geneid | 199857 |
---|---|
ensemblid | ENSG00000172339.10 |
hgncid | 28287 |
symbol | ALG14 |
name | ALG14 UDP-N-acetylglucosaminyltransferase subunit |
refseq_nuc | NM_144988.4 |
refseq_prot | NP_659425.1 |
ensembl_nuc | ENST00000370205.6 |
ensembl_prot | ENSP00000359224.4 |
mane_status | MANE Select |
chr | chr1 |
start | 94974405 |
end | 95072951 |
strand | - |
ver | v1.2 |
region | chr1:94974405-95072951 |
region5000 | chr1:94969405-95077951 |
regionname0 | ALG14_chr1_94974405_95072951 |
regionname5000 | ALG14_chr1_94969405_95077951 |
ahapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
alen | total | AFR | AMR | EAS | EUR | SAS | JPT | regionname | genename | aa | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001 | 1/1 | 216 | 387 | 90 | 74 | 173 | 14 | 34 | 133 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0002 | 0/0 | 216 | 1 | 0 | 0 | 1 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
chapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
c0001 | 1/1 | 651 | 381 | 90 | 74 | 168 | 14 | 33 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
c0002 | 0/0 | 651 | 4 | 0 | 0 | 4 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
c0003 | 0/0 | 651 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
c0004 | 0/0 | 651 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
c0005 | 0/0 | 651 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
thapid | grch38chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
t0001 | 0/0 | 8727 | 38 | 7 | 8 | 14 | 4 | 5 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0002 | 0/0 | 8730 | 18 | 0 | 0 | 17 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0003 | 0/0 | 8731 | 15 | 0 | 0 | 15 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0004 | 0/0 | 8726 | 13 | 0 | 4 | 7 | 0 | 2 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0005 | 0/0 | 8730 | 12 | 2 | 2 | 7 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0006 | 0/0 | 8731 | 8 | 1 | 3 | 0 | 2 | 2 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0007 | 0/0 | 8729 | 7 | 0 | 6 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0008 | 0/0 | 8724 | 6 | 6 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0009 | 0/0 | 8728 | 6 | 1 | 2 | 2 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0010 | 0/0 | 8732 | 5 | 0 | 0 | 5 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0011 | 0/0 | 8726 | 5 | 0 | 0 | 5 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0012 | 0/0 | 8725 | 5 | 1 | 2 | 0 | 1 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0013 | 0/0 | 8729 | 5 | 0 | 0 | 5 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0014 | 0/0 | 8729 | 5 | 2 | 1 | 2 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0015 | 0/0 | 8730 | 5 | 0 | 3 | 2 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0016 | 0/0 | 8732 | 4 | 3 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0017 | 0/0 | 8728 | 4 | 0 | 0 | 4 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0018 | 0/0 | 8732 | 4 | 0 | 4 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0019 | 0/0 | 8731 | 4 | 0 | 1 | 2 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0020 | 0/0 | 8729 | 4 | 4 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0021 | 0/0 | 8728 | 4 | 1 | 1 | 1 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0022 | 0/0 | 8731 | 4 | 0 | 4 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0023 | 0/0 | 8729 | 3 | 3 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0024 | 0/0 | 8728 | 3 | 3 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0025 | 0/0 | 8730 | 3 | 0 | 0 | 0 | 0 | 3 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0026 | 0/0 | 8730 | 3 | 0 | 0 | 1 | 0 | 2 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0027 | 0/0 | 8730 | 3 | 0 | 0 | 3 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0028 | 0/0 | 8727 | 2 | 2 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0029 | 0/0 | 8730 | 2 | 1 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0030 | 0/0 | 8731 | 2 | 2 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0031 | 1/0 | 8725 | 2 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0032 | 0/0 | 8730 | 2 | 0 | 0 | 2 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0033 | 0/0 | 8730 | 2 | 2 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0034 | 0/0 | 8732 | 2 | 0 | 0 | 2 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0035 | 0/0 | 8724 | 2 | 0 | 2 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0036 | 0/0 | 8725 | 2 | 2 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0037 | 0/0 | 8735 | 2 | 1 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0038 | 0/0 | 8736 | 2 | 2 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0039 | 0/0 | 8731 | 2 | 0 | 0 | 2 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0040 | 0/0 | 8730 | 2 | 2 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0041 | 0/0 | 8730 | 2 | 0 | 0 | 2 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0042 | 0/0 | 8728 | 2 | 2 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0043 | 0/0 | 8726 | 2 | 1 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0044 | 0/0 | 8728 | 2 | 0 | 1 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0045 | 0/1 | 8727 | 2 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0046 | 0/0 | 8731 | 2 | 0 | 0 | 2 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0047 | 0/0 | 8731 | 2 | 1 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0048 | 0/0 | 8732 | 2 | 0 | 1 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0049 | 0/0 | 8726 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0050 | 0/0 | 8730 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0051 | 0/0 | 8729 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0052 | 0/0 | 8730 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0053 | 0/0 | 8728 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0054 | 0/0 | 8729 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0055 | 0/0 | 8726 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0056 | 0/0 | 8725 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0057 | 0/0 | 8727 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0058 | 0/0 | 8728 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0059 | 0/0 | 8731 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0060 | 0/0 | 8729 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0061 | 0/0 | 8730 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0062 | 0/0 | 8731 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0063 | 0/0 | 8723 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0064 | 0/0 | 8733 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0065 | 0/0 | 8727 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0066 | 0/0 | 8725 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0067 | 0/0 | 8727 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0068 | 0/0 | 8730 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0069 | 0/0 | 8731 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0070 | 0/0 | 8727 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0071 | 0/0 | 8730 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0072 | 0/0 | 8726 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0073 | 0/0 | 8730 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0074 | 0/0 | 8729 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0075 | 0/0 | 8728 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0076 | 0/0 | 8728 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0077 | 0/0 | 8725 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0078 | 0/0 | 8727 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0079 | 0/0 | 8729 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0080 | 0/0 | 8729 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0081 | 0/0 | 8729 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0082 | 0/0 | 8734 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0083 | 0/0 | 8730 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0084 | 0/0 | 8733 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0085 | 0/0 | 8729 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0086 | 0/0 | 8730 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0087 | 0/0 | 8730 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0088 | 0/0 | 8731 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0089 | 0/0 | 8726 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0090 | 0/0 | 8725 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0091 | 0/0 | 8726 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0092 | 0/0 | 8726 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0093 | 0/0 | 8727 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0094 | 0/0 | 8726 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0095 | 0/0 | 8725 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0096 | 0/0 | 8725 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0097 | 0/0 | 8730 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0098 | 0/0 | 8731 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0099 | 0/0 | 8732 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0100 | 0/0 | 8733 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0101 | 0/0 | 8734 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0102 | 0/0 | 8730 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0103 | 0/0 | 8731 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0104 | 0/0 | 8727 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0105 | 0/0 | 8731 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0106 | 0/0 | 8730 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0107 | 0/0 | 8731 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0108 | 0/0 | 8731 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0109 | 0/0 | 8730 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0110 | 0/0 | 8731 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0111 | 0/0 | 8727 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0112 | 0/0 | 8728 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0113 | 0/0 | 8728 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0114 | 0/0 | 8730 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0115 | 0/0 | 8729 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0116 | 0/0 | 8730 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0117 | 0/0 | 8729 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0118 | 0/0 | 8730 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0119 | 0/0 | 8729 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0120 | 0/0 | 8732 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0121 | 0/0 | 8729 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0122 | 0/0 | 8728 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0123 | 0/0 | 8732 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0124 | 0/0 | 8731 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0125 | 0/0 | 8730 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0126 | 0/0 | 8729 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0127 | 0/0 | 8731 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0128 | 0/0 | 8729 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0129 | 0/0 | 8729 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0130 | 0/0 | 8730 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0131 | 0/0 | 8729 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0132 | 0/0 | 8731 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0133 | 0/0 | 8731 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0134 | 0/0 | 8731 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0135 | 0/0 | 8731 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0136 | 0/0 | 8730 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0137 | 0/0 | 8730 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0138 | 0/0 | 8730 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0139 | 0/0 | 8732 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0140 | 0/0 | 8731 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0141 | 0/0 | 8730 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0142 | 0/0 | 8732 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0143 | 0/0 | 8729 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0144 | 0/0 | 8733 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0145 | 0/0 | 8730 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0146 | 0/0 | 8729 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0147 | 0/0 | 8725 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0148 | 0/0 | 8726 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0149 | 0/0 | 8726 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0150 | 0/0 | 8728 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0151 | 0/0 | 8727 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0152 | 0/0 | 8728 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0153 | 0/0 | 8727 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0154 | 0/0 | 8727 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0155 | 0/0 | 8727 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0156 | 0/0 | 8727 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0157 | 0/0 | 8727 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0158 | 0/0 | 8727 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0159 | 0/0 | 8728 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0160 | 0/0 | 8727 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0161 | 0/0 | 8727 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0162 | 0/0 | 8728 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0163 | 0/0 | 8728 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0164 | 0/0 | 8731 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0165 | 0/0 | 8728 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0166 | 0/0 | 8733 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0167 | 0/0 | 8734 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0168 | 0/0 | 8725 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0169 | 0/0 | 8730 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0170 | 0/0 | 8731 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0171 | 0/0 | 8732 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0172 | 0/0 | 8732 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0173 | 0/0 | 8730 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0174 | 0/0 | 8731 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0175 | 0/0 | 8732 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0176 | 0/0 | 8734 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0177 | 0/0 | 8731 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0178 | 0/0 | 8732 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0179 | 0/0 | 8731 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0180 | 0/0 | 8732 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0181 | 0/0 | 8731 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0182 | 0/0 | 8733 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0183 | 0/0 | 8727 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0184 | 0/0 | 8731 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0185 | 0/0 | 8729 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0186 | 0/0 | 8732 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0187 | 0/0 | 8730 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0188 | 0/0 | 8728 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0189 | 0/0 | 8728 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0190 | 0/0 | 8729 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0191 | 0/0 | 8726 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0192 | 0/0 | 8732 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0193 | 0/0 | 8733 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0194 | 0/0 | 8734 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0195 | 0/0 | 8733 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0196 | 0/0 | 8736 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0197 | 0/0 | 8737 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
t0198 | 0/0 | 8729 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
ghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
g0001 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0331 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0372 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0384 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
achapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
clen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | cseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001 | 1/1 | 651 | 381 | 90 | 74 | 168 | 14 | 33 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0002 | 0/0 | 651 | 4 | 0 | 0 | 4 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0003 | 0/0 | 651 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0005 | 0/0 | 651 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0002c0004 | 0/0 | 651 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
acthapid | grch38chm13v2 | tlen | total | AFR | AMR | EAS | EUR | SAS | regionname | genename | tseq | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001 | 0/0 | 9377 | 38 | 7 | 8 | 14 | 4 | 5 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0002 | 0/0 | 9380 | 18 | 0 | 0 | 17 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0003 | 0/0 | 9381 | 15 | 0 | 0 | 15 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0004 | 0/0 | 9376 | 13 | 0 | 4 | 7 | 0 | 2 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0005 | 0/0 | 9380 | 12 | 2 | 2 | 7 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0006 | 0/0 | 9381 | 8 | 1 | 3 | 0 | 2 | 2 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0007 | 0/0 | 9379 | 7 | 0 | 6 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0008 | 0/0 | 9374 | 6 | 6 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0009 | 0/0 | 9378 | 6 | 1 | 2 | 2 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0010 | 0/0 | 9382 | 5 | 0 | 0 | 5 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0011 | 0/0 | 9376 | 5 | 0 | 0 | 5 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0012 | 0/0 | 9375 | 5 | 1 | 2 | 0 | 1 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0013 | 0/0 | 9379 | 5 | 0 | 0 | 5 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0014 | 0/0 | 9379 | 5 | 2 | 1 | 2 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0015 | 0/0 | 9380 | 5 | 0 | 3 | 2 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0016 | 0/0 | 9382 | 4 | 3 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0017 | 0/0 | 9378 | 4 | 0 | 0 | 4 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0018 | 0/0 | 9382 | 4 | 0 | 4 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0019 | 0/0 | 9381 | 3 | 0 | 1 | 2 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0020 | 0/0 | 9379 | 4 | 4 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0021 | 0/0 | 9378 | 4 | 1 | 1 | 1 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0022 | 0/0 | 9381 | 4 | 0 | 4 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0023 | 0/0 | 9379 | 3 | 3 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0024 | 0/0 | 9378 | 3 | 3 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0025 | 0/0 | 9380 | 3 | 0 | 0 | 0 | 0 | 3 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0026 | 0/0 | 9380 | 3 | 0 | 0 | 1 | 0 | 2 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0027 | 0/0 | 9380 | 3 | 0 | 0 | 3 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0028 | 0/0 | 9377 | 2 | 2 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0029 | 0/0 | 9380 | 2 | 1 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0030 | 0/0 | 9381 | 2 | 2 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0031 | 1/0 | 9375 | 2 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0032 | 0/0 | 9380 | 2 | 0 | 0 | 2 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0033 | 0/0 | 9380 | 2 | 2 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0034 | 0/0 | 9382 | 2 | 0 | 0 | 2 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0035 | 0/0 | 9374 | 2 | 0 | 2 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0036 | 0/0 | 9375 | 2 | 2 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0037 | 0/0 | 9385 | 2 | 1 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0038 | 0/0 | 9386 | 2 | 2 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0039 | 0/0 | 9381 | 2 | 0 | 0 | 2 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0040 | 0/0 | 9380 | 2 | 2 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0041 | 0/0 | 9380 | 2 | 0 | 0 | 2 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0042 | 0/0 | 9378 | 2 | 2 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0043 | 0/0 | 9376 | 2 | 1 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0044 | 0/0 | 9378 | 2 | 0 | 1 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0045 | 0/1 | 9377 | 2 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0046 | 0/0 | 9381 | 2 | 0 | 0 | 2 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0047 | 0/0 | 9381 | 2 | 1 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0048 | 0/0 | 9382 | 2 | 0 | 1 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0049 | 0/0 | 9376 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0050 | 0/0 | 9380 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0051 | 0/0 | 9379 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0052 | 0/0 | 9380 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0053 | 0/0 | 9378 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0054 | 0/0 | 9379 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0055 | 0/0 | 9376 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0056 | 0/0 | 9375 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0057 | 0/0 | 9377 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0058 | 0/0 | 9378 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0059 | 0/0 | 9381 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0060 | 0/0 | 9379 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0061 | 0/0 | 9380 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0062 | 0/0 | 9381 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0063 | 0/0 | 9373 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0064 | 0/0 | 9383 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0065 | 0/0 | 9377 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0066 | 0/0 | 9375 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0067 | 0/0 | 9377 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0068 | 0/0 | 9380 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0069 | 0/0 | 9381 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0070 | 0/0 | 9377 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0071 | 0/0 | 9380 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0072 | 0/0 | 9376 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0073 | 0/0 | 9380 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0074 | 0/0 | 9379 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0075 | 0/0 | 9378 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0076 | 0/0 | 9378 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0077 | 0/0 | 9375 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0078 | 0/0 | 9377 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0079 | 0/0 | 9379 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0080 | 0/0 | 9379 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0081 | 0/0 | 9379 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0082 | 0/0 | 9384 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0083 | 0/0 | 9380 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0084 | 0/0 | 9383 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0085 | 0/0 | 9379 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0086 | 0/0 | 9380 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0087 | 0/0 | 9380 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0088 | 0/0 | 9381 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0089 | 0/0 | 9376 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0090 | 0/0 | 9375 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0091 | 0/0 | 9376 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0092 | 0/0 | 9376 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0093 | 0/0 | 9377 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0094 | 0/0 | 9376 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0095 | 0/0 | 9375 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0096 | 0/0 | 9375 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0097 | 0/0 | 9380 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0098 | 0/0 | 9381 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0099 | 0/0 | 9382 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0100 | 0/0 | 9383 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0101 | 0/0 | 9384 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0102 | 0/0 | 9380 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0103 | 0/0 | 9381 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0104 | 0/0 | 9377 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0105 | 0/0 | 9381 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0106 | 0/0 | 9380 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0107 | 0/0 | 9381 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0109 | 0/0 | 9380 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0110 | 0/0 | 9381 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0111 | 0/0 | 9377 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0112 | 0/0 | 9378 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0113 | 0/0 | 9378 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0114 | 0/0 | 9380 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0115 | 0/0 | 9379 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0116 | 0/0 | 9380 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0117 | 0/0 | 9379 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0118 | 0/0 | 9380 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0119 | 0/0 | 9379 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0121 | 0/0 | 9379 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0122 | 0/0 | 9378 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0123 | 0/0 | 9382 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0124 | 0/0 | 9381 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0128 | 0/0 | 9379 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0129 | 0/0 | 9379 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0130 | 0/0 | 9380 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0131 | 0/0 | 9379 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0132 | 0/0 | 9381 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0133 | 0/0 | 9381 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0134 | 0/0 | 9381 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0135 | 0/0 | 9381 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0136 | 0/0 | 9380 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0137 | 0/0 | 9380 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0138 | 0/0 | 9380 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0140 | 0/0 | 9381 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0141 | 0/0 | 9380 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0142 | 0/0 | 9382 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0143 | 0/0 | 9379 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0144 | 0/0 | 9383 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0145 | 0/0 | 9380 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0146 | 0/0 | 9379 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0147 | 0/0 | 9375 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0148 | 0/0 | 9376 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0149 | 0/0 | 9376 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0150 | 0/0 | 9378 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0151 | 0/0 | 9377 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0152 | 0/0 | 9378 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0153 | 0/0 | 9377 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0154 | 0/0 | 9377 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0155 | 0/0 | 9377 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0156 | 0/0 | 9377 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0157 | 0/0 | 9377 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0158 | 0/0 | 9377 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0159 | 0/0 | 9378 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0160 | 0/0 | 9377 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0161 | 0/0 | 9377 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0162 | 0/0 | 9378 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0163 | 0/0 | 9378 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0164 | 0/0 | 9381 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0165 | 0/0 | 9378 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0166 | 0/0 | 9383 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0167 | 0/0 | 9384 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0168 | 0/0 | 9375 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0169 | 0/0 | 9380 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0170 | 0/0 | 9381 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0171 | 0/0 | 9382 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0172 | 0/0 | 9382 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0173 | 0/0 | 9380 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0174 | 0/0 | 9381 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0175 | 0/0 | 9382 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0176 | 0/0 | 9384 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0177 | 0/0 | 9381 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0178 | 0/0 | 9382 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0179 | 0/0 | 9381 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0180 | 0/0 | 9382 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0181 | 0/0 | 9381 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0182 | 0/0 | 9383 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0183 | 0/0 | 9377 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0184 | 0/0 | 9381 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0185 | 0/0 | 9379 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0186 | 0/0 | 9382 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0187 | 0/0 | 9380 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0188 | 0/0 | 9378 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0189 | 0/0 | 9378 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0190 | 0/0 | 9379 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0191 | 0/0 | 9376 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0192 | 0/0 | 9382 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0193 | 0/0 | 9383 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0194 | 0/0 | 9384 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0195 | 0/0 | 9383 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0196 | 0/0 | 9386 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0197 | 0/0 | 9387 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0001t0198 | 0/0 | 9379 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0002t0108 | 0/0 | 9381 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0002t0120 | 0/0 | 9382 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0002t0126 | 0/0 | 9379 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0002t0127 | 0/0 | 9381 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0003t0019 | 0/0 | 9381 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0001c0005t0139 | 0/0 | 9382 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
a0002c0004t0125 | 0/0 | 9380 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | copy fasta | chr1 | 94969405 | 95077951 |
actghapid | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
total | AFR | AMR | EAS | EUR | SAS | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
a0001c0001t0001g0115 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0194 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0276 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0278 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0282 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0284 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0289 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0293 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0295 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0296 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0300 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0301 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0304 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0307 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0308 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0309 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0313 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0314 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0317 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0318 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0319 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0321 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0322 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0330 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0334 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0335 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0340 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0341 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0342 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0347 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0352 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0353 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0356 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0357 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0358 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0359 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0362 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0001g0365 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0002g0213 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0002g0218 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0002g0221 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0002g0223 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0002g0227 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0002g0228 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0002g0230 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0002g0231 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0002g0244 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0002g0245 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0002g0247 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0002g0250 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0002g0251 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0002g0258 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0002g0259 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0002g0275 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0002g0298 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0002g0306 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0003g0002 | 0/0 | 2 | 0 | 0 | 2 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0003g0130 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0003g0133 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0003g0140 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0003g0141 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0003g0142 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0003g0145 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0003g0147 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0003g0148 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0003g0149 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0003g0150 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0003g0152 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0003g0178 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0003g0270 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0004g0004 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0004g0111 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0004g0153 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0004g0154 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0004g0155 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0004g0160 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0004g0162 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0004g0163 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0004g0164 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0004g0165 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0004g0166 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0004g0170 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0004g0256 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0005g0185 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0005g0189 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0005g0190 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0005g0191 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0005g0193 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0005g0196 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0005g0201 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0005g0203 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0005g0211 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0005g0264 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0005g0268 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0005g0269 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0006g0001 | 0/0 | 2 | 1 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0006g0035 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0006g0038 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0006g0039 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0006g0043 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0006g0044 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0006g0045 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0007g0212 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0007g0235 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0007g0236 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0007g0238 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0007g0239 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0007g0240 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0007g0252 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0008g0098 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0008g0099 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0008g0100 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0008g0101 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0008g0102 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0008g0103 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0009g0279 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0009g0291 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0009g0316 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0009g0324 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0009g0350 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0009g0364 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0010g0134 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0010g0135 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0010g0136 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0010g0137 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0010g0146 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0011g0280 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0011g0297 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0011g0303 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0011g0305 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0011g0310 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0012g0092 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0012g0093 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0012g0094 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0012g0095 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0012g0105 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0013g0053 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0013g0054 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0013g0059 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0013g0060 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0013g0073 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0014g0013 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0014g0014 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0014g0033 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0014g0062 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0014g0088 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0015g0046 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0015g0058 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0015g0072 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0015g0080 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0015g0085 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0016g0123 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0016g0124 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0016g0128 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0016g0267 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0017g0312 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0017g0378 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0017g0380 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0017g0381 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0018g0118 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0018g0119 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0018g0120 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0018g0121 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0019g0209 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0019g0216 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0019g0226 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0020g0074 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0020g0075 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0020g0076 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0020g0077 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0021g0285 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0021g0290 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0021g0294 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0021g0315 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0022g0082 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0022g0083 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0022g0084 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0022g0086 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0023g0029 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0023g0030 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0023g0263 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0024g0375 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0024g0376 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0024g0377 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0025g0026 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0025g0384 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0025g0385 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0026g0015 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0026g0017 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0026g0061 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0027g0199 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0027g0204 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0027g0207 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0028g0175 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0028g0176 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0029g0031 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0029g0032 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0030g0273 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0030g0274 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0031g0125 | 1/0 | 1 | 0 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0031g0354 