+2454C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73647496 | ||||||
chr14:73647669
|
C | A | 14 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3+2627C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73647669 | ||||||
chr14:73647711
|
C | G | 1 | a0001c0001t0099g0195 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.3+2669C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73647711 | ||||||
chr14:73647809
|
T | A | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3+2767T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73647809 | ||||||
chr14:73647822
|
C | T | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3+2780C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73647822 | ||||||
chr14:73647824
|
T | C | 1 | a0001c0001t0050g0012 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.3+2782T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73647824 | ||||||
chr14:73647870
|
G | A | 2 | a0001c0001t0007g0210a0001c0001t0007g0211 | 2 | NA18944.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.3+2828G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73647870 | ||||||
chr14:73648102
|
C | T | 1 | a0001c0001t0002g0194 | 1 | NA18957.hp1 | intron_variant | MODIFIER | c.3+3060C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73648102 | ||||||
chr14:73648134
|
C | T | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.3+3092C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73648134 | ||||||
chr14:73648268
|
G | A | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3+3226G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73648268 | ||||||
chr14:73648329
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3+3287C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73648329 | ||||||
chr14:73648334
|
G | A | 14 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.3+3292G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73648334 | ||||||
chr14:73648403
|
C | CATATATA others(1): Show |
3 | a0001c0001t0009g0153a0001c0001t0027g0002a0001c0001t0027g0152 | 4 | HG06807.hp1 NA18612.hp1 NA18747.hp1 others(1): Show |
intron_variant | MODIFIER | c.3+3368_3+3375dupAT others(6): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(5): Show |
92 | a0001c0001t0001g0004a0001c0001t0001g0245a0001c0001t0001g0246others(89): Show | 94 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(91): Show |
intron_variant | MODIFIER | c.3+3364_3+3375dupAT others(10): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(7): Show |
40 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0001t0001g0241others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.3+3362_3+3375dupAT others(12): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(9): Show |
8 | a0001c0001t0003g0053a0001c0001t0010g0072a0001c0001t0011g0236others(5): Show | 8 | HG00323.hp2 HG01934.hp2 HG01978.hp1 others(5): Show |
intron_variant | MODIFIER | c.3+3375_3+3376insAT others(14): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(11): Show |
6 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(3): Show | 6 | HG01099.hp1 HG02055.hp1 HG02257.hp2 others(3): Show |
intron_variant | MODIFIER | c.3+3375_3+3376insAT others(16): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(13): Show |
4 | a0001c0001t0009g0149a0001c0001t0009g0150a0001c0001t0009g0151others(1): Show | 4 | HG02258.hp2 HG02886.hp2 HG02897.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+3375_3+3376insAT others(18): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(15): Show |
1 | a0001c0001t0060g0009 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.3+3375_3+3376insAT others(20): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(17): Show |
2 | a0001c0001t0057g0234a0001c0001t0061g0008 | 2 | HG02258.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.3+3375_3+3376insAT others(22): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(19): Show |
6 | a0001c0001t0005g0147a0001c0001t0021g0317a0001c0001t0021g0318others(3): Show | 6 | HG01109.hp2 HG02559.hp1 HG03017.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+3375_3+3376insAT others(24): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(21): Show |
6 | a0001c0001t0004g0038a0001c0001t0008g0144a0001c0001t0008g0145others(3): Show | 6 | HG01515.hp1 HG01517.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.3+3375_3+3376insAT others(26): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(23): Show |
6 | a0001c0001t0015g0143a0001c0001t0020g0315a0001c0001t0023g0036others(3): Show | 6 | HG00423.hp1 HG00639.hp1 HG01496.hp2 others(3): Show |
intron_variant | MODIFIER | c.3+3375_3+3376insAT others(28): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(25): Show |
24 | a0001c0001t0004g0011a0001c0001t0004g0034a0001c0001t0004g0035others(21): Show | 24 | HG01069.hp2 HG01071.hp1 HG01081.hp2 others(21): Show |
intron_variant | MODIFIER | c.3+3375_3+3376insAT others(30): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(27): Show |
33 | a0001c0001t0004g0031a0001c0001t0004g0032a0001c0001t0005g0116others(30): Show | 33 | HG00544.hp2 HG00621.hp2 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.3+3375_3+3376insAT others(32): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(29): Show |
16 | a0001c0001t0004g0026a0001c0001t0005g0105a0001c0001t0005g0106others(13): Show | 16 | HG00558.hp1 HG01109.hp1 HG01167.hp2 others(13): Show |
intron_variant | MODIFIER | c.3+3375_3+3376insAT others(34): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(31): Show |
20 | a0001c0001t0004g0017a0001c0001t0004g0018a0001c0001t0004g0019others(17): Show | 20 | HG01074.hp2 HG01243.hp1 HG01255.hp1 others(17): Show |
intron_variant | MODIFIER | c.3+3375_3+3376insAT others(36): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(33): Show |
10 | a0001c0001t0005g0085a0001c0001t0007g0213a0001c0001t0009g0327others(7): Show | 10 | HG00438.hp1 HG02080.hp2 HG02148.hp2 others(7): Show |
intron_variant | MODIFIER | c.3+3375_3+3376insAT others(38): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(35): Show |
4 | a0001c0001t0004g0014a0001c0001t0004g0015a0001c0001t0004g0039others(1): Show | 4 | HG02055.hp2 HG02523.hp2 NA18973.hp2 others(1): Show |
intron_variant | MODIFIER | c.3+3375_3+3376insAT others(40): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(37): Show |
2 | a0001c0001t0005g0092a0001c0001t0009g0093 | 2 | HG02970.hp1 NA19064.hp1 |
intron_variant | MODIFIER | c.3+3375_3+3376insAT others(42): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(41): Show |
1 | a0001c0001t0004g0013 | 1 | HG01261.hp1 | intron_variant | MODIFIER | c.3+3375_3+3376insAT others(46): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648403
|
C | CATATATA others(47): Show |
1 | a0001c0001t0008g0090 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.3+3375_3+3376insAT others(52): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648403 | |||||
chr14:73648411
|
T | TATATATA others(8): Show |
1 | a0001c0001t0007g0212 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.3+3375_3+3376insAT others(13): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648411 | |||||
chr14:73648412
|
A | ATATATAT others(31): Show |
1 | a0001c0001t0029g0079 | 1 | HG03130.hp1 | intron_variant | MODIFIER | c.3+3375_3+3376insAT others(36): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648412 | |||||
chr14:73648412
|
A | ATATATAT others(29): Show |
1 | a0001c0001t0037g0080 | 1 | HG03041.hp1 | intron_variant | MODIFIER | c.3+3375_3+3376insAT others(34): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648412 | |||||
chr14:73648412
|
A | ATATATAT others(23): Show |
1 | a0001c0001t0029g0081 | 1 | HG03471.hp1 | intron_variant | MODIFIER | c.3+3375_3+3376insAT others(28): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648412 | |||||
chr14:73648417
|
T | TATATATA others(26): Show |
1 | a0001c0001t0005g0113 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.3+3375_3+3376insAT others(31): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73648417 | ||||||
chr14:73648417
|
T | TATATATA others(28): Show |
2 | a0001c0001t0004g0023a0001c0001t0067g0217 | 2 | HG03927.hp1 HG04204.hp1 |
intron_variant | MODIFIER | c.3+3375_3+3376insAT others(33): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73648417 | ||||||
chr14:73648417
|
T | TATATATA others(36): Show |
1 | a0001c0001t0005g0091 | 1 | NA19056.hp2 | intron_variant | MODIFIER | c.3+3375_3+3376insAT others(41): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73648417 | ||||||
chr14:73648452
|
A | G | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3+3410A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73648452 | ||||||
chr14:73648538
|
C | T | 3 | a0001c0001t0002g0191a0001c0001t0002g0192a0001c0001t0002g0193 | 3 | HG02056.hp2 NA18998.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.3+3496C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73648538 | ||||||
chr14:73648545
|
T | C | 58 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(55): Show | 58 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(55): Show |
intron_variant | MODIFIER | c.3+3503T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73648545 | ||||||
chr14:73648607
|
G | C | 43 | a0001c0001t0005g0085a0001c0001t0005g0091a0001c0001t0005g0092others(40): Show | 44 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.3+3565G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73648607 | ||||||
chr14:73648667
|
G | A | 10 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0054others(7): Show | 10 | HG00639.hp2 HG01070.hp2 HG01071.hp2 others(7): Show |
intron_variant | MODIFIER | c.3+3625G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73648667 | ||||||
chr14:73648680
|
G | A | 5 | a0001c0001t0033g0226a0001c0001t0033g0232a0001c0001t0064g0233others(2): Show | 5 | HG02559.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.3+3638G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73648680 | ||||||
chr14:73648711
|
A | G | 1 | a0001c0001t0034g0190 | 1 | HG00642.hp1 | intron_variant | MODIFIER | c.3+3669A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73648711 | ||||||
chr14:73648878
|
G | A | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3+3836G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73648878 | ||||||
chr14:73648894
|
A | AAT | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3+3861_3+3862dupAT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73648894 | |||||
chr14:73648969
|
G | A | 1 | a0001c0001t0023g0028 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.3+3927G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73648969 | ||||||
chr14:73649080
|
A | C | 2 | a0001c0001t0017g0208a0001c0001t0017g0209 | 2 | HG03486.hp2 NA18906.hp1 |
intron_variant | MODIFIER | c.3+4038A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73649080 | ||||||
chr14:73649088
|
C | T | 2 | a0001c0001t0048g0082a0001c0001t0049g0071 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.3+4046C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73649088 | ||||||
chr14:73649124
|
G | A | 1 | a0001c0001t0089g0124 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.3+4082G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73649124 | ||||||
chr14:73649274
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.3+4232G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73649274 | ||||||
chr14:73649286
|
A | AT | 7 | a0001c0001t0002g0189a0001c0001t0019g0307a0001c0001t0027g0152others(4): Show | 7 | HG03041.hp1 HG03130.hp1 HG03471.hp1 others(4): Show |
intron_variant | MODIFIER | c.3+4258dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73649286 | |||||
chr14:73649305
|
C | T | 1 | a0001c0001t0003g0047 | 1 | HG01256.hp1 | intron_variant | MODIFIER | c.3+4263C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73649305 | ||||||
chr14:73649313
|
C | T | 1 | a0001c0001t0005g0092 | 1 | NA19064.hp1 | intron_variant | MODIFIER | c.3+4271C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73649313 | ||||||
chr14:73649345
|
C | T | 8 | a0001c0001t0002g0188a0001c0001t0006g0006a0001c0001t0006g0301others(5): Show | 9 | HG00099.hp2 HG00438.hp2 HG02074.hp2 others(6): Show |
intron_variant | MODIFIER | c.3+4303C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73649345 | ||||||
chr14:73649431
|
T | C | 35 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.3+4389T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73649431 | ||||||
chr14:73649448
|
C | A | 280 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(277): Show | 283 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(280): Show |
intron_variant | MODIFIER | c.3+4406C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73649448 | ||||||
chr14:73649483
|
C | T | 59 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.3+4441C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73649483 | ||||||
chr14:73649484
|
A | G | 59 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.3+4442A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73649484 | ||||||
chr14:73649487
|
A | T | 59 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(56): Show | 59 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(56): Show |
intron_variant | MODIFIER | c.3+4445A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73649487 | ||||||
chr14:73649513
|
A | T | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.3+4471A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73649513 | ||||||
chr14:73649529
|
G | A | 2 | a0001c0001t0052g0235a0001c0001t0057g0234 | 2 | HG02886.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.3+4487G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73649529 | ||||||
chr14:73649569
|
A | G | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.3+4527A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73649569 | ||||||
chr14:73649605
|
A | G | 1 | a0001c0001t0001g0300 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.3+4563A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73649605 | ||||||
chr14:73650055
|
C | T | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4-4792C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73650055 | ||||||
chr14:73650057
|
C | T | 2 | a0001c0001t0002g0186a0001c0001t0002g0187 | 2 | HG02895.hp2 HG02897.hp1 |
intron_variant | MODIFIER | c.4-4790C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73650057 | ||||||
chr14:73650108
|
T | A | 7 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.4-4739T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73650108 | ||||||
chr14:73650190
|
A | T | 1 | a0001c0001t0003g0053 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.4-4657A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73650190 | ||||||
chr14:73650235
|
G | C | 1 | a0001c0001t0002g0154 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.4-4612G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73650235 | ||||||
chr14:73650237
|
C | T | 1 | a0001c0001t0004g0022 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.4-4610C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73650237 | ||||||
chr14:73650532
|
A | C | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.4-4315A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73650532 | ||||||
chr14:73650770
|
C | A | 1 | a0001c0001t0007g0219 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.4-4077C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73650770 | ||||||
chr14:73650969
|
AACTTT | A | 7 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.4-3876_4-3872delCT others(3): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73650969 | |||||
chr14:73651135
|
A | AT | 20 | a0001c0001t0007g0210a0001c0001t0007g0211a0001c0001t0007g0212others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.4-3703dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73651135 | |||||
chr14:73651397
|
T | TC | 68 | a0001c0001t0005g0085a0001c0001t0005g0091a0001c0001t0005g0092others(65): Show | 69 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(66): Show |
intron_variant | MODIFIER | c.4-3447dupC | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73651397 | |||||
chr14:73651405
|
T | C | 43 | a0001c0001t0005g0085a0001c0001t0005g0091a0001c0001t0005g0092others(40): Show | 44 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.4-3442T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73651405 | ||||||
chr14:73651620
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4-3227G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73651620 | ||||||
chr14:73651621
|
G | C | 109 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(106): Show | 111 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.4-3226G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73651621 | ||||||
chr14:73651622
|
G | A | 2 | a0001c0001t0052g0235a0001c0001t0057g0234 | 2 | HG02886.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.4-3225G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73651622 | ||||||
chr14:73651706
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.4-3141C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73651706 | ||||||
chr14:73651730
|
C | T | 6 | a0001c0001t0017g0205a0001c0001t0017g0207a0001c0001t0017g0208others(3): Show | 6 | HG01243.hp2 HG01891.hp1 HG02895.hp1 others(3): Show |
intron_variant | MODIFIER | c.4-3117C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73651730 | ||||||
chr14:73651794
|
A | C | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4-3053A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73651794 | ||||||
chr14:73651932
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4-2915C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73651932 | ||||||
chr14:73651937
|
G | A | 1 | a0001c0001t0002g0155 | 1 | NA18945.hp2 | intron_variant | MODIFIER | c.4-2910G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73651937 | ||||||
chr14:73652128
|
C | T | 43 | a0001c0001t0005g0085a0001c0001t0005g0091a0001c0001t0005g0092others(40): Show | 44 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(41): Show |
intron_variant | MODIFIER | c.4-2719C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73652128 | ||||||
chr14:73652269
|
A | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4-2578A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73652269 | ||||||
chr14:73652374
|
A | G | 4 | a0001c0001t0021g0317a0001c0001t0021g0318a0001c0001t0021g0319others(1): Show | 4 | HG01109.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-2473A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73652374 | ||||||
chr14:73652418
|
C | T | 1 | a0001c0001t0039g0197 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.4-2429C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73652418 | ||||||
chr14:73652676
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4-2171C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73652676 | ||||||
chr14:73652766
|
A | C | 2 | a0001c0001t0048g0082a0001c0001t0049g0071 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4-2081A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73652766 | ||||||
chr14:73652766
|
A | G | 2 | a0001c0001t0029g0079a0001c0001t0037g0080 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.4-2081A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73652766 | ||||||
chr14:73652782
|
A | C | 1 | a0001c0001t0096g0123 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.4-2065A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73652782 | ||||||
chr14:73653011
|
T | C | 19 | a0001c0001t0007g0210a0001c0001t0007g0211a0001c0001t0007g0212others(16): Show | 19 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.4-1836T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73653011 | ||||||
chr14:73653196
|
G | A | 1 | a0001c0001t0004g0243 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.4-1651G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73653196 | ||||||
chr14:73653289
|
A | G | 4 | a0001c0001t0021g0317a0001c0001t0021g0318a0001c0001t0021g0319others(1): Show | 4 | HG01109.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.4-1558A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73653289 | ||||||
chr14:73653353
|
A | G | 1 | a0001c0001t0082g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.4-1494A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73653353 | ||||||
chr14:73653527
|
T | A | 2 | a0001c0001t0023g0024a0001c0001t0084g0110 | 2 | HG01109.hp1 HG01167.hp2 |
intron_variant | MODIFIER | c.4-1320T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73653527 | ||||||
chr14:73653716
|
A | G | 2 | a0001c0001t0048g0082a0001c0001t0049g0071 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.4-1131A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73653716 | ||||||
chr14:73653787
|
A | T | 1 | a0001c0001t0002g0185 | 1 | NA19057.hp1 | intron_variant | MODIFIER | c.4-1060A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73653787 | ||||||
chr14:73653802
|
G | A | 5 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.4-1045G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73653802 | ||||||
chr14:73653845
|
T | G | 1 | a0001c0001t0090g0114 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.4-1002T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73653845 | ||||||
chr14:73654135
|
G | A | 41 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.4-712G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73654135 | ||||||
chr14:73654351
|
G | A | 2 | a0001c0001t0016g0320a0001c0001t0016g0321 | 2 | HG02055.hp1 NA20129.hp2 |
intron_variant | MODIFIER | c.4-496G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73654351 | ||||||
chr14:73654357
|
A | G | 110 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(107): Show | 112 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.4-490A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73654357 | ||||||
chr14:73654453
|
A | C | 3 | a0001c0001t0008g0130a0001c0001t0009g0086a0001c0001t0009g0153 | 3 | HG01081.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.4-394A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73654453 | ||||||
chr14:73654496
|
C | T | 8 | a0001c0001t0008g0144a0001c0001t0008g0145a0001c0001t0015g0121others(5): Show | 8 | HG01515.hp1 HG01517.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.4-351C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73654496 | ||||||
chr14:73654556