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0032g0171 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0032g0173 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0033g0034 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0033g0040 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0034g0139 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0034g0144 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0035g0096 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0035g0097 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0036g0107 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0036g0108 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0037g0009 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0037g0018 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0038g0007 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0038g0011 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0039g0249 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0039g0260 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0040g0065 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0040g0066 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0041g0188 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0041g0214 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0042g0217 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0042g0243 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0043g0277 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0043g0283 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0044g0327 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0044g0346 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0045g0326 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0045g0331 | 0/1 | 1 | 0 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0046g0222 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0046g0224 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0047g0241 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0047g0242 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0048g0006 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0048g0079 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0049g0019 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0050g0262 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0051g0020 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0052g0067 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0053g0023 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0054g0021 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0055g0156 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0056g0157 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0057g0159 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0058g0177 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0059g0272 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0060g0027 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0061g0022 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0062g0024 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0063g0104 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0064g0127 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0065g0110 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0066g0167 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0067g0050 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0068g0003 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0069g0366 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0070g0168 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0071g0174 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0072g0161 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0073g0172 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0074g0382 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0075g0012 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0076g0379 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0077g0169 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0078g0089 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0079g0374 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0080g0047 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0081g0025 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0082g0049 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0083g0122 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0084g0132 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0085g0151 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0086g0131 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0087g0138 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0088g0129 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0089g0106 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0090g0281 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0091g0302 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0092g0320 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0093g0286 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0094g0288 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0095g0091 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0096g0386 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0097g0186 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0098g0255 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0099g0037 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0100g0126 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0101g0008 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0102g0041 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0103g0042 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0104g0112 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0105g0036 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0106g0215 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0107g0233 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0109g0237 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0110g0070 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0111g0087 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0112g0051 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0113g0063 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0114g0016 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0115g0052 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0116g0048 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0117g0057 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0118g0055 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0119g0071 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0121g0253 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0122g0206 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0123g0117 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0124g0197 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0128g0200 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0129g0184 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0130g0195 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0131g0192 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0132g0265 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0133g0005 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0134g0202 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0135g0257 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0136g0261 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0137g0180 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0138g0248 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0140g0246 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0141g0069 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0142g0010 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0143g0234 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0144g0143 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0145g0266 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0146g0287 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0147g0271 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0148g0344 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0149g0337 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0150g0360 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0151g0339 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0152g0292 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0153g0351 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0154g0363 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0155g0349 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0156g0345 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0157g0343 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0158g0090 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0159g0332 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0160g0109 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0161g0323 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0162g0355 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0163g0325 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0164g0372 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0165g0158 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0166g0068 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0167g0254 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0168g0064 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0169g0056 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0170g0367 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0171g0369 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0172g0081 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0173g0329 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0174g0078 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0175g0371 | 0/0 | 1 | 0 | 0 | 0 | 1 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0176g0232 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0177g0198 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0178g0208 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0179g0205 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0180g0311 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0181g0220 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0182g0219 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0183g0028 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0184g0361 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0185g0333 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0186g0328 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0187g0336 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0188g0348 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0189g0187 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0190g0338 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0191g0299 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0192g0368 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0193g0370 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0194g0373 | 0/0 | 1 | 0 | 1 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0195g0113 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0196g0114 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0197g0116 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0001t0198g0383 | 0/0 | 1 | 1 | 0 | 0 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0002t0108g0179 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0002t0120g0181 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0002t0126g0183 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0002t0127g0182 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0003t0019g0210 | 0/0 | 1 | 0 | 0 | 0 | 0 | 1 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0001c0005t0139g0225 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
a0002c0004t0125g0229 | 0/0 | 1 | 0 | 0 | 1 | 0 | 0 | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
sampleid | ID haplotypeid
|
ahapid | chapid | thapid | ghapid | gpopname | popname | regionname | genename | chr | start | end |
---|---|---|---|---|---|---|---|---|---|---|---|---|
HG00099 | hp1 | a0001 | c0001 | t0164 | g0372 | EUR | GBR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00099 | hp2 | a0001 | c0001 | t0001 | g0335 | EUR | GBR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00140 | hp1 | a0001 | c0001 | t0170 | g0367 | EUR | GBR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00140 | hp2 | a0001 | c0001 | t0157 | g0343 | EUR | GBR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00323 | hp1 | a0001 | c0001 | t0001 | g0341 | EUR | FIN | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00323 | hp2 | a0001 | c0001 | t0097 | g0186 | EUR | FIN | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00408 | hp1 | a0001 | c0001 | t0151 | g0339 | EAS | CHS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00408 | hp2 | a0001 | c0001 | t0010 | g0137 | EAS | CHS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00423 | hp1 | a0001 | c0001 | t0002 | g0245 | EAS | CHS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00423 | hp2 | a0001 | c0001 | t0003 | g0141 | EAS | CHS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00438 | hp1 | a0001 | c0001 | t0138 | g0248 | EAS | CHS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00438 | hp2 | a0001 | c0001 | t0009 | g0364 | EAS | CHS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00544 | hp1 | a0001 | c0001 | t0027 | g0204 | EAS | CHS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00544 | hp2 | a0001 | c0001 | t0010 | g0136 | EAS | CHS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00558 | hp1 | a0001 | c0001 | t0001 | g0307 | EAS | CHS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00558 | hp2 | a0001 | c0001 | t0143 | g0234 | EAS | CHS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00597 | hp1 | a0001 | c0001 | t0123 | g0117 | EAS | CHS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00597 | hp2 | a0001 | c0001 | t0004 | g0166 | EAS | CHS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00609 | hp1 | a0001 | c0001 | t0046 | g0222 | EAS | CHS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00609 | hp2 | a0001 | c0001 | t0017 | g0312 | EAS | CHS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00621 | hp1 | a0001 | c0001 | t0001 | g0308 | EAS | CHS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00621 | hp2 | a0001 | c0001 | t0010 | g0135 | EAS | CHS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00639 | hp1 | a0001 | c0001 | t0103 | g0042 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00639 | hp2 | a0001 | c0001 | t0009 | g0316 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00642 | hp1 | a0001 | c0001 | t0009 | g0324 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00642 | hp2 | a0001 | c0001 | t0194 | g0373 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00673 | hp1 | a0001 | c0001 | t0065 | g0110 | EAS | CHS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00673 | hp2 | a0001 | c0001 | t0007 | g0235 | EAS | CHS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00735 | hp1 | a0001 | c0001 | t0051 | g0020 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00735 | hp2 | a0001 | c0001 | t0100 | g0126 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00741 | hp1 | a0001 | c0001 | t0162 | g0355 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG00741 | hp2 | a0001 | c0001 | t0047 | g0241 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01069 | hp1 | a0001 | c0001 | t0156 | g0345 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01069 | hp2 | a0001 | c0001 | t0035 | g0096 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01070 | hp1 | a0001 | c0001 | t0001 | g0313 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01070 | hp2 | a0001 | c0001 | t0005 | g0185 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01074 | hp1 | a0001 | c0001 | t0018 | g0121 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01074 | hp2 | a0001 | c0001 | t0001 | g0353 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01081 | hp1 | a0001 | c0001 | t0016 | g0123 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01081 | hp2 | a0001 | c0001 | t0015 | g0085 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01099 | hp1 | a0001 | c0001 | t0001 | g0317 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01099 | hp2 | a0001 | c0001 | t0035 | g0097 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01109 | hp1 | a0001 | c0001 | t0185 | g0333 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01109 | hp2 | a0001 | c0001 | t0037 | g0018 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01167 | hp1 | a0001 | c0001 | t0001 | g0321 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01167 | hp2 | a0001 | c0001 | t0018 | g0119 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01169 | hp1 | a0001 | c0001 | t0018 | g0118 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01169 | hp2 | a0001 | c0001 | t0004 | g0111 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01175 | hp1 | a0001 | c0001 | t0187 | g0336 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01175 | hp2 | a0001 | c0001 | t0134 | g0202 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01192 | hp1 | a0001 | c0001 | t0188 | g0348 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01192 | hp2 | a0001 | c0001 | t0005 | g0203 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01243 | hp1 | a0001 | c0001 | t0001 | g0342 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01243 | hp2 | a0001 | c0001 | t0006 | g0045 | AMR | PUR | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01255 | hp1 | a0001 | c0001 | t0031 | g0354 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01255 | hp2 | a0001 | c0001 | t0014 | g0033 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01257 | hp1 | a0001 | c0001 | t0004 | g0153 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01257 | hp2 | a0001 | c0001 | t0043 | g0283 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01258 | hp1 | a0001 | c0001 | t0004 | g0154 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01258 | hp2 | a0001 | c0001 | t0132 | g0265 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01261 | hp1 | a0001 | c0001 | t0007 | g0212 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01261 | hp2 | a0001 | c0001 | t0159 | g0332 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01346 | hp1 | a0001 | c0001 | t0155 | g0349 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01346 | hp2 | a0001 | c0001 | t0022 | g0086 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01358 | hp1 | a0001 | c0001 | t0007 | g0239 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01358 | hp2 | a0001 | c0001 | t0006 | g0044 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01361 | hp1 | a0001 | c0001 | t0109 | g0237 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01361 | hp2 | a0001 | c0001 | t0105 | g0036 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01433 | hp1 | a0001 | c0001 | t0192 | g0368 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01433 | hp2 | a0001 | c0001 | t0018 | g0120 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01496 | hp1 | a0001 | c0001 | t0012 | g0092 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01496 | hp2 | a0001 | c0001 | t0007 | g0238 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01516 | hp1 | a0001 | c0001 | t0001 | g0314 | EUR | IBS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01516 | hp2 | a0001 | c0001 | t0006 | g0001 | EUR | IBS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01517 | hp1 | a0001 | c0001 | t0001 | g0318 | EUR | IBS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01517 | hp2 | a0001 | c0001 | t0006 | g0035 | EUR | IBS | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01884 | hp1 | a0001 | c0001 | t0024 | g0377 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01884 | hp2 | a0001 | c0001 | t0008 | g0099 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01891 | hp1 | a0001 | c0001 | t0001 | g0278 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01891 | hp2 | a0001 | c0001 | t0082 | g0049 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01928 | hp1 | a0001 | c0001 | t0022 | g0082 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01928 | hp2 | a0001 | c0001 | t0019 | g0216 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01934 | hp1 | a0001 | c0001 | t0163 | g0325 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01934 | hp2 | a0001 | c0001 | t0022 | g0083 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01943 | hp1 | a0001 | c0001 | t0015 | g0080 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01943 | hp2 | a0001 | c0001 | t0006 | g0038 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01952 | hp1 | a0001 | c0001 | t0015 | g0058 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01952 | hp2 | a0001 | c0001 | t0044 | g0327 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01975 | hp1 | a0001 | c0001 | t0001 | g0322 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01975 | hp2 | a0001 | c0001 | t0048 | g0079 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01978 | hp1 | a0001 | c0001 | t0190 | g0338 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01978 | hp2 | a0001 | c0001 | t0171 | g0369 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01981 | hp1 | a0001 | c0001 | t0022 | g0084 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01981 | hp2 | a0001 | c0001 | t0189 | g0187 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01993 | hp1 | a0001 | c0001 | t0001 | g0352 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01993 | hp2 | a0001 | c0001 | t0193 | g0370 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02004 | hp1 | a0001 | c0001 | t0012 | g0094 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02004 | hp2 | a0001 | c0001 | t0007 | g0236 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02015 | hp1 | a0001 | c0001 | t0021 | g0315 | EAS | KHV | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02015 | hp2 | a0001 | c0001 | t0027 | g0199 | EAS | KHV | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02027 | hp1 | a0001 | c0001 | t0002 | g0223 | EAS | KHV | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02027 | hp2 | a0001 | c0001 | t0003 | g0150 | EAS | KHV | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02040 | hp1 | a0001 | c0001 | t0017 | g0380 | EAS | KHV | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02040 | hp2 | a0001 | c0001 | t0002 | g0275 | EAS | KHV | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02055 | hp1 | a0001 | c0001 | t0133 | g0005 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02055 | hp2 | a0001 | c0001 | t0058 | g0177 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02071 | hp1 | a0001 | c0001 | t0076 | g0379 | EAS | KHV | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02071 | hp2 | a0001 | c0001 | t0077 | g0169 | EAS | KHV | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02074 | hp1 | a0001 | c0002 | t0126 | g0183 | EAS | KHV | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02074 | hp2 | a0001 | c0001 | t0019 | g0209 | EAS | KHV | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02129 | hp1 | a0001 | c0001 | t0003 | g0130 | EAS | KHV | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02129 | hp2 | a0001 | c0001 | t0046 | g0224 | EAS | KHV | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02135 | hp1 | a0001 | c0001 | t0001 | g0330 | EAS | KHV | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02135 | hp2 | a0001 | c0001 | t0129 | g0184 | EAS | KHV | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02145 | hp1 | a0001 | c0001 | t0049 | g0019 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02145 | hp2 | a0001 | c0001 | t0167 | g0254 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02148 | hp1 | a0001 | c0001 | t0172 | g0081 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02148 | hp2 | a0001 | c0001 | t0021 | g0294 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02155 | hp1 | a0001 | c0001 | t0004 | g0256 | EAS | CDX | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02155 | hp2 | a0001 | c0001 | t0137 | g0180 | EAS | CDX | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02165 | hp1 | a0001 | c0001 | t0001 | g0282 | EAS | CDX | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02165 | hp2 | a0001 | c0001 | t0071 | g0174 | EAS | CDX | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02257 | hp1 | a0001 | c0001 | t0005 | g0193 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02257 | hp2 | a0001 | c0001 | t0099 | g0037 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02258 | hp1 | a0001 | c0001 | t0014 | g0013 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02258 | hp2 | a0001 | c0001 | t0038 | g0011 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02273 | hp1 | a0001 | c0001 | t0174 | g0078 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02273 | hp2 | a0001 | c0001 | t0173 | g0329 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02280 | hp1 | a0001 | c0001 | t0016 | g0128 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02280 | hp2 | a0001 | c0001 | t0093 | g0286 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02300 | hp1 | a0001 | c0001 | t0001 | g0293 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02300 | hp2 | a0001 | c0001 | t0007 | g0240 | AMR | PEL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02451 | hp1 | a0001 | c0001 | t0001 | g0115 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02451 | hp2 | a0001 | c0001 | t0078 | g0089 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02572 | hp1 | a0001 | c0001 | t0183 | g0028 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02572 | hp2 | a0001 | c0001 | t0008 | g0100 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02602 | hp1 | a0001 | c0001 | t0060 | g0027 | SAS | PJL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02602 | hp2 | a0001 | c0001 | t0006 | g0043 | SAS | PJL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02622 | hp1 | a0001 | c0001 | t0063 | g0104 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02622 | hp2 | a0001 | c0001 | t0142 | g0010 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02630 | hp1 | a0001 | c0001 | t0020 | g0075 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02630 | hp2 | a0001 | c0001 | t0094 | g0288 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02647 | hp1 | a0001 | c0001 | t0021 | g0285 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02647 | hp2 | a0001 | c0001 | t0024 | g0376 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02698 | hp1 | a0001 | c0001 | t0001 | g0356 | SAS | PJL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02698 | hp2 | a0001 | c0001 | t0081 | g0025 | SAS | PJL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02717 | hp1 | a0001 | c0001 | t0053 | g0023 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02717 | hp2 | a0001 | c0001 | t0195 | g0113 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02723 | hp1 | a0001 | c0001 | t0001 | g0340 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02723 | hp2 | a0001 | c0001 | t0029 | g0031 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02735 | hp1 | a0001 | c0001 | t0009 | g0291 | SAS | PJL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02735 | hp2 | a0001 | c0001 | t0025 | g0026 | SAS | PJL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02809 | hp1 | a0001 | c0001 | t0113 | g0063 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02809 | hp2 | a0001 | c0001 | t0023 | g0029 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02818 | hp1 | a0001 | c0001 | t0158 | g0090 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02818 | hp2 | a0001 | c0001 | t0050 | g0262 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02886 | hp1 | a0001 | c0001 | t0001 | g0276 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02886 | hp2 | a0001 | c0001 | t0059 | g0272 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02895 | hp1 | a0001 | c0001 | t0101 | g0008 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02895 | hp2 | a0001 | c0001 | t0147 | g0271 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02896 | hp1 | a0001 | c0001 | t0079 | g0374 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02896 | hp2 | a0001 | c0001 | t0196 | g0114 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02922 | hp1 | a0001 | c0001 | t0012 | g0105 | AFR | ESN | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02922 | hp2 | a0001 | c0001 | t0168 | g0064 | AFR | ESN | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02965 | hp1 | a0001 | c0001 | t0042 | g0217 | AFR | ESN | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02965 | hp2 | a0001 | c0001 | t0043 | g0277 | AFR | ESN | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02970 | hp1 | a0001 | c0001 | t0042 | g0243 | AFR | ESN | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02970 | hp2 | a0001 | c0001 | t0008 | g0101 | AFR | ESN | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03041 | hp1 | a0001 | c0001 | t0023 | g0263 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03041 | hp2 | a0001 | c0001 | t0054 | g0021 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03098 | hp1 | a0001 | c0001 | t0009 | g0279 | AFR | MSL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03098 | hp2 | a0001 | c0001 | t0160 | g0109 | AFR | MSL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03130 | hp1 | a0001 | c0001 | t0023 | g0030 | AFR | ESN | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03130 | hp2 | a0001 | c0001 | t0020 | g0074 | AFR | ESN | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03139 | hp1 | a0001 | c0001 | t0096 | g0386 | AFR | ESN | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03139 | hp2 | a0001 | c0001 | t0040 | g0065 | AFR | ESN | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03195 | hp1 | a0001 | c0001 | t0008 | g0098 | AFR | ESN | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03195 | hp2 | a0001 | c0001 | t0030 | g0274 | AFR | ESN | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03225 | hp1 | a0001 | c0001 | t0095 | g0091 | AFR | MSL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03225 | hp2 | a0001 | c0001 | t0047 | g0242 | AFR | MSL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03239 | hp1 | a0001 | c0001 | t0102 | g0041 | SAS | PJL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03239 | hp2 | a0001 | c0001 | t0029 | g0032 | SAS | PJL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03453 | hp1 | a0001 | c0001 | t0008 | g0103 | AFR | MSL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03453 | hp2 | a0001 | c0001 | t0024 | g0375 | AFR | MSL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03486 | hp1 | a0001 | c0001 | t0008 | g0102 | AFR | MSL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03486 | hp2 | a0001 | c0001 | t0145 | g0266 | AFR | MSL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03490 | hp1 | a0001 | c0001 | t0004 | g0170 | SAS | PJL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03490 | hp2 | a0001 | c0001 | t0025 | g0384 | SAS | PJL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03492 | hp1 | a0001 | c0001 | t0025 | g0385 | SAS | PJL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03492 | hp2 | a0001 | c0001 | t0152 | g0292 | SAS | PJL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03516 | hp1 | a0001 | c0001 | t0033 | g0034 | AFR | ESN | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03516 | hp2 | a0001 | c0001 | t0198 | g0383 | AFR | ESN | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03540 | hp1 | a0001 | c0001 | t0061 | g0022 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03540 | hp2 | a0001 | c0001 | t0075 | g0012 | AFR | GWD | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03579 | hp1 | a0001 | c0001 | t0062 | g0024 | AFR | MSL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03579 | hp2 | a0001 | c0001 | t0028 | g0176 | AFR | MSL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03669 | hp1 | a0001 | c0001 | t0128 | g0200 | SAS | PJL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03669 | hp2 | a0001 | c0001 | t0104 | g0112 | SAS | PJL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03688 | hp1 | a0001 | c0001 | t0021 | g0290 | SAS | STU | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03688 | hp2 | a0001 | c0001 | t0026 | g0017 | SAS | STU | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03710 | hp1 | a0001 | c0001 | t0006 | g0039 | SAS | PJL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03710 | hp2 | a0001 | c0001 | t0012 | g0095 | SAS | PJL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03831 | hp1 | a0001 | c0001 | t0002 | g0221 | SAS | BEB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03831 | hp2 | a0001 | c0001 | t0153 | g0351 | SAS | BEB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03834 | hp1 | a0001 | c0001 | t0161 | g0323 | SAS | BEB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03834 | hp2 | a0001 | c0001 | t0114 | g0016 | SAS | BEB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03927 | hp1 | a0001 | c0001 | t0001 | g0365 | SAS | BEB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03927 | hp2 | a0001 | c0001 | t0165 | g0158 | SAS | BEB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG04115 | hp1 | a0001 | c0003 | t0019 | g0210 | SAS | STU | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG04115 | hp2 | a0001 | c0001 | t0092 | g0320 | SAS | STU | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG04199 | hp1 | a0001 | c0001 | t0068 | g0003 | SAS | STU | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG04199 | hp2 | a0001 | c0001 | t0001 | g0194 | SAS | STU | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG04204 | hp1 | a0001 | c0001 | t0130 | g0195 | SAS | STU | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG04204 | hp2 | a0001 | c0001 | t0026 | g0015 | SAS | STU | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG04228 | hp1 | a0001 | c0001 | t0135 | g0257 | SAS | STU | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG04228 | hp2 | a0001 | c0001 | t0001 | g0319 | SAS | STU | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18522 | hp1 | a0001 | c0001 | t0020 | g0076 | AFR | YRI | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18522 | hp2 | a0001 | c0001 | t0197 | g0116 | AFR | YRI | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18612 | hp1 | a0001 | c0001 | t0014 | g0062 | EAS | CHB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18612 | hp2 | a0001 | c0005 | t0139 | g0225 | EAS | CHB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18747 | hp1 | a0001 | c0001 | t0019 | g0226 | EAS | CHB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18747 | hp2 | a0001 | c0001 | t0003 | g0178 | EAS | CHB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18939 | hp1 | a0001 | c0001 | t0001 | g0362 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18939 | hp2 | a0001 | c0001 | t0003 | g0140 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18941 | hp1 | a0001 | c0001 | t0001 | g0359 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18941 | hp2 | a0001 | c0001 | t0005 | g0190 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18942 | hp1 | a0001 | c0001 | t0002 | g0227 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18942 | hp2 | a0001 | c0001 | t0003 | g0148 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18943 | hp1 | a0001 | c0001 | t0003 | g0147 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18943 | hp2 | a0001 | c0001 | t0026 | g0061 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18944 | hp1 | a0001 | c0001 | t0110 | g0070 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18944 | hp2 | a0001 | c0001 | t0032 | g0173 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18945 | hp1 | a0001 | c0001 | t0011 | g0310 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18945 | hp2 | a0001 | c0002 | t0127 | g0182 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18946 | hp1 | a0001 | c0001 | t0001 | g0300 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18946 | hp2 | a0001 | c0001 | t0124 | g0197 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18949 | hp1 | a0001 | c0001 | t0013 | g0054 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18949 | hp2 | a0001 | c0001 | t0002 | g0259 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18951 | hp1 | a0001 | c0001 | t0117 | g0057 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18951 | hp2 | a0002 | c0004 | t0125 | g0229 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18952 | hp1 | a0001 | c0001 | t0011 | g0303 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18952 | hp2 | a0001 | c0001 | t0005 | g0189 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18953 | hp1 | a0001 | c0001 | t0009 | g0350 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18953 | hp2 | a0001 | c0001 | t0136 | g0261 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18954 | hp1 | a0001 | c0001 | t0116 | g0048 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18954 | hp2 | a0001 | c0001 | t0001 | g0304 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18956 | hp1 | a0001 | c0001 | t0034 | g0139 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18956 | hp2 | a0001 | c0001 | t0186 | g0328 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18957 | hp1 | a0001 | c0001 | t0106 | g0215 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18957 | hp2 | a0001 | c0001 | t0115 | g0052 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18959 | hp1 | a0001 | c0001 | t0107 | g0233 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18959 | hp2 | a0001 | c0001 | t0011 | g0305 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18960 | hp1 | a0001 | c0001 | t0013 | g0053 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18960 | hp2 | a0001 | c0001 | t0083 | g0122 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18961 | hp1 | a0001 | c0001 | t0005 | g0264 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18961 | hp2 | a0001 | c0001 | t0011 | g0280 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18962 | hp1 | a0001 | c0001 | t0086 | g0131 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18962 | hp2 | a0001 | c0001 | t0090 | g0281 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18964 | hp1 | a0001 | c0001 | t0073 | g0172 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18964 | hp2 | a0001 | c0001 | t0111 | g0087 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18966 | hp1 | a0001 | c0001 | t0048 | g0006 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18966 | hp2 | a0001 | c0001 | t0005 | g0191 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18967 | hp1 | a0001 | c0001 | t0166 | g0068 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18967 | hp2 | a0001 | c0001 | t0010 | g0146 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18969 | hp1 | a0001 | c0001 | t0148 | g0344 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18969 | hp2 | a0001 | c0001 | t0041 | g0188 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18970 | hp1 | a0001 | c0001 | t0003 | g0152 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18970 | hp2 | a0001 | c0001 | t0140 | g0246 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18972 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18972 | hp2 | a0001 | c0001 | t0178 | g0208 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18973 | hp1 | a0001 | c0001 | t0084 | g0132 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18973 | hp2 | a0001 | c0001 | t0181 | g0220 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18977 | hp1 | a0001 | c0001 | t0179 | g0205 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18977 | hp2 | a0001 | c0001 | t0013 | g0073 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18978 | hp1 | a0001 | c0001 | t0141 | g0069 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18978 | hp2 | a0001 | c0001 | t0039 | g0249 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18980 | hp1 | a0001 | c0001 | t0027 | g0207 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18980 | hp2 | a0001 | c0001 | t0001 | g0358 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18982 | hp1 | a0001 | c0001 | t0080 | g0047 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18982 | hp2 | a0001 | c0001 | t0032 | g0171 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18985 | hp1 | a0001 | c0001 | t0180 | g0311 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18985 | hp2 | a0001 | c0001 | t0182 | g0219 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18986 | hp1 | a0001 | c0001 | t0169 | g0056 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18986 | hp2 | a0001 | c0001 | t0131 | g0192 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18987 | hp1 | a0001 | c0001 | t0085 | g0151 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18987 | hp2 | a0001 | c0001 | t0150 | g0360 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18988 | hp1 | a0001 | c0001 | t0177 | g0198 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18988 | hp2 | a0001 | c0001 | t0119 | g0071 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18992 | hp1 | a0001 | c0001 | t0017 | g0378 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18992 | hp2 | a0001 | c0001 | t0057 | g0159 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18994 | hp1 | a0001 | c0001 | t0002 | g0247 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18994 | hp2 | a0001 | c0001 | t0144 | g0143 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18999 | hp1 | a0001 | c0001 | t0003 | g0270 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18999 | hp2 | a0001 | c0001 | t0015 | g0046 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19000 | hp1 | a0001 | c0002 | t0108 | g0179 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19000 | hp2 | a0001 | c0001 | t0074 | g0382 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19002 | hp1 | a0001 | c0001 | t0004 | g0163 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19002 | hp2 | a0001 | c0001 | t0002 | g0218 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19005 | hp1 | a0001 | c0001 | t0154 | g0363 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19005 | hp2 | a0001 | c0001 | t0002 | g0251 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19006 | hp1 | a0001 | c0001 | t0039 | g0260 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19006 | hp2 | a0001 | c0001 | t0015 | g0072 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19007 | hp1 | a0001 | c0001 | t0003 | g0002 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19007 | hp2 | a0001 | c0001 | t0098 | g0255 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19009 | hp1 | a0001 | c0001 | t0002 | g0250 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19009 | hp2 | a0001 | c0001 | t0001 | g0309 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19010 | hp1 | a0001 | c0001 | t0001 | g0295 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19010 | hp2 | a0001 | c0001 | t0034 | g0144 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19011 | hp1 | a0001 | c0001 | t0001 | g0301 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19011 | hp2 | a0001 | c0001 | t0002 | g0244 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19030 | hp1 | a0001 | c0001 | t0064 | g0127 | AFR | LWK | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19030 | hp2 | a0001 | c0001 | t0001 | g0284 | AFR | LWK | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19043 | hp1 | a0001 | c0001 | t0001 | g0289 | AFR | LWK | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19043 | hp2 | a0001 | c0001 | t0020 | g0077 | AFR | LWK | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19056 | hp1 | a0001 | c0001 | t0013 | g0060 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19056 | hp2 | a0001 | c0001 | t0004 | g0164 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19057 | hp1 | a0001 | c0001 | t0004 | g0165 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19057 | hp2 | a0001 | c0001 | t0191 | g0299 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19058 | hp1 | a0001 | c0001 | t0002 | g0213 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19058 | hp2 | a0001 | c0001 | t0087 | g0138 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19060 | hp1 | a0001 | c0001 | t0003 | g0149 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19060 | hp2 | a0001 | c0001 | t0002 | g0258 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19064 | hp1 | a0001 | c0001 | t0041 | g0214 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19064 | hp2 | a0001 | c0001 | t0001 | g0347 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19065 | hp1 | a0001 | c0001 | t0003 | g0142 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19065 | hp2 | a0001 | c0002 | t0120 | g0181 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19066 | hp1 | a0001 | c0001 | t0017 | g0381 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19066 | hp2 | a0001 | c0001 | t0091 | g0302 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19067 | hp1 | a0001 | c0001 | t0184 | g0361 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19067 | hp2 | a0001 | c0001 | t0176 | g0232 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19068 | hp1 | a0001 | c0001 | t0121 | g0253 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19068 | hp2 | a0001 | c0001 | t0014 | g0088 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19074 | hp1 | a0001 | c0001 | t0002 | g0298 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19074 | hp2 | a0001 | c0001 | t0118 | g0055 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19075 | hp1 | a0001 | c0001 | t0002 | g0230 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19075 | hp2 | a0001 | c0001 | t0066 | g0167 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19077 | hp1 | a0001 | c0001 | t0112 | g0051 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19077 | hp2 | a0001 | c0001 | t0072 | g0161 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19079 | hp1 | a0001 | c0001 | t0070 | g0168 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19079 | hp2 | a0001 | c0001 | t0002 | g0228 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19080 | hp1 | a0001 | c0001 | t0005 | g0196 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19080 | hp2 | a0001 | c0001 | t0004 | g0162 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19081 | hp1 | a0001 | c0001 | t0002 | g0231 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19081 | hp2 | a0001 | c0001 | t0044 | g0346 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19083 | hp1 | a0001 | c0001 | t0005 | g0211 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19083 | hp2 | a0001 | c0001 | t0056 | g0157 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19084 | hp1 | a0001 | c0001 | t0010 | g0134 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19084 | hp2 | a0001 | c0001 | t0088 | g0129 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19086 | hp1 | a0001 | c0001 | t0011 | g0297 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19086 | hp2 | a0001 | c0001 | t0003 | g0133 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19088 | hp1 | a0001 | c0001 | t0002 | g0306 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19088 | hp2 | a0001 | c0001 | t0005 | g0201 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19089 | hp1 | a0001 | c0001 | t0067 | g0050 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19089 | hp2 | a0001 | c0001 | t0149 | g0337 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19090 | hp1 | a0001 | c0001 | t0004 | g0160 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19090 | hp2 | a0001 | c0001 | t0003 | g0145 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19091 | hp1 | a0001 | c0001 | t0055 | g0156 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19091 | hp2 | a0001 | c0001 | t0013 | g0059 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19240 | hp1 | a0001 | c0001 | t0016 | g0124 | AFR | YRI | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA19240 | hp2 | a0001 | c0001 | t0037 | g0009 | AFR | YRI | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA20129 | hp1 | a0001 | c0001 | t0038 | g0007 | AFR | ASW | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA20129 | hp2 | a0001 | c0001 | t0146 | g0287 | AFR | ASW | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA20752 | hp1 | a0001 | c0001 | t0175 | g0371 | EUR | TSI | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA20752 | hp2 | a0001 | c0001 | t0005 | g0269 | EUR | TSI | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA20805 | hp1 | a0001 | c0001 | t0069 | g0366 | EUR | TSI | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA20805 | hp2 | a0001 | c0001 | t0012 | g0093 | EUR | TSI | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA20905 | hp1 | a0001 | c0001 | t0001 | g0296 | SAS | GIH | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA20905 | hp2 | a0001 | c0001 | t0004 | g0004 | SAS | GIH | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01123 | hp1 | a0001 | c0001 | t0004 | g0155 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG01123 | hp2 | a0001 | c0001 | t0007 | g0252 | AMR | CLM | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02109 | hp1 | a0001 | c0001 | t0028 | g0175 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02109 | hp2 | a0001 | c0001 | t0030 | g0273 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02486 | hp1 | a0001 | c0001 | t0014 | g0014 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02486 | hp2 | a0001 | c0001 | t0036 | g0108 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02559 | hp1 | a0001 | c0001 | t0006 | g0001 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG02559 | hp2 | a0001 | c0001 | t0052 | g0067 | AFR | ACB | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03471 | hp1 | a0001 | c0001 | t0089 | g0106 | AFR | MSL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG03471 | hp2 | a0001 | c0001 | t0040 | g0066 | AFR | MSL | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG06807 | hp1 | a0001 | c0001 | t0005 | g0268 | AFR | USA | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