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4-291G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73654556 | ||||||
chr14:73654630
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.4-217G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73654630 | ||||||
chr14:73654731
|
C | T | 1 | a0001c0001t0004g0011 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.4-116C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | chr14 | 73654731 | ||||||
chr14:73654765
|
A | AATAC | 14 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.4-59_4-56dupACAT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73654765 | |||||
chr14:73654828
|
C | CT | 6 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(3): Show | 6 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(3): Show |
splice_region_variant&intron_variant | LOW | c.4-5dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73654828 | |||||
chr14:73654828
|
CT | C | 14 | a0001c0001t0001g0245a0001c0001t0003g0060a0001c0001t0003g0061others(11): Show | 14 | HG01069.hp1 HG01167.hp1 HG01169.hp1 others(11): Show |
splice_region_variant&intron_variant | LOW | c.4-5delT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 1/7 | INFO_REALIGN_3_PRIME | chr14 | 73654828 | |||||
chr14:73655011
|
T | C | 5 | a0001c0001t0020g0310a0001c0001t0020g0311a0001c0001t0020g0313others(2): Show | 5 | HG01891.hp2 HG03139.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.42+126T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73655011 | ||||||
chr14:73655037
|
T | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.42+152T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73655037 | ||||||
chr14:73655058
|
T | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(81): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.42+173T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73655058 | ||||||
chr14:73655166
|
T | C | 1 | a0001c0001t0031g0227 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.42+281T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73655166 | ||||||
chr14:73655346
|
C | CT | 11 | a0001c0001t0002g0003a0001c0001t0002g0178a0001c0001t0002g0179others(8): Show | 12 | HG00558.hp2 HG01069.hp1 HG01255.hp2 others(9): Show |
intron_variant | MODIFIER | c.42+476dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 73655346 | |||||
chr14:73655437
|
C | T | 5 | a0001c0001t0004g0015a0001c0001t0004g0026a0001c0001t0051g0020others(2): Show | 5 | HG02074.hp1 HG02523.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.42+552C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73655437 | ||||||
chr14:73655445
|
A | G | 8 | a0001c0001t0008g0128a0001c0001t0008g0139a0001c0001t0081g0129others(5): Show | 8 | HG02486.hp1 HG02647.hp2 HG02717.hp2 others(5): Show |
intron_variant | MODIFIER | c.42+560A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73655445 | ||||||
chr14:73655520
|
T | A | 35 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.42+635T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73655520 | ||||||
chr14:73655535
|
T | C | 3 | a0001c0001t0021g0317a0001c0001t0021g0318a0001c0001t0021g0325 | 3 | HG02451.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.42+650T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73655535 | ||||||
chr14:73655538
|
T | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.42+653T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73655538 | ||||||
chr14:73655589
|
T | C | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.42+704T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73655589 | ||||||
chr14:73655590
|
G | A | 153 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(150): Show | 155 | HG00140.hp2 HG00423.hp1 HG00423.hp2 others(152): Show |
intron_variant | MODIFIER | c.42+705G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73655590 | ||||||
chr14:73655668
|
TATC | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.42+788_42+790delTC others(1): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | 73655668 | |||||
chr14:73655670
|
T | C | 3 | a0001c0001t0009g0149a0001c0001t0009g0150a0001c0001t0009g0151 | 3 | HG02258.hp2 HG02897.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.42+785T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73655670 | ||||||
chr14:73655710
|
T | C | 9 | a0001c0001t0028g0115a0001c0001t0028g0134a0001c0001t0028g0135others(6): Show | 9 | HG01496.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.42+825T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73655710 | ||||||
chr14:73655775
|
A | T | 2 | a0001c0001t0001g0296a0001c0001t0001g0297 | 2 | HG02083.hp2 NA18944.hp2 |
intron_variant | MODIFIER | c.42+890A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73655775 | ||||||
chr14:73656251
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.42+1366G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73656251 | ||||||
chr14:73656280
|
A | G | 2 | a0001c0001t0048g0082a0001c0001t0049g0071 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.42+1395A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73656280 | ||||||
chr14:73656326
|
C | G | 4 | a0001c0001t0021g0317a0001c0001t0021g0318a0001c0001t0021g0319others(1): Show | 4 | HG01109.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.42+1441C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73656326 | ||||||
chr14:73656465
|
G | A | 72 | a0001c0001t0005g0085a0001c0001t0005g0091a0001c0001t0005g0092others(69): Show | 73 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.42+1580G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73656465 | ||||||
chr14:73656480
|
C | T | 84 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(81): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.42+1595C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73656480 | ||||||
chr14:73656535
|
A | T | 1 | a0001c0001t0001g0298 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.42+1650A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73656535 | ||||||
chr14:73656989
|
G | C | 1 | a0001c0001t0008g0146 | 1 | HG02145.hp1 | intron_variant | MODIFIER | c.43-1858G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73656989 | ||||||
chr14:73657064
|
A | G | 2 | a0001c0001t0003g0061a0002c0002t0003g0070 | 2 | HG01069.hp1 HG01255.hp2 |
intron_variant | MODIFIER | c.43-1783A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73657064 | ||||||
chr14:73657283
|
C | T | 35 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.43-1564C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73657283 | ||||||
chr14:73657306
|
C | T | 1 | a0001c0001t0015g0109 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.43-1541C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73657306 | ||||||
chr14:73657686
|
C | G | 1 | a0001c0001t0015g0122 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.43-1161C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73657686 | ||||||
chr14:73657720
|
C | T | 32 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.43-1127C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73657720 | ||||||
chr14:73657826
|
C | T | 4 | a0001c0001t0009g0093a0001c0001t0009g0101a0001c0001t0009g0102others(1): Show | 4 | HG01074.hp2 HG01243.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.43-1021C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73657826 | ||||||
chr14:73657971
|
C | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.43-876C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73657971 | ||||||
chr14:73657980
|
G | C | 1 | a0001c0001t0061g0008 | 1 | HG02258.hp1 | intron_variant | MODIFIER | c.43-867G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73657980 | ||||||
chr14:73658065
|
T | C | 1 | a0001c0001t0009g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.43-782T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73658065 | ||||||
chr14:73658071
|
A | G | 5 | a0001c0001t0004g0015a0001c0001t0004g0026a0001c0001t0051g0020others(2): Show | 5 | HG02074.hp1 HG02523.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.43-776A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73658071 | ||||||
chr14:73658125
|
A | G | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-722A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73658125 | ||||||
chr14:73658431
|
T | C | 26 | a0001c0001t0007g0210a0001c0001t0007g0211a0001c0001t0007g0212others(23): Show | 26 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.43-416T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73658431 | ||||||
chr14:73658472
|
A | C | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.43-375A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73658472 | ||||||
chr14:73658731
|
G | A | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.43-116G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 2/7 | chr14 | 73658731 | ||||||
chr14:73658980
|
A | G | 1 | a0001c0001t0008g0127 | 1 | HG02683.hp2 | intron_variant | MODIFIER | c.152+24A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73658980 | ||||||
chr14:73659094
|
A | G | 4 | a0001c0001t0021g0317a0001c0001t0021g0318a0001c0001t0021g0319others(1): Show | 4 | HG01109.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+138A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73659094 | ||||||
chr14:73659154
|
T | C | 4 | a0001c0001t0021g0317a0001c0001t0021g0318a0001c0001t0021g0319others(1): Show | 4 | HG01109.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.152+198T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73659154 | ||||||
chr14:73659161
|
A | AT | 10 | a0001c0001t0004g0243a0001c0001t0009g0111a0001c0001t0026g0096others(7): Show | 10 | HG02486.hp1 HG03041.hp2 HG03942.hp2 others(7): Show |
intron_variant | MODIFIER | c.152+223dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 73659161 | |||||
chr14:73659161
|
AT | A | 32 | a0001c0001t0001g0237a0001c0001t0009g0149a0001c0001t0012g0198others(29): Show | 32 | HG01167.hp1 HG01168.hp1 HG01243.hp2 others(29): Show |
intron_variant | MODIFIER | c.152+223delT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 73659161 | |||||
chr14:73659161
|
ATTT | A | 41 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.152+221_152+223del others(3): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 73659161 | |||||
chr14:73659201
|
G | A | 1 | a0001c0001t0001g0246 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.152+245G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73659201 | ||||||
chr14:73659287
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.152+331G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73659287 | ||||||
chr14:73659405
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.152+449G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73659405 | ||||||
chr14:73659475
|
T | G | 2 | a0001c0001t0048g0082a0001c0001t0049g0071 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.152+519T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73659475 | ||||||
chr14:73659518
|
C | G | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.152+562C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73659518 | ||||||
chr14:73659544
|
C | T | 1 | a0001c0001t0103g0309 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.152+588C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73659544 | ||||||
chr14:73659719
|
G | A | 8 | a0001c0001t0008g0144a0001c0001t0008g0145a0001c0001t0015g0121others(5): Show | 8 | HG01515.hp1 HG01517.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.152+763G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73659719 | ||||||
chr14:73659966
|
A | G | 1 | a0001c0001t0001g0242 | 1 | HG02056.hp1 | intron_variant | MODIFIER | c.152+1010A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73659966 | ||||||
chr14:73660093
|
A | AT | 35 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.152+1145dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | 73660093 | |||||
chr14:73660330
|
T | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.152+1374T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73660330 | ||||||
chr14:73660389
|
G | A | 1 | a0001c0001t0002g0154 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.152+1433G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73660389 | ||||||
chr14:73660392
|
T | C | 34 | a0001c0001t0002g0003a0001c0001t0002g0154a0001c0001t0002g0155others(31): Show | 35 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(32): Show |
intron_variant | MODIFIER | c.152+1436T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73660392 | ||||||
chr14:73660483
|
T | C | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.153-1504T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73660483 | ||||||
chr14:73660714
|
A | T | 1 | a0001c0001t0015g0109 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.153-1273A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73660714 | ||||||
chr14:73660766
|
C | T | 1 | a0001c0001t0001g0297 | 1 | HG02083.hp2 | intron_variant | MODIFIER | c.153-1221C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73660766 | ||||||
chr14:73660788
|
A | G | 41 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.153-1199A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73660788 | ||||||
chr14:73660853
|
C | T | 5 | a0001c0001t0033g0226a0001c0001t0033g0232a0001c0001t0064g0233others(2): Show | 5 | HG02559.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.153-1134C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73660853 | ||||||
chr14:73660902
|
T | G | 1 | a0001c0001t0003g0040 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.153-1085T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73660902 | ||||||
chr14:73660954
|
A | C | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.153-1033A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73660954 | ||||||
chr14:73660987
|
G | A | 10 | a0001c0001t0014g0328a0001c0001t0014g0329a0001c0001t0014g0330others(7): Show | 10 | HG01168.hp1 HG01515.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.153-1000G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73660987 | ||||||
chr14:73661004
|
A | G | 1 | a0001c0001t0002g0171 | 1 | NA19010.hp2 | intron_variant | MODIFIER | c.153-983A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73661004 | ||||||
chr14:73661095
|
C | T | 2 | a0001c0001t0048g0082a0001c0001t0049g0071 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.153-892C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73661095 | ||||||
chr14:73661096
|
G | A | 9 | a0001c0001t0004g0017a0001c0001t0004g0034a0001c0001t0004g0035others(6): Show | 9 | HG01123.hp1 HG01167.hp2 HG01261.hp2 others(6): Show |
intron_variant | MODIFIER | c.153-891G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73661096 | ||||||
chr14:73661154
|
A | G | 1 | a0001c0001t0103g0309 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.153-833A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73661154 | ||||||
chr14:73661171
|
A | AT | 17 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(14): Show | 17 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(14): Show |
intron_variant | MODIFIER | c.153-816_153-815ins others(1): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73661171 | ||||||
chr14:73661171
|
A | T | 1 | a0001c0001t0013g0052 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.153-816A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73661171 | ||||||
chr14:73661173
|
T | A | 245 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(242): Show | 249 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(246): Show |
intron_variant | MODIFIER | c.153-814T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73661173 | ||||||
chr14:73661240
|
G | A | 306 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(303): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.153-747G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73661240 | ||||||
chr14:73661247
|
T | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.153-740T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73661247 | ||||||
chr14:73661635
|
C | T | 1 | a0001c0001t0063g0021 | 1 | NA18984.hp1 | intron_variant | MODIFIER | c.153-352C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73661635 | ||||||
chr14:73661668
|
C | G | 26 | a0001c0001t0007g0210a0001c0001t0007g0211a0001c0001t0007g0212others(23): Show | 26 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(23): Show |
intron_variant | MODIFIER | c.153-319C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73661668 | ||||||
chr14:73661674
|
G | A | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.153-313G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73661674 | ||||||
chr14:73661975
|
G | C | 1 | a0001c0001t0050g0012 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.153-12G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 3/7 | chr14 | 73661975 | ||||||
chr14:73662142
|
G | A | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.208+100G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73662142 | ||||||
chr14:73662161
|
A | G | 1 | a0001c0001t0007g0210 | 1 | NA18944.hp1 | intron_variant | MODIFIER | c.208+119A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73662161 | ||||||
chr14:73662208
|
TAG | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.208+170_208+171del others(2): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 73662208 | |||||
chr14:73662230
|
C | T | 3 | a0001c0001t0008g0099a0001c0001t0008g0126a0001c0001t0008g0146 | 3 | HG02145.hp1 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.208+188C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73662230 | ||||||
chr14:73662242
|
A | G | 54 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(51): Show | 54 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(51): Show |
intron_variant | MODIFIER | c.208+200A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73662242 | ||||||
chr14:73662415
|
C | A | 114 | a0001c0001t0002g0003a0001c0001t0002g0154a0001c0001t0002g0155others(111): Show | 116 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.208+373C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73662415 | ||||||
chr14:73662419
|
C | T | 2 | a0001c0001t0048g0082a0001c0001t0049g0071 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.208+377C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73662419 | ||||||
chr14:73662550
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.208+508G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73662550 | ||||||
chr14:73662566
|
T | C | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.208+524T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73662566 | ||||||
chr14:73662793
|
A | G | 1 | a0001c0001t0001g0293 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.208+751A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73662793 | ||||||
chr14:73662807
|
C | CT | 28 | a0001c0001t0001g0241a0001c0001t0001g0284a0001c0001t0004g0017others(25): Show | 28 | HG01069.hp2 HG01071.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.208+784dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 73662807 | |||||
chr14:73662807
|
C | CTT | 9 | a0001c0001t0001g0286a0001c0001t0001g0287a0001c0001t0001g0288others(6): Show | 9 | NA18747.hp2 NA18945.hp1 NA18946.hp1 others(6): Show |
intron_variant | MODIFIER | c.208+783_208+784dup others(2): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 73662807 | |||||
chr14:73662807
|
CT | C | 10 | a0001c0001t0001g0294a0001c0001t0002g0186a0001c0001t0020g0311others(7): Show | 10 | HG02559.hp1 HG02615.hp2 HG02683.hp1 others(7): Show |
intron_variant | MODIFIER | c.208+784delT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 73662807 | |||||
chr14:73662807
|
CTT | C | 30 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(27): Show | 30 | HG01109.hp2 HG01243.hp2 HG01884.hp2 others(27): Show |
intron_variant | MODIFIER | c.208+783_208+784del others(2): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 73662807 | |||||
chr14:73662807
|
CTTTT | C | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.208+781_208+784del others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 73662807 | |||||
chr14:73662826
|
T | G | 71 | a0001c0001t0005g0085a0001c0001t0005g0091a0001c0001t0005g0092others(68): Show | 72 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(69): Show |
intron_variant | MODIFIER | c.208+784T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73662826 | ||||||
chr14:73662841
|
C | A | 1 | a0001c0001t0031g0227 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.208+799C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73662841 | ||||||
chr14:73662842
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.208+800G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73662842 | ||||||
chr14:73662933
|
T | G | 1 | a0001c0001t0010g0075 | 1 | NA18947.hp2 | intron_variant | MODIFIER | c.208+891T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73662933 | ||||||
chr14:73663068
|
A | G | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.208+1026A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73663068 | ||||||
chr14:73663137
|
G | T | 1 | a0001c0001t0050g0012 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.208+1095G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73663137 | ||||||
chr14:73663202
|
A | AT | 70 | a0001c0001t0001g0283a0001c0001t0005g0091a0001c0001t0005g0092others(67): Show | 70 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(67): Show |
intron_variant | MODIFIER | c.208+1181dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 73663202 | |||||
chr14:73663202
|
AT | A | 17 | a0001c0001t0002g0003a0001c0001t0002g0157a0001c0001t0002g0178others(14): Show | 18 | HG00099.hp2 HG01167.hp2 HG01169.hp1 others(15): Show |
intron_variant | MODIFIER | c.208+1181delT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 73663202 | |||||
chr14:73663262
|
G | A | 1 | a0001c0001t0001g0247 | 1 | HG02293.hp2 | intron_variant | MODIFIER | c.208+1220G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73663262 | ||||||
chr14:73663394
|
T | C | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.208+1352T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73663394 | ||||||
chr14:73663406
|
A | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.208+1364A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73663406 | ||||||
chr14:73663431
|
C | T | 40 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.208+1389C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73663431 | ||||||