HG06807 | hp2 | a0001 | c0001 | t0036 | g0107 | AFR | USA | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18955 | hp1 | a0001 | c0001 | t0122 | g0206 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA18955 | hp2 | a0001 | c0001 | t0001 | g0357 | EAS | JPT | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA20300 | hp1 | a0001 | c0001 | t0033 | g0040 | AFR | USA | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA20300 | hp2 | a0001 | c0001 | t0045 | g0326 | AFR | USA | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA21309 | hp1 | a0001 | c0001 | t0001 | g0334 | AFR | LWK | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
NA21309 | hp2 | a0001 | c0001 | t0016 | g0267 | AFR | LWK | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
homoSapiens_chm13v2 | hp1 | a0001 | c0001 | t0045 | g0331 | REF | REF | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
homoSapiens_grch38 | hp1 | a0001 | c0001 | t0031 | g0125 | REF | REF | ALG14_chr1_94969405_95077951 | ALG14 | chr1 | 94969405 | 95077951 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:95027238
|
C | T | 1 | a0002 | 1 | NA18951.hp2 | missense_variant | MODERATE | c.311G>A | p.Arg104Gln | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/4 | 364/9375 | 311/651 | 104/216 | chr1 | 95027238 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:94983118
|
T | C | 1 | a0001c0005 | 1 | NA18612.hp2 | synonymous_variant | LOW | c.609A>G | p.Lys203Lys | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 662/9375 | 609/651 | 203/216 | chr1 | 94983118 | ||
chr1:95027258
|
A | G | 1 | a0001c0003 | 1 | HG04115.hp1 | splice_region_variant&synonymous_variant | LOW | c.291T>C | p.Tyr97Tyr | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/4 | 344/9375 | 291/651 | 97/216 | chr1 | 95027258 | ||
chr1:95064983
|
C | T | 1 | a0001c0002 | 4 | HG02074.hp1 NA18945.hp2 NA19000.hp1 others(1): Show |
synonymous_variant | LOW | c.171G>A | p.Gly57Gly | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/4 | 224/9375 | 171/651 | 57/216 | chr1 | 95064983 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:94974684
|
A | G | 4 | a0001c0001t0037a0001c0001t0038a0001c0001t0101others(1): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*8392T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 8392 | chr1 | 94974684 | |||||
chr1:94974747
|
A | T | 1 | a0001c0001t0103 | 1 | HG00639.hp1 | 3_prime_UTR_variant | MODIFIER | c.*8329T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 8329 | chr1 | 94974747 | |||||
chr1:94974890
|
C | G | 1 | a0001c0001t0145 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8186G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 8186 | chr1 | 94974890 | |||||
chr1:94975039
|
C | A | 1 | a0001c0001t0195 | 1 | HG02717.hp2 | 3_prime_UTR_variant | MODIFIER | c.*8037G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 8037 | chr1 | 94975039 | |||||
chr1:94975220
|
G | C | 2 | a0001c0001t0016a0001c0001t0100 | 5 | HG00735.hp2 HG01081.hp1 HG02280.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*7856C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7856 | chr1 | 94975220 | |||||
chr1:94975315
|
A | G | 43 | a0001c0001t0002a0001c0001t0005a0001c0001t0019others(40): Show | 79 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(76): Show |
3_prime_UTR_variant | MODIFIER | c.*7761T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7761 | chr1 | 94975315 | |||||
chr1:94975442
|
G | A | 2 | a0001c0001t0145a0001c0001t0154 | 2 | HG03486.hp2 NA19005.hp1 |
3_prime_UTR_variant | MODIFIER | c.*7634C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7634 | chr1 | 94975442 | |||||
chr1:94975555
|
A | G | 7 | a0001c0001t0037a0001c0001t0038a0001c0001t0082others(4): Show | 9 | HG01109.hp2 HG01891.hp2 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7521T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7521 | chr1 | 94975555 | |||||
chr1:94975723
|
G | A | 1 | a0001c0001t0092 | 1 | HG04115.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7353C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7353 | chr1 | 94975723 | |||||
chr1:94975736
|
C | T | 114 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(111): Show | 215 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(212): Show |
3_prime_UTR_variant | MODIFIER | c.*7340G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7340 | chr1 | 94975736 | |||||
chr1:94975772
|
G | A | 7 | a0001c0001t0037a0001c0001t0038a0001c0001t0082others(4): Show | 9 | HG01109.hp2 HG01891.hp2 HG02258.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*7304C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7304 | chr1 | 94975772 | |||||
chr1:94975849
|
A | C | 24 | a0001c0001t0004a0001c0001t0037a0001c0001t0038others(21): Show | 38 | HG00597.hp2 HG00673.hp1 HG01109.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*7227T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7227 | chr1 | 94975849 | |||||
chr1:94975853
|
C | A | 19 | a0001c0001t0017a0001c0001t0024a0001c0001t0028others(16): Show | 25 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(22): Show |
3_prime_UTR_variant | MODIFIER | c.*7223G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7223 | chr1 | 94975853 | |||||
chr1:94975861
|
A | C | 19 | a0001c0001t0004a0001c0001t0013a0001c0001t0018others(16): Show | 38 | HG00597.hp2 HG00673.hp1 HG01074.hp1 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*7215T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7215 | chr1 | 94975861 | |||||
chr1:94975873
|
C | T | 4 | a0001c0001t0006a0001c0001t0099a0001c0001t0103others(1): Show | 11 | HG00639.hp1 HG01243.hp2 HG01358.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*7203G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7203 | chr1 | 94975873 | |||||
chr1:94975939
|
C | A | 1 | a0001c0001t0096 | 1 | HG03139.hp1 | 3_prime_UTR_variant | MODIFIER | c.*7137G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7137 | chr1 | 94975939 | |||||
chr1:94975996
|
A | G | 4 | a0001c0001t0037a0001c0001t0038a0001c0001t0101others(1): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7080T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7080 | chr1 | 94975996 | |||||
chr1:94976016
|
C | CA | 58 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(55): Show | 118 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
3_prime_UTR_variant | MODIFIER | c.*7059dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7059 | chr1 | 94976016 | |||||
chr1:94976016
|
C | CAA | 23 | a0001c0001t0019a0001c0001t0030a0001c0001t0034others(20): Show | 27 | HG00597.hp1 HG01175.hp2 HG01258.hp2 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*7058_*7059dupTT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7059 | chr1 | 94976016 | |||||
chr1:94976016
|
C | CAAAA | 4 | a0001c0001t0037a0001c0001t0038a0001c0001t0101others(1): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*7056_*7059dupTTTT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7059 | chr1 | 94976016 | |||||
chr1:94976016
|
CA | C | 15 | a0001c0001t0008a0001c0001t0016a0001c0001t0018others(12): Show | 27 | HG00735.hp2 HG01074.hp1 HG01081.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*7059delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7059 | chr1 | 94976016 | |||||
chr1:94976016
|
CAA | C | 9 | a0001c0001t0004a0001c0001t0055a0001c0001t0056others(6): Show | 21 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*7058_*7059delTT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7058 | chr1 | 94976016 | |||||
chr1:94976037
|
A | G | 1 | a0001c0001t0152 | 1 | HG03492.hp2 | 3_prime_UTR_variant | MODIFIER | c.*7039T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 7039 | chr1 | 94976037 | |||||
chr1:94976364
|
A | C | 1 | a0001c0001t0068 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6712T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 6712 | chr1 | 94976364 | |||||
chr1:94976379
|
T | C | 3 | a0001c0001t0024a0001c0001t0075a0001c0001t0079 | 5 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6697A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 6697 | chr1 | 94976379 | |||||
chr1:94976504
|
C | T | 1 | a0001c0001t0166 | 1 | NA18967.hp1 | 3_prime_UTR_variant | MODIFIER | c.*6572G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 6572 | chr1 | 94976504 | |||||
chr1:94976653
|
C | T | 13 | a0001c0001t0003a0001c0001t0010a0001c0001t0032others(10): Show | 33 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*6423G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 6423 | chr1 | 94976653 | |||||
chr1:94976694
|
A | AG | 13 | a0001c0001t0003a0001c0001t0010a0001c0001t0032others(10): Show | 33 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(30): Show |
3_prime_UTR_variant | MODIFIER | c.*6381dupC | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 6381 | chr1 | 94976694 | |||||
chr1:94976730
|
C | G | 11 | a0001c0001t0004a0001c0001t0055a0001c0001t0056others(8): Show | 23 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*6346G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 6346 | chr1 | 94976730 | |||||
chr1:94976814
|
T | C | 3 | a0001c0001t0027a0001c0001t0122a0001c0001t0179 | 5 | HG00544.hp1 HG02015.hp2 NA18955.hp1 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*6262A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 6262 | chr1 | 94976814 | |||||
chr1:94976840
|
G | A | 18 | a0001c0001t0017a0001c0001t0024a0001c0001t0028others(15): Show | 24 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(21): Show |
3_prime_UTR_variant | MODIFIER | c.*6236C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 6236 | chr1 | 94976840 | |||||
chr1:94976986
|
G | T | 161 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(158): Show | 297 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(294): Show |
3_prime_UTR_variant | MODIFIER | c.*6090C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 6090 | chr1 | 94976986 | |||||
chr1:94977077
|
T | C | 3 | a0001c0001t0082a0001c0001t0196a0001c0001t0197 | 3 | HG01891.hp2 HG02896.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5999A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 5999 | chr1 | 94977077 | |||||
chr1:94977202
|
G | A | 3 | a0001c0001t0041a0001c0001t0181a0001c0001t0182 | 4 | NA18969.hp2 NA18973.hp2 NA18985.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5874C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 5874 | chr1 | 94977202 | |||||
chr1:94977205
|
C | A | 1 | a0001c0001t0071 | 1 | HG02165.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5871G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 5871 | chr1 | 94977205 | |||||
chr1:94977341
|
C | T | 1 | a0001c0001t0095 | 1 | HG03225.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5735G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 5735 | chr1 | 94977341 | |||||
chr1:94977356
|
A | G | 2 | a0001c0001t0128a0001c0001t0130 | 2 | HG03669.hp1 HG04204.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5720T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 5720 | chr1 | 94977356 | |||||
chr1:94977365
|
A | G | 1 | a0001c0001t0198 | 1 | HG03516.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5711T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 5711 | chr1 | 94977365 | |||||
chr1:94977394
|
T | C | 1 | a0001c0001t0174 | 1 | HG02273.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5682A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 5682 | chr1 | 94977394 | |||||
chr1:94977526
|
T | A | 2 | a0001c0001t0136a0001c0001t0137 | 2 | HG02155.hp2 NA18953.hp2 |
3_prime_UTR_variant | MODIFIER | c.*5550A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 5550 | chr1 | 94977526 | |||||
chr1:94977556
|
T | A | 3 | a0001c0001t0155a0001c0001t0156a0001c0001t0188 | 3 | HG01069.hp1 HG01192.hp1 HG01346.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5520A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 5520 | chr1 | 94977556 | |||||
chr1:94977573
|
G | A | 20 | a0001c0001t0002a0001c0001t0007a0001c0001t0039others(17): Show | 46 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(43): Show |
3_prime_UTR_variant | MODIFIER | c.*5503C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 5503 | chr1 | 94977573 | |||||
chr1:94977652
|
A | AT | 147 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(144): Show | 270 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(267): Show |
3_prime_UTR_variant | MODIFIER | c.*5423dupA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 5423 | chr1 | 94977652 | |||||
chr1:94977652
|
A | T | 1 | a0001c0001t0142 | 1 | HG02622.hp2 | 3_prime_UTR_variant | MODIFIER | c.*5424T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 5424 | chr1 | 94977652 | |||||
chr1:94977653
|
T | TA | 3 | a0001c0001t0047a0001c0001t0068a0001c0001t0138 | 4 | HG00438.hp1 HG00741.hp2 HG03225.hp2 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*5422_*5423insT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 5422 | chr1 | 94977653 | |||||
chr1:94977717
|
C | T | 1 | a0001c0001t0068 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*5359G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 5359 | chr1 | 94977717 | |||||
chr1:94977895
|
T | C | 15 | a0001c0001t0023a0001c0001t0025a0001c0001t0029others(12): Show | 21 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*5181A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 5181 | chr1 | 94977895 | |||||
chr1:94978070
|
T | C | 2 | a0001c0001t0054a0001c0001t0062 | 2 | HG03041.hp2 HG03579.hp1 |
3_prime_UTR_variant | MODIFIER | c.*5006A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 5006 | chr1 | 94978070 | |||||
chr1:94978237
|
A | AT | 13 | a0001c0001t0023a0001c0001t0029a0001c0001t0030others(10): Show | 17 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(14): Show |
3_prime_UTR_variant | MODIFIER | c.*4838dupA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 4838 | chr1 | 94978237 | |||||
chr1:94978297
|
G | A | 14 | a0001c0001t0004a0001c0001t0032a0001c0001t0055others(11): Show | 27 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*4779C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 4779 | chr1 | 94978297 | |||||
chr1:94978322
|
A | G | 14 | a0001c0001t0004a0001c0001t0032a0001c0001t0055others(11): Show | 27 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*4754T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 4754 | chr1 | 94978322 | |||||
chr1:94978341
|
G | A | 6 | a0001c0001t0016a0001c0001t0037a0001c0001t0038others(3): Show | 11 | HG00735.hp2 HG01081.hp1 HG01109.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4735C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 4735 | chr1 | 94978341 | |||||
chr1:94978351
|
A | G | 3 | a0001c0001t0117a0001c0001t0170a0001c0001t0192 | 3 | HG00140.hp1 HG01433.hp1 NA18951.hp1 |
3_prime_UTR_variant | MODIFIER | c.*4725T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 4725 | chr1 | 94978351 | |||||
chr1:94978352
|
T | C | 1 | a0001c0001t0117 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4724A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 4724 | chr1 | 94978352 | |||||
chr1:94978356
|
T | C | 1 | a0001c0001t0117 | 1 | NA18951.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4720A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 4720 | chr1 | 94978356 | |||||
chr1:94978646
|
G | A | 161 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(158): Show | 297 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(294): Show |
3_prime_UTR_variant | MODIFIER | c.*4430C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 4430 | chr1 | 94978646 | |||||
chr1:94978844
|
T | A | 1 | a0001c0001t0068 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4232A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 4232 | chr1 | 94978844 | |||||
chr1:94978844
|
T | TA | 50 | a0001c0001t0006a0001c0001t0013a0001c0001t0014others(47): Show | 86 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(83): Show |
3_prime_UTR_variant | MODIFIER | c.*4231dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 4231 | chr1 | 94978844 | |||||
chr1:94978844
|
T | TAA | 76 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(73): Show | 151 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(148): Show |
3_prime_UTR_variant | MODIFIER | c.*4230_*4231dupTT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 4231 | chr1 | 94978844 | |||||
chr1:94978844
|
T | TAAA | 10 | a0001c0001t0038a0001c0001t0050a0001c0001t0082others(7): Show | 11 | HG01891.hp2 HG02258.hp2 HG02818.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*4229_*4231dupTTT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 4231 | chr1 | 94978844 | |||||
chr1:94978855
|
A | C | 2 | a0001c0001t0189a0001c0001t0190 | 2 | HG01978.hp1 HG01981.hp2 |
3_prime_UTR_variant | MODIFIER | c.*4221T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 4221 | chr1 | 94978855 | |||||
chr1:94978857
|
A | AAC | 14 | a0001c0001t0004a0001c0001t0032a0001c0001t0055others(11): Show | 27 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*4218_*4219insGT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 4218 | chr1 | 94978857 | |||||
chr1:94979007
|
G | A | 1 | a0001c0001t0121 | 1 | NA19068.hp1 | 3_prime_UTR_variant | MODIFIER | c.*4069C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 4069 | chr1 | 94979007 | |||||
chr1:94979007
|
G | C | 14 | a0001c0001t0004a0001c0001t0032a0001c0001t0055others(11): Show | 27 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*4069C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 4069 | chr1 | 94979007 | |||||
chr1:94979072
|
T | C | 4 | a0001c0001t0037a0001c0001t0038a0001c0001t0101others(1): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*4004A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 4004 | chr1 | 94979072 | |||||
chr1:94979176
|
C | T | 1 | a0001c0001t0128 | 1 | HG03669.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3900G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 3900 | chr1 | 94979176 | |||||
chr1:94979223
|
A | G | 160 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(157): Show | 296 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(293): Show |
3_prime_UTR_variant | MODIFIER | c.*3853T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 3853 | chr1 | 94979223 | |||||
chr1:94979233
|
A | G | 1 | a0001c0001t0066 | 1 | NA19075.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3843T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 3843 | chr1 | 94979233 | |||||
chr1:94979289
|
C | T | 17 | a0001c0001t0017a0001c0001t0024a0001c0001t0028others(14): Show | 23 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*3787G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 3787 | chr1 | 94979289 | |||||
chr1:94979310
|
A | AAAAAG | 14 | a0001c0001t0026a0001c0001t0051a0001c0001t0052others(11): Show | 16 | HG00735.hp1 HG01361.hp2 HG01891.hp2 others(13): Show |
3_prime_UTR_variant | MODIFIER | c.*3761_*3765dupCTTT others(1): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 3765 | chr1 | 94979310 | |||||
chr1:94979310
|
A | AAAAG | 112 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(109): Show | 220 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(217): Show |
3_prime_UTR_variant | MODIFIER | c.*3765_*3766insCTTT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 3765 | chr1 | 94979310 | |||||
chr1:94979310
|
A | AAAG | 8 | a0001c0001t0037a0001c0001t0038a0001c0001t0078others(5): Show | 10 | HG01109.hp2 HG02258.hp2 HG02451.hp2 others(7): Show |
3_prime_UTR_variant | MODIFIER | c.*3765_*3766insCTT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 3765 | chr1 | 94979310 | |||||
chr1:94979310
|
A | G | 15 | a0001c0001t0004a0001c0001t0032a0001c0001t0055others(12): Show | 28 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(25): Show |
3_prime_UTR_variant | MODIFIER | c.*3766T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 3766 | chr1 | 94979310 | |||||
chr1:94979346
|
T | C | 15 | a0001c0001t0023a0001c0001t0025a0001c0001t0029others(12): Show | 21 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*3730A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 3730 | chr1 | 94979346 | |||||
chr1:94979364
|
C | T | 1 | a0001c0001t0059 | 1 | HG02886.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3712G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 3712 | chr1 | 94979364 | |||||
chr1:94979494
|
T | A | 1 | a0001c0001t0157 | 1 | HG00140.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3582A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 3582 | chr1 | 94979494 | |||||
chr1:94979619
|
T | A | 14 | a0001c0001t0004a0001c0001t0032a0001c0001t0055others(11): Show | 27 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(24): Show |
3_prime_UTR_variant | MODIFIER | c.*3457A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 3457 | chr1 | 94979619 | |||||
chr1:94979899
|
C | T | 1 | a0001c0001t0068 | 1 | HG04199.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3177G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 3177 | chr1 | 94979899 | |||||
chr1:94979912
|
G | A | 146 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(143): Show | 269 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(266): Show |
3_prime_UTR_variant | MODIFIER | c.*3164C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 3164 | chr1 | 94979912 | |||||
chr1:94979950
|
T | A | 1 | a0001c0001t0072 | 1 | NA19077.hp2 | 3_prime_UTR_variant | MODIFIER | c.*3126A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 3126 | chr1 | 94979950 | |||||
chr1:94980047
|
T | C | 1 | a0001c0001t0073 | 1 | NA18964.hp1 | 3_prime_UTR_variant | MODIFIER | c.*3029A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 3029 | chr1 | 94980047 | |||||
chr1:94980059
|
GA | G | 159 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(156): Show | 295 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(292): Show |
3_prime_UTR_variant | MODIFIER | c.*3016delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 3016 | chr1 | 94980059 | |||||
chr1:94980283
|
C | T | 1 | a0001c0001t0151 | 1 | HG00408.hp1 | 3_prime_UTR_variant | MODIFIER | c.*2793G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 2793 | chr1 | 94980283 | |||||
chr1:94980332
|
T | TA | 19 | a0001c0001t0004a0001c0001t0016a0001c0001t0018others(16): Show | 38 | HG00597.hp2 HG00673.hp1 HG00735.hp2 others(35): Show |
3_prime_UTR_variant | MODIFIER | c.*2743dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 2743 | chr1 | 94980332 | |||||
chr1:94980954
|
GT | G | 160 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(157): Show | 296 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(293): Show |
3_prime_UTR_variant | MODIFIER | c.*2121delA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 2121 | chr1 | 94980954 | |||||
chr1:94980965
|
A | G | 5 | a0001c0002t0108a0001c0002t0120a0001c0002t0126others(2): Show | 5 | HG02074.hp1 NA18945.hp2 NA18951.hp2 others(2): Show |
3_prime_UTR_variant | MODIFIER | c.*2111T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 2111 | chr1 | 94980965 | |||||
chr1:94981206
|
G | A | 47 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(44): Show | 90 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(87): Show |
3_prime_UTR_variant | MODIFIER | c.*1870C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1870 | chr1 | 94981206 | |||||
chr1:94981224
|
C | T | 1 | a0001c0001t0124 | 1 | NA18946.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1852G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1852 | chr1 | 94981224 | |||||
chr1:94981255
|
C | A | 1 | a0001c0001t0149 | 1 | NA19089.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1821G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1821 | chr1 | 94981255 | |||||
chr1:94981447
|
G | GT | 7 | a0001c0001t0055a0001c0001t0150a0001c0001t0160others(4): Show | 7 | HG01175.hp1 HG01934.hp1 HG02148.hp1 others(4): Show |
3_prime_UTR_variant | MODIFIER | c.*1628dupA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1628 | chr1 | 94981447 | |||||
chr1:94981456
|
G | T | 12 | a0001c0001t0107a0001c0001t0123a0001c0001t0144others(9): Show | 12 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1620C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1620 | chr1 | 94981456 | |||||
chr1:94981457
|
C | G | 12 | a0001c0001t0107a0001c0001t0123a0001c0001t0144others(9): Show | 12 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1619G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1619 | chr1 | 94981457 | |||||
chr1:94981457
|
CT | C | 72 | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(69): Show | 165 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(162): Show |
3_prime_UTR_variant | MODIFIER | c.*1618delA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1618 | chr1 | 94981457 | |||||
chr1:94981458
|
T | C | 12 | a0001c0001t0107a0001c0001t0123a0001c0001t0144others(9): Show | 12 | HG00099.hp1 HG00140.hp1 HG00597.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1618A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1618 | chr1 | 94981458 | |||||
chr1:94981467
|
TTA | T | 12 | a0001c0001t0067a0001c0001t0083a0001c0001t0085others(9): Show | 12 | HG02809.hp1 HG02922.hp2 HG03239.hp1 others(9): Show |
3_prime_UTR_variant | MODIFIER | c.*1607_*1608delTA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1607 | chr1 | 94981467 | |||||
chr1:94981468
|
T | A | 12 | a0001c0001t0022a0001c0001t0040a0001c0001t0045others(9): Show | 18 | HG01261.hp2 HG01346.hp2 HG01928.hp1 others(15): Show |
3_prime_UTR_variant | MODIFIER | c.*1608A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1608 | chr1 | 94981468 | |||||
chr1:94981468
|
T | TA | 11 | a0001c0001t0008a0001c0001t0012a0001c0001t0036others(8): Show | 21 | HG01496.hp1 HG01884.hp2 HG01891.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1607dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1607 | chr1 | 94981468 | |||||
chr1:94981468
|
TA | T | 11 | a0001c0001t0066a0001c0001t0076a0001c0001t0081others(8): Show | 11 | HG00323.hp2 HG02071.hp1 HG02698.hp2 others(8): Show |
3_prime_UTR_variant | MODIFIER | c.*1607delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1607 | chr1 | 94981468 | |||||
chr1:94981469
|
A | T | 1 | a0001c0001t0161 | 1 | HG03834.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1607T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1607 | chr1 | 94981469 | |||||
chr1:94981527
|
G | A | 1 | a0001c0001t0175 | 1 | NA20752.hp1 | 3_prime_UTR_variant | MODIFIER | c.*1549C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1549 | chr1 | 94981527 | |||||
chr1:94981579
|
T | C | 3 | a0001c0001t0036a0001c0001t0089a0001c0001t0160 | 4 | HG02486.hp2 HG03098.hp2 HG03471.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1497A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1497 | chr1 | 94981579 | |||||
chr1:94981646
|
G | A | 15 | a0001c0001t0023a0001c0001t0025a0001c0001t0029others(12): Show | 21 | HG00735.hp1 HG02109.hp2 HG02145.hp1 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*1430C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1430 | chr1 | 94981646 | |||||
chr1:94981683
|
G | GT | 10 | a0001c0001t0006a0001c0001t0010a0001c0001t0033others(7): Show | 22 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(19): Show |
3_prime_UTR_variant | MODIFIER | c.*1392dupA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1392 | chr1 | 94981683 | |||||
chr1:94981683
|
G | T | 1 | a0001c0001t0018 | 4 | HG01074.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*1393C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1393 | chr1 | 94981683 | |||||
chr1:94981683
|
GT | G | 48 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(45): Show | 91 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(88): Show |
3_prime_UTR_variant | MODIFIER | c.*1392delA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1392 | chr1 | 94981683 | |||||
chr1:94981688
|
T | G | 6 | a0001c0001t0054a0001c0001t0061a0001c0001t0062others(3): Show | 6 | HG00741.hp1 HG01934.hp1 HG03041.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1388A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1388 | chr1 | 94981688 | |||||
chr1:94981697
|
T | TG | 3 | a0001c0001t0080a0001c0001t0110a0001c0001t0141 | 3 | NA18944.hp1 NA18978.hp1 NA18982.hp1 |
3_prime_UTR_variant | MODIFIER | c.*1378dupC | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1378 | chr1 | 94981697 | |||||
chr1:94981892
|
AT | A | 4 | a0001c0001t0037a0001c0001t0038a0001c0001t0101others(1): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
3_prime_UTR_variant | MODIFIER | c.*1183delA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1183 | chr1 | 94981892 | |||||
chr1:94981949
|
C | T | 1 | a0001c0001t0075 | 1 | HG03540.hp2 | 3_prime_UTR_variant | MODIFIER | c.*1127G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 1127 | chr1 | 94981949 | |||||
chr1:94982111
|
T | C | 1 | a0001c0001t0020 | 4 | HG02630.hp1 HG03130.hp2 NA18522.hp1 others(1): Show |
3_prime_UTR_variant | MODIFIER | c.*965A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 965 | chr1 | 94982111 | |||||
chr1:94982120
|
G | GT | 35 | a0001c0001t0004a0001c0001t0006a0001c0001t0018others(32): Show | 62 | HG00597.hp2 HG00639.hp1 HG01074.hp1 others(59): Show |
3_prime_UTR_variant | MODIFIER | c.*955dupA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 955 | chr1 | 94982120 | |||||
chr1:94982120
|
G | GTT | 8 | a0001c0001t0016a0001c0001t0037a0001c0001t0038others(5): Show | 13 | HG00673.hp1 HG00735.hp2 HG01081.hp1 others(10): Show |
3_prime_UTR_variant | MODIFIER | c.*954_*955dupAA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 955 | chr1 | 94982120 | |||||
chr1:94982120
|
G | T | 2 | a0001c0001t0097a0001c0001t0098 | 2 | HG00323.hp2 NA19007.hp2 |
3_prime_UTR_variant | MODIFIER | c.*956C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 956 | chr1 | 94982120 | |||||
chr1:94982120
|
GT | G | 15 | a0001c0001t0023a0001c0001t0025a0001c0001t0029others(12): Show | 21 | HG00558.hp2 HG00735.hp1 HG02109.hp2 others(18): Show |
3_prime_UTR_variant | MODIFIER | c.*955delA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 955 | chr1 | 94982120 | |||||
chr1:94982126
|
T | G | 3 | a0001c0001t0082a0001c0001t0196a0001c0001t0197 | 3 | HG01891.hp2 HG02896.hp2 NA18522.hp2 |
3_prime_UTR_variant | MODIFIER | c.*950A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 950 | chr1 | 94982126 | |||||
chr1:94982128
|
T | G | 10 | a0001c0001t0003a0001c0001t0010a0001c0001t0034others(7): Show | 29 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(26): Show |
3_prime_UTR_variant | MODIFIER | c.*948A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 948 | chr1 | 94982128 | |||||
chr1:94982143
|
C | T | 1 | a0001c0001t0164 | 1 | HG00099.hp1 | 3_prime_UTR_variant | MODIFIER | c.*933G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 933 | chr1 | 94982143 | |||||
chr1:94982167
|
G | A | 1 | a0001c0001t0145 | 1 | HG03486.hp2 | 3_prime_UTR_variant | MODIFIER | c.*909C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 909 | chr1 | 94982167 | |||||
chr1:94982377
|
T | C | 150 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(147): Show | 275 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(272): Show |
3_prime_UTR_variant | MODIFIER | c.*699A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 699 | chr1 | 94982377 | |||||
chr1:94982666
|
T | C | 2 | a0001c0001t0183a0001c0001t0198 | 2 | HG02572.hp1 HG03516.hp2 |
3_prime_UTR_variant | MODIFIER | c.*410A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 410 | chr1 | 94982666 | |||||
chr1:94982699
|
C | CA | 80 | a0001c0001t0002a0001c0001t0005a0001c0001t0006others(77): Show | 162 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(159): Show |
3_prime_UTR_variant | MODIFIER | c.*376dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 376 | chr1 | 94982699 | |||||
chr1:94982699
|
C | CAA | 47 | a0001c0001t0001a0001c0001t0015a0001c0001t0021others(44): Show | 99 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(96): Show |
3_prime_UTR_variant | MODIFIER | c.*375_*376dupTT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 376 | chr1 | 94982699 | |||||
chr1:94982699
|
C | CAAA | 17 | a0001c0001t0009a0001c0001t0048a0001c0001t0184others(14): Show | 23 | HG00438.hp2 HG00639.hp2 HG00642.hp1 others(20): Show |
3_prime_UTR_variant | MODIFIER | c.*374_*376dupTTT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 376 | chr1 | 94982699 | |||||
chr1:94982699
|
CA | C | 11 | a0001c0001t0028a0001c0001t0029a0001c0001t0030others(8): Show | 14 | HG02055.hp2 HG02109.hp1 HG02109.hp2 others(11): Show |
3_prime_UTR_variant | MODIFIER | c.*376delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 376 | chr1 | 94982699 | |||||
chr1:94982699
|
CAA | C | 7 | a0001c0001t0023a0001c0001t0049a0001c0001t0050others(4): Show | 9 | HG00735.hp1 HG02145.hp1 HG02559.hp2 others(6): Show |
3_prime_UTR_variant | MODIFIER | c.*375_*376delTT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 4/4 | 375 | chr1 | 94982699 |
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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
chr1:94983477
|
T | C | 203 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(200): Show | 205 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(202): Show |
intron_variant | MODIFIER | c.421-171A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94983477 | ||||||
chr1:94983609
|
G | A | 27 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(24): Show | 27 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.421-303C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94983609 | ||||||
chr1:94983726
|
A | G | 308 | a0001c0001t0001g0115a0001c0001t0001g0276a0001c0001t0001g0278others(305): Show | 310 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(307): Show |
intron_variant | MODIFIER | c.421-420T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94983726 | ||||||
chr1:94983845
|
G | A | 28 | a0001c0001t0003g0002a0001c0001t0003g0130a0001c0001t0003g0133others(25): Show | 29 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.421-539C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94983845 | ||||||
chr1:94983894
|
A | G | 3 | a0001c0001t0082g0049a0001c0001t0196g0114a0001c0001t0197g0116 | 3 | HG01891.hp2 HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.421-588T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94983894 | ||||||
chr1:94983902
|
C | T | 1 | a0001c0001t0192g0368 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.421-596G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94983902 | ||||||
chr1:94983945
|
CA | C | 5 | a0001c0001t0018g0118a0001c0001t0018g0119a0001c0001t0018g0120others(2): Show | 5 | HG01074.hp1 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.421-640delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94983945 | ||||||
chr1:94984218
|
G | C | 6 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-912C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94984218 | ||||||
chr1:94984315
|
G | C | 27 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(24): Show | 27 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.421-1009C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94984315 | ||||||
chr1:94984367
|
A | G | 27 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(24): Show | 27 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.421-1061T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94984367 | ||||||
chr1:94984548
|
G | A | 1 | a0001c0001t0006g0044 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.421-1242C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94984548 | ||||||
chr1:94984862
|
G | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.421-1556C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94984862 | ||||||
chr1:94984939
|
T | TTTTG | 7 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(4): Show | 7 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.421-1634_421-1633i others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94984939 | ||||||
chr1:94985156
|
A | G | 1 | a0001c0001t0001g0115 | 1 | HG02451.hp1 | intron_variant | MODIFIER | c.421-1850T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94985156 | ||||||
chr1:94985211
|
C | CTCTA | 294 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(291): Show | 296 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.421-1906_421-1905i others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94985211 | ||||||
chr1:94985289
|
A | G | 3 | a0001c0001t0082g0049a0001c0001t0196g0114a0001c0001t0197g0116 | 3 | HG01891.hp2 HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.421-1983T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94985289 | ||||||
chr1:94985363
|
G | A | 1 | a0001c0002t0108g0179 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.421-2057C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94985363 | ||||||
chr1:94985471
|
C | A | 1 | a0001c0001t0010g0134 | 1 | NA19084.hp1 | intron_variant | MODIFIER | c.421-2165G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94985471 | ||||||
chr1:94985617
|
A | C | 21 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0100others(18): Show | 21 | HG01069.hp2 HG01099.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.421-2311T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94985617 | ||||||
chr1:94985619
|
T | C | 1 | a0001c0001t0044g0327 | 1 | HG01952.hp2 | intron_variant | MODIFIER | c.421-2313A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94985619 | ||||||
chr1:94985892
|
G | GA | 21 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0100others(18): Show | 21 | HG01069.hp2 HG01099.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.421-2587dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94985892 | ||||||
chr1:94985892
|
GA | G | 7 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(4): Show | 7 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.421-2587delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94985892 | ||||||
chr1:94986139
|
T | A | 2 | a0001c0001t0040g0065a0001c0001t0040g0066 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.421-2833A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94986139 | ||||||
chr1:94986296
|
T | C | 4 | a0001c0001t0028g0175a0001c0001t0028g0176a0001c0001t0058g0177others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-2990A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94986296 | ||||||
chr1:94986362
|
T | C | 1 | a0001c0001t0075g0012 | 1 | HG03540.hp2 | intron_variant | MODIFIER | c.421-3056A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94986362 | ||||||
chr1:94986370
|
G | A | 122 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(119): Show | 123 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(120): Show |
intron_variant | MODIFIER | c.421-3064C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94986370 | ||||||
chr1:94986672
|