chr14:73663813
|
G | T | 1 | a0001c0001t0101g0314 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.208+1771G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73663813 | ||||||
chr14:73663816
|
G | A | 2 | a0001c0001t0048g0082a0001c0001t0049g0071 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.208+1774G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73663816 | ||||||
chr14:73663836
|
A | G | 1 | a0001c0001t0001g0292 | 1 | NA18991.hp2 | intron_variant | MODIFIER | c.208+1794A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73663836 | ||||||
chr14:73663929
|
A | C | 4 | a0001c0001t0007g0216a0001c0001t0007g0223a0001c0001t0007g0224others(1): Show | 4 | NA18964.hp2 NA18980.hp2 NA18986.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+1887A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73663929 | ||||||
chr14:73663952
|
G | A | 306 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(303): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.208+1910G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73663952 | ||||||
chr14:73664039
|
A | C | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.208+1997A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73664039 | ||||||
chr14:73664087
|
A | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.208+2045A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73664087 | ||||||
chr14:73664455
|
T | C | 14 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(11): Show | 14 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(11): Show |
intron_variant | MODIFIER | c.208+2413T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73664455 | ||||||
chr14:73664518
|
A | G | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.208+2476A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73664518 | ||||||
chr14:73664536
|
A | G | 1 | a0001c0001t0042g0196 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.208+2494A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73664536 | ||||||
chr14:73664605
|
A | T | 3 | a0001c0001t0013g0051a0001c0001t0013g0052a0001c0001t0044g0050 | 3 | HG00323.hp2 HG02040.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.208+2563A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73664605 | ||||||
chr14:73664628
|
G | A | 4 | a0001c0001t0033g0232a0001c0001t0064g0233a0001c0001t0065g0218others(1): Show | 4 | HG02559.hp1 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+2586G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73664628 | ||||||
chr14:73664667
|
G | A | 1 | a0001c0001t0104g0312 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.208+2625G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73664667 | ||||||
chr14:73664859
|
TA | T | 111 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(108): Show | 113 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(110): Show |
intron_variant | MODIFIER | c.208+2828delA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 73664859 | |||||
chr14:73664872
|
A | T | 123 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(120): Show | 125 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(122): Show |
intron_variant | MODIFIER | c.208+2830A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73664872 | ||||||
chr14:73665002
|
C | T | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.208+2960C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73665002 | ||||||
chr14:73665022
|
A | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.208+2980A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73665022 | ||||||
chr14:73665036
|
T | C | 1 | a0001c0001t0001g0248 | 1 | HG01975.hp1 | intron_variant | MODIFIER | c.208+2994T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73665036 | ||||||
chr14:73665042
|
T | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(81): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.208+3000T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73665042 | ||||||
chr14:73665234
|
C | G | 1 | a0001c0001t0069g0282 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.208+3192C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73665234 | ||||||
chr14:73665261
|
C | T | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.208+3219C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73665261 | ||||||
chr14:73665519
|
G | A | 1 | a0001c0001t0005g0085 | 1 | HG00438.hp1 | intron_variant | MODIFIER | c.208+3477G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73665519 | ||||||
chr14:73665556
|
C | T | 2 | a0001c0001t0032g0088a0001c0001t0032g0089 | 2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.208+3514C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73665556 | ||||||
chr14:73665557
|
G | A | 4 | a0001c0001t0006g0249a0001c0001t0006g0250a0001c0001t0068g0251others(1): Show | 4 | HG00544.hp1 HG02071.hp1 NA18981.hp2 others(1): Show |
intron_variant | MODIFIER | c.208+3515G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73665557 | ||||||
chr14:73665561
|
C | T | 4 | a0001c0001t0009g0093a0001c0001t0009g0101a0001c0001t0009g0102others(1): Show | 4 | HG01074.hp2 HG01243.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.208+3519C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73665561 | ||||||
chr14:73665629
|
A | G | 1 | a0001c0001t0014g0333 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.208+3587A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73665629 | ||||||
chr14:73665833
|
C | G | 7 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(4): Show | 7 | HG01884.hp2 HG02055.hp1 HG02257.hp2 others(4): Show |
intron_variant | MODIFIER | c.208+3791C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73665833 | ||||||
chr14:73666050
|
A | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.208+4008A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73666050 | ||||||
chr14:73666398
|
A | G | 1 | a0001c0001t0001g0291 | 1 | NA18945.hp1 | intron_variant | MODIFIER | c.208+4356A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73666398 | ||||||
chr14:73666544
|
G | C | 3 | a0001c0001t0021g0317a0001c0001t0021g0318a0001c0001t0021g0319 | 3 | HG01109.hp2 HG03209.hp1 HG03225.hp2 |
intron_variant | MODIFIER | c.208+4502G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73666544 | ||||||
chr14:73666546
|
A | G | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.208+4504A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73666546 | ||||||
chr14:73666607
|
G | A | 1 | a0001c0001t0008g0099 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.208+4565G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73666607 | ||||||
chr14:73666695
|
G | A | 1 | a0001c0001t0074g0252 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.208+4653G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73666695 | ||||||
chr14:73666936
|
C | T | 8 | a0001c0001t0014g0328a0001c0001t0014g0329a0001c0001t0014g0330others(5): Show | 8 | HG01168.hp1 HG01515.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-4606C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73666936 | ||||||
chr14:73667154
|
CT | C | 8 | a0001c0001t0002g0186a0001c0001t0007g0223a0001c0001t0009g0101others(5): Show | 8 | HG01243.hp1 HG02109.hp1 HG02559.hp2 others(5): Show |
intron_variant | MODIFIER | c.209-4376delT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 73667154 | |||||
chr14:73667166
|
T | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.209-4376T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73667166 | ||||||
chr14:73667244
|
T | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.209-4298T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73667244 | ||||||
chr14:73667247
|
A | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.209-4295A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73667247 | ||||||
chr14:73667303
|
A | G | 1 | a0001c0001t0088g0112 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.209-4239A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73667303 | ||||||
chr14:73667343
|
T | C | 1 | a0001c0001t0001g0299 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.209-4199T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73667343 | ||||||
chr14:73667348
|
C | T | 7 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-4194C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73667348 | ||||||
chr14:73667490
|
A | T | 1 | a0001c0001t0014g0333 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.209-4052A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73667490 | ||||||
chr14:73667567
|
C | T | 5 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-3975C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73667567 | ||||||
chr14:73667767
|
T | G | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.209-3775T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73667767 | ||||||
chr14:73667782
|
G | A | 35 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.209-3760G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73667782 | ||||||
chr14:73667940
|
GACTT | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.209-3595_209-3592d others(6): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 73667940 | |||||
chr14:73668008
|
T | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.209-3534T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73668008 | ||||||
chr14:73668014
|
G | T | 35 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.209-3528G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73668014 | ||||||
chr14:73668059
|
A | T | 2 | a0001c0001t0032g0088a0001c0001t0032g0089 | 2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.209-3483A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73668059 | ||||||
chr14:73668078
|
G | C | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.209-3464G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73668078 | ||||||
chr14:73668242
|
T | TATC | 84 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(81): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.209-3299_209-3297d others(5): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 73668242 | |||||
chr14:73668384
|
G | A | 2 | a0001c0001t0008g0090a0001c0001t0008g0127 | 2 | HG00738.hp2 HG02683.hp2 |
intron_variant | MODIFIER | c.209-3158G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73668384 | ||||||
chr14:73668421
|
T | A | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.209-3121T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73668421 | ||||||
chr14:73668501
|
G | A | 19 | a0001c0001t0007g0210a0001c0001t0007g0211a0001c0001t0007g0212others(16): Show | 19 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.209-3041G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73668501 | ||||||
chr14:73668519
|
G | C | 114 | a0001c0001t0002g0003a0001c0001t0002g0154a0001c0001t0002g0155others(111): Show | 116 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.209-3023G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73668519 | ||||||
chr14:73668643
|
G | A | 13 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.209-2899G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73668643 | ||||||
chr14:73668762
|
C | T | 5 | a0001c0001t0020g0310a0001c0001t0020g0311a0001c0001t0020g0313others(2): Show | 5 | HG01891.hp2 HG03139.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.209-2780C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73668762 | ||||||
chr14:73668867
|
G | T | 2 | a0001c0001t0006g0280a0001c0001t0006g0281 | 2 | NA18979.hp1 NA18984.hp2 |
intron_variant | MODIFIER | c.209-2675G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73668867 | ||||||
chr14:73668916
|
A | G | 22 | a0001c0001t0008g0090a0001c0001t0008g0099a0001c0001t0008g0126others(19): Show | 22 | HG00738.hp2 HG01081.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.209-2626A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73668916 | ||||||
chr14:73668924
|
G | A | 2 | a0001c0001t0004g0026a0001c0001t0072g0027 | 2 | NA18978.hp2 NA18980.hp1 |
intron_variant | MODIFIER | c.209-2618G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73668924 | ||||||
chr14:73669010
|
G | C | 2 | a0001c0001t0034g0158a0001c0001t0034g0190 | 2 | HG00642.hp1 HG03688.hp2 |
intron_variant | MODIFIER | c.209-2532G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73669010 | ||||||
chr14:73669144
|
T | C | 1 | a0001c0001t0032g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.209-2398T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73669144 | ||||||
chr14:73669195
|
A | G | 1 | a0001c0001t0004g0035 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.209-2347A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73669195 | ||||||
chr14:73669214
|
C | G | 5 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-2328C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73669214 | ||||||
chr14:73669279
|
C | A | 35 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.209-2263C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73669279 | ||||||
chr14:73669338
|
G | A | 2 | a0001c0001t0001g0291a0001c0001t0092g0131 | 2 | HG03209.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.209-2204G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73669338 | ||||||
chr14:73669367
|
C | T | 5 | a0001c0001t0033g0226a0001c0001t0033g0232a0001c0001t0064g0233others(2): Show | 5 | HG02559.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.209-2175C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73669367 | ||||||
chr14:73669496
|
C | T | 2 | a0001c0001t0052g0235a0001c0001t0057g0234 | 2 | HG02886.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.209-2046C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73669496 | ||||||
chr14:73669510
|
C | T | 2 | a0001c0001t0032g0088a0001c0001t0032g0089 | 2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.209-2032C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73669510 | ||||||
chr14:73669540
|
G | T | 4 | a0001c0001t0032g0088a0001c0001t0032g0089a0001c0001t0060g0009others(1): Show | 4 | HG02258.hp1 HG02486.hp2 HG02970.hp2 others(1): Show |
intron_variant | MODIFIER | c.209-2002G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73669540 | ||||||
chr14:73669650
|
G | A | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.209-1892G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73669650 | ||||||
chr14:73669681
|
C | T | 1 | a0001c0001t0002g0154 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.209-1861C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73669681 | ||||||
chr14:73669692
|
A | T | 1 | a0001c0001t0002g0154 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.209-1850A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73669692 | ||||||
chr14:73669756
|
C | T | 3 | a0001c0001t0025g0169a0001c0001t0035g0168a0001c0001t0035g0170 | 3 | HG00738.hp1 HG01123.hp2 HG01358.hp1 |
intron_variant | MODIFIER | c.209-1786C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73669756 | ||||||
chr14:73669826
|
A | G | 2 | a0001c0001t0005g0107a0001c0001t0005g0108 | 2 | NA18971.hp1 NA19085.hp2 |
intron_variant | MODIFIER | c.209-1716A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73669826 | ||||||
chr14:73669836
|
A | T | 1 | a0001c0001t0002g0154 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.209-1706A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73669836 | ||||||
chr14:73669893
|
A | G | 2 | a0001c0001t0002g0167a0001c0001t0002g0194 | 2 | NA18950.hp2 NA18957.hp1 |
intron_variant | MODIFIER | c.209-1649A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73669893 | ||||||
chr14:73669984
|
T | TACAC | 4 | a0001c0001t0033g0232a0001c0001t0064g0233a0001c0001t0065g0218others(1): Show | 4 | HG02559.hp1 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-1544_209-1541d others(6): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 73669984 | |||||
chr14:73669984
|
TAC | T | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.209-1542_209-1541d others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | INFO_REALIGN_3_PRIME | chr14 | 73669984 | |||||
chr14:73670039
|
T | G | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.209-1503T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73670039 | ||||||
chr14:73670124
|
A | G | 1 | a0001c0001t0104g0312 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.209-1418A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73670124 | ||||||
chr14:73670130
|
G | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.209-1412G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73670130 | ||||||
chr14:73670535
|
A | G | 1 | a0001c0001t0009g0111 | 1 | NA19030.hp2 | intron_variant | MODIFIER | c.209-1007A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73670535 | ||||||
chr14:73670745
|
A | T | 2 | a0001c0001t0001g0279a0001c0001t0074g0252 | 2 | HG02602.hp2 HG03688.hp1 |
intron_variant | MODIFIER | c.209-797A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73670745 | ||||||
chr14:73670776
|
G | A | 1 | a0001c0001t0012g0198 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.209-766G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73670776 | ||||||
chr14:73670861
|
C | T | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.209-681C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73670861 | ||||||
chr14:73670978
|
C | T | 4 | a0001c0001t0009g0093a0001c0001t0009g0101a0001c0001t0009g0102others(1): Show | 4 | HG01074.hp2 HG01243.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.209-564C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73670978 | ||||||
chr14:73671027
|
C | T | 35 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.209-515C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73671027 | ||||||
chr14:73671081
|
C | A | 72 | a0001c0001t0005g0085a0001c0001t0005g0091a0001c0001t0005g0092others(69): Show | 73 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.209-461C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73671081 | ||||||
chr14:73671089
|
A | C | 307 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(304): Show | 311 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(308): Show |
intron_variant | MODIFIER | c.209-453A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73671089 | ||||||
chr14:73671097
|
T | G | 1 | a0001c0001t0025g0156 | 1 | NA20752.hp1 | intron_variant | MODIFIER | c.209-445T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73671097 | ||||||
chr14:73671157
|
T | C | 114 | a0001c0001t0002g0003a0001c0001t0002g0154a0001c0001t0002g0155others(111): Show | 116 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.209-385T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73671157 | ||||||
chr14:73671217
|
T | G | 1 | a0001c0001t0058g0220 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.209-325T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73671217 | ||||||
chr14:73671247
|
T | C | 7 | a0001c0001t0017g0205a0001c0001t0017g0207a0001c0001t0017g0208others(4): Show | 7 | HG01243.hp2 HG01891.hp1 HG02717.hp1 others(4): Show |
intron_variant | MODIFIER | c.209-295T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73671247 | ||||||
chr14:73671369
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.209-173G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73671369 | ||||||
chr14:73671444
|
C | T | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.209-98C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 4/7 | chr14 | 73671444 | ||||||
chr14:73671687
|
A | G | 2 | a0001c0001t0002g0157a0001c0001t0002g0188 | 2 | HG00099.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.264+90A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73671687 | ||||||
chr14:73671739
|
A | G | 40 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.264+142A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73671739 | ||||||
chr14:73671781
|
C | T | 2 | a0001c0001t0009g0327a0001c0001t0098g0326 | 2 | HG02622.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.264+184C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73671781 | ||||||
chr14:73671906
|
A | G | 4 | a0001c0001t0017g0207a0001c0001t0017g0208a0001c0001t0017g0209others(1): Show | 4 | HG02895.hp1 HG03486.hp2 HG03540.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+309A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73671906 | ||||||
chr14:73671962
|
A | C | 4 | a0001c0001t0021g0317a0001c0001t0021g0318a0001c0001t0021g0319others(1): Show | 4 | HG01109.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.264+365A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73671962 | ||||||
chr14:73672105
|
A | G | 6 | a0001c0001t0014g0328a0001c0001t0014g0329a0001c0001t0014g0330others(3): Show | 6 | HG01168.hp1 HG01515.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.264+508A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73672105 | ||||||
chr14:73672243
|
T | C | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+646T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73672243 | ||||||
chr14:73672303
|
G | GT | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+706_264+707ins others(1): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73672303 | ||||||
chr14:73672304
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+707C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73672304 | ||||||
chr14:73672372
|
G | A | 84 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(81): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.264+775G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73672372 | ||||||
chr14:73672480
|
C | T | 1 | a0001c0001t0050g0012 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.264+883C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73672480 | ||||||
chr14:73672501
|
G | T | 1 | a0001c0001t0010g0078 | 1 | HG03017.hp2 | intron_variant | MODIFIER | c.264+904G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73672501 | ||||||
chr14:73672564
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+967C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73672564 | ||||||
chr14:73672565
|
G | A | 1 | a0001c0001t0015g0121 | 1 | NA18957.hp2 | intron_variant | MODIFIER | c.264+968G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73672565 | ||||||
chr14:73672584
|
G | A | 1 | a0001c0001t0015g0334 | 1 | HG02922.hp1 | intron_variant | MODIFIER | c.264+987G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73672584 | ||||||
chr14:73672595
|
G | A | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.264+998G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73672595 | ||||||
chr14:73672607
|
CA | C | 288 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(285): Show | 292 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(289): Show |
intron_variant | MODIFIER | c.264+1029delA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73672607 | |||||
chr14:73672651
|
G | A | 1 | a0001c0001t0003g0041 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.264+1054G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73672651 | ||||||
chr14:73672759
|
A | AT | 49 | a0001c0001t0002g0159a0001c0001t0002g0193a0001c0001t0003g0001others(46): Show | 49 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(46): Show |
intron_variant | MODIFIER | c.264+1176dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73672759 | |||||
chr14:73672849
|
G | A | 72 | a0001c0001t0005g0085a0001c0001t0005g0091a0001c0001t0005g0092others(69): Show | 73 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.264+1252G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73672849 | ||||||
chr14:73673001
|
G | A | 1 | a0001c0001t0031g0227 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.264+1404G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73673001 | ||||||
chr14:73673141
|
G | GT | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+1544_264+1545i others(3): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73673141 | ||||||
chr14:73673333
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+1736C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73673333 | ||||||
chr14:73673402
|
C | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+1805C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73673402 | ||||||
chr14:73673508
|
C | T | 1 | a0001c0001t0001g0296 | 1 | NA18944.hp2 | intron_variant | MODIFIER | c.264+1911C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73673508 | ||||||
chr14:73673554
|
A | G | 22 | a0001c0001t0007g0210a0001c0001t0007g0211a0001c0001t0007g0212others(19): Show | 22 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(19): Show |
intron_variant | MODIFIER | c.264+1957A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73673554 | ||||||
chr14:73673561
|
G | A | 1 | a0001c0001t0088g0112 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.264+1964G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73673561 | ||||||
chr14:73673718
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+2121G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73673718 | ||||||
chr14:73673864
|
A | C | 4 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.264+2267A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73673864 | ||||||
chr14:73673886
|
G | A | 2 | a0001c0001t0002g0160a0001c0001t0015g0334 | 2 | HG02922.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.264+2289G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73673886 | ||||||
chr14:73673886
|
G | GA | 324 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(321): Show | 328 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(325): Show |
intron_variant | MODIFIER | c.264+2299dupA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73673886 | |||||
chr14:73673962
|
G | T | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.264+2365G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73673962 | ||||||
chr14:73674132
|
A | G | 2 | a0001c0001t0028g0135a0001c0001t0090g0114 | 2 | HG03098.hp2 HG03486.hp1 |
intron_variant | MODIFIER | c.264+2535A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73674132 | ||||||
chr14:73674231
|
A | G | 1 | a0001c0001t0009g0153 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.264+2634A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73674231 | ||||||
chr14:73674295
|
A | G | 4 | a0001c0001t0021g0317a0001c0001t0021g0318a0001c0001t0021g0319others(1): Show | 4 | HG01109.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.264+2698A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73674295 | ||||||
chr14:73674358
|
CTCCTCAA others(61): Show |
C | 6 | a0001c0001t0008g0090a0001c0001t0028g0115a0001c0001t0029g0079others(3): Show | 6 | HG00738.hp2 HG01884.hp1 HG03041.hp1 others(3): Show |
intron_variant | MODIFIER | c.264+2829_264+2896d others(70): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73674358 | |||||
chr14:73674426
|
T | C | 300 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(297): Show | 304 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(301): Show |
intron_variant | MODIFIER | c.264+2829T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73674426 | ||||||
chr14:73674449
|
G | A | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.264+2852G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73674449 | ||||||
chr14:73674613
|
C | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+3016C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73674613 | ||||||
chr14:73674726
|
A | G | 222 | a0001c0001t0002g0003a0001c0001t0002g0154a0001c0001t0002g0155others(219): Show | 224 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(221): Show |
intron_variant | MODIFIER | c.264+3129A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73674726 | ||||||
chr14:73674847
|
C | T | 1 | a0001c0001t0050g0012 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.264+3250C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73674847 | ||||||
chr14:73674849
|
T | C | 40 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.264+3252T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73674849 | ||||||
chr14:73675013
|
G | A | 1 | a0001c0001t0042g0196 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.264+3416G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675013 | ||||||
chr14:73675116
|
G | A | 2 | a0001c0001t0048g0082a0001c0001t0049g0071 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.264+3519G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675116 | ||||||
chr14:73675185
|
TTC | T | 34 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(31): Show | 34 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(31): Show |
intron_variant | MODIFIER | c.264+3605_264+3606d others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73675185 | |||||
chr14:73675202
|
T | A | 6 | a0001c0001t0002g0161a0001c0001t0022g0057a0001c0001t0022g0058others(3): Show | 6 | HG00639.hp2 HG01070.hp2 HG01071.hp2 others(3): Show |
intron_variant | MODIFIER | c.264+3605T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675202 | ||||||
chr14:73675204
|
A | T | 2 | a0001c0001t0029g0079a0001c0001t0037g0080 | 2 | HG03041.hp1 HG03130.hp1 |
intron_variant | MODIFIER | c.264+3607A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675204 | ||||||
chr14:73675209
|
C | A | 3 | a0001c0001t0022g0057a0001c0001t0022g0058a0001c0001t0022g0059 | 3 | HG00639.hp2 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.264+3612C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675209 | ||||||
chr14:73675211
|
A | AAC | 6 | a0001c0001t0014g0328a0001c0001t0021g0317a0001c0001t0021g0318others(3): Show | 6 | HG01109.hp2 HG02109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.264+3634_264+3635d others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73675211 | |||||
chr14:73675211
|
A | C | 3 | a0001c0001t0022g0057a0001c0001t0022g0058a0001c0001t0022g0059 | 3 | HG00639.hp2 HG01070.hp2 HG01071.hp2 |
intron_variant | MODIFIER | c.264+3614A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675211 | ||||||
chr14:73675211
|
AACACAC | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+3630_264+3635d others(8): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73675211 | |||||
chr14:73675213
|
C | T | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.264+3616C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675213 | ||||||
chr14:73675231
|
CAA | C | 4 | a0001c0001t0009g0093a0001c0001t0009g0101a0001c0001t0009g0102others(1): Show | 4 | HG01074.hp2 HG01243.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.264+3636_264+3637d others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73675231 | |||||
chr14:73675279
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.264+3682G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675279 | ||||||
chr14:73675310
|
G | A | 1 | a0001c0001t0081g0129 | 1 | HG02486.hp1 | intron_variant | MODIFIER | c.264+3713G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675310 | ||||||
chr14:73675338
|
C | T | 1 | a0001c0001t0003g0069 | 1 | HG03491.hp2 | intron_variant | MODIFIER | c.264+3741C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675338 | ||||||
chr14:73675357
|
A | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+3760A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675357 | ||||||
chr14:73675414
|
G | A | 7 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.264+3817G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675414 | ||||||
chr14:73675478
|
A | T | 114 | a0001c0001t0002g0003a0001c0001t0002g0154a0001c0001t0002g0155others(111): Show | 116 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.264+3881A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675478 | ||||||
chr14:73675479
|
T | A | 1 | a0001c0001t0104g0312 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.264+3882T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675479 | ||||||
chr14:73675728
|
A | G | 6 | a0001c0001t0014g0328a0001c0001t0014g0329a0001c0001t0014g0330others(3): Show | 6 | HG01168.hp1 HG01515.hp2 HG02109.hp2 others(3): Show |
intron_variant | MODIFIER | c.264+4131A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675728 | ||||||
chr14:73675755
|
C | T | 1 | a0001c0001t0066g0141 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.264+4158C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675755 | ||||||
chr14:73675812
|
C | T | 1 | a0001c0001t0014g0331 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.264+4215C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675812 | ||||||
chr14:73675820
|
G | C | 35 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.264+4223G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675820 | ||||||
chr14:73675887
|
T | C | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+4290T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675887 | ||||||
chr14:73675892
|
G | A | 1 | a0001c0001t0103g0309 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.264+4295G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675892 | ||||||
chr14:73675911
|
A | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+4314A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675911 | ||||||
chr14:73675968
|
T | C | 72 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(69): Show | 72 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.264+4371T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73675968 | ||||||
chr14:73676013
|
C | T | 2 | a0001c0001t0001g0276a0001c0001t0001g0277 | 2 | HG01070.hp1 HG01192.hp2 |
intron_variant | MODIFIER | c.264+4416C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676013 | ||||||
chr14:73676065
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+4468C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676065 | ||||||
chr14:73676093
|
G | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+4496G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676093 | ||||||
chr14:73676095
|
G | A | 1 | a0001c0001t0004g0023 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.264+4498G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676095 | ||||||
chr14:73676097
|
G | T | 1 | a0001c0001t0008g0128 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.264+4500G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676097 | ||||||
chr14:73676104
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+4507C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676104 | ||||||
chr14:73676200
|
C | T | 1 | a0001c0001t0104g0312 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.264+4603C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676200 | ||||||
chr14:73676233
|
C | CA | 6 | a0001c0001t0021g0317a0001c0001t0021g0318a0001c0001t0021g0319others(3): Show | 6 | HG01109.hp2 HG02451.hp2 HG03209.hp1 others(3): Show |
intron_variant | MODIFIER | c.264+4650dupA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73676233 | |||||
chr14:73676244
|
A | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+4647A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676244 | ||||||
chr14:73676286
|
G | A | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.264+4689G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676286 | ||||||
chr14:73676315
|
T | C | 5 | a0001c0001t0004g0013a0001c0001t0004g0022a0001c0001t0004g0031others(2): Show | 5 | HG00639.hp1 HG00735.hp2 HG01261.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+4718T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676315 | ||||||
chr14:73676448
|
ATG | A | 114 | a0001c0001t0002g0003a0001c0001t0002g0154a0001c0001t0002g0155others(111): Show | 116 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.264+4863_264+4864d others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73676448 | |||||
chr14:73676448
|
ATGTG | A | 5 | a0001c0001t0020g0310a0001c0001t0020g0311a0001c0001t0020g0313others(2): Show | 5 | HG01891.hp2 HG03139.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+4861_264+4864d others(6): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73676448 | |||||
chr14:73676466
|
T | C | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.264+4869T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676466 | ||||||
chr14:73676467
|
T | G | 5 | a0001c0001t0033g0226a0001c0001t0033g0232a0001c0001t0064g0233others(2): Show | 5 | HG02559.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+4870T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676467 | ||||||
chr14:73676536
|
A | G | 1 | a0001c0001t0004g0018 | 1 | HG01952.hp1 | intron_variant | MODIFIER | c.264+4939A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676536 | ||||||
chr14:73676551
|
C | G | 1 | a0001c0001t0005g0106 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.264+4954C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676551 | ||||||
chr14:73676590
|
G | A | 5 | a0001c0001t0020g0310a0001c0001t0020g0311a0001c0001t0020g0313others(2): Show | 5 | HG01891.hp2 HG03139.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+4993G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676590 | ||||||
chr14:73676663
|
G | A | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.264+5066G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676663 | ||||||
chr14:73676694
|
TTCTC | T | 4 | a0001c0001t0010g0253a0001c0001t0010g0254a0001c0001t0010g0255others(1): Show | 4 | HG01167.hp1 HG01169.hp2 HG01952.hp2 others(1): Show |
intron_variant | MODIFIER | c.264+5110_264+5113d others(6): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73676694 | |||||
chr14:73676761
|
A | G | 4 | a0001c0001t0011g0005a0001c0001t0011g0274a0001c0001t0011g0275others(1): Show | 5 | HG00140.hp2 HG00642.hp2 HG00735.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+5164A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676761 | ||||||
chr14:73676898
|
A | G | 2 | a0001c0001t0048g0082a0001c0001t0049g0071 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.264+5301A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676898 | ||||||
chr14:73676963
|
A | AT | 52 | a0001c0001t0001g0272a0001c0001t0002g0003a0001c0001t0002g0154others(49): Show | 53 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(50): Show |
intron_variant | MODIFIER | c.264+5387dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73676963 | |||||
chr14:73676963
|
A | ATT | 8 | a0001c0001t0002g0164a0001c0001t0002g0165a0001c0001t0002g0166others(5): Show | 8 | HG02155.hp1 NA18612.hp2 NA18950.hp2 others(5): Show |
intron_variant | MODIFIER | c.264+5386_264+5387d others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73676963 | |||||
chr14:73676963
|
AT | A | 49 | a0001c0001t0001g0256a0001c0001t0001g0257a0001c0001t0003g0001others(46): Show | 49 | HG00099.hp1 HG00323.hp1 HG00639.hp2 others(46): Show |
intron_variant | MODIFIER | c.264+5387delT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73676963 | |||||
chr14:73676984
|
T | A | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.264+5387T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73676984 | ||||||
chr14:73677033
|
T | C | 55 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(52): Show | 55 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(52): Show |
intron_variant | MODIFIER | c.264+5436T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677033 | ||||||
chr14:73677052
|
G | A | 1 | a0001c0001t0042g0196 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.264+5455G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677052 | ||||||
chr14:73677072
|
G | A | 1 | a0001c0001t0099g0195 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.264+5475G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677072 | ||||||
chr14:73677075
|
A | G | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.264+5478A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677075 | ||||||
chr14:73677116
|
G | A | 1 | a0001c0001t0049g0071 | 1 | HG03453.hp1 | intron_variant | MODIFIER | c.264+5519G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677116 | ||||||
chr14:73677269
|
C | T | 1 | a0001c0001t0003g0066 | 1 | HG02129.hp2 | intron_variant | MODIFIER | c.264+5672C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677269 | ||||||
chr14:73677353
|
A | G | 1 | a0001c0001t0055g0016 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.264+5756A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677353 | ||||||
chr14:73677366
|
C | T | 13 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.264+5769C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677366 | ||||||
chr14:73677455
|
G | A | 2 | a0001c0001t0032g0088a0001c0001t0032g0089 | 2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.264+5858G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677455 | ||||||
chr14:73677487
|
C | T | 11 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.264+5890C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677487 | ||||||
chr14:73677554
|
A | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+5957A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677554 | ||||||
chr14:73677558
|
A | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+5961A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677558 | ||||||
chr14:73677562
|
A | T | 303 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(300): Show | 307 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
intron_variant | MODIFIER | c.264+5965A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677562 | ||||||
chr14:73677565
|
T | A | 39 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(36): Show | 39 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(36): Show |
intron_variant | MODIFIER | c.264+5968T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677565 | ||||||
chr14:73677566
|
A | T | 1 | a0001c0001t0004g0038 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.264+5969A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677566 | ||||||
chr14:73677649
|
C | T | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.264+6052C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677649 | ||||||
chr14:73677707
|
C | T | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.264+6110C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677707 | ||||||
chr14:73677768
|
A | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+6171A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677768 | ||||||
chr14:73677792
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+6195C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677792 | ||||||
chr14:73677804
|
A | G | 3 | a0001c0001t0002g0160a0001c0001t0048g0082a0001c0001t0049g0071 | 3 | HG02886.hp1 HG03453.hp1 NA19058.hp2 |
intron_variant | MODIFIER | c.264+6207A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677804 | ||||||
chr14:73677808
|
T | C | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.264+6211T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677808 | ||||||
chr14:73677809
|
G | A | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.264+6212G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677809 | ||||||
chr14:73677866
|
A | T | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.264+6269A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677866 | ||||||
chr14:73677880
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0033g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.264+6284_264+6285i others(14): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677880 | |||||
chr14:73677880
|
A | ATTTGTGT others(7): Show |
1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.264+6284_264+6285i others(16): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677880 | |||||
chr14:73677880
|
ATATT | A | 12 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(9): Show | 12 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.264+6285_264+6288d others(6): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677880 | |||||
chr14:73677880
|
ATATTTGT others(3): Show |
A | 35 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.264+6285_264+6294d others(12): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677880 | |||||
chr14:73677880
|
ATATTTGT others(5): Show |
A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+6285_264+6296d others(14): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677880 | |||||
chr14:73677882
|
A | ATATATTT others(5): Show |
1 | a0001c0001t0014g0333 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.264+6286_264+6287i others(14): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677882 | |||||
chr14:73677882
|
A | ATATATTT others(7): Show |
1 | a0001c0001t0056g0332 | 1 | HG01168.hp1 | intron_variant | MODIFIER | c.264+6286_264+6287i others(16): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677882 | |||||
chr14:73677882
|
A | ATATT | 14 | a0001c0001t0007g0212a0001c0001t0007g0214a0001c0001t0007g0216others(11): Show | 14 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(11): Show |