C | T | 4 | a0001c0001t0028g0175a0001c0001t0028g0176a0001c0001t0058g0177others(1): Show | 4 | HG02055.hp2 HG02109.hp1 HG02451.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-3366G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94986672 | ||||||
chr1:94986701
|
G | T | 6 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-3395C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94986701 | ||||||
chr1:94986771
|
C | CT | 15 | a0001c0001t0004g0160a0001c0001t0008g0099a0001c0001t0021g0315others(12): Show | 15 | HG01109.hp2 HG01884.hp2 HG01891.hp2 others(12): Show |
intron_variant | MODIFIER | c.421-3466dupA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94986771 | ||||||
chr1:94986771
|
C | CTT | 11 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(8): Show | 12 | HG00639.hp1 HG01243.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.421-3467_421-3466d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94986771 | ||||||
chr1:94986771
|
CT | C | 9 | a0001c0001t0001g0318a0001c0001t0003g0133a0001c0001t0043g0277others(6): Show | 9 | HG01517.hp1 HG01975.hp2 HG02965.hp2 others(6): Show |
intron_variant | MODIFIER | c.421-3466delA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94986771 | ||||||
chr1:94986772
|
T | C | 7 | a0001c0001t0164g0372a0001c0001t0170g0367a0001c0001t0171g0369others(4): Show | 7 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(4): Show |
intron_variant | MODIFIER | c.421-3466A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94986772 | ||||||
chr1:94986900
|
T | A | 7 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(4): Show | 7 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.421-3594A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94986900 | ||||||
chr1:94986929
|
C | T | 7 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(4): Show | 7 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.421-3623G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94986929 | ||||||
chr1:94986930
|
G | A | 21 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0100others(18): Show | 21 | HG01069.hp2 HG01099.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.421-3624C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94986930 | ||||||
chr1:94986940
|
G | A | 42 | a0001c0001t0013g0053a0001c0001t0013g0054a0001c0001t0013g0059others(39): Show | 42 | HG01081.hp2 HG01255.hp2 HG01346.hp2 others(39): Show |
intron_variant | MODIFIER | c.421-3634C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94986940 | ||||||
chr1:94987030
|
G | A | 38 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(35): Show | 38 | HG00597.hp2 HG00673.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.421-3724C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94987030 | ||||||
chr1:94987139
|
A | G | 1 | a0001c0001t0015g0080 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.421-3833T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94987139 | ||||||
chr1:94987228
|
T | C | 1 | a0001c0001t0159g0332 | 1 | HG01261.hp2 | intron_variant | MODIFIER | c.421-3922A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94987228 | ||||||
chr1:94987305
|
T | TA | 7 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(4): Show | 7 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.421-4000dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94987305 | ||||||
chr1:94987601
|
C | G | 1 | a0001c0001t0129g0184 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.421-4295G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94987601 | ||||||
chr1:94987718
|
G | A | 7 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(4): Show | 7 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.421-4412C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94987718 | ||||||
chr1:94987750
|
C | G | 1 | a0001c0001t0195g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.421-4444G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94987750 | ||||||
chr1:94987757
|
G | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.421-4451C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94987757 | ||||||
chr1:94987942
|
C | A | 1 | a0001c0001t0067g0050 | 1 | NA19089.hp1 | intron_variant | MODIFIER | c.421-4636G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94987942 | ||||||
chr1:94988095
|
C | T | 6 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-4789G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94988095 | ||||||
chr1:94988111
|
C | A | 7 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(4): Show | 7 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.421-4805G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94988111 | ||||||
chr1:94988171
|
C | T | 64 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(61): Show | 64 | HG00597.hp2 HG00673.hp1 HG00735.hp1 others(61): Show |
intron_variant | MODIFIER | c.421-4865G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94988171 | ||||||
chr1:94988215
|
C | T | 1 | a0001c0001t0153g0351 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.421-4909G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94988215 | ||||||
chr1:94988414
|
T | C | 4 | a0001c0001t0027g0204a0001c0001t0027g0207a0001c0001t0122g0206others(1): Show | 4 | HG00544.hp1 NA18955.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.421-5108A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94988414 | ||||||
chr1:94988660
|
A | C | 6 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272others(3): Show | 6 | HG01891.hp2 HG02109.hp2 HG02886.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-5354T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94988660 | ||||||
chr1:94988844
|
TAC | T | 3 | a0001c0001t0082g0049a0001c0001t0196g0114a0001c0001t0197g0116 | 3 | HG01891.hp2 HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.421-5540_421-5539d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94988844 | ||||||
chr1:94988922
|
C | T | 1 | a0001c0001t0020g0075 | 1 | HG02630.hp1 | intron_variant | MODIFIER | c.421-5616G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94988922 | ||||||
chr1:94988981
|
G | C | 3 | a0001c0001t0004g0153a0001c0001t0004g0154a0001c0001t0004g0155 | 3 | HG01123.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.421-5675C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94988981 | ||||||
chr1:94989010
|
T | C | 27 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(24): Show | 27 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(24): Show |
intron_variant | MODIFIER | c.421-5704A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94989010 | ||||||
chr1:94989341
|
T | C | 1 | a0001c0001t0105g0036 | 1 | HG01361.hp2 | intron_variant | MODIFIER | c.421-6035A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94989341 | ||||||
chr1:94989401
|
A | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-6095T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94989401 | ||||||
chr1:94989450
|
G | T | 3 | a0001c0001t0082g0049a0001c0001t0196g0114a0001c0001t0197g0116 | 3 | HG01891.hp2 HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.421-6144C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94989450 | ||||||
chr1:94989559
|
G | A | 1 | a0001c0001t0003g0141 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.421-6253C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94989559 | ||||||
chr1:94989570
|
T | C | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-6264A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94989570 | ||||||
chr1:94989573
|
G | A | 1 | a0001c0001t0003g0152 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.421-6267C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94989573 | ||||||
chr1:94989597
|
G | A | 5 | a0001c0001t0024g0375a0001c0001t0024g0376a0001c0001t0024g0377others(2): Show | 5 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(2): Show |
intron_variant | MODIFIER | c.421-6291C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94989597 | ||||||
chr1:94989688
|
T | C | 19 | a0001c0001t0003g0002a0001c0001t0003g0130a0001c0001t0003g0133others(16): Show | 20 | HG02027.hp2 HG02129.hp1 NA18747.hp2 others(17): Show |
intron_variant | MODIFIER | c.421-6382A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94989688 | ||||||
chr1:94989752
|
A | G | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-6446T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94989752 | ||||||
chr1:94989758
|
T | C | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-6452A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94989758 | ||||||
chr1:94989790
|
T | C | 19 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(16): Show | 19 | HG00735.hp1 HG02145.hp1 HG02559.hp2 others(16): Show |
intron_variant | MODIFIER | c.421-6484A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94989790 | ||||||
chr1:94989928
|
A | G | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-6622T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94989928 | ||||||
chr1:94989976
|
G | C | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-6670C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94989976 | ||||||
chr1:94990125
|
A | G | 1 | a0001c0001t0191g0299 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.421-6819T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94990125 | ||||||
chr1:94990177
|
A | G | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-6871T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94990177 | ||||||
chr1:94990196
|
C | G | 1 | a0001c0001t0028g0176 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.421-6890G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94990196 | ||||||
chr1:94990230
|
G | A | 1 | a0001c0001t0021g0290 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.421-6924C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94990230 | ||||||
chr1:94990298
|
A | G | 1 | a0001c0001t0006g0044 | 1 | HG01358.hp2 | intron_variant | MODIFIER | c.421-6992T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94990298 | ||||||
chr1:94990349
|
C | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-7043G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94990349 | ||||||
chr1:94990376
|
T | C | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-7070A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94990376 | ||||||
chr1:94990504
|
T | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.421-7198A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94990504 | ||||||
chr1:94990753
|
T | C | 28 | a0001c0001t0003g0002a0001c0001t0003g0130a0001c0001t0003g0133others(25): Show | 29 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.421-7447A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94990753 | ||||||
chr1:94990874
|
C | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-7568G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94990874 | ||||||
chr1:94991029
|
G | A | 1 | a0001c0001t0133g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.421-7723C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94991029 | ||||||
chr1:94991121
|
G | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-7815C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94991121 | ||||||
chr1:94991273
|
C | T | 1 | a0001c0001t0010g0146 | 1 | NA18967.hp2 | intron_variant | MODIFIER | c.421-7967G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94991273 | ||||||
chr1:94991516
|
G | C | 76 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(73): Show | 76 | HG00597.hp2 HG00673.hp1 HG00735.hp2 others(73): Show |
intron_variant | MODIFIER | c.421-8210C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94991516 | ||||||
chr1:94991680
|
C | T | 273 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(270): Show | 275 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(272): Show |
intron_variant | MODIFIER | c.421-8374G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94991680 | ||||||
chr1:94991733
|
T | C | 2 | a0001c0001t0054g0021a0001c0001t0062g0024 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.421-8427A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94991733 | ||||||
chr1:94991747
|
T | C | 3 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0085g0151 | 3 | NA18942.hp2 NA18943.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.421-8441A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94991747 | ||||||
chr1:94991853
|
C | CT | 292 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(289): Show | 294 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(291): Show |
intron_variant | MODIFIER | c.421-8548dupA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94991853 | ||||||
chr1:94991878
|
T | C | 18 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(15): Show | 18 | HG00735.hp1 HG02145.hp1 HG02559.hp2 others(15): Show |
intron_variant | MODIFIER | c.421-8572A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94991878 | ||||||
chr1:94991979
|
A | G | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-8673T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94991979 | ||||||
chr1:94992038
|
CTT | C | 119 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(116): Show | 120 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.421-8734_421-8733d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94992038 | ||||||
chr1:94992236
|
T | C | 1 | a0001c0001t0013g0073 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.421-8930A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94992236 | ||||||
chr1:94992255
|
C | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-8949G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94992255 | ||||||
chr1:94992323
|
G | C | 3 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272 | 3 | HG02109.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.421-9017C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94992323 | ||||||
chr1:94992420
|
C | G | 1 | a0001c0001t0003g0150 | 1 | HG02027.hp2 | intron_variant | MODIFIER | c.421-9114G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94992420 | ||||||
chr1:94992554
|
A | AGGGTTGA others(16): Show |
1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-9249_421-9248i others(25): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94992554 | ||||||
chr1:94992647
|
G | A | 5 | a0001c0001t0001g0362a0001c0001t0009g0364a0001c0001t0150g0360others(2): Show | 5 | HG00438.hp2 NA18939.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.421-9341C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94992647 | ||||||
chr1:94992781
|
T | C | 1 | a0001c0001t0082g0049 | 1 | HG01891.hp2 | intron_variant | MODIFIER | c.421-9475A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94992781 | ||||||
chr1:94992828
|
C | G | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-9522G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94992828 | ||||||
chr1:94992944
|
A | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.421-9638T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94992944 | ||||||
chr1:94993161
|
T | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-9855A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94993161 | ||||||
chr1:94993164
|
T | C | 1 | a0001c0001t0031g0354 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.421-9858A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94993164 | ||||||
chr1:94993456
|
G | A | 1 | a0001c0001t0004g0256 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.421-10150C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94993456 | ||||||
chr1:94993519
|
C | A | 1 | a0001c0001t0102g0041 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.421-10213G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94993519 | ||||||
chr1:94993756
|
G | A | 1 | a0001c0001t0165g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.421-10450C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94993756 | ||||||
chr1:94993797
|
T | C | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-10491A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94993797 | ||||||
chr1:94993853
|
C | T | 2 | a0001c0001t0016g0123a0001c0001t0100g0126 | 2 | HG00735.hp2 HG01081.hp1 |
intron_variant | MODIFIER | c.421-10547G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94993853 | ||||||
chr1:94993917
|
C | T | 1 | a0001c0001t0020g0076 | 1 | NA18522.hp1 | intron_variant | MODIFIER | c.421-10611G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94993917 | ||||||
chr1:94994033
|
G | A | 1 | a0001c0001t0195g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.421-10727C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94994033 | ||||||
chr1:94994259
|
T | C | 1 | a0001c0001t0005g0269 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.421-10953A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94994259 | ||||||
chr1:94994301
|
C | T | 2 | a0001c0001t0005g0264a0001c0001t0019g0209 | 2 | HG02074.hp2 NA18961.hp1 |
intron_variant | MODIFIER | c.421-10995G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94994301 | ||||||
chr1:94994316
|
ATTTT | A | 3 | a0001c0001t0009g0350a0001c0001t0044g0346a0001c0001t0148g0344 | 3 | NA18953.hp1 NA18969.hp1 NA19081.hp2 |
intron_variant | MODIFIER | c.421-11014_421-1101 others(8): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94994316 | ||||||
chr1:94994327
|
T | C | 1 | a0001c0001t0039g0260 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.421-11021A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94994327 | ||||||
chr1:94994563
|
TC | T | 4 | a0001c0001t0007g0236a0001c0001t0007g0238a0001c0001t0007g0239others(1): Show | 4 | HG01358.hp1 HG01361.hp1 HG01496.hp2 others(1): Show |
intron_variant | MODIFIER | c.421-11258delG | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94994563 | ||||||
chr1:94994612
|
G | A | 6 | a0001c0001t0016g0123a0001c0001t0016g0124a0001c0001t0016g0128others(3): Show | 6 | HG00735.hp2 HG01081.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.421-11306C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94994612 | ||||||
chr1:94994746
|
G | A | 6 | a0001c0001t0016g0123a0001c0001t0016g0124a0001c0001t0016g0128others(3): Show | 6 | HG00735.hp2 HG01081.hp1 HG02280.hp1 others(3): Show |
intron_variant | MODIFIER | c.421-11440C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94994746 | ||||||
chr1:94994764
|
T | C | 38 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(35): Show | 38 | HG00597.hp2 HG00673.hp1 HG00735.hp2 others(35): Show |
intron_variant | MODIFIER | c.421-11458A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94994764 | ||||||
chr1:94994874
|
C | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.421-11568G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94994874 | ||||||
chr1:94995085
|
G | A | 1 | a0001c0001t0132g0265 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.421-11779C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94995085 | ||||||
chr1:94995313
|
GAGAC | G | 4 | a0001c0001t0036g0107a0001c0001t0036g0108a0001c0001t0089g0106others(1): Show | 4 | HG02486.hp2 HG03098.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.421-12011_421-1200 others(8): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94995313 | ||||||
chr1:94995439
|
G | A | 9 | a0001c0001t0002g0221a0001c0001t0002g0223a0001c0001t0041g0188others(6): Show | 9 | HG00609.hp1 HG02027.hp1 HG02129.hp2 others(6): Show |
intron_variant | MODIFIER | c.421-12133C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94995439 | ||||||
chr1:94995479
|
G | A | 33 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(30): Show | 33 | HG00597.hp2 HG00673.hp1 HG00735.hp2 others(30): Show |
intron_variant | MODIFIER | c.421-12173C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94995479 | ||||||
chr1:94995641
|
G | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-12335C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94995641 | ||||||
chr1:94995670
|
T | C | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-12364A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94995670 | ||||||
chr1:94995765
|
C | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-12459G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94995765 | ||||||
chr1:94995779
|
C | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-12473G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94995779 | ||||||
chr1:94995877
|
T | C | 57 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(54): Show | 57 | HG00597.hp2 HG00673.hp1 HG00735.hp1 others(54): Show |
intron_variant | MODIFIER | c.421-12571A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94995877 | ||||||
chr1:94995974
|
C | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-12668G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94995974 | ||||||
chr1:94995980
|
A | G | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-12674T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94995980 | ||||||
chr1:94996036
|
G | A | 6 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-12730C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94996036 | ||||||
chr1:94996174
|
C | T | 1 | a0001c0001t0001g0289 | 1 | NA19043.hp1 | intron_variant | MODIFIER | c.421-12868G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94996174 | ||||||
chr1:94996186
|
TTCTTTCT others(19): Show |
T | 2 | a0001c0001t0047g0241a0001c0001t0047g0242 | 2 | HG00741.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.421-12906_421-1288 others(30): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94996186 | ||||||
chr1:94996318
|
C | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-13012G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94996318 | ||||||
chr1:94996486
|
C | A | 1 | a0001c0001t0048g0079 | 1 | HG01975.hp2 | intron_variant | MODIFIER | c.421-13180G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94996486 | ||||||
chr1:94996508
|
C | A | 46 | a0001c0001t0013g0053a0001c0001t0013g0054a0001c0001t0013g0059others(43): Show | 46 | HG01081.hp2 HG01255.hp2 HG01346.hp2 others(43): Show |
intron_variant | MODIFIER | c.421-13202G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94996508 | ||||||
chr1:94996545
|
T | G | 89 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(86): Show | 89 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.421-13239A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94996545 | ||||||
chr1:94996556
|
G | T | 3 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272 | 3 | HG02109.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.421-13250C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94996556 | ||||||
chr1:94996658
|
C | T | 3 | a0001c0001t0014g0033a0001c0001t0015g0046a0001c0001t0015g0072 | 3 | HG01255.hp2 NA18999.hp2 NA19006.hp2 |
intron_variant | MODIFIER | c.421-13352G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94996658 | ||||||
chr1:94996680
|
T | C | 5 | a0001c0001t0006g0001a0001c0001t0006g0043a0001c0001t0006g0044others(2): Show | 6 | HG00639.hp1 HG01243.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.421-13374A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94996680 | ||||||
chr1:94996767
|
C | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-13461G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94996767 | ||||||
chr1:94996829
|
C | T | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(13): Show | 16 | HG00735.hp1 HG02602.hp1 HG02698.hp2 others(13): Show |
intron_variant | MODIFIER | c.421-13523G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94996829 | ||||||
chr1:94996861
|
T | C | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-13555A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94996861 | ||||||
chr1:94996873
|
G | A | 2 | a0001c0001t0189g0187a0001c0001t0190g0338 | 2 | HG01978.hp1 HG01981.hp2 |
intron_variant | MODIFIER | c.421-13567C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94996873 | ||||||
chr1:94996882
|
G | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-13576C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94996882 | ||||||
chr1:94996906
|
T | C | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-13600A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94996906 | ||||||
chr1:94996911
|
G | A | 5 | a0001c0001t0001g0362a0001c0001t0009g0364a0001c0001t0150g0360others(2): Show | 5 | HG00438.hp2 NA18939.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.421-13605C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94996911 | ||||||
chr1:94996921
|
G | A | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(13): Show | 16 | HG00735.hp1 HG02602.hp1 HG02698.hp2 others(13): Show |
intron_variant | MODIFIER | c.421-13615C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94996921 | ||||||
chr1:94997323
|
G | T | 3 | a0001c0001t0002g0298a0001c0001t0002g0306a0001c0001t0180g0311 | 3 | NA18985.hp1 NA19074.hp1 NA19088.hp1 |
intron_variant | MODIFIER | c.421-14017C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94997323 | ||||||
chr1:94997415
|
T | G | 270 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(267): Show | 272 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.421-14109A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94997415 | ||||||
chr1:94997420
|
T | C | 117 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(114): Show | 118 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(115): Show |
intron_variant | MODIFIER | c.421-14114A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94997420 | ||||||
chr1:94997975
|
T | G | 1 | a0001c0001t0015g0046 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.421-14669A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94997975 | ||||||
chr1:94998308
|
T | C | 2 | a0001c0001t0033g0034a0001c0001t0033g0040 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.421-15002A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94998308 | ||||||
chr1:94998429
|
A | G | 294 | a0001c0001t0001g0289a0001c0001t0002g0213a0001c0001t0002g0218others(291): Show | 296 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.421-15123T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94998429 | ||||||
chr1:94998527
|
C | T | 1 | a0001c0001t0002g0244 | 1 | NA19011.hp2 | intron_variant | MODIFIER | c.421-15221G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94998527 | ||||||
chr1:94999265
|
A | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.421-15959T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94999265 | ||||||
chr1:94999284
|
T | TA | 11 | a0001c0001t0001g0335a0001c0001t0002g0259a0001c0001t0015g0072others(8): Show | 11 | HG00099.hp2 HG01175.hp1 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.421-15979dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94999284 | ||||||
chr1:94999284
|
TA | T | 64 | a0001c0001t0001g0317a0001c0001t0001g0357a0001c0001t0003g0002others(61): Show | 65 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(62): Show |
intron_variant | MODIFIER | c.421-15979delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94999284 | ||||||
chr1:94999343
|
A | AT | 63 | a0001c0001t0001g0276a0001c0001t0001g0284a0001c0001t0001g0289others(60): Show | 64 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(61): Show |
intron_variant | MODIFIER | c.421-16038dupA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94999343 | ||||||
chr1:94999343
|
A | ATT | 8 | a0001c0001t0003g0130a0001c0001t0003g0133a0001c0001t0003g0140others(5): Show | 8 | HG00735.hp1 HG02129.hp1 HG02970.hp2 others(5): Show |
intron_variant | MODIFIER | c.421-16039_421-1603 others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94999343 | ||||||
chr1:94999343
|
AT | A | 63 | a0001c0001t0001g0115a0001c0001t0001g0322a0001c0001t0004g0004others(60): Show | 63 | HG00323.hp2 HG00597.hp2 HG00673.hp1 others(60): Show |
intron_variant | MODIFIER | c.421-16038delA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94999343 | ||||||
chr1:94999343
|
ATTTTTTT | A | 18 | a0001c0001t0017g0312a0001c0001t0017g0380a0001c0001t0017g0381others(15): Show | 18 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.421-16044_421-1603 others(11): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94999343 | ||||||
chr1:94999344
|
T | A | 1 | a0001c0001t0028g0176 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.421-16038A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94999344 | ||||||
chr1:94999345
|
T | A | 40 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(37): Show | 40 | HG00597.hp2 HG00673.hp1 HG00735.hp2 others(37): Show |
intron_variant | MODIFIER | c.421-16039A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94999345 | ||||||
chr1:94999730
|
G | C | 5 | a0001c0001t0018g0118a0001c0001t0018g0119a0001c0001t0018g0120others(2): Show | 5 | HG01074.hp1 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.421-16424C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94999730 | ||||||
chr1:94999771
|
A | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-16465T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94999771 | ||||||
chr1:94999821
|
C | A | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(14): Show | 17 | HG00735.hp1 HG02572.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.421-16515G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 94999821 | ||||||
chr1:95000127
|
T | C | 1 | a0001c0001t0053g0023 | 1 | HG02717.hp1 | intron_variant | MODIFIER | c.421-16821A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95000127 | ||||||
chr1:95000159
|
A | C | 1 | a0001c0001t0195g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.421-16853T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95000159 | ||||||
chr1:95000176
|
C | T | 28 | a0001c0001t0003g0002a0001c0001t0003g0130a0001c0001t0003g0133others(25): Show | 29 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.421-16870G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95000176 | ||||||
chr1:95000304
|
G | A | 4 | a0001c0001t0001g0362a0001c0001t0150g0360a0001c0001t0154g0363others(1): Show | 4 | NA18939.hp1 NA18987.hp2 NA19005.hp1 others(1): Show |
intron_variant | MODIFIER | c.421-16998C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95000304 | ||||||
chr1:95000325
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.421-17019G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95000325 | ||||||
chr1:95000365
|
G | A | 8 | a0001c0001t0007g0212a0001c0001t0007g0235a0001c0001t0007g0236others(5): Show | 8 | HG00673.hp2 HG01123.hp2 HG01261.hp1 others(5): Show |
intron_variant | MODIFIER | c.421-17059C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95000365 | ||||||
chr1:95000535
|
T | TA | 135 | a0001c0001t0001g0289a0001c0001t0001g0342a0001c0001t0001g0358others(132): Show | 136 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(133): Show |
intron_variant | MODIFIER | c.421-17230dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95000535 | ||||||
chr1:95000535
|
T | TAA | 13 | a0001c0001t0013g0054a0001c0001t0018g0118a0001c0001t0018g0119others(10): Show | 13 | HG01074.hp1 HG01167.hp2 HG01169.hp1 others(10): Show |
intron_variant | MODIFIER | c.421-17231_421-1723 others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95000535 | ||||||
chr1:95000535
|
TA | T | 6 | a0001c0001t0001g0352a0001c0001t0001g0359a0001c0001t0043g0283others(3): Show | 6 | HG01257.hp2 HG01993.hp1 NA18941.hp1 others(3): Show |
intron_variant | MODIFIER | c.421-17230delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95000535 | ||||||
chr1:95000554
|
A | G | 10 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0037g0009others(7): Show | 10 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(7): Show |
intron_variant | MODIFIER | c.421-17248T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95000554 | ||||||
chr1:95000674
|
G | A | 1 | a0001c0001t0007g0235 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.421-17368C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95000674 | ||||||
chr1:95000777
|
T | TA | 45 | a0001c0001t0001g0284a0001c0001t0001g0308a0001c0001t0001g0347others(42): Show | 45 | HG00438.hp2 HG00621.hp1 HG00735.hp1 others(42): Show |
intron_variant | MODIFIER | c.421-17472dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95000777 | ||||||
chr1:95000777
|
TA | T | 37 | a0001c0001t0001g0317a0001c0001t0001g0342a0001c0001t0005g0190others(34): Show | 37 | HG00323.hp2 HG00609.hp2 HG01069.hp1 others(34): Show |
intron_variant | MODIFIER | c.421-17472delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95000777 | ||||||
chr1:95000777
|
TAAAAAAA others(3): Show |
T | 39 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(36): Show | 39 | HG00597.hp2 HG00673.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.421-17481_421-1747 others(14): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95000777 | ||||||
chr1:95000843
|
G | A | 87 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(84): Show | 87 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.421-17537C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95000843 | ||||||
chr1:95000906
|
C | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-17600G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95000906 | ||||||
chr1:95000944
|
T | C | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-17638A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95000944 | ||||||
chr1:95001123
|
G | A | 1 | a0001c0001t0002g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.421-17817C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95001123 | ||||||
chr1:95001133
|
G | C | 1 | a0001c0001t0194g0373 | 1 | HG00642.hp2 | intron_variant | MODIFIER | c.421-17827C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95001133 | ||||||
chr1:95001146
|
C | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-17840G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95001146 | ||||||
chr1:95001284
|
A | G | 1 | a0001c0001t0024g0377 | 1 | HG01884.hp1 | intron_variant | MODIFIER | c.421-17978T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95001284 | ||||||
chr1:95001333
|
C | G | 1 | a0001c0001t0006g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.421-18027G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95001333 | ||||||
chr1:95001413
|
C | T | 7 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(4): Show | 7 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(4): Show |
intron_variant | MODIFIER | c.421-18107G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95001413 | ||||||
chr1:95001551
|
A | C | 13 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(10): Show | 14 | HG00639.hp1 HG01243.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.421-18245T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95001551 | ||||||
chr1:95001583
|
C | T | 1 | a0001c0001t0195g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.421-18277G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95001583 | ||||||
chr1:95001596
|
A | T | 3 | a0001c0001t0054g0021a0001c0001t0061g0022a0001c0001t0062g0024 | 3 | HG03041.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.421-18290T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95001596 | ||||||
chr1:95001696
|
A | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.421-18390T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95001696 | ||||||
chr1:95001750
|
C | T | 1 | a0001c0001t0141g0069 | 1 | NA18978.hp1 | intron_variant | MODIFIER | c.421-18444G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95001750 | ||||||
chr1:95001850
|
G | A | 1 | a0001c0001t0114g0016 | 1 | HG03834.hp2 | intron_variant | MODIFIER | c.421-18544C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95001850 | ||||||
chr1:95001917
|
T | G | 3 | a0001c0001t0028g0175a0001c0001t0028g0176a0001c0001t0058g0177 | 3 | HG02055.hp2 HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.421-18611A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95001917 | ||||||
chr1:95001971
|
G | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-18665C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95001971 | ||||||
chr1:95002052
|
T | G | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(14): Show | 17 | HG00735.hp1 HG02572.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.421-18746A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95002052 | ||||||
chr1:95002089
|
T | C | 1 | a0001c0001t0015g0080 | 1 | HG01943.hp1 | intron_variant | MODIFIER | c.421-18783A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95002089 | ||||||
chr1:95002246
|
G | T | 3 | a0001c0001t0011g0310a0001c0001t0024g0376a0001c0001t0024g0377 | 3 | HG01884.hp1 HG02647.hp2 NA18945.hp1 |
intron_variant | MODIFIER | c.421-18940C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95002246 | ||||||
chr1:95002247
|
G | A | 116 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(113): Show | 117 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.421-18941C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95002247 | ||||||
chr1:95002336
|
C | T | 87 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(84): Show | 87 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.421-19030G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95002336 | ||||||
chr1:95002341
|
T | G | 1 | a0001c0001t0174g0078 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.421-19035A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95002341 | ||||||
chr1:95002403
|
C | A | 1 | a0001c0001t0195g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.421-19097G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95002403 | ||||||
chr1:95002412
|
G | A | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(14): Show | 17 | HG00735.hp1 HG02572.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.421-19106C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95002412 | ||||||
chr1:95002560
|
C | T | 1 | a0001c0001t0003g0142 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.421-19254G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95002560 | ||||||
chr1:95002607
|
G | A | 1 | a0001c0001t0052g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.421-19301C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95002607 | ||||||
chr1:95002945
|
A | G | 1 | a0001c0001t0051g0020 | 1 | HG00735.hp1 | intron_variant | MODIFIER | c.421-19639T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95002945 | ||||||
chr1:95003380
|
T | C | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-20074A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95003380 | ||||||
chr1:95003450
|
C | CT | 21 | a0001c0001t0017g0312a0001c0001t0017g0378a0001c0001t0017g0380others(18): Show | 21 | HG00609.hp2 HG01109.hp2 HG01884.hp1 others(18): Show |
intron_variant | MODIFIER | c.421-20145dupA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95003450 | ||||||
chr1:95003450
|
CT | C | 151 | a0001c0001t0001g0194a0001c0001t0001g0282a0001c0001t0001g0317others(148): Show | 151 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(148): Show |
intron_variant | MODIFIER | c.421-20145delA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95003450 | ||||||
chr1:95003519
|
G | A | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(14): Show | 17 | HG00735.hp1 HG02572.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.421-20213C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95003519 | ||||||
chr1:95003584
|
A | G | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-20278T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95003584 | ||||||
chr1:95003592
|
G | A | 1 | a0001c0001t0128g0200 | 1 | HG03669.hp1 | intron_variant | MODIFIER | c.421-20286C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95003592 | ||||||
chr1:95003607
|
C | A | 83 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(80): Show | 84 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.421-20301G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95003607 | ||||||
chr1:95003622
|
A | T | 1 | a0001c0001t0174g0078 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.421-20316T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95003622 | ||||||
chr1:95003702
|
C | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-20396G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95003702 | ||||||
chr1:95003714
|
C | G | 2 | a0001c0001t0001g0284a0001c0001t0094g0288 | 2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.421-20408G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95003714 | ||||||
chr1:95004112
|
A | T | 1 | a0001c0001t0057g0159 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.421-20806T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95004112 | ||||||
chr1:95004115
|
T | A | 1 | a0001c0001t0005g0185 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.421-20809A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95004115 | ||||||
chr1:95004215
|
C | CT | 23 | a0001c0001t0001g0289a0001c0001t0001g0330a0001c0001t0002g0247others(20): Show | 23 | HG00408.hp1 HG00735.hp1 HG01109.hp2 others(20): Show |
intron_variant | MODIFIER | c.421-20910dupA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95004215 | ||||||
chr1:95004215
|
CT | C | 25 | a0001c0001t0001g0115a0001c0001t0001g0300a0001c0001t0003g0140others(22): Show | 25 | HG00735.hp2 HG01081.hp1 HG01081.hp2 others(22): Show |
intron_variant | MODIFIER | c.421-20910delA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95004215 | ||||||
chr1:95004261
|
A | C | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.421-20955T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95004261 | ||||||
chr1:95004432
|
G | C | 1 | a0001c0001t0005g0201 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.421-21126C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95004432 | ||||||
chr1:95004636
|
A | G | 2 | a0001c0001t0020g0076a0001c0001t0020g0077 | 2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.421-21330T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95004636 | ||||||
chr1:95004752
|
C | T | 116 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(113): Show | 117 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.421-21446G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95004752 | ||||||
chr1:95004786
|
C | T | 1 | a0001c0001t0151g0339 | 1 | HG00408.hp1 | intron_variant | MODIFIER | c.421-21480G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95004786 | ||||||
chr1:95004793
|
C | A | 2 | a0001c0001t0055g0156a0001c0001t0057g0159 | 2 | NA18992.hp2 NA19091.hp1 |
intron_variant | MODIFIER | c.421-21487G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95004793 | ||||||
chr1:95004797
|
G | C | 1 | a0001c0001t0195g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.421-21491C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95004797 | ||||||
chr1:95004837
|
G | A | 1 | a0001c0001t0077g0169 | 1 | HG02071.hp2 | intron_variant | MODIFIER | c.421-21531C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95004837 | ||||||
chr1:95004954
|
T | C | 28 | a0001c0001t0003g0002a0001c0001t0003g0130a0001c0001t0003g0133others(25): Show | 29 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.421-21648A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95004954 | ||||||
chr1:95004981
|
A | T | 269 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(266): Show | 271 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(268): Show |
intron_variant | MODIFIER | c.421-21675T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95004981 | ||||||
chr1:95005160
|
G | A | 1 | a0001c0001t0001g0335 | 1 | HG00099.hp2 | intron_variant | MODIFIER | c.421-21854C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95005160 | ||||||
chr1:95005227
|
C | G | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(14): Show | 17 | HG00735.hp1 HG02572.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.420+21902G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95005227 | ||||||
chr1:95005255
|
C | T | 42 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(39): Show | 42 | HG00597.hp2 HG00673.hp1 HG00735.hp2 others(39): Show |
intron_variant | MODIFIER | c.420+21874G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95005255 | ||||||
chr1:95005416
|
G | C | 1 | a0001c0001t0001g0307 | 1 | HG00558.hp1 | intron_variant | MODIFIER | c.420+21713C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95005416 | ||||||
chr1:95005417
|
G | T | 1 | a0001c0001t0083g0122 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.420+21712C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95005417 | ||||||
chr1:95005419
|
C | CACTGGTC others(97): Show |
6 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.420+21709_420+2171 others(108): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95005419 | ||||||
chr1:95005420
|
T | C | 6 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.420+21709A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95005420 | ||||||
chr1:95005425
|