intron_variant | MODIFIER | c.264+6286_264+6287i others(6): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677882 | |||||
chr14:73677882
|
A | ATATTTGT others(1): Show |
7 | a0001c0001t0007g0213a0001c0001t0008g0139a0001c0001t0014g0328others(4): Show | 7 | HG02080.hp2 HG02109.hp2 HG02486.hp2 others(4): Show |
intron_variant | MODIFIER | c.264+6286_264+6287i others(10): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677882 | |||||
chr14:73677882
|
A | ATATTTGT others(3): Show |
5 | a0001c0001t0014g0329a0001c0001t0014g0330a0001c0001t0052g0235others(2): Show | 5 | HG01515.hp2 HG02886.hp2 HG03195.hp1 others(2): Show |
intron_variant | MODIFIER | c.264+6286_264+6287i others(12): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677882 | |||||
chr14:73677882
|
A | ATGTGTGT others(3): Show |
3 | a0001c0001t0033g0232a0001c0001t0064g0233a0001c0001t0080g0225 | 3 | HG02559.hp1 HG02723.hp1 HG02922.hp2 |
intron_variant | MODIFIER | c.264+6286_264+6287i others(12): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677882 | |||||
chr14:73677882
|
A | ATGTGTGT others(5): Show |
1 | a0001c0001t0065g0218 | 1 | HG02615.hp2 | intron_variant | MODIFIER | c.264+6286_264+6287i others(14): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677882 | |||||
chr14:73677882
|
A | G | 4 | a0001c0001t0033g0226a0001c0001t0038g0084a0001c0001t0048g0082others(1): Show | 4 | HG02886.hp1 HG03139.hp1 HG03453.hp1 others(1): Show |
intron_variant | MODIFIER | c.264+6285A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677882 | ||||||
chr14:73677882
|
A | T | 1 | a0001c0001t0101g0314 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.264+6285A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677882 | ||||||
chr14:73677884
|
T | G | 42 | a0001c0001t0007g0210a0001c0001t0007g0211a0001c0001t0007g0212others(39): Show | 42 | HG01069.hp2 HG01071.hp1 HG01168.hp1 others(39): Show |
intron_variant | MODIFIER | c.264+6287T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677884 | ||||||
chr14:73677884
|
T | TTG | 7 | a0001c0001t0004g0013a0001c0001t0004g0022a0001c0001t0004g0031others(4): Show | 7 | HG00423.hp1 HG00639.hp1 HG00735.hp2 others(4): Show |
intron_variant | MODIFIER | c.264+6318_264+6319d others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677884 | |||||
chr14:73677884
|
T | TTGTG | 78 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(75): Show | 80 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(77): Show |
intron_variant | MODIFIER | c.264+6316_264+6319d others(6): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677884 | |||||
chr14:73677884
|
T | TTGTGTG | 13 | a0001c0001t0001g0276a0001c0001t0001g0277a0001c0001t0001g0298others(10): Show | 13 | HG01070.hp1 HG01074.hp1 HG01074.hp2 others(10): Show |
intron_variant | MODIFIER | c.264+6314_264+6319d others(8): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677884 | |||||
chr14:73677884
|
T | TTGTGTGT others(1): Show |
50 | a0001c0001t0001g0257a0001c0001t0005g0091a0001c0001t0005g0092others(47): Show | 51 | HG00544.hp2 HG00558.hp1 HG00621.hp2 others(48): Show |
intron_variant | MODIFIER | c.264+6312_264+6319d others(10): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677884 | |||||
chr14:73677884
|
T | TTGTGTGT others(3): Show |
30 | a0001c0001t0002g0003a0001c0001t0002g0154a0001c0001t0002g0159others(27): Show | 31 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(28): Show |
intron_variant | MODIFIER | c.264+6310_264+6319d others(12): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677884 | |||||
chr14:73677884
|
T | TTGTGTGT others(5): Show |
12 | a0001c0001t0002g0161a0001c0001t0002g0165a0001c0001t0002g0166others(9): Show | 12 | HG00733.hp2 HG00738.hp1 HG01123.hp2 others(9): Show |
intron_variant | MODIFIER | c.264+6308_264+6319d others(14): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677884 | |||||
chr14:73677884
|
T | TTGTGTGT others(7): Show |
6 | a0001c0001t0002g0167a0001c0001t0008g0090a0001c0001t0008g0127others(3): Show | 6 | HG00738.hp2 HG02683.hp2 HG02897.hp2 others(3): Show |
intron_variant | MODIFIER | c.264+6306_264+6319d others(16): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677884 | |||||
chr14:73677884
|
T | TTGTGTGT others(9): Show |
2 | a0001c0001t0002g0157a0001c0001t0059g0176 | 2 | HG01175.hp2 HG02257.hp1 |
intron_variant | MODIFIER | c.264+6304_264+6319d others(18): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677884 | |||||
chr14:73677884
|
T | TTGTGTGT others(11): Show |
1 | a0001c0001t0009g0151 | 1 | HG02258.hp2 | intron_variant | MODIFIER | c.264+6302_264+6319d others(20): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677884 | |||||
chr14:73677884
|
TTG | T | 13 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(10): Show | 13 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(10): Show |
intron_variant | MODIFIER | c.264+6318_264+6319d others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73677884 | |||||
chr14:73677886
|
G | T | 12 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(9): Show | 12 | HG01891.hp2 HG02055.hp1 HG02257.hp2 others(9): Show |
intron_variant | MODIFIER | c.264+6289G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677886 | ||||||
chr14:73677892
|
G | T | 35 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.264+6295G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677892 | ||||||
chr14:73677894
|
G | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+6297G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677894 | ||||||
chr14:73677919
|
G | A | 2 | a0001c0001t0014g0333a0001c0001t0056g0332 | 2 | HG01168.hp1 HG03492.hp2 |
intron_variant | MODIFIER | c.264+6322G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73677919 | ||||||
chr14:73678060
|
G | C | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+6463G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73678060 | ||||||
chr14:73678131
|
C | T | 10 | a0001c0001t0014g0328a0001c0001t0014g0329a0001c0001t0014g0330others(7): Show | 10 | HG01168.hp1 HG01515.hp2 HG02109.hp2 others(7): Show |
intron_variant | MODIFIER | c.264+6534C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73678131 | ||||||
chr14:73678144
|
C | T | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.264+6547C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73678144 | ||||||
chr14:73678149
|
C | T | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.264+6552C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73678149 | ||||||
chr14:73678157
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+6560C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73678157 | ||||||
chr14:73678224
|
T | A | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.264+6627T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73678224 | ||||||
chr14:73678241
|
GA | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+6647delA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73678241 | |||||
chr14:73678322
|
C | T | 306 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(303): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.264+6725C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73678322 | ||||||
chr14:73678433
|
G | GATA | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+6838_264+6839i others(5): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73678433 | |||||
chr14:73678511
|
C | CT | 90 | a0001c0001t0001g0240a0001c0001t0001g0242a0001c0001t0001g0272others(87): Show | 91 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(88): Show |
intron_variant | MODIFIER | c.264+6936dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73678511 | |||||
chr14:73678511
|
CT | C | 51 | a0001c0001t0001g0256a0001c0001t0001g0258a0001c0001t0002g0194others(48): Show | 51 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(48): Show |
intron_variant | MODIFIER | c.264+6936delT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73678511 | |||||
chr14:73678970
|
G | A | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.264+7373G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73678970 | ||||||
chr14:73679007
|
A | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.264+7410A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73679007 | ||||||
chr14:73679052
|
A | C | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.264+7455A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73679052 | ||||||
chr14:73679237
|
G | T | 32 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(29): Show | 32 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(29): Show |
intron_variant | MODIFIER | c.264+7640G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73679237 | ||||||
chr14:73679242
|
C | A | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.264+7645C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73679242 | ||||||
chr14:73679250
|
T | C | 3 | a0001c0001t0009g0149a0001c0001t0009g0150a0001c0001t0009g0151 | 3 | HG02258.hp2 HG02897.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.264+7653T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73679250 | ||||||
chr14:73679283
|
C | T | 5 | a0001c0001t0004g0015a0001c0001t0004g0026a0001c0001t0051g0020others(2): Show | 5 | HG02074.hp1 HG02523.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.264+7686C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73679283 | ||||||
chr14:73679319
|
G | A | 40 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.264+7722G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73679319 | ||||||
chr14:73679445
|
G | A | 5 | a0001c0001t0004g0015a0001c0001t0004g0026a0001c0001t0051g0020others(2): Show | 5 | HG02074.hp1 HG02523.hp2 NA18978.hp2 others(2): Show |
intron_variant | MODIFIER | c.265-7814G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73679445 | ||||||
chr14:73679501
|
A | C | 2 | a0001c0001t0032g0088a0001c0001t0032g0089 | 2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.265-7758A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73679501 | ||||||
chr14:73679612
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.265-7647C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73679612 | ||||||
chr14:73679732
|
G | A | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.265-7527G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73679732 | ||||||
chr14:73679798
|
C | CTTTT | 306 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(303): Show | 310 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(307): Show |
intron_variant | MODIFIER | c.265-7459_265-7458i others(6): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73679798 | |||||
chr14:73679856
|
G | C | 11 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.265-7403G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73679856 | ||||||
chr14:73679865
|
C | T | 3 | a0001c0001t0002g0191a0001c0001t0002g0192a0001c0001t0002g0193 | 3 | HG02056.hp2 NA18998.hp1 NA19055.hp2 |
intron_variant | MODIFIER | c.265-7394C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73679865 | ||||||
chr14:73679866
|
G | A | 4 | a0001c0001t0009g0093a0001c0001t0009g0101a0001c0001t0009g0102others(1): Show | 4 | HG01074.hp2 HG01243.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.265-7393G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73679866 | ||||||
chr14:73679879
|
CT | C | 86 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(83): Show | 88 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(85): Show |
intron_variant | MODIFIER | c.265-7368delT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73679879 | |||||
chr14:73679995
|
G | A | 1 | a0001c0001t0067g0217 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.265-7264G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73679995 | ||||||
chr14:73680119
|
G | A | 1 | a0001c0001t0050g0012 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.265-7140G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73680119 | ||||||
chr14:73680221
|
T | C | 17 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(14): Show | 17 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.265-7038T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73680221 | ||||||
chr14:73680265
|
G | A | 13 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.265-6994G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73680265 | ||||||
chr14:73680296
|
T | C | 1 | a0001c0001t0009g0102 | 1 | HG01074.hp2 | intron_variant | MODIFIER | c.265-6963T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73680296 | ||||||
chr14:73680384
|
A | G | 1 | a0001c0001t0033g0226 | 1 | NA18522.hp2 | intron_variant | MODIFIER | c.265-6875A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73680384 | ||||||
chr14:73680536
|
A | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.265-6723A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73680536 | ||||||
chr14:73680543
|
T | C | 7 | a0001c0001t0028g0115a0001c0001t0028g0134a0001c0001t0083g0104others(4): Show | 7 | HG01496.hp2 HG01884.hp1 HG02145.hp2 others(4): Show |
intron_variant | MODIFIER | c.265-6716T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73680543 | ||||||
chr14:73680583
|
G | A | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.265-6676G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73680583 | ||||||
chr14:73680630
|
C | CACTT | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.265-6628_265-6627i others(6): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73680630 | |||||
chr14:73680660
|
ATCTTC | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.265-6592_265-6588d others(7): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73680660 | |||||
chr14:73680762
|
A | G | 1 | a0001c0001t0103g0309 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.265-6497A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73680762 | ||||||
chr14:73680825
|
G | C | 1 | a0001c0001t0019g0259 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.265-6434G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73680825 | ||||||
chr14:73680842
|
G | C | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.265-6417G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73680842 | ||||||
chr14:73680855
|
A | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.265-6404A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73680855 | ||||||
chr14:73681092
|
TTTG | T | 38 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.265-6155_265-6153d others(5): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681092 | |||||
chr14:73681138
|
C | CT | 27 | a0001c0001t0001g0269a0001c0001t0001g0270a0001c0001t0001g0271others(24): Show | 27 | HG00423.hp2 HG01070.hp1 HG01074.hp1 others(24): Show |
intron_variant | MODIFIER | c.265-6108dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681138 | |||||
chr14:73681202
|
C | T | 3 | a0001c0001t0008g0130a0001c0001t0009g0086a0001c0001t0009g0153 | 3 | HG01081.hp1 HG03098.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.265-6057C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681202 | ||||||
chr14:73681210
|
T | C | 1 | a0001c0001t0019g0307 | 1 | NA19090.hp1 | intron_variant | MODIFIER | c.265-6049T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681210 | ||||||
chr14:73681219
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.265-6040C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681219 | ||||||
chr14:73681295
|
G | A | 1 | a0001c0001t0014g0329 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.265-5964G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681295 | ||||||
chr14:73681433
|
T | TCCGCAAC others(4): Show |
3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.265-5826_265-5825i others(13): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681433 | ||||||
chr14:73681539
|
G | A | 42 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(39): Show | 42 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(39): Show |
intron_variant | MODIFIER | c.265-5720G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681539 | ||||||
chr14:73681539
|
G | T | 2 | a0001c0001t0009g0093a0001c0001t0009g0102 | 2 | HG01074.hp2 HG02970.hp1 |
intron_variant | MODIFIER | c.265-5720G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681539 | ||||||
chr14:73681605
|
CA | C | 7 | a0001c0001t0004g0015a0001c0001t0004g0022a0001c0001t0004g0026others(4): Show | 7 | HG01167.hp2 HG02074.hp1 HG02523.hp2 others(4): Show |
intron_variant | MODIFIER | c.265-5625delA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681605 | |||||
chr14:73681605
|
CAA | C | 7 | a0001c0001t0004g0031a0001c0001t0004g0032a0001c0001t0004g0243others(4): Show | 7 | HG00639.hp1 HG00735.hp2 HG03130.hp1 others(4): Show |
intron_variant | MODIFIER | c.265-5626_265-5625d others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681605 | |||||
chr14:73681605
|
CAAA | C | 7 | a0001c0001t0014g0329a0001c0001t0014g0330a0001c0001t0014g0331others(4): Show | 7 | HG01168.hp1 HG01515.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.265-5627_265-5625d others(5): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681605 | |||||
chr14:73681605
|
CAAAAAAA others(6): Show |
C | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.265-5637_265-5625d others(15): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681605 | |||||
chr14:73681605
|
CAAAAAAA others(8): Show |
C | 2 | a0001c0001t0049g0071a0001c0001t0052g0235 | 2 | HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.265-5639_265-5625d others(17): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681605 | |||||
chr14:73681605
|
CAAAAAAA others(10): Show |
C | 3 | a0001c0001t0013g0051a0001c0001t0013g0052a0001c0001t0044g0050 | 3 | HG00323.hp2 HG02040.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.265-5641_265-5625d others(19): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681605 | |||||
chr14:73681618
|
AAAAAAAA others(10): Show |
A | 25 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0046others(22): Show | 25 | HG00140.hp1 HG00323.hp1 HG00639.hp2 others(22): Show |
intron_variant | MODIFIER | c.265-5639_265-5623d others(19): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681618 | |||||
chr14:73681619
|
AAAAAAAA others(11): Show |
A | 1 | a0001c0001t0003g0045 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.265-5638_265-5621d others(20): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681619 | |||||
chr14:73681620
|
AAAAAAAA others(8): Show |
A | 1 | a0001c0001t0048g0082 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.265-5637_265-5623d others(17): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681620 | |||||
chr14:73681620
|
AAAAAAAA others(10): Show |
A | 6 | a0001c0001t0003g0040a0001c0001t0003g0041a0001c0001t0003g0042others(3): Show | 6 | HG00099.hp1 HG01175.hp1 HG01256.hp1 others(3): Show |
intron_variant | MODIFIER | c.265-5637_265-5621d others(19): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681620 | |||||
chr14:73681621
|
A | AATATATA others(3): Show |
1 | a0001c0001t0007g0224 | 1 | NA18986.hp2 | intron_variant | MODIFIER | c.265-5637_265-5636i others(12): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681621 | |||||
chr14:73681621
|
A | AATATATA others(5): Show |
2 | a0001c0001t0007g0211a0001c0001t0018g0215 | 2 | HG01934.hp1 NA19079.hp2 |
intron_variant | MODIFIER | c.265-5637_265-5636i others(14): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681621 | |||||
chr14:73681621
|
A | AATATATA others(9): Show |
1 | a0001c0001t0016g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.265-5637_265-5636i others(18): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681621 | |||||
chr14:73681621
|
A | AT | 4 | a0001c0001t0002g0157a0001c0001t0002g0166a0001c0001t0002g0171others(1): Show | 4 | HG00099.hp2 HG02257.hp1 NA18952.hp1 others(1): Show |
intron_variant | MODIFIER | c.265-5638_265-5637i others(3): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681621 | ||||||
chr14:73681621
|
A | T | 10 | a0001c0001t0002g0174a0001c0001t0007g0219a0001c0001t0021g0317others(7): Show | 10 | HG01074.hp1 HG01099.hp2 HG01175.hp2 others(7): Show |
intron_variant | MODIFIER | c.265-5638A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681621 | ||||||
chr14:73681623
|
A | AATATATA others(5): Show |
1 | a0001c0001t0067g0217 | 1 | HG04204.hp1 | intron_variant | MODIFIER | c.265-5635_265-5634i others(14): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681623 | |||||
chr14:73681623
|
A | AATATATA others(7): Show |
1 | a0001c0001t0031g0227 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.265-5635_265-5634i others(16): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681623 | |||||
chr14:73681623
|
A | AATATATA others(23): Show |
1 | a0001c0001t0043g0204 | 1 | HG02895.hp1 | intron_variant | MODIFIER | c.265-5635_265-5634i others(32): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681623 | |||||
chr14:73681623
|
A | AT | 15 | a0001c0001t0002g0003a0001c0001t0002g0159a0001c0001t0002g0160others(12): Show | 16 | HG02056.hp2 HG04184.hp2 NA18612.hp2 others(13): Show |
intron_variant | MODIFIER | c.265-5636_265-5635i others(3): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681623 | ||||||
chr14:73681623
|
A | ATAT | 3 | a0001c0001t0002g0162a0001c0001t0002g0179a0001c0001t0002g0184 | 3 | HG00558.hp2 NA18988.hp1 NA18994.hp1 |
intron_variant | MODIFIER | c.265-5636_265-5635i others(5): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681623 | ||||||
chr14:73681623
|
A | ATATAT | 3 | a0001c0001t0033g0232a0001c0001t0034g0190a0001c0001t0035g0170 | 3 | HG00642.hp1 HG01123.hp2 HG02723.hp1 |
intron_variant | MODIFIER | c.265-5636_265-5635i others(7): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681623 | ||||||
chr14:73681623
|
A | ATATATAT others(10): Show |
1 | a0001c0001t0016g0320 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.265-5636_265-5635i others(19): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681623 | ||||||
chr14:73681623
|
A | T | 28 | a0001c0001t0002g0157a0001c0001t0002g0166a0001c0001t0002g0171others(25): Show | 28 | HG00099.hp2 HG00733.hp2 HG01074.hp1 others(25): Show |
intron_variant | MODIFIER | c.265-5636A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681623 | ||||||
chr14:73681625
|
A | AATATATA others(3): Show |
1 | a0001c0001t0007g0212 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.265-5633_265-5632i others(12): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681625 | |||||
chr14:73681625
|
A | AATATATA others(13): Show |