C | G | 6 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.420+21704G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95005425 | ||||||
chr1:95005427
|
T | C | 6 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.420+21702A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95005427 | ||||||
chr1:95005483
|
T | A | 1 | a0001c0001t0057g0159 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.420+21646A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95005483 | ||||||
chr1:95005761
|
C | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+21368G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95005761 | ||||||
chr1:95005773
|
T | C | 1 | a0001c0001t0078g0089 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.420+21356A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95005773 | ||||||
chr1:95005809
|
T | A | 1 | a0001c0001t0057g0159 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.420+21320A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95005809 | ||||||
chr1:95005900
|
C | T | 116 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(113): Show | 117 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.420+21229G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95005900 | ||||||
chr1:95005951
|
C | T | 61 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(58): Show | 61 | HG00597.hp2 HG00673.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.420+21178G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95005951 | ||||||
chr1:95006091
|
T | A | 28 | a0001c0001t0003g0002a0001c0001t0003g0130a0001c0001t0003g0133others(25): Show | 29 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.420+21038A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95006091 | ||||||
chr1:95006185
|
T | A | 13 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(10): Show | 14 | HG00639.hp1 HG01243.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.420+20944A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95006185 | ||||||
chr1:95006219
|
T | G | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+20910A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95006219 | ||||||
chr1:95006377
|
GAAAAGGC others(7): Show |
G | 8 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(5): Show | 8 | HG00735.hp1 HG02572.hp1 HG02717.hp1 others(5): Show |
intron_variant | MODIFIER | c.420+20738_420+2075 others(18): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95006377 | ||||||
chr1:95006406
|
T | C | 1 | a0001c0001t0019g0226 | 1 | NA18747.hp1 | intron_variant | MODIFIER | c.420+20723A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95006406 | ||||||
chr1:95006421
|
C | T | 1 | a0001c0001t0001g0341 | 1 | HG00323.hp1 | intron_variant | MODIFIER | c.420+20708G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95006421 | ||||||
chr1:95006707
|
G | A | 1 | a0001c0001t0001g0321 | 1 | HG01167.hp1 | intron_variant | MODIFIER | c.420+20422C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95006707 | ||||||
chr1:95006772
|
C | A | 6 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.420+20357G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95006772 | ||||||
chr1:95006939
|
A | T | 3 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272 | 3 | HG02109.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.420+20190T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95006939 | ||||||
chr1:95007082
|
G | C | 13 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(10): Show | 14 | HG00639.hp1 HG01243.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.420+20047C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95007082 | ||||||
chr1:95007138
|
T | A | 1 | a0001c0001t0057g0159 | 1 | NA18992.hp2 | intron_variant | MODIFIER | c.420+19991A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95007138 | ||||||
chr1:95007191
|
T | C | 1 | a0001c0001t0048g0006 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.420+19938A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95007191 | ||||||
chr1:95007229
|
G | A | 1 | a0001c0001t0012g0095 | 1 | HG03710.hp2 | intron_variant | MODIFIER | c.420+19900C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95007229 | ||||||
chr1:95007471
|
G | A | 1 | a0001c0001t0152g0292 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.420+19658C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95007471 | ||||||
chr1:95007488
|
C | T | 1 | a0001c0001t0003g0270 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.420+19641G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95007488 | ||||||
chr1:95007625
|
T | C | 1 | a0001c0001t0008g0101 | 1 | HG02970.hp2 | intron_variant | MODIFIER | c.420+19504A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95007625 | ||||||
chr1:95007698
|
C | T | 3 | a0001c0001t0001g0330a0001c0001t0149g0337a0001c0001t0151g0339 | 3 | HG00408.hp1 HG02135.hp1 NA19089.hp2 |
intron_variant | MODIFIER | c.420+19431G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95007698 | ||||||
chr1:95007885
|
C | T | 11 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(8): Show | 12 | HG00639.hp1 HG01243.hp2 HG01358.hp2 others(9): Show |
intron_variant | MODIFIER | c.420+19244G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95007885 | ||||||
chr1:95008068
|
T | C | 2 | a0001c0001t0170g0367a0001c0001t0192g0368 | 2 | HG00140.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.420+19061A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95008068 | ||||||
chr1:95008189
|
G | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.420+18940C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95008189 | ||||||
chr1:95008641
|
T | C | 1 | a0001c0001t0026g0015 | 1 | HG04204.hp2 | intron_variant | MODIFIER | c.420+18488A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95008641 | ||||||
chr1:95008750
|
T | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+18379A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95008750 | ||||||
chr1:95008752
|
G | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+18377C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95008752 | ||||||
chr1:95008754
|
G | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+18375C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95008754 | ||||||
chr1:95008918
|
A | G | 1 | a0001c0001t0088g0129 | 1 | NA19084.hp2 | intron_variant | MODIFIER | c.420+18211T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95008918 | ||||||
chr1:95008989
|
G | T | 7 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0100others(4): Show | 7 | HG01884.hp2 HG02572.hp2 HG02622.hp1 others(4): Show |
intron_variant | MODIFIER | c.420+18140C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95008989 | ||||||
chr1:95009205
|
T | C | 1 | a0001c0001t0192g0368 | 1 | HG01433.hp1 | intron_variant | MODIFIER | c.420+17924A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95009205 | ||||||
chr1:95009386
|
T | C | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+17743A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95009386 | ||||||
chr1:95009388
|
T | C | 1 | a0001c0003t0019g0210 | 1 | HG04115.hp1 | intron_variant | MODIFIER | c.420+17741A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95009388 | ||||||
chr1:95009566
|
A | T | 1 | a0001c0001t0183g0028 | 1 | HG02572.hp1 | intron_variant | MODIFIER | c.420+17563T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95009566 | ||||||
chr1:95009927
|
T | C | 1 | a0001c0001t0078g0089 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.420+17202A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95009927 | ||||||
chr1:95009971
|
T | G | 30 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(27): Show | 30 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.420+17158A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95009971 | ||||||
chr1:95010050
|
C | G | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+17079G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95010050 | ||||||
chr1:95010776
|
A | G | 65 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(62): Show | 66 | HG00639.hp1 HG01081.hp2 HG01243.hp2 others(63): Show |
intron_variant | MODIFIER | c.420+16353T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95010776 | ||||||
chr1:95011027
|
C | T | 2 | a0001c0001t0017g0312a0001c0001t0076g0379 | 2 | HG00609.hp2 HG02071.hp1 |
intron_variant | MODIFIER | c.420+16102G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95011027 | ||||||
chr1:95011133
|
A | G | 3 | a0001c0001t0005g0196a0001c0001t0005g0211a0001c0001t0178g0208 | 3 | NA18972.hp2 NA19080.hp1 NA19083.hp1 |
intron_variant | MODIFIER | c.420+15996T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95011133 | ||||||
chr1:95011179
|
G | A | 62 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(59): Show | 62 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(59): Show |
intron_variant | MODIFIER | c.420+15950C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95011179 | ||||||
chr1:95011293
|
T | TC | 8 | a0001c0001t0001g0289a0001c0001t0016g0123a0001c0001t0016g0124others(5): Show | 8 | HG00735.hp2 HG01081.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.420+15835dupG | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95011293 | ||||||
chr1:95011465
|
G | A | 2 | a0001c0001t0001g0335a0001c0001t0145g0266 | 2 | HG00099.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.420+15664C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95011465 | ||||||
chr1:95011601
|
G | T | 1 | a0001c0001t0004g0170 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.420+15528C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95011601 | ||||||
chr1:95011672
|
C | G | 6 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.420+15457G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95011672 | ||||||
chr1:95011702
|
G | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+15427C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95011702 | ||||||
chr1:95011806
|
T | C | 1 | a0001c0001t0021g0315 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.420+15323A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95011806 | ||||||
chr1:95011821
|
T | C | 1 | a0001c0001t0147g0271 | 1 | HG02895.hp2 | intron_variant | MODIFIER | c.420+15308A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95011821 | ||||||
chr1:95012094
|
CTT | C | 3 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0085g0151 | 3 | NA18942.hp2 NA18943.hp1 NA18987.hp1 |
intron_variant | MODIFIER | c.420+15033_420+1503 others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95012094 | ||||||
chr1:95012204
|
G | A | 1 | a0001c0001t0028g0176 | 1 | HG03579.hp2 | intron_variant | MODIFIER | c.420+14925C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95012204 | ||||||
chr1:95012204
|
G | C | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+14925C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95012204 | ||||||
chr1:95012370
|
T | C | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(14): Show | 17 | HG00735.hp1 HG02572.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.420+14759A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95012370 | ||||||
chr1:95012570
|
T | C | 61 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(58): Show | 61 | HG00597.hp2 HG00673.hp1 HG00735.hp1 others(58): Show |
intron_variant | MODIFIER | c.420+14559A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95012570 | ||||||
chr1:95012651
|
T | C | 1 | a0001c0001t0167g0254 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.420+14478A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95012651 | ||||||
chr1:95012655
|
T | C | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+14474A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95012655 | ||||||
chr1:95012662
|
C | T | 1 | a0001c0001t0006g0035 | 1 | HG01517.hp2 | intron_variant | MODIFIER | c.420+14467G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95012662 | ||||||
chr1:95012839
|
C | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+14290G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95012839 | ||||||
chr1:95012908
|
G | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+14221C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95012908 | ||||||
chr1:95013115
|
TA | T | 7 | a0001c0001t0001g0352a0001c0001t0003g0178a0001c0001t0013g0073others(4): Show | 7 | HG01257.hp2 HG01993.hp1 HG04115.hp2 others(4): Show |
intron_variant | MODIFIER | c.420+14013delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95013115 | ||||||
chr1:95013147
|
C | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+13982G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95013147 | ||||||
chr1:95013306
|
G | A | 1 | a0001c0001t0022g0082 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.420+13823C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95013306 | ||||||
chr1:95013341
|
A | T | 2 | a0001c0001t0029g0031a0001c0001t0145g0266 | 2 | HG02723.hp2 HG03486.hp2 |
intron_variant | MODIFIER | c.420+13788T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95013341 | ||||||
chr1:95013345
|
T | A | 126 | a0001c0001t0001g0284a0001c0001t0001g0296a0001c0001t0004g0004others(123): Show | 127 | HG00099.hp1 HG00140.hp1 HG00597.hp2 others(124): Show |
intron_variant | MODIFIER | c.420+13784A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95013345 | ||||||
chr1:95013527
|
G | T | 1 | a0001c0001t0001g0317 | 1 | HG01099.hp1 | intron_variant | MODIFIER | c.420+13602C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95013527 | ||||||
chr1:95013599
|
G | A | 1 | a0001c0001t0102g0041 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.420+13530C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95013599 | ||||||
chr1:95013624
|
C | T | 26 | a0001c0001t0003g0002a0001c0001t0003g0130a0001c0001t0003g0133others(23): Show | 27 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(24): Show |
intron_variant | MODIFIER | c.420+13505G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95013624 | ||||||
chr1:95013667
|
C | G | 34 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(31): Show | 34 | HG00597.hp2 HG00673.hp1 HG00735.hp2 others(31): Show |
intron_variant | MODIFIER | c.420+13462G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95013667 | ||||||
chr1:95013670
|
C | T | 1 | a0001c0001t0002g0245 | 1 | HG00423.hp1 | intron_variant | MODIFIER | c.420+13459G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95013670 | ||||||
chr1:95013929
|
TA | T | 217 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(214): Show | 218 | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(215): Show |
intron_variant | MODIFIER | c.420+13199delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95013929 | ||||||
chr1:95013929
|
TAA | T | 31 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(28): Show | 31 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(28): Show |
intron_variant | MODIFIER | c.420+13198_420+1319 others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95013929 | ||||||
chr1:95013946
|
C | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+13183G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95013946 | ||||||
chr1:95014063
|
C | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+13066G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95014063 | ||||||
chr1:95014150
|
C | A | 1 | a0001c0001t0155g0349 | 1 | HG01346.hp1 | intron_variant | MODIFIER | c.420+12979G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95014150 | ||||||
chr1:95014239
|
G | A | 6 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0049g0019others(3): Show | 6 | HG01891.hp2 HG02109.hp2 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.420+12890C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95014239 | ||||||
chr1:95014304
|
G | A | 83 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(80): Show | 84 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.420+12825C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95014304 | ||||||
chr1:95014615
|
A | G | 1 | a0001c0001t0005g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.420+12514T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95014615 | ||||||
chr1:95015020
|
T | C | 290 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(287): Show | 292 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(289): Show |
intron_variant | MODIFIER | c.420+12109A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95015020 | ||||||
chr1:95015427
|
G | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+11702C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95015427 | ||||||
chr1:95015544
|
A | G | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+11585T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95015544 | ||||||
chr1:95015624
|
G | A | 385 | a0001c0001t0001g0115a0001c0001t0001g0194a0001c0001t0001g0276others(382): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.420+11505C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95015624 | ||||||
chr1:95015630
|
G | A | 1 | a0001c0001t0069g0366 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.420+11499C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95015630 | ||||||
chr1:95015633
|
C | T | 2 | a0001c0001t0001g0284a0001c0001t0094g0288 | 2 | HG02630.hp2 NA19030.hp2 |
intron_variant | MODIFIER | c.420+11496G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95015633 | ||||||
chr1:95015736
|
A | C | 1 | a0001c0001t0030g0274 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.420+11393T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95015736 | ||||||
chr1:95015792
|
A | C | 3 | a0001c0001t0080g0047a0001c0001t0110g0070a0001c0001t0141g0069 | 3 | NA18944.hp1 NA18978.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.420+11337T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95015792 | ||||||
chr1:95015807
|
G | GCATGAAA others(5): Show |
1 | a0001c0001t0003g0178 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.420+11310_420+1132 others(16): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95015807 | ||||||
chr1:95016020
|
G | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.420+11109C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016020 | ||||||
chr1:95016044
|
C | T | 1 | a0001c0001t0158g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.420+11085G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016044 | ||||||
chr1:95016202
|
G | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+10927C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016202 | ||||||
chr1:95016595
|
C | T | 39 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(36): Show | 39 | HG00597.hp2 HG00673.hp1 HG00735.hp2 others(36): Show |
intron_variant | MODIFIER | c.420+10534G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016595 | ||||||
chr1:95016664
|
T | G | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+10465A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016664 | ||||||
chr1:95016942
|
G | GGT | 27 | a0001c0001t0001g0194a0001c0001t0001g0282a0001c0001t0001g0308others(24): Show | 27 | HG00099.hp2 HG00621.hp1 HG01257.hp2 others(24): Show |
intron_variant | MODIFIER | c.420+10185_420+1018 others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016942 | ||||||
chr1:95016942
|
G | GGTGT | 17 | a0001c0001t0001g0276a0001c0001t0003g0142a0001c0001t0003g0150others(14): Show | 17 | HG00597.hp1 HG00621.hp2 HG00673.hp2 others(14): Show |
intron_variant | MODIFIER | c.420+10183_420+1018 others(8): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016942 | ||||||
chr1:95016942
|
G | GGTGTGT | 15 | a0001c0001t0001g0278a0001c0001t0013g0054a0001c0001t0015g0072others(12): Show | 15 | HG00140.hp2 HG00642.hp2 HG01891.hp1 others(12): Show |
intron_variant | MODIFIER | c.420+10181_420+1018 others(10): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016942 | ||||||
chr1:95016942
|
G | GGTGTGTG others(1): Show |
6 | a0001c0001t0009g0350a0001c0001t0014g0033a0001c0001t0021g0315others(3): Show | 6 | HG01255.hp2 HG02015.hp1 HG02145.hp1 others(3): Show |
intron_variant | MODIFIER | c.420+10179_420+1018 others(12): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016942 | ||||||
chr1:95016942
|
G | GGTGTGTG others(3): Show |
2 | a0001c0001t0153g0351a0001c0001t0161g0323 | 2 | HG03831.hp2 HG03834.hp1 |
intron_variant | MODIFIER | c.420+10177_420+1018 others(14): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016942 | ||||||
chr1:95016942
|
G | GGTGTGTG others(5): Show |
3 | a0001c0001t0026g0015a0001c0001t0026g0061a0001c0001t0118g0055 | 3 | HG04204.hp2 NA18943.hp2 NA19074.hp2 |
intron_variant | MODIFIER | c.420+10175_420+1018 others(16): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016942 | ||||||
chr1:95016942
|
G | GTGT | 3 | a0001c0001t0001g0304a0001c0001t0002g0245a0001c0001t0193g0370 | 3 | HG00423.hp1 HG01993.hp2 NA18954.hp2 |
intron_variant | MODIFIER | c.420+10186_420+1018 others(7): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016942 | ||||||
chr1:95016942
|
G | T | 1 | a0001c0001t0013g0073 | 1 | NA18977.hp2 | intron_variant | MODIFIER | c.420+10187C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016942 | ||||||
chr1:95016942
|
GGT | G | 54 | a0001c0001t0001g0115a0001c0001t0001g0284a0001c0001t0001g0289others(51): Show | 56 | HG00408.hp2 HG00639.hp1 HG00639.hp2 others(53): Show |
intron_variant | MODIFIER | c.420+10185_420+1018 others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016942 | ||||||
chr1:95016942
|
GGTGT | G | 45 | a0001c0001t0001g0314a0001c0001t0001g0318a0001c0001t0001g0340others(42): Show | 45 | HG00323.hp1 HG00408.hp1 HG00741.hp1 others(42): Show |
intron_variant | MODIFIER | c.420+10183_420+1018 others(8): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016942 | ||||||
chr1:95016942
|
GGTGTGT | G | 62 | a0001c0001t0001g0296a0001c0001t0002g0221a0001c0001t0002g0223others(59): Show | 62 | HG00323.hp2 HG00423.hp2 HG00438.hp1 others(59): Show |
intron_variant | MODIFIER | c.420+10181_420+1018 others(10): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016942 | ||||||
chr1:95016942
|
GGTGTGTG others(1): Show |
G | 43 | a0001c0001t0001g0334a0001c0001t0004g0153a0001c0001t0004g0154others(40): Show | 43 | HG00597.hp2 HG00673.hp1 HG01070.hp2 others(40): Show |
intron_variant | MODIFIER | c.420+10179_420+1018 others(12): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016942 | ||||||
chr1:95016942
|
GGTGTGTG others(3): Show |
G | 9 | a0001c0001t0004g0111a0001c0001t0007g0212a0001c0001t0007g0240others(6): Show | 9 | HG01169.hp2 HG01261.hp1 HG02300.hp2 others(6): Show |
intron_variant | MODIFIER | c.420+10177_420+1018 others(14): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016942 | ||||||
chr1:95016942
|
GGTGTGTG others(5): Show |
G | 12 | a0001c0001t0004g0004a0001c0001t0016g0123a0001c0001t0016g0124others(9): Show | 12 | HG00735.hp2 HG01081.hp1 HG01978.hp1 others(9): Show |
intron_variant | MODIFIER | c.420+10175_420+1018 others(16): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016942 | ||||||
chr1:95016942
|
GGTGTGTG others(7): Show |
G | 7 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(4): Show | 7 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(4): Show |
intron_variant | MODIFIER | c.420+10173_420+1018 others(18): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016942 | ||||||
chr1:95016942
|
GGTGTGTG others(9): Show |
G | 2 | a0001c0001t0059g0272a0001c0001t0101g0008 | 2 | HG02886.hp2 HG02895.hp1 |
intron_variant | MODIFIER | c.420+10171_420+1018 others(20): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016942 | ||||||
chr1:95016942
|
GGTGTGTG others(11): Show |
G | 1 | a0001c0001t0090g0281 | 1 | NA18962.hp2 | intron_variant | MODIFIER | c.420+10169_420+1018 others(22): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016942 | ||||||
chr1:95016942
|
GGTGTGTG others(17): Show |
G | 1 | a0001c0001t0001g0356 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.420+10163_420+1018 others(28): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016942 | ||||||
chr1:95016985
|
G | A | 6 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.420+10144C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95016985 | ||||||
chr1:95017011
|
T | G | 1 | a0001c0001t0060g0027 | 1 | HG02602.hp1 | intron_variant | MODIFIER | c.420+10118A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95017011 | ||||||
chr1:95017034
|
C | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+10095G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95017034 | ||||||
chr1:95017066
|
T | A | 1 | a0001c0001t0030g0274 | 1 | HG03195.hp2 | intron_variant | MODIFIER | c.420+10063A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95017066 | ||||||
chr1:95017105
|
G | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+10024C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95017105 | ||||||
chr1:95017112
|
T | C | 83 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(80): Show | 84 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.420+10017A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95017112 | ||||||
chr1:95017371
|
CA | C | 18 | a0001c0001t0017g0312a0001c0001t0017g0378a0001c0001t0017g0380others(15): Show | 18 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(15): Show |
intron_variant | MODIFIER | c.420+9757delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95017371 | ||||||
chr1:95017470
|
G | A | 1 | a0001c0001t0007g0235 | 1 | HG00673.hp2 | intron_variant | MODIFIER | c.420+9659C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95017470 | ||||||
chr1:95017651
|
C | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+9478G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95017651 | ||||||
chr1:95017729
|
C | T | 1 | a0001c0001t0094g0288 | 1 | HG02630.hp2 | intron_variant | MODIFIER | c.420+9400G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95017729 | ||||||
chr1:95017826
|
C | A | 1 | a0001c0001t0039g0260 | 1 | NA19006.hp1 | intron_variant | MODIFIER | c.420+9303G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95017826 | ||||||
chr1:95017861
|
A | G | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+9268T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95017861 | ||||||
chr1:95017871
|
G | C | 1 | a0001c0001t0186g0328 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.420+9258C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95017871 | ||||||
chr1:95018075
|
A | G | 1 | a0001c0001t0001g0319 | 1 | HG04228.hp2 | intron_variant | MODIFIER | c.420+9054T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95018075 | ||||||
chr1:95018169
|
A | G | 25 | a0001c0001t0005g0185a0001c0001t0005g0189a0001c0001t0005g0190others(22): Show | 25 | HG00323.hp2 HG00544.hp1 HG01070.hp2 others(22): Show |
intron_variant | MODIFIER | c.420+8960T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95018169 | ||||||
chr1:95018312
|
G | C | 6 | a0001c0001t0044g0327a0001c0001t0045g0326a0001c0001t0045g0331others(3): Show | 6 | HG01261.hp2 HG01934.hp1 HG01952.hp2 others(3): Show |
intron_variant | MODIFIER | c.420+8817C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95018312 | ||||||
chr1:95018365
|
G | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+8764C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95018365 | ||||||
chr1:95018447
|
A | G | 2 | a0001c0001t0033g0034a0001c0001t0033g0040 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.420+8682T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95018447 | ||||||
chr1:95018492
|
T | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.420+8637A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95018492 | ||||||
chr1:95018577
|
C | T | 21 | a0001c0001t0004g0162a0001c0001t0008g0098a0001c0001t0008g0099others(18): Show | 21 | HG01069.hp2 HG01099.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.420+8552G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95018577 | ||||||
chr1:95018669
|
G | GAGAGCAG others(16): Show |
1 | a0001c0001t0006g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.420+8459_420+8460i others(25): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95018669 | ||||||
chr1:95018819
|
T | C | 1 | a0001c0001t0195g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.420+8310A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95018819 | ||||||
chr1:95018841
|
G | T | 1 | a0001c0001t0116g0048 | 1 | NA18954.hp1 | intron_variant | MODIFIER | c.420+8288C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95018841 | ||||||
chr1:95019262
|
T | A | 87 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(84): Show | 87 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(84): Show |
intron_variant | MODIFIER | c.420+7867A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95019262 | ||||||
chr1:95019451
|
A | G | 1 | a0001c0001t0032g0171 | 1 | NA18982.hp2 | intron_variant | MODIFIER | c.420+7678T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95019451 | ||||||
chr1:95019570
|
C | A | 1 | a0001c0001t0004g0163 | 1 | NA19002.hp1 | intron_variant | MODIFIER | c.420+7559G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95019570 | ||||||
chr1:95019619
|
G | C | 3 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272 | 3 | HG02109.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.420+7510C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95019619 | ||||||
chr1:95019623
|
A | G | 119 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(116): Show | 120 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.420+7506T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95019623 | ||||||
chr1:95019639
|
G | T | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(14): Show | 17 | HG00735.hp1 HG02572.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.420+7490C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95019639 | ||||||
chr1:95019837
|
G | A | 83 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(80): Show | 84 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.420+7292C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95019837 | ||||||
chr1:95019868
|
A | G | 270 | a0001c0001t0001g0289a0001c0001t0002g0213a0001c0001t0002g0218others(267): Show | 272 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(269): Show |
intron_variant | MODIFIER | c.420+7261T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95019868 | ||||||
chr1:95019920
|
G | T | 21 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0100others(18): Show | 21 | HG01069.hp2 HG01099.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.420+7209C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95019920 | ||||||
chr1:95020048
|
T | C | 259 | a0001c0001t0001g0289a0001c0001t0002g0213a0001c0001t0002g0218others(256): Show | 261 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(258): Show |
intron_variant | MODIFIER | c.420+7081A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95020048 | ||||||
chr1:95020123
|
A | G | 242 | a0001c0001t0001g0289a0001c0001t0002g0213a0001c0001t0002g0218others(239): Show | 244 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.420+7006T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95020123 | ||||||
chr1:95020172
|
A | C | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+6957T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95020172 | ||||||
chr1:95020269
|
A | C | 242 | a0001c0001t0001g0289a0001c0001t0002g0213a0001c0001t0002g0218others(239): Show | 244 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(241): Show |
intron_variant | MODIFIER | c.420+6860T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95020269 | ||||||
chr1:95020287
|
C | T | 7 | a0001c0001t0016g0123a0001c0001t0016g0124a0001c0001t0016g0128others(4): Show | 7 | HG00735.hp2 HG01081.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.420+6842G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95020287 | ||||||
chr1:95020312
|
T | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.420+6817A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95020312 | ||||||
chr1:95020429
|
C | T | 28 | a0001c0001t0003g0002a0001c0001t0003g0130a0001c0001t0003g0133others(25): Show | 29 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.420+6700G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95020429 | ||||||
chr1:95020431
|
A | C | 3 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272 | 3 | HG02109.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.420+6698T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95020431 | ||||||
chr1:95020699
|
T | C | 1 | a0001c0001t0186g0328 | 1 | NA18956.hp2 | intron_variant | MODIFIER | c.420+6430A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95020699 | ||||||
chr1:95020712
|
T | C | 5 | a0001c0001t0018g0118a0001c0001t0018g0119a0001c0001t0018g0120others(2): Show | 5 | HG01074.hp1 HG01167.hp2 HG01169.hp1 others(2): Show |
intron_variant | MODIFIER | c.420+6417A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95020712 | ||||||
chr1:95020738
|
C | CA | 258 | a0001c0001t0001g0289a0001c0001t0002g0213a0001c0001t0002g0218others(255): Show | 259 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(256): Show |
intron_variant | MODIFIER | c.420+6390dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95020738 | ||||||
chr1:95020738
|
C | CAA | 16 | a0001c0001t0003g0130a0001c0001t0003g0141a0001c0001t0003g0142others(13): Show | 16 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(13): Show |
intron_variant | MODIFIER | c.420+6389_420+6390d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95020738 | ||||||
chr1:95020738
|
C | CAAA | 16 | a0001c0001t0003g0002a0001c0001t0003g0133a0001c0001t0003g0140others(13): Show | 17 | HG02027.hp2 NA18747.hp2 NA18939.hp2 others(14): Show |
intron_variant | MODIFIER | c.420+6388_420+6390d others(5): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95020738 | ||||||
chr1:95021195
|
A | C | 83 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(80): Show | 84 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(81): Show |
intron_variant | MODIFIER | c.420+5934T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95021195 | ||||||
chr1:95021280
|
C | T | 3 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272 | 3 | HG02109.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.420+5849G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95021280 | ||||||
chr1:95021310
|
A | G | 30 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(27): Show | 30 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(27): Show |
intron_variant | MODIFIER | c.420+5819T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95021310 | ||||||
chr1:95021380
|
C | T | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.420+5749G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95021380 | ||||||
chr1:95021767
|
G | A | 3 | a0001c0001t0049g0019a0001c0001t0052g0067a0001c0001t0082g0049 | 3 | HG01891.hp2 HG02145.hp1 HG02559.hp2 |
intron_variant | MODIFIER | c.420+5362C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95021767 | ||||||
chr1:95022067
|
C | T | 14 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(11): Show | 14 | HG00735.hp1 HG02572.hp1 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.420+5062G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95022067 | ||||||
chr1:95022171
|
A | C | 1 | a0001c0001t0021g0290 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.420+4958T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95022171 | ||||||
chr1:95022532
|
G | A | 21 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0100others(18): Show | 21 | HG01069.hp2 HG01099.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.420+4597C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95022532 | ||||||
chr1:95022756
|
T | C | 1 | a0001c0001t0021g0285 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.420+4373A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95022756 | ||||||
chr1:95022967
|
A | T | 2 | a0001c0001t0033g0034a0001c0001t0033g0040 | 2 | HG03516.hp1 NA20300.hp1 |
intron_variant | MODIFIER | c.420+4162T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95022967 | ||||||
chr1:95022993
|
A | G | 1 | a0001c0001t0195g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.420+4136T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95022993 | ||||||
chr1:95023366
|
C | T | 1 | a0001c0002t0126g0183 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.420+3763G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95023366 | ||||||
chr1:95023413
|
C | T | 1 | a0001c0001t0002g0247 | 1 | NA18994.hp1 | intron_variant | MODIFIER | c.420+3716G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95023413 | ||||||
chr1:95023414
|
G | A | 3 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272 | 3 | HG02109.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.420+3715C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95023414 | ||||||
chr1:95023504
|
A | T | 4 | a0001c0001t0018g0118a0001c0001t0018g0119a0001c0001t0018g0120others(1): Show | 4 | HG01074.hp1 HG01167.hp2 HG01169.hp1 others(1): Show |
intron_variant | MODIFIER | c.420+3625T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95023504 | ||||||
chr1:95023664
|
A | G | 8 | a0001c0001t0001g0289a0001c0001t0016g0123a0001c0001t0016g0124others(5): Show | 8 | HG00735.hp2 HG01081.hp1 HG02280.hp1 others(5): Show |
intron_variant | MODIFIER | c.420+3465T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95023664 | ||||||
chr1:95024034
|
T | A | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(14): Show | 17 | HG00735.hp1 HG02572.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.420+3095A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95024034 | ||||||
chr1:95024158
|
T | C | 2 | a0001c0001t0004g0111a0001c0001t0104g0112 | 2 | HG01169.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.420+2971A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95024158 | ||||||
chr1:95024263
|
G | C | 101 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(98): Show | 102 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.420+2866C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95024263 | ||||||
chr1:95024269
|
G | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.420+2860C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95024269 | ||||||
chr1:95024482
|
T | C | 3 | a0001c0001t0010g0134a0001c0001t0010g0146a0001c0001t0083g0122 | 3 | NA18960.hp2 NA18967.hp2 NA19084.hp1 |
intron_variant | MODIFIER | c.420+2647A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95024482 | ||||||
chr1:95024504
|
T | C | 1 | a0001c0001t0164g0372 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.420+2625A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95024504 | ||||||
chr1:95024741
|
C | T | 1 | a0001c0001t0009g0350 | 1 | NA18953.hp1 | intron_variant | MODIFIER | c.420+2388G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95024741 | ||||||
chr1:95025045
|
C | A | 1 | a0001c0001t0015g0046 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.420+2084G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95025045 | ||||||
chr1:95025073
|
C | A | 3 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272 | 3 | HG02109.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.420+2056G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95025073 | ||||||
chr1:95025198
|
C | T | 7 | a0001c0001t0017g0312a0001c0001t0017g0378a0001c0001t0017g0380others(4): Show | 7 | HG00609.hp2 HG02040.hp1 HG02071.hp1 others(4): Show |
intron_variant | MODIFIER | c.420+1931G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95025198 | ||||||
chr1:95025270
|
A | C | 3 | a0001c0001t0001g0284a0001c0001t0021g0285a0001c0001t0094g0288 | 3 | HG02630.hp2 HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.420+1859T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95025270 | ||||||
chr1:95025474
|
G | C | 4 | a0001c0001t0002g0247a0001c0001t0107g0233a0001c0001t0138g0248others(1): Show | 4 | HG00438.hp1 NA18959.hp1 NA18994.hp1 others(1): Show |
intron_variant | MODIFIER | c.420+1655C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95025474 | ||||||
chr1:95025694
|
C | G | 385 | a0001c0001t0001g0115a0001c0001t0001g0194a0001c0001t0001g0276others(382): Show | 387 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(384): Show |
intron_variant | MODIFIER | c.420+1435G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95025694 | ||||||
chr1:95025705
|
T | C | 64 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(61): Show | 65 | HG00639.hp1 HG01081.hp2 HG01243.hp2 others(62): Show |
intron_variant | MODIFIER | c.420+1424A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95025705 | ||||||
chr1:95025761
|
T | G | 14 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(11): Show | 14 | HG00735.hp1 HG02572.hp1 HG02602.hp1 others(11): Show |
intron_variant | MODIFIER | c.420+1368A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95025761 | ||||||
chr1:95025795
|
T | C | 1 | a0001c0001t0074g0382 | 1 | NA19000.hp2 | intron_variant | MODIFIER | c.420+1334A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95025795 | ||||||
chr1:95026174
|
C | T | 1 | a0001c0001t0003g0141 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.420+955G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95026174 | ||||||
chr1:95026462
|
A | ATG | 85 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0001g0317others(82): Show | 86 | HG00408.hp1 HG00597.hp1 HG00597.hp2 others(83): Show |
intron_variant | MODIFIER | c.420+665_420+666dup others(2): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95026462 | ||||||
chr1:95026462
|
A | ATGTG | 18 | a0001c0001t0004g0170a0001c0001t0009g0316a0001c0001t0014g0033others(15): Show | 18 | HG00140.hp1 HG00544.hp1 HG00639.hp2 others(15): Show |
intron_variant | MODIFIER | c.420+663_420+666dup others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95026462 | ||||||
chr1:95026462
|
A | ATGTGTG | 6 | a0001c0001t0033g0034a0001c0001t0078g0089a0001c0001t0104g0112others(3): Show | 6 | HG00099.hp1 HG01978.hp2 HG01993.hp2 others(3): Show |
intron_variant | MODIFIER | c.420+661_420+666dup others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95026462 | ||||||
chr1:95026462
|
A | ATGTGTGT others(1): Show |
9 | a0001c0001t0024g0375a0001c0001t0024g0376a0001c0001t0024g0377others(6): Show | 9 | HG00642.hp2 HG01433.hp1 HG01884.hp1 others(6): Show |
intron_variant | MODIFIER | c.420+659_420+666dup others(8): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95026462 | ||||||
chr1:95026462
|
A | ATGTGTGT others(3): Show |
4 | a0001c0001t0017g0312a0001c0001t0017g0380a0001c0001t0017g0381others(1): Show | 4 | HG00609.hp2 HG02040.hp1 NA19000.hp2 others(1): Show |
intron_variant | MODIFIER | c.420+657_420+666dup others(10): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95026462 | ||||||
chr1:95026462
|
ATG | A | 74 | a0001c0001t0001g0194a0001c0001t0001g0282a0001c0001t0001g0293others(71): Show | 75 | HG00408.hp2 HG00423.hp2 HG00621.hp2 others(72): Show |
intron_variant | MODIFIER | c.420+665_420+666del others(2): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95026462 | ||||||
chr1:95026462
|
ATGTG | A | 16 | a0001c0001t0005g0203a0001c0001t0012g0092a0001c0001t0012g0093others(13): Show | 16 | HG01069.hp2 HG01099.hp2 HG01192.hp2 others(13): Show |
intron_variant | MODIFIER | c.420+663_420+666del others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95026462 | ||||||
chr1:95026462
|
ATGTGTG | A | 6 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(3): Show | 6 | HG00735.hp1 HG01109.hp2 HG02258.hp2 others(3): Show |
intron_variant | MODIFIER | c.420+661_420+666del others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95026462 | ||||||
chr1:95026504
|
A | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.420+625T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95026504 | ||||||
chr1:95026515
|
A | T | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.420+614T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95026515 | ||||||
chr1:95026570
|
G | A | 2 | a0001c0001t0004g0170a0001c0001t0165g0158 | 2 | HG03490.hp1 HG03927.hp2 |
intron_variant | MODIFIER | c.420+559C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95026570 | ||||||
chr1:95026655
|
G | A | 3 | a0001c0001t0026g0015a0001c0001t0026g0017a0001c0001t0114g0016 | 3 | HG03688.hp2 HG03834.hp2 HG04204.hp2 |
intron_variant | MODIFIER | c.420+474C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95026655 | ||||||
chr1:95026662
|
CT | C | 100 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(97): Show | 101 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(98): Show |
intron_variant | MODIFIER | c.420+466delA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95026662 | ||||||
chr1:95026674
|
A | T | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.420+455T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95026674 | ||||||
chr1:95026699
|
C | T | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.420+430G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95026699 | ||||||
chr1:95026700
|
G | A | 1 | a0001c0001t0001g0359 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.420+429C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95026700 | ||||||
chr1:95026916
|
C | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.420+213G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95026916 | ||||||
chr1:95027110
|
T | C | 2 | a0001c0001t0004g0165a0001c0001t0070g0168 | 2 | NA19057.hp1 NA19079.hp1 |
intron_variant | MODIFIER | c.420+19A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 3/3 | chr1 | 95027110 | ||||||
chr1:95027351
|
C | T | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-91G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95027351 | ||||||
chr1:95027620
|
C | T | 1 | a0001c0001t0038g0007 | 1 | NA20129.hp1 | intron_variant | MODIFIER | c.289-360G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95027620 | ||||||
chr1:95027705
|
C | T | 119 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(116): Show | 120 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(117): Show |
intron_variant | MODIFIER | c.289-445G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95027705 | ||||||
chr1:95027723
|
C | T | 1 | a0001c0001t0195g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.289-463G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95027723 | ||||||
chr1:95027749
|
G | A | 1 | a0001c0001t0001g0334 | 1 | NA21309.hp1 | intron_variant | MODIFIER | c.289-489C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95027749 | ||||||
chr1:95027977
|
A | G | 2 | a0001c0001t0020g0076a0001c0001t0020g0077 | 2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.289-717T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95027977 | ||||||
chr1:95028017
|
T | A | 1 | a0001c0001t0036g0108 | 1 | HG02486.hp2 | intron_variant | MODIFIER | c.289-757A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95028017 | ||||||
chr1:95028419
|
G | A | 1 | a0001c0001t0037g0009 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.289-1159C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95028419 | ||||||
chr1:95028474
|
C | T | 1 | a0001c0001t0160g0109 | 1 | HG03098.hp2 | intron_variant | MODIFIER | c.289-1214G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95028474 | ||||||
chr1:95028497
|
C | T | 1 | a0001c0001t0076g0379 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.289-1237G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95028497 | ||||||
chr1:95028566
|
C | T | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(14): Show | 17 | HG00735.hp1 HG02572.hp1 HG02602.hp1 others(14): Show |
intron_variant | MODIFIER | c.289-1306G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95028566 | ||||||
chr1:95028670
|
A | T | 101 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(98): Show | 102 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.289-1410T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95028670 | ||||||
chr1:95028673
|
G | GTTGGGTG others(1): Show |
101 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(98): Show | 102 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.289-1414_289-1413i others(10): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95028673 | ||||||
chr1:95028680
|
T | G | 2 | a0001c0001t0040g0065a0001c0001t0040g0066 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.289-1420A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95028680 | ||||||
chr1:95028780
|
T | C | 2 | a0001c0001t0007g0239a0001c0001t0109g0237 | 2 | HG01358.hp1 HG01361.hp1 |
intron_variant | MODIFIER | c.289-1520A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95028780 | ||||||
chr1:95029208
|
A | AT | 260 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(257): Show | 262 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(259): Show |
intron_variant | MODIFIER | c.289-1949_289-1948i others(3): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95029208 | ||||||
chr1:95029275
|
T | C | 21 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0100others(18): Show | 21 | HG01069.hp2 HG01099.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.289-2015A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95029275 | ||||||
chr1:95029718
|
G | T | 1 | a0001c0001t0002g0306 | 1 | NA19088.hp1 | intron_variant | MODIFIER | c.289-2458C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95029718 | ||||||
chr1:95029769
|
G | A | 1 | a0001c0001t0164g0372 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.289-2509C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95029769 | ||||||
chr1:95030113
|
A | C | 1 | a0001c0001t0153g0351 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.289-2853T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95030113 | ||||||
chr1:95030267
|
T | C | 1 | a0001c0001t0152g0292 | 1 | HG03492.hp2 | intron_variant | MODIFIER | c.289-3007A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95030267 | ||||||
chr1:95030407
|
T | C | 1 | a0001c0001t0001g0194 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.289-3147A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95030407 | ||||||
chr1:95030456
|
G | C | 20 | a0001c0001t0001g0282a0001c0001t0001g0295a0001c0001t0001g0300others(17): Show | 20 | HG00558.hp1 HG00621.hp1 HG02165.hp1 others(17): Show |
intron_variant | MODIFIER | c.289-3196C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95030456 | ||||||
chr1:95030673
|
C | T | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-3413G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95030673 | ||||||
chr1:95030736
|
G | A | 10 | a0001c0001t0004g0160a0001c0001t0004g0162a0001c0001t0004g0163others(7): Show | 10 | HG00597.hp2 HG00673.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.289-3476C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95030736 | ||||||
chr1:95030752
|
A | G | 3 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272 | 3 | HG02109.hp2 HG02886.hp2 HG03195.hp2 |
intron_variant | MODIFIER | c.289-3492T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95030752 | ||||||
chr1:95030770
|
C | A | 1 | a0001c0001t0001g0276 | 1 | HG02886.hp1 | intron_variant | MODIFIER | c.289-3510G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95030770 | ||||||
chr1:95030783
|
C | T | 2 | a0001c0001t0040g0065a0001c0001t0040g0066 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.289-3523G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95030783 | ||||||
chr1:95030898
|
G | C | 2 | a0001c0001t0054g0021a0001c0001t0062g0024 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.289-3638C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95030898 | ||||||
chr1:95030935
|
G | C | 2 | a0001c0001t0131g0192a0001c0001t0177g0198 | 2 | NA18986.hp2 NA18988.hp1 |
intron_variant | MODIFIER | c.289-3675C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95030935 | ||||||
chr1:95031029
|
C | T | 4 | a0001c0001t0171g0369a0001c0001t0175g0371a0001c0001t0193g0370others(1): Show | 4 | HG00642.hp2 HG01978.hp2 HG01993.hp2 others(1): Show |
intron_variant | MODIFIER | c.289-3769G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95031029 | ||||||
chr1:95031460
|
G | T | 3 | a0001c0001t0001g0284a0001c0001t0021g0285a0001c0001t0094g0288 | 3 | HG02630.hp2 HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.289-4200C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95031460 | ||||||
chr1:95031601
|
C | T | 1 | a0001c0001t0103g0042 | 1 | HG00639.hp1 | intron_variant | MODIFIER | c.289-4341G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95031601 | ||||||
chr1:95031645
|
T | C | 1 | a0001c0001t0029g0031 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.289-4385A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95031645 | ||||||
chr1:95031674
|
G | A | 1 | a0001c0001t0005g0191 | 1 | NA18966.hp2 | intron_variant | MODIFIER | c.289-4414C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95031674 | ||||||
chr1:95031831
|
G | A | 1 | a0001c0001t0063g0104 | 1 | HG02622.hp1 | intron_variant | MODIFIER | c.289-4571C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95031831 | ||||||
chr1:95031880
|
C | A | 1 | a0001c0001t0163g0325 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.289-4620G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95031880 | ||||||
chr1:95031945
|
A | G | 7 | a0001c0001t0014g0013a0001c0001t0014g0014a0001c0001t0020g0074others(4): Show | 7 | HG02258.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.289-4685T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95031945 | ||||||
chr1:95031957
|
C | T | 2 | a0001c0001t0069g0366a0001c0001t0123g0117 | 2 | HG00597.hp1 NA20805.hp1 |
intron_variant | MODIFIER | c.289-4697G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95031957 | ||||||
chr1:95031971
|
C | T | 1 | a0001c0001t0167g0254 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.289-4711G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95031971 | ||||||
chr1:95032039
|
C | T | 1 | a0001c0001t0001g0293 | 1 | HG02300.hp1 | intron_variant | MODIFIER | c.289-4779G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95032039 | ||||||
chr1:95032089
|
G | T | 4 | a0001c0001t0003g0140a0001c0001t0034g0139a0001c0001t0086g0131others(1): Show | 4 | NA18939.hp2 NA18956.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.289-4829C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95032089 | ||||||
chr1:95032099
|
G | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-4839C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95032099 | ||||||
chr1:95032174
|
T | TA | 9 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(6): Show | 9 | HG01109.hp2 HG02071.hp1 HG02258.hp2 others(6): Show |
intron_variant | MODIFIER | c.289-4915dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95032174 | ||||||
chr1:95032189
|
T | A | 8 | a0001c0001t0001g0347a0001c0001t0044g0327a0001c0001t0045g0326others(5): Show | 8 | HG01261.hp2 HG01934.hp1 HG01952.hp2 others(5): Show |
intron_variant | MODIFIER | c.289-4929A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95032189 | ||||||
chr1:95032237
|
A | C | 1 | a0001c0001t0018g0118 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.289-4977T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95032237 | ||||||
chr1:95032245
|
C | A | 1 | a0001c0001t0007g0252 | 1 | HG01123.hp2 | intron_variant | MODIFIER | c.289-4985G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95032245 | ||||||
chr1:95032300
|
A | G | 1 | a0001c0001t0018g0118 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.289-5040T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95032300 | ||||||
chr1:95032327
|
A | G | 1 | a0001c0001t0018g0118 | 1 | HG01169.hp1 | intron_variant | MODIFIER | c.289-5067T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95032327 | ||||||
chr1:95032338
|
C | T | 1 | a0001c0001t0003g0152 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.289-5078G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95032338 | ||||||
chr1:95032503
|
T | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-5243A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95032503 | ||||||
chr1:95032572
|
G | A | 1 | a0001c0001t0001g0359 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.289-5312C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95032572 | ||||||
chr1:95033063
|
A | G | 1 | a0001c0001t0003g0141 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.289-5803T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033063 | ||||||
chr1:95033064
|
T | C | 101 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(98): Show | 102 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.289-5804A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033064 | ||||||
chr1:95033402
|
C | CAT | 34 | a0001c0001t0001g0115a0001c0001t0001g0276a0001c0001t0001g0278others(31): Show | 35 | HG00639.hp1 HG01069.hp2 HG01099.hp2 others(32): Show |
intron_variant | MODIFIER | c.289-6144_289-6143d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033402 | ||||||
chr1:95033408
|
T | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-6148A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033408 | ||||||
chr1:95033418
|
TATAC | T | 13 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0004g0256others(10): Show | 13 | HG01258.hp2 HG02074.hp1 HG02135.hp2 others(10): Show |
intron_variant | MODIFIER | c.289-6162_289-6159d others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033418 | ||||||
chr1:95033418
|
TATACACA others(3): Show |
T | 7 | a0001c0001t0016g0123a0001c0001t0016g0124a0001c0001t0016g0128others(4): Show | 7 | HG00735.hp2 HG01081.hp1 HG02280.hp1 others(4): Show |
intron_variant | MODIFIER | c.289-6168_289-6159d others(12): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033418 | ||||||
chr1:95033420
|
T | C | 44 | a0001c0001t0013g0053a0001c0001t0013g0054a0001c0001t0013g0059others(41): Show | 44 | HG01081.hp2 HG01109.hp2 HG01255.hp2 others(41): Show |
intron_variant | MODIFIER | c.289-6160A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033420 | ||||||
chr1:95033420
|
T | TAC | 12 | a0001c0001t0001g0321a0001c0001t0010g0134a0001c0001t0010g0135others(9): Show | 12 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(9): Show |
intron_variant | MODIFIER | c.289-6162_289-6161d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033420 | ||||||
chr1:95033420
|
T | TACACAC | 13 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(10): Show | 13 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(10): Show |
intron_variant | MODIFIER | c.289-6166_289-6161d others(8): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033420 | ||||||
chr1:95033420
|
T | TACACACA others(3): Show |
2 | a0001c0001t0054g0021a0001c0001t0062g0024 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.289-6170_289-6161d others(12): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033420 | ||||||
chr1:95033420
|
TAC | T | 57 | a0001c0001t0001g0319a0001c0001t0001g0347a0001c0001t0002g0245others(54): Show | 57 | HG00140.hp1 HG00423.hp1 HG00597.hp1 others(54): Show |
intron_variant | MODIFIER | c.289-6162_289-6161d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033420 | ||||||
chr1:95033420
|
TACAC | T | 58 | a0001c0001t0002g0221a0001c0001t0002g0223a0001c0001t0002g0227others(55): Show | 58 | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(55): Show |
intron_variant | MODIFIER | c.289-6164_289-6161d others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033420 | ||||||
chr1:95033420
|
TACACACA others(3): Show |
T | 1 | a0001c0001t0019g0216 | 1 | HG01928.hp2 | intron_variant | MODIFIER | c.289-6170_289-6161d others(12): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033420 | ||||||
chr1:95033422
|
C | T | 6 | a0001c0001t0040g0065a0001c0001t0040g0066a0001c0001t0057g0159others(3): Show | 6 | HG02886.hp2 HG03139.hp2 HG03471.hp2 others(3): Show |
intron_variant | MODIFIER | c.289-6162G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033422 | ||||||
chr1:95033424
|
C | T | 20 | a0001c0001t0002g0245a0001c0001t0005g0196a0001c0001t0005g0211others(17): Show | 20 | HG00140.hp1 HG00423.hp1 HG00609.hp2 others(17): Show |
intron_variant | MODIFIER | c.289-6164G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033424 | ||||||
chr1:95033426
|
C | T | 3 | a0001c0001t0005g0268a0001c0001t0068g0003a0001c0001t0078g0089 | 3 | HG02451.hp2 HG04199.hp1 HG06807.hp1 |
intron_variant | MODIFIER | c.289-6166G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033426 | ||||||
chr1:95033442
|
C | T | 2 | a0001c0001t0047g0241a0001c0001t0047g0242 | 2 | HG00741.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.289-6182G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033442 | ||||||
chr1:95033446
|
T | C | 8 | a0001c0001t0001g0282a0001c0001t0016g0123a0001c0001t0016g0124others(5): Show | 8 | HG00735.hp2 HG01081.hp1 HG02165.hp1 others(5): Show |
intron_variant | MODIFIER | c.289-6186A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033446 | ||||||
chr1:95033456
|
T | C | 2 | a0001c0001t0047g0241a0001c0001t0047g0242 | 2 | HG00741.hp2 HG03225.hp2 |
intron_variant | MODIFIER | c.289-6196A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033456 | ||||||
chr1:95033458
|
C | T | 1 | a0001c0001t0010g0135 | 1 | HG00621.hp2 | intron_variant | MODIFIER | c.289-6198G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033458 | ||||||
chr1:95033599
|
C | G | 2 | a0001c0001t0095g0091a0001c0001t0158g0090 | 2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.289-6339G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033599 | ||||||
chr1:95033625
|
T | C | 1 | a0001c0001t0002g0230 | 1 | NA19075.hp1 | intron_variant | MODIFIER | c.289-6365A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033625 | ||||||
chr1:95033630
|
T | C | 1 | a0001c0001t0193g0370 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.289-6370A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033630 | ||||||
chr1:95033716
|
T | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-6456A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033716 | ||||||
chr1:95033787
|
C | G | 8 | a0001c0001t0001g0115a0001c0001t0001g0276a0001c0001t0001g0278others(5): Show | 8 | HG01891.hp1 HG02280.hp2 HG02451.hp1 others(5): Show |
intron_variant | MODIFIER | c.289-6527G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033787 | ||||||
chr1:95033892
|
A | C | 2 | a0001c0001t0054g0021a0001c0001t0062g0024 | 2 | HG03041.hp2 HG03579.hp1 |
intron_variant | MODIFIER | c.289-6632T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033892 | ||||||
chr1:95033938
|
C | T | 1 | a0001c0001t0026g0017 | 1 | HG03688.hp2 | intron_variant | MODIFIER | c.289-6678G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033938 | ||||||
chr1:95033973
|
G | A | 1 | a0001c0001t0146g0287 | 1 | NA20129.hp2 | intron_variant | MODIFIER | c.289-6713C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95033973 | ||||||
chr1:95034020
|
C | T | 33 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(30): Show | 33 | HG00423.hp1 HG00438.hp1 HG00558.hp2 others(30): Show |
intron_variant | MODIFIER | c.289-6760G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95034020 | ||||||
chr1:95034162
|
T | C | 265 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0221others(262): Show | 267 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(264): Show |
intron_variant | MODIFIER | c.289-6902A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95034162 | ||||||
chr1:95034191
|
C | T | 1 | a0001c0001t0066g0167 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.289-6931G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95034191 | ||||||
chr1:95034192
|
TCA | T | 6 | a0001c0001t0001g0295a0001c0001t0001g0300a0001c0001t0001g0301others(3): Show | 6 | HG00621.hp1 NA18946.hp1 NA18954.hp2 others(3): Show |
intron_variant | MODIFIER | c.289-6934_289-6933d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95034192 | ||||||
chr1:95034534
|
G | A | 2 | a0001c0001t0170g0367a0001c0001t0192g0368 | 2 | HG00140.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.289-7274C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95034534 | ||||||
chr1:95034593
|
C | T | 101 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(98): Show | 102 | HG00099.hp1 HG00140.hp1 HG00609.hp2 others(99): Show |
intron_variant | MODIFIER | c.289-7333G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95034593 | ||||||
chr1:95034724
|
A | G | 1 | a0001c0001t0062g0024 | 1 | HG03579.hp1 | intron_variant | MODIFIER | c.289-7464T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95034724 | ||||||
chr1:95034800
|
C | T | 1 | a0001c0001t0185g0333 | 1 | HG01109.hp1 | intron_variant | MODIFIER | c.289-7540G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95034800 | ||||||
chr1:95034882
|
GA | G | 7 | a0001c0001t0011g0280a0001c0001t0011g0297a0001c0001t0011g0303others(4): Show | 7 | NA18945.hp1 NA18952.hp1 NA18959.hp2 others(4): Show |
intron_variant | MODIFIER | c.289-7623delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95034882 | ||||||
chr1:95034890
|
C | T | 2 | a0001c0001t0040g0065a0001c0001t0040g0066 | 2 | HG03139.hp2 HG03471.hp2 |
intron_variant | MODIFIER | c.289-7630G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95034890 | ||||||
chr1:95034938
|
G | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.289-7678C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95034938 | ||||||
chr1:95034957
|
C | T | 1 | a0001c0001t0071g0174 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.289-7697G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95034957 | ||||||
chr1:95034986
|
C | T | 1 | a0001c0001t0044g0346 | 1 | NA19081.hp2 | intron_variant | MODIFIER | c.289-7726G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95034986 | ||||||
chr1:95034999
|
G | A | 2 | a0001c0001t0170g0367a0001c0001t0192g0368 | 2 | HG00140.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.289-7739C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95034999 | ||||||
chr1:95035174
|
T | TTTTTG | 6 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.289-7919_289-7915d others(7): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95035174 | ||||||
chr1:95035174
|
TTTTTGTT others(3): Show |
T | 4 | a0001c0001t0036g0107a0001c0001t0036g0108a0001c0001t0089g0106others(1): Show | 4 | HG02486.hp2 HG03098.hp2 HG03471.hp1 others(1): Show |
intron_variant | MODIFIER | c.289-7924_289-7915d others(12): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95035174 | ||||||
chr1:95035208
|
T | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-7948A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95035208 | ||||||
chr1:95035225
|
T | C | 1 | a0001c0001t0195g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.289-7965A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95035225 | ||||||
chr1:95035355
|
A | G | 378 | a0001c0001t0001g0115a0001c0001t0001g0194a0001c0001t0001g0276others(375): Show | 380 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(377): Show |
intron_variant | MODIFIER | c.289-8095T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95035355 | ||||||
chr1:95035416
|
C | T | 1 | a0001c0001t0040g0066 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.289-8156G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95035416 | ||||||
chr1:95035462
|
C | T | 1 | a0001c0001t0016g0267 | 1 | NA21309.hp2 | intron_variant | MODIFIER | c.289-8202G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95035462 | ||||||
chr1:95035499
|
A | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-8239T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95035499 | ||||||
chr1:95035501
|
A | G | 1 | a0001c0001t0012g0093 | 1 | NA20805.hp2 | intron_variant | MODIFIER | c.289-8241T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95035501 | ||||||
chr1:95035502
|
T | C | 1 | a0001c0001t0003g0141 | 1 | HG00423.hp2 | intron_variant | MODIFIER | c.289-8242A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95035502 | ||||||
chr1:95035626
|
C | A | 4 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272others(1): Show | 4 | HG02109.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.289-8366G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95035626 | ||||||
chr1:95035754
|
G | T | 6 | a0001c0001t0018g0118a0001c0001t0018g0119a0001c0001t0018g0120others(3): Show | 6 | HG00597.hp1 HG01074.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.289-8494C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95035754 | ||||||
chr1:95035846
|
C | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-8586G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95035846 | ||||||
chr1:95036002
|
C | T | 1 | a0001c0001t0031g0354 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.289-8742G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036002 | ||||||
chr1:95036047
|
T | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.289-8787A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036047 | ||||||
chr1:95036120
|
A | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-8860T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036120 | ||||||
chr1:95036177
|
T | C | 4 | a0001c0001t0024g0375a0001c0001t0024g0376a0001c0001t0024g0377others(1): Show | 4 | HG01884.hp1 HG02647.hp2 HG02896.hp1 others(1): Show |
intron_variant | MODIFIER | c.289-8917A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036177 | ||||||
chr1:95036228
|
T | C | 1 | a0001c0001t0003g0142 | 1 | NA19065.hp1 | intron_variant | MODIFIER | c.289-8968A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036228 | ||||||
chr1:95036419
|
CT | C | 69 | a0001c0001t0001g0300a0001c0001t0001g0307a0001c0001t0001g0313others(66): Show | 70 | HG00140.hp1 HG00323.hp1 HG00408.hp2 others(67): Show |
intron_variant | MODIFIER | c.289-9160delA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036419 | ||||||
chr1:95036419
|
CTT | C | 218 | a0001c0001t0001g0194a0001c0001t0002g0213a0001c0001t0002g0218others(215): Show | 219 | HG00099.hp1 HG00423.hp1 HG00438.hp1 others(216): Show |
intron_variant | MODIFIER | c.289-9161_289-9160d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036419 | ||||||
chr1:95036419
|
CTTT | C | 13 | a0001c0001t0002g0230a0001c0001t0018g0121a0001c0001t0020g0077others(10): Show | 13 | HG00323.hp2 HG01074.hp1 HG02109.hp2 others(10): Show |
intron_variant | MODIFIER | c.289-9162_289-9160d others(5): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036419 | ||||||
chr1:95036419
|
CTTTTTTT others(8): Show |
C | 2 | a0001c0001t0004g0111a0001c0001t0104g0112 | 2 | HG01169.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.289-9174_289-9160d others(17): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036419 | ||||||
chr1:95036462
|
T | C | 15 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(12): Show | 15 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.289-9202A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036462 | ||||||
chr1:95036481
|
C | T | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-9221G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036481 | ||||||
chr1:95036522
|
A | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-9262T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036522 | ||||||
chr1:95036558
|
T | C | 3 | a0001c0001t0001g0314a0001c0001t0001g0317a0001c0001t0001g0318 | 3 | HG01099.hp1 HG01516.hp1 HG01517.hp1 |
intron_variant | MODIFIER | c.289-9298A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036558 | ||||||
chr1:95036587
|
C | T | 1 | a0001c0001t0001g0194 | 1 | HG04199.hp2 | intron_variant | MODIFIER | c.289-9327G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036587 | ||||||
chr1:95036702
|
A | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-9442T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036702 | ||||||
chr1:95036703
|
G | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-9443C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036703 | ||||||
chr1:95036718
|
C | T | 3 | a0001c0001t0040g0065a0001c0001t0040g0066a0001c0001t0068g0003 | 3 | HG03139.hp2 HG03471.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.289-9458G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036718 | ||||||
chr1:95036772
|
A | T | 15 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(12): Show | 15 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(12): Show |
intron_variant | MODIFIER | c.289-9512T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036772 | ||||||
chr1:95036805
|
T | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-9545A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036805 | ||||||
chr1:95036872
|
T | C | 3 | a0001c0001t0001g0357a0001c0001t0001g0358a0001c0001t0001g0359 | 3 | NA18941.hp1 NA18955.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.289-9612A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95036872 | ||||||
chr1:95037047
|
C | G | 9 | a0001c0001t0001g0115a0001c0001t0001g0276a0001c0001t0001g0278others(6): Show | 9 | HG01891.hp1 HG02280.hp2 HG02451.hp1 others(6): Show |
intron_variant | MODIFIER | c.289-9787G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95037047 | ||||||
chr1:95037137
|
TTC | T | 26 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(23): Show | 26 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.289-9879_289-9878d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95037137 | ||||||
chr1:95037309
|
G | C | 43 | a0001c0001t0002g0259a0001c0001t0002g0275a0001c0001t0003g0002others(40): Show | 44 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.289-10049C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95037309 | ||||||
chr1:95037335
|
C | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-10075G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95037335 | ||||||
chr1:95037377
|
G | A | 1 | a0001c0001t0036g0107 | 1 | HG06807.hp2 | intron_variant | MODIFIER | c.289-10117C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95037377 | ||||||
chr1:95037531
|
G | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-10271C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95037531 | ||||||
chr1:95037548
|
A | C | 1 | a0001c0001t0043g0283 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.289-10288T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95037548 | ||||||
chr1:95037740
|
A | T | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-10480T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95037740 | ||||||
chr1:95037745
|
A | G | 1 | a0001c0002t0126g0183 | 1 | HG02074.hp1 | intron_variant | MODIFIER | c.289-10485T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95037745 | ||||||
chr1:95037792
|
T | C | 1 | a0001c0001t0097g0186 | 1 | HG00323.hp2 | intron_variant | MODIFIER | c.289-10532A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95037792 | ||||||
chr1:95037807
|
C | T | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-10547G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95037807 | ||||||
chr1:95038012
|
G | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-10752C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038012 | ||||||
chr1:95038121
|
T | C | 292 | a0001c0001t0001g0194a0001c0001t0002g0213a0001c0001t0002g0218others(289): Show | 294 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(291): Show |
intron_variant | MODIFIER | c.289-10861A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038121 | ||||||
chr1:95038132
|
C | CAAGAGTT others(338): Show |
1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-10873_289-1087 others(349): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038132 | ||||||
chr1:95038205
|
G | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-10945C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038205 | ||||||
chr1:95038278
|
A | G | 3 | a0001c0001t0014g0013a0001c0001t0014g0014a0001c0001t0075g0012 | 3 | HG02258.hp1 HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.289-11018T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038278 | ||||||
chr1:95038355
|
A | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-11095T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038355 | ||||||
chr1:95038411
|
C | T | 1 | a0001c0001t0001g0308 | 1 | HG00621.hp1 | intron_variant | MODIFIER | c.289-11151G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038411 | ||||||
chr1:95038444
|
G | A | 1 | a0001c0001t0076g0379 | 1 | HG02071.hp1 | intron_variant | MODIFIER | c.289-11184C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038444 | ||||||
chr1:95038603
|
T | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-11343A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038603 | ||||||
chr1:95038634
|
T | G | 6 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.289-11374A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038634 | ||||||
chr1:95038681
|
C | CA | 122 | a0001c0001t0001g0194a0001c0001t0001g0293a0001c0001t0002g0213others(119): Show | 123 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.289-11422dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038681 | ||||||
chr1:95038681
|
C | CAA | 7 | a0001c0001t0003g0130a0001c0001t0003g0145a0001c0001t0003g0270others(4): Show | 7 | HG02055.hp1 HG02129.hp1 HG04115.hp1 others(4): Show |
intron_variant | MODIFIER | c.289-11423_289-1142 others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038681 | ||||||
chr1:95038681
|
CA | C | 95 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(92): Show | 96 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(93): Show |
intron_variant | MODIFIER | c.289-11422delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038681 | ||||||
chr1:95038716
|
G | GT | 53 | a0001c0001t0001g0321a0001c0001t0001g0347a0001c0001t0001g0365others(50): Show | 53 | HG00438.hp1 HG00735.hp1 HG00735.hp2 others(50): Show |
intron_variant | MODIFIER | c.289-11457dupA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038716 | ||||||
chr1:95038716
|
GT | G | 15 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(12): Show | 16 | HG00639.hp1 HG01358.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.289-11457delA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038716 | ||||||
chr1:95038726
|
T | TG | 4 | a0001c0001t0002g0213a0001c0001t0002g0218a0001c0001t0002g0258others(1): Show | 4 | NA18978.hp2 NA19002.hp2 NA19058.hp1 others(1): Show |
intron_variant | MODIFIER | c.289-11467_289-1146 others(5): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038726 | ||||||
chr1:95038729
|
T | G | 1 | a0001c0001t0157g0343 | 1 | HG00140.hp2 | intron_variant | MODIFIER | c.289-11469A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038729 | ||||||
chr1:95038770
|
G | A | 1 | a0001c0001t0004g0170 | 1 | HG03490.hp1 | intron_variant | MODIFIER | c.289-11510C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038770 | ||||||
chr1:95038776
|
C | T | 6 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.289-11516G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038776 | ||||||
chr1:95038811
|
T | C | 1 | a0001c0001t0193g0370 | 1 | HG01993.hp2 | intron_variant | MODIFIER | c.289-11551A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038811 | ||||||
chr1:95038859
|
C | T | 2 | a0001c0001t0017g0378a0001c0001t0067g0050 | 2 | NA18992.hp1 NA19089.hp1 |
intron_variant | MODIFIER | c.289-11599G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038859 | ||||||
chr1:95038869
|
C | T | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-11609G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038869 | ||||||
chr1:95038896
|
AC | A | 4 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272others(1): Show | 4 | HG02109.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.289-11637delG | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038896 | ||||||
chr1:95038911
|
G | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-11651C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038911 | ||||||
chr1:95038929
|
C | T | 43 | a0001c0001t0002g0259a0001c0001t0002g0275a0001c0001t0003g0002others(40): Show | 44 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(41): Show |
intron_variant | MODIFIER | c.289-11669G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95038929 | ||||||
chr1:95039013
|
C | T | 1 | a0001c0001t0005g0196 | 1 | NA19080.hp1 | intron_variant | MODIFIER | c.289-11753G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95039013 | ||||||
chr1:95039014
|
G | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-11754C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95039014 | ||||||
chr1:95039016
|
C | T | 293 | a0001c0001t0001g0194a0001c0001t0002g0213a0001c0001t0002g0218others(290): Show | 295 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(292): Show |
intron_variant | MODIFIER | c.289-11756G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95039016 | ||||||
chr1:95039040
|
A | G | 21 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0100others(18): Show | 21 | HG01069.hp2 HG01099.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.289-11780T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95039040 | ||||||
chr1:95039080
|
T | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-11820A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95039080 | ||||||
chr1:95039156
|
C | T | 81 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.289-11896G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95039156 | ||||||
chr1:95039168
|
T | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-11908A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95039168 | ||||||
chr1:95039177
|
T | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-11917A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95039177 | ||||||
chr1:95039213
|
G | T | 1 | a0001c0001t0039g0249 | 1 | NA18978.hp2 | intron_variant | MODIFIER | c.289-11953C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95039213 | ||||||
chr1:95039354
|
A | G | 2 | a0001c0001t0025g0384a0001c0001t0025g0385 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.289-12094T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95039354 | ||||||
chr1:95039434
|
A | G | 18 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(15): Show | 18 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.289-12174T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95039434 | ||||||
chr1:95039475
|
G | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-12215C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95039475 | ||||||
chr1:95039481
|
T | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-12221A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95039481 | ||||||
chr1:95039529
|
C | T | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-12269G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95039529 | ||||||
chr1:95039551
|
C | T | 40 | a0001c0001t0002g0259a0001c0001t0002g0275a0001c0001t0003g0002others(37): Show | 41 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(38): Show |
intron_variant | MODIFIER | c.289-12291G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95039551 | ||||||
chr1:95039552
|
G | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-12292C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95039552 | ||||||
chr1:95039768
|
G | A | 78 | a0001c0001t0001g0194a0001c0001t0002g0213a0001c0001t0002g0218others(75): Show | 78 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(75): Show |
intron_variant | MODIFIER | c.289-12508C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95039768 | ||||||
chr1:95039895
|
G | A | 2 | a0001c0001t0019g0216a0001c0001t0068g0003 | 2 | HG01928.hp2 HG04199.hp1 |
intron_variant | MODIFIER | c.289-12635C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95039895 | ||||||
chr1:95040071
|
T | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-12811A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95040071 | ||||||
chr1:95040086
|
A | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-12826T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95040086 | ||||||
chr1:95040103
|
A | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-12843T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95040103 | ||||||
chr1:95040172
|
A | AAAAT | 145 | a0001c0001t0001g0301a0001c0001t0001g0342a0001c0001t0001g0358others(142): Show | 146 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(143): Show |
intron_variant | MODIFIER | c.289-12916_289-1291 others(8): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95040172 | ||||||
chr1:95040172
|
A | AAAATAAA others(1): Show |
20 | a0001c0001t0001g0284a0001c0001t0004g0111a0001c0001t0004g0163others(17): Show | 20 | HG00558.hp2 HG01169.hp2 HG02109.hp2 others(17): Show |
intron_variant | MODIFIER | c.289-12920_289-1291 others(12): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95040172 | ||||||
chr1:95040172
|
AAAAT | A | 7 | a0001c0001t0001g0282a0001c0001t0037g0009a0001c0001t0037g0018others(4): Show | 7 | HG01109.hp2 HG02165.hp1 HG02258.hp2 others(4): Show |
intron_variant | MODIFIER | c.289-12916_289-1291 others(8): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95040172 | ||||||
chr1:95040172
|
AAAATAAA others(1): Show |
A | 10 | a0001c0001t0001g0115a0001c0001t0001g0276a0001c0001t0001g0278others(7): Show | 10 | HG01891.hp1 HG02280.hp2 HG02451.hp1 others(7): Show |
intron_variant | MODIFIER | c.289-12920_289-1291 others(12): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95040172 | ||||||
chr1:95040279
|
A | G | 102 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(99): Show | 103 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(100): Show |
intron_variant | MODIFIER | c.289-13019T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95040279 | ||||||
chr1:95040503
|
A | G | 18 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(15): Show | 18 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.289-13243T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95040503 | ||||||
chr1:95040517
|
A | G | 1 | a0001c0001t0001g0359 | 1 | NA18941.hp1 | intron_variant | MODIFIER | c.289-13257T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95040517 | ||||||
chr1:95040568
|
TA | T | 18 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(15): Show | 18 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.289-13309delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95040568 | ||||||
chr1:95040613
|
G | A | 1 | a0001c0001t0004g0155 | 1 | HG01123.hp1 | intron_variant | MODIFIER | c.289-13353C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95040613 | ||||||
chr1:95040616
|
G | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-13356C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95040616 | ||||||
chr1:95040632
|
C | A | 122 | a0001c0001t0001g0194a0001c0001t0002g0213a0001c0001t0002g0218others(119): Show | 123 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.289-13372G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95040632 | ||||||
chr1:95040687
|
A | T | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-13427T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95040687 | ||||||
chr1:95040705
|
T | A | 294 | a0001c0001t0001g0115a0001c0001t0001g0194a0001c0001t0002g0213others(291): Show | 296 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(293): Show |
intron_variant | MODIFIER | c.289-13445A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95040705 | ||||||
chr1:95040719
|
A | G | 18 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(15): Show | 18 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.289-13459T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95040719 | ||||||
chr1:95040829
|
C | T | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-13569G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95040829 | ||||||
chr1:95041124
|
T | C | 1 | a0001c0001t0168g0064 | 1 | HG02922.hp2 | intron_variant | MODIFIER | c.289-13864A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95041124 | ||||||
chr1:95041171
|
T | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-13911A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95041171 | ||||||
chr1:95041176
|
C | T | 1 | a0001c0001t0158g0090 | 1 | HG02818.hp1 | intron_variant | MODIFIER | c.289-13916G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95041176 | ||||||
chr1:95041335
|
T | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-14075A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95041335 | ||||||
chr1:95041392
|
TGGGAGGC others(9): Show |
T | 1 | a0001c0001t0191g0299 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.289-14148_289-1413 others(20): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95041392 | ||||||
chr1:95041500
|
T | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-14240A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95041500 | ||||||
chr1:95041616
|
T | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-14356A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95041616 | ||||||
chr1:95041628
|
A | G | 4 | a0001c0001t0027g0204a0001c0001t0027g0207a0001c0001t0122g0206others(1): Show | 4 | HG00544.hp1 NA18955.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.289-14368T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95041628 | ||||||
chr1:95041699
|
C | A | 1 | a0001c0001t0164g0372 | 1 | HG00099.hp1 | intron_variant | MODIFIER | c.289-14439G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95041699 | ||||||
chr1:95041794
|
T | C | 3 | a0001c0001t0003g0130a0001c0001t0003g0270a0001c0001t0088g0129 | 3 | HG02129.hp1 NA18999.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.289-14534A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95041794 | ||||||