1 | a0001c0001t0040g0206 | 1 | HG01891.hp1 | intron_variant | MODIFIER | c.265-5633_265-5632i others(22): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681625 | |||||
chr14:73681625
|
A | AATATATA others(15): Show |
1 | a0001c0001t0017g0209 | 1 | NA18906.hp1 | intron_variant | MODIFIER | c.265-5633_265-5632i others(24): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681625 | |||||
chr14:73681625
|
A | AT | 5 | a0001c0001t0002g0154a0001c0001t0002g0164a0001c0001t0002g0167others(2): Show | 5 | HG01358.hp1 HG02155.hp1 HG02165.hp2 others(2): Show |
intron_variant | MODIFIER | c.265-5634_265-5633i others(3): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681625 | ||||||
chr14:73681625
|
A | ATATATAT others(12): Show |
2 | a0001c0001t0017g0205a0001c0001t0101g0314 | 2 | HG01243.hp2 HG01884.hp2 |
intron_variant | MODIFIER | c.265-5634_265-5633i others(21): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681625 | ||||||
chr14:73681625
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0016g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.265-5634_265-5633i others(23): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681625 | ||||||
chr14:73681625
|
A | ATATATAT others(16): Show |
2 | a0001c0001t0016g0323a0001c0001t0017g0207 | 2 | HG02451.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.265-5634_265-5633i others(25): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681625 | ||||||
chr14:73681625
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0016g0322 | 1 | HG02615.hp1 | intron_variant | MODIFIER | c.265-5634_265-5633i others(27): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681625 | ||||||
chr14:73681625
|
A | T | 64 | a0001c0001t0002g0003a0001c0001t0002g0157a0001c0001t0002g0159others(61): Show | 65 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(62): Show |
intron_variant | MODIFIER | c.265-5634A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681625 | ||||||
chr14:73681627
|
A | AATATATA others(9): Show |
1 | a0001c0001t0066g0141 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.265-5631_265-5630i others(18): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681627 | |||||
chr14:73681627
|
A | AT | 10 | a0001c0001t0001g0257a0001c0001t0001g0258a0001c0001t0001g0276others(7): Show | 10 | HG01070.hp1 HG01192.hp2 HG01517.hp1 others(7): Show |
intron_variant | MODIFIER | c.265-5632_265-5631i others(3): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681627 | ||||||
chr14:73681627
|
A | ATATATAT others(14): Show |
1 | a0001c0001t0017g0208 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.265-5632_265-5631i others(23): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681627 | ||||||
chr14:73681627
|
A | T | 84 | a0001c0001t0001g0299a0001c0001t0002g0003a0001c0001t0002g0154others(81): Show | 85 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(82): Show |
intron_variant | MODIFIER | c.265-5632A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681627 | ||||||
chr14:73681629
|
A | AAT | 9 | a0001c0001t0001g0246a0001c0001t0001g0292a0001c0001t0001g0296others(6): Show | 9 | HG00544.hp1 HG01169.hp2 HG01952.hp2 others(6): Show |
intron_variant | MODIFIER | c.265-5629_265-5628i others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681629 | |||||
chr14:73681629
|
A | AATAT | 9 | a0001c0001t0005g0107a0001c0001t0026g0096a0001c0001t0028g0135others(6): Show | 9 | HG01496.hp2 HG01884.hp1 HG02145.hp2 others(6): Show |
intron_variant | MODIFIER | c.265-5629_265-5628i others(6): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681629 | |||||
chr14:73681629
|
A | AATATATA others(3): Show |
2 | a0001c0001t0008g0126a0001c0001t0008g0144 | 2 | HG01515.hp1 HG03130.hp2 |
intron_variant | MODIFIER | c.265-5629_265-5628i others(12): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681629 | |||||
chr14:73681629
|
A | AT | 46 | a0001c0001t0001g0004a0001c0001t0001g0240a0001c0001t0001g0241others(43): Show | 48 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(45): Show |
intron_variant | MODIFIER | c.265-5630_265-5629i others(3): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681629 | ||||||
chr14:73681629
|
A | ATAT | 11 | a0001c0001t0001g0286a0001c0001t0005g0085a0001c0001t0005g0097others(8): Show | 11 | HG00438.hp1 HG02976.hp1 NA18954.hp1 others(8): Show |
intron_variant | MODIFIER | c.265-5630_265-5629i others(5): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681629 | ||||||
chr14:73681629
|
A | ATATAT | 8 | a0001c0001t0005g0091a0001c0001t0005g0106a0001c0001t0005g0108others(5): Show | 8 | HG00558.hp1 HG00621.hp2 NA18942.hp2 others(5): Show |
intron_variant | MODIFIER | c.265-5630_265-5629i others(7): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681629 | ||||||
chr14:73681629
|
A | ATATATAT | 4 | a0001c0001t0005g0117a0001c0001t0015g0109a0001c0001t0015g0122others(1): Show | 4 | HG00544.hp2 HG02027.hp1 HG03017.hp1 others(1): Show |
intron_variant | MODIFIER | c.265-5630_265-5629i others(9): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681629 | ||||||
chr14:73681629
|
A | ATATATAT others(2): Show |
3 | a0001c0001t0005g0098a0001c0001t0008g0099a0001c0001t0008g0145 | 3 | HG01517.hp2 HG02630.hp2 NA18991.hp1 |
intron_variant | MODIFIER | c.265-5630_265-5629i others(11): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681629 | ||||||
chr14:73681629
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0099g0195 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.265-5630_265-5629i others(13): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681629 | ||||||
chr14:73681629
|
A | ATATATAT others(18): Show |
1 | a0001c0001t0039g0197 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.265-5630_265-5629i others(27): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681629 | ||||||
chr14:73681629
|
A | T | 114 | a0001c0001t0001g0237a0001c0001t0001g0257a0001c0001t0001g0258others(111): Show | 115 | HG00099.hp2 HG00423.hp1 HG00558.hp2 others(112): Show |
intron_variant | MODIFIER | c.265-5630A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681629 | ||||||
chr14:73681631
|
A | AATATATA others(1): Show |
6 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(3): Show | 6 | HG01891.hp2 HG02559.hp2 HG02723.hp2 others(3): Show |
intron_variant | MODIFIER | c.265-5627_265-5626i others(10): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681631 | |||||
chr14:73681631
|
A | AATATATA others(5): Show |
1 | a0001c0001t0082g0140 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.265-5627_265-5626i others(14): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681631 | |||||
chr14:73681631
|
A | AATATATA others(7): Show |
1 | a0001c0001t0094g0100 | 1 | HG03041.hp2 | intron_variant | MODIFIER | c.265-5627_265-5626i others(16): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681631 | |||||
chr14:73681631
|
A | ATAT | 5 | a0001c0001t0005g0116a0001c0001t0005g0137a0001c0001t0009g0149others(2): Show | 5 | HG02027.hp2 HG02897.hp2 NA18952.hp2 others(2): Show |
intron_variant | MODIFIER | c.265-5628_265-5627i others(5): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681631 | ||||||
chr14:73681631
|
A | ATATAT | 5 | a0001c0001t0005g0136a0001c0001t0027g0002a0001c0001t0027g0152others(2): Show | 6 | HG01081.hp2 NA18612.hp1 NA18747.hp1 others(3): Show |
intron_variant | MODIFIER | c.265-5628_265-5627i others(7): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681631 | ||||||
chr14:73681631
|
A | ATATATAT others(4): Show |
1 | a0001c0001t0088g0112 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.265-5628_265-5627i others(13): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681631 | ||||||
chr14:73681631
|
A | ATATATAT others(6): Show |
1 | a0001c0001t0008g0139 | 1 | NA20300.hp2 | intron_variant | MODIFIER | c.265-5628_265-5627i others(15): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681631 | ||||||
chr14:73681631
|
A | ATATATAT others(8): Show |
1 | a0001c0001t0008g0090 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.265-5628_265-5627i others(17): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681631 | ||||||
chr14:73681631
|
A | T | 218 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(215): Show | 221 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(218): Show |
intron_variant | MODIFIER | c.265-5628A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681631 | ||||||
chr14:73681633
|
A | AAAAAATA others(3): Show |
1 | a0001c0001t0042g0196 | 1 | HG02818.hp2 | intron_variant | MODIFIER | c.265-5625_265-5624i others(12): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681633 | |||||
chr14:73681633
|
A | AAAATATA others(27): Show |
1 | a0001c0001t0104g0312 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.265-5625_265-5624i others(36): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681633 | |||||
chr14:73681633
|
A | AAATATAT others(4): Show |
3 | a0001c0001t0008g0130a0001c0001t0081g0129a0001c0001t0097g0007 | 3 | HG01081.hp1 HG02486.hp1 NA19240.hp1 |
intron_variant | MODIFIER | c.265-5625_265-5624i others(13): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681633 | |||||
chr14:73681633
|
A | AAATATAT others(6): Show |
3 | a0001c0001t0008g0128a0001c0001t0009g0111a0001c0001t0085g0125 | 3 | HG02647.hp2 HG03195.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.265-5625_265-5624i others(15): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681633 | |||||
chr14:73681633
|
A | AATATATA others(3): Show |
4 | a0001c0001t0009g0327a0001c0001t0041g0203a0001c0001t0089g0124others(1): Show | 4 | HG02622.hp1 HG02630.hp1 HG02717.hp2 others(1): Show |
intron_variant | MODIFIER | c.265-5613_265-5604d others(12): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681633 | |||||
chr14:73681633
|
A | AATATATA others(5): Show |
1 | a0001c0001t0009g0086 | 1 | HG03098.hp1 | intron_variant | MODIFIER | c.265-5615_265-5604d others(14): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681633 | |||||
chr14:73681633
|
A | AATATATA others(7): Show |
1 | a0001c0001t0084g0110 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.265-5617_265-5604d others(16): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73681633 | |||||
chr14:73681633
|
A | ATATATAT others(4): Show |
3 | a0001c0001t0009g0153a0001c0001t0012g0202a0001c0001t0015g0334 | 3 | HG02109.hp1 HG02922.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.265-5626_265-5625i others(13): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681633 | ||||||
chr14:73681633
|
A | ATATATAT others(8): Show |
2 | a0001c0001t0008g0127a0001c0001t0102g0316 | 2 | HG02683.hp2 NA19240.hp2 |
intron_variant | MODIFIER | c.265-5626_265-5625i others(17): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681633 | ||||||
chr14:73681633
|
A | T | 260 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(257): Show | 264 | HG00099.hp2 HG00140.hp2 HG00423.hp1 others(261): Show |
intron_variant | MODIFIER | c.265-5626A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681633 | ||||||
chr14:73681635
|
T | A | 1 | a0001c0001t0055g0016 | 1 | HG02148.hp2 | intron_variant | MODIFIER | c.265-5624T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681635 | ||||||
chr14:73681698
|
A | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.265-5561A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681698 | ||||||
chr14:73681733
|
T | C | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.265-5526T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681733 | ||||||
chr14:73681850
|
C | T | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.265-5409C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73681850 | ||||||
chr14:73682092
|
A | G | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.265-5167A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73682092 | ||||||
chr14:73682171
|
C | CT | 35 | a0001c0001t0001g0258a0001c0001t0002g0162a0001c0001t0012g0198others(32): Show | 35 | HG00738.hp1 HG01123.hp2 HG01243.hp2 others(32): Show |
intron_variant | MODIFIER | c.265-5071dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73682171 | |||||
chr14:73682171
|
C | CTTT | 31 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.265-5073_265-5071d others(5): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73682171 | |||||
chr14:73682171
|
CT | C | 7 | a0001c0001t0006g0302a0001c0001t0009g0093a0001c0001t0028g0135others(4): Show | 7 | HG02970.hp1 HG02976.hp1 HG03017.hp1 others(4): Show |
intron_variant | MODIFIER | c.265-5071delT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73682171 | |||||
chr14:73682240
|
A | G | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.265-5019A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73682240 | ||||||
chr14:73682252
|
C | T | 1 | a0001c0001t0001g0298 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.265-5007C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73682252 | ||||||
chr14:73682337
|
A | AT | 50 | a0001c0001t0002g0157a0001c0001t0002g0159a0001c0001t0002g0160others(47): Show | 50 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(47): Show |
intron_variant | MODIFIER | c.265-4899dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73682337 | |||||
chr14:73682337
|
A | ATT | 6 | a0001c0001t0003g0056a0001c0001t0029g0079a0001c0001t0029g0081others(3): Show | 6 | HG01928.hp1 HG03041.hp1 HG03130.hp1 others(3): Show |
intron_variant | MODIFIER | c.265-4900_265-4899d others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73682337 | |||||
chr14:73682337
|
AT | A | 105 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(102): Show | 106 | HG00438.hp2 HG00544.hp1 HG00621.hp1 others(103): Show |
intron_variant | MODIFIER | c.265-4899delT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73682337 | |||||
chr14:73682337
|
ATTTTTTT others(2): Show |
A | 12 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.265-4907_265-4899d others(11): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73682337 | |||||
chr14:73682337
|
ATTTTTTT others(5): Show |
A | 1 | a0001c0001t0080g0225 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.265-4910_265-4899d others(14): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73682337 | |||||
chr14:73682369
|
A | G | 72 | a0001c0001t0005g0085a0001c0001t0005g0091a0001c0001t0005g0092others(69): Show | 73 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.265-4890A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73682369 | ||||||
chr14:73682422
|
C | T | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.265-4837C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73682422 | ||||||
chr14:73682485
|
G | A | 5 | a0001c0001t0001g0240a0001c0001t0001g0261a0001c0001t0001g0262others(2): Show | 5 | HG02080.hp1 HG02129.hp1 NA19011.hp2 others(2): Show |
intron_variant | MODIFIER | c.265-4774G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73682485 | ||||||
chr14:73682587
|
TTTTC | T | 3 | a0001c0001t0004g0243a0001c0001t0038g0084a0001c0001t0072g0027 | 3 | HG03139.hp1 NA18978.hp1 NA18978.hp2 |
intron_variant | MODIFIER | c.265-4664_265-4661d others(6): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73682587 | |||||
chr14:73682595
|
C | A | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.265-4664C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73682595 | ||||||
chr14:73682633
|
T | C | 17 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(14): Show | 17 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.265-4626T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73682633 | ||||||
chr14:73682788
|
T | G | 114 | a0001c0001t0002g0003a0001c0001t0002g0154a0001c0001t0002g0155others(111): Show | 116 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.265-4471T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73682788 | ||||||
chr14:73682867
|
TTA | T | 12 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(9): Show | 12 | HG01243.hp2 HG01891.hp1 HG02559.hp2 others(9): Show |
intron_variant | MODIFIER | c.265-4390_265-4389d others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73682867 | |||||
chr14:73682868
|
TA | T | 3 | a0001c0001t0012g0201a0001c0001t0012g0202a0001c0001t0032g0088 | 3 | HG02109.hp1 HG03516.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.265-4390delA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73682868 | ||||||
chr14:73682869
|
A | T | 1 | a0001c0001t0032g0089 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.265-4390A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73682869 | ||||||
chr14:73682869
|
AT | A | 112 | a0001c0001t0001g0240a0001c0001t0001g0258a0001c0001t0001g0270others(109): Show | 113 | HG00423.hp2 HG00438.hp1 HG00544.hp2 others(110): Show |
intron_variant | MODIFIER | c.265-4365delT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73682869 | |||||
chr14:73682869
|
ATT | A | 122 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0241others(119): Show | 124 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(121): Show |
intron_variant | MODIFIER | c.265-4366_265-4365d others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73682869 | |||||
chr14:73682869
|
ATTTTTTT others(1): Show |
A | 42 | a0001c0001t0002g0003a0001c0001t0002g0154a0001c0001t0002g0155others(39): Show | 43 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.265-4372_265-4365d others(10): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73682869 | |||||
chr14:73682880
|
T | A | 1 | a0001c0001t0002g0154 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.265-4379T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73682880 | ||||||
chr14:73682881
|
T | A | 1 | a0001c0001t0101g0314 | 1 | HG01884.hp2 | intron_variant | MODIFIER | c.265-4378T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73682881 | ||||||
chr14:73683027
|
T | C | 41 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.265-4232T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73683027 | ||||||
chr14:73683127
|
C | T | 1 | a0001c0001t0057g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.265-4132C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73683127 | ||||||
chr14:73683128
|
G | A | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.265-4131G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73683128 | ||||||
chr14:73683185
|
C | T | 1 | a0001c0001t0011g0274 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.265-4074C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73683185 | ||||||
chr14:73683485
|
T | C | 15 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(12): Show | 15 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.265-3774T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73683485 | ||||||
chr14:73683491
|
T | C | 38 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.265-3768T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73683491 | ||||||
chr14:73683611
|
C | T | 5 | a0001c0001t0033g0226a0001c0001t0033g0232a0001c0001t0064g0233others(2): Show | 5 | HG02559.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.265-3648C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73683611 | ||||||
chr14:73683627
|
C | G | 35 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.265-3632C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73683627 | ||||||
chr14:73683657
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.265-3602G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73683657 | ||||||
chr14:73683662
|
C | A | 41 | a0001c0001t0002g0003a0001c0001t0002g0154a0001c0001t0002g0155others(38): Show | 42 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(39): Show |
intron_variant | MODIFIER | c.265-3597C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73683662 | ||||||
chr14:73683684
|
T | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.265-3575T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73683684 | ||||||
chr14:73683697
|
T | TTTA | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.265-3544_265-3542d others(5): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73683697 | |||||
chr14:73683710
|
T | G | 1 | a0001c0001t0095g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.265-3549T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73683710 | ||||||
chr14:73683815
|
C | G | 3 | a0001c0001t0009g0149a0001c0001t0009g0150a0001c0001t0009g0151 | 3 | HG02258.hp2 HG02897.hp2 HG03516.hp2 |
intron_variant | MODIFIER | c.265-3444C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73683815 | ||||||
chr14:73683883
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.265-3376G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73683883 | ||||||
chr14:73683895
|
C | T | 1 | a0001c0001t0057g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.265-3364C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73683895 | ||||||
chr14:73683912
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.265-3347G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73683912 | ||||||
chr14:73684072
|
T | C | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.265-3187T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73684072 | ||||||
chr14:73684159
|
G | A | 2 | a0001c0001t0036g0095a0001c0001t0036g0119 | 2 | NA18961.hp2 NA19012.hp1 |
intron_variant | MODIFIER | c.265-3100G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73684159 | ||||||
chr14:73684280
|
G | A | 72 | a0001c0001t0005g0085a0001c0001t0005g0091a0001c0001t0005g0092others(69): Show | 73 | HG00438.hp1 HG00544.hp2 HG00558.hp1 others(70): Show |
intron_variant | MODIFIER | c.265-2979G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73684280 | ||||||
chr14:73684352
|
T | C | 2 | a0001c0001t0005g0138a0001c0001t0096g0123 | 2 | HG00621.hp2 NA18942.hp2 |
intron_variant | MODIFIER | c.265-2907T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73684352 | ||||||
chr14:73684444
|
A | G | 5 | a0001c0001t0001g0284a0001c0001t0001g0286a0001c0001t0001g0288others(2): Show | 5 | NA18946.hp1 NA19010.hp1 NA19055.hp1 others(2): Show |
intron_variant | MODIFIER | c.265-2815A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73684444 | ||||||
chr14:73684635
|
G | A | 4 | a0001c0001t0001g0298a0001c0001t0029g0079a0001c0001t0029g0081others(1): Show | 4 | HG03041.hp1 HG03130.hp1 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.265-2624G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73684635 | ||||||
chr14:73684741
|
T | A | 1 | a0001c0001t0103g0309 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.265-2518T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73684741 | ||||||