chr1:95041802
|
T | A | 1 | a0001c0001t0165g0158 | 1 | HG03927.hp2 | intron_variant | MODIFIER | c.289-14542A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95041802 | ||||||
chr1:95041961
|
A | G | 18 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(15): Show | 18 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.289-14701T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95041961 | ||||||
chr1:95042104
|
A | C | 4 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272others(1): Show | 4 | HG02109.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.289-14844T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95042104 | ||||||
chr1:95042122
|
T | C | 6 | a0001c0001t0025g0026a0001c0001t0025g0384a0001c0001t0025g0385others(3): Show | 6 | HG02602.hp1 HG02698.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.289-14862A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95042122 | ||||||
chr1:95042305
|
T | TAC | 21 | a0001c0001t0001g0362a0001c0001t0008g0098a0001c0001t0008g0099others(18): Show | 21 | HG00438.hp2 HG01175.hp1 HG01255.hp1 others(18): Show |
intron_variant | MODIFIER | c.289-15047_289-1504 others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95042305 | ||||||
chr1:95042305
|
T | TACAC | 7 | a0001c0001t0001g0335a0001c0001t0012g0092a0001c0001t0012g0093others(4): Show | 7 | HG00099.hp2 HG01099.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.289-15049_289-1504 others(8): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95042305 | ||||||
chr1:95042305
|
TAC | T | 251 | a0001c0001t0001g0115a0001c0001t0001g0194a0001c0001t0002g0213others(248): Show | 252 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(249): Show |
intron_variant | MODIFIER | c.289-15047_289-1504 others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95042305 | ||||||
chr1:95042305
|
TACAC | T | 6 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.289-15049_289-1504 others(8): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95042305 | ||||||
chr1:95042828
|
T | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-15568A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95042828 | ||||||
chr1:95042866
|
C | T | 21 | a0001c0001t0013g0053a0001c0001t0013g0054a0001c0001t0013g0059others(18): Show | 21 | HG01952.hp1 NA18612.hp1 NA18943.hp2 others(18): Show |
intron_variant | MODIFIER | c.289-15606G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95042866 | ||||||
chr1:95042891
|
T | C | 3 | a0001c0001t0001g0284a0001c0001t0021g0285a0001c0001t0094g0288 | 3 | HG02630.hp2 HG02647.hp1 NA19030.hp2 |
intron_variant | MODIFIER | c.289-15631A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95042891 | ||||||
chr1:95043017
|
T | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-15757A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95043017 | ||||||
chr1:95043028
|
A | C | 19 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(16): Show | 19 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.289-15768T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95043028 | ||||||
chr1:95043059
|
T | C | 1 | a0001c0001t0195g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.289-15799A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95043059 | ||||||
chr1:95043239
|
A | G | 19 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(16): Show | 19 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.289-15979T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95043239 | ||||||
chr1:95043434
|
G | A | 1 | a0001c0001t0027g0199 | 1 | HG02015.hp2 | intron_variant | MODIFIER | c.289-16174C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95043434 | ||||||
chr1:95043573
|
G | A | 1 | a0001c0001t0022g0082 | 1 | HG01928.hp1 | intron_variant | MODIFIER | c.289-16313C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95043573 | ||||||
chr1:95043614
|
G | A | 18 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(15): Show | 18 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.289-16354C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95043614 | ||||||
chr1:95043667
|
G | A | 18 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(15): Show | 18 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.289-16407C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95043667 | ||||||
chr1:95043709
|
G | A | 1 | a0001c0001t0002g0218 | 1 | NA19002.hp2 | intron_variant | MODIFIER | c.289-16449C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95043709 | ||||||
chr1:95043727
|
A | C | 1 | a0001c0001t0006g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.289-16467T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95043727 | ||||||
chr1:95043786
|
A | G | 18 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(15): Show | 18 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.289-16526T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95043786 | ||||||
chr1:95043806
|
G | T | 1 | a0001c0001t0134g0202 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.289-16546C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95043806 | ||||||
chr1:95043831
|
A | T | 1 | a0001c0001t0163g0325 | 1 | HG01934.hp1 | intron_variant | MODIFIER | c.289-16571T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95043831 | ||||||
chr1:95043919
|
A | T | 81 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.289-16659T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95043919 | ||||||
chr1:95044215
|
C | T | 9 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0039others(6): Show | 10 | HG00639.hp1 HG01243.hp2 HG01358.hp2 others(7): Show |
intron_variant | MODIFIER | c.289-16955G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95044215 | ||||||
chr1:95044358
|
T | C | 1 | a0001c0001t0045g0331 | 1 | homoSapiens_chm13v2.hp1 | intron_variant | MODIFIER | c.289-17098A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95044358 | ||||||
chr1:95044409
|
A | C | 1 | a0001c0001t0002g0227 | 1 | NA18942.hp1 | intron_variant | MODIFIER | c.289-17149T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95044409 | ||||||
chr1:95044472
|
T | C | 4 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0009g0279others(1): Show | 4 | HG01891.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.289-17212A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95044472 | ||||||
chr1:95044586
|
A | G | 18 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(15): Show | 18 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.289-17326T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95044586 | ||||||
chr1:95044787
|
G | T | 1 | a0001c0001t0006g0039 | 1 | HG03710.hp1 | intron_variant | MODIFIER | c.289-17527C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95044787 | ||||||
chr1:95044866
|
C | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-17606G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95044866 | ||||||
chr1:95044881
|
T | TAAA | 12 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(9): Show | 12 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(9): Show |
intron_variant | MODIFIER | c.289-17622_289-1762 others(7): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95044881 | ||||||
chr1:95044881
|
T | TAAAA | 6 | a0001c0001t0025g0026a0001c0001t0025g0384a0001c0001t0025g0385others(3): Show | 6 | HG02602.hp1 HG02698.hp2 HG02735.hp2 others(3): Show |
intron_variant | MODIFIER | c.289-17622_289-1762 others(8): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95044881 | ||||||
chr1:95044882
|
T | A | 19 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(16): Show | 19 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.289-17622A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95044882 | ||||||
chr1:95044883
|
A | T | 8 | a0001c0001t0030g0273a0001c0001t0037g0009a0001c0001t0037g0018others(5): Show | 8 | HG01109.hp2 HG02109.hp2 HG02258.hp2 others(5): Show |
intron_variant | MODIFIER | c.289-17623T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95044883 | ||||||
chr1:95044935
|
G | T | 4 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0009g0279others(1): Show | 4 | HG01891.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.289-17675C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95044935 | ||||||
chr1:95045197
|
T | G | 3 | a0001c0001t0002g0247a0001c0001t0107g0233a0001c0001t0176g0232 | 3 | NA18959.hp1 NA18994.hp1 NA19067.hp2 |
intron_variant | MODIFIER | c.289-17937A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045197 | ||||||
chr1:95045280
|
C | T | 18 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(15): Show | 18 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.289-18020G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045280 | ||||||
chr1:95045463
|
T | A | 1 | a0001c0001t0184g0361 | 1 | NA19067.hp1 | intron_variant | MODIFIER | c.289-18203A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045463 | ||||||
chr1:95045643
|
T | A | 6 | a0001c0001t0014g0062a0001c0001t0015g0058a0001c0001t0080g0047others(3): Show | 6 | HG01952.hp1 NA18612.hp1 NA18944.hp1 others(3): Show |
intron_variant | MODIFIER | c.289-18383A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045643 | ||||||
chr1:95045650
|
A | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.289-18390T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045650 | ||||||
chr1:95045664
|
G | GTATACTA others(17): Show |
1 | a0001c0001t0195g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.289-18428_289-1840 others(28): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045664 | ||||||
chr1:95045664
|
GTATACTA others(17): Show |
G | 40 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0100others(37): Show | 40 | HG00735.hp1 HG01069.hp2 HG01099.hp2 others(37): Show |
intron_variant | MODIFIER | c.289-18428_289-1840 others(28): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045664 | ||||||
chr1:95045665
|
T | C | 4 | a0001c0001t0006g0035a0001c0001t0006g0039a0001c0001t0099g0037others(1): Show | 4 | HG01361.hp2 HG01517.hp2 HG02257.hp2 others(1): Show |
intron_variant | MODIFIER | c.289-18405A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045665 | ||||||
chr1:95045777
|
C | T | 377 | a0001c0001t0001g0194a0001c0001t0001g0276a0001c0001t0001g0278others(374): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.289-18517G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045777 | ||||||
chr1:95045791
|
T | G | 91 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0282others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.289-18531A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045791 | ||||||
chr1:95045810
|
C | T | 7 | a0001c0001t0014g0013a0001c0001t0014g0014a0001c0001t0020g0074others(4): Show | 7 | HG02258.hp1 HG02486.hp1 HG02630.hp1 others(4): Show |
intron_variant | MODIFIER | c.289-18550G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045810 | ||||||
chr1:95045843
|
C | T | 377 | a0001c0001t0001g0194a0001c0001t0001g0276a0001c0001t0001g0278others(374): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.289-18583G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045843 | ||||||
chr1:95045907
|
G | GGTATACT others(24): Show |
5 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272others(2): Show | 5 | HG02109.hp2 HG02886.hp2 HG02895.hp2 others(2): Show |
intron_variant | MODIFIER | c.289-18678_289-1864 others(35): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045907 | ||||||
chr1:95045907
|
G | GGTATACT others(55): Show |
82 | a0001c0001t0001g0282a0001c0001t0001g0284a0001c0001t0001g0293others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(79): Show |
intron_variant | MODIFIER | c.289-18709_289-1864 others(66): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045907 | ||||||
chr1:95045907
|
G | GGTATACT others(86): Show |
9 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0289others(6): Show | 9 | HG01891.hp1 HG02280.hp2 HG02886.hp1 others(6): Show |
intron_variant | MODIFIER | c.289-18648_289-1864 others(97): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045907 | ||||||
chr1:95045907
|
GGTATACT others(24): Show |
G | 81 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.289-18678_289-1864 others(35): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045907 | ||||||
chr1:95045938
|
A | G | 4 | a0001c0001t0003g0140a0001c0001t0034g0139a0001c0001t0086g0131others(1): Show | 4 | NA18939.hp2 NA18956.hp1 NA18962.hp1 others(1): Show |
intron_variant | MODIFIER | c.289-18678T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045938 | ||||||
chr1:95045945
|
T | C | 1 | a0001c0001t0167g0254 | 1 | HG02145.hp2 | intron_variant | MODIFIER | c.289-18685A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045945 | ||||||
chr1:95045957
|
T | C | 1 | a0001c0001t0005g0185 | 1 | HG01070.hp2 | intron_variant | MODIFIER | c.289-18697A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95045957 | ||||||
chr1:95046277
|
C | T | 13 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(10): Show | 14 | HG00639.hp1 HG01243.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.288+18589G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95046277 | ||||||
chr1:95046341
|
T | C | 1 | a0001c0001t0153g0351 | 1 | HG03831.hp2 | intron_variant | MODIFIER | c.288+18525A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95046341 | ||||||
chr1:95046442
|
A | G | 1 | a0001c0001t0078g0089 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.288+18424T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95046442 | ||||||
chr1:95046775
|
T | C | 19 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(16): Show | 19 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(16): Show |
intron_variant | MODIFIER | c.288+18091A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95046775 | ||||||
chr1:95046835
|
C | T | 18 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(15): Show | 18 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.288+18031G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95046835 | ||||||
chr1:95046973
|
A | AAACAT | 90 | a0001c0001t0001g0115a0001c0001t0001g0194a0001c0001t0001g0295others(87): Show | 91 | HG00140.hp2 HG00323.hp1 HG00423.hp2 others(88): Show |
intron_variant | MODIFIER | c.288+17888_288+1789 others(9): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95046973 | ||||||
chr1:95046973
|
A | AAACATAA others(3): Show |
21 | a0001c0001t0001g0293a0001c0001t0002g0223a0001c0001t0003g0148others(18): Show | 21 | HG00544.hp1 HG00735.hp2 HG01074.hp1 others(18): Show |
intron_variant | MODIFIER | c.288+17883_288+1789 others(14): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95046973 | ||||||
chr1:95046973
|
A | AAACATAA others(8): Show |
6 | a0001c0001t0001g0356a0001c0001t0002g0227a0001c0001t0002g0228others(3): Show | 6 | HG02698.hp1 NA18942.hp1 NA18970.hp1 others(3): Show |
intron_variant | MODIFIER | c.288+17878_288+1789 others(19): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95046973 | ||||||
chr1:95046973
|
A | AAACATAA others(13): Show |
1 | a0001c0001t0035g0097 | 1 | HG01099.hp2 | intron_variant | MODIFIER | c.288+17873_288+1789 others(24): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95046973 | ||||||
chr1:95046973
|
AAACAT | A | 43 | a0001c0001t0001g0309a0001c0001t0001g0313a0001c0001t0001g0359others(40): Show | 43 | HG00597.hp1 HG00597.hp2 HG00639.hp2 others(40): Show |
intron_variant | MODIFIER | c.288+17888_288+1789 others(9): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95046973 | ||||||
chr1:95046973
|
AAACATAA others(3): Show |
A | 29 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0289others(26): Show | 30 | HG00323.hp2 HG00408.hp1 HG00609.hp2 others(27): Show |
intron_variant | MODIFIER | c.288+17883_288+1789 others(14): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95046973 | ||||||
chr1:95046973
|
AAACATAA others(8): Show |
A | 16 | a0001c0001t0006g0038a0001c0001t0006g0039a0001c0001t0006g0044others(13): Show | 16 | HG01243.hp2 HG01358.hp2 HG01361.hp2 others(13): Show |
intron_variant | MODIFIER | c.288+17878_288+1789 others(19): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95046973 | ||||||
chr1:95046973
|
AAACATAA others(13): Show |
A | 47 | a0001c0001t0013g0053a0001c0001t0013g0054a0001c0001t0013g0059others(44): Show | 47 | HG01081.hp2 HG01255.hp2 HG01346.hp2 others(44): Show |
intron_variant | MODIFIER | c.288+17873_288+1789 others(24): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95046973 | ||||||
chr1:95046973
|
AAACATAA others(18): Show |
A | 12 | a0001c0001t0024g0375a0001c0001t0024g0376a0001c0001t0024g0377others(9): Show | 12 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(9): Show |
intron_variant | MODIFIER | c.288+17868_288+1789 others(29): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95046973 | ||||||
chr1:95047007
|
A | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+17859T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95047007 | ||||||
chr1:95047463
|
C | A | 19 | a0001c0001t0001g0282a0001c0001t0001g0295a0001c0001t0001g0300others(16): Show | 19 | HG00558.hp1 HG00621.hp1 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.288+17403G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95047463 | ||||||
chr1:95047598
|
C | T | 122 | a0001c0001t0001g0194a0001c0001t0002g0213a0001c0001t0002g0218others(119): Show | 123 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.288+17268G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95047598 | ||||||
chr1:95047666
|
T | G | 18 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0023g0263others(15): Show | 18 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.288+17200A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95047666 | ||||||
chr1:95047718
|
G | A | 6 | a0001c0001t0018g0118a0001c0001t0018g0119a0001c0001t0018g0120others(3): Show | 6 | HG00597.hp1 HG01074.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.288+17148C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95047718 | ||||||
chr1:95047736
|
T | A | 1 | a0001c0001t0005g0201 | 1 | NA19088.hp2 | intron_variant | MODIFIER | c.288+17130A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95047736 | ||||||
chr1:95047836
|
T | C | 3 | a0001c0001t0054g0021a0001c0001t0061g0022a0001c0001t0062g0024 | 3 | HG03041.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.288+17030A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95047836 | ||||||
chr1:95047909
|
G | A | 122 | a0001c0001t0001g0194a0001c0001t0002g0213a0001c0001t0002g0218others(119): Show | 123 | HG00323.hp2 HG00408.hp2 HG00423.hp1 others(120): Show |
intron_variant | MODIFIER | c.288+16957C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95047909 | ||||||
chr1:95048083
|
T | C | 2 | a0001c0001t0011g0280a0001c0001t0090g0281 | 2 | NA18961.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.288+16783A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95048083 | ||||||
chr1:95048124
|
T | C | 1 | a0001c0001t0021g0285 | 1 | HG02647.hp1 | intron_variant | MODIFIER | c.288+16742A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95048124 | ||||||
chr1:95048252
|
G | C | 63 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(60): Show | 64 | HG00639.hp1 HG01081.hp2 HG01243.hp2 others(61): Show |
intron_variant | MODIFIER | c.288+16614C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95048252 | ||||||
chr1:95048294
|
T | G | 8 | a0001c0001t0023g0263a0001c0001t0037g0009a0001c0001t0037g0018others(5): Show | 8 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.288+16572A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95048294 | ||||||
chr1:95048641
|
G | T | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+16225C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95048641 | ||||||
chr1:95048808
|
T | C | 21 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0100others(18): Show | 21 | HG01069.hp2 HG01099.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.288+16058A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95048808 | ||||||
chr1:95048825
|
CCTTT | C | 3 | a0001c0001t0032g0171a0001c0001t0032g0173a0001c0001t0073g0172 | 3 | NA18944.hp2 NA18964.hp1 NA18982.hp2 |
intron_variant | MODIFIER | c.288+16037_288+1604 others(8): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95048825 | ||||||
chr1:95049060
|
T | A | 89 | a0001c0001t0001g0194a0001c0001t0002g0213a0001c0001t0002g0218others(86): Show | 89 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.288+15806A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95049060 | ||||||
chr1:95049288
|
G | A | 1 | a0001c0001t0031g0354 | 1 | HG01255.hp1 | intron_variant | MODIFIER | c.288+15578C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95049288 | ||||||
chr1:95049330
|
C | T | 1 | a0001c0001t0181g0220 | 1 | NA18973.hp2 | intron_variant | MODIFIER | c.288+15536G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95049330 | ||||||
chr1:95049349
|
A | G | 1 | a0001c0001t0102g0041 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.288+15517T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95049349 | ||||||
chr1:95049433
|
A | G | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(14): Show | 17 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+15433T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95049433 | ||||||
chr1:95049568
|
C | T | 91 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0282others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.288+15298G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95049568 | ||||||
chr1:95049663
|
A | G | 1 | a0001c0001t0014g0062 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.288+15203T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95049663 | ||||||
chr1:95049769
|
G | C | 20 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(17): Show | 21 | HG00639.hp1 HG01243.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.288+15097C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95049769 | ||||||
chr1:95049818
|
C | A | 81 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.288+15048G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95049818 | ||||||
chr1:95050081
|
T | G | 112 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0282others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.288+14785A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95050081 | ||||||
chr1:95050105
|
C | T | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+14761G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95050105 | ||||||
chr1:95050222
|
G | T | 10 | a0001c0001t0003g0002a0001c0001t0003g0140a0001c0001t0003g0147others(7): Show | 11 | NA18939.hp2 NA18942.hp2 NA18943.hp1 others(8): Show |
intron_variant | MODIFIER | c.288+14644C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95050222 | ||||||
chr1:95050253
|
A | G | 1 | a0001c0001t0195g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.288+14613T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95050253 | ||||||
chr1:95050572
|
G | A | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(14): Show | 17 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+14294C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95050572 | ||||||
chr1:95050687
|
G | A | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+14179C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95050687 | ||||||
chr1:95050862
|
A | AT | 12 | a0001c0001t0001g0278a0001c0001t0003g0147a0001c0001t0007g0235others(9): Show | 12 | HG00673.hp2 HG00735.hp2 HG01175.hp1 others(9): Show |
intron_variant | MODIFIER | c.288+14003dupA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95050862 | ||||||
chr1:95050862
|
A | ATT | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+14002_288+1400 others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95050862 | ||||||
chr1:95050862
|
AT | A | 64 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(61): Show | 65 | HG00639.hp1 HG01081.hp2 HG01243.hp2 others(62): Show |
intron_variant | MODIFIER | c.288+14003delA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95050862 | ||||||
chr1:95051174
|
G | A | 8 | a0001c0001t0023g0263a0001c0001t0037g0009a0001c0001t0037g0018others(5): Show | 8 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.288+13692C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95051174 | ||||||
chr1:95051222
|
C | A | 4 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272others(1): Show | 4 | HG02109.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.288+13644G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95051222 | ||||||
chr1:95051232
|
GT | G | 377 | a0001c0001t0001g0194a0001c0001t0001g0276a0001c0001t0001g0278others(374): Show | 379 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(376): Show |
intron_variant | MODIFIER | c.288+13633delA | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95051232 | ||||||
chr1:95051245
|
T | G | 2 | a0001c0001t0001g0313a0001c0001t0009g0316 | 2 | HG00639.hp2 HG01070.hp1 |
intron_variant | MODIFIER | c.288+13621A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95051245 | ||||||
chr1:95051422
|
A | T | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+13444T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95051422 | ||||||
chr1:95051587
|
C | A | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(14): Show | 17 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+13279G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95051587 | ||||||
chr1:95051928
|
C | T | 4 | a0001c0001t0027g0204a0001c0001t0027g0207a0001c0001t0122g0206others(1): Show | 4 | HG00544.hp1 NA18955.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.288+12938G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95051928 | ||||||
chr1:95051967
|
C | T | 1 | a0001c0001t0002g0223 | 1 | HG02027.hp1 | intron_variant | MODIFIER | c.288+12899G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95051967 | ||||||
chr1:95051983
|
C | A | 81 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.288+12883G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95051983 | ||||||
chr1:95052140
|
T | C | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+12726A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95052140 | ||||||
chr1:95052192
|
C | T | 1 | a0001c0001t0017g0312 | 1 | HG00609.hp2 | intron_variant | MODIFIER | c.288+12674G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95052192 | ||||||
chr1:95052266
|
G | A | 10 | a0001c0001t0004g0160a0001c0001t0004g0162a0001c0001t0004g0163others(7): Show | 10 | HG00597.hp2 HG00673.hp1 HG02071.hp2 others(7): Show |
intron_variant | MODIFIER | c.288+12600C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95052266 | ||||||
chr1:95052307
|
A | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+12559T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95052307 | ||||||
chr1:95052321
|
A | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+12545T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95052321 | ||||||
chr1:95052362
|
A | T | 1 | a0001c0001t0195g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.288+12504T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95052362 | ||||||
chr1:95052452
|
C | G | 3 | a0001c0001t0054g0021a0001c0001t0061g0022a0001c0001t0062g0024 | 3 | HG03041.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.288+12414G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95052452 | ||||||
chr1:95052502
|
G | A | 4 | a0001c0001t0013g0053a0001c0001t0013g0059a0001c0001t0013g0060others(1): Show | 4 | NA18957.hp2 NA18960.hp1 NA19056.hp1 others(1): Show |
intron_variant | MODIFIER | c.288+12364C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95052502 | ||||||
chr1:95052541
|
T | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+12325A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95052541 | ||||||
chr1:95052608
|
AC | A | 3 | a0001c0001t0054g0021a0001c0001t0061g0022a0001c0001t0062g0024 | 3 | HG03041.hp2 HG03540.hp1 HG03579.hp1 |
intron_variant | MODIFIER | c.288+12257delG | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95052608 | ||||||
chr1:95052677
|
T | A | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(14): Show | 17 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+12189A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95052677 | ||||||
chr1:95052857
|
GA | G | 230 | a0001c0001t0001g0194a0001c0001t0001g0276a0001c0001t0001g0278others(227): Show | 231 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(228): Show |
intron_variant | MODIFIER | c.288+12008delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95052857 | ||||||
chr1:95052857
|
GAA | G | 7 | a0001c0001t0001g0300a0001c0001t0001g0313a0001c0001t0009g0316others(4): Show | 7 | HG00639.hp2 HG01070.hp1 HG03041.hp2 others(4): Show |
intron_variant | MODIFIER | c.288+12007_288+1200 others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95052857 | ||||||
chr1:95052927
|
C | T | 32 | a0001c0001t0003g0002a0001c0001t0003g0130a0001c0001t0003g0133others(29): Show | 33 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(30): Show |
intron_variant | MODIFIER | c.288+11939G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95052927 | ||||||
chr1:95053048
|
C | T | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(14): Show | 17 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+11818G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95053048 | ||||||
chr1:95053112
|
C | T | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(14): Show | 17 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+11754G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95053112 | ||||||
chr1:95053257
|
T | C | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(14): Show | 17 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+11609A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95053257 | ||||||
chr1:95053281
|
T | A | 1 | a0001c0001t0040g0066 | 1 | HG03471.hp2 | intron_variant | MODIFIER | c.288+11585A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95053281 | ||||||
chr1:95053473
|
C | G | 1 | a0001c0001t0021g0315 | 1 | HG02015.hp1 | intron_variant | MODIFIER | c.288+11393G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95053473 | ||||||
chr1:95053480
|
C | G | 6 | a0001c0001t0010g0134a0001c0001t0010g0135a0001c0001t0010g0136others(3): Show | 6 | HG00408.hp2 HG00544.hp2 HG00621.hp2 others(3): Show |
intron_variant | MODIFIER | c.288+11386G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95053480 | ||||||
chr1:95053530
|
C | T | 9 | a0001c0001t0023g0263a0001c0001t0037g0009a0001c0001t0037g0018others(6): Show | 9 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.288+11336G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95053530 | ||||||
chr1:95053622
|
A | G | 89 | a0001c0001t0001g0194a0001c0001t0002g0213a0001c0001t0002g0218others(86): Show | 89 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.288+11244T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95053622 | ||||||
chr1:95053788
|
A | C | 6 | a0001c0001t0018g0118a0001c0001t0018g0119a0001c0001t0018g0120others(3): Show | 6 | HG00597.hp1 HG01074.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.288+11078T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95053788 | ||||||
chr1:95054174
|
T | C | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(14): Show | 17 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+10692A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95054174 | ||||||
chr1:95054197
|
C | T | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+10669G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95054197 | ||||||
chr1:95054244
|
T | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+10622A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95054244 | ||||||
chr1:95054274
|
G | A | 18 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0101others(15): Show | 18 | HG01069.hp2 HG01099.hp2 HG01496.hp1 others(15): Show |
intron_variant | MODIFIER | c.288+10592C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95054274 | ||||||
chr1:95054475
|
GC | G | 91 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0282others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.288+10390delG | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95054475 | ||||||
chr1:95054575
|
A | T | 81 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.288+10291T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95054575 | ||||||
chr1:95054590
|
T | C | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+10276A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95054590 | ||||||
chr1:95054800
|
T | C | 21 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0100others(18): Show | 21 | HG01069.hp2 HG01099.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.288+10066A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95054800 | ||||||
chr1:95054867
|
G | C | 1 | a0001c0001t0195g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.288+9999C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95054867 | ||||||
chr1:95055301
|
T | C | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(14): Show | 17 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+9565A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95055301 | ||||||
chr1:95055336
|
A | T | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(14): Show | 17 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+9530T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95055336 | ||||||
chr1:95055374
|
T | C | 6 | a0001c0001t0018g0118a0001c0001t0018g0119a0001c0001t0018g0120others(3): Show | 6 | HG00597.hp1 HG01074.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.288+9492A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95055374 | ||||||
chr1:95055774
|
C | T | 1 | a0001c0001t0134g0202 | 1 | HG01175.hp2 | intron_variant | MODIFIER | c.288+9092G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95055774 | ||||||
chr1:95055828
|
T | TA | 26 | a0001c0001t0001g0293a0001c0001t0002g0245a0001c0001t0003g0002others(23): Show | 27 | HG00408.hp2 HG00423.hp1 HG00423.hp2 others(24): Show |
intron_variant | MODIFIER | c.288+9037dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95055828 | ||||||
chr1:95055828
|
T | TAA | 13 | a0001c0001t0003g0147a0001c0001t0003g0148a0001c0001t0003g0149others(10): Show | 13 | HG01261.hp1 HG02027.hp2 HG02280.hp1 others(10): Show |
intron_variant | MODIFIER | c.288+9036_288+9037d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95055828 | ||||||
chr1:95055828
|
TA | T | 132 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0282others(129): Show | 132 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(129): Show |
intron_variant | MODIFIER | c.288+9037delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95055828 | ||||||
chr1:95055828
|
TAA | T | 137 | a0001c0001t0001g0194a0001c0001t0001g0300a0001c0001t0001g0341others(134): Show | 138 | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(135): Show |
intron_variant | MODIFIER | c.288+9036_288+9037d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95055828 | ||||||
chr1:95055828
|
TAAA | T | 6 | a0001c0001t0006g0043a0001c0001t0008g0098a0001c0001t0013g0053others(3): Show | 6 | HG02602.hp2 HG02717.hp2 HG02896.hp1 others(3): Show |
intron_variant | MODIFIER | c.288+9035_288+9037d others(5): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95055828 | ||||||
chr1:95055828
|
TAAAAAAA others(3): Show |
T | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+9028_288+9037d others(12): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95055828 | ||||||
chr1:95055831
|
A | T | 1 | a0001c0001t0078g0089 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.288+9035T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95055831 | ||||||
chr1:95055885
|
C | T | 9 | a0001c0001t0023g0263a0001c0001t0037g0009a0001c0001t0037g0018others(6): Show | 9 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.288+8981G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95055885 | ||||||
chr1:95055958
|
G | A | 1 | a0001c0001t0140g0246 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.288+8908C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95055958 | ||||||
chr1:95056008
|
C | CA | 49 | a0001c0001t0001g0309a0001c0001t0005g0203a0001c0001t0006g0001others(46): Show | 50 | HG00639.hp1 HG01069.hp2 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.288+8857dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056008 | ||||||
chr1:95056008
|
C | CAA | 17 | a0001c0001t0012g0105a0001c0001t0023g0029a0001c0001t0023g0030others(14): Show | 17 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+8856_288+8857d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056008 | ||||||
chr1:95056017
|
A | C | 11 | a0001c0001t0001g0319a0001c0001t0005g0268a0001c0001t0016g0267others(8): Show | 11 | HG00741.hp2 HG01928.hp2 HG02040.hp1 others(8): Show |
intron_variant | MODIFIER | c.288+8849T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056017 | ||||||
chr1:95056027
|
C | T | 1 | a0001c0001t0191g0299 | 1 | NA19057.hp2 | intron_variant | MODIFIER | c.288+8839G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056027 | ||||||
chr1:95056045
|
A | C | 2 | a0001c0001t0009g0316a0001c0002t0126g0183 | 2 | HG00639.hp2 HG02074.hp1 |
intron_variant | MODIFIER | c.288+8821T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056045 | ||||||
chr1:95056059
|
A | G | 1 | a0001c0001t0121g0253 | 1 | NA19068.hp1 | intron_variant | MODIFIER | c.288+8807T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056059 | ||||||
chr1:95056087
|
G | A | 1 | a0001c0001t0140g0246 | 1 | NA18970.hp2 | intron_variant | MODIFIER | c.288+8779C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056087 | ||||||
chr1:95056210
|
G | A | 2 | a0001c0001t0017g0381a0001c0001t0074g0382 | 2 | NA19000.hp2 NA19066.hp1 |
intron_variant | MODIFIER | c.288+8656C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056210 | ||||||
chr1:95056250
|
T | C | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+8616A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056250 | ||||||
chr1:95056373
|
G | A | 1 | a0001c0001t0052g0067 | 1 | HG02559.hp2 | intron_variant | MODIFIER | c.288+8493C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056373 | ||||||
chr1:95056460
|
C | T | 3 | a0001c0001t0003g0130a0001c0001t0003g0270a0001c0001t0088g0129 | 3 | HG02129.hp1 NA18999.hp1 NA19084.hp2 |
intron_variant | MODIFIER | c.288+8406G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056460 | ||||||
chr1:95056642
|
C | CA | 6 | a0001c0001t0018g0118a0001c0001t0018g0119a0001c0001t0018g0120others(3): Show | 6 | HG00597.hp1 HG01074.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.288+8223dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056642 | ||||||
chr1:95056703
|
ACCTTTAA others(3670): Show |
A | 28 | a0001c0001t0003g0002a0001c0001t0003g0130a0001c0001t0003g0133others(25): Show | 29 | HG00408.hp2 HG00423.hp2 HG00544.hp2 others(26): Show |
intron_variant | MODIFIER | c.288+4486_288+8162d others(2): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056703 | ||||||
chr1:95056788
|
G | C | 1 | a0001c0001t0014g0062 | 1 | NA18612.hp1 | intron_variant | MODIFIER | c.288+8078C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056788 | ||||||
chr1:95056796
|
C | T | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+8070G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056796 | ||||||
chr1:95056840
|
C | T | 5 | a0001c0001t0001g0362a0001c0001t0009g0364a0001c0001t0150g0360others(2): Show | 5 | HG00438.hp2 NA18939.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.288+8026G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056840 | ||||||
chr1:95056864
|
CTGGCCAA others(18): Show |
C | 44 | a0001c0001t0013g0053a0001c0001t0013g0054a0001c0001t0013g0059others(41): Show | 44 | HG01081.hp2 HG01255.hp2 HG01346.hp2 others(41): Show |
intron_variant | MODIFIER | c.288+7977_288+8001d others(27): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056864 | ||||||
chr1:95056921
|
G | C | 4 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272others(1): Show | 4 | HG02109.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.288+7945C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056921 | ||||||
chr1:95056969
|
T | C | 2 | a0001c0001t0004g0004a0001c0001t0009g0350 | 2 | NA18953.hp1 NA20905.hp2 |
intron_variant | MODIFIER | c.288+7897A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95056969 | ||||||
chr1:95057055
|
C | CA | 106 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0284others(103): Show | 106 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(103): Show |
intron_variant | MODIFIER | c.288+7810dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95057055 | ||||||
chr1:95057055
|
C | CAA | 21 | a0001c0001t0001g0313a0001c0001t0008g0098a0001c0001t0008g0099others(18): Show | 21 | HG00609.hp2 HG00639.hp2 HG01069.hp2 others(18): Show |
intron_variant | MODIFIER | c.288+7809_288+7810d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95057055 | ||||||
chr1:95057085
|
C | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+7781G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95057085 | ||||||
chr1:95057252
|
C | T | 1 | a0001c0001t0037g0009 | 1 | NA19240.hp2 | intron_variant | MODIFIER | c.288+7614G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95057252 | ||||||
chr1:95057480
|
G | A | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+7386C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95057480 | ||||||
chr1:95057507
|
G | A | 18 | a0001c0001t0001g0334a0001c0001t0023g0029a0001c0001t0023g0030others(15): Show | 18 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(15): Show |
intron_variant | MODIFIER | c.288+7359C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95057507 | ||||||
chr1:95057546
|
G | C | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+7320C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95057546 | ||||||
chr1:95057622
|
C | CTG | 117 | a0001c0001t0001g0194a0001c0001t0001g0335a0001c0001t0002g0213others(114): Show | 117 | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(114): Show |
intron_variant | MODIFIER | c.288+7242_288+7243d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95057622 | ||||||
chr1:95057622
|
C | CTGTG | 202 | a0001c0001t0001g0282a0001c0001t0001g0284a0001c0001t0001g0293others(199): Show | 203 | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(200): Show |
intron_variant | MODIFIER | c.288+7240_288+7243d others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95057622 | ||||||
chr1:95057622
|
C | CTGTGTG | 19 | a0001c0001t0001g0296a0001c0001t0001g0313a0001c0001t0001g0356others(16): Show | 19 | HG00597.hp1 HG00609.hp1 HG00639.hp2 others(16): Show |
intron_variant | MODIFIER | c.288+7238_288+7243d others(8): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95057622 | ||||||
chr1:95057648
|
A | G | 38 | a0001c0001t0013g0053a0001c0001t0013g0054a0001c0001t0013g0059others(35): Show | 38 | HG01081.hp2 HG01255.hp2 HG01346.hp2 others(35): Show |
intron_variant | MODIFIER | c.288+7218T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95057648 | ||||||
chr1:95057656
|
A | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+7210T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95057656 | ||||||
chr1:95057875
|
C | A | 1 | a0001c0001t0022g0083 | 1 | HG01934.hp2 | intron_variant | MODIFIER | c.288+6991G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95057875 | ||||||
chr1:95057887
|
G | A | 3 | a0001c0001t0080g0047a0001c0001t0110g0070a0001c0001t0141g0069 | 3 | NA18944.hp1 NA18978.hp1 NA18982.hp1 |
intron_variant | MODIFIER | c.288+6979C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95057887 | ||||||
chr1:95057921
|
G | A | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+6945C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95057921 | ||||||
chr1:95058242
|
C | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.288+6624G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058242 | ||||||
chr1:95058243
|
G | A | 4 | a0001c0001t0027g0204a0001c0001t0027g0207a0001c0001t0122g0206others(1): Show | 4 | HG00544.hp1 NA18955.hp1 NA18977.hp1 others(1): Show |
intron_variant | MODIFIER | c.288+6623C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058243 | ||||||
chr1:95058284
|
G | GA | 101 | a0001c0001t0001g0194a0001c0001t0001g0293a0001c0001t0001g0341others(98): Show | 101 | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
intron_variant | MODIFIER | c.288+6581dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058284 | ||||||
chr1:95058284
|
G | GAA | 15 | a0001c0001t0001g0289a0001c0001t0002g0247a0001c0001t0005g0211others(12): Show | 15 | HG00438.hp1 HG01884.hp1 HG01981.hp2 others(12): Show |