chr14:73684747
|
T | A | 1 | a0001c0001t0004g0023 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.265-2512T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73684747 | ||||||
chr14:73684776
|
T | C | 1 | a0001c0001t0001g0246 | 1 | HG03654.hp1 | intron_variant | MODIFIER | c.265-2483T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73684776 | ||||||
chr14:73684931
|
CATTT | C | 38 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.265-2327_265-2324d others(6): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73684931 | ||||||
chr14:73685133
|
CAT | C | 42 | a0001c0001t0002g0003a0001c0001t0002g0154a0001c0001t0002g0155others(39): Show | 43 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.265-2124_265-2123d others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73685133 | |||||
chr14:73685224
|
T | C | 2 | a0001c0001t0032g0088a0001c0001t0032g0089 | 2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.265-2035T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73685224 | ||||||
chr14:73685259
|
C | T | 19 | a0001c0001t0007g0210a0001c0001t0007g0211a0001c0001t0007g0212others(16): Show | 19 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.265-2000C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73685259 | ||||||
chr14:73685348
|
A | G | 5 | a0001c0001t0020g0310a0001c0001t0020g0311a0001c0001t0020g0313others(2): Show | 5 | HG01891.hp2 HG03139.hp2 HG03471.hp2 others(2): Show |
intron_variant | MODIFIER | c.265-1911A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73685348 | ||||||
chr14:73685370
|
T | C | 5 | a0001c0001t0005g0138a0001c0001t0015g0109a0001c0001t0036g0095others(2): Show | 5 | HG00621.hp2 HG02027.hp1 NA18942.hp2 others(2): Show |
intron_variant | MODIFIER | c.265-1889T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73685370 | ||||||
chr14:73685382
|
A | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.265-1877A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73685382 | ||||||
chr14:73685401
|
C | T | 2 | a0001c0001t0004g0018a0001c0001t0053g0037 | 2 | HG00423.hp1 HG01952.hp1 |
intron_variant | MODIFIER | c.265-1858C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73685401 | ||||||
chr14:73685433
|
C | T | 1 | a0001c0001t0057g0234 | 1 | NA19043.hp2 | intron_variant | MODIFIER | c.265-1826C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73685433 | ||||||
chr14:73685460
|
A | AT | 28 | a0001c0001t0001g0270a0001c0001t0001g0300a0001c0001t0003g0056others(25): Show | 28 | HG00735.hp2 HG01167.hp1 HG01167.hp2 others(25): Show |
intron_variant | MODIFIER | c.265-1782dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73685460 | |||||
chr14:73685460
|
A | ATT | 76 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(73): Show | 78 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(75): Show |
intron_variant | MODIFIER | c.265-1783_265-1782d others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73685460 | |||||
chr14:73685460
|
A | T | 1 | a0001c0001t0104g0312 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.265-1799A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73685460 | ||||||
chr14:73685460
|
AT | A | 9 | a0001c0001t0002g0178a0001c0001t0005g0138a0001c0001t0007g0223others(6): Show | 9 | HG00639.hp1 HG01070.hp2 HG01168.hp1 others(6): Show |
intron_variant | MODIFIER | c.265-1782delT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73685460 | |||||
chr14:73685498
|
C | T | 35 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.265-1761C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73685498 | ||||||
chr14:73685521
|
G | A | 4 | a0001c0001t0033g0232a0001c0001t0064g0233a0001c0001t0065g0218others(1): Show | 4 | HG02559.hp1 HG02615.hp2 HG02723.hp1 others(1): Show |
intron_variant | MODIFIER | c.265-1738G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73685521 | ||||||
chr14:73685610
|
C | T | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.265-1649C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73685610 | ||||||
chr14:73685613
|
C | T | 35 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.265-1646C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73685613 | ||||||
chr14:73685621
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.265-1638G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73685621 | ||||||
chr14:73685643
|
T | C | 19 | a0001c0001t0007g0210a0001c0001t0007g0211a0001c0001t0007g0212others(16): Show | 19 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(16): Show |
intron_variant | MODIFIER | c.265-1616T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73685643 | ||||||
chr14:73685854
|
G | A | 1 | a0001c0001t0008g0130 | 1 | HG01081.hp1 | intron_variant | MODIFIER | c.265-1405G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73685854 | ||||||
chr14:73685897
|
C | T | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.265-1362C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73685897 | ||||||
chr14:73686081
|
A | G | 38 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.265-1178A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73686081 | ||||||
chr14:73686469
|
C | T | 3 | a0001c0001t0008g0099a0001c0001t0008g0126a0001c0001t0008g0146 | 3 | HG02145.hp1 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.265-790C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73686469 | ||||||
chr14:73686641
|
G | A | 1 | a0001c0001t0004g0038 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.265-618G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73686641 | ||||||
chr14:73686808
|
G | A | 4 | a0001c0001t0009g0093a0001c0001t0009g0101a0001c0001t0009g0102others(1): Show | 4 | HG01074.hp2 HG01243.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.265-451G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73686808 | ||||||
chr14:73687010
|
A | AT | 57 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(54): Show | 57 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(54): Show |
intron_variant | MODIFIER | c.265-234dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | INFO_REALIGN_3_PRIME | chr14 | 73687010 | |||||
chr14:73687067
|
G | A | 4 | a0001c0001t0021g0317a0001c0001t0021g0318a0001c0001t0021g0319others(1): Show | 4 | HG01109.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.265-192G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 5/7 | chr14 | 73687067 | ||||||
chr14:73687394
|
A | G | 3 | a0001c0001t0008g0099a0001c0001t0008g0126a0001c0001t0008g0146 | 3 | HG02145.hp1 HG02630.hp2 HG03130.hp2 |
intron_variant | MODIFIER | c.391+9A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73687394 | ||||||
chr14:73687451
|
A | G | 8 | a0001c0001t0014g0328a0001c0001t0014g0329a0001c0001t0014g0330others(5): Show | 8 | HG01168.hp1 HG01515.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.391+66A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73687451 | ||||||
chr14:73687661
|
A | G | 7 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(4): Show | 7 | HG02109.hp1 HG02559.hp2 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.391+276A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73687661 | ||||||
chr14:73687717
|
A | C | 1 | a0001c0001t0002g0157 | 1 | HG02257.hp1 | intron_variant | MODIFIER | c.391+332A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73687717 | ||||||
chr14:73687754
|
T | G | 1 | a0001c0001t0045g0044 | 1 | HG04184.hp1 | intron_variant | MODIFIER | c.391+369T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73687754 | ||||||
chr14:73687790
|
G | A | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.391+405G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73687790 | ||||||
chr14:73687947
|
C | T | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.391+562C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73687947 | ||||||
chr14:73687983
|
A | G | 13 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.391+598A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73687983 | ||||||
chr14:73688034
|
G | C | 35 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.391+649G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73688034 | ||||||
chr14:73688126
|
A | G | 15 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(12): Show | 15 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.391+741A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73688126 | ||||||
chr14:73688198
|
T | A | 1 | a0001c0001t0001g0240 | 1 | NA19085.hp1 | intron_variant | MODIFIER | c.391+813T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73688198 | ||||||
chr14:73688213
|
A | G | 3 | a0001c0001t0048g0082a0001c0001t0049g0071a0001c0001t0052g0235 | 3 | HG02886.hp1 HG02886.hp2 HG03453.hp1 |
intron_variant | MODIFIER | c.391+828A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73688213 | ||||||
chr14:73688441
|
T | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.392-934T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73688441 | ||||||
chr14:73688479
|
C | T | 4 | a0001c0001t0021g0317a0001c0001t0021g0318a0001c0001t0021g0319others(1): Show | 4 | HG01109.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.392-896C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73688479 | ||||||
chr14:73688653
|
G | A | 72 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(69): Show | 72 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(69): Show |
intron_variant | MODIFIER | c.392-722G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73688653 | ||||||
chr14:73688858
|
T | A | 1 | a0001c0001t0066g0141 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.392-517T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73688858 | ||||||
chr14:73688869
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.392-506C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73688869 | ||||||
chr14:73688894
|
G | A | 1 | a0001c0001t0001g0237 | 1 | HG03704.hp1 | intron_variant | MODIFIER | c.392-481G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73688894 | ||||||
chr14:73689026
|
G | GT | 18 | a0001c0001t0004g0014a0001c0001t0004g0018a0001c0001t0004g0035others(15): Show | 18 | HG01123.hp1 HG01891.hp1 HG01952.hp1 others(15): Show |
intron_variant | MODIFIER | c.392-324dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr14 | 73689026 | |||||
chr14:73689026
|
GT | G | 105 | a0001c0001t0001g0237a0001c0001t0001g0242a0001c0001t0001g0261others(102): Show | 105 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(102): Show |
intron_variant | MODIFIER | c.392-324delT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr14 | 73689026 | |||||
chr14:73689026
|
GTT | G | 137 | a0001c0001t0001g0004a0001c0001t0001g0240a0001c0001t0001g0241others(134): Show | 140 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(137): Show |
intron_variant | MODIFIER | c.392-325_392-324del others(2): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr14 | 73689026 | |||||
chr14:73689026
|
GTTT | G | 9 | a0001c0001t0007g0210a0001c0001t0014g0330a0001c0001t0018g0215others(6): Show | 9 | HG01515.hp2 HG01934.hp1 HG02258.hp1 others(6): Show |
intron_variant | MODIFIER | c.392-326_392-324del others(3): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr14 | 73689026 | |||||
chr14:73689026
|
GTTTT | G | 17 | a0001c0001t0007g0211a0001c0001t0007g0212a0001c0001t0007g0213others(14): Show | 17 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(14): Show |
intron_variant | MODIFIER | c.392-327_392-324del others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | INFO_REALIGN_3_PRIME | chr14 | 73689026 | |||||
chr14:73689029
|
T | G | 5 | a0001c0001t0003g0047a0001c0001t0003g0055a0001c0001t0003g0056others(2): Show | 5 | HG01168.hp2 HG01175.hp1 HG01256.hp1 others(2): Show |
intron_variant | MODIFIER | c.392-346T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73689029 | ||||||
chr14:73689030
|
T | G | 33 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(30): Show | 33 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(30): Show |
intron_variant | MODIFIER | c.392-345T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73689030 | ||||||
chr14:73689062
|
C | T | 1 | a0001c0001t0007g0214 | 1 | HG02083.hp1 | intron_variant | MODIFIER | c.392-313C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73689062 | ||||||
chr14:73689063
|
G | C | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.392-312G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73689063 | ||||||
chr14:73689063
|
G | T | 41 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(38): Show | 41 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(38): Show |
intron_variant | MODIFIER | c.392-312G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73689063 | ||||||
chr14:73689072
|
C | T | 1 | a0001c0001t0002g0164 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.392-303C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73689072 | ||||||
chr14:73689120
|
G | A | 1 | a0001c0001t0007g0231 | 1 | NA19009.hp1 | intron_variant | MODIFIER | c.392-255G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73689120 | ||||||
chr14:73689254
|
G | A | 1 | a0001c0001t0013g0052 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.392-121G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73689254 | ||||||
chr14:73689290
|
C | G | 4 | a0001c0001t0021g0317a0001c0001t0021g0318a0001c0001t0021g0319others(1): Show | 4 | HG01109.hp2 HG02451.hp2 HG03209.hp1 others(1): Show |
intron_variant | MODIFIER | c.392-85C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73689290 | ||||||
chr14:73689312
|
G | A | 20 | a0001c0001t0007g0210a0001c0001t0007g0211a0001c0001t0007g0212others(17): Show | 20 | HG01069.hp2 HG01071.hp1 HG01192.hp1 others(17): Show |
intron_variant | MODIFIER | c.392-63G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73689312 | ||||||
chr14:73689328
|
G | A | 8 | a0001c0001t0014g0328a0001c0001t0014g0329a0001c0001t0014g0330others(5): Show | 8 | HG01168.hp1 HG01515.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.392-47G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 6/7 | chr14 | 73689328 | ||||||
chr14:73689526
|
C | T | 8 | a0001c0001t0008g0144a0001c0001t0008g0145a0001c0001t0015g0121others(5): Show | 8 | HG01515.hp1 HG01517.hp2 HG03017.hp1 others(5): Show |
intron_variant | MODIFIER | c.532+11C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73689526 | ||||||
chr14:73689542
|
A | G | 25 | a0001c0001t0008g0090a0001c0001t0008g0099a0001c0001t0008g0126others(22): Show | 25 | HG00738.hp2 HG01081.hp1 HG01109.hp1 others(22): Show |
intron_variant | MODIFIER | c.532+27A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73689542 | ||||||
chr14:73689568
|
T | A | 1 | a0001c0001t0014g0329 | 1 | HG03704.hp2 | intron_variant | MODIFIER | c.532+53T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73689568 | ||||||
chr14:73689613
|
C | T | 38 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.532+98C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73689613 | ||||||
chr14:73689719
|
C | T | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.532+204C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73689719 | ||||||
chr14:73689819
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.532+304G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73689819 | ||||||
chr14:73689975
|
G | C | 1 | a0001c0001t0011g0236 | 1 | NA18950.hp1 | intron_variant | MODIFIER | c.532+460G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73689975 | ||||||
chr14:73690037
|
CAA | C | 11 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(8): Show | 11 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(8): Show |
intron_variant | MODIFIER | c.532+535_532+536del others(2): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73690037 | |||||
chr14:73690050
|
AAG | A | 73 | a0001c0001t0002g0003a0001c0001t0002g0154a0001c0001t0002g0155others(70): Show | 74 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(71): Show |
intron_variant | MODIFIER | c.532+537_532+538del others(2): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73690050 | |||||
chr14:73690051
|
AG | A | 213 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(210): Show | 216 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(213): Show |
intron_variant | MODIFIER | c.532+537delG | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73690051 | ||||||
chr14:73690052
|
G | A | 3 | a0001c0001t0009g0149a0001c0001t0026g0096a0001c0001t0060g0009 | 3 | HG02897.hp2 HG02970.hp2 NA18979.hp2 |
intron_variant | MODIFIER | c.532+537G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73690052 | ||||||
chr14:73690075
|
T | A | 5 | a0001c0001t0033g0226a0001c0001t0033g0232a0001c0001t0064g0233others(2): Show | 5 | HG02559.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.532+560T>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73690075 | ||||||
chr14:73690176
|
T | C | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.532+661T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73690176 | ||||||
chr14:73690177
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.532+662G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73690177 | ||||||
chr14:73690241
|
T | C | 1 | a0001c0001t0088g0112 | 1 | HG03195.hp1 | intron_variant | MODIFIER | c.532+726T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73690241 | ||||||
chr14:73690262
|
G | T | 2 | a0001c0001t0048g0082a0001c0001t0049g0071 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.532+747G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73690262 | ||||||
chr14:73690367
|
G | T | 40 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(37): Show | 40 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(37): Show |
intron_variant | MODIFIER | c.532+852G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73690367 | ||||||
chr14:73690410
|
G | T | 334 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(331): Show | 338 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
intron_variant | MODIFIER | c.532+895G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73690410 | ||||||
chr14:73690521
|
G | C | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.532+1006G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73690521 | ||||||
chr14:73690576
|
C | T | 1 | a0001c0001t0021g0325 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.532+1061C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73690576 | ||||||
chr14:73690652
|
C | CA | 6 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080others(3): Show | 6 | HG03041.hp1 HG03130.hp1 HG03139.hp1 others(3): Show |
intron_variant | MODIFIER | c.532+1151dupA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73690652 | |||||
chr14:73690652
|
CA | C | 6 | a0001c0001t0002g0174a0001c0001t0021g0317a0001c0001t0021g0318others(3): Show | 6 | HG01070.hp2 HG01109.hp2 HG02451.hp2 others(3): Show |
intron_variant | MODIFIER | c.532+1151delA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73690652 | |||||
chr14:73690673
|
G | T | 1 | a0001c0001t0014g0331 | 1 | HG02622.hp2 | intron_variant | MODIFIER | c.532+1158G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73690673 | ||||||
chr14:73690675
|
T | C | 1 | a0001c0001t0099g0195 | 1 | NA18946.hp2 | intron_variant | MODIFIER | c.532+1160T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73690675 | ||||||
chr14:73690713
|
A | G | 1 | a0001c0001t0073g0083 | 1 | HG02698.hp2 | intron_variant | MODIFIER | c.532+1198A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73690713 | ||||||
chr14:73691042
|
T | C | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.532+1527T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73691042 | ||||||
chr14:73691066
|
A | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.532+1551A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73691066 | ||||||
chr14:73691163
|
A | G | 4 | a0001c0001t0010g0075a0001c0001t0010g0076a0001c0001t0010g0077others(1): Show | 4 | HG03017.hp2 NA18947.hp2 NA18971.hp2 others(1): Show |
intron_variant | MODIFIER | c.532+1648A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73691163 | ||||||
chr14:73691315
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.532+1800C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73691315 | ||||||
chr14:73691347
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.532+1832C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73691347 | ||||||
chr14:73691348
|
G | A | 42 | a0001c0001t0002g0003a0001c0001t0002g0154a0001c0001t0002g0155others(39): Show | 43 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.532+1833G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73691348 | ||||||
chr14:73691422
|
G | T | 17 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(14): Show | 17 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.532+1907G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73691422 | ||||||
chr14:73691754
|
C | T | 17 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(14): Show | 17 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(14): Show |
intron_variant | MODIFIER | c.532+2239C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73691754 | ||||||
chr14:73691787
|
G | A | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.532+2272G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73691787 | ||||||
chr14:73691846
|
A | AC | 57 | a0001c0001t0004g0013a0001c0001t0004g0014a0001c0001t0004g0018others(54): Show | 57 | HG00423.hp1 HG00544.hp2 HG00738.hp2 others(54): Show |
intron_variant | MODIFIER | c.532+2343dupC | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73691846 | |||||
chr14:73691846
|
AC | A | 28 | a0001c0001t0003g0042a0001c0001t0003g0064a0001c0001t0003g0308others(25): Show | 28 | HG00558.hp1 HG01074.hp2 HG01175.hp1 others(25): Show |
intron_variant | MODIFIER | c.532+2343delC | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73691846 | |||||
chr14:73691846
|
ACC | A | 35 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.532+2342_532+2343d others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73691846 | |||||
chr14:73691854
|
C | CCG | 18 | a0001c0001t0001g0004a0001c0001t0001g0242a0001c0001t0001g0270others(15): Show | 18 | HG00140.hp2 HG00621.hp1 HG02027.hp2 others(15): Show |
intron_variant | MODIFIER | c.532+2340_532+2341i others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73691854 | |||||
chr14:73691854
|
C | CG | 66 | a0001c0001t0001g0237a0001c0001t0001g0240a0001c0001t0001g0241others(63): Show | 68 | HG00423.hp2 HG00438.hp2 HG00544.hp1 others(65): Show |