intron_variant | MODIFIER | c.288+6580_288+6581d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058284 | ||||||
chr1:95058284
|
GA | G | 25 | a0001c0001t0001g0313a0001c0001t0001g0314a0001c0001t0004g0153others(22): Show | 25 | HG01069.hp1 HG01070.hp1 HG01109.hp2 others(22): Show |
intron_variant | MODIFIER | c.288+6581delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058284 | ||||||
chr1:95058284
|
GAA | G | 9 | a0001c0001t0025g0026a0001c0001t0025g0384a0001c0001t0025g0385others(6): Show | 9 | HG00735.hp1 HG02602.hp1 HG02698.hp2 others(6): Show |
intron_variant | MODIFIER | c.288+6580_288+6581d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058284 | ||||||
chr1:95058284
|
GAAAAAAA others(4): Show |
G | 1 | a0001c0001t0195g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.288+6571_288+6581d others(13): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058284 | ||||||
chr1:95058284
|
GAAAAAAA others(5): Show |
G | 4 | a0001c0001t0028g0175a0001c0001t0028g0176a0001c0001t0058g0177others(1): Show | 4 | HG02055.hp1 HG02055.hp2 HG02109.hp1 others(1): Show |
intron_variant | MODIFIER | c.288+6570_288+6581d others(14): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058284 | ||||||
chr1:95058285
|
A | G | 1 | a0001c0001t0190g0338 | 1 | HG01978.hp1 | intron_variant | MODIFIER | c.288+6581T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058285 | ||||||
chr1:95058324
|
GAGATGAT others(10): Show |
G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+6525_288+6541d others(19): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058324 | ||||||
chr1:95058477
|
C | T | 4 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272others(1): Show | 4 | HG02109.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.288+6389G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058477 | ||||||
chr1:95058481
|
G | C | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+6385C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058481 | ||||||
chr1:95058511
|
G | C | 94 | a0001c0001t0001g0194a0001c0001t0002g0213a0001c0001t0002g0218others(91): Show | 94 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(91): Show |
intron_variant | MODIFIER | c.288+6355C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058511 | ||||||
chr1:95058600
|
G | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+6266C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058600 | ||||||
chr1:95058600
|
G | C | 112 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0282others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.288+6266C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058600 | ||||||
chr1:95058601
|
A | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+6265T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058601 | ||||||
chr1:95058616
|
TA | T | 50 | a0001c0001t0001g0357a0001c0001t0001g0358a0001c0001t0002g0213others(47): Show | 50 | HG00639.hp1 HG00735.hp1 HG01099.hp2 others(47): Show |
intron_variant | MODIFIER | c.288+6249delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058616 | ||||||
chr1:95058670
|
T | C | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.288+6196A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058670 | ||||||
chr1:95058691
|
C | CA | 83 | a0001c0001t0005g0191a0001c0001t0006g0001a0001c0001t0006g0035others(80): Show | 84 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(81): Show |
intron_variant | MODIFIER | c.288+6174dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058691 | ||||||
chr1:95058691
|
CA | C | 20 | a0001c0001t0001g0295a0001c0001t0007g0212a0001c0001t0023g0029others(17): Show | 20 | HG00735.hp1 HG01261.hp1 HG02145.hp1 others(17): Show |
intron_variant | MODIFIER | c.288+6174delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058691 | ||||||
chr1:95058947
|
G | T | 81 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.288+5919C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058947 | ||||||
chr1:95058995
|
T | C | 349 | a0001c0001t0001g0194a0001c0001t0001g0276a0001c0001t0001g0278others(346): Show | 350 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(347): Show |
intron_variant | MODIFIER | c.288+5871A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058995 | ||||||
chr1:95058998
|
C | A | 4 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272others(1): Show | 4 | HG02109.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.288+5868G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95058998 | ||||||
chr1:95059000
|
A | G | 6 | a0001c0001t0018g0118a0001c0001t0018g0119a0001c0001t0018g0120others(3): Show | 6 | HG00597.hp1 HG01074.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.288+5866T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059000 | ||||||
chr1:95059055
|
T | C | 1 | a0001c0001t0135g0257 | 1 | HG04228.hp1 | intron_variant | MODIFIER | c.288+5811A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059055 | ||||||
chr1:95059075
|
T | C | 1 | a0001c0001t0132g0265 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.288+5791A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059075 | ||||||
chr1:95059143
|
A | T | 4 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272others(1): Show | 4 | HG02109.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.288+5723T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059143 | ||||||
chr1:95059152
|
G | A | 1 | a0001c0001t0015g0085 | 1 | HG01081.hp2 | intron_variant | MODIFIER | c.288+5714C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059152 | ||||||
chr1:95059181
|
G | A | 9 | a0001c0001t0023g0263a0001c0001t0037g0009a0001c0001t0037g0018others(6): Show | 9 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(6): Show |
intron_variant | MODIFIER | c.288+5685C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059181 | ||||||
chr1:95059195
|
G | A | 21 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0100others(18): Show | 21 | HG01069.hp2 HG01099.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.288+5671C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059195 | ||||||
chr1:95059254
|
G | T | 3 | a0001c0001t0028g0175a0001c0001t0028g0176a0001c0001t0058g0177 | 3 | HG02055.hp2 HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.288+5612C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059254 | ||||||
chr1:95059326
|
C | T | 2 | a0001c0001t0008g0102a0001c0001t0008g0103 | 2 | HG03453.hp1 HG03486.hp1 |
intron_variant | MODIFIER | c.288+5540G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059326 | ||||||
chr1:95059333
|
G | A | 1 | a0001c0001t0066g0167 | 1 | NA19075.hp2 | intron_variant | MODIFIER | c.288+5533C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059333 | ||||||
chr1:95059397
|
C | CA | 62 | a0001c0001t0001g0289a0001c0001t0001g0295a0001c0001t0002g0250others(59): Show | 62 | HG00408.hp1 HG00673.hp1 HG00735.hp2 others(59): Show |
intron_variant | MODIFIER | c.288+5468dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059397 | ||||||
chr1:95059397
|
C | CAA | 10 | a0001c0001t0008g0101a0001c0001t0018g0118a0001c0001t0018g0119others(7): Show | 10 | HG00597.hp1 HG01074.hp1 HG01167.hp2 others(7): Show |
intron_variant | MODIFIER | c.288+5467_288+5468d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059397 | ||||||
chr1:95059397
|
CA | C | 17 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0001g0352others(14): Show | 18 | HG00323.hp1 HG00639.hp1 HG01243.hp2 others(15): Show |
intron_variant | MODIFIER | c.288+5468delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059397 | ||||||
chr1:95059397
|
CAAAAAAA others(6): Show |
C | 27 | a0001c0001t0001g0194a0001c0001t0005g0185a0001c0001t0005g0189others(24): Show | 27 | HG00323.hp2 HG00544.hp1 HG01070.hp2 others(24): Show |
intron_variant | MODIFIER | c.288+5456_288+5468d others(15): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059397 | ||||||
chr1:95059413
|
A | AC | 14 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(11): Show | 14 | HG02145.hp1 HG02572.hp1 HG02698.hp2 others(11): Show |
intron_variant | MODIFIER | c.288+5452_288+5453i others(3): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059413 | ||||||
chr1:95059415
|
A | C | 5 | a0001c0001t0017g0312a0001c0001t0024g0375a0001c0001t0024g0376others(2): Show | 5 | HG00609.hp2 HG01884.hp1 HG02647.hp2 others(2): Show |
intron_variant | MODIFIER | c.288+5451T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059415 | ||||||
chr1:95059450
|
C | T | 19 | a0001c0001t0001g0282a0001c0001t0001g0295a0001c0001t0001g0300others(16): Show | 19 | HG00558.hp1 HG00621.hp1 HG02165.hp1 others(16): Show |
intron_variant | MODIFIER | c.288+5416G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059450 | ||||||
chr1:95059594
|
G | A | 4 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0029g0031others(1): Show | 4 | HG02572.hp1 HG02723.hp2 HG02809.hp2 others(1): Show |
intron_variant | MODIFIER | c.288+5272C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059594 | ||||||
chr1:95059646
|
T | C | 1 | a0001c0001t0002g0258 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.288+5220A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059646 | ||||||
chr1:95059857
|
A | G | 26 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(23): Show | 26 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.288+5009T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059857 | ||||||
chr1:95059860
|
C | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+5006G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95059860 | ||||||
chr1:95060007
|
T | C | 1 | a0001c0001t0098g0255 | 1 | NA19007.hp2 | intron_variant | MODIFIER | c.288+4859A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060007 | ||||||
chr1:95060035
|
AC | A | 219 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0282others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.288+4830delG | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060035 | ||||||
chr1:95060071
|
T | A | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+4795A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060071 | ||||||
chr1:95060129
|
AAC | A | 19 | a0001c0001t0004g0111a0001c0001t0004g0153a0001c0001t0004g0154others(16): Show | 19 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(16): Show |
intron_variant | MODIFIER | c.288+4735_288+4736d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060129 | ||||||
chr1:95060129
|
AACAC | A | 18 | a0001c0001t0001g0115a0001c0001t0004g0170a0001c0001t0008g0098others(15): Show | 18 | HG01069.hp2 HG01884.hp2 HG02004.hp1 others(15): Show |
intron_variant | MODIFIER | c.288+4733_288+4736d others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060129 | ||||||
chr1:95060129
|
AACACAC | A | 20 | a0001c0001t0008g0102a0001c0001t0008g0103a0001c0001t0012g0092others(17): Show | 20 | HG00597.hp1 HG01099.hp2 HG01109.hp2 others(17): Show |
intron_variant | MODIFIER | c.288+4731_288+4736d others(8): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060129 | ||||||
chr1:95060129
|
AACACACA others(1): Show |
A | 7 | a0001c0001t0001g0293a0001c0001t0012g0105a0001c0001t0018g0121others(4): Show | 7 | HG01074.hp1 HG02148.hp2 HG02300.hp1 others(4): Show |
intron_variant | MODIFIER | c.288+4729_288+4736d others(10): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060129 | ||||||
chr1:95060129
|
AACACACA others(3): Show |
A | 7 | a0001c0001t0001g0295a0001c0001t0001g0296a0001c0001t0001g0352others(4): Show | 7 | HG01255.hp1 HG01993.hp1 HG03041.hp1 others(4): Show |
intron_variant | MODIFIER | c.288+4727_288+4736d others(12): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060129 | ||||||
chr1:95060129
|
AACACACA others(5): Show |
A | 82 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0282others(79): Show | 82 | HG00099.hp2 HG00140.hp2 HG00408.hp1 others(79): Show |
intron_variant | MODIFIER | c.288+4725_288+4736d others(14): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060129 | ||||||
chr1:95060129
|
AACACACA others(7): Show |
A | 12 | a0001c0001t0001g0340a0001c0001t0001g0341a0001c0001t0001g0342others(9): Show | 12 | HG00323.hp1 HG00735.hp1 HG01243.hp1 others(9): Show |
intron_variant | MODIFIER | c.288+4723_288+4736d others(16): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060129 | ||||||
chr1:95060129
|
AACACACA others(9): Show |
A | 78 | a0001c0001t0005g0191a0001c0001t0006g0001a0001c0001t0006g0035others(75): Show | 79 | HG00639.hp1 HG01081.hp2 HG01243.hp2 others(76): Show |
intron_variant | MODIFIER | c.288+4721_288+4736d others(18): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060129 | ||||||
chr1:95060129
|
AACACACA others(11): Show |
A | 104 | a0001c0001t0001g0194a0001c0001t0002g0213a0001c0001t0002g0218others(101): Show | 104 | HG00099.hp1 HG00140.hp1 HG00323.hp2 others(101): Show |
intron_variant | MODIFIER | c.288+4719_288+4736d others(20): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060129 | ||||||
chr1:95060129
|
AACACACA others(13): Show |
A | 1 | a0001c0001t0078g0089 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.288+4717_288+4736d others(22): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060129 | ||||||
chr1:95060214
|
C | A | 1 | a0001c0001t0071g0174 | 1 | HG02165.hp2 | intron_variant | MODIFIER | c.288+4652G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060214 | ||||||
chr1:95060319
|
A | G | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(14): Show | 17 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+4547T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060319 | ||||||
chr1:95060454
|
C | T | 2 | a0001c0001t0005g0189a0001c0001t0005g0190 | 2 | NA18941.hp2 NA18952.hp2 |
intron_variant | MODIFIER | c.288+4412G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060454 | ||||||
chr1:95060461
|
A | C | 1 | a0001c0001t0133g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.288+4405T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060461 | ||||||
chr1:95060552
|
T | TAA | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+4312_288+4313d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060552 | ||||||
chr1:95060552
|
TA | T | 32 | a0001c0001t0001g0352a0001c0001t0004g0004a0001c0001t0004g0111others(29): Show | 32 | HG00323.hp2 HG00597.hp2 HG00673.hp1 others(29): Show |
intron_variant | MODIFIER | c.288+4313delT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060552 | ||||||
chr1:95060640
|
T | C | 1 | a0001c0001t0033g0040 | 1 | NA20300.hp1 | intron_variant | MODIFIER | c.288+4226A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060640 | ||||||
chr1:95060674
|
C | T | 6 | a0001c0001t0018g0118a0001c0001t0018g0119a0001c0001t0018g0120others(3): Show | 6 | HG00597.hp1 HG01074.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.288+4192G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060674 | ||||||
chr1:95060703
|
G | C | 1 | a0001c0001t0004g0256 | 1 | HG02155.hp1 | intron_variant | MODIFIER | c.288+4163C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060703 | ||||||
chr1:95060715
|
A | T | 80 | a0001c0001t0001g0282a0001c0001t0001g0293a0001c0001t0001g0295others(77): Show | 80 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.288+4151T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060715 | ||||||
chr1:95060775
|
T | C | 1 | a0001c0001t0078g0089 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.288+4091A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95060775 | ||||||
chr1:95061004
|
A | G | 1 | a0001c0001t0009g0291 | 1 | HG02735.hp1 | intron_variant | MODIFIER | c.288+3862T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95061004 | ||||||
chr1:95061046
|
C | T | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.288+3820G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95061046 | ||||||
chr1:95061107
|
G | A | 6 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.288+3759C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95061107 | ||||||
chr1:95061128
|
C | T | 1 | a0001c0001t0021g0290 | 1 | HG03688.hp1 | intron_variant | MODIFIER | c.288+3738G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95061128 | ||||||
chr1:95061136
|
G | C | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+3730C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95061136 | ||||||
chr1:95061384
|
A | G | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(14): Show | 17 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+3482T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95061384 | ||||||
chr1:95061405
|
T | C | 20 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(17): Show | 21 | HG00639.hp1 HG01243.hp2 HG01358.hp2 others(18): Show |
intron_variant | MODIFIER | c.288+3461A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95061405 | ||||||
chr1:95061480
|
T | TGA | 8 | a0001c0001t0005g0268a0001c0001t0016g0267a0001c0001t0018g0118others(5): Show | 8 | HG00597.hp1 HG01074.hp1 HG01167.hp2 others(5): Show |
intron_variant | MODIFIER | c.288+3384_288+3385d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95061480 | ||||||
chr1:95061480
|
T | TGAGA | 6 | a0001c0001t0037g0009a0001c0001t0037g0018a0001c0001t0038g0007others(3): Show | 6 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(3): Show |
intron_variant | MODIFIER | c.288+3382_288+3385d others(6): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95061480 | ||||||
chr1:95061520
|
G | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+3346C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95061520 | ||||||
chr1:95061549
|
T | C | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+3317A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95061549 | ||||||
chr1:95061628
|
T | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+3238A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95061628 | ||||||
chr1:95061890
|
C | T | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+2976G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95061890 | ||||||
chr1:95061902
|
G | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+2964C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95061902 | ||||||
chr1:95061975
|
A | G | 26 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(23): Show | 26 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.288+2891T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95061975 | ||||||
chr1:95061978
|
T | TA | 89 | a0001c0001t0001g0194a0001c0001t0002g0213a0001c0001t0002g0218others(86): Show | 89 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.288+2887dupT | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95061978 | ||||||
chr1:95061979
|
A | T | 1 | a0001c0001t0083g0122 | 1 | NA18960.hp2 | intron_variant | MODIFIER | c.288+2887T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95061979 | ||||||
chr1:95062010
|
T | C | 80 | a0001c0001t0001g0282a0001c0001t0001g0293a0001c0001t0001g0295others(77): Show | 80 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(77): Show |
intron_variant | MODIFIER | c.288+2856A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95062010 | ||||||
chr1:95062194
|
G | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+2672C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95062194 | ||||||
chr1:95062357
|
G | A | 4 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0009g0279others(1): Show | 4 | HG01891.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.288+2509C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95062357 | ||||||
chr1:95062483
|
T | G | 82 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(79): Show | 83 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(80): Show |
intron_variant | MODIFIER | c.288+2383A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95062483 | ||||||
chr1:95062514
|
T | C | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(14): Show | 17 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+2352A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95062514 | ||||||
chr1:95062530
|
A | G | 1 | a0001c0001t0129g0184 | 1 | HG02135.hp2 | intron_variant | MODIFIER | c.288+2336T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95062530 | ||||||
chr1:95062660
|
T | C | 1 | a0001c0001t0102g0041 | 1 | HG03239.hp1 | intron_variant | MODIFIER | c.288+2206A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95062660 | ||||||
chr1:95062736
|
T | C | 91 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0282others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.288+2130A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95062736 | ||||||
chr1:95062742
|
T | G | 1 | a0001c0001t0029g0031 | 1 | HG02723.hp2 | intron_variant | MODIFIER | c.288+2124A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95062742 | ||||||
chr1:95062870
|
G | A | 4 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0009g0279others(1): Show | 4 | HG01891.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.288+1996C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95062870 | ||||||
chr1:95063005
|
G | C | 1 | a0001c0001t0002g0258 | 1 | NA19060.hp2 | intron_variant | MODIFIER | c.288+1861C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95063005 | ||||||
chr1:95063025
|
T | C | 5 | a0001c0001t0006g0001a0001c0001t0006g0043a0001c0001t0006g0044others(2): Show | 6 | HG00639.hp1 HG01243.hp2 HG01358.hp2 others(3): Show |
intron_variant | MODIFIER | c.288+1841A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95063025 | ||||||
chr1:95063045
|
G | A | 112 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0282others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.288+1821C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95063045 | ||||||
chr1:95063139
|
A | G | 8 | a0001c0001t0023g0263a0001c0001t0037g0009a0001c0001t0037g0018others(5): Show | 8 | HG01109.hp2 HG02258.hp2 HG02622.hp2 others(5): Show |
intron_variant | MODIFIER | c.288+1727T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95063139 | ||||||
chr1:95063227
|
T | C | 3 | a0001c0001t0002g0259a0001c0001t0002g0275a0001c0001t0039g0260 | 3 | HG02040.hp2 NA18949.hp2 NA19006.hp1 |
intron_variant | MODIFIER | c.288+1639A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95063227 | ||||||
chr1:95063289
|
T | C | 1 | a0001c0001t0022g0086 | 1 | HG01346.hp2 | intron_variant | MODIFIER | c.288+1577A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95063289 | ||||||
chr1:95063372
|
T | C | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(14): Show | 17 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+1494A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95063372 | ||||||
chr1:95063373
|
G | A | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.288+1493C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95063373 | ||||||
chr1:95063451
|
C | T | 1 | a0001c0001t0015g0046 | 1 | NA18999.hp2 | intron_variant | MODIFIER | c.288+1415G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95063451 | ||||||
chr1:95063466
|
T | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+1400A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95063466 | ||||||
chr1:95063506
|
C | T | 3 | a0001c0001t0004g0153a0001c0001t0004g0154a0001c0001t0004g0155 | 3 | HG01123.hp1 HG01257.hp1 HG01258.hp1 |
intron_variant | MODIFIER | c.288+1360G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95063506 | ||||||
chr1:95063510
|
T | C | 2 | a0001c0001t0023g0263a0001c0001t0050g0262 | 2 | HG02818.hp2 HG03041.hp1 |
intron_variant | MODIFIER | c.288+1356A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95063510 | ||||||
chr1:95063570
|
C | G | 6 | a0001c0001t0012g0092a0001c0001t0012g0093a0001c0001t0012g0094others(3): Show | 6 | HG01069.hp2 HG01099.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.288+1296G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95063570 | ||||||
chr1:95063619
|
C | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+1247G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95063619 | ||||||
chr1:95064165
|
T | A | 6 | a0001c0001t0012g0092a0001c0001t0012g0093a0001c0001t0012g0094others(3): Show | 6 | HG01069.hp2 HG01099.hp2 HG01496.hp1 others(3): Show |
intron_variant | MODIFIER | c.288+701A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95064165 | ||||||
chr1:95064177
|
T | C | 2 | a0001c0001t0043g0283a0001c0001t0157g0343 | 2 | HG00140.hp2 HG01257.hp2 |
intron_variant | MODIFIER | c.288+689A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95064177 | ||||||
chr1:95064284
|
C | A | 9 | a0001c0001t0017g0378a0001c0001t0017g0380a0001c0001t0017g0381others(6): Show | 9 | HG01884.hp1 HG02040.hp1 HG02071.hp1 others(6): Show |
intron_variant | MODIFIER | c.288+582G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95064284 | ||||||
chr1:95064393
|
T | G | 1 | a0001c0001t0136g0261 | 1 | NA18953.hp2 | intron_variant | MODIFIER | c.288+473A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95064393 | ||||||
chr1:95064447
|
T | C | 1 | a0001c0001t0006g0045 | 1 | HG01243.hp2 | intron_variant | MODIFIER | c.288+419A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95064447 | ||||||
chr1:95064457
|
C | A | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.288+409G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95064457 | ||||||
chr1:95064467
|
A | T | 17 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(14): Show | 17 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(14): Show |
intron_variant | MODIFIER | c.288+399T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95064467 | ||||||
chr1:95064649
|
T | C | 1 | a0001c0001t0005g0268 | 1 | HG06807.hp1 | intron_variant | MODIFIER | c.288+217A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95064649 | ||||||
chr1:95064706
|
A | G | 1 | a0001c0001t0012g0092 | 1 | HG01496.hp1 | intron_variant | MODIFIER | c.288+160T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95064706 | ||||||
chr1:95064855
|
T | C | 2 | a0001c0001t0001g0352a0001c0001t0001g0353 | 2 | HG01074.hp2 HG01993.hp1 |
intron_variant | MODIFIER | c.288+11A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 2/3 | chr1 | 95064855 | ||||||
chr1:95065035
|
A | T | 13 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(10): Show | 14 | HG00639.hp1 HG01243.hp2 HG01358.hp2 others(11): Show |
intron_variant | MODIFIER | c.137-18T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95065035 | ||||||
chr1:95065059
|
A | G | 2 | a0001c0001t0170g0367a0001c0001t0192g0368 | 2 | HG00140.hp1 HG01433.hp1 |
intron_variant | MODIFIER | c.137-42T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95065059 | ||||||
chr1:95065114
|
G | A | 16 | a0001c0001t0001g0347a0001c0001t0001g0352a0001c0001t0001g0353others(13): Show | 16 | HG00438.hp2 HG01069.hp1 HG01074.hp2 others(13): Show |
intron_variant | MODIFIER | c.137-97C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95065114 | ||||||
chr1:95065153
|
G | A | 64 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(61): Show | 65 | HG00639.hp1 HG01081.hp2 HG01243.hp2 others(62): Show |
intron_variant | MODIFIER | c.137-136C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95065153 | ||||||
chr1:95065227
|
T | TAAAAATA others(350): Show |
1 | a0001c0001t0029g0032 | 1 | HG03239.hp2 | intron_variant | MODIFIER | c.137-211_137-210ins others(357): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95065227 | ||||||
chr1:95065334
|
A | G | 6 | a0001c0001t0018g0118a0001c0001t0018g0119a0001c0001t0018g0120others(3): Show | 6 | HG00597.hp1 HG01074.hp1 HG01167.hp2 others(3): Show |
intron_variant | MODIFIER | c.137-317T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95065334 | ||||||
chr1:95065405
|
T | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.137-388A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95065405 | ||||||
chr1:95065752
|
A | G | 1 | a0001c0001t0043g0283 | 1 | HG01257.hp2 | intron_variant | MODIFIER | c.137-735T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95065752 | ||||||
chr1:95065817
|
A | C | 219 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0282others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.137-800T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95065817 | ||||||
chr1:95066089
|
T | C | 2 | a0001c0001t0031g0354a0001c0001t0162g0355 | 2 | HG00741.hp1 HG01255.hp1 |
intron_variant | MODIFIER | c.137-1072A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95066089 | ||||||
chr1:95066247
|
G | C | 21 | a0001c0001t0008g0098a0001c0001t0008g0099a0001c0001t0008g0100others(18): Show | 21 | HG01069.hp2 HG01099.hp2 HG01496.hp1 others(18): Show |
intron_variant | MODIFIER | c.137-1230C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95066247 | ||||||
chr1:95066292
|
C | T | 7 | a0001c0001t0012g0092a0001c0001t0012g0093a0001c0001t0012g0094others(4): Show | 7 | HG01069.hp2 HG01099.hp2 HG01496.hp1 others(4): Show |
intron_variant | MODIFIER | c.137-1275G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95066292 | ||||||
chr1:95066327
|
G | A | 1 | a0001c0001t0003g0152 | 1 | NA18970.hp1 | intron_variant | MODIFIER | c.137-1310C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95066327 | ||||||
chr1:95066330
|
T | C | 89 | a0001c0001t0001g0194a0001c0001t0002g0213a0001c0001t0002g0218others(86): Show | 89 | HG00323.hp2 HG00423.hp1 HG00438.hp1 others(86): Show |
intron_variant | MODIFIER | c.137-1313A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95066330 | ||||||
chr1:95066338
|
C | A | 1 | a0001c0001t0001g0356 | 1 | HG02698.hp1 | intron_variant | MODIFIER | c.137-1321G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95066338 | ||||||
chr1:95066528
|
T | A | 3 | a0001c0001t0001g0357a0001c0001t0001g0358a0001c0001t0001g0359 | 3 | NA18941.hp1 NA18955.hp2 NA18980.hp2 |
intron_variant | MODIFIER | c.137-1511A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95066528 | ||||||
chr1:95066589
|
A | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.137-1572T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95066589 | ||||||
chr1:95066618
|
T | A | 81 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(78): Show | 82 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(79): Show |
intron_variant | MODIFIER | c.137-1601A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95066618 | ||||||
chr1:95066653
|
C | T | 2 | a0001c0001t0095g0091a0001c0001t0158g0090 | 2 | HG02818.hp1 HG03225.hp1 |
intron_variant | MODIFIER | c.137-1636G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95066653 | ||||||
chr1:95066802
|
G | A | 26 | a0001c0001t0004g0004a0001c0001t0004g0111a0001c0001t0004g0153others(23): Show | 26 | HG00597.hp2 HG00673.hp1 HG01123.hp1 others(23): Show |
intron_variant | MODIFIER | c.137-1785C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95066802 | ||||||
chr1:95066868
|
A | C | 1 | a0001c0001t0137g0180 | 1 | HG02155.hp2 | intron_variant | MODIFIER | c.137-1851T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95066868 | ||||||
chr1:95066948
|
C | T | 1 | a0001c0001t0014g0033 | 1 | HG01255.hp2 | intron_variant | MODIFIER | c.137-1931G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95066948 | ||||||
chr1:95067034
|
A | T | 3 | a0001c0001t0001g0115a0001c0001t0196g0114a0001c0001t0197g0116 | 3 | HG02451.hp1 HG02896.hp2 NA18522.hp2 |
intron_variant | MODIFIER | c.137-2017T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95067034 | ||||||
chr1:95067116
|
A | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.137-2099T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95067116 | ||||||
chr1:95067181
|
T | C | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.137-2164A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95067181 | ||||||
chr1:95067238
|
T | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.137-2221A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95067238 | ||||||
chr1:95067272
|
C | A | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.137-2255G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95067272 | ||||||
chr1:95067458
|
A | T | 1 | a0001c0001t0195g0113 | 1 | HG02717.hp2 | intron_variant | MODIFIER | c.137-2441T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95067458 | ||||||
chr1:95067570
|
T | G | 3 | a0001c0001t0001g0278a0001c0001t0009g0279a0001c0001t0043g0277 | 3 | HG01891.hp1 HG02965.hp2 HG03098.hp1 |
intron_variant | MODIFIER | c.137-2553A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95067570 | ||||||
chr1:95067576
|
T | TAA | 219 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0282others(216): Show | 220 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(217): Show |
intron_variant | MODIFIER | c.137-2560_137-2559i others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95067576 | ||||||
chr1:95067789
|
T | A | 3 | a0001c0001t0014g0013a0001c0001t0014g0014a0001c0001t0075g0012 | 3 | HG02258.hp1 HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.137-2772A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95067789 | ||||||
chr1:95067910
|
G | A | 91 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0282others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.137-2893C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95067910 | ||||||
chr1:95068090
|
C | T | 2 | a0001c0001t0004g0111a0001c0001t0104g0112 | 2 | HG01169.hp2 HG03669.hp2 |
intron_variant | MODIFIER | c.137-3073G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95068090 | ||||||
chr1:95068171
|
T | C | 3 | a0001c0001t0028g0175a0001c0001t0028g0176a0001c0001t0058g0177 | 3 | HG02055.hp2 HG02109.hp1 HG03579.hp2 |
intron_variant | MODIFIER | c.137-3154A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95068171 | ||||||
chr1:95068205
|
T | A | 5 | a0001c0001t0001g0362a0001c0001t0009g0364a0001c0001t0150g0360others(2): Show | 5 | HG00438.hp2 NA18939.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.137-3188A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95068205 | ||||||
chr1:95068206
|
T | A | 5 | a0001c0001t0001g0362a0001c0001t0009g0364a0001c0001t0150g0360others(2): Show | 5 | HG00438.hp2 NA18939.hp1 NA18987.hp2 others(2): Show |
intron_variant | MODIFIER | c.137-3189A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95068206 | ||||||
chr1:95068342
|
C | G | 1 | a0001c0001t0001g0282 | 1 | HG02165.hp1 | intron_variant | MODIFIER | c.137-3325G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95068342 | ||||||
chr1:95068348
|
G | A | 1 | a0001c0001t0003g0178 | 1 | NA18747.hp2 | intron_variant | MODIFIER | c.137-3331C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95068348 | ||||||
chr1:95068363
|
G | T | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.137-3346C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95068363 | ||||||
chr1:95068390
|
G | A | 1 | a0001c0001t0001g0365 | 1 | HG03927.hp1 | intron_variant | MODIFIER | c.137-3373C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95068390 | ||||||
chr1:95068438
|
G | A | 16 | a0001c0001t0023g0029a0001c0001t0023g0030a0001c0001t0025g0026others(13): Show | 16 | HG00735.hp1 HG02145.hp1 HG02572.hp1 others(13): Show |
intron_variant | MODIFIER | c.137-3421C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95068438 | ||||||
chr1:95068628
|
G | A | 85 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(82): Show | 86 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(83): Show |
intron_variant | MODIFIER | c.137-3611C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95068628 | ||||||
chr1:95069147
|
T | A | 1 | a0001c0001t0005g0264 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.136+3616A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95069147 | ||||||
chr1:95069148
|
C | A | 1 | a0001c0001t0005g0264 | 1 | NA18961.hp1 | intron_variant | MODIFIER | c.136+3615G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95069148 | ||||||
chr1:95069161
|
A | G | 1 | a0001c0001t0174g0078 | 1 | HG02273.hp1 | intron_variant | MODIFIER | c.136+3602T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95069161 | ||||||
chr1:95069351
|
A | G | 1 | a0001c0002t0108g0179 | 1 | NA19000.hp1 | intron_variant | MODIFIER | c.136+3412T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95069351 | ||||||
chr1:95069588
|
T | TAG | 65 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(62): Show | 66 | HG00639.hp1 HG01081.hp2 HG01243.hp2 others(63): Show |
intron_variant | MODIFIER | c.136+3173_136+3174d others(4): Show |
ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95069588 | ||||||
chr1:95069711
|
A | T | 19 | a0001c0001t0017g0378a0001c0001t0017g0380a0001c0001t0017g0381others(16): Show | 19 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(16): Show |
intron_variant | MODIFIER | c.136+3052T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95069711 | ||||||
chr1:95069723
|
C | A | 2 | a0001c0001t0020g0076a0001c0001t0020g0077 | 2 | NA18522.hp1 NA19043.hp2 |
intron_variant | MODIFIER | c.136+3040G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95069723 | ||||||
chr1:95069848
|
A | G | 16 | a0001c0001t0017g0378a0001c0001t0017g0380a0001c0001t0017g0381others(13): Show | 16 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.136+2915T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95069848 | ||||||
chr1:95069877
|
A | T | 1 | a0001c0001t0132g0265 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.136+2886T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95069877 | ||||||
chr1:95069878
|
C | G | 1 | a0001c0001t0132g0265 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.136+2885G>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95069878 | ||||||
chr1:95069879
|
C | T | 1 | a0001c0001t0132g0265 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.136+2884G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95069879 | ||||||
chr1:95069880
|
T | G | 1 | a0001c0001t0132g0265 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.136+2883A>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95069880 | ||||||
chr1:95069882
|
T | A | 1 | a0001c0001t0132g0265 | 1 | HG01258.hp2 | intron_variant | MODIFIER | c.136+2881A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95069882 | ||||||
chr1:95069890
|
A | C | 91 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0282others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.136+2873T>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95069890 | ||||||
chr1:95070011
|
C | T | 2 | a0001c0001t0011g0280a0001c0001t0090g0281 | 2 | NA18961.hp2 NA18962.hp2 |
intron_variant | MODIFIER | c.136+2752G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95070011 | ||||||
chr1:95070090
|
G | A | 1 | a0001c0001t0145g0266 | 1 | HG03486.hp2 | intron_variant | MODIFIER | c.136+2673C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95070090 | ||||||
chr1:95070115
|
G | C | 16 | a0001c0001t0017g0378a0001c0001t0017g0380a0001c0001t0017g0381others(13): Show | 16 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.136+2648C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95070115 | ||||||
chr1:95070316
|
C | A | 10 | a0001c0001t0015g0080a0001c0001t0015g0085a0001c0001t0022g0082others(7): Show | 10 | HG01081.hp2 HG01346.hp2 HG01928.hp1 others(7): Show |
intron_variant | MODIFIER | c.136+2447G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95070316 | ||||||
chr1:95070461
|
G | C | 2 | a0001c0001t0005g0268a0001c0001t0016g0267 | 2 | HG06807.hp1 NA21309.hp2 |
intron_variant | MODIFIER | c.136+2302C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95070461 | ||||||
chr1:95070475
|
G | C | 1 | a0001c0001t0005g0269 | 1 | NA20752.hp2 | intron_variant | MODIFIER | c.136+2288C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95070475 | ||||||
chr1:95070509
|
C | T | 3 | a0001c0001t0014g0013a0001c0001t0014g0014a0001c0001t0075g0012 | 3 | HG02258.hp1 HG02486.hp1 HG03540.hp2 |
intron_variant | MODIFIER | c.136+2254G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95070509 | ||||||
chr1:95070524
|
G | C | 308 | a0001c0001t0001g0194a0001c0001t0001g0276a0001c0001t0001g0278others(305): Show | 309 | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(306): Show |
intron_variant | MODIFIER | c.136+2239C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95070524 | ||||||
chr1:95070611
|
C | T | 4 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0009g0279others(1): Show | 4 | HG01891.hp1 HG02886.hp1 HG02965.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+2152G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95070611 | ||||||
chr1:95070651
|
C | A | 1 | a0001c0001t0003g0270 | 1 | NA18999.hp1 | intron_variant | MODIFIER | c.136+2112G>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95070651 | ||||||
chr1:95070928
|
A | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.136+1835T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95070928 | ||||||
chr1:95070984
|
G | A | 2 | a0001c0001t0014g0088a0001c0001t0111g0087 | 2 | NA18964.hp2 NA19068.hp2 |
intron_variant | MODIFIER | c.136+1779C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95070984 | ||||||
chr1:95070993
|
G | A | 1 | a0001c0001t0078g0089 | 1 | HG02451.hp2 | intron_variant | MODIFIER | c.136+1770C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95070993 | ||||||
chr1:95071034
|
C | T | 1 | a0001c0001t0065g0110 | 1 | HG00673.hp1 | intron_variant | MODIFIER | c.136+1729G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95071034 | ||||||
chr1:95071067
|
A | T | 112 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0282others(109): Show | 112 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(109): Show |
intron_variant | MODIFIER | c.136+1696T>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95071067 | ||||||
chr1:95071077
|
G | C | 4 | a0001c0001t0030g0273a0001c0001t0030g0274a0001c0001t0059g0272others(1): Show | 4 | HG02109.hp2 HG02886.hp2 HG02895.hp2 others(1): Show |
intron_variant | MODIFIER | c.136+1686C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95071077 | ||||||
chr1:95071159
|
A | G | 99 | a0001c0001t0006g0001a0001c0001t0006g0035a0001c0001t0006g0038others(96): Show | 100 | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(97): Show |
intron_variant | MODIFIER | c.136+1604T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95071159 | ||||||
chr1:95071425
|
TC | T | 5 | a0001c0001t0037g0009a0001c0001t0038g0007a0001c0001t0038g0011others(2): Show | 5 | HG02258.hp2 HG02622.hp2 HG02895.hp1 others(2): Show |
intron_variant | MODIFIER | c.136+1337delG | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95071425 | ||||||
chr1:95071436
|
C | T | 16 | a0001c0001t0017g0378a0001c0001t0017g0380a0001c0001t0017g0381others(13): Show | 16 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.136+1327G>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95071436 | ||||||
chr1:95071500
|
G | A | 1 | a0001c0001t0002g0275 | 1 | HG02040.hp2 | intron_variant | MODIFIER | c.136+1263C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95071500 | ||||||
chr1:95071584
|
G | T | 1 | a0001c0001t0048g0006 | 1 | NA18966.hp1 | intron_variant | MODIFIER | c.136+1179C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95071584 | ||||||
chr1:95071887
|
G | T | 1 | a0001c0001t0133g0005 | 1 | HG02055.hp1 | intron_variant | MODIFIER | c.136+876C>A | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95071887 | ||||||
chr1:95072236
|
G | A | 91 | a0001c0001t0001g0276a0001c0001t0001g0278a0001c0001t0001g0282others(88): Show | 91 | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(88): Show |
intron_variant | MODIFIER | c.136+527C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95072236 | ||||||
chr1:95072391
|
G | A | 1 | a0001c0001t0069g0366 | 1 | NA20805.hp1 | intron_variant | MODIFIER | c.136+372C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95072391 | ||||||
chr1:95072402
|
T | A | 16 | a0001c0001t0017g0378a0001c0001t0017g0380a0001c0001t0017g0381others(13): Show | 16 | HG00099.hp1 HG00140.hp1 HG00642.hp2 others(13): Show |
intron_variant | MODIFIER | c.136+361A>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95072402 | ||||||
chr1:95072467
|
T | C | 1 | a0001c0001t0198g0383 | 1 | HG03516.hp2 | intron_variant | MODIFIER | c.136+296A>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95072467 | ||||||
chr1:95072529
|
A | G | 1 | a0001c0001t0004g0004 | 1 | NA20905.hp2 | intron_variant | MODIFIER | c.136+234T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95072529 | ||||||
chr1:95072627
|
G | A | 2 | a0001c0001t0025g0384a0001c0001t0025g0385 | 2 | HG03490.hp2 HG03492.hp1 |
intron_variant | MODIFIER | c.136+136C>T | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95072627 | ||||||
chr1:95072658
|
G | C | 1 | a0001c0001t0096g0386 | 1 | HG03139.hp1 | intron_variant | MODIFIER | c.136+105C>G | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95072658 | ||||||
chr1:95072692
|
A | G | 1 | a0001c0001t0068g0003 | 1 | HG04199.hp1 | intron_variant | MODIFIER | c.136+71T>C | ALG14 | ENSG00000172339.10 | transcript | ENST00000370205.6 | protein_coding | 1/3 | chr1 | 95072692 |