intron_variant | MODIFIER | c.532+2339_532+2340i others(3): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73691854 | ||||||
chr14:73691854
|
C | G | 8 | a0001c0001t0014g0328a0001c0001t0014g0329a0001c0001t0014g0330others(5): Show | 8 | HG01168.hp1 HG01515.hp2 HG02109.hp2 others(5): Show |
intron_variant | MODIFIER | c.532+2339C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73691854 | ||||||
chr14:73691856
|
C | CG | 6 | a0001c0001t0002g0157a0001c0001t0002g0160a0001c0001t0002g0180others(3): Show | 6 | HG01074.hp1 HG01175.hp2 HG02257.hp1 others(3): Show |
intron_variant | MODIFIER | c.532+2341_532+2342i others(3): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73691856 | ||||||
chr14:73691856
|
C | G | 38 | a0001c0001t0002g0003a0001c0001t0002g0154a0001c0001t0002g0155others(35): Show | 39 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(36): Show |
intron_variant | MODIFIER | c.532+2341C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73691856 | ||||||
chr14:73691973
|
G | A | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.532+2458G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73691973 | ||||||
chr14:73691975
|
CG | C | 335 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(332): Show | 339 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(336): Show |
intron_variant | MODIFIER | c.532+2462delG | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73691975 | |||||
chr14:73691996
|
CT | C | 114 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(111): Show | 116 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(113): Show |
intron_variant | MODIFIER | c.532+2500delT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73691996 | |||||
chr14:73691996
|
CTT | C | 146 | a0001c0001t0002g0003a0001c0001t0002g0154a0001c0001t0002g0155others(143): Show | 148 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(145): Show |
intron_variant | MODIFIER | c.532+2499_532+2500d others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73691996 | |||||
chr14:73691996
|
CTTT | C | 35 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(32): Show | 35 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(32): Show |
intron_variant | MODIFIER | c.532+2498_532+2500d others(5): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73691996 | |||||
chr14:73692031
|
T | C | 1 | a0001c0001t0006g0305 | 1 | HG02074.hp2 | intron_variant | MODIFIER | c.532+2516T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692031 | ||||||
chr14:73692052
|
C | G | 1 | a0001c0001t0027g0152 | 1 | NA18981.hp1 | intron_variant | MODIFIER | c.532+2537C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692052 | ||||||
chr14:73692083
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.532+2568C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692083 | ||||||
chr14:73692084
|
G | A | 2 | a0001c0001t0052g0235a0001c0001t0057g0234 | 2 | HG02886.hp2 NA19043.hp2 |
intron_variant | MODIFIER | c.532+2569G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692084 | ||||||
chr14:73692162
|
C | T | 1 | a0001c0001t0005g0117 | 1 | HG00544.hp2 | intron_variant | MODIFIER | c.532+2647C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692162 | ||||||
chr14:73692204
|
G | A | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.532+2689G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692204 | ||||||
chr14:73692336
|
G | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.532+2821G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692336 | ||||||
chr14:73692337
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.532+2822C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692337 | ||||||
chr14:73692338
|
T | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.532+2823T>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692338 | ||||||
chr14:73692339
|
G | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.532+2824G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692339 | ||||||
chr14:73692340
|
C | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.532+2825C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692340 | ||||||
chr14:73692340
|
C | T | 1 | a0001c0001t0004g0014 | 1 | HG02055.hp2 | intron_variant | MODIFIER | c.532+2825C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692340 | ||||||
chr14:73692341
|
G | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.532+2826G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692341 | ||||||
chr14:73692610
|
GA | G | 8 | a0001c0001t0020g0310a0001c0001t0020g0311a0001c0001t0020g0313others(5): Show | 8 | HG01891.hp2 HG03041.hp1 HG03130.hp1 others(5): Show |
intron_variant | MODIFIER | c.532+3109delA | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73692610 | |||||
chr14:73692642
|
C | T | 1 | a0001c0001t0016g0321 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.532+3127C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692642 | ||||||
chr14:73692757
|
A | G | 1 | a0001c0001t0016g0324 | 1 | HG02257.hp2 | intron_variant | MODIFIER | c.533-3145A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692757 | ||||||
chr14:73692840
|
C | CT | 15 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(12): Show | 15 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.533-3048dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73692840 | |||||
chr14:73692869
|
C | T | 2 | a0001c0001t0008g0144a0001c0001t0008g0145 | 2 | HG01515.hp1 HG01517.hp2 |
intron_variant | MODIFIER | c.533-3033C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692869 | ||||||
chr14:73692897
|
C | T | 1 | a0001c0001t0001g0269 | 1 | NA19009.hp2 | intron_variant | MODIFIER | c.533-3005C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692897 | ||||||
chr14:73692935
|
C | T | 5 | a0001c0001t0033g0226a0001c0001t0033g0232a0001c0001t0064g0233others(2): Show | 5 | HG02559.hp1 HG02615.hp2 HG02723.hp1 others(2): Show |
intron_variant | MODIFIER | c.533-2967C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692935 | ||||||
chr14:73692941
|
A | G | 38 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(35): Show | 38 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(35): Show |
intron_variant | MODIFIER | c.533-2961A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73692941 | ||||||
chr14:73693100
|
C | T | 1 | a0001c0001t0058g0220 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.533-2802C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693100 | ||||||
chr14:73693123
|
C | T | 7 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0010g0075others(4): Show | 7 | HG01358.hp2 HG01978.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.533-2779C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693123 | ||||||
chr14:73693277
|
A | AG | 56 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(53): Show | 56 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(53): Show |
intron_variant | MODIFIER | c.533-2625_533-2624i others(3): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693277 | ||||||
chr14:73693315
|
T | C | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.533-2587T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693315 | ||||||
chr14:73693332
|
A | T | 2 | a0001c0001t0026g0096a0001c0001t0026g0120 | 2 | NA18979.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.533-2570A>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693332 | ||||||
chr14:73693333
|
A | C | 2 | a0001c0001t0026g0096a0001c0001t0026g0120 | 2 | NA18979.hp2 NA18994.hp2 |
intron_variant | MODIFIER | c.533-2569A>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693333 | ||||||
chr14:73693365
|
C | T | 42 | a0001c0001t0002g0003a0001c0001t0002g0154a0001c0001t0002g0155others(39): Show | 43 | HG00099.hp2 HG00558.hp2 HG00642.hp1 others(40): Show |
intron_variant | MODIFIER | c.533-2537C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693365 | ||||||
chr14:73693366
|
G | A | 7 | a0001c0001t0010g0072a0001c0001t0010g0073a0001c0001t0010g0075others(4): Show | 7 | HG01358.hp2 HG01978.hp1 HG03017.hp2 others(4): Show |
intron_variant | MODIFIER | c.533-2536G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693366 | ||||||
chr14:73693498
|
G | A | 1 | a0001c0001t0007g0223 | 1 | NA18964.hp2 | intron_variant | MODIFIER | c.533-2404G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693498 | ||||||
chr14:73693559
|
AG | A | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.533-2342delG | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693559 | ||||||
chr14:73693589
|
C | T | 114 | a0001c0001t0002g0003a0001c0001t0002g0154a0001c0001t0002g0155others(111): Show | 116 | HG00099.hp2 HG00438.hp1 HG00544.hp2 others(113): Show |
intron_variant | MODIFIER | c.533-2313C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693589 | ||||||
chr14:73693636
|
G | A | 13 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(10): Show | 13 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(10): Show |
intron_variant | MODIFIER | c.533-2266G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693636 | ||||||
chr14:73693684
|
C | T | 1 | a0001c0001t0001g0279 | 1 | HG02602.hp2 | intron_variant | MODIFIER | c.533-2218C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693684 | ||||||
chr14:73693742
|
G | A | 1 | a0001c0001t0008g0128 | 1 | HG02647.hp2 | intron_variant | MODIFIER | c.533-2160G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693742 | ||||||
chr14:73693758
|
T | C | 2 | a0001c0001t0032g0088a0001c0001t0032g0089 | 2 | HG02486.hp2 NA18906.hp2 |
intron_variant | MODIFIER | c.533-2144T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693758 | ||||||
chr14:73693792
|
C | G | 15 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(12): Show | 15 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(12): Show |
intron_variant | MODIFIER | c.533-2110C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693792 | ||||||
chr14:73693851
|
C | T | 1 | a0001c0001t0047g0067 | 1 | HG00140.hp1 | intron_variant | MODIFIER | c.533-2051C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693851 | ||||||
chr14:73693852
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.533-2050G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693852 | ||||||
chr14:73693864
|
G | A | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.533-2038G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693864 | ||||||
chr14:73693920
|
G | A | 1 | a0001c0001t0031g0227 | 1 | HG03942.hp2 | intron_variant | MODIFIER | c.533-1982G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693920 | ||||||
chr14:73693924
|
C | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.533-1978C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693924 | ||||||
chr14:73693949
|
C | T | 1 | a0001c0001t0008g0090 | 1 | HG00738.hp2 | intron_variant | MODIFIER | c.533-1953C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693949 | ||||||
chr14:73693972
|
T | C | 1 | a0001c0001t0010g0253 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.533-1930T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73693972 | ||||||
chr14:73694032
|
C | T | 22 | a0001c0001t0008g0090a0001c0001t0008g0099a0001c0001t0008g0126others(19): Show | 22 | HG00738.hp2 HG01081.hp1 HG01109.hp1 others(19): Show |
intron_variant | MODIFIER | c.533-1870C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73694032 | ||||||
chr14:73694076
|
A | G | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.533-1826A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73694076 | ||||||
chr14:73694146
|
C | G | 1 | a0001c0001t0038g0084 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.533-1756C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73694146 | ||||||
chr14:73694151
|
G | C | 110 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(107): Show | 112 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(109): Show |
intron_variant | MODIFIER | c.533-1751G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73694151 | ||||||
chr14:73694237
|
T | TATAA | 72 | a0001c0001t0001g0242a0001c0001t0001g0246a0001c0001t0001g0247others(69): Show | 73 | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(70): Show |
intron_variant | MODIFIER | c.533-1615_533-1612d others(6): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73694237 | |||||
chr14:73694237
|
T | TATAAATA others(1): Show |
83 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(80): Show | 84 | HG00423.hp2 HG00544.hp1 HG00544.hp2 others(81): Show |
intron_variant | MODIFIER | c.533-1619_533-1612d others(10): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73694237 | |||||
chr14:73694237
|
T | TATAAATA others(5): Show |
29 | a0001c0001t0001g0248a0001c0001t0001g0258a0001c0001t0001g0262others(26): Show | 30 | HG00639.hp2 HG01070.hp2 HG01071.hp2 others(27): Show |
intron_variant | MODIFIER | c.533-1623_533-1612d others(14): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73694237 | |||||
chr14:73694237
|
T | TATAAATA others(9): Show |
4 | a0001c0001t0001g0298a0001c0001t0005g0092a0001c0001t0028g0115others(1): Show | 4 | HG00423.hp1 HG04228.hp2 NA18522.hp1 others(1): Show |
intron_variant | MODIFIER | c.533-1627_533-1612d others(18): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73694237 | |||||
chr14:73694237
|
TATAA | T | 38 | a0001c0001t0002g0154a0001c0001t0002g0161a0001c0001t0002g0183others(35): Show | 38 | HG00323.hp1 HG00558.hp2 HG00738.hp2 others(35): Show |
intron_variant | MODIFIER | c.533-1615_533-1612d others(6): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73694237 | |||||
chr14:73694237
|
TATAAATA others(1): Show |
T | 47 | a0001c0001t0002g0003a0001c0001t0002g0155a0001c0001t0002g0159others(44): Show | 48 | HG00642.hp1 HG00738.hp1 HG01074.hp1 others(45): Show |
intron_variant | MODIFIER | c.533-1619_533-1612d others(10): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73694237 | |||||
chr14:73694237
|
TATAAATA others(5): Show |
T | 1 | a0001c0001t0008g0099 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.533-1623_533-1612d others(14): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73694237 | |||||
chr14:73694237
|
TATAAATA others(9): Show |
T | 6 | a0001c0001t0002g0157a0001c0001t0002g0188a0001c0001t0032g0088others(3): Show | 6 | HG00099.hp2 HG02257.hp1 HG02258.hp1 others(3): Show |
intron_variant | MODIFIER | c.533-1627_533-1612d others(18): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73694237 | |||||
chr14:73694300
|
G | C | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.533-1602G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73694300 | ||||||
chr14:73694497
|
C | T | 1 | a0001c0001t0023g0028 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.533-1405C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73694497 | ||||||
chr14:73694544
|
A | AT | 270 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(267): Show | 274 | HG00099.hp2 HG00140.hp2 HG00423.hp2 others(271): Show |
intron_variant | MODIFIER | c.533-1349dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73694544 | |||||
chr14:73694544
|
A | ATTT | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.533-1351_533-1349d others(5): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73694544 | |||||
chr14:73694567
|
A | G | 3 | a0001c0001t0001g0237a0001c0001t0032g0088a0001c0001t0032g0089 | 3 | HG02486.hp2 HG03704.hp1 NA18906.hp2 |
intron_variant | MODIFIER | c.533-1335A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73694567 | ||||||
chr14:73694591
|
T | C | 1 | a0001c0001t0004g0019 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.533-1311T>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73694591 | ||||||
chr14:73694643
|
A | G | 84 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(81): Show | 86 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(83): Show |
intron_variant | MODIFIER | c.533-1259A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73694643 | ||||||
chr14:73694692
|
C | CTT | 12 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(9): Show | 12 | HG01884.hp2 HG01891.hp2 HG02055.hp1 others(9): Show |
intron_variant | MODIFIER | c.533-1196_533-1195d others(4): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73694692 | |||||
chr14:73694692
|
CT | C | 8 | a0001c0001t0003g0046a0001c0001t0005g0113a0001c0001t0014g0330others(5): Show | 8 | HG00323.hp1 HG01109.hp2 HG01515.hp2 others(5): Show |
intron_variant | MODIFIER | c.533-1195delT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73694692 | |||||
chr14:73694729
|
G | A | 1 | a0001c0001t0050g0012 | 1 | HG03540.hp1 | intron_variant | MODIFIER | c.533-1173G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73694729 | ||||||
chr14:73694756
|
C | G | 14 | a0001c0001t0012g0198a0001c0001t0012g0199a0001c0001t0012g0200others(11): Show | 14 | HG01243.hp2 HG01891.hp1 HG02109.hp1 others(11): Show |
intron_variant | MODIFIER | c.533-1146C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73694756 | ||||||
chr14:73694897
|
C | G | 1 | a0001c0001t0002g0184 | 1 | HG00558.hp2 | intron_variant | MODIFIER | c.533-1005C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73694897 | ||||||
chr14:73694984
|
C | T | 2 | a0001c0001t0048g0082a0001c0001t0049g0071 | 2 | HG02886.hp1 HG03453.hp1 |
intron_variant | MODIFIER | c.533-918C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73694984 | ||||||
chr14:73695048
|
C | CT | 41 | a0001c0001t0001g0245a0001c0001t0001g0256a0001c0001t0001g0277others(38): Show | 41 | HG00735.hp2 HG01168.hp2 HG01192.hp2 others(38): Show |
intron_variant | MODIFIER | c.533-829dupT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73695048 | |||||
chr14:73695048
|
C | CTT | 31 | a0001c0001t0001g0242a0001c0001t0003g0001a0001c0001t0003g0010others(28): Show | 31 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(28): Show |
intron_variant | MODIFIER | c.533-830_533-829dup others(2): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73695048 | |||||
chr14:73695048
|
C | CTTT | 14 | a0001c0001t0003g0042a0001c0001t0003g0063a0001c0001t0003g0308others(11): Show | 14 | HG00639.hp2 HG00733.hp1 HG01891.hp1 others(11): Show |
intron_variant | MODIFIER | c.533-831_533-829dup others(3): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73695048 | |||||
chr14:73695048
|
CT | C | 53 | a0001c0001t0001g0271a0001c0001t0001g0287a0001c0001t0002g0003others(50): Show | 54 | HG00099.hp2 HG00438.hp1 HG00558.hp2 others(51): Show |
intron_variant | MODIFIER | c.533-829delT | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73695048 | |||||
chr14:73695048
|
CTT | C | 61 | a0001c0001t0005g0091a0001c0001t0005g0092a0001c0001t0005g0097others(58): Show | 62 | HG00544.hp2 HG00558.hp1 HG01074.hp2 others(59): Show |
intron_variant | MODIFIER | c.533-830_533-829del others(2): Show |
DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | INFO_REALIGN_3_PRIME | chr14 | 73695048 | |||||
chr14:73695119
|
A | G | 1 | a0001c0001t0004g0017 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.533-783A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73695119 | ||||||
chr14:73695138
|
C | G | 109 | a0001c0001t0001g0004a0001c0001t0001g0237a0001c0001t0001g0240others(106): Show | 111 | HG00140.hp2 HG00423.hp2 HG00438.hp2 others(108): Show |
intron_variant | MODIFIER | c.533-764C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73695138 | ||||||
chr14:73695196
|
A | G | 3 | a0001c0001t0013g0051a0001c0001t0013g0052a0001c0001t0044g0050 | 3 | HG00323.hp2 HG02040.hp2 HG03239.hp1 |
intron_variant | MODIFIER | c.533-706A>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73695196 | ||||||
chr14:73695295
|
C | T | 5 | a0001c0001t0016g0320a0001c0001t0016g0321a0001c0001t0016g0322others(2): Show | 5 | HG02055.hp1 HG02257.hp2 HG02451.hp1 others(2): Show |
intron_variant | MODIFIER | c.533-607C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73695295 | ||||||
chr14:73695375
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.533-527C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73695375 | ||||||
chr14:73695376
|
G | T | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.533-526G>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73695376 | ||||||
chr14:73695405
|
C | T | 2 | a0001c0001t0024g0172a0001c0001t0024g0173 | 2 | HG01074.hp1 HG01099.hp2 |
intron_variant | MODIFIER | c.533-497C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73695405 | ||||||
chr14:73695500
|
G | A | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.533-402G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73695500 | ||||||
chr14:73695519
|
C | T | 4 | a0001c0001t0025g0163a0001c0001t0025g0169a0001c0001t0035g0168others(1): Show | 4 | HG00733.hp2 HG00738.hp1 HG01123.hp2 others(1): Show |
intron_variant | MODIFIER | c.533-383C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73695519 | ||||||
chr14:73695614
|
C | T | 3 | a0001c0001t0029g0079a0001c0001t0029g0081a0001c0001t0037g0080 | 3 | HG03041.hp1 HG03130.hp1 HG03471.hp1 |
intron_variant | MODIFIER | c.533-288C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73695614 | ||||||
chr14:73695661
|
C | G | 1 | a0001c0001t0002g0192 | 1 | NA19055.hp2 | intron_variant | MODIFIER | c.533-241C>G | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73695661 | ||||||
chr14:73695674
|
C | T | 2 | a0001c0001t0006g0268a0001c0001t0085g0125 | 2 | HG03195.hp2 NA19058.hp1 |
intron_variant | MODIFIER | c.533-228C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73695674 | ||||||
chr14:73695679
|
G | A | 1 | a0001c0001t0095g0148 | 1 | HG03017.hp1 | intron_variant | MODIFIER | c.533-223G>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73695679 | ||||||
chr14:73695749
|
G | C | 37 | a0001c0001t0003g0001a0001c0001t0003g0010a0001c0001t0003g0040others(34): Show | 37 | HG00099.hp1 HG00140.hp1 HG00323.hp1 others(34): Show |
intron_variant | MODIFIER | c.533-153G>C | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73695749 | ||||||
chr14:73695808
|
C | T | 1 | a0001c0001t0005g0097 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.533-94C>T | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73695808 | ||||||
chr14:73695817
|
C | A | 4 | a0001c0001t0009g0093a0001c0001t0009g0101a0001c0001t0009g0102others(1): Show | 4 | HG01074.hp2 HG01243.hp1 HG02818.hp1 others(1): Show |
intron_variant | MODIFIER | c.533-85C>A | DNAL1 | ENSG00000119661.15 | transcript | ENST00000553645.7 | protein_coding | 7/7 | chr14 | 73695817 |